Refining Processes

Refining
Processes
2002
www.HydrocarbonProcessing.com
Refining 2002
Processes
Process Index
Alkylation . . . . . . . . . . . . . . . 86, 88, 89, 90
Alkylationfeed preparation . . . . . . . . 90
Aromatics extraction . . . . . . . . . . . . . . . 91
Aromatics extractive distillation . . . . . . 91
Aromatics recovery . . . . . . . . . . . . . . . . 92
Benzene reduction . . . . . . . . . . . . . . . . . 92
Catalytic cracking . . . . . . . . . . . . . . . . . . 94
Catalytic dewaxing . . . . . . . . . . . . . . 94, 95
Catalytic reforming . . . . . . . . . . . . . 95, 96
Catalytic SOx removal . . . . . . . . . . . . . . . 97
Coking . . . . . . . . . . . . . . . . . . . . . . . . 97, 98
Crude distillation . . . . . . . . . . . . . . 99, 100
Dearomatization
middle distillate . . . . . . . . . . . . . . . 100
Deasphalting . . . . . . . . . . . . . . . . . . . . 101
Deep catalytic cracking . . . . . . . . . . . . 102
Deep thermal conversion . . . . . . . . . . 102
Desulfurization . . . . . . . . . . . . . . . . . . . 103
Dewaxing/wax deoiling . . . . . . . . . . . . 104
Diesel desulfurization . . . . . . . . . . . . . 104
Diesel hydrotreatment . . . . . . . . . . . . . 105
Electrical desalting . . . . . . . . . . . . . . . . 105
Ethers . . . . . . . . . . . . . . . . . . . . . . . . . . 106
Ethers-MTBE . . . . . . . . . . . . . . . . . . . . . 108
Fluid catalytic
cracking . . . . . . . . . . 108, 110, 111, 112
Gas treatingH2S removal . . . . . . . . . 112
Gasification . . . . . . . . . . . . . . . . . . . . . . 113
Gasoline desulfurization . . . . . . . . . . . 113

Gasoline desulfurization,
ultra-deep . . . . . . . . . . . . . . . . . . . . 114
H2S and SWS gas conversion . . . . . . . . 114
Hydrocracking . . . . . . . . . . . 115, 116, 117
Hydrocracking, residue . . . . . . . . . . . . 118
Hydrocracking/
hydrotreatingVGO . . . . . . . . . . . 118
Hydrocracking (mild)/
VGO hydrotreating . . . . . . . . . . . . . 119
Hydrodearomatization . . . . . . . . . . . . 119
Hydrodesulfurization . . . . . . . . . . 120, 121
Hydrodesulfurization,
ultra-low-sulfur diesel . . . . . . . . . . 121
Hydrodesulfurization
pretreatment . . . . . . . . . . . . . . . . . 122
HydrodesulfurizationUDHDS . . . . . . 122
Hydrofinishing/hydrotreating . . . . . . . 123
Hydrogen . . . . . . . . . . . . . . . . . . . . . . . 123
Hydrogenation . . . . . . . . . . . . . . . . . . . 124
Hydrotreating . . . . 124, 125, 126, 127, 128
Hydrotreatingaromatic
saturation . . . . . . . . . . . . . . . . . . . . 128
Hydrotreatingcatalytic
dewaxing . . . . . . . . . . . . . . . . . . . . . 129
Hydrotreatingresid . . . . . . . . . . . . . . 129
Isomerization . . . . . . . . . . . . 130, 131, 132
Isooctane /isooctene . . . . . . . . . . . 132, 133
Isooctene /Isooctane/ETBE . . . . . . . . . 133

Low-temperature NOx reduction . . . . 134
LPG recovery . . . . . . . . . . . . . . . . . . . . . 134
Lube hydroprocessing . . . . . . . . . . . . . 135
Lube treating . . . . . . . . . . . . 135, 136, 137
NOx abatement . . . . . . . . . . . . . . . . . . 137
Olefins . . . . . . . . . . . . . . . . . . . . . . . . . . 138
Olefins recovery . . . . . . . . . . . . . . . . . . 139
Oligomerization of C3C4 cuts . . . . . . . . 139
Oligomerizationpolynaphtha . . . . . 140
Prereforming with feed
ultrapurification . . . . . . . . . . . . . . . 140
Resid catalytic cracking . . . . . . . . . . . . 142
Residue hydroprocessing . . . . . . . . . . . 142
SO2 removal . . . . . . . . . . . . . . . . . . . . . 143
Sour gas treatment . . . . . . . . . . . . . . . 143
Spent acid recovery . . . . . . . . . . . . . . . 144
Sulfur degassing . . . . . . . . . . . . . . . . . . 144
Thermal gasoil process . . . . . . . . . . . . . 145
Treating . . . . . . . . . . . . . . . . . . . . . . . . 145
Vacuum distillation . . . . . . . . . . . . . . . 146
Visbreaking . . . . . . . . . . . . . . . . . . 146, 147
Wet scrubbing system . . . . . . . . . . . . . 147
Wet-chemistry NOx reduction . . . . . . . 148
White oil and wax
hydrotreating . . . . . . . . . . . . . . . . . 148
Licensor Index
ABB Lummus Global Inc. . . . . . . . . .86, 97,
108, 127, 128, 130
ABB Lummus Global B.V. . . .102, 145, 146
Aker Kvaerner . . . . . . . . . . . . . . . . . . . 133
Akzo Nobel Catalysts B.V. . . . .86, 122, 129
Axens . . . . . . . . . . . . . . . . . . . . . 90, 92, 95,
105, 106, 111, 114, 115,
118, 129, 130, 139, 140, 142
Axens NA . . . . . . . . . . . . . . . . . . 90, 92, 95,
105, 106, 114, 115, 118,
129, 130, 139, 140
BARCO . . . . . . . . . . . . . . . . . . . . . . . . . . 94
BASF . . . . . . . . . . . . . . . . . . . . . . . . . . . 148
Bechtel Corp. . . . . . . . . . . . . . 98, 104, 135
Belco Technologies
Corp. . . . . . . . . . . . . 134, 143, 147, 148
Black & Veatch Pritchard, Inc. . . . 134, 144
BOC Group, Inc. . . . . . . . . . . . . . . . . . . 134
Cansolv Technologies Inc. . . . . . . . . . . 148
CDTECH . . . . . . . . . 106, 124, 131, 133, 146
Chevron Lummus Global LLC . . . . 115, 116
Chicago Bridge & Iron Co. . . . 96, 105, 125
Conoco Inc. . . . . . . . . . . . . . . . . . . . . . . . 98
ConocoPhillips Co., Fuels Technology

Division . . . . . . . . . . . 88, 104, 113, 131
Criterion Catalyst and
Technologies Co. . . . . . . . . . . . 127, 128
Davy Process Technology . . . . . . . . . . . 140
Engelhard Corp. . . . . . . . . . . . . . . . . . . 100
ExxonMobil Research & Engineering
Co. . . . . 86, 94, 110, 112, 120, 136, 137
Fina Research S.A. . . . . . . . . . . . . . . . . 129
Fortum Oil and Gas OY . . . . . . . . . 86, 132
Foster Wheeler . . . . . 98, 99, 101, 123, 147
GTC Technology Inc. . . . . . . . . . . . . 92, 103
Haldor Topse A/S . . . . . . . . . . . 88, 95, 97,
114, 119, 121, 125, 143, 144
Howe-Baker Engineers, Ltd. . 96, 105, 125
IFP Group Technologies . . . . . . . . 111, 142
JGC . . . . . . . . . . . . . . . . . . . . . . . . . . . . 126
Kellogg Brown & Root, Inc. . 101, 110, 132
Linde BOC Process Plants, LLC . . 126, 139
Lyondell Chemical Co. . . . . . . . . . 131, 133
Merichem Chemicals & Refinery
Services LLC . . . . . . . . . . . . . . . . . . . 145
Process Dynamics . . . . . . . . . . . . . . . . . 126
PDVSA-INTEVEP . . . . . . . . . . . . . . . . . . .121
Research Institute of Petroleum
Processing . . . . . . . . . . . . . . . . . . . . 102
Shell Global Solutions
International B.V. . . . . . . . 99, 102, 111,
113, 116, 127, 128,
135, 142, 145, 146
SK Corp . . . . . . . . . . . . . . . . . . . . . 122, 137
Snamprogetti SpA . . . . . . . . . . . . 106, 133
Stone & Webster Inc. . . . . . . 102, 111, 142
Stratco, Inc. . . . . . . . . . . . . . . . . . . . . . . . 89
Synetix . . . . . . . . . . . . . . . . . . . . . . . . . .140
Technip-Coflexip . . . . . . . . . . . . . . . . . 100
TOTAL FINA ELF . . . . . . . . . . . . . . . . . . 100
Udhe Edeleanu GmbH . . . . 108, 123, 136,
146, 148
Udhe GmbH . . . . . . . . . . . . . . . . . . 91, 138
UniPure Corp. . . . . . . . . . . . . . . . . . . . . 103
UOP LLC . . . . . . . . . . . . . . . . . . . 89, 90, 94,
96, 98, 101, 112, 117,
121, 127, 128, 132, 147
VEBA OEL GmbH . . . . . . . . . . . . . . . . . 117
Washington Group
International . . . . . . . . . . 100, 122, 137
HYDROCARBON PROCESSING NOVEMBER 2002
I 85
Refining Processes 2002

Propane product
Isobutane
Reactor
system
(1)
Olefin feed
Hydrogen
Product
distillation
(3)
Recycle
isobutane
Refrigerant
Butane
product
n-Butane
Alkylate
product
Hydrogen
Isobutane feed
Catalyst
regeneration
(2)
4
5
Olefin
feed
START
Recycle acid
Makeup
isobutane
Alkylate
product
Alkylation
Alkylation
Application: The AlkyClean process converts light olefins into alkylate by reacting the olefins with isobutane over a true solid acid catalyst.
AlkyCleans unique catalyst, reactor design and process scheme allows operation at low external isobutene to olefin ratios while maintaining excellent product quality.
Application: Combines propylene, butylene and pentylene with

isobutane, in the presence of sulfuric acid catalyst, to form a high-octane,
mogas component.
Products: A highly isoparaffinic, low Rvp, high-octane gasoline blendstock is produced from the alkylation process.
Description: Olefin feed and recycled isobutane are introduced into
the stirred, autorefrigerated reactor (1). Mixers provide intimate contact
between the reactants and the acid catalyst. Reaction heat is removed from
the reactor by the highly efficient autorefrigeration method. The hydrocarbons that are vaporized from the reactor, and that provide cooling to
the 40F level, are routed to the refrigeration compressor (2) where they
are compressed, condensed and returned to the reactor. A depropanizer
(3), which is fed by a slipstream from the refrigeration section, is designed
to remove any propane introduced to the plant with the feeds. The reactor product is sent to the settler (4), where the hydrocarbons are separated
from the acid that is recycled. The hydrocarbons are then sent to the
deisobutanizer (5) along with makeup isobutane. The isobutane-rich overhead is recycled to the reactor. The bottoms are then sent to a debutanizer
(6) to produce a low Rvp alkylate product with an FBP less than 400F.
Major features of the reactor are:
Use of the autorefrigeration method of cooling is thermodynamically efficient. It also allows lower temperatures, which are favorable for producing high product quality with low power requirements.
Use of a staged reactor system results in a high average isobutane concentration, which favors high product quality.
Use of low space velocity in the reactor design results in high product quality and eliminates any corrosion problems in the fractionation
section associated with the formation of esters.
Use of low reactor operating pressure means high reliability for the
mechanical seals for the mixers.
Use of simple reactor internals translates to low cost.
Yields:
Products: Alkylate is a high-octane, low-Rvp gasoline component

used for blending in all grades of gasoline.
Description: The light olefin feed is combined with the isobutene
make-up and recycle and sent to the alkylation reactors which convert the
olefins into alkylate using a solid acid catalyst (1). The AlkyClean process uses a true solid acid catalyst to produce alkylate eliminating the safety
and environmental hazards associated with liquid acid technologies.
Simultaneously, reactors are undergoing a mild liquid-phase regeneration
using isobutene and hydrogen and, periodically, a reactor undergoes a
higher temperature vapor phase hydrogen strip (2). The reactor and
mild regeneration effluent is sent to the product-fractionation section,
which produces propane, n-butane and alkylate, while also recycling
isobutene and recovering hydrogen used in regeneration for reuse in
other refinery hydroprocessing units (3). AlkyClean does not produce any
acid soluble oils (ASO) or require post treatment of the reactor effluent
or final products.
Product: The C 5+ alkylate has a RON of 9398 depending on processing conditions and feed composition.
Economics:
Investment (basis 10,000 -bpsd Unit) $/bpsd
Operating cost, $/gal
3,100
0.47
Installation: Demonstration unit at Fortums Porvoo, Finland Refinery.

Reference: The Process: A new solid acid catalyst gasoline alkylation
technology, NPRA 2002 Annual Meeting, March 1719, 2002.
Licensor: ABB Lummus Global Inc., Akzo Nobel Catalysts and Fortum Oil and Gas.
Alkylate yield
Isobutane (pure) required
Alkylate quality
1.78 bbl C5+/bbl butylene feed

1.17 bbl/bbl butylene feed
96 RON/94 MON
Economics:
Utilities, typical per barrel of alkylate produced:
Water, cooling (20F rise), 1,000 gal
2.1
Power, kWh
10.5
Steam, 60 psig, lb
200
19
H2SO4, lb
NaOH, 100%, lb
0.1
Installation: 115,000-bpd capacity at 11 locations with the sizes

ranging from 2,000 to 30,000 bpd. Single reactor/settle trains with
capacities up to 9,500 bpsd.
Reference: Lerner, H., Exxon sulfuric acid alkylation technology,
Handbook of Petroleum Refining Processes, 2nd ed., R. A. Meyers, Ed., pp.
1.31.14.
Licensor: ExxonMobil Research & Engineering Co.
Circle 275 on Reader Service Card
86
Isobutane recycle
Propane
Isobutane
Isobutane recycle
n-Butane
Propane
Olefin feed
Olefin feed
START
2
Motor fuel butane
Alkylate
Isobutane
Alkylate
START
Alkylation
Alkylation
Application: The Topse fixed-bed alkylation (FBA) technology

applies a unique fixed-bed reactor system with a liquid superacid catalyst
absorbed on a solid support. FBA converts isobutane with propylene, butylene and amylenes to produce branched chain hydrocarbons. As an alternative, FBA can conveniently be used to alkylate isopentane as a means
of disposing isopentane for RVP control purpose.
Application: Convert propylene, amylenes, butylenes and isobutane

to the highest quality motor fuel using ReVAP alkylation.
Products: A high-octane, low-RVP and ultra-low-sulfur blending

stock for motor and aviation gasoline.
Description: The FBA process combines the benefits of a liquid catalyst with the advantages of a fixed-bed reactor system. Olefin and isobutane feedstocks are mixed with a recycle stream of isobutane and charged
to the reactor section (1). The olefins are fully converted over a supportedliquid-phase catalyst confined within a mobile, well-defined catalyst
zone. The simple fixed-bed reactor system allows easy monitoring and
maintenance of the catalyst zone with no handling of solids.
Traces of dissolved acid in the net reactor effluent are removed quantitatively in a compact and simple-to-operate effluent treatment unit (2).
In the fractionation section (3), the acid-free net reactor effluent is split into
propane, isobutane, n-butane and alkylate. The unique reactor concept
allows an easy and selective withdrawal of small amounts of passivated
acid. The acid catalyst is fully recovered in a compact catalyst activity
maintenance unit (4). The integrated, inexpensive, on-site catalyst activity maintenance is a distinct feature of the FBA process. Other significant features of FBA include:
High flexibility (feedstock, operation temperature)
Low operating costs
Low catalyst consumption.
Process performance:
Olefin feed type
C3C5 cut
MTBE raffinate FCC C4 cut
Alkylate product
98
95
93
RON (C 5+)
95
92
91
MON (C 5+)
Economics: (Basis: MTBE raffinate, inclusive feed pretreatment and

on-site catalyst activity maintenance)
Investment (basis: 6,000 bpsd unit), $ per bpsd
Utilities, typical per bbl alkylate:
Electricity, kWh
Steam, MP (150 psig), lb
Steam, LP (50 psig), lb
Water, cooling (20F rise), gal103
Licensor: Haldor Topse A/S.
5,600
10
60
200
2.2
Products: An ultra-low-sulfur, high-octane and low-Rvp blending

stock for motor and aviation fuels.
Description: Dry liquid feed containing olefins and isobutane is charged
to a combined reactor-settler (1). The reactor uses the principle of differential gravity head to effect catalyst circulation through a cooler prior to contacting highly dispersed hydrocarbon in the reactor pipe. The hydrocarbon
phase that is produced in the settler is fed to the main fractionator (2), which
separates LPG-quality propane, isobutane recycle, n-butane and alkylate products. Small amount of dissolved catalyst is removed from the propane product by a small stripper tower (3). Major process features are:
Gravity catalyst circulation (no catalyst circulation pumps required)
Low catalyst consumption
Low operating cost
Superior alkylate qualities from propylene, isobutylene and amylene feedstocks
Onsite catalyst regeneration
Environmentally responsible (very low emissions/waste)
Between 60% and 90% reduction in airborne catalyst release over
traditional catalysts
Can be installed in all licensors HF alkylation units.
With the proposed reduction of MTBE in gasoline, ReVAP offers
significant advantages over sending the isobutylene to a sulfuric-acidalkylation unit or a dimerization plant. ReVAP alkylation produces higher
octane, lower RVP and endpoint product than a sulfuric-acid-alkylation
unit and nearly twice as many octane barrels as can be produced from a
dimerization unit.
Yields:
Feed type
PropyleneButylene
butylene mix
Composition (lv%)
Propylene
Propane
Butylene
i-Butane
n-Butane
i-Pentane
Alkylate product
Gravity, API
RVP, psi
ASTM 10%, F
ASTM 90%, F
RONC
Per bbl olefin converted
i-Butane consumed, bbl
Alkylate produced, bbl
0.8
1.5
47.0
33.8
14.7
2.2
24.6
12.5
30.3
21.8
9.5
1.3
70.1
67
185
236
96.0
71.1
67
170
253
93.5
1.139
1.780
1.175
1.755
Installation: 107 alkylation units licensed worldwide.

Licensor: Fuels Technology Division of ConocoPhillips Co.
88

Propane
product
Light ends
LPG
3
6
n-Butane
product
i-C4/H2
2
Alkylate
product
Olefin feed
Olefin feed
Alkylate
i-C4/H2
START
i-Butane
Isobutane recycle
START
Alkylation
Alkylation
Application: To combine propylene, butylenes and amylenes with

isobutane in the presence of strong sulfuric acid to produce high-octane
branched chain hydrocarbons using the Effluent Refrigeration Alkylation
process.
Application: The Alkylene process uses a solid catalyst to react isobutane with light olefins (C3 to C5) to produce a branched-chain paraffinic
fuel. The performance characteristics of this catalyst and novel process
design have yielded a technology that is competitive with traditional liquid-acid-alkylation processes. Unlike liquid-acid-catalyzed technologies,
significant opportunities to continually advance the catalytic activity
and selectivity of this exciting new technology are possible. This process
meets todays demand for both improved gasoline formulations and a more
environmentally friendly light olefin upgrading technology.
Products: Branched chain hydrocarbons for use in high-octane motor

fuel and aviation gasoline.
Description: Plants are designed to process a mixture of propylene,
butylenes and amylenes. Olefins and isobutane-rich streams along with
a recycle stream of H2SO4 are charged to the STRATCO Contactor reactor (1). The liquid contents of the Contactor reactor are circulated at high
velocities and an extremely large amount of interfacial area is exposed
between the reacting hydrocarbons and the acid catalyst from the acid settler (2). The entire volume of the liquid in the Contactor reactor is
maintained at a uniform temperature, less than 1F between any two points
within the reaction mass. Contractor reactor products pass through a flash
drum (3) and deisobutanizer (4). The refrigeration section consists of a
compressor (5) and depropanizer (6).
The overhead from the deisobutanizer (4) and effluent refrigerant
recycle (6) constitutes the total isobutane recycle to the reaction zone.
This total quantity of isobutane and all other hydrocarbons is maintained
in the liquid phase throughout the Contactor reactor, thereby serving to
promote the alkylation reaction. Onsite acid regeneration technology is
also available.
Product quality: The total debutanized alkylate has RON of 92 to
96 clear and MON of 90 to 94 clear. When processing straight butylenes,
the debutanized total alkylate has RON as high as 98 clear. Endpoint of
the total alkylate from straight butylene feeds is less than 390F, and less
than 420F for mixed feeds containing amylenes in most cases.
Economics (basis: butylene feed):
Investment (basis: 10,000-bpsd unit), $ per bpsd 3,500
Utilities, typical per bbl alkylate:
Electricity, kWh
13.5
Steam, 150 psig, lb
180
1.85
Water, cooling (20 oF rise), 10 3 gal
Acid, lb
15
Caustic, lb
0.1
Installation: Nearly 600,000 bpsd installed capacity.
Description: Olefin charge is first treated to remove impurities such

as diolefins and oxygenates (1). The olefin feed and isobutane recycle are
mixed with reactivated catalyst at the bottom of the reactor vessel riser
(2). The reactants and catalyst flow up the riser in a cocurrent manner
where the alkylation reaction occurs. Upon exiting the riser, the catalyst
separates easily from the hydrocarbon effluent liquid by gravity and
flows downward into the cold reactivation zone of the reactor. The
hydrocarbon effluent flows to the fractionation section (3), where the alkylate product is separated from the LPG product. There is no acid soluble oil (ASO) or heavy polymer to dispose of as with liquid acid technology.
The catalyst flows slowly down the annulus section of the reactor
around the riser as a packed bed. Isobutane saturated with hydrogen is
injected to reactivate the catalyst. The reactivated catalyst then flows
through standpipes back into the bottom of the riser. The reactivation
in this section is nearly complete, but some strongly adsorbed material
remains on the catalyst surface. This is removed by processing a small
portion of the circulating catalyst in the reactivation vessel (4), where the
temperature is elevated for complete reactivation. The reactivated catalyst
then flows back to the bottom of the riser.
Product quality: Alkylate has ideal gasoline properties such as: high
research and motor octane numbers, low Reid vapor pressure (Rvp), and
no aromatics, olefins or sulfur. The alkylate from an Alkylene unit has
the particular advantage of lower 50% and 90% distillation temperatures,
which is important for new reformulated gasoline specifications.
Economics: (basis: FCC source C4 olefin feed)
Investment (basis: 6,000-bpsd unit), $ per bpsd

Operating cost ($/gal)
6,100
0.45
Licensor: UOP LLC.
Reference: Hydrocarbon Processing, Vol. 64, No. 9, September 1985,

pp. 6771.
Licensor: Stratco, Inc.

I 89

Polymerization Debutanizer
reactors
column
Olefin
feed
Saturation
reactor
Product
stripper
Offgas
Reactor
Raffinate
1
2
Stripper
Fuel gas
5
Hydrogen
Hydroisomerized
C4s to alkylation
C4 feed
Alkylate
Makeup hydrogen
Alkylation
Alkylationfeed preparation
Application: The UOP Indirect Alkylation (InAlk) process uses solid

catalysts to react isobutylene with light olefins (C3 to C5) to produce a
high-octane, low-vapor pressure, paraffinic gasoline component similar
in quality to traditional motor alkylate.
Application: Upgrades alkylation plant feeds with Alkyfining process.
Description: The InAlk process combines two, commercially proven

technologies: polymerization and olefin saturation. Isobutylene is reacted
with light olefins (C3 to C5 ) in the polymerization reactor (1), the resulting mixture is stabilized (2) and the isooctane-rich stream is saturated in
the saturation reactor (3). Recycle hydrogen is removed (4) and the
product is stripped (5) to remove light-ends.
The InAlk process is more flexible than the traditional alkylation processes. Using a direct alkylation process, refiners must match the isobutane
requirement with olefin availability. The InAlk process does not require
isobutane to produce a high-quality product. Additional flexibility comes
from being able to revamp existing catalytic condensation and MTBE
units easily to the InAlk process.
The flexibility of the InAlk process is in both the polymerization and
saturation sections. Both sections have different catalyst options based
on specific operating objectives and site conditions. This flexibility allows
existing catalytic condensation units to revamp to the InAlk process with
the addition of the saturation section and optimized processing conditions. Existing MTBE units can be converted to the InAlk process with
only minor modifications.
Product quality: High-octane, low Rvp, mid-boiling-range paraffinic gasoline blending component with no aromatic content, low-sulfur content and adjustable olefin content.
Economics: (basis: C4 feed from FCC unit)
Investment (basis: 2,800-bpsd unit), $/bpsd

Grassroots
Revamp of MTBE unit
Utilities (per bbl alkylate)
Hydrogen, lb
Power, kW
Steam, HP, lb
Steam, LP, lb
Licensor: UOP LLC.
3,000
1,580
5.2
7.5
385
50
Description: Diolefins and acetylenes in the C 4 (or C3 C 4 ) feed react

selectively with hydrogen in the liquid-phase, fixed-bed reactor under mild
temperature and pressure conditions. Butadiene and, if C3 s are present,
methylacetylene and propadiene are converted to olefins.
The high isomerization activity of the catalyst transforms 1-butene
into cis- and trans-2-butenes, which affords higher octane-barrel production.
Good hydrogen distribution and reactor design eliminate channeling while enabling high turndown ratios. Butene yields are maximized,
hydrogen is completely consumed, and essentially, no gaseous byproducts or heavier compounds are formed. Additional savings are possible
when pure hydrogen is available eliminating the need for a stabilizer. The
process integrates easily with the C3 /C4 splitter.
Alkyfining performance and impact on HF alkylation
product:
The results of an Alkyfining unit treating an FCC C4 HF alkylation unit feed containing 0.8% 1,3-butadiene are:
Butadiene in alkylate, ppm
< 10
1-butene isomerization, %
70
Butenes yield, %
100.5
RON increase in alkylate
2
MON increase in alkylate
1
Alkylate end point reduction, C
20
The increases in MON, RON and butenes yield are reflected in a

substantial octane-barrel increase while the lower alkylate end point
reduces ASO production and HF consumption.
Economics:
Investment:
Grassroots ISBL cost:
For an HF unit, $/ bpsd
For an H 2SO4 unit, $/ bpsd
430
210
Annual savings for a 10,000-bpsd alkylation unit:

HF unit
4.1 million U.S.$
5.5 million U.S.$
H2SO4 unit
Installation: Over 80 units are operating with a total installed capacity of 700,000 bpsd
Licensor: Axens, Axens NA.

90

Nonaromatics
Washer
Extractor
Water &
solvent
Extractive
distillation
column
Nonaromatics
Extractive
distillation
column
Water
Aromatics
fraction
Feed BTXfraction
Side
stripper
Aromatics
Stripper
column
Water
Aromatics
Light nonaromatics
Solvent
Solvent+aromatics
Aromatics extraction
Aromatics extractive distillation
Application: Simultaneous recovery of benzene, toluene and xylenes

(BTX) from reformate or pyrolysis gasoline (pygas) using liquid-liquid
extraction.
Application: Recovery of high-purity aromatics from reformate,

pyrolysis gasoline or coke-oven light oil using extractive distillation.
Description: At the top of extractor operating at 30C to 50C and

1 to 3 bar, the solvent, N-Formylmorpholin with 4% to 6% water, is fed
as a continuous phase. The feedstockreformate or pygasenters several stages above the base of the column. Due to density differences, the
feedstock bubbles upwards, countercurrent to the solvent. Aromatics
pass into the solvent, while the nonaromatics move to the top, remaining in the light phase. Low-boiling nonaromatics from the top of the extractive distillation (ED) column enter the base of the extractor as countersolvent.
Aromatics and solvent from the bottom of the extractor enter the ED,
which is operated at reduced pressure due to the boiling-temperature
threshold. Additional solvent is fed above the aromatics feed containing
small amounts of nonaromatics that move to the top of the column. In the
bottom section, as well as in the side rectifier, aromatics and practically
water-free solvent are separated.
The water is produced as a second subphase in the reflux drum after
azeotropic distillation in the top section of the ED. This water is then
fed to the solvent-recovery stage of the extraction process.
Economics:
Consumption per ton of feedstock
Steam (20 bar), t/t
Water, cooling (T=10C), m3/t
Electric power, kWh/t
Production yield
Benzene, %
Toluene, %
EB, Xylenes,%
Purity
Benzene, wt%
Toluene, wt%
EB, Xylenes, wt%
0.46
12
18
~100
99.7
94.0
99.999
>99.99
>99.99
Description: In the extractive distillation (ED) process, a singlecompound solvent, N-Formylmorpholin (NFM) alters the vapor pressure of the components being separated. The vapor pressure of the aromatics is lowered more than that of the less soluble nonaromatics.
Nonaromatics vapors leave the top of the ED column with some solvent, which is recovered in a small column that can either be mounted on
the main column or installed separately.
Bottom product of the ED column is fed to the stripper to separate
pure aromatics from the solvent. After intensive heat exchange, the lean
solvent is recycled to the ED column. NFM perfectly satisfies the necessary solvent properties needed for this process including high selectivity,
thermal stability and a suitable boiling point.
Economics:
Pygas feedstock:
Production yield
Benzene
Toluene
Quality
Benzene
Toluene
Consumption
Steam
Benzene
Benzene/toluene
99.95%
99.95%
99.98%
30 wt ppm NA*
80 wt ppm NA*
600 wt ppm NA*
475 kg/t ED feed
680 kg/t ED feed**
Reformate feedstock with low aromatics content (20wt%):

Benzene
Quality
Benzene
10 wt ppm NA*
Consumption
Steam
320 kg/t ED feed
*Maximum content of nonaromatics.
**Including benzene/toluene splitter.
Installation: One Morphylex plant was erected.
Installation: 45 Morphylane plants (total capacity of more than 6

MMtpa).
Reference: Emmrich, G., F. Ennenbach and U. Ranke, Krupp Uhde

Processes for Aromatics Recovery, European Petrochemical Technology
Conference, June 2122, 1999, London.
Reference: Emmrich, G., F. Ennenbach and U. Ranke, Krupp Uhde

Processes for Aromatics Recovery, European Petrochemical Technology
Conference, June 2122, 1999, London.
Licensor: Uhde GmbH.

I 91

Offgas
C5/C6
Water
Lean solvent
Hydrocarbon
feed
START
Splitter
Raffinate
Extractive
distillation
column
Solvent
recovery
column
Aromatics to
downstream
fractionation
C5-C9
Reformate
H2
Light
reformate
2
Steam
Heavy
reformate
Aromatics-rich solvent
Aromatics recovery
Benzene reduction
Application: GT-BTX is an aromatics recovery process. The technology uses extractive distillation to remove benzene, toluene and xylene
(BTX) from refinery or petrochemical aromatics streams such as catalytic
reformate or pyrolysis gasoline. The process is superior to conventional liquid-liquid and other extraction processes in terms of lower capital and operating costs, simplicity of operation, range of feedstock and solvent performance. Flexibility of design allows its use for grassroots aromatics recovery
units, debottlenecking or expansion of conventional extraction systems.
Description: The technology has several advantages:
Less equipment required, thus, significantly lower capital cost compared to conventional liquid-liquid extraction systems
Energy integration reduces operating costs
Higher product purity and aromatic recovery
Recovers aromatics from full-range BTX feedstock without prefractionation
Distillation-based operation provides better control and simplified
operation
Proprietary formulation of commercially available solvents exhibits
high selectivity and capacity
Low solvent circulation rates
Insignificant fouling due to elimination of liquid-liquid
contactors
Fewer hydrocarbon emission sources for environmental benefits
Flexibility of design options for grassroots plants or expansion of
existing liquid-liquid extraction units.
Hydrocarbon feed is preheated with hot circulating solvent and fed at
a midpoint into the extractive distillation column (EDC). Lean solvent is
fed at an upper point to selectively extract the aromatics into the column
bottoms in a vapor/liquid distillation operation. The nonaromatic hydrocarbons exit the top of the column and pass through a condenser. A portion of the overhead stream is returned to the top of the column as reflux
to wash out any entrained solvent. The balance of the overhead stream is
the raffinate product, requiring no further treatment.
Rich solvent from the bottom of the EDC is routed to the solvent-recovery column (SRC), where the aromatics are stripped overhead. Stripping
steam from a closed-loop water circuit facilitates hydrocarbon removal. The
SRC is operated under a vacuum to reduce the boiling point at the base of
the column. Lean solvent from the bottom of the SRC is passed through
heat exchange before returning to the EDC. A small portion of the lean circulating solvent is processed in a solvent-regeneration step to remove heavy
decomposition products.
The SRC overhead mixed aromatics product is routed to the purification section, where it is fractionated to produce chemical-grade benzene, toluene and xylenes.
Economics: Estimated installed cost for a 15,000-bpd GT-BTX
extraction unit processing BT-Reformate feedstock is $12 million (U.S.
Gulf Coast 2002 basis).
Installations: Three grassroots applications.
Licensor: GTC Technology Inc.
Application: Benzene reduction from reformate, with the Benfree process, using integrated reactive distillation.

92
Description: Full-range reformate from either a semiregenerative or

CCR reformer is fed to the reformate splitter column, shown above. The
splitter operates as a dehexanizer lifting C 6 and lower-boiling components
to the overhead section of the column. Benzene is lifted with the light ends,
but toluene is not. Since benzene forms azeotropic mixtures with some
C 7 paraffin isomers, these fractions are also entrained with the light
fraction.
Above the feed injection tray, a benzene-rich light fraction is withdrawn and pumped to the hydrogenation reactor outside the column. A
pump enables the reactor to operate at higher pressure than the column,
thus ensuring increased solubility of hydrogen in the feed.
A slightly higher-than-chemical stoichiometric ratio of hydrogen to
benzene is added to the feed to ensure that the benzene content of the
resulting gasoline pool is below mandated levels, i.e., below 1.0 vol% for
many major markets. The low hydrogen flow minimizes losses of gasoline
product in the offgas of the column. Benzene conversion to cyclohexane
can easily be increased if even lower benzene content is desired. The reactor effluent, essentially benzene-free, is returned to the column.
The absence of benzene disrupts the benzene-iso-C 7 azeotropes,
thereby ensuring that the latter components leave with the bottoms fraction of the column. This is particularly advantageous when the light reformate is destined to be isomerized, because iso-C 7 paraffins tend to be
cracked to C 3 and C4 components, thus leading to a loss of gasoline production.
Economics:
Investment, Grassroots ISBL cost , $/bpsd:
300
Combined utilities, $/bbl
0.17
Hydrogen
Stoichiometric to benzene
Catalyst, $/bbl
0.01
Installation: Eighteen benzene reduction units have been licensed.

.

Makeup
H2
Regenerator
Water
wash
M/U
HDW
Rxr
HDT
Rxr
Feed
Rec
Water
wash
Waxy
feed
Water
LT
HT sep
sep
MSCC reactor
Fuel ags to LP absorber
Purge
Wild naphtha
HP
Sour water
stripper
MP steam
Vacuum system
Vac
strip.
Sour
water
Oily
water
Distillate
MP steam
Lube product
Vac
dryer
Catalytic cracking
Catalytic dewaxing
Application: To selectively convert gas oils and residual feedstocks to

higher-value cracked products such as light olefins, gasoline and distillates.
Application: Use the ExxonMobil Selective Catalytic Dewaxing

(MSDW) process to make high VI lube base stock.
Description: The Milli-Second Catalytic Cracking (MSCC) process

uses a fluid catalyst and a novel contacting arrangement to crack heavier materials into a highly selective yield of light olefins, gasoline and distillates. A distinguishing feature of the process is that the initial contact
of oil and catalyst occurs without a riser in a very short residence time
followed by a rapid separation of initial reaction products. Because there
is no riser and the catalyst is downflowing, startup and operability are outstanding.
The configuration of an MSCC unit has the regenerator (1) at a higher
elevation than the reactor (2). Regenerated catalyst falls down a standpipe (3), through a shaped opening (4) that creates a falling curtain of
catalyst, and across a well-distributed feed stream. The products from
this initial reaction are quickly separated from the catalyst. The catalyst then
passes into a second reaction zone (5), where further reaction and stripping
occurs. This second zone can be operated at a higher temperature, which
is achieved through contact with regenerated catalyst.
Since a large portion of the reaction product is produced under very
short time conditions, the reaction mixture maintains good product
olefinicity and retains hydrogen content in the heavier liquid products.
Additional reaction time is available for the more-difficult-to-crack species
in the second reaction zone/stripper.
Stripped catalyst is airlifted back to the regenerator where coke deposits
are burned, creating clean, hot catalyst to begin the sequence again.
Products: High VI/low-aromatics lube base oils (light neutral through

bright stocks). Byproducts include fuel gas, naphtha and low-pour diesel.
Installations: A new MSCC unit began operation earlier this year.

Four MSCC units are currently in operation.
Description: MSDW is targeted for hydrocracked or severely

hydrotreated stocks. The improved selectivity of MSDW for the highly
isoparaffinic-lube components, which results in higher lube yields and VIs.
The process uses multiple catalyst systems with multiple reactors. Internals are proprietary (the Spider Vortex Quench Zone technology is
used). Feed and recycle gases are preheated and contact the catalyst in a
down-flow-fixed-bed reactor. Reactor effluent is cooled, and the remaining aromatics are saturated in a post-treat reactor. The process can be integrated into a lube hydrocracker or lube hydrotreater. Postfractionation is
targeted for client needs.
Operating conditions:
Temperatures, F
Hydrogen partial pressures, psig
LHSV
550 to 800
500 to 2,500
0.4 to 3.0
Conversion depends on feed wax content

Pour point reduction as needed.
Yields:
Lube yield, wt%
C1 to C4, wt%
C5 400F, wt%
400F Lube, wt%
H 2 cons, scf/bbl
Light neutral
94.5
1.5
2.7
1.5
100300
Heavy neutral
96.5
1.0
1.8
1.0
100300
Reference: Short-Contact-Time FCC, AIChE 1998 Spring Meeting, New Orleans.
Economics: $3,0005,500 per bpsd installed cost (U. S. Gulf Coast).
Licensor: UOP LLC (in cooperation with BARCO).
Installation: Three units are operating, one under construction and

one being converted.

94

Hydrogen makeup
Furnace
Dewaxing
reactor
Hydrotreating
reactor
Absorber
Lean amine
Offgas
Feed
START
4
3
Rich amine
H2-rich
gas
Fresh feed
HP
separator
Wild
naphtha
LP separator Product
stripper
Reformate
Diesel
Catalytic dewaxing
Catalytic reforming
Application: Catalytic dewaxing process improves the cold flow

properties (pour point, CFPP) of distillate fuels so that deeper cuts can
be made at the crude unit. Thus, middle-distillate fuel production can
be increased. The waxy n-paraffins are selectively cracked to produce a
very high yield of distillate with some fuel gas, LPG and naphtha.
Application: Upgrade various types of naphtha to produce high-octane

reformate, BTX and LPG.
Description: Two different designs are offered. One design is conventional where the catalyst is regenerated in place at the end of each cycle. Operating normally in a pressure range of 12 to 25 kg/cm2 (170 to 350 psig)
and with low pressure drop in the hydrogen loop, the product is 90 to 100
RONC. With its higher selectivity, trimetallic catalyst RG582 and RG682
make an excellent catalyst replacement for semi-regenerative reformers.
The second, the advanced Octanizing process, uses continuous catalyst regeneration allowing operating pressures as low as 3.5 kg/cm2 (50
psig). This is made possible by smooth-flowing moving bed reactors (13)
which use a highly stable and selective catalyst suitable for continuous
regeneration (4). Main features of Axenss regenerative technology are:
Side-by-side reactor arrangement, which is very easy to erect and consequently leads to low investment cost.
The Regen C catalyst regeneration system featuring the dry burn
loop, completely restores the catalyst activity while maintaining its specific
area for more than 600 cycles.
Finally, with the new CR401 (gasoline mode) and AR501 (aromatics
production) catalysts specifically developed for ultra-low operating pressure and the very effective catalyst regeneration system, refiners operating
Octanizing or Aromizing processes can obtain the highest hydrogen, C5+
and aromatics yields over the entire catalyst life.
Yields: Typical for a 90C to 170C (176F to 338F) cut from light
Arabian feedstock:
Description: The heart of the dewaxing process is the zeolitic catalyst, which operates at typical distillate hydrotreating conditions. This feature allows low-cost revamp for existing hydrotreaters into a HDS/DW
unit by adding reactor volume. The dewaxing step requires a very small
increase in hydrogen consumption; thus, the incremental operating cost
is low. Since the dewaxing catalyst is tolerant of sulfur and nitrogen
components in the feed, it can be located upstream of the HDS catalyst.
The run length for the dewaxing catalyst can be designed to match the
HDS catalyst.
Economics: The cost of a new HDS/DW is estimated at 1,000-2,000
$/bbl depending primarily on hydrotreating requirements.
Installation: One unit is operating, and one ultra-low-sulfur/dewaxing unit is under design.
Oper. press., kg/cm2

Yield, wt% of feed
Hydrogen
C5+
RONC
MONC
Conventional
1015
Octanizing
<5
2.8
83
100
89
3.8
88
102
90.5
Economics:
Investment (basis 25,000 bpsd continuous octanizing unit,
battery limits, erected cost, mid-2002 Gulf Coast), U.S.$ per
bpsd
1,800
Utilities: typical per bbl feed:
65
Fuel, 103 kcal
Electricity, kWh
0.96
Steam, net, HP, kg
12.5
0.03
Water, boiler feed, m3
Installation: Of 110 units licensed, 60 units are designed with continuous regeneration technology capability.
Reference: Continuing Innovation In Cat Reforming, NPRA
Annual Meeting, March 1517, 1998, San Antonio.
Fixed Bed Reformer Revamp Solutions for Gasoline Pool Improvement,Petroleum Technology Quarterly, Summer 2000.
Increase reformer performance through catalytic solutions, ERTC
2002, Paris.

I 95

BFW
Net gas to fuel
Spent catalyst
Steam
Heaters
Net gas to
H2 users
2
Reactors
Hot
feed
START
4
Net gas
CW
Highpressure
flash
To fractionator
Lowpressure
flash
Charge
Liquid to stabilizer
START
Catalytic reforming
Catalytic reforming
Application: Increase the octane of straight-run or cracked naphthas

for gasoline production.
Application: Upgrade naphtha for use as a gasoline blendstock or feed

to a petrochemical complex with the UOP CCR Platforming process. The
unit is also a reliable, continuous source of high-purity hydrogen.
Products: High-octane gasoline and hydrogen-rich gas. Byproducts may

be LPG, fuel gas and steam.
Description: Semi-regenerative multibed reforming over platinum or
bimetallic catalysts. Hydrogen recycled to reactors at the rate of 3 to 7
mols/mol of feed. Straight-run and/or cracked feeds are typically
hydrotreated, but low-sulfur feeds (<10 ppm) may be reformed without
hydrotreatment.
Operating conditions: 875F to 1,000F and 150 to 400 psig reactor conditions.
Yields: Depend on feed characteristics, product octane and reactor pressure. The following yields are one example. The feed contains 51.4% paraffins, 41.5% naphthenes and 7.1% aromatics, and boils from 208F to
375F (ASTM D86). Product octane is 99.7 RONC and average reactor pressure is 200 psig.
Component
H2
C1
C2
C3
iC4
nC4
C5+
LPG
Reformate
wt%
2.3
1.1
1.8
3.2
1.6
2.3
87.1
vol%
1,150 scf/bbl
3.7
83.2
Economics:
Utilities, (per bbl feed)
Fuel, 103 Btu release
Electricity, kWh
Water, cooling (20F rise), gal
Steam produced (175 psig sat), lb
275
7.2
216
100
Licensor: Howe-Baker Engineers, Ltd., a subsidiary of Chicago Bridge

& Iron Co.
Description: Constant product yields and onstream availability distinguish the CCR Platforming process featuring catalyst transfer with minimum lifts, no valves closing on catalyst and gravity flow from reactor to
reactor (2,3,4). The CycleMax regenerator (1) provides simplified operation and enhanced performance at a lower cost than other designs. The
product recovery section downstream of the separator (7) is customized
to meet site-specific requirements. The R-270 series catalysts offer the highest C5+ and hydrogen yields while also providing the R-230 series
attributes of CCR Platforming process unit flexibility through reduced
coke make.
Semiregenerative reforming units also benefit from the latest UOP
catalysts. R-86 catalyst provides the high stability with excellent yields at
low cost. Refiners use UOP engineering and technical service experience
to tune operations, plan the most cost-effective revamps, and implement
a stepwise approach for conversion of semiregenerative units to obtain
the full benefits of CCR Platforming technology.
Yields:
Operating mode
Semiregen.
Onstream availability, days/yr
330
Feedstock, P/N/A LV%
63/25/12
IBP/EP,F
200/360
Operating conditions
Reactor pressure, psig
200
100
C5+ octane, RONC
Catalyst
R-86
Yield information
Hydrogen, scfb
1,270
84.8
C 5 +, wt%
1,690
91.6
Investment (basis: 20,000 bpsd CCR Platforming unit, 50 psig

reactor pressure, 100 C5+ RONC, 2002, U.S. Gulf Coast ISBL):
$ per bpsd
2,100
Installation: UOP has licensed more than 800 platforming units; 37

customers have selected CCR platforming for two or more catalytic
reforming units. Twenty-nine refiners operate 100 of the 173 operating
units. Twenty units are designed for initial semiregenerative operation with
the future installation of a CCR regeneration section.
Operating Design & const.
173
47
44
31
29
5
14
Licensor: UOP LLC.
50
100
R-274
Economics:
Total CCR Platforming units

Ultra-low 50 psig units
Units at 35,000+ bpsd
Semiregenerative units
with a stacked reactor
96
Continuous
360
63/25/12
200/360

Fuel gas
Hot air Stack gas
Oil
Products
C3/C4 LP
4
Blower
SO2
Air converter
Coker naphtha
WSA condenser
FCCU
Offgas
CO boiler
Oil feed
Lift
air
Dust
filter
Stm.
Stm.
Blower
Acid pump
Heat
exchanger
Support
heat
BFW
Light gas oil
BFW
Heavy gas oil
Acid cooler
Fresh feed
Product acid
START
Stm.
Catalytic SOx removal
Coking
Application: The Wet gas Sulfuric Acid (WSA) process catalytically

removes more than 99% + of sulfurous compounds from moist acid gases
without prior drying and recovers concentrated sulfuric acid.
WSA combined with selective catalytic reduction, the SNOX process, efficiently removes nitrogen oxides (up to 95%) and sulfur oxides from
flue gases and offgases. The main applications in refineries are H2S gases,
onsite regeneration of alkylation acid (spent acid recovery (SAR)), FCC
regenerator offgases (example below), and boiler offgases, especially flue
gases from petroleum coke and heavy residual oil fired boilers.
Application: Conversion of vacuum residues (virgin and hydrotreated),

various petroleum tars and coal tar pitch through delayed coking.
Description: Flue gas from the FCC regenerator is cooled to 430F

(220C) in the waste-heat boiler. By means of an electrostatic precipitator, catalyst and coke particulates are reduced to less than 0.18 lb/MMscf.
The flue gas is heated to approximately 770F (410C) before entering
the SO2 reactor. In the SO2 reactor, SO2 is oxided to SO3, and all
remaining particulates are deposited in the catalyst panels. The reactor
consists of several parallel catalyst panels, which can be individually
cleaned and reloaded without interrupting plant operation.
After the SO2 converter, the gas is cooled to near the acid dew point.
In the last step, concentrated sulfuric acid is condensed, and flue gas is
cooled in the WSA condenser. Hot cooling air from the condenser may be
used for preheating of boiler feedwater or as preheated air for the FCC
regenerator/CO boiler.
All equipment, except the condenser, is made of carbon steel or low
alloy steel. The WSA process has few moving parts, low maintenance
costs and high onstream availability. The process can be applied to new or
revamp installations.
The WSA process is characterized by:
99% or more of the flue gas sulfur is recovered as commercial grade
concentrated sulfuric acid
Particulates are essentially completely removed
No waste solids or wastewater is produced. No absorbents or auxiliary chemicals are used
Operating costs decrease with increasing sulfur content in flue gas
Process is fully automated, contains few moving parts and does not
use a circulation of slurries or solids
Simple operation allows wide flexibility in operating loads.
Installation: More than 40 units worldwide.
Products: Fuel gas, LPG, naphtha, gas oils and fuel, anode or needle
grade coke (depending on feedstock and operating conditions).
Description: Feedstock is introduced (after heat exchange) to the bottom of the coker fractionator (1) where it mixes with condensed recycle.
The mixture is pumped through the coker heater (2) where the desired coking temperature is achieved, to one of two coke drums (3). Steam or boiler
feedwater is injected into the heater tubes to prevent coking in the furnace
tubes. Coke drum overhead vapors flow to the fractionator (1) where they
are separated into an overhead stream containing the wet gas, LPG and naphtha; two gas oil sidestreams; and the recycle that rejoins the feed.
The overhead stream is sent to a vapor recovery unit (4) where the
individual product streams are separated. The coke that forms in one of
at least two (parallel connected) drums is then removed using high-pressure water. The plant also includes a blow-down system, coke handling and
a water recovery system.
Heater outlet temperature, F
Coke drum pressure, psig
Recycle ratio, vol/vol feed, %
900950
1590
0100
Yields:
Feedstock
Gravity, API
Sulfur, wt%
Conradson
carbon, wt%
Products, wt%
Gas + LPG
Naphtha
Gas oils
Coke
Vacuum residue of
Middle East hydrotreated Coal tar
vac. residue
bottoms
pitch
7.4
1.3
211.0
4.2
2.3
0.5
20.0
27.6
7.9
12.6
50.8
28.7
9.0
11.1
44.0
35.9
3.9
31.0
65.1
Economics:
Investment (basis: 20,000 bpsd straight-run vacuum residue
feed, U.S. Gulf Coast 2002, fuel-grade coke, includes vapor recovery), U.S. $ per bpsd (typical)
4,000
Utilities, typical/bbl of feed:
145
Fuel, 103 Btu
Electricity, kWh
3.9
Steam (exported), lb
20
Water, cooling, gal
180
Installation: More than 55 units.

Reference: Mallik, Ram, Gary and Hamilton, Delayed coker design
considerations and project execution, NPRA 2002 Annual Meeting,
March 1719, 2002.
Licensor: ABB Lummus Global Inc.

I 97

Gas
Gas and naphtha

to gas plant
Distillate
Coke
drums
Naphtha
Gas oil
Feed
Green coke
Steam
Light gas oil
Furnace
Fractionator
Feed
Heavy gas oil
START
Coking
Coking
Application: Upgrading of petroleum residues (vacuum residue,

bitumen, solvent-deasphalter pitch and fuel oil) to more valuable liquid
products (LPG, naphtha, distillate and gas oil). Fuel gas and petroleum
coke are also produced.
Application: Manufacture petroleum coke and upgrade residues to

lighter hydrocarbon fractions using the Selective Yield Delayed Coking
(SYDEC) process.
Description: The delayed coking process is a thermal process and consists of fired heater(s), coke drums and main fractionator. The cracking
and coking reactions are initiated in the fired heater under controlled timetemperature-pressure conditions. The reactions continue as the process
stream moves to the coke drums. Being highly endothermic, the cokingreaction rate drops dramatically as coke-drum temperature decreases. Coke
is deposited in the coke drums. The vapor is routed to the fractionator,
where it is condensed and fractionated into product streamstypically
fuel gas, LPG, naphtha, distillate and gas oil.
When one of the pair of coke drums is full of coke, the heater outlet
stream is directed to the other coke drum. The full drum is taken offline,
cooled with steam and water and opened. The coke is removed by
hydraulic cutting. The empty drum is then closed, warmed-up and made
ready to receive feed while the other drum becomes full.
Benefits of Conoco-Bechtels delayed coking technology are:
Maximum liquid-product yields and minimum coke yield through
low-pressure operation, patented distillate recycle technology and zero
(patented) or minimum natural recycle operation
Maximum flexibility; distillate recycle operation can be used to
adjust the liquid-product slate or can be withdrawn to maximize unit
capacity
Extended furnace runlengths between decokings
Ultra-low-cycle-time operation maximizes capacity and asset utilization
Higher reliability and maintainability enables higher onstream time
and lowers maintenance costs
Lower investment cost.
Economics: For a delayed coker processing 35,000 bpsd of heavy, highsulfur vacuum residue, the U.S. Gulf Coast investment cost is approximately U.S.$145160 million.
Installation: Low investment cost and attractive yield structure has
made delayed coking the technology of choice for bottom-of-the-barrel
upgrading. Numerous delayed coking units are operating in petroleum
refineries worldwide.
Licensor: Bechtel Corp. and Conoco Inc.
Products: Coke, gas, LPG, naphtha and gas oils.

Description: Charge is fed directly to the fractionator (1) where it combines with recycle and is pumped to the coker heater where it is heated
to coking temperature, causing partial vaporization and mild cracking.
The vapor-liquid mix enters a coke drum (2 or 3) for further cracking.
Drum overhead enters the fractionator (1) to be separated into gas,
naphtha, and light and heavy gas oils. There are at least two coking drums,
one coking while the other is decoked using high-pressure water jets.
Operating conditions: Typical ranges are:
Coke drum pressure, psig
Recycle ratio, equiv. fresh feed
900950
15100
0.051.0
Increased coking temperature decreases coke production; increases

liquid yield and gas oil end point. Increasing pressure and/or recycle ratio
increases gas and coke make, decreases liquid yield and gas oil end point.
Yields:
Feed, source
Venezuela
Type
Vac. resid
Gravity, API
2.6
Sulfur, wt%
4.4
Concarbon, wt%
23.3
Operation
Max dist.
products, wt%
Gas
8.7
Naphtha
10.0
Gas oil
50.3
Coke
31.0
N. Africa
Vac. resid
15.2
0.7
16.7
Anode coke
Decant oil
0.7
0.5
Needle coke
7.7
19.9
46.0
26.4
9.8
8.4
41.6
40.2
Economics:
Investment (basis: 65,00010,000 bpsd,
4Q 1999, U.S. Gulf), $ per bpsd
Utilities, typical per bbl feed:
Fuel, 103 Btu
Electricity, kWh
Steam (exported), lb
Water, cooling, gal
2,5004,000
120
3.6
(40)
36
Installation: More than 58,000 tpd of fuel, anode and needle coke.
Reference: Handbook of Petroleum Refining Processes, 2nd Ed., pp.
12.2512.82; Oil & Gas Journal, Feb. 4, 1991, pp. 4144; Hydrocarbon
Processing, Vol. 71, No. 1, January 1992, pp. 7584.
Licensor: Foster Wheeler/UOP LLC

98

Flash gas
FG
6
Light naphtha
Rec
Heavy naphtha
Kerosine
8
9
Diesel
Cracker feed
10
To vac. system
Lt. vac. gas oil

Stm.
Stm.
Hvy. vac.
gas oil
12
11
Crude
LPG
Crude
C
D
U
Tops
H
D
F
HDS
Kero
LGO
HGO
Vac
VGO
H
LR V WD
U
Storage
Vac. gas oil

Stm. (cracker feed)
START
NHT
Naphtha
Kero
GO
HCU
VBU
Flash column
VBU
Bleed
Residue
Asphalt
Crude distillation
Crude distillation
Application: Separates and recovers the relatively lighter fractions from

a fresh crude oil charge (e.g., naphtha, kerosine, diesel and cracking
stock). The vacuum flasher processes the crude distillation bottoms to produce an increased yield of liquid distillates and a heavy residual material.
Application: The Shell Bulk CDU is a highly integrated concept. It

separates the crude in long residue, waxy distillate, middle distillates
and a naphtha minus fraction. Compared with stand-alone units, the overall integration of a crude distillation unit (CDU), hydrodesulfurization
unit (HDS), high vacuum unit (HVU) and a visbreaker (VBU) results
in a 50% reduction in equipment count and significantly reduced operating costs. A prominent feature embedded in this design is the Shell deepflash HVU technology. This technology can also be provided in cost-effective process designs for both feedprep and lube oil HVUs as stand-alone
units. For each application, tailor-made designs can be produced.
Description: The charge is preheated (1), desalted (2) and directed

to a preheat train (3) where it recovers heat from product and reflux
streams. The typical crude fired heater (4) inlet temperature is on the order
of 550F, while the outlet temperature is on the order of 675F to 725F.
Heater effluent then enters a crude distillation column (5) where light
naphtha is drawn off the tower overhead (6); heavy naphtha, kerosine,
diesel and cracking stock are sidestream drawoffs. External reflux for the
tower is provided by pumparound streams (710). The atmospheric
residue is charged to a fired heater (11) where the typical outlet temperature is on the order of 750F to 775F.
From the heater outlet, the stream is fed into a vacuum tower (12),
where the distillate is condensed in two sections and withdrawn as two
sidestreams. The two sidestreams are combined to form cracking feedstock. An asphalt base stock is pumped from the bottom of the tower.
Two circulating reflux streams serve as heat removal media for the tower.
Yields: Typical for Merey crude oil:
Crude unit products
Overhead & naphtha
Kerosine
Diesel
Gas oil
Lt. vac. gas oil
Hvy. vac. gas oil
Vac. bottoms
Total
wt%
API
6.2
4.5
18.0
3.9
2.6
10.9
53.9
100.0
58.0
41.4
30.0
24.0
23.4
19.5
5.8
8.7
Pour, F
85
10
20
35
85
(120)*
85
*Softening point, F
Note: Crude unit feed is 2.19 wt% sulfur. Vacuum unit feed is 2.91 wt% sulfur.
Economics:
Investment (basis: 100,00050,000 bpsd,
2nd Q, 2002, U.S. Gulf), $ per bpsd
8901,100
Utility requirements, typical per bbl fresh feed
Steam, lb
24
(80120)
Fuel (liberated), 103 Btu
Power, kWh
0.6
Water, cooling, gal
300400
Installation: Foster Wheeler has designed and constructed crude

units having a total crude capacity in excess of 10 MMbpsd.
Reference: Encyclopedia of Chemical Processing and Design, MarcelDekker, 1997, pp. 230249.
Description: The basic concept of the bulk CDU is the separation

of the naphtha minus and the long residue from the middle distillate fraction which is routed to the HDS. After desulfurization in the HDS
unit, final product separation of the bulk middle distillate stream from
the CDU takes place in the HDS fractionator (HDF), which consists of
a main atmospheric fractionator with side strippers.
The long residue is routed hot to a feedprep HVU, which recovers
the waxy distillate fraction from long residue as the feedstock for a cat
cracker or hydrocracker unit (HCU). Typical flashzone conditions are
415C and 24 mbara. The Shell design features a deentrainment section,
spray sections to obtain a lower flashzone pressure, and a VGO recovery
section to recover up to 10 wt% of as automotive diesel. The Shell furnace
design prevents excessive cracking and enables a 5-year run length between
decoke.
Yields: Typical for Arabian light crude
Products
Gas
Gasoline
Kerosine
Gasoil (GO)
VGO
Waxy distillate (WD)
Residue
C1C4
C5150C
150250C
250350C
350370C
370575C
575C+
% wt
0.7
15.2
17.4
18.3
3.6
28.8
16.0
Economics: Due to the incorporation of Shell high capacity internals

and the deeply integrated designs, an attractive CAPEX reduction can be
achieved. Investment costs are dependent on the required configuration
and process objectives.
Installation: Over 100 Shell CDUs have been designed and operated
since the early 1900s. Additionally, a total of some 50 HVU units have
been built while a similar number has been debottlenecked, including
many third-party designs of feedprep and lube oil HVUs.
Licensor: Shell Global Solutions International B.V.
Licensor: Foster Wheeler.

I 99

LPG
Feed
Light naphtha
START
Medium naphtha
RX feed
heater
One or two kerosine cut
Stm.
1
2
Two kerosine cut

5
Vacuum gas oil
Distillate
WTR
HDS
F/E
exch.
Feed
heater
Makeup
comp.
Amine
wash
HP-LT
separator
Feed
heater
Distillate for FCC

Vacuum
residue
Recycle
comp.
HDS
reactor
Heavy naphtha
REDAR
production
HP-HT
separator
Steam
Sour
water
Product fractionation section

Gasoil feed
Diesel
Wild naphtha
Fuel gas
Hydrogen
Crude distillation
Dearomatizationmiddle distillate
Application: The D2000 process is progressive distillation to minimize the total energy consumption required to separate crude oils or condensates into hydrocarbon cuts, which number and properties are optimized to fit with sophisticated refining schemes and future regulations.
This process is applied normally for new topping units or new integrated
topping/vacuum units but the concept can be used for debottlenecking
purpose.
Application: Deep dearomatization of middle distillates and upgrading of light cycle oil (LCO).
Products: This process is particularly suitable when more than two

naphtha cuts are to be produced. Typically the process is optimized to produce three naphtha cuts or more, one or two kerosine cuts, two atmospheric gas oil cuts, one vacuum gas oil cut, two vacuum distillates cuts,
and one vacuum residue.
Description: The crude is preheated and desalted (1). It is fed to a
first dry reboiled pre-flash tower (2) and then to a wet pre-flash tower (3).
The overhead products of the two pre-flash towers are then fractionated
as required in a gas plant and rectification towers (4).
The topped crude typically reduced by 23 of the total naphtha cut is
then heated in a conventional heater and conventional topping column
(5). If necessary the reduced crude is fractionated in one deep vacuum
column designed for a sharp fractionation between vacuum gas oil, two
vacuum distillates (6) and a vacuum residue, which could be also a road
bitumen.
Extensive use of pinch technology minimizes heat supplied by heaters
and heat removed by air and water coolers.
This process is particularly suitable for large crude capacity from
150,000 to 250,000 bpsd.
It is also available for condensates and light crudes progressive distillation with a slightly adapted scheme.
Economics:
Investment (basis 230,000 bpsd including atmospheric and
vacuum distillation, gas plant and rectification tower) 750 to
950 $ per bpsd (U.S. Gulf Coast 2000).
Utility requirements, typical per bbl of crude feed:
5065
Fuel fired, 103 btu
Power, kWh
0.91.2
Steam 65 psig, lb
05
Water cooling, (15C rise) gal
50100
Total primary energy consumption:
for Arabian Light or Russian
Export Blend:
1.25 tons of fuel
per 100 tons of Crude
for Arabian Heavy
1.15 tons of fuel
per 100 tons of Crude
Description: The process uses the REDAR catalyst, developed by

Engelhard Corp. It is capable of aromatics hydrogenation in presence of
sulfur and nitrogen at low-operating pressure and temperature. The process operates in conjunction with a conventional hydrotreating step to
remove sulfur. Therefore, it is ideal as an add-on to existing hydrotreaters
with sulfur levels reaching 250 ppm-wt and nitrogen levels up to 100 ppmwt.
The process also offers an excellent cost-effective opportunity to
upgrade LCOs from FCC units. Depending on the LCO blend ratio in
the feed, the first stage reactor may require a highly active NiMo catalyst
followed by the REDAR catalyst in the second stage. A hot-hydrogen
stripper is recommended for both applications. An important feature of
this process is cascading of treat gas from the REDAR stage to the
hydrotreating stage, thereby taking advantage of higher hydrogen partial
pressure in the REDAR stage.
Key features of the process are: low gas and naphtha make, sulfur in
product meets all proposed fuel regulations, significant aromatics reduction and boiling point shift, which allows higher boiling point LCO in the
feed.
Typical product properties: (LCO upgrading)
Properties
Feed HDS stage REDAR stage
Sulfur, ppm-wt
8,800
83
4
Density, @60F, API
18.0
24.5
32.7
5% BP, D-86, F
361
345
310
95% BP, D-86, F
675
650
630
Cetane index, D-4737
24
31
40
Mono aromatics, IP 391/95 wt% 16.7
53.1
7.5
Di aromatics, IP 391/95, wt%
32.2
8.2
0.2
Tri and higher, IP 391/95, wt%
13.0
4.0
0.0
Total aromatics
61.9
65.3
7.7
Gas yield, Wt% on feed
<0.5
<0.1
<1.0
<3.0
C5 392F, Wt% on feed
Economics: Investment cost for a grassroots 15,000-bpsd LCO

upgrading unit is approximately $35 million on U.S.GC, 2Q 2002
basis. Cost of retrofitting an existing 40,000-bpsd hydrotreater will be significantly less and is estimated at $15 million for U.S.GC, 2Q, 2002.
Licensor: Badger Technology Center of Washington Group International, in association with Engelhard Corp.
Installation: Technip has designed and constructed one crude unit

and one condensate unit with the D2000 concept. The latest revamp project currently in operation shows an increase of capacity of the existing
crude unit of 30% without heater addition.
Licensor: TOTALFINAELF, Technip-Coflexip.
100

E-2
P-1
E-1
E-4
Vacuum
residue
charge
Extractor
E-3
Residuum
Pitch
stripper
M-1
Hot
oil
Hot
oil
T-3
V-3
T-2
S-1
V-2
T-1
E-6
V-1
START
DAO
separator
2
1
Oils
DAO
stripper
P-2
Asphaltenes
Resins
Pitch
DAO
Deasphalting
Deasphalting
Application: Extract lubricating oil blend stocks and FCCU or

hydrocracker feedstocks with low metal and Conradson carbon contents from atmospheric and vacuum resid using ROSE Supercritical
Fluid Technology. Can be used to upgrade existing solvent deasphalters.
ROSE may also be used to economically upgrade heavy crude oil.
Products: Lube blend stocks, FCCU feed, hydrocracker feed, resins
and asphaltenes.
Description: Resid is charged through a mixer (M-1), where it is mixed
with solvent before entering the asphaltene separator (V-1). Countercurrent
solvent flow extracts lighter components from the resid while rejecting
asphaltenes with a small amount of solvent. Asphaltenes are then heated
and stripped of solvent (T-1). Remaining solvent solution goes overhead
(V-1) through heat exchange (E-1) and a second separation (V-2), yielding an intermediate product (resins) that is stripped of solvent (T-2). The
overhead is heated (E-4, E-6) so the solvent exists as a supercritical fluid
in which the oil is virtually insoluble. Recovered solvent leaves the separator top (V-3) to be cooled by heat exchange (E-4, E-1) and a cooler
(E-2). Deasphalted oil from the oil separator (V-3) is stripped (T-3) of
dissolved solvent. The only solvent vaporized is a small amount dissolved in fractions withdrawn in the separators. This solvent is recovered
in the product strippers. V-1, V-2 and V-3 are equipped with high-performance ROSEMAX internals. These high-efficiency, high-capacity
internals offer superior product yield and quality while minimizing vessel size and capital investment. They can also debottleneck and improve
operations of existing solvent deasphalting units.
The system can be simplified by removing equipment in the outlined
box to make two products. The intermediate fraction can be shifted into
the final oil fraction by adjusting operating conditions. Only one exchanger
(E-6) provides heat to warm the resid charge and the small amount of
extraction solvent recovered in the product strippers.
Yields: The extraction solvent composition and operating conditions
are adjusted to provide the product quality and yields required for downstream processing or to meet finished product specifications. Solvents range
from propane through hexane and include blends normally produced in
refineries.
Economics:
Application: Prepare quality feed for FCC units and hydrocrackers

from vacuum residue and blending stocks for lube oil and asphalt manufacturing.
Investment (basis: 30,000 bpsd, U.S. Gulf Coast),

$ per bpsd
1,250
3
80110
Fuel absorbed, 10 Btu
Electricity, kWh
2.0
Steam, 150-psig, lb
12
Installation: Thirty-three licensed units with a combined capacity of

over 600,000 bpd.
Reference: Northup, A. H., and H. D. Sloan, Advances in solvent
deasphalting technology, 1996 NPRA Annual Meeting, San Antonio.
Licensor: Kellogg Brown & Root, Inc.
Products: Deasphalted oil (DAO) for catalytic cracking and hydrocracking feedstocks, resins for specification asphalts, and pitch for specification asphalts and residue fuels.
Description: Feed and light paraffinic solvent are mixed then charged
to the extractor (1). The DAO and pitch phases, both containing solvents,
exit the extractor. The DAO and solvent mixture is separated under
supercritical conditions (2). Both the pitch and DAO products are
stripped of entrained solvent (3,4). A second extraction stage is utilized
if resins are to be produced.
Operating conditions: Typical ranges are: solvent, various blends
of C3C7 hydrocarbons including light naphthas. Pressure: 300 to 600
psig. Temp.: 120F to 450F. Solvent-to-oil ratio: 4/1 to 13/1.
Yields:
Feed, type
Gravity, API
Sulfur, wt.%
CCR, wt%
Visc, SSU@ 210F
NI/V, wppm
Lube oil
6.6
4.9
20.1
7,300
29/100
Cracking stock
6.5
3.0
21.8
8,720
46/125
DAO
Yield, vol.% of Feed
Gravity, API
Sulfur, wt%
CCR, wt%
Visc., SSU@ 210F
Ni/V, wppm
30
20.3
2.7
1.4
165
0.25/0.37
53
17.6
1.9
3.5
307
1.8/3.4
65
15.1
2.2
6.2
540
4.5/10.3
149
12
226
0
240
0
Pitch
Softening point, R&B,F
Penetration@77F
Economics:
Investment (basis: 2,000 40,000 bpsd
4Q 2000, U.S. Gulf), $/bpsd
800 3,000
Lube oil Cracking stock
81
56
Fuel, 103 Btu
Electricity, kWh
1.5
1.8
Steam, 150-psig, lb
116
11
15
nil
Installations: 50+. This also includes both UOP and Foster Wheeler
units originally licensed separately before the merging the technologies
in 1996.
Reference: Handbook of Petroleum Refining Processes, 2nd Ed., McGraw
Hill, 1997, pp.10.1510.60.
Licensor: UOP LLC/Foster Wheeler.

I 101

Product vapors
Gas
Reactor
Naptha
Vapor and catalyst

distributor
Stripper
Flue gas
4
LGO
Steam
Regenerator
HGO
3
Combustion air
Reactor riser
2
Regen. cat. standpipe
Riser steam
Feed nozzles (FIT)
Feed
Steam
5
Vacuum flashed
cracked residue
Deep catalytic cracking
Deep thermal conversion
Application: Selective conversion of gasoil and paraffinic residual feedstocks.
Application: The Shell Deep Thermal Conversion process closes the

gap between visbreaking and coking. The process yields a maximum of
distillates by applying deep thermal conversion of the vacuum residue feed
and by vacuum flashing the cracked residue. High-distillate yields are
obtained, while still producing a stable liquid residual product, referred
to as liquid coke. The liquid coke, not suitable for blending to commercial
fuel, is used for speciality products, gasification and/or combustion, e.g.,
to generate power and/or hydrogen.
Products: C2 C5 olefins, aromatic-rich, high-octane gasoline and

distillate.
Description: DCC is a fluidized process for selectively cracking a wide
variety of feedstocks to light olefins. Propylene yields over 24 wt% are
achievable with paraffinic feeds. A traditional reactor/regenerator unit
design uses a catalyst with physical properties similar to traditional FCC
catalyst. The DCC unit may be operated in two operational modes: maximum propylene (Type I) or maximum iso-olefins (Type II).
Each operational mode utilizes unique catalyst as well as reaction conditions. Maximum propylene DCC uses both riser and bed cracking at
severe reactor conditions while Type II DDC uses only riser cracking like
a modern FCC unit at milder conditions.
The overall flow scheme of DCC is very similar to that of a conventional FCC. However, innovations in the areas of catalyst development,
process variable selection and severity and gas plant design enables the
DCC to produce significantly more olefins than FCC in a maximum
olefins mode of operation.
This technology is quite suitable for revamps as well as grassroot applications. Feed enters the unit through nozzles proprietary feed as shown in
the schematic. Integrating DCC technology into existing refineries as
either a grassroots or revamp application can offer an attractive opportunity to produce large quantities of light olefins.
In a market requiring both proplylene and ethylene, use of both thermal and catalytic processes is essential, due to the fundamental differences in the reaction mechanisms involved. The combination of thermal
and catalytic cracking mechanisms is the only way to increase total olefins
from heavier feeds while meeting the need for an increased propylene to
ethylene ratio. The integrated DCC/steam cracking complex offers significant capital savings over a conventional standalone refinery for propylene production.
Products (wt%)
Ethylene
Propylene
Butylene
in which IC4=
Amylene
in which IC5=
DCC Type I
6.1
20.5
14.3
5.4
DCC Type II
2.3
14.3
14.6
6.1
9.8
6.5
FCC
0.9
6.8
11.0
3.3
8.5
4.3
Installation: Five units are curently operating in China and one in

Thailand. Several more units are under design in China.
Reference: Chapin, Letzsch and Zaiting, Petrochemical options
from deep catalytic cracking and the FCCU, NPRA Annual Meeting ,
March 1998.
Description: The preheated short residue is charged to the heater (1)

and from there to the soaker (2), where the deep conversion takes place.
The conversion is maximized by controlling the operating temperature
and pressure. The soaker effluent is routed to a cyclone (3). The cyclone
overheads are charged to an atmospheric fractionator (4) to produce the
desired products like gas, LPG, naphtha, kero and gasoil. The cyclone and
fractionator bottoms are subsequently routed to a vacuum flasher (5),
which recovers additional gasoil and waxy distillate. The residual liquid
coke is routed for further processing depending on the outlet.
Yields: Depend on feed type and product specifications.
Feed, vacuum residue
Viscosity, cSt @ 100C
Products in % wt. on feed
Gas
Gasoline ECP 165C
Gas oil ECP 350C
Waxy distillate ECP 520C
Residue ECP 520C+
Middle East
770
Economics: The investment ranges from 1,300 to 1,600 U.S.$/bbl

installed excl. treating facilities and depending on the capacity and configuration (basis: 1998)
Utilities, typical per bbl @ 180C
Fuel, Mcal
Electricity, kWh
Net steam production, kg
Water, cooling, m3
26
0.5
20
0.15
Installation: To date, four Deep Thermal Conversion units have

been licensed. In two cases this involved a revamp of an existing Shell
Soaker Visbreaker unit. In addition, two units are planned for revamp,
while one grassroots unit is currently under construction. Post startup services and technical services on existing units are available from Shell.
Reference: Visbreaking Technology, Erdl and Kohle, January 1986.
Licensor: Shell Global Solutions International B.V. and ABB Lummus
Global B.V.
Licensor: Stone & Webster Inc., a Shaw Group Co., and Research Institute of Petroleum Processing, Sinopec
102
4.0
8.0
18.1
22.5
47.4

Diesel fuel
500 ppm S
FCC
gasoline
feed
START
Desulfurized/
de-aromatised
olefin-rich gasoline
Extractive
distillation Solvent
recovery
column
column
Reactor
START
Diesel
Adsorption
Separator
Aqueous
oxidant (H2O2)
Hydrogenation
Water
Extraction
Methanol
START
2
Steam
Desulfurized
aromatic
extract
Clean diesel
product
Acid
recycle
Spent acid
+ sulfones
Methanol
recovery
Sulfones
byproduct
Lean solvent
Desulfurization
Desulfurization
Application: GT-DeSulf addresses overall plant profitability by desulfurizing the FCC stream with no octane loss and decreased hydrogen consumption by using a proprietary solvent in an extractive distillation system. This process also recovers valuable aromatics compounds.
Application: To produce ultra-low sulfur fuels, having less than 10

ppm sulfur, from distillate feeds containing 20 to 3,000 ppm sulfur. The
UniPure ASR-2 process is based on oxidation chemistry. It requires no
hydrogen and uses no fired heaters. The process also reduces nitrogen compounds to ultra-low levels.
Applications are anticipated in refineries and stand-alone plants. Skidmounted or truck-mounted units can remediate off spec products at distribution terminals. Extensions are under development for other refinery hydrocarbon streams and for lube oils.
Description: FCC gasoline, with endpoint up to 210C, is fed to the

GT-DeSulf unit, which extracts sulfur and aromatics from the hydrocarbon
stream. The sulfur and aromatic components are processed in a conventional hydrotreater to convert the sulfur into H2S. Because the portion of gasoline being hydrotreated is reduced in volume and free of olefins,
hydrogen consumption and operating costs are greatly reduced. In contrast, conventional desulfurization schemes process the majority of the gasoline through hydrotreating and caustic-washing units to eliminate the sulfur. That method inevitably results in olefin saturation, octane downgrade
and yield loss.
GT-DeSulf has these advantages:
Segregates and eliminates FCC-gasoline sulfur species to meet a
pool gasoline target of 20 ppm
Preserves more than 90% of the olefins from being hydrotreated
in the HDS unit; and thus, prevents significant octane loss and reduces
hydrogen consumption
Fewer components (only those boiling higher than 210C and the
aromatic concentrate from ED unit) are sent to the HDS unit; consequently, a smaller HDS unit is needed and there is less yield loss
High-purity BTX products can be produced from the aromaticrich extract stream after hydrotreating
Olefin-rich raffinate stream (from the ED unit) can be recycled to
the FCC unit to increase the light olefin production.
FCC gasoline is fed to the extractive distillation column (EDC). In a
vapor-liquid operation, the solvent extracts the sulfur compounds into
the bottoms of the column along with the aromatic components, while
rejecting the olefins and nonaromatics into the overhead as raffinate.
Nearly all of the nonaromatics, including olefins, are effectively separated
into the raffinate stream. The raffinate stream can be optionally caustic
washed before routing to the gasoline pool, or to a C3= producing unit.
Rich solvent, containing aromatics and sulfur compounds, is routed
to the solvent recovery column, (SRC), where the hydrocarbons and sulfur species are separated, and lean solvent is recovered in columns bottoms. The SRC overhead is hydrotreated by conventional means and
used as desulfurized gasoline, or processed through an aromatics recovery
unit. Lean solvent from the SRC bottoms are treated and recycled back to
the EDC.
Description: Diesel fuel, or other distillate feed, is introduced at

about 200F into the oxidation reactor operating at about 1 bar pressure.
An aqueous oxidizing solution comprised primarily of recycled formic acid
containing a small amount of hydrogen peroxide and water is also introduced into the reactor. After a short residence time, the sulfur species are
completely oxidized to the corresponding sulfones. The acid extracts about
half of the oxidized sulfur compounds and is separated from the hydrocarbon in a gravity separator. Spent acid and sulfones are processed further to reject the sulfones and regenerate the acid by removing water introduced in the process.
The oxidized diesel from the gravity separator, which contains no
residual peroxide, is water-washed, dried and then passed over a solid
alumina adsorbing bed to extract the remaining sulfones. The product
stream typically has less than 5 ppm sulfur. Two alumina columns are
operated in cycles. While one is being used for adsorption of oxidized
sulfur, the other is regenerated with methanol. The methanol extract containing sulfones is then flash distilled to separate the methanol from the
mixed sulfones. The sulfones recovered from the alumina extraction are
combined with those recovered from the spent acid to form a small
byproduct stream.
Product quality: Product properties other than sulfur and nitrogen
are virtually unchanged. Initial indications are that diesel lubricity is not
reduced. The process can achieve sulfur and nitrogen levels below 1
ppm. The diesel product is usually water white.
Economics: (basis: 25,000-bpsd unit, 500 ppm S feed)
Investment, $/bpsd
Operating cost (utilities and reagents), $/bbl
1,000
0.700.90
Commercialization status: A demonstration plant with a 50- bpd

capacity will start up at a Gulf Coast refinery by early 2003. Commercial readiness for diesel is anticipated before mid-2003.
Economics: Estimated installed cost of $1,000/bpd of feed and production cost of $0.50/bbl of feed for desulfurization and dearomatization.
Reference: Hydrocarbon Engineering, Vol. 7, No. 7, July 2002, pp.

2528.
Licensor: GTC Technology Inc.
Licensor: UniPure Corp.

I 103

SO2
5
Reactor 1
Refrigerant
Air
2
Regen.
Refrigerant 2
Hydrogen
Solvent
recovery
Water
Steam
Waxy
feed
Soft wax
Dewaxed
oil
Steam
Water
Nitrogen
Sorbent flow
8
Hard wax
Fuel gas
Charge
heater
Recycle
comp.
Diesel
stream
Refrigerant
Process steam
Stabilizer
Heater
Desulfurized
product
Product
separator
Dewaxing/wax deoiling
Diesel desulfurization
Application: Bechtels dewaxing/wax fractionation processes remove

waxy components from lubrication base-oil streams to simultaneously meet
desired low-temperture properties for dewaxed oils and produce hard wax
as a premium byproduct.
Application: Convert high-sulfur diesel streams into a very-low sulfur diesel product using S Zorb sulfur removal technology.
Description: The two-stage, solvent-dewaxing process can be expanded

to simultaneously produce hard wax by adding a third deoiling stage using
the wax fractionation process.
Waxy feedstock (raffinate, distillate or deasphalted oil) is mixed with
a binary-solvent system and chilled in a very closely controlled manner in
scraped-surface double-pipe exchangers (1) and refrigerated chillers (2) to
form a wax/oil/solvent slurry. This slurry is filtered through the primaryfilter stage (3) and dewaxed-oil mixture is routed to the dewaxed-oilrecovery section (6) for separation of solvent from the oil. Prior to solvent recovery, the primary filtrate is used to cool the feed/solvent mixture
(1). Wax from the primary stage is slurried with cold solvent and filtered
again in the repulp filter (4) to reduce the oil content to approximately
10%. The repulp filtrate is reused as dilution solvent in the feed-chilling
train.
The low-oil-content slack wax is then warmed by mixing with warm
solvent to melt the low-melting-point waxes (soft wax) and is filtered in
a third stage of filtration (5) to separate the hard wax from the soft wax.
The hard and soft wax mixtures are each routed to solvent-recovery sections (7,8) to strip solvent from the product streams (hard wax and soft
wax). The recovered solvent is collected, dried and recycled back to the
chilling and filtration sections.
Description: Diesel-weight streams from a variety of refinery sources

is combined with a small hydrogen stream and heated. Stream enters the
expanded fluid-bed reactor (1), where the proprietary sorbent removes
sulfur from the feed. The process can be designed to operate with no net
chemical hydrogen consumption.
Economics:
Investment (basis: 7,000-bpsd feedrate
capacity, 2002 U.S. Gulf Coast), $/bpsd
Fuel, 103 Btu (absorbed)
Electricity, kWh
Steam, lb
Installation: Seven in service.

Licensor: Bechtel Corp.
10,500
280
46
60
1,500
Products: A zero sulfur product for diesel motor fuels.
Regeneration: The sorbent is continuously withdrawn from the reactor and transferred to the regenerator section (2), where the sulfur is
removed as S02. The cleansed sorbent is reconditioned and returned to
the reactor. The rate of sorbent circulation is controlled to help maintain the desired sulfur concentration in the product.
General operating conditions:
Reactor temperature, F
700800
275500
The following example case studies show the performance of
S Zorb technology for processing various distillate streams.
Feed properties:
Sulfur ppm
API gravity
523
33.20
460
36.05
2,000
41.27
2,400
20.38
D86 IBP, F
385
346
291
409
10%
440
402
318
480
50%
513
492
401
537
90%
604
573
496
611
Product properties:
Sulfur, ppm API gravity
6
33.22
<1
36.23
<1
41.51
10
21.99
D86 IBP, F
380
347
290
409
10%
438
403
317
480
50%
513
491
400
537
90%
603
574
495
611
LHSV
2
2
6
1
H2 consumption, scf/bbl
5
15
42
186
Installation: Licensed for use at 28 sites, as of 2Q 2002.


104

3
Hydrocarbon
feedstock
Offgas
Additional
catalyst
volume
Electrical
power unit
START
7
4
1
Low-sulfur
product
Internal
electrodes
Demulsifier
chemical
PSA purified
hydrogen
Amine
absorber
New amine
absorber
H2S
LC
Effluent
water
6
H2 recycle
Feed
Desalted product
Alternate
Mixing
device
Process water
Diesel hydrotreatment
Electrical desalting
Application: Produce ultra-low sulfur diesel and high quality diesel

fuel (low aromatics, high cetane) via Prime-D toolbox of proven stateof-the art technology, catalysts and services.
Application: For removal of undesirable impurities such as salt,

water, suspended solids and metallic contaminants from unrefined crude
oil, residuums and FCC feedstocks.
Description: In the basic process as shown above, feed and hydrogen are
heated in the feed-reactor effluent exchanger (1) and furnace (2) and enter
the reaction section (3), with possible added volume for revamp cases. The
reaction effluent is cooled by exchanger (1) and air cooler (4) and separated
in the separator (5). The hydrogen-rich gas phase is treated in an existing
or new amine absorber for H2S removal (6) and recycled to the reactor. The
liquid phase is sent to the stripper (7) where small amounts of gas and naphtha are removed and high-quality product diesel is recovered.
Whether the need is for a new unit or for maximum reuse of existing
diesel HDS units, the Prime-D hydrotreating toolbox of solutions meets
the challenge. Process objectives ranging from low-sulfur, ultra-low sulfur, lowaromatics, and/or high cetane number are met with minimum cost by:
Selection of the proper catalyst from the HR 400 series, based on
the feed analysis and processing objectives. HR 400 catalysts cover the range
of ULSD requirements with highly active and stable catalysts. HR 426
CoMo exhibits high desulfurization rates at low-to-medium pressures,
HR 448 NiMo has higher hydrogenation activity at higher pressures, and
HR 468 NiCoMo is very effective for ULSD in the case of moderate pressures.
Use of proven, efficient reactor internals, EquiFlow, that allow nearperfect gas and liquid distribution and outstanding radial temperature
profiles.
Loading catalyst in the reactor(s) with the Catapac dense loading
technique for up to 20% more reactor capacity. Over 8,000 tons of catalyst have been loaded quickly and safely in recent years using the Catapac technique.
Application of Advanced Process Control for dependable operation and longer catalyst life.
Sound engineering design based on years of R&D, process design
and technical service feed-back to ensure the right application of the right
technology for new and revamp projects.
Whatever the diesel quality goalsULSD, high cetane or low aromaticsPrime-Ds Hydrotreating Toolbox approach will attain your
goals in a cost-effective manner.
Description: Salts such as sodium, calcium and magnesium chlorides

are generally contained in the residual water suspended in the oil phase
of hydrocarbon feedstocks. All feedstocks also contain, as mechanical suspensions, such impurities as silt, iron oxides, sand and crystalline salt. These
undesirable components can be removed from hydrocarbon feedstocks
by dissolving them in washwater or causing them to be water-wetted.
Emulsion formation is the best way to produce highly intimate contact
between the oil and washwater phases.
The electrical desalting process consists of adding process (wash) water
to the feedstock, generating an emulsion to assure maximum contact and
then utilizing a highly efficient AC electrical field to resolve the emulsion. The impurity-laden water phase can then be easily withdrawn as
underflow.
Depending on the characteristics of the hydrocarbon feedstock being
processed, optimum desalting temperatures will be in the range of 150F
to 300F. For unrefined crude feedstocks, the desalter is located in the
crude unit preheat train such that the desired temperature is achieved by
heat exchange with the crude unit products or pumparound reflux. Washwater, usually 3 to 6 vol%, is added upstream and/or downstream of the
heat exchanger(s). The combined streams pass through a mixing device
thereby creating a stable water-in-oil emulsion. Properties of the emulsion
are controlled by adjusting the pressure drop across the mixing device.
The emulsion enters the desalter vessel where it is subjected to a high
voltage electrostatic field. The electrostatic field causes the dispersed water
droplets to coalesce, agglomerate and settle to the lower portion of the
vessel. The water phase, containing the various impurities removed from
the hydrocarbon feedstock, is continuously discharged to the effluent
system. A portion of the water stream may be recycled back to the desalter
to assist in water conservation efforts. Clean, desalted hydrocarbon product flows from the top of the desalter vessel to subsequent processing
facilities.
Desalting and dehydration efficiency of the oil phase is enhanced by
using EDGE (Enhanced Deep-Grid Electrode) technology which creates both high and low intensity AC electrical fields inside the vessel.
Demulsifying chemicals may be used in small quantities to assist in
oil/water separation and to assure low oil contents in the effluent water.
Installation: Over 100 middle distillate hydrotreaters have been

licensed or revamped. They include 23 low- and ultra-low sulfur diesel
units ( < 50 ppm ), as well as a number of cetane boosting units. Most
of those units are equipped with Equiflow internals.
References: Getting Total Performance with Hydrotreating,
Petroleum Technology Quarterly, Spring 2002.
Premium Performance Hydrotreating with Axens HR 400 Series
Hydrotreating Catalysts, NPRA Annual Meeting, March 2002, San
Antonio.
The Hydrotreating Toolbox Approach, Harts European Fuel News,
May 29, 2002.

& Iron Co.


I 105

C4 raffinate
Methanol
Raffinate
Recycle methanol
START
Mixed C4s
START
C4 - C6
feed
4
2
3
5
Alcohol
Ethers
Water
1
MTBE
Ethers
Ethers
Application: Production of high-octane reformulated gasoline components (MTBE, ETBE, TAME and/or higher molecular-weight ethers)
from C1 to C2 alcohols and reactive hydrocarbons in C4 to C6 cuts.
Application: To produce high-octane, low-vapor-pressure oxygenates

such as methyl tertiary butyl ether (MTBE), tertiary amyl methyl ether
(TAME) or heavier tertiary ethers for gasoline blending to reduce olefin
content and/or meet oxygen/octane/vapor pressure specifications. The processes use boiling-point/tubular reactor and catalytic distillation (CD) technologies to react methanol (MeOH) or ethanol with tertiary isoolefins
to produce respective ethers.
Description: Different arrangements have been demonstrated depending on the nature of the feeds. All use acid resins in the reaction section.
The process includes alcohol purification (1), hydrocarbon purification
(2), followed by the main reaction section. This main reactor (3) operates under adiabatic upflow conditions using an expanded-bed technology and cooled recycle. Reactants are converted at moderate well-controlled
temperatures and moderate pressures, maximizing yield and catalyst life.
The main effluents are purified for further applications or recycle.
More than 90% of the total per pass conversion occurs in the expandedbed reactor. The effluent then flows to a reactive distillation system (4),
Catacol. This system, operated like a conventional distillation column,
combines catalysis and distillation. The catalytic zones of the Catacol use
fixed-bed arrangements of an inexpensive acidic resin catalyst that is available in bulk quantities and easy to load and unload.
The last part of the unit removes alcohol from the crude raffinate
using a conventional waterwash system (5) and a standard distillation
column (6).
Yields: Ether yields are not only highly dependent on the reactive olefins
content and the alcohols chemical structure, but also on operating goals:
maximum ether production and/or high final raffinate purity (for instance,
for downstream 1-butene extraction) are achieved.
Economics: Plants and their operations are simple. The same inexpensive (purchased in bulk quantities) and long lived, non-sophisticated
catalysts are used in the main reactor section catalytic region of the Catacol column, if any.
Installation: Over 25 units, including ETBE and TAME, have been
licensed. Twenty-four units, including four Catacol units, are in operation.
Description: For an MTBE unit, the process can be described as follows. Process description is similar for production of heavier ethers. The
C4s and methanol are fed to the boiling-point reactor (1)a fixed-bed,
downflow adiabatic reactor. In the reactor, the liquid is heated to its boiling point by the heat of reaction, and limited vaporization occurs. System pressure is controlled to set the boiling point of the reactor contents
and hence, the maximum temperatures. An isothermal tubular reactor is
used, when optimum, to allow maximum temperature control. The
equilibrium-converted reactor effluent flows to the CD column (2)
where the reaction continues. Concurrently, MTBE is separated from unreacted C4s as the bottom product.
This scheme can provide overall isobutylene conversions up to 99.99%.
Heat input to the column is reduced due to the heat produced in the boilingpoint reactor and reaction zone. Over time, the boiling-reactor catalyst loses
activity. As the boiling-point reactor conversion decreases, the CD reaction column recovers lost conversion, so that high overall conversion is sustained.
CD column overhead is washed in an extraction column (3) with a countercurrent water stream to extract methanol. The water extract stream is sent
to a methanol recovery column (4) to recycle both methanol and water.
C4s ex-FCCU require a well-designed feed waterwash to remove catalyst poisons for economic catalyst life and MTBE production.
Conversion: The information below is for 98% isobutylene conversion, typical for refinery feedstocks. Conversion is slightly less for ETBE
than for MTBE. For TAME and TAEE, isoamylene conversions of
95%+ are achievable. For heavier ethers, conversion to equilibrium limits are achieved.
Economics: Based on a 1,500-bpsd MTBE unit, (6,460-bpsd C4s exFCCU, 19% vol. isobutylene, 520-bpsd MeOH feeds) located on the U.S.
Gulf Coast, the inside battery limits investment is:
Investment, $ per bpsd of MTBE product
Typical utility requirements, per bbl of product
Electricity, kWh
Steam, 150-psig, lb
Steam, 50-psig, lb
Water, cooling (30 F rise), gal
3,500
0.5
210
35
1,050
Installation: Over 60 units are in operation using catalytic distillation

to produce MTBE, TAME and ETBE. More than 100 ether projects
have been awarded to CDTECH since the first unit came onstream in 1981.
Snamprogetti has over 20 operating ether units using tubular reactors.
Licensor: CDTECH (CDTECH and Snamprogetti are cooperating
to further develop and license their ether technologies.)
106

MTBE reactor Debutanizer
Water
wash
Methanol/water
separation
BB raffinate
4
9
8
2
C4 feedstock
10
Methanol
11
MTBE product
EthersMTBE
Fluid catalytic cracking
Application: The Uhde EDELEANU MTBE process combines

methanol and isobutene to produce the high-octane oxygenatemethyl
tertiary butyl ether (MTBE).
Application: Selective conversion of a wide range of gas oils into highvalue products. Typical feedstocks are virgin or hydrotreated gas oils but
may also include lube oil extract, coker gas oil and resid.
Feeds: C4 -cuts from steam cracker and FCC units with isobutene
contents range from 12% to 30%.
Products: High-octane gasoline, light olefins and distillate. Flexibillity of mode of operation allows for maximizing the most desirable product. The new Selective Component Cracking (SCC) technology maximizes propylene production.
Products: MTBE and other tertiary alkyl ethers are primarily used in
gasoline blending as an octane enhancer to improve hydrocarbon combustion efficiency.
Description: The Uhde Edeleanu technology features a two-stage reactor system of which the first reactor is operated in the recycle mode. With
this method, a slight expansion of the catalyst bed is achieved which ensures
very uniform concentration profiles within the reactor and, most important, avoids hot spot formation. Undesired side reactions such as the formation of dimethyl ether (DME) is minimized.
The reactor inlet temperature ranges from 45C at start-of-run to
about 60C at end-of-run conditions. One important factor of the twostage system is that the catalyst may be replaced in each reactor separately,
without shutting down the MTBE unit.
The catalyst used in this process is a cation-exchange resin and is available from several catalyst manufacturers. Isobutene conversions of 97% are
typical for FCC feedstocks. Higher conversions are attainable when processing steam-cracker C4-cuts that contain isobutene concentrations of
25%.
MTBE is recovered as the bottoms product of the distillation unit.
The methanol-rich C4-distillate is sent to the methanol-recovery section.
Water is used to extract excess methanol and recycle it back to process. The
isobutene-depleted C4-stream may be sent to a raffinate stripper or to a
molsieve-based unit to remove other oxygenates such as DME, MTBE,
methanol and tert-butanol.
Very high isobutene conversion, in excess of 99%, can be achieved
through a debutanizer column with structured packings containing additional catalyst. This reactive distillation technique is particularly suited
when the raffinate-stream from the MTBE unit will be used to produce
a high-purity butene-1 product.
For a C4-cut containing 22% isobutene, the isobutene conversion
may exceed 98% at a selectivity for MTBE of 99.5%.
Utility requirements, (C4-feed containing 21% isobutene; per ton
of MTBE):
Steam, MP, kg
Electricity, kWh
Water, cooling, m 3
Steam, LP, kg
100
35
15
900
Description: The Lummus process incorporates an advanced reaction

system, high-efficiency catalyst stripper and a mechanically robust, single-stage fast fluidized bed regenerator. Oil is injected into the base of the
riser via proprietary Micro-Jet feed injection nozzles (1). Catalyst and oil
vapor flow upwards through a short-contact time, all-vertical riser (2) where
raw oil feedstock is cracked under optimum conditions.
Reaction products exiting the riser are separated from the spent catalyst in a patented, direct-coupled cyclone system (3). Product vapors are
routed directly to fractionation, thereby eliminating nonselective, post-riser
cracking and maintaining the optimum product yield slate. Spent catalyst
containing only minute quantities of hydrocarbon is discharged from the
diplegs of the direct-coupled cyclones into the cyclone containment vessel (4). The catalyst flows down into the stripper (5).
Trace hydrocarbons entrained with spent catalyst are removed in the
stripper using stripping steam. The net stripper vapors are routed to the
fractionator via specially designed vents in the direct-coupled cyclones. Catalyst from the stripper flows down the spent-catalyst standpipe and through
the slide valve (6). The spent catalyst is then transported in dilute phase
to the center of the regenerator (8) through a unique square-bend-spent
catalyst transfer line (7). This arrangement provides the lowest overall
unit elevation. Catalyst is regenerated by efficient contacting with air for
complete combustion of coke. For resid-containing feeds, the optional
catalyst cooler is integrated with the regenerator. The resulting flue gas exists
via cyclones (9) to energy recovery/flue gas treating. The hot regenerated
catalyst is withdrawn via an external withdrawal well (10). The well allows
independent optimization of catalyst density in the regenerated catalyst
standpipe, maximizes slide valve (11) pressure drop and ensures stable
catalyst flow back to the riser feed injection zone.
Economics:
Investment (basis: 30,000 bpsd including reaction/regeneration
system and product recovery. Excluding offsites, power recovery and flue gas scrubbing U.S. Gulf Coast 2001.)
$/bpsd (typical)
2,2003,000
Utilities, typical per bbl fresh feed:
Electricity, kWh
0.81.0
Steam, 600 psig (produced)
50200
Maintenance, % of investment per year
23
Installation: Uhde Edeleanus proprietary MTBE process has been successfully applied in five refineries. The accumulated licensed capacity
exceeds 1 MMtpy.
Installation: Fourteen grassroots units in operation and one in design

stage. Fifteen units revamped and two in design stage.
Licensor: Uhde Edeleanu GmbH.

108

Vapor to fractionator
Vapor to fractionator
Flue gas
4
7
Flue gas
5
6
7
5
2
8
10
Feed
START
9
8
Application: FLEXICRACKING IIIR converts high-boiling hydrocarbons including residues, gasoils, lube extracts, and/or deasphalted
oils to higher value products.
Application: Conversion of gas oils and residues to high-value products using the efficient and flexible Orthoflow catalytic cracking process.
Products: Light olefins for gasoline processes and petrochemicals,

LPG, blend stocks for high-octane gasoline, distillates, and fuel oils.
Description: The FLEXICRACKING IIIR technology includes process design, hardware details, special mechanical and safety features,
control systems, flue gas processing options, and a full range of technical services and support. The reactor (1) incorporates many features to
enhance performance, reliability, and flexibility, including a riser (2)
with patented high efficiency close-coupled riser termination (3), enhanced
feed injection system (4), and efficient stripper design (5). The reactor
design and operation maximizes the selectivity of desired products, such
as naphtha and propylene.
The technology uses an improved catalyst circulation system with
advanced control features, including cold-walled slide valves (6). The single vessel regenerator (7) has proprietary process and mechanical features
for maximum reliability and efficient air/catalyst distribution and contacting (8). Either full or partial combustion is used. With increasing
residue processing and the need for additional heat balance control, partial burn operation with outboard CO combustion is possible, or KBR
dense phase catalyst cooler technology may be applied. The ExxonMobil
wet gas scrubbing or the ExxonMobil-KBR Cyclofines TSS technologies
can meet flue gas emission requirements.
Yields: Typical examples:
Resid feed VGO+lube extracts
mogas
distillate
operation
operation
VGO feed
mogas
operation
Feed
Gravity, API
22.9
22.2
25.4
Con carbon, wt%
3.9
0.7
0.4
Quality
80% Atm. Resid 20% Lube Extracts 50% TBP 794F
(Hydrotreated)
Product yields
Naphtha, lv% ff
78.2
40.6
77.6
(C4 /430F)
(C4 /260F)
(C4 /430F)
(C4 /FBP)
Mid Dist., lv% ff
13.7
49.5
19.2
(IBP/FBP)
(430/645F)
(260/745F)
(430/629F)
Products: Light olefins, high-octane gasoline, and distillate.

Description: The converter is a one-piece modularized unit that efficiently combines KBRs proven Orthoflow features with ExxonMobils
advanced design features. Regenerated catalyst flows through a wye (1)
to the base of the external vertical riser (2). Feed enters through the proprietary ATOMAX-2 feed injection system. Reaction vapors pass through
a patented right-angle turn (3) and are quickly separated from the catalyst in a patented closed-cyclone system (4). Spent catalyst flows through
a two-stage stripper equipped with DynaFlux baffles (5) to the regenerator (6) where advanced catalyst distribution and air distribution are used.
Either partial or complete CO combustion may be used in the regenerator, depending on the coke-forming tendency of the feedstock. The system uses a patented external flue gas plenum (7) to improve mechanical
reliability. Catalyst flow is controlled by one slide valve (8) and one plug
valve (9). An advanced dense-phase catalyst cooler (10) is used to optimize profitability when heavier feeds are processed.
Economics:
Investment (basis: 50,000-bpsd fresh feed including converter,
fractionator, vapor recovery and amine treating, but not
power recovery; battery limit, direct material and labor, 2002
Gulf Coast)
$ per bpsd
1,9502,150
Utilities, typical per bbl fresh feed
Electricity, kWh
0.71.0
Steam, 600 psig (produced) lb
40200
Catalyst, makeup, lb/bbl
0.100.15
Maintenance, % of plant replacement cost / yr
3
Installation: More than 150, resulting in a total of over 4 million bpd

fresh feed, with 20 designed in the past 12 years.
References: New developments in FCC feed injection and stripping
technologies, NPRA 2000 Annual Meeting, March 2000.
RegenMax technology: staged combustion in a single regenerator,
NPRA 1999 Annual Meeting, March 1999.
Licensor: Kellogg Brown & Root, Inc.
Installation: More than 70 units with a design capacity of over 2.5million bpd fresh feed.
References: Ladwig, P. K., Exxon FLEXICRACKING IIIR fluid catalytic cracking technology, Handbook of Petroleum Refining Processes, Second Ed., R. A. Meyers, Ed., pp. 3.33.28.
Licensor: ExxonMobil Research & Engineering Co. and Kellogg
Brown & Root, Inc.

110

Shell 2 vessel design
Shell external reactor design

External
cyclones
To fractionator
Integral
TSS
Reactor
Prestripping
reactor
cyclone
Close
coupled
cyclones
Advanced
spent cat
inlet device
Staged
stripping
Riser
internals
Counter
current
regen.
Coldwall
construction
High
preformance
nozzles
Product vapors
To fractionator
Proprietary riser
termination device
Packed stripper
Regenerator
Staged
stripping
Counter
current
regen
Riser
internals
High preformance
nozzles
4
Combustion air
Regen. cat. standpipe
1
2
Coldwall
construction
Reactor riser
MTC system
Feed nozzles
Application: The Shell FCC process converts heavy petroleum distillates and residues to high-value products. Profitability is increased by a reliable and robust process, which has flexibility to process heavy feeds and maximize product upgrading including propylene production where required.
Application: Selective conversion of gas oil feedstocks.
Products: Light olefins, LPG, high-octane gasoline, distillate and

propylene.
Description: Hydrocarbon is fed to a short contact-time-riser by
Shells high performance feed nozzle system, ensuring good mixing and
rapid vaporisation. Proprietary riser internals lower pressure drop and
reduce back mixing. The riser termination design provides rapid catalyst/hydrocarbon separation to maximise desired product yields and a
staged stripper achieves low hydrogen in coke without excessive gas or coke
formation. A single stage partial burn regenerator delivers excellent performance at low cost (full burn can also be applied). Cat coolers can be
added for feedstock flexibility. Flue gas cleanup is by Shells third stage
separator and power recovery can be incorporated if justified.
There are currently two FCC design configurations. The Shell 2 Vessel
design is recommended for feeds (including residue) with mild coking tendencies, the incorporation of reactor and regenerator elements within the
vessels leads to low capital expenditure. The Shell External Reactor design is
the preferred option for heavy feeds with high coking tendencies, delivering
improved robustness.The pre-stripping cyclone positioned inside the roughcut cyclones prevents post riser coke make and the external reactor design eliminates stagnant areas for coke growth. Cost effectiveness is achieved through
a simple, low-elevation design. Proprietary catalyst circulation enhancement
techniques are vital in achieving that. The designs have proven to be reliable due to incorporation of Shells extensive operating experience.
Shell can also provide advanced distillation designs, advanced process control and optimizers as part of an integrated FCC design solution.
Installation: Shell has designed and licensed over 30 grassroots units,
including seven for residue feed. Shell has revamped over 30 units, including the designs of other licensors. Shell has converted seven existing distillate units to residue operation. A Shell close-coupled riser termination
system has been designed for 14 units, Shells high performance feed
nozzles for 15 units, catalyst circulation enhancement for 8 units and thirdstage separators for 58 units. Many licenses are for non-Shell customers.
Shell has over 1,000+ years of own FCC operational experience.
Reference: Chapter FCC, Handbook Fluidization, Wen-Cing Yang,
Ed., 2002.
FCC cyclonesa vital elment in profitability, Petroleum Technology Quarterly, Spring, 2001.
New advances in third-stage separators, World Refining, October
2000.
Update on Shell Residue FCC Process and Operation, AIChE 1998
Spring Meeting.Design and Operation of Shells Residue Catalytic Crackers in East Asia, ARTC 1998 Conference.
Products: High-octane gasoline, distillate and C3 C4 olefins.

Description: Catalytic and selective cracking in a short-contact-time
riser (1) where oil feed is effectively dispersed and vaporized through a
proprietary feed-injection system. Operation is carried out at a temperature consistent with targeted yields. The riser temperature profile can
be optimized with the proprietary mixed temperature control (MTC) system (2). Reaction products exit the riser-reactor through a high-efficiency,
close-coupled, proprietary riser termination device RS2 (Riser Separator
Stripper) (3). Spent catalyst is pre-stripped followed by an advanced
high-efficiency packed stripper prior to regeneration. The reaction product vapor may be quenched using Amocos proprietary technology to give
the lowest possible dry gas and maximum gasoline yield. Final recovery
of catalyst particles occurs in cyclones before the product vapor is transferred to the fractionation section.
Catalyst regeneration is carried out in a single regenerator (4) equipped
with proprietary air and catalyst distribution systems, and may be operated for either full or partial CO combustion. Heat removal for heavier
feedstocks may be accomplished by using reliable dense-phase catalyst
cooler, which has been commercially proven in over 24 units and is
licensed exclusively by Stone & Webster/Axens. As an alternative to catalyst cooling, this unit can easily be retrofitted to a two-regenerator system in the event that a future resid operation is desired.
The converter vessels use a cold-wall design that results in minimum
capital investment and maximum mechanical reliability and safety. Reliable operation is ensured through the use of advanced fluidization technology combined with a proprietary reaction system. Unit design is tailored to the refiners needs and can include wide turndown flexibility.
Available options include power recovery, wasteheat recovery, flue gas
treatment and slurry filtration. Revamps incorporating proprietary feed
injection and riser termination devices and vapor quench result in substantial improvements in capacity, yields and feedstock flexibility within
the mechanical limits of the existing unit.
Installation: Stone & Webster and Axens have licensed 26 full-technology units and performed more than 100 revamp projects.
Reference: Letzsch, W. S., 1999 FCC Technology Advances, 1999
Stone & Webster Eleventh Annual Refining Seminar at NPRA Q&A, Dallas, Oct. 5, 1999.
Licensor: Stone & Webster Inc., a Shaw Group Co./Axens, IFP Group
Technologies


I 111

To fractionation
FCC
Combustor-style
regenerator
Flue gas
Combuster
riser
12
Primary
1st
air
stage
2nd stage
3
Feed
2
1
Air
Lift media
Lean amine
Feed gas
10
Catalyst
transfer line
Secondary
air
Acid gas
to Claus
Rich amine
11
6
Treated gas
Flue gas
Hot-catalyst
circulation
Catalyst
cooler
To fractionation
RFCC
Two-stage
regenerator
Catalyst 3
cooler
2
Feed
2
1
Lift media
Gas treatingH2S removal
Application: Selectively convert gas oils and resid feedstocks into

higher-value products using the FCC/RFCC/PETROFCC process.
Products: Light olefins (for alkylation, polymerization, etherification
or petrochemicals), LPG, high-octane gasoline, distillates and fuel oils.
Description: The combustor-style unit is used to process gas oils and
moderately contaminated resids, while the two-stage unit is used for
more contaminated resids.
In either unit style, the reactor section is similar. A lift media of light
hydrocarbons, steam or a mixture of both contacts regenerated catalyst at
the base of the riser (1). This patented acceleration zone (2), with elevated Optimix feed distributors (3), enhances the yield structure by effectively contacting catalyst with finely atomized oil droplets.
The reactor zone features a short-contact-time riser and a state-of-the-art
riser termination device (4) for quick separation of catalyst and vapor, with
high hydrocarbon containment (VSS/VDS technology). This design offers
high gasoline yields and selectivity with low dry gas yields. Steam is used in
an annular stripper (5) to displace and remove entrained hydrocarbons from
the catalyst. Existing units can be revamped to include these features (15).
The combustor-style regenerator (6) burns coke, in a fast-fluidized
environment, completely to CO2 with very low levels of CO. The circulation of hot catalyst (7) from the upper section to the combustor provides added control over the burn-zone temperature and kinetics and
enhances radial mixing. Catalyst coolers (8) can be added to new and
existing units to reduce catalyst temperature and increase unit flexibility
for commercial operations of feeds up to 6 wt% Conradson carbon.
For heavier resid feeds, the two-stage regenerator is used. In the first
stage, upper zone (9), the bulk of the carbon is burned from the catalyst,
forming a mixture of CO and CO2. Catalyst is transferred to the second
stage, lower zone (10), where the remaining coke is burned in complete
combustion, producing low levels of carbon on regenerated catalyst. A catalyst cooler (11) is located between the stages. This configuration maximizes
oxygen use, requires only one train of cyclones and one flue gas stream (12),
avoids costly multiple flue gas systems and creates a hydraulically-simple
and well-circulating layout. The two-stage regenerator system has processed
feeds up to 10 wt% Conradson carbon.
PETROFCC is a customized application using mechanical features such
as RxCAT technology for recontacting carbonized catalyst, high-severity
processing conditions and selected catalyst and additives to produe high
yields of propylene, light olefins and aromatics for petrochemical applications.
Installations: All of UOPs technology and equipment are commercially
proven for both process performance and mechanical reliability. UOP has been
an active designer and licensor of FCC technology since the early 1940s and has
licensed more than 210 FCC, Resid FCC, and MSCC process units. Today, more
than 150 of these units are operating worldwide. In addition to applying our
technology and skills to new units, UOP is also extensively involved in the revamping of existing units. During the past 15 years, UOPs FCC Engineering department has undertaken 40 to 60 revamp projects or studies per year.
Application: Remove H2S selectively, or remove a group of acidic

impurities (H2S, CO2, COS, CS2 and mercaptans) from a variety of
streams, depending on the solvent used. FLEXSORB SE technology
has been used in refineries, natural gas production facilities and petrochemical operations.
Licensor: UOP LLC.

112
FLEXSORB SE or SE Plus solvent is used on: hydrogenated Claus plant

tail gas to give H2S, ranging down to H2S <10 ppmv; pipeline natural
gas to give H2S <0.25 gr/100 scf; or Flexicoking low Btu fuel gas. The
resulting acid gas byproduct stream is rich in H2S.
Hybrid FLEXSORB SE solvent is used to selectively remove H2S, as
well as organic sulfur impurities commonly found in natural gas.
FLEXSORB PS solvent yields a treated gas with: H2S <0.25 gr/100 scf,
CO2 <50 ppmv, COS and CS2 <1 ppmv, mercaptans removal >95%.
This solvent is primarily aimed at natural gas or syngas cleanup. The
byproduct stream is concentrated acid gases.
Description: A typical amine system flow scheme is used. The feed
gas contacts the treating solvent in the absorber (1). The resulting rich
solvent bottom stream is heated and sent to the regenerator (2). Regenerator heat is supplied by any suitable heat source. Lean solvent from the
regenerator is sent through rich/lean solvent exchangers and coolers
before returning to the absorber.
FLEXSORB SE solvent is an aqueous solution of a hindered amine.
FLEXSORB SE Plus solvent is an enhanced aqueous solution, which has
improved H2S regenerability yielding <10 vppm H2S in the treated gas.
Hybrid FLEXSORB SE solvent is a hybrid solution containing FLEXSORB
SE amine, a physical solvent and water. FLEXSORB PS solvent is a hybrid
consisting of a different hindered amine, a physical solvent and water.
Economics: Lower investment and energy requirements based primarily
on requiring 30% to 50% lower solution circulation rates.
Installations: Total gases treated by FLEXSORB solvents are about
2 billion scfd and the total sulfur recovery is about 900 long tpd.
FLEXSORB SE26 plants operating, two startups in 2002, one in
design
FLEXSORB SE Plus14 plants operating, one startup in 2002, one
in design
Hybrid FLEXSORB SEtwo plants operating
FLEXSORB PSfour plants operating and one startup scheduled
in 2000.
Reference: Garrison, J., et al, Keyspan Energy Canada Rimbey acid
gas enrichment with FLEXSORB SE Plus technology, 2002 Laurance
Reid Gas Conditioning Conference, Norman, Oklahoma.
Adams-Smith, J., et al, Chevron USA Production Company Carter
Creek Gas Plant FLEXSORB tail gas treating unit, 2002 GPA Annual
Meeting, Dallas.
Licensor: ExxonMobil Research and Engineering Co.

SO2 & CO2
Oil
Scrubber
Syngas
Sorber 1
Steam
2
Regen.
Oxygen
Boiler
Reactor
BFW
Fuel gas
Nitrogen
Bleed to SWS
Filtercake
work up
Effluent
boiler
Soot
quench
To SRU
Air
Ni/V
ash
Filtration
Hydrogen
Charge
heater
Recycle
compressor
Stabilizer
Process
steam
Steam
Cat.
gasoline
Product
separator
Desulfurized
product
Gasification
Gasoline desulfurization
Application: The Shell Gasification Process (SGP) converts the heaviest residual liquid hydrocarbon streams with high-sulfur and metals
content into a clean synthesis gas and valuable metal oxides. Sulfur (S)
is removed by normal gas treating processes and sold as elemental S.
The process converts residual streams with virtually zero value as fuelblending components into valuable, clean gas and byproducts. This gas can
be used to generate power in gas turbines and for making H2 by the wellknown shift and PSA technology. It is one of the few ultimate, environmentally acceptable solutions for residual hydrocarbon streams.
Application: Convert high-sulfur gasoline streams into a low-sulfur

gasoline blendstock using S Zorb sulfur-removal technology.
Products: Synthesis gas (CO+H2), sulfur and metal oxides.
Regeneration: The sorbent (catalyst) is continuously withdrawn

from the reactor and transferred to the regenerator section (2), where the
sulfur is removed as SO2 and sent to a sulfur-recovery unit. The cleansed
sorbent is reconditioned and returned to the reactor. The rate of sorbent
circulation is controlled to help maintain the desired sulfur concentration in the product.
Process description: Liquid hydrocarbon feedstock (from very

light such as natural gas to very heavy such as vacuum flashed cracked
residue, VFCR and ashphalt ) is fed into a reactor, and gasified with pure
O2 and steam. The net reaction is exothermic and produces a gas primarily
containing CO and H2. Depending on the final syngas application,
operating pressures, ranging from atmospheric up to 65 bar, can easily
be accommodated. SGP uses refractory-lined reactors that are fitted
with both burners and a heat-recovery-steam generator, designed to produce high-pressure steamover 100 bar (about 2.5 tons per ton feedstock).
Gases leaving the steam generator are at a temperature approaching the
steam temperature; thus further heat recovery occurrs in an economizer.
Soot (unconverted carbon) and ash are removed from the raw gas by
a two-stage waterwash. After the final scrubbing, the gas is virtually particulate-free; it is then routed to a selective-acid-gas-removal system. Net
water from the scrubber section is routed to the soot ash removal unit
(SARU ) to filter out soot and ash from the slurry. By controlled oxidation
of the filtercake, the ash components are recovered as valuable oxides
principally vanadium pentoxide. The (clean) filtrate is returned to the
scrubber.
A related processthe Shell Coal Gasification Process (SCGP)gasifies solids such as coal or petroleum coke. The reactor is different, but
main process layout and work-up are similar.
Installation: Over the past 40 years, more than 150 SGP units have
been installed, that convert residue feedstock into synthesis gas for chemical applications. The latest, flagship installation is in the Shell Pernis refinery near Rotterdam, The Netherlands. This highly complex refinery
depends on the SGP process for its H2 supply. Similar projects are underway in India and Italy.
The Demkolec Power plant at Buggenum, The Netherlands produces
250 Mwe based on the SCGP process. The Shell middle distillate synthesis
plant in Bintulu, Malaysia, uses SGP to convert 100 million scfd of natural gas into synthesis gas used for petrochemical applications.
Products: A zero sulfur blending stock for gasoline motor fuels.

Description: Gasoline from the fluid catalytic cracker unit is combined
with a small hydrogen stream and heated. Vaporized gasoline is injected
into the expanded fluid-bed reactor (1), where the proprietary sorbent
removes sulfur from the feed. A disengaging zone in the reactor removes
suspended sorbent from the vapor, which exits the reactor to be cooled.
Economics:
General operating conditions:
Temperature, F
650775
Pressure, psig
100300
Space velocity, whsv
410
Hydrogen purity, %
7099
4060
Total H2 usage, scf/bbl
Case study premises:
25,000-bpd feed
775-ppm feed sulfur
25-ppm product sulfur (97% removal)
No cat gasoline splitter
Results:
~ 100
C5+ yield, vol% of feed
Lights yield, wt% of feed
< 0.2
(R+M) Loss
2
0.6 (or <0.6)
Capital cost, $/bbl
900
Operating cost, /gal *
0.9
* Includes utilities, 4% per year maintenance and sorbent costs.
Installation: Forty-three sites licensed as of 2Q 2002.

Reference: Shell Gasification Process, AIChE Spring National

Meeting, March 59, 2000. Shell Pernis Netherlands Refinery Residue
Gasification Project, 1999 Gasification Technologies Conference, San
Francisco, Oct. 1720, 1999.

I 113

Air Steam
LCN to TAME or alky. unit

Fuel gas
Splitter
(optional)
Prime-G+
dual catalyst
reactor system
Selective
hydro.
Feed
START
HCN
H2S gas
Clean gas
SO2
Furnace/
boiler
NH3
Absorber
AHS soln.
Stabilizer
SWS gas (H2S, NH3)
ATS
reactor
Ultra-low
sulfur
gasoline
NH3
60% ATS soln.

NH4HSO3
Absorber: SO2 + NH3 + H2O
ATS reactor: 4 NH4HSO3 + 2 H2S + 2 NH3
Hydrogen
makeup
H2O
3 (NH4)2S2O3 + 3 H2O
Gasoline desulfurization, ultra-deep
H2S and SWS gas conversion
Application: Ultra-deep desulfurization of FCC gasoline with minimal octane penalty using Prime-G+ process.
Application: The ATS process recovers H2S and NH3 in amine

regenerator offgas and sour water stripper gas (SWS gas) as a 60% aqueous solution of ATSammonium thiosulfate, (NH3)2S2O3, which is the
standard commercial specification. The ATS process can be combined with
a Claus unit; thus increasing processing capacity while obtaining a total
sulfur recovery of >99.95%.
ATS is increasingly used as a fertilizer (12-0-0-26S) for direct application and as component in liquid fertilizer formulations.
Description: FCC debutanizer bottoms are fed directly to a first

reactor wherein, under mild conditions diolefins are selectively hydrogenated and mercaptans are converted to heavier sulfur species. The
selective hydrogenation reactor effluent is then usually split to produce
a LCN (light cat naphtha) cut and a HCN (heavy cat naphtha).
The LCN stream is mercaptans free with a low sulfur and diolefin
concentration enabling further processing in an etherification or alkylation unit. The HCN then enters the main Prime-G+ section where it
undergoes in a dual catalyst reactor system; a deep HDS with very limited
olefins saturation and no aromatics losses produces an ultra-low sulfur
gasoline.
The process provides flexibility to advantageously co-process other
sulfur containing naphthas such as light coker naphtha, steam cracker
naphtha or light straight-run naphtha.
Industrial results:
Full-range FCC Gasoline,
40C220C
Sulfur, ppm
(RON + MON)/2
(RON + MON)/2
% HDS
30 ppm pool sulfur after blending
Feed
2100
87.5
Prime-G+
Product
50*
86.5
1.0
97.6
Pool sulfur specifications as low as less than 10 ppm are attained with
the Prime-G+ process in two units in Germany.
Economics:
Investment:
Grassroots ISBL cost, $/bpsd
600800
Description: Amine regenerator off gas is combusted in a burner/wasteheat boiler. The resulting SO2 with ammonia is absorbed in a two-stage
absorber to form ammonium hydrogen sulfate (AHS). NH3 and H2S contained in the SWS gas plus imported ammonia (if required) is reacted with
the AHS solution in the ATS reactor. The ATS product is withdrawn as
a 60% aqueous solution that meets all commercial specifications for
usage as a fertilizer. Unreacted H2S is vented to the H2S burner.
Except for the H2S burner/waste-heat boiler, all process steps occurs
in the water phase at moderate temperatures and neutral pressure. The
AHS absorber and ATS reactor systems are chilled with cooling water.
More than 99.95% of the sulfur and practically 100% of the ammonia contained in the feed-gas streams are recovered. Typical emission values are:
SOx
NOx
H2S
NH3
<100 ppmv
<50 ppmv
<1 ppmv
<20 ppmv
Installation: One Topse 30,000-mtpy ATS plant is operating in

Northern Europe.
Installation: Fifty-three units have been licensed for a total capacity

of 1.4 million bpsd. Four Prime-G+ units are already in operation, producing ultra-low sulfur gasoline. Four other units will come onstream at
the end of 2002.
OATS process: In addition to the Prime-G+ technology, the OATS
(olefins alkylation of thiophenic sulfur), initially developed by BP, is
also exclusively offered for license by Axens for ultra-low sulfur gasoline
production.
Reference: Prime-G+: From pilot to start-up of worlds first commercial 10 ppm FCC gasoline desulfurization process, NPRA Annual
Meeting, March 1719, 2002, San Antonio.

114

Fuel gas
Fuel gas
High-pressure
section
H2
makeup
Light
gas oil
LC-Fining
reactor
Makeup hydrogen
Recycle
H2
Stm.
6
2
5
1
Low-pressure
section
Diesel
Wild naphtha
Hydrocarbon
feed
Feed
Low-sulfur VGO
START
START
Products
Hydrocracking
Hydrocracking
Application: Upgrade vacuum gas oil alone or blended with various

feedstocks (light-cycle oil, deasphalted oil, visbreaker or coker-gas oil).
Application: Desulfurization, demetallization, CCR reduction, and

hydrocracking of atmospheric and vacuum resids using the LC-Fining process.
Products: Middle distillates, very-low-sulfur fuel oil, extra-quality

FCC feed with limited or no FCC gasoline post-treatment or high VI lube
base stocks.
Description: This process uses a refining catalyst usually followed by
a zeolite-type hydrocracking catalyst. Main features of this process are:
High tolerance toward feedstock nitrogen
High selectivity toward middle distillates
High activity of the zeolite, allowing for 34 year cycle lengths and
products with low aromatics content until end of cycle.
Three different process arrangements are available: single-step/oncethrough; single-step/total conversion with liquid recycle; and two-step
hydrocracking. The process consists of: reaction section (1, 2), gas separator (3), stripper (4) and product fractionator (5).
Product quality: Typical for HVGO (50/50 Arabian light/heavy):
Sp. gr.
TBP cut point, C
Sulfur, ppm
Nitrogen, ppm
Metals, ppm
Cetane index
Flash pt., C
Smoke pt., mm, EOR
Aromatics, vol%, EOR
Viscosity @ 38C, cSt
PAH, wt%, EOR
Feed,
HVGO
0.932
405565
31,700
853
<2
110
Jet
fuel
0.800
140225
<10
<5
40
2628
< 12
Diesel
0.826
225360
<10
<5
62
125
<8
5.3
<2
Economics:
Investment (basis: 40,000-bpsd unit, once-through, 90% conversion, battery limits, erected, engineering fees included, 2000
Gulf Coast), $ per bpsd
2,000 2,500
Fuel oil, kg
5.3
Electricity, kWh
6.9
0.64
Water, cooling, m3
Steam, MP
balance
Installation: Fifty references, cumulative capacity exceeding 1 million bpsd, conversion ranging from 20% to 99%.
Products: Full range of high quality distillates. Residual products can

be used as fuel oil, synthetic crude or feedstock for a resid FCC, coker,
visbreaker or solvent deasphalter.
Description: Fresh hydrocarbon liquid feed is mixed with hydrogen
and reacted within an expanded catalyst bed (1) maintained in turbulence
by liquid upflow to achieve efficient isothermal operation. Product quality is maintained constant and at a high level by intermittent catalyst addition and withdrawal. Reactor products flow to a high-pressure separator
(2), low-pressure separator (3) and product fractionator (4). Recycle
hydrogen is separated (5) and purified (6).
Process features include on stream catalyst addition and withdrawal.
Recovering and purifying the recycled H2 at low pressure rather than at
high pressure can result in lower capital cost and allows design at lower gas
rates.
Operating conditions: Typical reactor temp., 725F to 840F; reactor press., 1,400 to 3,500 psig; H2 part. press., 1,000 to 2,700 psig; LHSV,
0.1 to 0.6; conversion, 40% to 97+%; desulfurization, 60% to 90%;
demetallization, 50% to 98%; CCR reduction, 35% to 80%.
Yields: For Arabian Heavy/Arabian Light blends:
Feed
Atm. resid
Gravity, API
12.40
Sulfur, wt%
3.90
Ni/ V, ppmw
18/65
Conversion vol%
(1,022F+)
45
Products, vol%
1.11
C4
6.89
C5350F
350700F (650F) (15.24)
700 (650F)1,022F (55.27)
25.33
1,022F+
23.7/0.54
C5+API/wt%S
4.73
4.97
39/142
Vac. resid
4.73
4.97
39/142
4.73
4.97
39/142
60
75
95
2.35
12.60
30.62
21.46
40.00
22.5/0.71
3.57
18.25
42.65
19.32
25.00
26.6/0.66
5.53
23.86
64.81
11.92
5.0
33.3/0.33
Economics: Investment,estimated (U.S. Gulf Coast, 2000)

Size, bpsd fresh feed
92,000
49,000
$ per bpsd
(typical) fresh feed
2,200 3,500
4,200
5,200
Utilities, per bbl fresh feed
3
56.1
62.8
69.8
88.6
Fuel fired, 10 Btu
Electricity, kWh
8.4
13.9
16.5
22.9
Steam (export), lb
35.5
69.2
97.0
97.7
Water, cooling, gal
64.2 163
164
248
Installation: Four LC-Fining units in operation, one LC-Fining unit

in construction and two LC-Fining units in engineering.
Licensor: Chevron Lummus Global LLC.

I 115

Fresh gas
Recycle gas
Quench gas
Process gas
Wash
water
START
CHP
separator
Light naphtha
Feed
Heavy naphtha
6
7
Kerosine
Diesel
Fractionator
HHP
separator
HLP
separator
Feed
Makeup
hydrogen
370
Recycle
compressor
H2S
CLP
separator
370+
Bleed
START
Sour water
Hydrocracking
Hydrocracking
Application: Convert naphthas, AGO, VGO and cracked oils from

FCCs, cokers, hydroprocessing plants and SDA plants using the Chevron
Isocracking process.
Application: The Shell hydrocracking process converts heavy VGO

and other low-cost cracked and extracted feedstocks to high-value, highquality products. Profitability is maximized by careful choice of process
configuration, conditions and catalyst system to match refiners product
quality and selectivity requirements.
Products: Lighter, high-quality, more valuable products: LPG, gasoline, catalytic reformer feed, jet fuel, kerosine, diesel, lube oils and feeds
for FCC or ethylene plants.
Description: A broad range of both amorphous/zeolite and zeolite catalysts are used to obtain an exact match with the refiners process objective. An extensive range of proprietary amorphous/zeolitic catalysts and
various process configurations are used to match the refiners process objectives. Generally, a staged reactor system consists of one reactor (1, 4) and
one HP separator (2, 5) per stage optional recycle scrubber (3), LP separator (6) and fractionator (7) to provide flexibility to vary the light-toheavy product ratio and obtain maximum catalytic efficiency. Single-stage
options (both once-through and recycle) are also used when economical.
Yields: Typical from various feeds:
Feed
Naphtha
Catalyst stages
1
Gravity, API
72.5
ASTM 10%/EP, F
154/290
Sulfur, wt%
0.005
Nitrogen, ppm
0.1
Yields, vol%
Propane
55
iso-Butane
29
n-Butane
19
Light naphtha
23
Heavy naphtha
Kerosine
Diesel
Product quality
Kerosine smoke pt., mm
Diesel Cetane index
Kerosine freeze pt., F
Diesel pour pt., F
LCO
VGO
VGO
2
2
2
24.6
25.8
21.6
478/632 740/1,050 740/1,100
0.6
1.0
2.5
500
1,000
900
3.4
9.1
4.5
30.0
78.7
3.0
3.0
11.9
14.2
86.8
28
65
2.5
2.5
7.0
7.0
48.0
50.0
28
58
75
10
Economics:
Investment (basis: 30,000 bpsd maximum conversion unit, MidEast VGO feed, includes only on-plot facilities and first catalyst
charge, 2002 U.S. Gulf Coast), $ per bpsd
3,000
Fuel, equiv. fuel oil, gal
1
Electricity, kWh
7
Steam, 150 psig (net produced), lb
(50)
Water, cooling, gal
330
Products: Low-sulfur diesel and jet fuel with excellent combustion properties, high-octane light gasoline, and high-quality reformer, cat cracker,
ethylene cracker or lube oil feedstocks.
Description: Heavy hydrocarbons are discharged to the reactor circuit and preheated with reactor effluent (1). Fresh hydrogen is discharged
to the reactor circuit and combined with recycle gas from the cold highpressure separator. The mixed gas is supplied as quench for reactor
interbed cooling with the balance first preheated with reactor effluent followed by further heating in a single phase furnace. After mixing with the
liquid feed, the reactants pass in trickle flow through the multi-bed reactor(s) which contains proprietary pre-treat, cracking and post-treat catalysts (2). Interbed ultra-flat quench internals and high dispersion nozzle trays combine excellent quench, mixing and liquid flow distribution
at the top of each catalyst bed while maximizing reactor volume utilization. After cooling by incoming feed streams, reactor effluent enters a fourseparator system from which hot effluent is routed to the fractionator (3).
Wash water is applied via the cold separators in a novel countercurrent
configuration to scrub the effluent of corrosive salts and avoid equipment
corrosion.
Two-stage, series flow and single-stage unit design configurations are
all available including the single reactor stacked catalyst bed which is suitable for capacities up to 10,000 tpd in partial or full conversion modes. The
catalyst system is carefully tailored for the desired product slate and cycle
run length.
Installation: Over 20 new distillate and lube oil units including two
recent single-reactor high-capacity stacked bed units. Over a dozen
revamps have been carried out on own and other licensor designs usually to debottleneck and increase feed heaviness.
References: Performance optimisation of trickle bed processes,
European Refining Technology Conference, Berlin, November 1998;
Design and operation of Shell single reactor hydrocrackers, 3rd International Petroleum Conference, New Delhi, January 1999.
Installation: More than 50 units exceeding 750,000 bpsd total capacity.

Licensor: Chevron Lummus Global LLC.

116

Straight run distillates
Wash
water
Makeup
hydrogen
Vacuum residue
Recycle
gas
Additive
1
2
Flash gas
5
Fresh feed
To fractionator
START
Offgas
Sour water
Recycle oil
Syncrude
Waste water
Hydrogen
Hydrogenation residue
To fractionator
Hydrocracking
Hydrocracking
Application: Convert a wide variety of feedstocks into lower-molecular-weight products using the Unicracking and HyCycle Unicracking
process.
Application: Upgrading of heavy and extra heavy crudes as well as residual oils.
Feed: Feedstocks include atmospheric gas oil, vacuum gas oil, FCC/RCC
cycle oil, coker gas oil, deasphalted oil and naphtha for production of LPG.
Products: Processing objectives include production of gasoline, jet fuel,
diesel fuel, lube stocks, ethylene-plant feedstock, high-quality FCC feedstock and LPG.
Description: Feed and hydrogen are contacted with catalysts, which
induce desulfurization, denitrogenation and hydrocracking. Catalysts
are based upon both amorphous and molecular-sieve containing supports.
Process objectives determine catalyst selection for a specific unit. Product from the reactor section is condensed, separated from hydrogen-rich
gas and fractionated into desired products. Unconverted oil is recycled
or used as lube stock, FCC feedstock or ethylene-plant feedstock.
Yields: Example:
FCC cycle
Feed type
oil blend
Gravity, API
27.8
Boiling, 10%, F
481
End pt., F
674
Sulfur, wt%
0.54
Nitrogen, wt%
0.024
Principal products
Gasoline
Yields, vol% of feed
Butanes
16.0
Light gasoline
33.0
Heavy naphtha
75.0
Jet fuel
Diesel fuel
600F + gas oil
H2 consump., scf/bbl 2,150
Vacuum
Fluid coker
gas oil
gas oil
22.7
8.4
690
640
1,015
1,100
2.4
4.57
0.08
0.269
Jet
Diesel FCC feed
6.3
12.9
11.0
89.0
1,860
3.8
7.9
9.4
5.2
8.8
31.8
94.1
33.8
35.0
2,500
1,550
Economics: Example:
Investment, $ per bpsd capacity
Fuel, 103 Btu
Electricity, kWh
2,000 4,000
70 120
710
Installation: Selected for 151 commercial units, including several converted from competing technologies. Total capacity exceeds 3.4 million
bpsd.
Licensor: UOP LLC.
Products: Full-range high-quality syncrude.

Description: A hydrogen addition process applying the principles of
thermal hydrocracking in liquid-phase hydrogenation reactors (LPH) (1)
for primary conversion directly coupled with an integrated catalytical
hydrofinishing step (GPH). In the LPH slurry phase reactors, residue is
converted up to 95% at temperatures between 440C and 500C. In the
hot separator (HS) (2), light distillates are separated from the unconverted
material. By vacuum-flash distillation (3), the HS bottoms distillates are
recovered. For further hydrotreating, the HS overheads, together with the
recovered HS bottoms distillates and straight-run distillates (optional),
are routed to the catalytical fixed-bed reactors of the GPH (4), which operates at the same pressure as the LPH. GPH pressure is typically above
hydrocracking conditions, therefore, GPH mild hydrocracking can also
be applied to allow a shift in yield structure to lighter products. Separation of syncrude and associated gases is performed in a cold separator system (5). The syncrude after separation is sent to a stabilizer (6) and a fractionation unit. After being washed in a lean oil scrubber (7), the gases are
recycled to the LPH section.
Feed: Feedstock quality ranges covered are:
Gravity, API
Sulfur, wt%
Metals (Ni,V), ppm
Asphaltenes, wt%
3 to 14
0.7 to 7
up to 2,180
2 to 80
Yields:
Naphtha <180C, wt%
Middle distillates, wt%
Vac. gasoil >350C, wt%
1530
3540
1530
Product qualities:
Naphtha: Sulfur < 5 ppm, Nitrogen < 5 ppm
Kerosine: Smoke point >20 mm, Cloud point <-50C
Diesel: Sulfur <50 ppm, Cetane no. > 45
Vac. gasoil: Sulfur <150 ppm, CCR <0.1wt%, Metals <1 ppm
Economics: Plant capacity 23,000 bpsd.

Investment U.S. MM$190 (U.S. Gulf Coast, 1st Q. 1994)
Utilities:
Fuel oil, MW
12
Power, MW
17
Steam, tph
34
3
2,000
Water, cooling, m /h
Installation: Two licenses have been granted.

Licensor: VEBA OEL Technologie und Automatisierung GmbH.

I 117

Recycle hydrogen
compressor
Purge to
H2 recovery
Catalyst
Recycle hydrogen
Makeup hydrogen
H2
makeup
VGO feed T-star

reactor
START
Fuel gas
Naphtha
Middle distillate
to diesel pool
VGO to FCC
1
3
START
Vacuum residue
feedstock
Catalyst
withdrawal
Vacuum bottoms to
fuel oil, coker, etc.
Fuel gas
High
pressure
separator
Naphtha S=
<2 wppm
Stabilizer
Diesel S=
<50 wppm
Oil feed
heater
Hydrogen
heater
Amine
absorber
Fixed-bed
HDS
Gas-oil
stripper
FCC feed S=
1,000-1,500 wppm
Ebullating
pump
Hydrocracking, residue
Hydrocracking/hydrotreatingVGO
Application: Catalytic hydrocracking and desulfurization of residua

and heavy oils in an ebullated-bed reactor using the H-Oil process.
Application: The T-Star Process is an ebullated-bed process for the

hydrotreatment/hydrocracking of vacuum gas oils. The T-Star Process is
best suited for difficult feedstocks (coker VGO, DAO), high-severity operations and applications requiring a long run length.
Products: Full-range distillates and upgraded residue, transportation

fuels, FCC or coker feed, low-sulfur-fuel oil.
Description: A one, two or three stage ebullated-bed (1) reactor system. Feed consists of atmospheric or vacuum residue, recycle from downstream fractionation (3), hydrogen-rich recycle gas and makeup hydrogen. Combined feed is fed to the bottom of the reactor and expands the
catalyst bed resulting in good mixing, near isothermal operation and allows
for onstream catalyst replacement to maintain catalyst activity and 3 to
4 year run lengths between turnarounds. Two-phase reactor effluent is sent
to high-pressure separator (2); liquid is sent to fractionation (3) to recover
light liquid products and vacuum bottoms for recycle.
Operating conditions: Temperature, 770F 840F; hydrogen
partial pressure, psi 1,0002,500; LHSV, 0.11.0 hr 1 ; conversion
40%90%.
Process performance and yields: From commercial two-stage
processing:
Vacuum residue conversion 52 W%
70 W%
Processing objective
LSFO
Conversion
Feed
Ural VR
Arab H VR+FCC slurry
Gravity, API
13
3.6
+
85
85
1,000F , vol%
Sulfur, wt%
2.8
5.2
Performance, yields and product qualities
HDS, wt%
85
83
HDN, wt%
40
38
920
1,540
Chem. H2 Cons, scf/bbl
Naphtha, vol%
7
8
Diesel, vol%
25
33
VGO, vol%
31
38
Residue, vol%
41
25
Diesel sulfur, wppm
400
2,000
VGO sulfur, wt%
0.18
0.9
Residue sulfur, wt%
0.8
2.0
Residue gravity, API
14
4.0
Economics: Basis 2002 U.S. Gulf Coast

Investment$ per bpsd
Utilitiesper bbl of feed
Fuel, 10 3 Btu
Power, kWh
Catalyst makeup, $
3,5005,500
40100
915
100200
0.21.5
Description: A T-Star process flow diagram, which includes integrated

mid-distillate hydrotreating, is shown above. The typical
T-Star battery limits include oil/hydrogen fired heaters, an advanced
hot high-pressure design for product separation and for providing recycle to the ebullating pump, recycle gas scrubbing and product separation.
Catalyst is replaced periodically from the reactor, without shutdown. This
ensures the maintenance of constant, optimal catalyst activity and consistent product slate and quality. After high-pressure recovery of the
effluent and recycle gas, the products are separated and stabilized through
fractionation. A T-Star unit can operate for four-year run lengths with
conversion in the 20%60% range and hydrodesulfurization in the
93%99% range.
Temperature, F
Hydrogen partial pressure, psi
LHSV, hr 1
VGO conversion, %
750 820
6001,500
0.5 3.0
20 60
Examples: In Case 1, a deep-cut Arab heavy VGO is processed at 40

wt% conversion with objectives of mild conversion and preparing specification diesel and FCC unit feed. In Case 2, a VGO blend containing
20% coker material is processed at lower conversion to also obtain specification FCC unit feedstock and high-quality diesel.
Economics: Basis 2002 U.S. Gulf Coast
Investment in $ per bpsd
Utilities, per bbl of feed
Fuel, 103 Btu
Power, kWh
Catalyst makeup, $
1,200 2,500
60
3
0.05 0.20
Installation: The T-Star process is commercially demonstrated based

on the ebullated-bed reactor. Axens has licensed more than 1.3 MMbpsd
of capacity in gas oil, VGO and residue. Axens has seven commercially
operating ebullated-bed units and one is under construction that will process a variety of VGO feedstocks.
Reference: A novel approach to attain new fuel specifications,
Petroleum Technology Quarterly, Winter 1999/2000.
Installation: Seven units currently in operation.


118

Makeup hydrogen
Furnace
Pretreating
reactor
Mild
hydrocracking
reactor
Absorber
Lean amine
Rich amine
H2-rich
gas
Product
fractionator
Fresh feed
HP
separator
LP separator
First
stage
HDS
reactor
Wash
water
HDS
stripper
Process gas
Overhead
vapor
Sour
water
Water
Naphtha
Middle
distillate
Second
stage
Application: The Topse mild hydrocracking / VGO hydrotreating

process upgrades, and if required, converts a variety of vacuum gasoil feedstocks including straight run (SR) and cracked components from an
FCC, Coker, and visbreaker as well as deasphalting units.
Products: Low-sulfur naphtha, diesel and vacuum gasoil. The vacuum
gasoil sulfur is adjusted such that when processed by the FCC, it will produce low-sulfur gasoline that does not require post treatment and can be
blended directly in the gasoline pool.
Description: This process uses a combination of process conditions
and hydrotreating and hydrocracking catalyst to meet the required conversion as well as required product quality specifications. Topse has developed amorphous and zeolitic cracking catalysts specifically designed for
mild hydrocracking applications. Topse s engineers utilize their process
design experience to adjust the unit flow configuration to meet product
quality requirements and provide a cost-effective design.
The unit design also features an industry leader graded-bed design
for reactor pressure-drop control as well as state of the art reactor internals
design. For FCC pretreater revamps, Topse has further developed the
Aroshift process that considerably improves FCC profitability at little
investment.
Operating conditions: Typical operating pressures range from
55 to 110 barg (800 to 1,600 psig). Typical operating temperatures
range from 340C to 410C (644F to 770F).
Installation: Four units designed by Topse for Mild Hydrocracking/VGO Hydrotreating are in service.
Wild
naphtha
Product
diesel
stripper
HDA
reactor
Steam
Diesel product
HDA
separator
FCC feed
Hydrocracking (mild)/
VGO hydrotreating
HDS
stripper
Diesel
feed
HDS separator
Recycle gas Amine

compressor scrubber
Hydrogen makeup
Diesel cooler
Hydrodearomatization
Application: Topses two-stage hydrodesulfurization hydrodearomatization (HDS/HDA) process is designed to produce low-aromatics
distillate products. This process enables refiners to meet the new, stringent standards for environmentally friendly fuels.
Products: Ultra-low sulfur, ultra-low nitrogen, low-aromatics diesel,
kerosine and solvents (ultra-low aromatics).
Description: The process consists of four sections: initial hydrotreating,
intermediate stripping, final hydrotreating and product stripping. The initial hydrotreating step, or the first stage of the two-stage reaction process,
is similar to conventional Topse hydrotreating, using a Topse high-activity base metal catalyst such as TK-573 to perform deep desulfurization and
deep denitrification of the distillate feed. Liquid effluent from this first stage
is sent to an intermediate stripping section, in which H2S and ammonia are
removed using steam or recycle hydrogen. Stripped distillate is sent to the
final hydrotreating reactor, or the second stage. In this reactor, distillate
feed undergoes saturation of aromatics using a Topse noble metal catalyst,
either TK-907/TK-908 or TK-915, a high-activity dearomatization catalyst. Finally, the desulfurized, dearomatized distillate product is steam
stripped in the product stripping column to remove H2S, dissolved gases and
a small amount of naphtha formed.
Like the conventional Topse hydrotreating process, the HDS/HDA
process uses Topses graded bed loading and high-efficiency patented reactor internals to provide optimum reactor performance and catalyst use leading to the longest possible catalyst cycle lengths. Topses high efficiency
internals have a low sensitivity to unlevelness and are designed to ensure the
most effective mixing of liquid and vapor streams and maximum utilization of catalyst. These internals are effective at high of liquid loadings, thereby
enabling high turndown ratios. Topses graded-bed technology and the use
of shape-optimized inert topping and catalysts minimize the build-up of
pressure drop, thereby enabling longer catalyst cycle length.
Operating conditions: Typical operating pressures range from 20 to
60 barg (300 to 900 psig), and typical operating temperatures range from
320C to 400C (600F to 750F) in the first stage reactor, and from 260C
to 330C (500F to 625F) in the second stage reactor. The Topse
HDS/HDA treatment of a heavy straight-run gas oil feed yielded these
product specifications:
Specific gravity
Sulfur, ppmw
Nitrogen, ppmw
Total aromatics, wt%
Cetane index, D-976
Feed
0.86
3,000
400
30
49
Product
0.83
1
<1
<10
57
References: Cooper, Hannerup and Sgaard-Andersen, Reduction

of aromatics in diesel, Oil and Gas, September 1994
Sgaard-Andersen, Cooper and Hannerup, Topses process for
improving diesel quality, NPRA Annual Meeting, 1992.
de la Fuente, E., P. Christensen, and M. Johansen, Options for meeting EU year 2005 fuel specifications.
Installation: A total of five, two in Europe and three in North America.

I 119

Recycle gas
compressor
Makeup gas
compressor
Makeup gas
Makeup gas
Purge
Hydrogen-rich
gas
Quench
Feed
Lowtemperature
separator
Reactor
Purge
Preheater
Light ends
Product
stripper
Low-sulfur,
low-olefins,
high-octane
gasoline
Preheater
Feed
HDS
reactor
Pretreat
reactor
Amine
scrubber
Light ends
Cooler
Separator
Product
stripper
Low-sulfur
naphtha
High-temperature
separator
Application: Reduce sulfur in gasoline to less than 10 ppm by

hydrodesulfurization followed by cracking and isomerization to recover
octane.
Application: Reduce sulfur in FCC gasoline to less than 10 ppm by

selective hydrotreating to maximize octane preservation.
Description: The basic flow scheme is similar to that of a conventional

naphtha hydrotreater. Feed and recycle hydrogen mix is preheated in
feed/effluent exchangers and a fired heater then introduced into a fixedbed reactor. Over the first catalyst bed, the sulfur in the feed is converted
to hydrogen sulfide with near complete olefin saturation. In the second
bed, over a different catalyst, octane is recovered by cracking and isomerization reactions. The reactor effluent is cooled and the liquid product separated from the recycle gas using high- and-low temperature separators.
The vapor from the separators is combined with makeup gas, compressed and recycled. The liquid from the separators is sent to the product stripper where the light ends are recovered overhead and desulfurized
naphtha from the bottoms. The product sulfur level can be as low as 5
ppm. The OCTGAIN process can be retrofitted into existing refinery
hydrotreating units. The design and operation permit the desired level
of octane recovery and yields.
Yields: Yield depends on feed olefins and desired product octane.
Installations: Commercial experience with two operating units.
Reference: Halbert, T., et al., Technology Options For Meeting
Low Sulfur Mogas Targets, NPRA Annual Meeting, March, 2000.
Description: The feed is mixed with recycle hydrogen, heated with

reactor effluent and passed through the pretreat reactor for diolefin saturation. After further heat exchange with reactor effluent and preheat using
a utility, the hydrocarbon/hydrogen mixture enters the HDS reactor
containing proprietary RT-225 catalyst. In the reactor, the sulfur is converted to H2S under conditions which strongly favor hydrodesulfurization while minimizing olefin saturation.
The reactor effluent is cooled and the liquid separated from gas that is
amine scrubbed and recycled to the reactor along with makeup gas. The
liquid product is stabilized in a product stripper before being sent to storage/blending.
For high-sulfur feeds and/or very low-sulfur product, variations in
the design are available to minimize octane loss and hydrogen consumption. The feed may be full range, intermediate or heavy fractions. SCANfining can be retrofitted to existing refinery units such as naphtha or
diesel hydrotreaters and reformers.
Yields: Yield of C5 plus liquid product typically over 100 LV%.
Installations: Twenty-four units under design, construction or operation.
Reference: Sweed, N., et al., Low sulfur technology, Hydrocarbon
Engineering, July 2002.
Ellis,E., et al., Meeting the low sulfur mogas challenge, World Refining Association Third European Fuels Conference, March 2002.

120

Fresh feed
Makeup
hydrogen
Lean DEA
Furnace
Light ends
Absorber
Reactor
Wash water
Rich DEA
4
2
H2 rich gas
Fresh feed
START
Hydrogen makeup
Low-sulfur
naphtha
Sour water
Product
High-pressure
separator
Low-pressure separator
Application: The ISAL process enables refiners to meet the worlds
most stringent specifications for gasoline sulfur while also controlling product octane.
This moderate-pressure, fixed-bed hydroprocessing technology desulfurizes gasoline-range olefinic feedstocks and selectively reconfigures lower
octane components to control product octane. This process can be applied
as a standalone unit or as part of an overall integrated flow scheme for
gasoline desulfurization.
Description: The flow scheme of the ISAL process is very similar to
that of a conventional hydrotreating process. The naphtha feed is mixed
with hydrogen-rich recycle gas and processed across fixed catalyst beds
at moderate temperatures and pressures. Following heat exchange and separation, the reactor effluent is stabilized. The similarity of an ISAL unit
to a conventional naphtha hydrotreating unit makes new unit and revamp
implementation both simple and straightforward. The technology can be
applied to idle reforming and hydrotreating units.
Product quality: The ISAL units operation can be adjusted to
achieve various combinations of desulfurization, product octane and
yield. Typical yield/octane relationships for an integrated flow scheme processing an FBR FCC naphtha containing 400 wppm sulfur and 20 wt%
olefins are:
%Desulfurization,
93%
wt% C5+ product
Yield, vol%
99.5
97.4
Sulfur, wppm
30
30
Olefins, wt%
15.3
15.7
(R + M)/2 change
1.9
0
98%
99.5
10
14.9
2.1
97.2
10
15.3
0
Hydrodesulfurization,
ultra-low-sulfur diesel
Application: Topse ULSD process is designed to produce ultra-lowsulfur diesel (ULSD)5 wppm Sfrom cracked and straight-run distillates. By selecting the proper catalyst and operating conditions, the process can be designed to produce 5 wppm S diesel at low reactor pressures
(<500 psig) or at higher reactor pressure when products with improved
density, cetane, and polyaromatics are required.
Description: Topse ULSD process is a hydrotreating process that combines Topses understanding of deep-desulfurization kinetics, highactivity catalyst, state-of-the-art reactor internal, and engineering expertise in the design of new and revamped ULSD units. The ULSD process
can be applied over a very wide range of reactor pressures.
Our highest activity CoMo catalyst is specifically formulated with
high-desulfurization activity and stability at low reactor pressure (~ 500
psig) to produce 5 wppm diesel. This catalyst is suitable for revamping
existing low-pressure hydrotreaters or in new units when minimizing
hydrogen consumption.
The highest activity NiMo catalyst is suitable at higher pressure when
secondary objectives such as cetane improvement and density reduction
are required. Topse offers a wide range of engineering deliverables to
meet the needs of the refiners. Our offerings include process scoping
study, reactor design package, process design package, or engineering
design package.
Installation: Topse has licensed 21 ULSD hydrotreaters with 11
revamps. Our reactor internals are installed in more than 60 units.
Economics: The capital and operating costs of an ISAL unit are

slightly higher than those of a typical naphtha hydrotreating unit. With
this process, refiners benefit from the ability to produce a higher-octane
product at incremental additional operating cost primarily related to
additional hydrogen consumption.
References: Cost-Effectively Improve Hydrotreater Designs, Hydrocarbon Processing, November 2001 pp. 4346.
The importance of good liquid distribution and proper selection of
catalyst for ultra deep diesel HDS, JPI Petroleum Refining Conference,
October 2000, Tokyo.
Installation: Two ISAL applications have been implemented in the

U.S. Engineering work has also been completed on three additional
ISAL units, with an additional two ISAL units currently in the process
design stage.
Licensor: UOP LLC (in cooperation with PDVSA-INTEVEP).

I 121

Recycle
compressor
Water wash
LGO+LCO
Solvent
Rich amine
Heater
To HDS
unit
NPC
Tower A: Adsorption
Tower B: Desorption
Tower A: Desorption
Tower B: Adsorption
pretreatment
Application: The SK HDS pretreatment process allows a refiner to
use the existing diesel HDS unit with minor modifications to produce
ultra-low-sulfur diesel (ULSD) at less than 10 ppm sulfur. Modifications
to older, existing low-pressure HDS units usually require catalyst replacement and installation of a recycle gas scrubber, if not already in place.
Description: The primary goal of this process is to improve performance of the HDS unit by removing most of the nitrogen-bearing natural polar compounds (NPC) from the mid-boiling range distillate
streams. This is achieved by selectively adsorbing the NPC in an adsorption bed followed by desorption of NPC by a solvent. The process uses
twin adsorbers, a desorption-solvent circulation system, two stripping
columns and associated pumps and an overhead system.
Diesel blend feedstock is passed through one adsorbent vessels, which
is then stripped to remove a small amount of desorption solvent. The
adsorbed NPC is removed from the adsorber bed by desorption solvent and
is stripped in the second stripper column.
Pretreated diesel blend from diesel stripper is sent to the downstream
HDS unit for sulfur removal. The byproduct, NPC stream, from the
NPC stripper may be used as a blend stock in either marine diesel or in
high-sulfur fuel oil.
Economics: Total investment cost (ISBL) is $400 to $450/bbl for a
30,000-bpsd unit, U.S.GC, 3Q 2002.
Utilities per barrel of feed:
Fuel gas, fired, FOEB
Water, cooling, mt
Electricity, kWh
Absorber
Hot separator
Adsorber B
Adsorber A
Stripper
A/B
Pretreated
LGO+LCO
0.01
1.5
0.4
An alternate steam stripping design can be provided if required.

Cost of adsorbent: Less than $0.10/bbl
Distillate
feed
Cold Sour water

separator
Steam
Charge
pump
Hydrogen
Makeup
compressor
Application: A versatile family of premium distillates technologies is

used to meet all current and possible future premium diesel upgrading
requirements. Ultra-deep hydrodesulfurization (UDHDS) process can produce distillate products with sulfur levels below 10 wppm from a wide
range of distillate feedstocks.
Products: High volume yield of ultra-low-sulfur distillate is produced.
Cetane and API gravity uplift together with the reduction of polyaromatics
to less than 6 wt% or as low as 2 wt% can be economically achieved.
Description: The UDHDS reactor and catalyst technology is offered
through Akzo Nobel Catalysts bv. A single-stage, single-reactor process
incorporates proprietary high-performance-distribution and quench
internals. Feed and combined recycle and makeup gas are preheated and
contact the catalyst in a downflow-concurrent-fixed-bed reactor. The reactor effluent is flashed in a high- and a low-pressure separator. An amineabsorber tower is used to remove H2S from the recycle gas. In the example shown, a steam stripper is used for final product recovery. The
UDHDS technology is equally applicable to revamp and grassroots
applications.
Economics:
Investment (basis: 25,000 to 35,000 bpsd, 1Q 2000 U.S. Gulf Coast)
New unit, $ per bpsd
1,000 to 1,800
Installation: Over 60 distillate-upgrading units have applied the

Akzo Nobel HDS Technology. Eleven of these applications produce or
will produce <10ppm sulfur, using UDHDS technology.
Reference: Technology for premium distillates, ERTC Low Sulfur
Fuels Workshop, February/March 2002, London.
Licensor: Akzo Nobel Catalysts bv.
Licensor: The Badger Technology Center of Washington Group International, on behalf of SK Corp.
Low-sulfur
diesel
HydrodesulfurizationUDHDS
Installation: One 1,000-bpd demonstration unit has been operating

successfully since May 2002. A larger commercial-scale unit is currently
being studied for SK Corp.
Naphtha
Product
stripper
Hydrogen: Approximately 1020% less hydrogen consumption in

hydrotreating unit for feed processed in the SK Pretreatment Unit.
122
Fuel
gas
Lean amine
UDHDS
reactor

Reactor
Stm
Reactor
feed heater
Stm
Vent gas
to heater
Stripper
Hydrocarbon
feed
Steam
HP separator
Makeup Recycle
gas comp. gas comp.
To fuel
gas (H2S
absorption)
Drier
Steam
Stm
Steam
Product
hydrogen
Sour water
LP separator
Makeup
hydrogen
Slop oil
Feed
Oil product
Fuel gas
Purge gas
Hydrofinishing/hydrotreating
Hydrogen
Application: Process to produce finished lube-base oils and special oils.
Application: To produce hydrogen from light hydrocarbons using

steam-methane reforming.
Feedstock: Natural gas, refinery gas, LPG and naphtha.
Product: High-purity hydrogen and steam.
Description: Light hydrocarbon feed (1) is heated prior to passing through
two fixed-catalyst beds. Organic sulfur compounds present in feed gas (e.g., mercaptans) are converted to hydrogen sulfide (H2S) and mono-olefins in the gas
phase are hydrogenated in the first bed of cobalt molybdenum oxide catalyst
(2). The second bed contains zinc oxide to remove H2S by adsorption. This
sulfur-removal stage is necessary to avoid poisoning of the reforming catalysts.
Treated feed gas is mixed with steam and heated before passing to the reformer
where the hydrocarbons and steam react to form synthesis gas (syngas).
Foster Wheeler supplies proprietary side-fired Terrace Wall reformers, with natural draft mode for increased reliability, compact plot layout with convection section mounted directly above the radiant section and
modular fabrication option. Top-fired reformers are options for large
capacity plants.
Syngas containing hydrogen, methane, carbon dioxide (CO2), carbon
monoxide (CO) and water leaves the reformer and passes through the wasteheat boiler to the shift reactor (3) where most of the CO is converted to
CO2 and hydrogen by reaction with steam. For heavier feedstocks, prereforming is used for conversion of feedstock upstream of the reformer. The
syngas is cooled through a series of heat-recovery exchangers before free
water is recovered in a knockout drum. The resultant raw hydrogen stream
passes to the pressure swing adsorption (PSA) unit for purification (4) to
99.9% hydrogen product quality. Tail gas from the PSA unit provides a substantial proportion of the firing duty for the reformer. The remaining fuel is
supplied from feed gas or other sources (e.g. refinery fuel gas).
Saturated and superheated steam is raised by heat exchange with the
reformed gas and flue gas in the convection section of the reformer. Steam
export quantities can be varied between 1,250 and 5,750 lb/ MMscfd of
hydrogen produced using air pre-heat and auxiliary firing options.
Economics: Plant design configurations are optimized to suit the
clients economic requirements, using discounted cash-flow modeling to
establish the lowest lifecycle cost of hydrogen production.
Feeds: Dewaxed solvent or hydrogen-refined lube stocks or raw vacuum distillates for lubricating oils ranging from spindle oil to machine
oil and bright stock.
Products: Finished lube oils (base grades or intermediate lube oils) and
special oils with specified color, thermal and oxidation stability.
Description: Feedstock is fed together with make-up and recycle
hydrogen over a fixed-bed catalyst at moderate temperature and pressure.
The treated oil is separated from unreacted hydrogen, which is recycled.
Very high yields product are obtained.
For lube-oil hydrofinishing, the catalytic hydrogenation process is operated at medium hydrogen pressure, moderate temperature and low hydrogen consumption. The catalyst is easily regenerated with steam and air.
Operating pressures for hydrogen-finishing processes range from 25 to
80 bar. The higher-pressure range enables greater flexibility with regard to
base-stock source and product qualities. Oil color and thermal stability
depend on treating severity. Hydrogen consumption depends on the feed
stock and desired product quality.
Utility requirements, (typical, Middle East Crude), units per m 3
of feed:
Electricity, kWh
Steam, MP, kg
Steam, LP, kg
Fuel oil, kg
Water, cooling, m3
15
25
45
3
10
Installation: Numerous installations using the Uhde Edeleanu proprietary technology are in operation worldwide. The most recent reference is a complete lube-oil production facility licensed to the state of Turkmenistan, which successfully passed performance testing in 2002.
Investment: 10100 MMscfd, 3rd Q 2002, U.S.GC$955 million

Utilities, typical per MMscfd of hydrogen produced (natural gas
feedstock):
Feed + fuel, lb
960
Water, demineralized, lb
4,420
Steam, export, lb
3,320
Water, cooling, U.S. gal
1,180
Electricity, kWh
12
Reference: Ward, R. D. and N. Sears, Hydrogen plants for the new

millenium, Hydrocarbon Engineering, Vol. 7, June 2002.
Installation: Over 100 plants, ranging from 1 MMscfd to 95 MMscfd
in a single-train configuration and numerous multi-train configurations.
Licensor: Foster Wheeler.

I 123

Hydrogen recycle
LCN
CW
Offgas
CDHydro
Hydrogen
Hydrogen
MCN
FCC C5 + gasoline
CDHDS
FCC C4+
MCN/HCN
MP
steam
Reflux
Treated FCC C4s

Hydrogen
FCC C5+ gasoline
HCN
Depentanizer
Hydrogenation
Hydrotreating
Application: CDHydro is used to selectively hydrogenate diolefins

in the top section of a hydrocarbon distillation column. Additional
applicationsincluding mercaptan removal, hydroisomerization and
hydrogenation of olefins and aromatics are also available.
Application: CDHydro and CDHDS are used to selectively desulfurize FCC gasoline with minimum octane loss.
Description: The patented process CDHydro combines fractionation

with hydrogenation. Proprietary devices containing catalyst are installed
in the fractionation columns top section (1). Hydrogen is introduced
beneath the catalyst zone. Fractionation carries light components into the
catalyst zone where the reaction with hydrogen occurs. Fractionation also
sends heavy materials to the bottom. This prevents foulants and heavy
catalyst poisons in the feed from contacting the catalyst. In addition, clean
hydrogenated reflux continuously washes the catalyst zone. These factors
combine to give a long catalyst life. Additionally, mercaptans can react
with diolefins to make heavy, thermally-stable sulfides. The sulfides are
fractionated to the bottoms product. This can eliminate the need for a
separate mercaptan removal step. The distillate product is ideal feedstock
for alkylation or etherification processes.
The heat of reaction evaporates liquid, and the resulting vapor is condensed in the overhead condenser (2) to provide additional reflux. The natural temperature profile in the fractionation column results in a virtually
isothermal catalyst bed rather than the temperature increase typical of
conventional reactors.
The CDHydro process can operate at much lower pressure than conventional processes. Pressures for CDHydro are typically set by the fractionation requirements. Additionally, the elimination of a separate hydrogenation reactor and hydrogen stripper offer significant capital cost
reduction relative to conventional technologies.
Feeding CDHydro with reformate and light-straight run for benzene
saturation provides the refiner with increased flexibility to produce RFG.
Isomerization of the resulting C5 /C6 overhead stream provides higher
octane and yield due to reduced benzene and C 7+ content compared to typical isomerization feedstocks.
Economics: Fixed-bed hydrogenation requires a distillation column
followed by a fixed-bed hydrogenation unit. CDHydro eliminates the
fixed-bed unit by incorporating catalyst in the column. When a new distillation column is used, capital cost of the column is only 5% to 20%
more than for a standard column depending on the CDHydro application. Elimination of the fixed-bed reactor and stripper can reduce capital cost by as much as 50%.
Products: Ultra-low-sulfur FCC gasoline with maximum retention of

olefins and octane.
Description: The light, mid and heavy cat naphthas (LCN, MCN,
HCN) are treated separately, under optimal conditions for each. The fullrange FCC gasoline sulfur reduction begins with fractionation of the light
naphtha overhead in a CDHydro column. Mercaptan sulfur reacts quantitatively with excess diolefins to product heavier sulfur compounds,
and the remaining diolefins are partially saturated to olefins by reaction
with hydrogen. Bottoms from the CDHydro column, containing the
reacted mercaptans, are fed to the CDHDS column where the MCN and
HCN are catalytically desulfurized in two separate zones. HDS conditions are optimized for each fraction to achieve the desired sulfur reduction with minimal olefin saturation. Olefins are concentrated at the top
of the column, where conditions are mild, while sulfur is concentrated
at the bottom where the conditions result in very high levels of HDS.
No cracking reactions occur at the mild conditions, so that yield losses
are easily minimized with vent-gas recovery. The three product streams are
stabilized together or separately, as desired, resulting in product streams
appropriate for their subsequent use. The two columns are heat integrated to minimize energy requirements. Typical reformer hydrogen is
used in both columns without makeup compression. The sulfur reduction
achieved will allow the blending of gasoline that meets current and future
regulations.
Catalytic distillation essentially eliminates catalyst fouling because
the fractionation removes heavy-coke precursors from the catalyst zone
before coke can form and foul the catalyst pores. Thus, catalyst life in
catalytic distillation is increased significantly beyond typical fixed-bed
life. The CDHydro/CDHDS units can operate throughout an FCC
turnaround cycle up to five years without requiring a shutdown to regenerate or to replace catalyst. Typical fixed-bed processes will require a mid
FCC shutdown to regenerate/replace catalyst, requiring higher capital
cost for feed, storage, pumping and additional feed capacity.
Economics: The estimated ISBL capital cost for a 35,000 bpd CDHydro/CDHDS unit with 95% desulfurization is $26 million (2000 U.S.
Gulf Coast). Direct operating costsincluding utilities, catalyst, hydrogen and octane replacementare estimated at $0.04/gal of full-range FCC
gasoline.
Installation: Eighteen CDHydro units are in commercial operation

for C4, C5, C6 and benzene hydrogenation applications. Ten units have
been in operation for more than five years and total commercial operating time now exceeds 80 years for CDHydro technologies. Seventeen additional units are currently in engineering/construction.
Installation: Five CDHydro units are in operation treating FCC gasoline and 17 more units are currently in engineering/construction. Three
CDHDS units are in operation with 17 additional units currently in engineering/construction.
Licensor: CDTECH.
Licensor: CDTECH.

124

Makeup
hydrogen
Absorber
Fired
heater
Lean DEA
Furnace
Liquid
feed
Reactor
Rich DEA
H2 rich gas
Fresh feed
START
Feed/effluent
exchangers
START
Makeup
Hydrogen makeup compressor
Recycle compressor
Flash gas to fuel
Product
High-pressure
separator
Low-pressure separator
Liquid to stripper
Low-pressure
flash
Highpressure
flash
Hydrotreating
Hydrotreating
Application: Topse hydrotreating technology has a wide range of

applications, including the purification of naphtha, distillates and residue,
as well as the deep desulfurization and color improvement of diesel fuel
and pretreatment of FCC and hydrocracker feedstocks.
Application: Reduction of the sulfur, nitrogen, and metals content

of naphthas, kerosines, diesel or gas oil streams.
Products: Ultra-low-sulfur diesel fuel, and clean feedstocks for FCC

and hydrocracker units.
Description: Single or multibed catalytic treatment of hydrocarbon

liquids in the presence of hydrogen converts organic sulfur to hydrogen
sulfide and organic nitrogen to ammonia. Naphtha treating normally
occurs in the vapor phase, and heavier oils usually operate in mixed-phase.
Multiple beds may be placed in a single reactor shell for purposes of redistribution and/or interbed quenching for heat removal. Hydrogen-rich gas
is usually recycled to the reactor(s) (1) to maintain adequate hyrogen-tofeed ratio. Depending on the sulfur level in the feed, H2S may be
scrubbed from the recycle gas. Product stripping is done with either a
reboiler or with steam. Catalysts are cobalt-molybdenum, nickel-molybdenum, nickel-tungsten or a combination of the three.
Description: Topses hydrotreating process design incorporates our

industrially proven high-activity TK catalysts with optimized graded-bed
loading and high-performance, patented reactor internals. The combination of these features and custom design of hydrotreating units result
in process solutions that meet the refiners objectives in the most economic
way.
In the Topse hydrotreater, feed is mixed with hydrogen, heated and
partially evaporated in a feed/effluent exchanger before it enters the reactor. In the reactor, Topses high-efficiency internals have a low sensitivity to unlevelness and are designed to ensure the most effective mixing
of liquid and vapor streams and the maximum utilization of the catalyst
volume. These internals are effective at a high range of liquid loadings,
thereby enabling high turndown ratios. Topses graded-bed technology
and the use of shape-optimized inert topping and catalysts minimize the
build-up of pressure drop, thereby enabling longer catalyst cycle length.
The hydrotreating catalysts themselves are of the Topse TK series, and
have proven their high activities and outstanding performance in numerous operating units throughout the world. The reactor effluent is cooled
in the feed-effluent exchanger, and the gas and liquid are separated. The
hydrogen gas is sent to an amine wash for removal of hydrogen sulfide
and is then recycled to the reactor. Cold hydrogen recycle is used as quench
gas between the catalyst beds, if required. The liquid product is steam
stripped in a product stripper column to remove hydrogen sulfide, dissolved
gases and light ends.
Products: Low-sulfur products for sale or additional processing.
Operating conditions: 550F to 750F and 400 to 1,500 psig reactor conditions.
Yields: Depend on feed characteristics and product specifications.
Recovery of desired product almost always exceeds 98.5 wt% and usually exceeds 99%.
Economics:
Utilities, (per bbl feed)
Fuel, 103 Btu release
Electricity, kWh
Naphtha
48
0.65
35
Diesel
59.5
1.60
42

& Iron Co.
Operating conditions: Typical operating pressures range from

20 to 80 barg (300 to 1,200 psig), and typical operating temperatures range
from 320C to 400C (600F to 750F).
References: Cooper, B. H. and K. G. Knudsen, Production of ULSD:
Catalyst, kinetics and reactor design, World Petroleum Congress, 2002.
Bingham, Muller, Christensen and Moyse, Performance focused reactor design to maximize benefits of high activity hydrotreating catalysts,
European Refining Technology Conference, 1997.
Cooper, Meeting the challenge for middle distillates: scientific and
industrial aspects, Petrotech, 1997.
de la Fuente, E., P. Christensen and M. Johansen, Options for meeting EU year 2005 fuel specifications.
Installation: More than 35 Topse hydrotreating units for the various applications above are in operation or in the design phase.

I 125

LPG
JUST
hydrotreating
Crude
oil
Go and
lighter
Amine treating and

LPG recover
LPG
Makeup hydrogen
LN
HTR
and
fractionation
H2
HN
Crude
prefraction
Reformate
Cat.
reformer
Integrated
utility facility
Diesel S = 50 ppm
Fresh feed
Mixer
R1
Mixer
R2
Isotherming 2
reactor 1
Isotherming 4
reactor 2
Existing
6 hydrotreating
reactor
Fuel oil S = 3.2 wt%
AR
Acid gas from refinery
Jet/kerosine
S = 15 ppm wt%
Kerosine
Gasoil
Gasoline
RON=93
Sulfur
Sulfur
recovery
Low-sulfur
treated
product
Simplified
offsite facility
Recycle pump
Hydrotreating
Hydrotreating
Application: The JUST Refinery process is a stand-alone refinery concept that uses new technologies to enable a 30% reduction of CAPEX over
conventional refineries with similar functions; thus, improving ROI by
5%. The JUST concept is a low-cost technology option for new refineries. Benefits include:
Minimizes the initial investment cost through a phased approach
Improves the competitiveness of small- to medium-sized refineries.
Application: The IsoTherming process, when installed in a pre-treat

configuration ahead of an existing hydrotreating reactor, provides refiners an economical means to produce ultra-low-sulfur diesel (ULSD). In
addition, cat-cracker feeds can be desulfurized to the extent that gasoline
post-treating is not required to meet low-sulfur gasoline specifications.
Products: Ultra-low-sulfur diesel, low-sulfur cat feed and low-sulfur
gasoline.
Description: This process uses a novel approach to introduce hydrogen
into the reactor; it enables much higher space velocities than conventional
hydrotreating reactors. The IsoTherming process removes the hydrogen mass
transfer limitation and operates in a kinetically limited mode since hydrogen is delivered to the reactor in the liquid phase as soluble hydrogen.
The technology can be installed as a simple pre-treat unit ahead of an
existing hydrotreater reactor. Fresh feed, after heat exchange, is combined
with hydrogen in Reactor One mixer (1). The feed liquid with soluble
hydrogen is fed to IsoTherming Reactor One (2) where partial desulfurization takes place. The stream is combined with additional hydrogen in
Reactor Two Mixer (3), and fed to IsoTherming Reactor Two (4) where
further desulfurization takes place. Treated oil is recycled (5) back to the
inlet of Reactor One. This recycle stream is used to deliver more hydrogen
to the reactors and also acts as a heat sink, which results in a nearly isothermal reactor operation. The treated oil from IsoTherming Reactor Two (4)
is fed to the existing Hydrotreating Reactor (6) which functions in a polishing
mode to produce an ultra-low-sulfur product. The process can also be configured as a grass roots hydrotreater.
Operating conditions: Typical diesel IsoTherming conditions
are:
Description: The key technologies for the JUST program include JUST
Hydrotreating, which consists of a crude prefractionator, single hydrotreator
and product fractionator. The simplified crude prefractionator separates
crude into only two fractions: gasoil/lighter fraction and a residue. The
gasoil/lighter fraction is topped off by crude prefractionator and is
hydrotreated, in its entirety, by one hydrotreator. All products are
hydrotreated to meet individual sulfur specification. The single hydrodesulfurization step of the combined streams tremedously reduces the CAPEX
and OPEX; it eliminates using multiple (naphtha, kerosine and gasoil)
hydrodesulfurization systems.
The heavy-naphtha fraction is processed through a catalytic-reforming unit and produces reformate for gasoline blending. The hydrotreater
(HTR) uses hydrogen from the catalytic reformer and is, therefore, hydrogen self-sufficient.
The integrated utility unit and simplified offsite facility also lower
total refinery CAPEX and OPEX expenses. A comparison illustrating the
JUST Refinery advantages is presented:
Conventional scheme JUST Refinery
Process
No. of process units
9
6
No. of major equipt in HTR
12
4
Utility
Power and steam system
BTG/Boiler
GTG/HRSG*
Surface condenser
Yes
No
Independent air compressor
Yes
No
Offsite (no.of tanks)
13
28
Initial CAPEX
Base
30%
Area requirement
Base
34%
Economics (IRR)
Base
+5%
* HRSG: heat recovery steam generator
Reference: The Piping Engineering, Extra Edition, 1997, p. 39.

30th Petroleum-Petrochemical Symposium of Japan Petroleum Institute, C38, 2000.
Licensor: JGC.
Diesel
feed
LCO, vol%
40
SR, vol%
60
Sulfur, ppm
1985
Nitrogen, ppm
388
Cetane
46.50
Relative hydrogen
consumption *
LHSV, Hr-1 **
Relative catalyst
volume *
Reactor T
IsoTherming Treated product

pre-treat
from existing
reactor
conventional reactor
140
24
47.80
10
3
48.60
100%
15
18%
3
25%
15
600
100%
10
600
* Based on existing reactor producing 500 ppm sulfur diesel.

** Based on fresh feedrate without recycle.
Economics: Investment (Basis 15,00020,000 bpsd, 2Q 2002, U.S.

Gulf Coast)
$ per bpsd diesel
500
Installation: First commercial diesel unit onstream October 2002.

Licensor: Linde BOC Process Plants, LLC and Process Dynamics.
126
First stage
reactor
Vapor/liquid
separation recycle
Light components
Interstage Second stage

stripper
reactor
Makeup
hydrogen
1
H2
rich gas
Product
Feed
START
Product to
stripping
Feed oil
Hydrotreating
Hydrotreating
Application: Hydroprocessing of middle distillates, including cracked

materials (coker/visbreaker gas oils and LCO) using SynTechnology, maximizes distillate yield while producing ultra-low-sulfur diesel with improved
cetane and API gain, reduced aromatics, T95 reduction and cold-flow
improvement through selective ring opening, saturation and/or isomerization.
Various process configurations are available for revamps and new unit
design to stage investments to meet changing diesel specifications.
Products: Maximum yield of improved quality distillate while minimizing fuel gas and naphtha. Diesel properties include less than 10ppm sulfur, with aromatics content (total and/or PNA), cetane, density
and T95 dependent on product objectives and feedstock.
Description: SynTechnology includes SynHDS for ultra-deep desulfurization and SynShift/SynSat for cetane improvement, aromatics saturation and density/T95 reduction. SynFlow for cold flow improvement can be added as required. The process combines ABB Lummus
Globals cocurrent and/or patented countercurrent reactor technology with
special SynCat catalysts from Criterion Catalyst Co. LP. It incorporates
design and operations experience from Shell Global Solutions, to maximize reactor performance by using advanced reactor internals.
A single-stage or integrated two-stage reactor system provides various process configuration options and revamp opportunities. In a two-stage reactor system, the feed, makeup and recycle gas are heated and fed to a first-stage cocurrent reactor. Effluent from the first stage is stripped to remove impurities and
light ends before being sent to the second-stage countercurrent reactor. When
a countercurrent reactor is used, fresh makeup hydrogen can be introduced at
the bottom of the catalyst bed to achieve optimum reaction conditions.
Operating conditions: Typical operating conditions range from
5001,000 psig and 600F750F. Feedstocks range from straight-run gas
oils to feed blends containing up to 70% cracked feedstocks that have been
commercially processed. For example, the SynShift upgrading of a feed
blend containing 72% LCO and LCGO gave these performance figures:
Application: Hydrodesulfurization, hydrodenitrogenation and hydrogenation of petroleum and chemical feedstocks using the Unionfining and
MQD Unionfining processes.
Gravity, API
Sulfur, wt% (wppm)
Nitrogen, wppm
Aromatics, vol%
Cetane index
Liquid yield on feed, vol%
Feed blend
25
1.52
631
64.7
34.2
Product
33.1
(2)
<1
34.3
43.7
107.5
Economics: SynTechnology encompasses a family of low-to-moderate

pressure processes. Investment cost will be greatly dependent on feed quality and hydroprocessing objectives. For a 30,000 to 35,000-bpsd unit, the
typical ISBL investment cost in U.S.$/bpsd (U.S. Gulf Coast 2000) are:
Revamp existing unit
New unit for deep HDS
New unit for cetane improvement and HDA
450950
1,1001,200
1,5001,600
Installation: SynTechnology has been selected for more than 30 units,

with half of the projects being revamps. Seven units are in operation.
Licensor: ABB Lummus Global, Inc., on behalf of the SynAlliance,
which includes Criterion Catalyst and Technologies Co., and Shell
Global Solutions.
Products: Ultra-low-sulfur diesel fuel; feed for catalytic reforming, FCC

pretreat; upgrading distillates (higher cetane, lower aromatics); desulfurization, denitrogenation and demetallization of vacuum and atmospheric gas oils, coker gas oils and chemical feedstocks.
Description: Feed and hydrogen-rich gas are mixed, heated and contacted with regenerable catalyst (1). Reactor effluent is cooled and separated (2). Hydrogen-rich gas is recycled or used elsewhere. Liquid is
stripped (3) to remove light components and remaining hydrogen sulfide, or fractionated for splitting into multiple products.
Operating conditions: Operating conditions depend on feedstock and desired level of impurities removal. Pressures range from 500
to 2,000 psi. Temperatures and space velocities are determined by process objectives.
Yields:
Purpose
FCC feed
Feed, source
VGO + Coker
Gravity, API
17.0
Boiling range, F 400/1,000
Sulfur, wt%
1.37
Nitrogen, ppmw
6,050
Bromine number
Naphtha, vol%
4.8
Gravity, API
45.0
Boiling range, F 180/400
Sulfur, ppmw
50
Nitrogen, ppmw
30
Distillate, vol%
97.2
Gravity, API
24.0
Boiling range, F
400+
Sulfur, wt%
0.025
700
H2 consump., scf/bbl
Desulf. Desulf. Desulf.

AGO
VGO
DSL
25.7
24.3
32.9
310/660 540/1,085 380/700
1.40
3
1.1
400
1,670
102
26
4.2
3.9
1.6
50.0
54.0
51
C4 /356
C5 /300
C4 /325
<2
<2
<1
<1
<2
<0.5
97.6
98.0
99.0
26.9
27.8
35.2
325/660
300+
300
0.001
0.002
0.001
350
620
300
Economics:
Investment, $ per bpsd
Fuel, 103 Btu
Electricity, kWh
1,200 2,000
40100
0.51.5
Installation: Several hundred units installed.

Reference: UOP, LLC., Diesel fuel specifications and demand for the
21st Century, 1998 by UOP LLC.
Licensor: UOP LLC.

I 127

Guard Main reactors (2-4)
reactor
Resid
charge
First stage
reactor
START
HHPS
Recycle
Makeup gas comp.
hydrogen
Recycle
gas heater
Interstage Second stage

stripper
reactor
Gas
Fuel gas
Lean amine
H2
rich gas
Naphtha
Distillate
Treated
atm. resid
Rich amine
Amine
scrubber
Vapor/liquid
separation recycle
Hot low
Cold high Cold low
press. sep. press. flash press. flash Fractionator
Product to
stripping
Feed oil
Hydrotreating
Hydrotreatingaromatic saturation
Application: RCD Unionfining process reduces the sulfur, nitrogen,

Conradson carbon, asphaltene and organometallic contents of heavier
residue-derived feedstocks to allow them to be used as either specification
fuel oils or as feedstocks for downstream processing units such as hydrocrackers, fluidized catalytic crackers, resid catalytic crackers and cokers.
Application: Hydroprocessing of middle distillates, including cracked

materials (coker/visbreaker gas oils and LCO) using SynTechnology, maximizes distillate yield while producing ultra-low-sulfur diesel with improved
cetane and API gain, reduced aromatics, T95 reduction and cold-flow
improvement through selective ring opening, saturation and/or isomerization. Various process configurations are available for revamps and new unit
design to stage investments to meet changing diesel specifications.
Products: Maximum yield of improved quality distillate while minimizing fuel gas and naphtha. Diesel properties include less than 10ppm sulfur, with aromatics content (total and/or PNA), cetane, density
and T95 dependent on product objectives and feedstock.
Description: SynTechnology includes SynHDS for ultra-deep desulfurization and SynShift/SynSat for cetane improvement, aromatics saturation and density/T95 reduction. SynFlow for cold flow improvement can be added as required. The process combines ABB Lummus
Globals cocurrent and/or patented countercurrent reactor technology with
special SynCat catalysts from Criterion Catalyst Co. LP. It incorporates
design and operations experience from Shell Global Solutions, to maximize reactor performance by using advanced reactor internals.
A single-stage or integrated two-stage reactor system provides various
process configuration options and revamp opportunities. In a two-stage
reactor system, the feed, makeup and recycle gas are heated and fed to a
first-stage cocurrent reactor. Effluent from the first stage is stripped to
remove impurities and light ends before being sent to the second-stage
countercurrent reactor. When a countercurrent reactor is used, fresh
makeup hydrogen can be introduced at the bottom of the catalyst bed
to achieve optimum reaction conditions.
Operating conditions: Typical operating conditions range from
5001,000 psig and 600F750F. Feedstocks range from straight-run gas
oils to feed blends containing up to 70% cracked feedstocks that have been
commercially processed. For example, the SynShift upgrading of a feed blend
containing 72% LCO and LCGO gave these performance figures:
Feed: Feedstocks range from solvent-derived materials to atmospheric

and vacuum residues.
Description: The process uses a fixed-bed catalytic system that operates at moderate temperatures and moderate to high hydrogen partial pressures. Typically, moderate levels of hydrogen are consumed with minimal production of light gaseous and liquid products. However, adjustments
can be made to the units operating conditions, flowscheme configuration or catalysts to increase conversion to distillate and lighter products.
Fresh feed is combined with makeup hydrogen and recycled gas, and
then heated by exchange and fired heaters before entering the units reactor section. Simple downflow reactors incorporating a graded bed catalyst
system designed to accomplish the desired reactions while minimizing
side reactions and pressure drop buildup are used. Reactor effluent flows
to a series of separators to recover recycle gas and liquid products. The
hydrogen-rich recycle gas is scrubbed to remove H2S and recycled to the
reactors while finished products are recovered in the fractionation section. Fractionation facilities may be designed to simply recover a fullboiling range product or to recover individual fractions of the hydrotreated
product.
Economics:
Investment (basis: 15,000 to 20,000 bpsd, 2Q 2002,
U.S. Gulf Coast)
$ per bpsd
2,0003,500
Utilities, typical per barrel of fresh feed (20,000 bpsd basis)
Fuel, MMBtu/hr
46
Electricity, kWh
5,100
Steam, HP, lb/hr
8,900
Steam, LP, lb/hr
1,500
Installation: Twenty-six licensed units with a combined licensed

capacity of approximately 900,000 bpsd. Commercial applications have
included processing of atmospheric and vacuum residues and solventderived feedstocks.
Reference: Thompson, G. J., UOP RCD Unionfining Process, R.
A. Meyers, Ed., Handbook of Petroleum Refining Processes, 2nd ed., New
York, McGraw-Hill, 1996.
Licensor: UOP LLC.
Gravity, API
Sulfur, wt% (wppm)
Nitrogen, wppm
Aromatics, vol%
Cetane index
Liquid yield on feed, vol%
Feed blend
25
1.52
631
64.7
34.2
Product
33.1
(2)
<1
34.3
43.7
107.5
Economics: SynTechnology encompasses a family of low-to-moderate

pressure processes. Investment cost will be greatly dependent on feed quality and hydroprocessing objectives. For a 30,000 to 35,000-bpsd unit, the
typical ISBL investment cost in U.S.$/bpsd (U.S. Gulf Coast 2002) are:
Revamp existing unit
New unit for deep HDS
New unit for cetane improvement and HDA
450950
1,1001,200
1,5001,600
Installation: Eleven SynTechnology units are in operation with an additional seven units in design and construction.
Licensor: ABB Lummus Global, Inc., on behalf of the SynAlliance,
which includes Criterion Catalyst Co., LP, and Shell Global Solutions.
128

Recycle
compressor
Water wash
Lean amine
CFI
reactor
Fuel
gas
Feed
Absorber
Hot separator
Rich amine
Heater
Distillate
feed
Cold Sour water

separator
HDM-HDS
reaction
section
Naphtha
Steam
Charge
pump
Hydrogen
Product
stripper
Makeup
compressor
Product
Guard reactors
Low-sulfur, low
cold flow diesel
Hydrotreatingcatalytic dewaxing
Hydrotreatingresid
Application: A versatile family of premium distillates technologies is

used to meet all current and possible future premium diesel upgrading
requirements. The addition of selective normal paraffin hydrocracking
(CFI) function to the deep hydrodesulfurization (UDHDS) reactor will
improve the diesel product cold flow properties for a wide range of waxy
distillate feedstocks.
Application: Upgrade or convert atmospheric and vacuum residues

using the Hyvahl fixed-bed process.
Products: Ultra-low-sulfur distillate is produced with modest amounts

of lighter products. Low-cloud point, or pour point product quality
diesel can be achieved with the CFI processes.
Description: Residue feed and hydrogen, heated in a feed/effluent

exchangers and furnace, enter a reactor sectiontypically comprising of
a guard-reactor section, main HDM and HDS reactors.
The guard reactors are onstream at the same time in series, and they
protect downstream reactors by removing or converting sediment, metals and asphaltenes. For heavy feeds, they are permutable in operation
(PRS technology) and allow catalyst reloading during the run. Permutation frequency is adjusted according to feed-metals content and process
objectives. Regular catalyst changeout allows a high and constant protection of downstream reactors.
Following the guard reactors, the HDM section carries out the remaining demetallization and conversion functions. With most of the contaminants removed, the residue is sent to the HDS section where the sulfur level is reduced to the design specification.
The PRS technology associated with the high stability of the HDS
catalytic system leads to cycle runs exceeding a year even when processing
VR-type feeds to produce ultra-low- sulfur fuel oil.
Description: This Akzo-Fina CFI technology is offered through the

alliance between Akzo Nobel Catalysts and Fina Research S.A. When the
distillate product must meet stringent fluidity specifications, Akzo Nobel
can offer this selective normal paraffin cracking based CFI dewaxing technology. Dewaxing is generally a higher cost process but delivers higher
total product quality. This technology can be closely integrated with UDHDS and other functions to achieve the full upgrading requirements in
low-cost-integrated designs. The CFI process uses a single-stage design
even with high levels of heteroatoms in the feed. The Akzo Fina CFI Technology is equally applicable to revamp and grassroots applications.
Economics:
Investment (basis: 15,000 to 25,000 bpsd, 1Q 2000 U.S. Gulf Coast)
Grassroots unit, $ per bpsd1,000 to 2,000
Products: Low-sulfur fuels (0.3% to 1.0% sulfur) and RFCC feeds

(removal of metals, sulfur and nitrogen, reduction of carbon residue).
Thirty percent to 50% conversion of the 565C+ fraction into distillates.
Installation: Over 15 distillate-upgrading units have applied the

Akzo Fina CFI Technology.
Yields: Typical HDS and HDM rates are above 90%. Net production
of 12% to 25% of diesel + naphtha.
Reference: MAKFining-Premium Distillates Technology : The

future of distillate upgrading, NPRA Annual Meeting, March 2000, San
Antonio.
Economics:
Licensor: Akzo Nobel Catalysts bv and Fina Research S.A.
Investments (basis: 40,000 bpsd, AR to VR feeds, 2002 Gulf

coast), U.S.$/ bpsd
3,500 5,500
Utilities, per bbl feed:
Fuel, equiv. fuel oil, kg
0.3
Power, kWhr
10
Steam production, MP, kg
25
Steam consumption, HP, kg
10
3
1.1
Water, cooling, m
Installation: Two units are in operation (one on atmospheric-residue

feed, the other on vacuum residue) and a third unit using VR feed will
come onstream at the end of 2002; thus, the total installed capacity will
reach 134,000 bpsd.
References: Option for Resid Conversion, BBTC, Oct. 89, 2002,
Istanbul.
Maintaining On-spec products with residue hydroprocessing, 2000
NPRA Annual Meeting, March 2628, 2000, San Antonio.

I 129

Isobutane product
Deisobutanizer
Isomerization
reactors Stabilizer
Fluel gas
Circulating
caustic
n-Butane
Dryer
4 Scrubber
CW
Offgas
C5/C6 feed
START
Isomerate
Spent
caustic
C4 feed
C5+ to blend
Makeup H2
(via guard dryer)
Isomerate
(iC4/nC4 mix)
Hydrogen
Recycle
Isomerization
Isomerization
Application: Converting n-butane to isobutene using the Lummus

butane isomerization process. Isobutane is typically the feedstock for downstream alkylation units or MTBE complexes.
Application: C 5 /C 6 paraffin-rich hydrocarbon streams are isomerized to produce high RON and MON product suitable for addition to
the gasoline pool.
Products: Isobutane, fuel gas. The Lummus butane isomerization

process has high per pass conversion (>60%) and selectivity (>99%), which
provides the highest total yield of isobutene.
Description: Several variations of the C5 /C 6 isomerization process are

available. With either a zeolite or chlorinated alumina catalyst, the choice
can be a once-through reaction for an inexpensive-but-limited octane boost,
or, for substantial octane improvement, the Ipsorb Isom scheme shown
above to recycle the normal paraffins for their complete conversion. The
Hexorb Isom configuration achieves a complete normal paraffin conversion
plus substantial conversion of low (75) octane methyl pentanes gives the
maximum octane results. The product octanes from five process schemes
for treating a light naphtha feed (70 RON) containing a 50/50 mixture
of C5 /C 6 paraffins are:
Description: The Lummus butane process uses Akzo Nobels AT

series catalyst to isomerize n-butane into isobutene. The high-activity chlorided alumina catalyst allows operation at low temperature, which
increases both conversion and selectivity while minimizing capital costs.
The reaction is vapor phase at mild temperatures with the presence of a
small amount of hydrogen. The high stability of the catalyst at low
H2:HC ratios allows operation without a recycle compressor.
The n-butane feed and makeup hydrogen streams are dried over molecular sieves (1), combined, heated to reaction temperatures in feed/effluent exchangers followed by a trim heater and sent to two reactors in series
(2). The two reactors are used to allow operational flexibility and lower the
temperature in the second reactor for higher conversion. The reactor
effluent is sent to a stabilizer column to remove hydrogen and light ends
(3). The stabilizer overhead is directed to fuel gas via a caustic scrubber (4).
The stabilized bottoms is sent to the deisobutanizer which produces the
final isobutene product, recycles n-butane back to the reactors, and
removes any C5+ material that entered the unit in the feed (5).
Economics:
Investment (basis 10,000 bpsd unit) $/bpsd
1,900
Installation: 12,000 bpd DUGAS Dubai, United Arab Emirates.

Zeolite
Process configuration
catalyst
Once-through
80
Deisopentanizer and once-through
82
Deisohexanizer and recycle
86
Normal recycle-Ipsorb
88
Normal and deisohex. recycle-Hexorb
92
Chlorinated
alumina
catalyst
83
84
88
90
92
Operating conditions: The Ipsorb Isom process uses a deisopentanizer (1) to separate the isopentane from the reactor feed. A small
amount of hydrogen is also added to reactor (2) feed. The isomerization
reaction proceeds at moderate temperature producing an equilibrium mixture of normal and isoparaffins. The catalyst has a long service life. The
reactor products are separated into isomerate product and normal paraffins in the Ipsorb molecular sieve separation section (3) which features
a novel vapor phase PSA technique. This enables the product to consist
entirely of branched isomers.
Economics: (basis: Ipsorb A Isomerization unit with a 5,000-bpsd
70 RONC feed needing a 20 point octane boost):
Investment*, million U.S.$
Utilities:
Steam, HP, tph
Steam, MP, tph
Steam, LP, tph
Power, kWh/h
Cooling water, m3/h
13
1.0
8.5
6.8
310
100
* Mid-2002, Gulf coast, excluding cost of noble metals.
Installation: Of 24 licenses issued for C5 /C 6 isomerization plants, 11

units are operating including one Ipsorb unit.

130

Light-ends
separator
2
C4s to MTBE unit
3
4
Hydrogen
C5+
MTBE unit raffinate
Reactor
feed
heater
Overhead
condenser
Vent
Drain
Reflux pump
Reboiler
Olefin
Reactor
START
Olefin
feed pump
HF alkylation or etherification unit feed
Isomerization
Isomerization
Application: Convert normal olefins to isoolefins.
Application: Hydrisom is ConocoPhillips Co.s selective diolefin

hydrogenation process, with specific isomerization of butene-1 to butene2 and 3-methyl-butene-1 to 2-methyl-butene-1 and 2-methyl-butene-2.
The Hydrisom process uses a liquid-phase reaction over a commercially
available catalyst in a fixed-bed reactor.
Description:
C4 olefin skeletal isomerization (IsomPlus)
A zeolite-based catalyst especially developed for this process provides

near equilibrium conversion of normal butenes to isobutylene at high
selectivity and long process cycle times. A simple process scheme and
moderate process conditions result in low capital and operating costs.
Hydrocarbon feed containing n-butenes, such as C 4 raffinate, can be processed without steam or other diluents, nor the addition of catalyst activation agents to promote the reaction. Near-equilibrium conversion levels up to 44% of the contained n-butenes are achieved at greater than
90% selectivity to isobutylene. During the process cycle, coke gradually
builds up on the catalyst, reducing the isomerization activity. At the end
of the process cycle, the feed is switched to a fresh catalyst bed, and the
spent catalyst bed is regenerated by oxidizing the coke with an air/nitrogen mixture. The butene isomerate is suitable for making high purity
isobutylene product.
C5 olefin skeletal isomerization (IsomPlus)
A zeolite-based catalyst especially developed for this process provides

near-equilibrium conversion of normal pentenes to isoamylene at high
selectivity and long process cycle times. Hydrocarbon feeds containing
n-pentenes, such as C5 raffinate, are processed in the skeletal isomerization reactor without steam or other diluents, nor the addition of catalyst
activation agents to promote the reaction. Near-equilibrium conversion
levels up to 72% of the contained normal pentenes are observed at greater
than 95% selectivity to isoamylenes.
Economics: The Lyondell isomerization process offers the advantages of low capital investment and operating costs coupled with a high
yield of isobutylene. Also, the small quantity of heavy byproducts formed
can easily be blended into the gasoline pool. Capital costs (equipment,
labor and detailed engineering) for three different plant sizes are:
Total installed cost: Feedrate, Mbpd ISBL cost, $MM
10
8
15
11
30
30
Utility costs: per barrel of feed (assuming an electric-motordriven compressor) are:
Power, kWh
3.2
Fuel gas, MMBtu
0.44
Steam, MP, MMBtu
0.002
Water, cooling, MMBtu
0.051
Nitrogen, scf
57250
Description: The Hydrisom process is a once-through reaction and,

for typical cat cracker streams, requires no recycle or cooling. Hydrogen
is added downstream of the olefin feed pump on ratio control and the
feed mixture is preheated by exchange with the fractionator bottoms and/or
low-pressure steam. The feed then flows downward over a fixed bed of
commercial catalyst.
The reaction is liquid-phase, at a pressure just above the bubble point
of the hydrocarbon/hydrogen mixture. The rise in reactor temperature
is a function of the quantity of butadiene in the feed and the amount of
butene saturation that occurs.
The Hydrisom process can also be configured using a proprietary catalyst to upgrade streams containing diolefins up to 50% or more, e.g.,
steam cracker C4 steams, producing olefin-rich streams for use as chemical, etherification and/or alkylation feedstocks.
Installation of a Hydrisom unit upstream of an etherification and/or
alkylation unit can result in a very quick payout of the investment due to:
Improved etherification unit operations
Increased ether production
Increased alkylate octane number
Increased alkylate yield
Reduced chemical and HF acid costs
Reduced ASO handling
Reduced alkylation unit utilities
Upgraded steam cracker or other high diolefin streams (30% to
50%) for further processing.
Installation: Ten units licensed worldwide, including an installation
at ConocoPhillips Refinery, Sweeny, Texas.
Installation: One plant is in operation. Three licensed units are in

various stages of design.
Licensor: CDTECH and Lyondell Chemical Co.

I 131

Makeup hydrogen
Gas to scrubbing
and fuel
C4 raffinate to
alky or dehydro
C4 feed/
isobutylene
Isobutylene
dimerization
Isooctene
Isooctene
product recovery
3
TBA recycle
Hydrogenation
Isooctane
1
C5/C6 charge
Penex isomerate
START
Hydrogen
Isomerization
Isooctane
Application: Paraffin isomerization technology for light naphtha

offers a wide variety of processing options that allow refiners to tailor performance to their specific needs. Applications include octane enhancement and benzene reduction. The Penex process is specifically designed
for continuous catalytic isomerization of pentanes, hexanes and mixtures
of the two. The reactions take place in a hydrogen atmosphere, over a fixed
catalyst bed, and at operating conditions that promote isomerization and
minimize hydrocracking.
Application: Conversion of isobutylene contained in mixed-C4 feeds

to isooctane (2,2,4 tri-methyl pentane) to produce a high-quality gasoline blendstock. The full range of MTBE plant feeds can be processed
from refinery FCC, olefin-plant raffinate and isobutane dehydrogenation
processes. The NExOCTANE process is specifically developed to minimize conversion costs of existing MTBE units and offers a cost-effective
alternative to MTBE production.
Products: A typical C5 /C6 light naphtha feedstock can be upgraded to

82-84 RONC in hydrocarbon once-through operation. This can be
increased to about 87-93 RONC by recycling unconverted normal pentane, normal hexane and/or methylpentanes. Some systems for separating
the components for recycle are: vapor phase adsorptive separation (IsoSiv
process), liquid phase adsorptive separation (Molex process), fractionation
in a deisohexanizer column or a combination of fractionation and selective adsorption. The Par-Isom process is a lower cost isomerization option.
It provides a 12 lower octane-number product with regenerable catalyst.
Dryers are not required; recycle hydrogen is needed. The metal oxide catalyst is an ideal replacement for zeolitic catalyst. This process is a cost-effective revamp option.
Description: Hydrogen recycle is not required for the Penex process,
and high conversion is achieved at low temperature with negligible yield
loss. A fired heater is not required. The flow diagram represents the
Hydrogen-Once-Through (HOT) Penex process. A two reactor in series
flow configuration is normally used with the total required catalyst being
equally distributed between the two vessels. This allows the catalyst to be
fully utilized.
Feed and makeup hydrogen are dried (1) over adsorbent and then
mixed. The mixture is heated against reactor effluent and sent to the reactors (2). Reactor effluent passes directly to the stabilizer (3) after heat
exchange. Stabilizer bottoms are sent to gasoline blending in a oncethrough operation or to separation (adsorption or fractionation) in a recycle operation. The light ends are sent to a caustic-scrubber column and then
to fuel.
Economics: The typical estimated erected costs for 2Q 2002 ISBL,
U.S. Gulf Coast for a 10,000-bpsd unit are:
Flowscheme
Penex
Penex/Molex
Penex/DIH
EEC, $MM
10.1
25
17.1
Products: Isooctene and isooctane can be produced, depending on the

refiners gasoline pool. Typical product properties are:
RONC
MONC
Specific gravity
Vapor pressure, psia
ASTM EP, F
Isooctene
101103
8587
0.7010.704
1.8
380390
Description: In the NExOCTANE process, reuse of existing equipment from the MTBE unit is maximized. The process consists of three
sections. First, isobutylene is dimerized to isooctene in the reaction section. The dimerization reaction occurs in the liquid phase over an acidic
ion-exchange resin catalyst, and it uses simple liquid-phase-fixed-bed reactors. The isooctene product is recovered in a distillation system, for
which generally the existing fractionation equipment can be reused. The
recovered isooctene product can be further hydrogenated to produce isooctane. A highly efficient trickle-bed hydrogenation technology is offered
with the NExOCTANE process. This compact and cost-effective technology does not require recirculation of hydrogen. In the refinery, the NExOCTANE process fits as a replacement to MTBE production, thus associated refinery operations are mostly unaffected.
Economics:
Investment cost for revamps depend on the existing MTBE plant
design, capacity and feedstock composition. Typical utility requirements per bbl product:
Steam, 150-psig, lb
700
Electricity, kWh
2.3
1.2
Water, cooling, ft3
Installation: Process has been commercially demonstrated.

Licensor: Kellogg Brown & Root, Inc., and Fortum Oil and Gas OY.
Installation: UOP is the worlds leading licensor in C5/C6 isomerization technology. The first Penex unit was placed on stream in 1958.
Over 188 UOP C5 /C6 isomerization units have been commissioned as
of 2Q 2002.
Licensor: UOP LLC.

132
Isooctane
99100
9699
0.7260.729
1.8
370380

C4 raffinate
MeOH recovery
Isooctene product
Hydrogen
Makeup
methanol
iC4=
recycle
iC4=
H2
Raff. 2 to
alkylation
Existing
MTBE
reactors
Hydrogenation
Makeup water
C4 feed
Isooctane recycle
Modifier
Selectivator recycle
Isooctane
product
Isooctene
product
Dimerization
Isooctane
product
Hydrogenation
Isooctane/isooctene
Isooctene/Isooctane/ETBE
Application: CDIsoether is used for manufacture of high-octane, lowvapor pressure, MTBE-free isooctene and/or isooctane for gasoline
blending. Coproduction of MTBE and isooctene/isooctane in the desired
ratio is also possible.
Application: To produce isooctene or isooctane from isobutylene both

stepsvia catalytic dimerization followed by hydrogenation; with intermediate and final fractionation as required to meet final product specifications. Ideally, it is a drop-in to an existing MTBE reactor with
patented use of modifier to improve selectivity and prolong catalyst life.
Feed: Hydrocarbon streams containing reactive tertiary olefins such as:

FCC C4s, steamcracker C4s or isobutane dehydrogenation product.
Products: Isooctene or isooctane stream containing at least 85% of C8s,
with less than 5,000 ppm oligomers higher than C12 s.
Description: Depending on conversion and investment requirements, various options are available. CDIsoether can provide isobutylene
conversion of up to 99%. The C 4 feed is mixed with a recycle stream containing oxygenates (such as TBA and MTBE), used as selectivator and
heated before entering the reactor. The reactor (1) is a water-cooled
tubular reactor (WCTR) or a boiling-point reactor (BPR).
The heat of reaction is removed by circulating water through the shell
of the WCTR, while the heat of reaction remains in the two-phase BPR
effluent. There is no product recycle. The reactor effluent flows, along
with the selectivator, to the reaction column (2), where isobutene conversion is maximized using catalytic distillation and isooctene product is
fractionated as bottoms product.
Unreacted C4s are taken as column overhead and the selectivator is
drawn as a side stream for recycle together with some C4 hydrocarbons.
The isooctene product can be sent to storage or fed to the hydrogenation
unit to produce saturated hydrocarbonisooctane.
Economics:
Investment (basis grassroots CDIsoethers unit, charging FCC C4s)
5,0007,000 U.S.$ per bpsd of isooctene product
Investment for retrofitting an existing MTBE unit to isooctene production
500750 U.S.$ per bpsd of isooctene produced
Utilities, per bbl of isooctene:
Steam, (300 psig), lb
200250
Water, cooling, gal
1,5002,000
Power, kWh
1.62.0
The process can be easily modified to make ETBE from ethanol and
isobutylene as well.
Description: The process produces an isooctene intermediate or final
product starting with either a mixed C4 feed or on-purpose isobutylene
production. It is based on a highly selective conversion of isobutylene to
isooctene followed by hydrogenation, which will convert over 99.5% of
the isooctene to isooctane. The product has high-gasoline blending quality with superior octane rating and low Rvp. The design has the added
advantage of being inter-convertible between isooctene/isooctane and
MTBE production.
Economics: The drop-in design capability offers an efficient and costeffective approach to conversion of existing MTBE units. In retro-fit applications, this feature allows for maximum utilization of existing equipment
and hardware, thus reducing the capital costs of conversion to an alternate process/production technology. For the production of isooctane, the
process uses low-risk conventional hydrogenation with slight design
enhancements for conversion of isooctene.
The unit can be designed to be inter-convertible between MTBE,
isooctene/isooctane and /or ETBE operations. Thus, economics, as well
as changes in regulations, can dictate changes in the mode of operation over
time.
Commercial plants: Preliminary engineering and licensing is under
evaluation at several MTBE producers worldwide.
Licensor: Lyondell Chemical and Aker Kvaerner.
Licensor: Snamprogetti SpA and CDTECH.

I 133

Sales gas/
fuel gas
EDV scrubber stack
EDV quench
Reagent
Feed gas from

dehydration
Propane
absorber
Purge
LoTOx
injection
Deethanizer
C3+
Low-temperature NOx reduction
LPG recovery
Application: The LoTOx low-temperature oxidation process removes

NOx from flue gases in conjunction with BELCOs EDV wet scrubbing
system. Ozone is a very selective oxidizing agent; it converts relatively insoluble NO and NO2 to higher, more soluble nitrogen oxides. These oxides
are easily captured in a wet scrubber that is controlling sulfur compounds and/or particulates simultaneously.
Application: Recovery of propane and heavier components from

various refinery offgas streams and from low-pressure associated natural
gas. Propane recovery levels approaching 100% are typical.
Description: In the LoTOx process, ozone is added to oxidize insoluble NO and NO2 to highly oxidized, highly soluble species of NOx that
can be effectively removed by a variety of wet or semi-dry scrubbers. Ozone,
a highly effective oxidizing agent, is produced onsite and ondemand by
passing oxygen through an ozone generatoran electric corona device
with no moving parts. The rapid reaction rate of ozone with NOx results
in high selectivity for NOx over other components within the gas stream.
Thus, the NOx in the gas phase is converted to soluble ionic compounds in the aqueous phase; the reaction is driven to completion, thus
removing NOx with no secondary gaseous pollutants. The ozone is consumed by the process or destroyed within the system scrubber. All system components are proven, well-understood technologies with a history of safe and reliable performance.
Operating conditions: Ozone injection typically occurs in the fluegas stream upstream of the scrubber, near atmospheric pressure and at temperatures up to roughly 160C. For higher-temperature streams, the
ozone is injected after a quench section of the scrubber, at adiabatic saturation, typically 60C to 75C. High-particulate and sulfur loading (SOx
or TRS) do not cause problems.
Description: Low-pressure hydrocarbon gas is compressed and dried

before being chilled by cross-exchange and propane refrigerant. The
chilled feed stream is then contacted with a recycled liquid ethane stream
in the propane absorber. The absorber bottoms is pumped to the deethanizer, which operates at higher pressure than the absorber. The tower overhead is condensed with propane refrigerant to form a reflux stream composed primarily of ethane. A slip stream of the reflux is withdrawn and
recycled back to the propane absorber. The deethanizer bottoms stream
contains the valuable propane and heavier components which may be further processed as required by conventional fractionation.
Economics: Compared to other popular LPG recovery processes,
PRO-MAX typically requires 10-25% less refrigeration horsepower.
Installation: First unit under construction for Pertamina.
Reference: U.S. Patent 6,405,561 issued June 18, 2002.
Licensor: Black & Veatch Pritchard, Inc.
Economics: The costs for NOx control using this technology are
especially low when used as a part of a multi-pollutant control scenario.
Sulfurous and particulate-laden streams can be treated attractively as no
pretreatment is required by the LoTOx system. Typical costs range from
$1,500 to $4,000/t of NOx controlled.
Installation: The technology has been developed and commercialized
over the past seven years, winning the prestigious 2001 Kirkpatrick
Chemical Engineering Technology Award. As of early 2002, four full-scale
commercial installations are operating successfully. Pilot-scale demonstrations have been completed on coal- and petroleum-coke fired boilers, as well as, many other combustion and process sources. An FCCU
pilot demonstration is contracted to occur in the fall 2002.
Licensor: Belco Technologies Corp., as a sub-licensor for The BOC
Group, Inc.

134

Vacuum
Solvent
distillation extraction
Hydrotreating
and redistillation
Dewaxing
125 neutral
Atmospheric
residue
250 neutral
500 neutral
2
Feed
4
5
START
Stm.
Extracts
Stm.
Water
Bright stock
Deasphalting
Refined oil
Extract
Asphalt
Tops
Waxes/LPG
Lube hydroprocessing
Lube treating
Application: The Hybrid base oil manufacturing process is an optimized combination of solvent extraction and one-stage hydroprocessing.
It is particularly suited to the revamping/debottlenecking of existing
solvent extraction lube oil plants; capacity increases as great as 60% can
be achieved. Solvent extraction also liensed by Shell.
Application: Bechtels MP Refining process is a solvent extraction

process that uses N-methyl-2-pyrrolidone (NMP) as the solvent to
selectively remove undesirable components of low lubrication oil quality, which are naturally present in crude oil distillate and residual stocks.
The unit produces paraffinic or naphthenic raffinates that are suitable
for further processing into lube-base stocks. This process selectively
removes aromatics and compounds containing heteroatoms (e.g., oxygen, nitrogen and sulfur).
Feed: Derived from a wider range of crudes than can be used with solvent extraction. Yields and capacity are less sensitive to feedstock than when
the solvent extraction process is applied.
Description: Two separate upgrading units are used; solvent extraction
and one-stage hydroprocessing. Individual waxy distillate streams are either
mildly solvent-extracted and then hydroprocessed or are solvent extracted
at normal severity. Deasphalted oil is either mildly solvent extracted and
then hydroprocessed or is only hydroprocessed. The choice of solvent
extraction and hydroprocessing depends upon the feedstock and the objectives of debottlenecking (min. capital expenditure or max. capacity increase).
When the Shell process is used to debottleneck a lube oil plant, it is necessary to construct two new units: a hydrotreating/redistillation unit and an additional dewaxing unit (the existing dewaxing unit usually has insufficient spare
capacity). There is normally no need to construct additional vacuum distillation/deasphalting/solvent extraction units. However, some modifications will
be required to the existing vacuum distillation and solvent extraction units.
Yields: Depend upon the grade of base oil and the crude origin of the
feedstock. Shell Hybrid gives a significantly higher yield of base oil crude
and the yield is much less sensitive to feedstock origin than with solvent
extraction process.
Base oils obtained via the Shell Hybrid process are lighter in color
and have lower Conradson carbon residue contents than their solvent
extracted counterparts and can more advantageously be used in a number
of special applications. Moreover, the low-sulfur, low-pour-point gas oil
byproducts from the hydrotreating unit can have enhanced value in special markets, while the quantity of low-value byproducts (e.g., extracts) is
substantially reduced.
Economics: The following table compares the economics of debottlenecking a 300 ktpy solvent extraction complex to 500 ktpy with the
economics of a new 200 ktpy solvent extraction complex.
Solvent extraction
200 ktpy grass-roots
Capital charge
36% of total
Fixed costs
20% of total
Variable costs
8% of total
Hydrocarbon cost
36% of total
Total
100% of total
Hybrid debottlenecking
(from 300 to 500 ktpy)
24 36% of solvex total
79% of solvex total
8% of solvex total
11% of solvex total
5064% of solvex total
Installation: The process has been commercially applied in Shells Geelong refinery since 1980. Pertamina is applying the Shell Hybrid technology to debottleneck its Cilacap refinerythe successful start occurred
in the second half of 1998.
Products: A raffinate that may be dewaxed to produce a high-quality,

lube-base oil, characterized by high-viscosity index, good thermal and oxidation stability, light color and excellent additive response. The byproduct extracts, having a high aromatic content, can be used, in some cases,
for carbon black feedstocks, rubber extender oils and other nonlube
applications where this feature is desirable.
Description: The distillate or residual feedstock and solvent are contacted in the extraction tower (1) at controlled temperatures and flowrates
required for optimum countercurrent, liquid-liquid extraction of the
feedstock. The extract stream, containing the bulk of the solvent, exits
the bottom of the extraction tower. It is routed to a recovery section to
remove solvent contained in this stream. The solvent is separated from
the extract oil by multiple-effect evaporation (2) at various pressures, followed by vacuum flashing and steam stripping (3) under vacuum. The
raffinate stream exits the overhead of the extraction tower and is routed
to a recovery section for removal of the NMP solvent contained in this
stream by flashing and steam stripping (4) under vacuum.
Overhead vapors from the steam strippers are condensed and combined with solvent condensate from the recovery sections and are distilled at low pressure to remove water from the solvent (5). Solvent is
recovered in a single tower because NMP does not form an azeotrope
with water, as does furfural. The water is drained to the oily-water sewer.
The solvent is cooled and recycled to the extraction section.
Economics:
Investment (basis: 10,000-bpsd feedrate
capacity, 2002 U.S. Gulf Coast), $/bpsd
Fuel, 103 Btu (absorbed)
Electricity, kWh
Steam, lb
2,500
130
0.8
8
550
Installation: This process is being used in 15 licensed units to produce high-quality lubricating oils. Of this number, eight are units converted from phenol or furfural, with another two units being planned for
conversion from furfural. Presently, two new units that will refine used
oil have been designed.
Licensor: Bechtel Corp.


I 135
Waxy feed
Dichill
Scraped
crystallizer(s) surface
chillers
Dewaxing filters
1 or 2 stages
Warm-up
deoiling heater
START
Wax slurry
Precoolers
Extraction
tower
Raffinate
mix buffer
Fresh
solvent
Refrigeration
system
Cold-wash
solvent
Raffinate
flasher
stripper
Cold-wash solvent
Raffinate
Stm
Extract
mix
settler
Extract
flasher
stripper
Extract
flash
system
Stm
Extract
Solvent
Solvent
recovery
Solvent
recovery
Deoiling filters
(2 stages)
Solvent
recovery
Dewaxed oil Dewaxed wax Foots oil
Stm
Feed
deaerator
Furfural
stripper
buffer
Solvent
drying
system
Decanter
Feed
Water
stripper
Stm
Stm
Sewer
Lube treating
Lube treating
Application: Lube raffinates from extraction are dewaxed to provide

basestocks having low pour points (as low as 35C). Basestocks range
from light stocks (60N) to higher viscosity grades (600N and bright stock).
Byproduct waxes can also be upgraded for use in food applications.
Application: Process to produce lube oil raffinates with high viscosity index from vacuum distillates and deasphalted oil.
Feeds: DILCHILL dewaxing can be used for a wide range of stocks that
boil above 550F, from 60N up through bright stock. In addition to raffinates from extraction, DILCHILL dewaxing can be applied to hydrocracked stocks and to other stocks from raffinate hydroconversion processes.
Products: Lube oil raffinates of high viscosity indices. The raffinates

contain substantially all of the desirable lubricating oil components present in the feedstock. The extract contains a concentrate of aromatics that
may be utilized as rubber oil or cracker feed.
Processes: Lube basestocks having low pour points. Although slack

waxes containing 210 wt.% residual oil are the typical byproducts,
lower-oil-content waxes can be produced by using additional dewaxing
and/or warm-up deoiling stages.
Description: DILCHILL is a novel dewaxing technology in which wax
crystals are formed by cooling waxy oil stocks, which have been diluted
with ketone solvents, in a proprietary crystallizer tower that has a number of mixing stages. This nucleation environment provides crystals that
filter more quickly and retain less oil. This technology has the following
advantages over conventional incremental dilution dewaxing in scrapedsurface exchangers: less filter area is required, less washing of the filter cake
to achieve the same oil-in-wax content is required, refrigeration duty is
lower, and only scraped surface chillers are required which means that unit
maintenance costs are lower. No wax recrystallization is required for
deoiling.
Warm waxy feed is cooled in a prechiller before it enters the
DILCHILL crystallizer tower. Chilled solvent is then added in the crystallizer tower under highly agitated conditions. Most of the crystallization occurs in the crystallizer tower. The slurry of wax/oil/ketone is further cooled in scraped-surface chillers and the slurry is then filtered in
rotary vacuum filters. Flashing and stripping of products recover solvent.
Additional filtration stages can be added to recover additional oil or produce low-oil content saleable waxes.
Feeds: Vacuum distillate lube cuts and deasphalted oils.
Description: This liquid-liquid extraction process uses furfural as

the selective solvent to remove aromatics and other impurities present in
the distillates and deasphalted oils. Furfural has a high solvent power for
those components that are unstable to oxygen as well as for other undesirable materials including color bodies, resins, carbon-forming constituents and sulfur compounds. In the extraction tower, the feed oil is
introduced below the top at a predetermined temperature. The raffinate
phase leaves at the top of the tower and the extract, which contains the
bulk of the furfural, is withdrawn from the bottom. The extract phase is
cooled and a so-called pseudo raffinate may be sent back to the extraction tower. Multi-stage solvent recovery systems for raffinate and extract
solutions secure energy efficient operation.
Utility requirements, (typical, Middle East Crude), units per m 3
of feed:
Electricity, kWh
Steam, MP, kg
Steam, LP, kg
Fuel oil, kg
Water, cooling, m 3
10
10
35
20
20
Installation: Numerous installations using the Uhde Edeleanu proprietary technology are in operation worldwide. The most recent is a complete lube-oil production facility licensed to the state of Turkmenistan,
which successfully passed performance testing in 2002.
Economics: Depend on the slate of stocks to be dewaxed, the pour

point targets and the required oil-in-wax content.
Utilities: Depend on the slate of stocks to be dewaxed, the pour point
targets and the required oil-in-wax content.
Installation: The first application of DILCHILL dewaxing was the
conversion of an ExxonMobil affiliate unit on the U.S. Gulf Coast in 1972.
Since that time, 10 other applications have been constructed. These
applications include both grassroots units and conversions of incremental dilution plants. Six applications use warming-up deoiling.

136

Excess distillates
Heater load
Lights to
refinery
NH3 flow
controller
Pressure
controller
NOx
analyzer
Intermediate
storage
Injectors
Anhydrous NH3
storage
Flow controller
Unconverted oil (UCO)

Lube
Catalytic
dewaxing products
START
Distillation
NH3
vaporizer
Heater
Heater load
Fuel
Hydrogen
Carrier supply
Combustion air
Lube treating
NOx abatement
Application: Unconverted oil from a fuels hydrocracker is used to produce higher quality lube base stocks at lower investment and operating
costs than either solvent refining or lube oil hydrocracking utilizing the
SK UCO Lube Process.
Application: Flue gases are treated with ammonia via ExxonMobils

proprietary selective noncatalytic NOx reduction technology Thermal
DeNOx. NOx plus ammonia (NH3) are converted to elemental nitrogen
and water if temperature and residence time are appropriate. The technology has been widely applied since it was first commercialized in 1974.
Description: The base oils manufactured by the SK UCO Lube Process have many desirable properties as lube base stocks over those produced
by conventional solvent-refining or lube hydrocracking processes.
Unconverted oil from the existing fractionator in a fuels hydrocracker
is processed and separated into grades having the desired viscosity, which
are then cooled and sent to intermediate storage. The various grades of base
oil are then catalytically dewaxed and isomerized in blocked operation.
Excess distillates are sent back to the hydrocracker.
Since the withdrawn UCO can usually be replaced with an equal
amount of additional fresh vacuum distillate feed, the hydrocracker fuels
production is maintained. The hydrocracking and catalytic dewaxing
steps are not included in the SK UCO Lube Process, but are readily available from others.
Properties:
Test item
Viscosity @100C, cSt
Viscosity index
Pour point, C
CCS vis @20C, cP
Flash point, C
NOACK volatility, wt%
Aromatics, wt%
Sulfur content, wt%
Test method
ASTM D 445
ASTM D 2270
ASTM D 97
ASTM D 2602
ASTM D 92
DIN 51581
ASTM D 2549
ANTEC
Solvent
refining
5.2
97
12
2,100
218
17.0
27.7
0.58
Lube
SK
hydro- UCO Lube
cracking Process
5.1
6.0
99
130
12
12
2,000
1,440
220
234
16.6
7.8
3.5
1.0
0.03
0.00
Economics: Investment (Basis: 5,000 bpd of lube base oils excluding

fuels hydrocracker, 1998 U.S. Gulf Coast) $80 million.
Installation: 5,000 bpd of VHVI lube base oils at SK Corporations
Ulsan, Korea refinery.
Reference: Andre, J. P., S. H. Kwon and S. K. Hahn, Yukongs new
lube base oil plant, Hydrocarbon Engineering, November 1997.
An economical route to high quality lubricants, NPRA 1996 Annual
Meeting, March 1996.
Products: If conditions are appropriate, the flue gas is treated to

achieve NOx reductions of 40% to 70%+ with minimal NH3 slip or leakage.
Description: The technology involves the gas-phase reaction of NO
with NH3 (either aqueous or anhydrous) to produce elemental nitrogen
if conditions are favorable. Ammonia is injected into the flue gas using
steam or air as a carrier gas into a zone where the temperature is 1,600F
to 2,000F. This range can be extended down to 1,300F with a small
amount of hydrogen added to the injected gas. For most applications, wall
injectors are used for simplicity of operation.
Yield: Cleaned flue gas with 40% to 70%+ NOx reduction and less than
10-ppm NH3 slip.
Economics: Considerably less costly than catalytic systems but relatively variable depending on scale and site specifics. Third-party studies
have estimated the all-in cost at about 600 U.S.$/ton of NOx removed.
Installation: Over 135 applications on all types of fired heaters, boilers and incinerators with a wide variety of fuels (gas, oil, coal, coke, wood
and waste).
Reference: McIntyre, A. D., Applications of the THERMAL DeNOx
process to utility and independent power production boilers, ASME Joint
International Power Generation Conference, Phoenix, 1994.
McIntyre, A. D., The THERMAL DeNOx process: Liquid fuels
applications, International Flame Research Foundations 11th Topic
Oriented Technical Meeting, Biarritz, France, 1995.
McIntyre, A. D., Applications of the THERMAL DeNOx process
to FBC boilers, CIBO 13th Annual Fluidized Bed Conference, Lake
Charles, Louisiana, 1997.
Licensor: The Badger Technology Center of Washington Group International, under exclusive arrangement with SK Corp.

I 137

C4 paraffins
Process
steam
Fuel gas
C4 olefins
Extractive
distillation
column
C4
fraction
Stripper
column
Fresh
feed
Reaction
section
Heat
recovery
Gas compression
Gas
separation
Frac- Product
tionation
Recycle
Solvent
Solvent + olefins
Olefins
Olefins
Application: Separation of pure C4 olefins from olefinic/paraffinic C4

mixtures via extractive distillation using a selective solvent. BUTENEX
is the Uhde technology to separate light olefins from various C4 feedstocks,
which include ethylene cracker and FCC sources.
Application: Dehydrogenation of C4 or C 3 paraffins to pure olefins

using steam-active reforming over a noble metal catalyst. STAR, the steam
active reforming process, is the Uhde technology to dehydrogenate light
paraffins into olefins.
Description: In the extractive distillation (ED) process, a singlecompound solvent, N-Formylmorpholine (NFM), or NFM in a mixture
with further morpholine derivatives, alters the vapor pressure of the
components being separated. The vapor pressure of the olefins is lowered
more than that of the less soluble paraffins. Paraffinic vapors leave the top
of the ED column, and solvent with olefins leave the bottom of the ED
column.
The bottom product of the ED column is fed to the stripper to separate pure olefins (mixtures) from the solvent. After intensive heat exchange,
the lean solvent is recycled to the ED column. The solvent, which can
be either NFM, or a mixture including NFM, perfectly satisfies the solvent properties needed for this process, including high selectivity, thermal
stability and a suitable boiling point.
Description: Fresh paraffin feed is combined with internally generated steam and passed after preheating to the reactora fixed-bed, tubular top-fired reformer type. Dehydrogenation reactions occurs at 4 to 6
bar at 500C to 580C. In a subsequent fixed-bed reactor, oxygen (or air)
is admixed to enhance olefins yield by partial combustion of the hydrogen generated in the upstream reactor. The reaction section operates in
sequential mode (7 hours on-stream, 1 hour regeneration). Product flow
is balanced by a parallel reactor arrangement for continuous production.
After heat recovery, the gas is compressed, and the pure olefin product
is separated from non-converted paraffins and light ends. Apart from fuel
gas, which is used within the unit, high-purity olefin is the only product.
Economics:
Consumption per ton of FCC C4 fraction feedstock:
Steam, t/t
0.50.8
15.0
Water, cooling ( T = 10C), m3/t
25.0
Product purity:
n-Butene content
99.+ wt.% min.
Solvent content
1 wt. ppm max.
Installation: Two commercial plants for the recovery of n-butenes have

been installed since 1998.
Economics:
Consumption per ton of propylene product based on standard
grade propane feedstock:
Feedstock, t/t
1.20
Fuel, Gcal/t
1.18
200
Water, cooling (T = 10 C), m3/t
170
Product purity:
Propylene
99.70 wt.% min.
Installation: Two commercial plants for the dehydrogenation of

butane have been commissioned since 1992.
Reference: Preusser, G., Separation of n-Butanes and Butene-2 by

extractive distillation, Achema, June 1986, Frankfurt.
Reference: Thiagarajan, N., Ranke, U. and Ennenbach, F.,

Propane /butane dehydrogenation by steam active reforming, Achema,
May 2000, Frankfurt.

138

Residue gas
to fuel
Expander
Inlet heat
3 exchanger
Reaction
section
C3
Catalyst
removal
Stabilization
2b
LPG
CW
HEFC
2a
Expander
compressor
C3
Cold
separator
Catalyst
5
LEFC
Inlet gas
from
dehydration
Stm.
Condensate
Feedstock
Caustic
Process
water
Liquid product
Dimate to
gasoline pool
Olefins recovery
Oligomerization of C3C4 cuts
Application: Linde BOC Process Plants Cryo-Plus process recovers

ethylene or propylene and heavier components from refinery offgas
streams. Typical applications are on cat crackers, cokers or reformers downstream of the existing gas-recovery systems. Incremental valuable hydrocarbons that are currently being lost to the refinery fuel system can now
be economically recovered.
Application: To dimerize light olefins such as ethylene, propylene and

butylenes using the Dimersol process. The main applications are:
Dimerization of propylene, producing a high-octane, low-boiling
point gasoline called Dimate
Dimerization of n-butylene producing C8 olefins for plasticizer
synthesis.
The C3 feeds are generally the propylene cuts from catalytic cracking
units. The C4 cut source is mainly the raffinate from butadiene and
isobutylene extraction.
Description: Refinery offgases from cat crackers, cokers or other

sources are first dehydrated by molecular sieve (1). The expander/compressor (2a) compresses the gas stream, which is then cooled by heat
exchange with internal process streams (3). Depending on the richness
of the feed gas, supplemental refrigeration (4) may be used to further cool
the gas stream prior to primary vapor/liquid separation (5). Light gases
are fed to a turboexpander (2b) where the pressure is reduced resulting
in a low discharge temperature. The expander discharge is fed to the bottom of the LEFC (6). The HEFC (7) overhead is cooled and fed to the
top of the LEFC. The recovered ethylene or propylene and heavier liquid stream exit the bottom of the HEFC (7). Process advantages include:
Low capital cost
High propylene or high ethylene recovery (up to 99%)
Low energy usage
Small footprintcan be modularized
Simple to operate
Wide range of turndown capability.
Economics: Typically, the payback time for plant investment is one
to two years.
Installation: Sixteen plants operating in U.S. refineries, with two under
construction. The first plant was installed in 1984.
References: Buck, L., Separating hydrocarbon gases, U.S. Patent
No. 4,617,039, Oct. 14, 1986.
Key, R., and Z. Malik, Technology advances improve liquid recovery
from refinery offgases, NPRA Annual Meeting, San Antonio, March
2628, 2000.
Licensor: Linde BOC Process Plants LLC, a member of Linde Engineering Division.
Description: Dimerization is achieved in the liquid phase at ambient temperature by means of a soluble catalytic complex. One or several
reactors (1) in series are used. After elimination of catalyst (2, 3), the products are separated in an appropriate distillation section (4).
Product quality: For gasoline production, typical properties of the
Dimate are:
Specific gravity, @15C
End point, C
70% vaporized, C
Rvp, bar
RONC
MONC
RON blending value, avg.
0.70
205
80
0.5
96
81
103
Economics: For a plant charging 100,000 tpy of C3 cut (% propylene)

and producing 71,000 tpy of Dimate gasoline:
Investment for a 2002 ISBL Gulf Coast erected cost, excluding
engineering fees, U.S.
$7 million
Utilities per ton of feed
Electric power, kWh
10.8
Steam, HP, t
0.14
Water, cooling, t
28.5
Catalyst + chemicals, U.S.D
9.3
Installation: Twenty-seven units have been built or are under construction.

Reference: Olefin oligomerization with homogeneous catalysis,
1999 Dewitt Petrochemical Conference, Houston.

I 139

Steam
Raffinate
Preheat
Preheat
3
Product
gas
2
C4 feed
Polynaphtha
product
Oligomerizationpolynaphtha
Application: To produce C6+ isoolefin fractions that can be used as
high-octane blending stocks for the gasoline pool and high-smoke-point
blending stocks for kerosine and jet fuel. The Polynaphtha and Selectopol
processes achieve high conversions of light olefinic fractions into higher
value gasoline and kerosine from propylene and mixed-butene fractions
such as C3 and C4 cuts from cracking processes.
Description: Propylene or mixed butenes (or both) are oligomerized
catalytically in a series of fixed-bed reactors (1). Conversion and selectivity
are controlled by reactor temperature adjustment while the heat of reaction is removed by intercooling (2). The reactor section effluent is fractionated (3) producing raffinate, gasoline and kerosine.
The Selectopol process is a variant of the polynaphtha process where
the operating conditions are adjusted to convert selectively the isobutene
portion of an olefinic C4 fraction to high-octane, low-Rvp gasoline blending stock. It provides a low cost means of debottlenecking existing alkylation units by converting all of the isobutene and a small percentage of
the n-butenes, without additional isobutane.
Polynaphtha and Selectopol processes have the following features: low
investment, regenerable solid catalyst, no catalyst disposal problems, long
catalyst life, mild operating conditions, versatile product range, good
quality motor fuels and kerosine following a simple hydrogenation step and
the possibility of retrofitting old phosphoric acid units.
The polygasoline RON and MON obtained from FCC C4 cuts are significantly higher than those of FCC gasoline and, in addition, are sulfur-free. Hydrogenation improves the MON, whereas the RON remains
high and close to that of C4 alkylate.
Kerosine product characteristics such as oxidation stability, freezing
point and smoke point are excellent after hydrogenation of the polynaphtha product. The kerosine is also sulfur-free and low in aromatics.
The Polynaphtha process has operating conditions very close to those
of phosphoric acid poly units. Therefore, an existing units major equipment items can be retained with only minor changes to piping and instrumentation. Some pretreatment may be needed if sulfur, nitrogen, or water
contents in the feed warrant; however, the equipment cost is low.
Economics: Typical ISBL Gulf Coast investments for 5,000-bpd of
FCC C4 cut for polynaphtha (of maximum flexibility) and Selectopol (for
maximum gasoline) units are U.S.$8.5 and $3.0 million, respectively.
Respective utility costs are U.S.$4.4 and 1.8 per ton of feed while catalyst costs are U.S.$0.2 per ton of feed for both processes.
HDS vessel
Lead
desulfurization
vessel
Hydrocarbon feed
Lag
desulfurization
vessel
Prereforming with feed

ultrapurification
Application: Ultra-desulfurization and adiabatic-steam reforming of
hydrocarbon feed from refinery offgas or natural gas through LPG to naphtha feeds as a prereforming step in the route to hydrogen production.
Description: Sulfur components contained in the hydrocarbon feed
are converted to H2S in the HDS vessel and then fed to two desulfurization
vessels in series. Each vessel contains two catalyst typesthe first for bulk
sulfur removal and the second for ultrapurification down to sulfur levels of less than 1 ppb.
The two-desulfurization vessels are arranged in series in such a way
that either may be located in the lead position allowing online change
out of the catalysts. The novel interchanger between the two vessels
allows for the lead and lag vessels to work under different optimized conditions for the duties that require two catalyst types. This arrangement may
be retrofitted to existing units.
Desulfurized feed is then fed to a fixed bed of nickel-based catalyst
that converts the hydrocarbon feed, in the presence of steam, to a product stream containing only methane together with H2 , CO, CO2 and
unreacted steam which is suitable for further processing in a conventional
fired reformer. The CRG prereformer enables capital cost savings in primary reforming due to reductions in the radiant box heat load. It also
allows high-activity gas-reforming catalyst to be used. The ability to
increase preheat temperatures and transfer radiant duty to the convection section of the primary reformer can minimize involuntary steam
production.
Operating conditions: The desulfurization section typically operates between 170C and 420C and the CRG prereformer will operate
over a wide range of temperatures from 250C to 650C and at pressures
up to 75 bara.
Installation: CRG process technology covers 40 years of experience
with over 150 plants built and operated. Ongoing development of the
catalyst has lead to almost 50 such units since 1990.
Catalyst: The CRG catalyst is manufactured under license by Synetix.
Licensor: The process and CRG catalyst are licensed by Davy Process
Technology.
Installations: Five Selectopol and polynaphtha units have been

licensed (four in operation), with a cumulative operating experience
exceeding 40 years.

140
CRG
prereformer

Number 2 flue gas
Fresh gas
Product vapors
Cat.
Cat.
Quench gas to reactors

Cat.
Withdrawal well
3
Air ring
Number 1 flue gas
HHPS
Packed stripper
First stage
regenerator
Air ring
Lift air
Riser termination device
1
2
CHPS
Reactor riser
CLPS
HLPS
MTC system
Gasoil or resid. feed
Cat.
START
Feed
Cat. Cat.
HDM section
HCON section
To fractionator
Resid catalytic cracking
Residue hydroprocessing
Application: Selective conversion of gas oil and heavy residual feedstocks.
Application: Produces maximum distillates and low-sulfur fuel oil,

or low-sulfur LR-CCU feedstock, with very tight sulfur, vanadium and
CCR specifications, using moving bed bunker and fixed-bed technologies. Bunker units are available as a retrofit option to existing fixedbed residue HDS units.
Products: High-octane gasoline, distillate and C3C4 olefins.

Description: For residue cracking the process is known as R2R (reactor2 regenerators). Catalytic and selective cracking occurs in a short-contact-time riser (1) where oil feed is effectively dispersed and vaporized
through a proprietary feed-injection system. Operation is carried out at
a temperature consistent with targeted yields. The riser temperature profile can be optimized with the proprietary mixed temperature control
(MTC) system (2).
Reaction products exit the riser-reactor through a high-efficiency, closecoupled, proprietary riser termination device RS2 (riser separator stripper) (3).
Spent catalyst is pre-stripped followed by an advanced high-efficiency packed
stripper prior to regeneration. The reaction product vapor may be quenched
using Amocos proprietary technology to give the lowest dry gas and maximum gasoline yield. Final recovery of catalyst particles occurs in cyclones
before the product vapor is transferred to the fractionation section.
Catalyst regeneration is carried out in two independent stages (4, 5)
equipped with proprietary air and catalyst distribution systems resulting in
fully regenerated catalyst with minimum hydrothermal deactivation, plus
superior metals tolerance relative to single-stage systems. These benefits
are derived by operating the first-stage regenerator in a partial-burn mode,
the second-stage regenerator in a full-combustion mode and both regenerators in parallel with respect to air and flue gas flows. The resulting system is capable of processing feeds up to about 6 wt% ConC without additional catalyst cooling means, with less air, lower catalyst deactivation and
smaller regenerators than a single-stage regenerator design. Heat removal
for heavier feedstocks (above 6 CCR) may be accomplished by using a
reliable dense-phase catalyst cooler, which has been commercially proven
in over 24 units and is licensed exclusively by Stone & Webster/Axens.
The converter vessels use a cold-wall design that results in minimum
capital investment and maximum mechanical reliability and safety. Reliable
operation is ensured through the use of advanced fluidization technology
combined with a proprietary reaction system. Unit design is tailored to
refiners needs and can include wide turndown flexibility. Available options
include power recovery, wasteheat recovery, flue-gas treatment and slurry
filtration.
Existing gas oil units can be easily retrofitted to this technology. Revamps
incorporating proprietary feed injection and riser termination devices and
vapor quench result in substantial improvements in capacity, yields and feedstock flexibility within the mechanical limits of the existing unit.
Installation: Stone & Webster and Axens have licensed 26 full-technology R2R units and performed more than 100 revamp projects.
Reference: Letzsch, W. S., Commercial performance of the latest FCC
technology advances, NPRA Annual Meeting, March 2000.
Licensor: Stone & Webster Inc., a Shaw Group Co., and Axens, IFP
Group Technologies.
142
Description: At limited feed metal contents, the process typically uses

all fixed-bed reactors. With increasing feed metal content, one or more
moving-bed bunker reactors are added up-front of the fixed-bed reactors to ensure a fixed-bed catalyst life of at least one year. A steady state
is developed by continuous catalyst addition and withdrawal: the catalyst aging is fully compensated by catalyst replacement, at typically 0.5
to 2 vol% of inventory per day.
An all bunker option, which eliminates the need for catalyst changeout, is also available. A hydrocracking reactor, which converts the synthetic vacuum gasoil into distillates, can be efficiently integrated into the
unit. A wide range of residue feeds, like atmospheric or vacuum residues
and deasphalted oils, can be processed using Shell residue hydroprocessing technologies.
Reactor pressures:
Reactor temperatures:
100200 bar
1,4503,000 psi
370420C
700790F
Yields: Typical yields for an SR HYCON unit on Kuwait feed:

Feedstock
Yields:
Gases
Naphtha
Kero + gasoil
VGO
Residue
H2 cons.
C1 C4
C5 165C
165370C
370580C
580C+
SR
with
(95% 520C+) integrated HCU
[%wof]
[%wof]
3
5
4
18
20
43
41
4
29
29
2
3
Economics: Investment costs for the various options depend strongly

on feed properties and process objectives of the residue hydroprocessing
unit. Investment costs for a typical new single string 5,000 tpsd SR-Hycon
unit will range from 200300 MM US $, the higher figure includes an
integrated hydrocracker.
Installation: There is one unit with both bunker reactors and fixedbed reactors, operating on short residue (vacuum residue) at 4,300 tpd
or 27 kbpsd capacity, and two all-fixed bed units of 7,700 and 7,000 tpd
(48 and 44 kbpsd resp.), the latter one in one single string. Commercial
experiences range from low-sulfur atmospheric residues to high-metal,
high-sulfur vacuum residues with over 300 ppmw metals.
Reference: Scheffer, B., et al, The Shell Residue Hydroconversion
Process: Development and achievements, The European Refining Technology Conference, London, November 1997.

Reclaimed SO2
Quench column
pre-scrubber
Condenser
Cleaned
gas
H2S gas
Stripper
Vapor/
liquid
separator
Absorber
Buffer
makeup
Flue gas
Combustion air
SO2
Steam
Steam
converter
Buffer tank
Particulates
Blower
Stack gas
Blower
Air
Incinerator
WSA
condenser
Salt
circulation
system
LP
steam
Heat
exch.
Salt Salt
pump Tank
Condensate
Oxidation
product removal
Acid
pump
Acid cooler
Product acid
SO2 removal
Sour gas treatment
Application: Regenerative scrubbing system to recover SO2 from

flue gas containing high SO2 levels such as gas from FCC regenerator or
incinerated SRU tail gas and other high SO2 applications. The LABSORB
process is a low-pressure drop system and is able to operate under varying conditions and not sensitive to variations in the upstream processes.
Application: The WSA process (Wet gas Sulfuric Acid) process treats
all types of sulfur-containing gases such as amine and Rectisol regenerator offgas, SWS gas and Claus plant tail gas in refineries, gas treatment
plants, petrochemicals and coke chemicals plants. This process can also
be applied for SOx removal and regeneration of spent sulfuric acid.
Sulfur, in any form, is efficiently recovered as concentrated commercial-quality sulfuric acid.
Products: The product from the LABSORB process is a concentrated

SO2 stream consisting of approximately 90% SO2 and 10% moisture. This
stream can be sent to the front of the SRU to be mixed with H2S and form
sulfur, or it can be concentrated for other marketable uses.
Description: Hot dirty flue gas is cooled in a flue-gas cooler or wasteheat recovery boiler prior to entering the systems. Steam produced can
be used in the LABSORB plant. The gas is then quenched to adiabatic
saturation (typically 50C 75C) in a quencher/pre-scrubber; it proceeds
to the absorption tower where the SO2 is removed from the gas. The tower
incorporates multiple internal and re-circulation stages to ensure sufficient absorption.
A safe, chemically stable and regenerable buffer solution is contacted
with the SO2-rich gas for absorption. The rich solution is then piped to
a LABSORB buffer regeneration section where the solution is regenerated
for re-use in the scrubber. Regeneration is achieved using low-pressure
steam and conventional equipment such as strippers, condensers and heat
exchangers.
Economics: This process is very attractive at higher SO2 concentrations or when liquid or solid effluents are not allowed. The systems
buffer loss is very low, contributing to a very low operating cost. Additionally, when utilizing LABSORB as an SRU tail-gas treater, many
components normally associated with the SCOT process are not required
thus saving considerable capital.
Installations: One SRU tail-gas system and two FCCU scrubbing systems.
Description: Feed gas is combusted and cooled to approximately 420C

in a waste-heat boiler. The gas then enters the SO2 converter containing
one or several beds of SO2 oxidation catalyst to convert SO2 to SO3. The
gas is cooled in the gas cooler whereby SO3 hydrates to H2SO4 (gas), which
is finally condensed as concentrated sulfuric acid (typically 98% w/w).
The WSA condenser is cooled by ambient air; the heated air may be
used as combustion air in the burner for increased thermal efficiency.
The heat of reaction released in the reactor and gas cooler is transferred by
a heat displacement system to a boiler where it is recovered as steam. The
process operates without removing water from the gas. Therefore, the
number of equipment items is minimized, and generation of waste condensate is eliminated. Cleaned process gas leaving the WSA condenser
is sent to stack without further treatment.
More than 99% recovery of sulfur as commercial-grade sulfuric
acid.
No generation of waste solids or wastewater.
No consumption of absorbents or auxiliary chemicals.
Efficient heat recovery thus, ensuring economical operation.
Simple and fully automated operation allows adaptation to variations
in feed gas flow and composition.
Installation: More than 40 units worldwide
Reference: Confuorto, Weaver and Pedersen, LABSORB regenerative scrubbing operating history, design and economics, Sulfur 2000,
San Francisco, October 2000.
Confuorto, Eagleson and Pedersen, LABSORB, A regenerable wet
scrubbing process for controlling SO2 emissions, Petrotech-2001, New
Delhi, January 2001.
Licensor: Belco Technologies Corp. (LABSORB was developed by Prof.
Olav Erga of NTNU in Trondheim, Norway.)

I 143

Stack gas
Dust
removal
Spent acid
+ fuel feed
DENOX
SO2
converter
Sweep gas to
SRU process
Air
Vent
eductor
Incinerator
Export steam
WSA
condenser
Heat exchange system
Sulfur cooler
Steam
LP
LP Sulfur
condensate steam pumps
Overflow
Degassed
sulfur product
Air
Molten sulfur
from SRU
condensers
Cooler
Steam coils
Acid
Spent acid recovery
Sulfur degassing
Application: The WSA process (Wet gas Sulfuric Acid) treats spent
sulfuric acid from alkylation as well as other types of waste sulfuric acid
in the petrochemical and coke chemicals industry. Amine regenerator offgas and /or refinery gas may be used as auxiliary fuel. The regenerated
acid will contain min. 98% H2SO4 and can be recycled directly to the
alkylation process.
The WSA process is also applied for conversion of H2S and removal
of SOx.
Application: Hydrogen sulfide (H2S) removal from sulfur.
Description: Spent acid is decomposed to SO2 and water in a burner

using amine regenerator offgas or refinery gas as fuel. The SO2 containing flue gas is cooled in a waste-heat boiler; solid matter originating from
the acid feed is separated in an electrostatic precipitator. By adding preheated air, the process gas temperature and oxygen content are adjusted
before the catalytic converter when converting SO2 to SO3. The gas is
cooled in the gas cooler whereby SO3 is hydrated to H2SO4 (gas), which
is finally condensed as 98% sulfuric acid.
The WSA condenser is cooled by ambient air; the heated air may be
used as combustion air in the burner for increased thermal efficiency.
The heat of reaction released in the reactor and the gas cooler is transferred by a heat displacement system to a boiler where it is recovered as
steam.
The process operates without removing water from the gas. Therefore, the number of equipment items is minimized and generation of
condensate is eliminated. This is especially important in spent-acid regeneration where SO3 formed by the acid decomposition will otherwise be lost
with the condensate as wastewater.
More than 99% recovery of sulfuric acid
No generation of waste solids or wastewater
No consumption of absorbents or auxiliary chemicals
Efficient heat recovery ensuring economical operation
Simple and fully automated operation enables variations in feed
flow and composition.
Installation: More than 40 WSA units worldwide, including six for
spent-acid recovery.
Description: Sulfur, as produced by the Claus process, typically contains from about 200 to 500 ppmw H2S. The H2S may be contained in
the molten sulfur as H2S or as hydrogen polysulfides (H2S x ). The dissolved H2S separates from the molten sulfur readily, but the H2Sx does
not.
The sulfur degassing process accelerates the decomposition of hydrogen polysulfides to H2S and elemental sulfur (S). The dissolved H2S gas
is released in a controlled manner. Sulfur temperature, residence time,
and the degree of agitation all influence the degassing process. Chemical catalysts, including oxygen (air) that accelerate the rate of H2Sx decomposition are known to improve the degassing characteristics.
In fact, the majority of successful commercial degassing processes use
compressed air, in some fashion, as the degassing medium. Research performed by Alberta Sulphur Research Ltd. has demonstrated that air is a
superior degassing agent when compared to nitrogen, steam or other inert
gases. Oxygen present in air promotes a level of direct oxidation of H2S
to elemental S, which reduces the gaseous H2S partial pressure and increases
the driving force for H2Sx decomposition to the more easily removed
gaseous phase H2S.
The MAG degassing system concept was developed to use the benefits of degassing in the presence of air without relying on a costly compressed air source. With the MAG system, motive pressure from a recirculated degassed sulfur stream is converted to energy in a mixing assembly
within the undegassed sulfur. The energy of the recirculated sulfur creates
a high air-to-sulfur interfacial area by generating intense turbulence within
the jet plume turning over the contents many times, thus exposing the
molten sulfur to the sweep air. Intimate mixing is achieved along with
turbulence to promote degassing. This sulfur degassing system can readily meet a 10 ppmw total H2S (H2S + H2Sx ) specification.
Tests show degassing rate constants nearly identical to traditional air
sparging for well-mixed, air-swept degassing systems. Thus, comparable
degassing to air sparging can be achieved without using a compressed air
source. The assemblies are designed to be self-draining of molten sulfur and
to be easily slipped in and out for maintenance through the pit nozzles provided. The mixing assemblies require no moving parts or ancillary equipment other than the typical sulfur-product-transfer pump that maximizes
unit reliability and simplifies operations.
The process is straightforward; it is inherently safer than systems using
spray nozzles and/or impingement plates because no free fall of sulfur is
allowed.
Economics: Typically does not require changes to existing sulfur processing infrastructure.
Installation: Several units are in design.
Reference: U.S. Patent 5935548 issued Aug. 10, 1999.
Licensor: Black & Veatch Pritchard, Inc.

144

Gas
Naptha
Air
Catalyst in (batch)
Jet fuel
START
Steam
Gasoil
Recycle
LC
3
2
Waxy
distillate
5
Steam
Recycle
Recycle
2
LC
LC
Jet fuel
6
M
Charge
Vacuum flashed
cracked residue
Caustic out
Water in
Caustic in
Water out
Thermal gasoil process
Treating
Application: The Shell Thermal Gasoil process is a combined residue

and waxy distillate conversion unit. The process is an attractive low-cost
conversion option for hydroskimming refineries in gasoil-driven markets
or for complex refineries with constrained waxy distillate conversion
capacity. The typical feedstock is atmospheric residue, which eliminates
the need for an upstream vacuum flasher. This process features Shell Soaker
Visbreaking technology for residue conversion and an integrated recycle
heater system for the conversion of waxy distillate.
Application: Treating gas, LPG, butane, propane, gasoline, condensate, kerosine, diesel and light crude oil with caustic, amine, water and
acid using the following technologies that use the FIBER-FILM contactor.
Description: The preheated atmospheric (or vacuum) residue is

charged to the visbreaker heater (1) and from there to the soaker (2). The
conversion takes place in both the heater and soaker and is controlled by
the operating temperature and pressure. The soaker effluent is routed to
a cyclone (3). The cyclone overheads are charged to an atmospheric
fractionator (4) to produce the desired products including a light waxy
distillate. The cyclone and fractionator bottoms are routed to a vacuum
flasher (6), where waxy distillate is recovered. The combined waxy distillates are fully converted in the distillate heater (5) at elevated pressure.
Yields: Depend on feed type and product specifications.
Feed atmospheric residue
Viscosity, cSt @ 100C
Products, % wt.
Gas
Gasoline ECP 165C
Gasoil ECP 350C
Residue ECP 520C+
Viscosity 165C plus, cSt @100C
Middle East
31
6.4
12.9
38.6
42.1
7.7
Economics: The investment amounts to 1,4001,600 U.S.$/bbl

installed excluding treating facilities and depending on capacity and
configuration (basis: 1998)
Utilities, typical consumption per bbl of feed @ 180C:
34
Fuel, 103 cal
Electricity, kWh
0.8
29
3
0.17
Water, cooling, m
Installation: Thirteen Shell thermal gasoil units have been built or

are under construction. Post startup services and technical services on existing units are available from Shell.
Reference: Thermal Conversion Technology in Modern Power Integrated Refinery Schemes, 1999 NPRA Annual Meeting.
Licensor: Shell Global Solutions International B.V., and ABB Lummus Global B.V.
Description: A proprietary FIBER-FILM contactor is used in treating processes to achieve co-current contacting between the hydrocarbon
feed and aqueous solution. The FIBER-FILM contactor is comprised of
a bundle of long, continuous, small diameter fibers contained in a cylinder. The large, interfacial area created by the contactor greatly enhances
mass transfer without dispersion of one phase into the other as is necessary for typical conventional mixing systems. Process advantages include:
Low capital costs
Flexibility to operate over a wide range of hydrocarbon flowrates
Small sized equipment and low space requirement
Low pressure drop
Can be retrofitted into existing systems or skid mounted for easy system installation
Low guaranteed aqueous carryover.
AQUAFINING uses water to remove amines and caustic contaminants from hydrocarbon streams.
THIOLEX removes H2S, COS and mercaptans from gas, LPG, butane
and gasoline with caustic.
AMINEX removes H2S, COS and CO2 from gas, LPG, propane and
butane with amine.
THIOLEX coupled with REGEN, a caustic regeneration process, is
used for mercaptan extraction with minimal caustic consumption. One or
more stages of caustic extraction are used to remove H2S, COS and mercaptans from gas, LPG, propane, butane and gasoline. The catalyst-containing caustic solution then is sent to a tower for regeneration with air.
The disulfides formed are either gravity separated and/or solvent extracted.
The regenerated solution is then reused in the extraction unit.
MERICAT uses a catalyst-containing caustic solution and air to oxidize mercaptans to disulfides in gasoline.
MERICAT II sweetens kerosine/jet fuel by combining MERICAT
with a catalyst impregnated carbon bed.
NAPFINING uses caustic to reduce the acidity of kerosine/jet fuel
and heavier middle distillates.
CHLOREX uses dilute caustic to remove HCl and NH 4Cl from
reformer gas and liquid products.
ESTEREX uses sulfuric acid to remove neutral and acidic esters from
alkylation reactor effluent streams.
MERICON oxidizes and/or neutralizes spent caustics containing sulfides, mercaptans, napthenic acids and phenols.
EXOMER removes recombinant mercaptans from selectively
hydrotreated gasoline with a proprietary treating solution to reduce its
total sulfur content.
Installation: Over 540 installations treating 6.0 million bpsd and 21
million scfd in 39 countries.
Licensor: Merichem Chemicals & Refinery Services LLC.

I 145

Vacuum tower
Side strippers
Gas
To vacuum system
Vacuum gasoil
Heater
Naphtha
Stm
Low visc.
Stm
Medium visc.
High visc.
BFW
Metals cut
Steam
Residue
charge
Steam
Gas oil
Vacuum system
Vacuum gas oil
START
Visbroken residue
Vacuum resid.
Cutter stock
Feed
Vacuum distillation
Visbreaking
Application: Process to produce vacuum distillates that are suitable

for lubricating oil production by downstream units.
Application: The Shell Soaker Visbreaking process is most suitable

to reduce the viscosity of vacuum (and atmospheric) residues in (semi)
complex refineries. The products are primarily distillates and stable fuel
oil. The total fuel oil production is reduced by decreasing the quantity
of cutter stock required. Optionally, a Shell vacuum flasher may be
installed to recover additional gas oil and waxy distillates as cat cracker
or hydrocracker feed from the cracked residue. The Shell Soaker Visbreaking technology has also proven to be a very cost-effective revamp
option for existing units.
Feeds: Atmospheric bottoms from crude oils (atmospheric residue) or

hydrocracker bottoms.
Products: Vacuum distillates of precisely defined viscosities and flash
points as well as vacuum residue with specified softening point, penetration
and flash point.
Description: Feed is preheated in a heat-exchanger train and fed to
the fired heater. The heater-coil temperature is controlled to produce the
required quality of vacuum distillates and residue. Uhde Edeleanudesigned units ensure that vaporization occurs in the furnace coils to minimize superheating the residue. Circulating reflux streams enable maximum heat recovery and reduced column diameter.
Wash trays minimze the metals content in the heaviest vacuum distillate
to avoid difficulties in downstream lubricating oil production plants.
Heavy distillate from the wash trays is recycled to the heater inlet or withdrawn as metals cut.
When processing naphthenic residues, a neutralization section may be
added to the fractionator.
Utility requirements, (typical, Middle East Crude), units per m3
of feed:
Electricity, kWh
Steam, MP, kg
Steam production, LP, kg
Fuel oil, kg
Water, cooling, m3
7
30
35
15
10
Installation. Numerous installations using the Uhde Edeleanu proprietary technology are in operation worldwide. The most recent reference is a complete lube-oil production facility licensed to the state of Turkmenistan, which successfully passed performance testing in 2002.
Description: The preheated vacuum residue is charged to the visbreaker

heater (1) and from there to the soaker (2). The conversion takes place
in both the heater and the soaker. The operating temperature and pressure are controlled such as to reach the desired conversion level and/or
unit capacity. The cracked feed is then charged to an atmospheric fractionator (3) to produce the desired products like gas, LPG, naphtha, kerosine, gas oil, waxy distillates and cracked residue. If a vacuum flasher is
installed, additional gas oil and waxy distillates are recovered from the
cracked residue.
Yields: Vary with feed type and product specifications.
Feed, vacuum residue
Viscosity, cSt @100C
Products, wt%
Gas
Gasoline, 165C EP
Gas oil, 350C EP
Waxy distillate, 520C EP
Residue, 520C+
Viscosity, 165C plus, cSt @100C
Middle East
770
2.3
4.7
14.0
20.0
59.0
97
Economics: The investment amounts to 1,000 to 1,400 U.S.$/bbl

installed excluding treating facilities and depending on capacity and the
presence of a vacuum flasher (basis: 1998).
Utilities, typical consumption per bbl feed @180C:
Fuel, 103 kcal
Electricity, kWh
Water, cooling, m3
16
0.5
18
0.1
Installation: Eighty-six Shell Soaker Visbreaking units have been

built or are under construction. Post startup services and technical services for existing units are available from Shell.
Reference: Visbreaking Technology, Erdl und Kohle, January 1986.
Licensor: Shell Global Solutions International B.V. and ABB Lummus
Global B.V.

146

Gas
Cleaned gas
Stack
Droplet
separators
Reagent addition
Gasoline
Reduced
crude charge
Filtering
modules
Absorber
Steam
START
Gas oil
Tar
Flue gas
Quench
Slipstream to purge
treatment unit
Recirculation
pumps
Visbreaking
Wet scrubbing system
Application: Manufacture incremental gas and distillate products and

simultaneously reduce fuel oil viscosity and pour point. Also, reduce the
amount of cutter stock required to dilute the resid to meet the fuel oil
specifications. Foster Wheeler/UOP offer coil type visbreaking process.
Application: EDV Technology is a low-pressure drop scrubbing system, to scrub particulate matter (including PM2.5), SO2 and SO3 from
flue gases. It is especially well suited where the application requires high
reliability, flexibility and the ability to operate for 36 years continuously
without maintenance shutdowns. The EDV technology is highly suited
for FCCU regenerator flue-gas applications.
Products: Gas, naphtha, gas oil, visbroken resid (tar).

Description: In a coil type operation, charge is fed to the visbreaker heater (1) where it is heated to a high temperature, causing partial vaporization and mild cracking. The heater outlet stream is quenched
with gas oil or fractionator bottoms to stop the cracking reaction. The
vapor-liquid mixture enters the fractionator (2) to be separated into gas,
naphtha, gas oil and visbroken resid (tar).
Operating conditions: Typical ranges are:
Quenched temperature, F
850910
710800
An increase in heater outlet temperature will result in an increase in overall severity.

Yields:
Feed, source
Light Arabian
Type
Atm. resid
Gravity, API
15.9
Sulfur, wt%
3.0
Concarbon, wt%
8.5
Viscosity, CKS @ 130F
150
CKS @ 210F
25
Products, wt%
Gas
3.1
7.9
Naphtha (C5 330F)
Gas oil (330600F)
14.5
Visbroken resid (600F+)
74.5
(1)
(2)
Light Arabian
Vac. resid
7.1
4.0
20.3
30,000
900
2.4
6.0
15.5(1)
76.1(2)
330662F cut for Light Arabian vacuum residue.

662F+ cut for Light Arabian vacuum residue.
Economics:
Investment (basis: 40,000 10,000 bpsd, 4Q 1999, U.S. Gulf),
$ per bpsd
7851,650
Fuel, MMBtu
0.1195
Power, kW/bpsd
0.0358
Steam, MP, lb
6.4
Water, cooling, gal
71.0
Installation: Over 50 units worldwide.

Reference: Handbook of Petroleum Refining Processes, 2nd Ed., McGrawHill, 1997, pp. 12.8312.97.
Licensor: Foster Wheeler/UOP LLC.
Products: The effluents from the process will vary based on the
reagent selected for use with the scrubber. In the case where a sodiumbased reagent is used, the product will be a solution of sodium salts. Similarly, a magnesium-based reagent will result in magnesium salts. A
lime/limestone-based system will produce a gypsum waste. The EDV technology can also be used with the LABSORB buffer thus making the system regenerative. The product, in that case, would be a usable condensed SO2 stream.
Description: The flue gas enters the spray tower through the quench
section where it is immediately quenched to saturation temperature. It
proceeds to the absorber section for particulate and SO2 reduction. The
spray tower is an open tower with multiple levels of BELCO-G-Nozzles.
These nonplugging and abrasion-resistant nozzles remove particulates by
impacting on the water/reagent curtains. At the same time, these curtains
also reduce SO2 and SO3 emissions. The BELCO-G-Nozzles are designed
not to produce mist; thus a conventional mist eliminator is not required
these units can be prone to plugage.
Upon leaving the absorber section, the saturated gases are directed to
the EDV filtering modules to remove the fine particulates and additional
SO3. The filtering module is designed to cause condensation of the saturated gas onto the fine particles and onto the acid mist, thus allowing it
to be collected by the BELCO-F-nozzle located at the top.
To ensure droplet-free stack, the flue gas enters a droplet separator.
This is an open design that contains fixed-spin vanes that induce a cyclonic
flow of the gas. As the gases spiral down the droplet separator, the centrifugal forces drive any free droplets to the wall, separating them from the
gas stream.
Economics: The EDV wet scrubbing system has been extremely successful in the incineration and refining industries due to the very high
scrubbing capabilities, very reliable operation and reasonable price.
Installation: More than 200 applications worldwide on various processes including 25 FCCU applications, 3 CDU applications and 1 fluidized coker application to date.
Reference: Confuorto and Weaver, Flue gas scrubbing of FCCU
regenerator flue gasperformance, reliability, and flexibilitya case
history, Hydrocarbon Engineering, 1999.
Eagleson and Dharia, Controlling FCCU emissions, 11th Refining Technology Meeting, HPCL, Hyderabad, 2000.
Licensor: Belco Technologies Corp.

I 147

Makeup hydrogen
EDV scrubber
stack
Purge
Reactor
H2
recycle
Crystalizer
Oil
stripper
Tailgas
Purge
Reactor
H2
recycle
EDV quench
Stm
Waste
Food or
medicinalgrade
white oil
Reagent
Thickner
Solids
Stripped oil
Feed
First stage
Technical white oil
or fully refined wax
Second stage
Food or medicinalgrade white oil
Technical grade white

oil or fully-refined wax
Wet-chemistry NOx reduction
White oil and wax hydrotreating
Application: When AquaNOx is applied to BELCOs EDV wet

scrubbing system, one can achieve simultaneous high-efficiency SOx
and NOx removal from FCCU regenerator gas or flue gases.
Application. Process to produce white oils and waxes.
Description: A NOx absorbing additive to a caustic scrubbing DeSOx

unit enables simultaneous removal of both pollutants. The SO2 of the feed
gas, plus additional reducing reagent at low SO2 levels, converts NO to
N2 and gives a sodium-salt-waste byproduct. This byproduct is removed
from the recirculating solvent as a solid by low-temperature crystallization. The process operating conditions are chosen to regenerate the additive for continued high-efficiency scrubbing. SO2 removal is nearly complete, while the NO removal can be >90% if sufficient mass transfer
capability is provided in the absorber. The process can be easily retrofitted
to an existing caustic scrubber by installing the liquid side equipment to
maintain solvent quality. The equipment footprint is small.
Operating conditions: Most applications would use atmospheric
pressure scrubbing, at the adiabatic saturation temperature of the feed gas
in the range up to 160F.
Economics: The costs additional to caustic DeSOx costs for a unit treating 440,000 scfm of 115 ppm NO and 230 ppm SO2 are about $4 million capital + royalty fee and $800,000 operating cost/yr.
Development status: The process has been pilot tested at small
scale on FCCU regenerator offgas. One or more large-scale pilot plant
tests are planned for late 2002.
Licensor: Belco Technologies Corp., and Cansolv Technologies Inc.
Feeds: Non-refined as well as solvent- or hydrogen-refined naphthenic

or paraffinic vacuum distillates or deoiled waxes.
Products: Technical- and medical-grade white oils and waxes for plasticizer, textile, cosmetic, pharmaceutical and food industries. Products are
in accordance with the U.S. Food and Drug Administration (FDA) regulations and the German Pharmacopoeia (DAB 8 and DAB 9) specifications.
Description: This catalytic hydrotreating process uses two reactors.
Hydrogen and feed are heated upstream of the first reaction zone (containing a special presulfided NiMo/ alumina catalyst) and are separated
downstream of the reactors into the main product and byproducts
(hydrogen sulfide and light hydrocarbons). A stripping column permits
adjusting product specifications for technical-grade white oil or feed to
the second hydrogenation stage.
When hydrotreating waxes, however, medical quality is obtained in the
one-stage process. In the second reactor, the feed is passed over a highly
active hydrogenation catalyst to achieve a very low level of aromatics,
especially of polynuclear compounds. This scheme permits each stage to
operate independently and to produce technical- or medical-grade white
oils separately. Yields after the first stage range from 85% to 99% depending on feedstock. Yields from the second hydrogenation step are nearly
100%. When treating waxes, the yield is approximately 98%.
Utility requirements, (typical, Middle East Crude), units per m3
of feed:
Electricity, kWh
Steam, LP, kg
Water, cooling, m3
Hydrogen, kg
1st stage
for techn.
white oil
197
665
48
10.0
2nd stage
for med.
white oil
130
495
20
2.6
Foodgrade
wax
70
140
7
1.6
Installation: Four installations use the Uhde Edeleanu proprietary technology, one of which has the largest capacity worldwide.
Licensor: Uhde Edeleanu GmbH and through sublicense agreement
with BASF.

148

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Refining

Gasoline desulfurization . . . . . . . . . . . 113

Isooctene /Isooctane/ETBE . . . . . . . . . 133

ConocoPhillips Co., Fuels Technology

Refining Processes 2002

Application: Combines propylene, butylene and pentylene with

Products: Alkylate is a high-octane, low-Rvp gasoline component

Installation: Demonstration unit at Fortums Porvoo, Finland Refinery.

1.78 bbl C5+/bbl butylene feed

Installation: 115,000-bpd capacity at 11 locations with the sizes

HYDROCARBON PROCESSING NOVEMBER 2002

Circle 276 on Reader Service Card

Refining Processes 2002

Application: The Topse fixed-bed alkylation (FBA) technology

Application: Convert propylene, amylenes, butylenes and isobutane

Products: A high-octane, low-RVP and ultra-low-sulfur blending

Economics: (Basis: MTBE raffinate, inclusive feed pretreatment and

Licensor: Haldor Topse A/S.

Products: An ultra-low-sulfur, high-octane and low-Rvp blending

Installation: 107 alkylation units licensed worldwide.

HYDROCARBON PROCESSING NOVEMBER 2002

Circle 278 on Reader Service Card

Refining Processes 2002

Application: To combine propylene, butylenes and amylenes with

Products: Branched chain hydrocarbons for use in high-octane motor

Installation: Nearly 600,000 bpsd installed capacity.

Description: Olefin charge is first treated to remove impurities such

Investment (basis: 6,000-bpsd unit), $ per bpsd

Licensor: UOP LLC.

Reference: Hydrocarbon Processing, Vol. 64, No. 9, September 1985,

Circle 279 on Reader Service Card

Circle 280 on Reader Service Card

Refining Processes 2002

Application: The UOP Indirect Alkylation (InAlk) process uses solid

Application: Upgrades alkylation plant feeds with Alkyfining process.

Description: The InAlk process combines two, commercially proven

Investment (basis: 2,800-bpsd unit), $/bpsd

Licensor: UOP LLC.

Description: Diolefins and acetylenes in the C 4 (or C3 C 4 ) feed react

The increases in MON, RON and butenes yield are reflected in a

Annual savings for a 10,000-bpsd alkylation unit:

Circle 281 on Reader Service Card

HYDROCARBON PROCESSING NOVEMBER 2002

Circle 282 on Reader Service Card

Refining Processes 2002

Aromatics extractive distillation

Application: Simultaneous recovery of benzene, toluene and xylenes

Application: Recovery of high-purity aromatics from reformate,

Description: At the top of extractor operating at 30C to 50C and

475 kg/t ED feed

680 kg/t ED feed**

Reformate feedstock with low aromatics content (20wt%):

Installation: One Morphylex plant was erected.

Installation: 45 Morphylane plants (total capacity of more than 6

Reference: Emmrich, G., F. Ennenbach and U. Ranke, Krupp Uhde

Reference: Emmrich, G., F. Ennenbach and U. Ranke, Krupp Uhde

Licensor: Uhde GmbH.

Licensor: Uhde GmbH.

Circle 283 on Reader Service Card