CLL703 - Report 02 - Group08 PDF

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REPORT 02: LITERATURE SURVEY OF PROCESS DESIGNS

DESIGN 01: DIRECT SYNTHESIS


Almost 15% of total world production of HCl is through free chlorine and hydrogen. The gas formed after the
Direct synthesis3. In this process, elemental H2 and Cl2 react reaction contains 92% HCl by volume. It is then passed
directly to form HCl. through an absorbed which then gives a solution with
30-32% acid. This type of acid is generally called burner
! 2 + Cl 2 HCl H = 184k J
H grade HCl.4
Since this reaction is very exothermic, large amount heat is
generated inside the adiabatic reactor which raises the Generally, for small scale units, absorber and burner
temperature of mixture to as high as 2490oC. Here the equal chamber are a part of same unit. Whereas, in large scale
proportions of hydrogen and chlorine are mixed. At this production, they are separate units.Preferred material used
temperature, 4.2% free chlorine is present. Then the feed during construction of burner is Silica. Also, HCl gas
temperature is suddenly brought down to 200oC to convert produced through this method is very pure. It can even be
used to make pure acid through absorption processes.

!
Figure 1: Direct synthesis of HCl from H2 and Cl2 (CW stands for cold water)

DESIGN 02: RECOVERY BY ABSORPTION


Production of large amounts of hydrochloric acid are treated in various ways. For a purer product, fractional
integrated with formation of chlorinated products. This is distillation can be used, for e.g. products from cracking of
the most widely used approach for HCl production. Formed dichloroethane may be liquified and distilled into vinyl
HCl gas is either reused or absorbed resulting in HCl acid. chloride and HCl. HCl recovery can also be done through
Example reactions include : aqueous absorption of HCl. When HCl acid is the primary
product, water is used as absorption medium; else, if the
RH + Cl2 RCl + HCl demand for HCl acid is low, 20% azeotropic HCl acid is
used.
C + 2H2O + 2Cl2 4HCl + CO2
CHC is removed from concentrated HCl acid. The it is
Production of vinyl chloride (chloroethylenes) from 1,2-
passed through HCl desorption column to give HCl gas and
dichloroethane is a major source of hydrogen chloride. azeotropic HCl acid.
Hydrogen chloride produced through methods can be
!
Figure 2 Flow diagram showing recovery of HCl as a byproduct of chlorination in aqueous absorption (CHC: chlorinated
hydrocarbons). a) HCl absorption column. b) chlorinated hydrocarbon stripping column. c) HCl desorption column

DESIGN 03: INCINERATION OF WASTE ORGANICS


Of the several existing process designs, we choose to present the production of hydrochloric acid by incineration of
chlorocarbons owing to its idiosyncratic advantages viz. very cheap production costs5,6 and ability of the process to curb
environmental pollution by utilising a malign class of compounds as its reactants.7

Figure 3: A simplified block diagram of incineration process


Combustion: Incineration or pyrolysis of hydrocarbons Separation: These gases are then separated by scrubbing in
produce carbon dioxide and water. In case of chlorocarbons an absorption column. Water easily forms an azeotrope with
additional chlorine based simple products are obtained. hydrochloric acid above 20% concentration. Although the
Combustion of chlorocarbons takes place in a refractory- product gases are fully separated from the combustion
lined furnace at a temperature of 1000-1200 oC. gases. The inlet to the absorption column is the outlet of
the Sub X. All the liquid is transported using pumps and
The high heat in the furnace ensures complete combustion fresh water is added from the top in a countercurrent
at stoichiometric conditions. The exhaust gases are cooled fashion. The columns is divided into sections based on the
down to a temperature less than 100 oC in a submerged concentration needed. The non soluble components from the
exhaust (Sub X) which cools the gases down without using absorber include nitrogen carbon dioxide which do not
a heat exchanger. Quenching reduces the temperature.10 dissolve appreciably in water at atmospheric conditions.
The materials used in this construction must not corrode The recovery is enhanced by removing traces of hydrochloric
and and must be able to resist high temperatures. acid and chlorine using an alkaline liquid for absorption.11

3. HCl Synthesis: Improved overall performance with Micro Motion Zirconium 8. R. W. Bach, H. A. Friedrichs, H. Rau, High Temp. High Pressures 9 (1977)
Density Fork http://www.emerson.com/documents/automation/66802.pdf 305 312.
4. See reference 1 9. See reference 8
5. Y.-R. Chin, SRI International, Menlo Park, Calif., private communication, 10. S. Ezaki, U.S. Pat 3,58 9,864, "Process for Recovering HCl From a Spent Organic-
Chlorine Compound," June 2 9 ,1971.
1994.
11. See reference 5
6. includes labor costs, variable costs, overhead, taxes, and depreciation
7. See reference 1

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