MDEP Ethanol Spill Response Report

LARGE VOLUME ETHANOL SPILLS – ENVIRONMENTAL
IMPACTS AND RESPONSE OPTIONS
Prepared for:
Prepared by:
Shaw’s Environmental and Infrastructure Group

11 Northeastern Boulevard
Salem, New Hampshire 03079
July 2011
ACKNOWLEDGEMENTS
The project team instrumental in the development of this document includes the following from
Massachusetts Department of Environmental Protection (MassDEP): Nick Child, Central
Regional Office, Chief Emergency Response; Dan Crafton, Southeast Regional Office, Chief
Emergency Response; Kingsley Ndi, Northeast Regional Office, Chief Emergency Response;
David Slowick, Western Regional Office, Chief Emergency Response; Albe Simenas, Boston
Office, Chief Emergency Response; and the following from Shaw: Joanne Perwak; Guy
Gallello; Vikas Tandon; Dorothy Small; and Charles Schaefer.
MassDEP would also like to acknowledge the support and assistance of numerous government
agencies and other parties in the development of this report.
Local Level
Blackstone Fire Department, MA
Blackstone Emergency Management, MA
Fitchburg Fire Department, MA
Everett Fire Department, MA
Woonsocket Fire Department, HazMat and Training Divisions
Providence Fire Department, RI
New London Fire Department, CT
Mystic Fire Department, CT
State Level
Massachusetts Department of Environmental Protection, Emergency Response
Massachusetts Department of Environmental Protection, Field Assessment Support Team
Massachusetts Department of Environmental Protection, Office of Research and Standards
Massachusetts Department of Fire Service, Hazmat
Massachusetts Emergency Management Agency
Massachusetts State Police Hazmat/Tactical Operations/IMAT
Massachusetts Department of Conservation and Recreation, Emergency Response
Massachusetts Water Resource Authority, Emergency Response
Massachusetts Department of Energy Resources, Alternate Transportation Program/Mass Clean
Cities
Massachusetts Fish & Wildlife
Massachusetts State Emergency Response Commission
Rhode Island Department of Environmental Management, Emergency Response
Rhode Island Emergency Management Agency
Connecticut Department of Environmental Protection, Emergency Response
Connecticut Department of Emergency Management and Homeland Security
Connecticut Fire Academy
Connecticut State Emergency Response Commission
Ohio Environmental Protection Agency (state), Emergency Response
i
Pennsylvania Department of Environmental Protection, Emergency Response
Illinois Environmental Protection Agency (state), Emergency Response
USF&WS, Environmental Contamination Program, Illinois, USF&WS
Oregon Department of Environmental Quality, Emergency Response
Federal
USEPA Region 1, Emergency Planning and Response
USEPA Region 1, Emergency Planning and Community Right-To-Know Act
Mike Brazel, NIMS/HazMat Coordinator, US FEMA
Federal Railroad Administration, HazMat Division US DOT
US Coast Guard, Marine Safety Lab
US Coast Guard, Waterways Management, Sector Boston
US Coast Guard/National Office of Atmosphere Scientific Support Coordinator, Sector Boston
Private Sector/Other
Renewable Fuels Association
Providence & Worcester Railroad, Rules and Safety
Motiva Providence, New England Complex
Husky Energy Refinery - NW Ohio, Emergency Response
ExxonMobil, Everett, MA
Central Mass Homeland Security Advisory Council
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iii
Table of Contents________________________________________________
Executive Summary
1.0 Introduction ..................................................................................................................................... 1-1
1.1 Objectives............................................................................................................................. 1-1
1.2 Scope of Document .............................................................................................................. 1-1
2.0 Physical and Chemical Characteristics of Ethanol/Gasoline Blends ............................................... 2-1
2.1 Physical/Chemical Properties ............................................................................................... 2-1
2.2 DOT Placards ....................................................................................................................... 2-3
3.0 Summary of Case Studies .............................................................................................................. 3-1
4.0 Fate and Transport Characteristics ................................................................................................. 4-1
4.1 Ethanol Migration Pathways ................................................................................................. 4-2
4.2 Ethanol Degradation Rates .................................................................................................. 4-2
4.3 Methane Generation in Soil/Groundwater ............................................................................ 4-3
4.4 Ethanol Partitioning Between Environmental Media ............................................................. 4-3
4.5 Media Fate and Transport Characteristics............................................................................ 4-3
4.5.1 Soil .......................................................................................................................... 4-3
4.5.2 Groundwater............................................................................................................ 4-5
4.5.3 Surface Water ......................................................................................................... 4-8
4.5.4 Air/Vapor ............................................................................................................... 4-11
5.0 Health Effects and Environmental Risks ......................................................................................... 5-1
5.1 Environmental Risks – Fire and Explosion ........................................................................... 5-1
5.2 Potential Exposure Pathways in Spill Situations ................................................................... 5-2
5.3 Human Health Effects........................................................................................................... 5-2
5.3.1 Short-Term (Acute) Effects ...................................................................................... 5-2
5.3.2 Long-Term (Chronic) Effects ................................................................................... 5-3
5.3.3 Health Protective Concentrations ............................................................................ 5-4
5.4 Environmental Effects........................................................................................................... 5-5
5.4.1 Aquatic Systems...................................................................................................... 5-5
5.4.2 Terrestrial Systems.................................................................................................. 5-7
5.5 Health and Safety Considerations for Responders ............................................................... 5-9
5.5.1 Recognizing Product Spilled .................................................................................... 5-9
5.5.2 Exposure Limits ....................................................................................................... 5-9
5.5.3 Protective Clothing ................................................................................................ 5-10
5.5.4 Other Health and Safety Considerations ............................................................... 5-10
6.0 Spill Assessment and Delineation ................................................................................................... 6-1
6.1 Field Sampling ...................................................................................................................... 6-1
6.2 Screening Methods............................................................................................................... 6-2
6.3 Analytical Methods ............................................................................................................... 6-6
7.0 Response Options .......................................................................................................................... 7-1
7.1 General Description .............................................................................................................. 7-1
7.1.1 Short Term Response Priorities .............................................................................. 7-1
7.1.2 Longer Term Response Priorities ............................................................................ 7-2
7.2 Media Specific Options ......................................................................................................... 7-2
7.2.1 Soil .......................................................................................................................... 7-2
iv
7.2.2 Groundwater............................................................................................................ 7-5
7.2.3 Surface water .......................................................................................................... 7-6
7.2.4 Wetlands ................................................................................................................. 7-9
7.2.5 Marine Areas ......................................................................................................... 7-10
8.0 References ..................................................................................................................................... 8-1
List of Tables ___________________________________________________
Table 1-1 Ethanol and Blends and Their Uses _____________________________________________ 1-2
Table 2-1 Chemical/Physical Properties of Ethanol _________________________________________ 2-1
Table 2-2 Comparison of Properties for Ethanol/Gasoline Blends ______________________________ 2-2
Table 3-1 Ethanol Spill Incident Summaries _______________________________________________ 3-1
Table 4-1 Comparison of Fate and Transport of Neat Ethanol with E-Blends______________________ 4-1
Table 4-2 Fate of Ethanol after Major Release _____________________________________________ 4-2
Table 4-3 Effect of Ethanol on Gasoline Fate and Transport in Groundwater _____________________ 4-6
Table 5-1 Human Health Effects of Ethanol _______________________________________________ 5-3
Table 5-2 Health Protective Concentrations _______________________________________________ 5-4
Table 5-3 Water Quality Benchmarks for Ethanol ___________________________________________ 5-5
Table 5-4 Ethanol Concentrations Able to Deplete Stream Dissolved Oxygen _____________________ 5-6
Table 5-5 Ethanol Effects on Wildlife (Select Results) _______________________________________ 5-8
Table 5-6 Ethanol Wildlife Benchmarks (Based on No Observed Effect Levels) ___________________ 5-8
Table 5-7 Occupational Limits for Ethanol in Air ____________________________________________ 5-9
Table 5-8 Health and Safety Recommendations for Spills of Fuel Grade Ethanol and E85 __________ 5-10
Table 6-1 Sampling Techniques ________________________________________________________ 6-2
Table 6-2 Ethanol Spill Screening Techniques _____________________________________________ 6-3
Table 6-3 Analytical Methods __________________________________________________________ 6-7
Table 7-1 Response Options for Surface Soil Spills _________________________________________ 7-4
Table 7-2 Response Options for Spills Impacting Groundwater ________________________________ 7-5
Table 7-3 Response Options for Surface Water Spills _______________________________________ 7-6
List of Figures __________________________________________________
Figure 2-1 Flashpoint as a Function of Water Content _______________________________________ 2-1

Figure 2-2 Ethanol Vapor Pressure vs. Temperature ________________________________________ 2-2
Appendices
Appendix A Case Studies

Appendix B Fate and Transport Literature Review
Appendix C Health Effects Literature Review
Appendix D Draft SOP Field Hydrometer Gross Measurement of Ethanol and/or Denatured
Ethanol
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LARGE VOLUME ETHANOL SPILLS – ENVIRONMENTAL IMPACTS AND RESPONSE OPTIONS JULY 2011
Executive Summary
In the last ten years, the production of ethanol has increased dramatically due to the demand for
ethanol-blend fuels. Current production (2010) in the United States is 13 billion gallons.
Denatured ethanol (approximately 95% ethanol, 5% gasoline) is largely shipped from production
facilities by rail and is now the largest volume hazardous material shipped by rail.
Large volumes of ethanol are commonly shipped by unit trains, up to 3.2 million gallons, and the
larger barges can transport up to 2.5 million gallons. In Massachusetts, two to three ethanol unit
trains currently travel through the state per week, as well as an ethanol barge per week. The
number of trains and barges transporting denatured ethanol (95% - 98% ethanol) through the
state are anticipated to increase in the future, especially if the use of higher ethanol blends
becomes more prevalent. The high volume of ethanol transported and the differences in the
chemical properties, and the fate and transport of ethanol as compared to standard gasoline, led
to the need for additional consideration of spill response actions. In particular, this document
considers the assessment and response actions for rail and barge spills of denatured ethanol.
Ethanol is a flammable colorless liquid; a polar solvent that is completely miscible in water. It is
heavier than air, and has a wider flammable range than gasoline, with a Lower Explosive Limit
(LEL) to an Upper Explosive Limit (UEL) range of 3.3% to 19%. The flash point for pure
ethanol is 55°F, and for denatured ethanol it is much lower (-5°F). Ethanol is still considered a
flammable liquid in solutions as dilute as 20%, with a flash point of 97°F. At colder
temperatures (below about 51°F), the vapor pressure of ethanol is outside the flammable range.
Denatured ethanol is shipped with a flammable liquids placard and North American 1987
designation.
A number of large volume ethanol incidents have occurred. Some of these have resulted in
significant fires, most of which have been allowed to burn. Water has been used in some
incidents, primarily to protect nearby structures or tanks. Alcohol-resistant foam has also been
used, primarily to extinguish fires within tanker cars. Sampling and analysis of environmental
media that has occurred in connection with spill response activities have shown impacts related
to these spills, although they are generally of relatively short duration. The most significant
documented impact was a large fish kill that occurred in Kentucky as a result of a bourbon spill.
This effect was related to oxygen deficiency resulting from ethanol biodegradation, rather than
direct toxicity. Another fish kill was observed subsequent to a spill in Illinois, but it has not been
definitively attributed to the spill.
In general, ethanol in the environment degrades rapidly. Biodegradation is rapid in soil,

groundwater and surface water, with predicted half lives ranging from 0.1 to 10 days. Ethanol
will completely dissolve in water, and once in solution, volatilization and adsorption are not
likely to be significant transport pathways in soil/groundwater or surface water. Once oxygen is
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-1
depleted as a result of aerobic degradation, anaerobic biodegradation of ethanol in groundwater

results in the production of methane, which can result in an explosion hazard upon accumulating
in a confined space. For an ethanol spill in typical aerobic environments, the depletion of
oxygen and production of methane may take several months. Several case studies of significant
spills have shown that ethanol has been completely degraded in groundwater within two to three
years. The presence of ethanol can reduce the rate of biodegradation of gasoline constituents
(benzene, toluene, ethylbenzene, and xylenes – BTEX) in groundwater, and thus potentially
increase the persistence and dimensions of BTEX plumes. However, there is contradictory
evidence that suggests that ethanol may actually enhance the rate of benzene biodegradation.
Biodegradation of ethanol in surface water can result in complete depletion of dissolved oxygen,
as evidenced by the fish kill documented in Kentucky.
One of the greatest hazards of ethanol is its flammability. Ethanol can conduct electricity, so
electrocution hazards and possible ignition hazards are present during transloading operations.
Human exposure to ethanol during spill situations could occur by inhalation, contact with the
skin, or ingestion if ethanol reaches water supplies (surface water intakes or groundwater). The
odor threshold for ethanol is 100 ppm in air. No significant acute effects have been observed
upon exposure to ethanol in air at 1000 ppm, and this is the OSHA Permissible Exposure Level.
Effects have been observed from concentrations in air ranging from 3000 ppm to 10,000 ppm,
including headaches, and eye and respiratory system irritation. Acute ingestion doses of 0.1 to
0.5 g/kg body weight are considered the threshold for central nervous system effects. Chronic
effects associated with ethanol exposure are well documented, primarily associated with alcohol
abuse. A dose of 0.2 g/kg body weight/day is considered the threshold for neurological effects in
fetuses, and liver effects are observed at doses of 2 g/kg/day. In addition, the consumption of
both alcoholic beverages and ethanol have been identified as carcinogenic in humans by the
World Health Organization. However, chronic exposures to ethanol are unlikely to occur as a
result of a spill, due to the rapid biodegradation of ethanol and the monitoring associated with a
typical spill incident.
Water quality benchmarks (for the protection of aquatic life) have been developed: 63 mg/L for
the protection against chronic effects, and 564 mg/L for acute effects. However, modeling has
suggested that oxygen depletion can occur at lower concentrations. This is supported by the
Kentucky spill, where the fish kill was attributed to oxygen depletion, rather than direct toxicity.
The occupational exposure limit for ethanol is 1000 ppm in air (general industry), and the
concentration deemed to be Immediately Dangerous to Life or Health (IDLH) is 3300 ppm,
which is 10% of the LEL. Self-contained breathing apparatus (SCBA) is necessary for spill
response. For large spills with fire, evacuation of about ½ mile in all directions should be
considered.

Methods for assessment and analysis of ethanol are somewhat limited due to its high solubility.
A simple open flame test can be used to determine the presence of ethanol at relatively high
concentrations. A hydrometer can be used to determine approximate concentrations of ethanol in
water. The best option for screening is a portable Fourier Transform Infared (FT-IR)
spectrometer that has relatively low detection limits and can specify ethanol. A relatively recent
analytical method (SW-846 8261) has been developed that provides low detection limits for
ethanol.
Consideration of past ethanol incidents provides some insight into fate and transport in a spill
situation, as well as response activities that have been effective. Consideration of these
incidents, as well as conducted and possible response actions leads to the following conclusions:
In some cases, ethanol rail incidents result in fire. In many cases, these fires have been
significant, involving multiple rail cars and large volumes of ethanol;
First responders generally have been local fire fighters that have focused on necessary
evacuations, containing the fire, and protecting nearby structures and/or tanks;
In most cases, if not all, ethanol fires have been allowed to burn, although most have not
occurred in highly populated areas. Cooling water has been used to protect structures,
tanks, and uninvolved rail cars;
In some cases, where large amounts of water usage were necessary, run-off to nearby
streams occurred. In one case, the stream was subsequently dammed, and 500,000
gallons of impacted water were removed for disposal;
Alcohol resistant foam (AR-AFFF) has had limited use in these large spill and fire
situations, probably due to the limited volume generally available to local fire-fighters
and concerns with migration and/or recovery of the foam/ethanol. Most use has been to
extinguish specific breached and burning cars that were blocking passage, or to
extinguish fires inside tankers prior to removal of the contents and movement of the
tanker. The use of AR-AFFF has been effective in these circumstances;
The fires have consumed large volumes of ethanol, thus limiting impacts to
environmental media;
The most significant impacts related to ethanol spills have been to surface water. In some
cases, surface water impacts have resulted in fish kills several days after the spill as a
result of oxygen depletion. These impacts have occurred some distance from the site of
the original spill;

Due to concerns of surface water impacts, response activities have more recently
involved efforts to prevent discharge to surface water through damming. Aeration of
small creeks and large rivers has also been used to improve dissolved oxygen content;
and
Migration of spilled ethanol from the surface through soil to groundwater is also of
concern, due to possible groundwater contamination and discharge to surface water, as
well as methane generation. Where possible, spilled material has been recovered by
pumping. In some cases, spilled material was not identified, and migration to
groundwater and surface water occurred. In cases where groundwater impacts have
occurred, ethanol has degraded relatively rapidly, although gasoline constituents have
been more persistent.
As a result of the above observations, the following recommendations can be made:
Contained burning is an effective response to an ethanol spill incident. It has been used
in numerous spill incidents, albeit they have not generally occurred in highly populated
areas;
The use of cooling water may be necessary to protect structures, tanks, or uninvolved rail
cars. Runoff from water use should be contained and/or recovered to the extent possible
to prevent infiltration to groundwater and impacts to surface water;
The local fire department stocks of alcohol resistant foam could be increased, as its use is
effective. When used where the ethanol/foam can be recovered, environmental impacts
will be limited. Foam not recovered and reaching surface water can increase the
biochemical oxygen demand loading to streams. In addition, foam use on unpaved
surfaces does not limit the migration of ethanol to groundwater;
Ethanol pools or impacts to soils should be identified as quickly as possible to prevent

infiltration to groundwater and runoff to surface water. The high solubility of ethanol can
result in rapid transport in these media. Recovery and excavation have largely been used
to address such situations. Controlled burn has not been used, but could be considered in
some situations;
Ethanol impacts to surface water are a significant concern. Ethanol spills reaching
ditches or small creeks can be addressed by damming, thus allowing time for
biodegradation and preventing releases to larger water bodies. Aeration of these smaller
water bodies can be used to improve their dissolved oxygen content and enhance
biodegradation, but these actions may not reduce ethanol content sufficiently prior to
discharge to a large water body;

Once ethanol is discharged to a larger river, response options are limited. Monitoring of
both dissolved oxygen and ethanol should be conducted in order to determine whether
concentrations are approaching anoxic or toxic levels. Barge aerators can be used to
improve dissolved oxygen levels; and
Ethanol incidents in the marine environment have been rare, with none of a significant
volume occurring in harbors or near-shore areas. Response options in such cases are
similarly limited to the use of aeration to improve dissolved oxygen levels, although this
would only be effective in smaller areas, such as inlets.


1.0 Introduction
1.1 Objectives
In the last ten years the production of ethanol has increased dramatically due to the demand for
ethanol-blend fuels. The US currently has 204 biorefineries in 29 states, and produced more than
13 billion gallons of ethanol in 2010 (Dinneen, 2011). This is up from 10.6 billion gallons in
2009 (RFA, 2011).
In 2009, 75% of the nation‟s gasoline was blended with gasoline as 10% ethanol and 90%
gasoline (E10). Denatured ethanol is largely shipped from production facilities by rail (70%),
and is now the #1 hazardous material transported by rail (Rudolph, 2009). As a result of this
increased production and transportation, several ethanol incidents have occurred in the United
States since 2000, including 26 significant fires, 5 train derailments, and 3 ethanol tank fires
(Rudner, 2009).
As a result of concerns related to the increased prevalence of rail transport of ethanol, and the
potential magnitude of spills, the Massachusetts Department of Environmental Protection
(MassDEP) requested that Shaw‟s Environmental and Infrastructure Group (Shaw) prepare a
document containing information on the environmental impacts of and emergency response
techniques for ethanol and ethanol blends. Shaw, in consultation with MassDEP, and with
information provided by Ohio DEP, Illinois DEP, and Pennsylvania DEP, assembled the best
information, research, and field techniques available. The anticipated users of this document are
local, state, and federal responders.
1.2 Scope of Document

As discussed above, ethanol is the largest volume hazardous material transported by rail. The
primary mode of ethanol transport is rail. In many cases, denatured ethanol is being transported
in large (80 to 100 cars) unit trains, throughout the U.S., including the northeast. Such a unit
train can transport up to 2,900,000 gallons of ethanol (approximately 29,000 gallons per rail car).
About 10% of ethanol is transported by barge, typically in 630,000 gallon tanker barges;
although a large petroleum 2-barge unit tow can transport 2.52 million gallons. Tanker trucks
(about 8000 gallons) are also used to transport ethanol, although primarily ethanol blends
(USDA, 2007).
This document focuses on larger volume releases of denatured ethanol or ethanol blends during
transportation by rail or barge. In Massachusetts, it is estimated that there are 2-3 ethanol unit
trains traversing the state per week, as well as an ethanol barge every other day. This document
does not specifically address releases during production, storage, transfer, or during smaller
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 1-1

volume transport by highway cargo tankers, although much of the information presented is also
relevant to these types of releases.
Table 1-1 shows the most common ethanol blends and their uses. There are also mid-level
blends (20%, 30% and 40% by volume), although these are less common than those shown
below. As shown in the table, the ethanol blends are commonly referred to as E-blends, with the
numbers indicating the percentage of ethanol in the blend.
TABLE 1-1 ETHANOL AND BLENDS AND THEIR USES
Ethanol Blend Composition Use
E100 100% ethanol, also known as neat Used in the production of blends, not
ethanol or fuel grade ethanol generally transported in large
quantities
E95 – E99 95% - 99% ethanol, balance gasoline, Transported in large quantities to bulk
also known as denatured ethanol terminals for production of general use
blends
E85 85% ethanol, 15 % gasoline Used in flex-fuel vehicles (< 2% ethanol

consumed for this use)
E10 10% ethanol, 90% gasoline 70 % of nation’s gasoline (98% ethanol

consumed for this use)
This document provides the following information:
Physical and chemical characteristics of ethanol and blends (Section 2.0);
Summary of case studies of incidents involving ethanol (Section 3.0);
Fate and transport characteristics of ethanol and blends (Section 4.0);
Health effects and environmental risks associated with ethanol and blends (Section 5.0);
Spill assessment and delineation, including screening and analytical methods (Section
6.0);
Response options for ethanol spills by environmental medium (Section 7.0); and
Summary and recommendations (Section 8.0).

2.0 Physical and Chemical Characteristics of Ethanol/Gasoline Blends

TABLE 2-1 CHEMICAL/PHYSICAL PROPERTIES OF PURE
2.1 Physical/Chemical Properties ETHANOL
Ethanol is a flammable colorless liquid. It Formula •C2-H6-O
is a polar solvent that is volatile and
Molecular Weight •46.07
completely miscible (mixes) in water.
Vapors of ethanol are characterized as Color/Form •Clear, colorless, very mobile liquid
having a vinous or wine-like odor (HSDB, •Mild, like wine or whiskey (vinous)
Odor
2011). Table 2-1 shows the
chemical/physical properties of ethanol. Ionization potential •10.47eV
The vapor density of 1.59 indicates that it is Boiling Point •173 F (78.5 C)
heavier than air and will seek lower
Melting Point •-173 F (-114 C)
altitudes (tend to collect closer to the floor
level) (IFCA, 2008). Its specific gravity Liquid Density •0.79 at 20 C
indicates that it is lighter than water, but it
Vapor Density •1.59
will thoroughly mix with water. Once
mixed, it will not separate. It has a wider Flammable Range •3.3 - 19%
flammable range than gasoline, has a blue Solubility •Miscible in water and organic solvents
flame, and does not produce visible smoke
Vapor Pressure •59.3 mm Hg at 25 C
(IFCA, 2008) unless denatured with
gasoline. Flash Point •55 F (13 C)
The flammability of ethanol is affected by Source: HSDB 2011

mixture with water, but remains flammable even with the presence of 80% water, as shown in
Figure 2-1. At this concentration, the flash point is 97°F (36°C), and it is still considered a
flammable liquid. The flash point is the lowest temperature at which vapor formed above liquid
ignites in air at standard pressure (1
FIGURE 2-1 FLASHPOINT AS A atmosphere). This is not the same as the
FUNCTION OF WATER CONTENT temperature at which combustion will
120 continue. This is known as the fire point, or
97 (36)
FLASH POINT F ( C)
100 Flammable Liquid the lowest temperature at which heating

80 68 (20) beyond the flash point will support
55 I12.8)
60 combustion for 5 seconds. This characteristic
40
is not commonly measured, and no
20
information on the fire point of ethanol was
0
found.
Pure Ethanol 80% 20%
Ethanol/Water Ethanol/Water
Source: NFPA 2002

Ethanol blends will have properties affected by the percentage of ethanol in the blend. A
comparison of some of the relevant properties is found in Table 2-2. This table shows the flash
point for both ethanol and gasoline. As shown in Table 2-2, once gasoline is added to ethanol for
denaturing (E95), the flashpoint decreases dramatically from 55°F to -5°F. The flash point
continues to decline with a greater content of gasoline.
TABLE 2-2 COMPARISON OF PROPERTIES FOR ETHANOL/GASOLINE BLENDS
PROPERTY ETHANOL E95 E85 E10 Gasoline

Flammable Range 3.3%-19% 3.3%-19% 1.4%-19% 1.4%-7.6% 1.4%-7.6%
Flash Point 55°F (12.8°C) -5°F (-20°C) -20°F- -5°F -45°F (-43°C) -45°F (-43°C)
(-29°C- -20°C)
Source: HSDB (2011), Speedway (2004),NRT (2010), IFCA 2009
Properties are also affected by temperature. Figure 2-2 shows the vapor pressure of ethanol as it
varies with temperature. This figure also shows the flammability range at standard pressure. As
shown in Figure 2-2, at colder
FIGURE 2-2 ETHANOL VAPOR PRESSURE VS. temperatures (below 10.7°C
TEMPERATURE (51°F), the vapor pressure of
1000
ethanol is outside the
Vapor Pressure, mm Hg
flammable range. As
UEL = 19% discussed above, the addition
100 41.3°C (106°F)
of gasoline would change this
Flammability Range
graph, decreasing the
LEL = 3%
temperature at which, for
10 10.7°C (51°F)
example, E95 would be
outside the flammable range.
1
-10 0 10 20 30 40 50 60 70 80
Temperature °C

2.2 DOT Placards

DOT (2008) issued new and revised shipping names and identification numbers (ID) to be used
for fuel mixtures of ethanol and gasoline in 2008. The proper shipping names, labels, and
identification numbers are shown below:
Gasohol, NA 1203; Gasoline, UN 1203 (E1-E10)
Ethanol and gasoline mixture, UN 3475 (E11-E99)
Denatured Alcohol, NA 1987 (E95-E99)
Ethanol or Ethyl alcohol, UN1170 (E100)


3.0 Summary of Case Studies
Although ethanol has been produced and transported in large volumes for several decades there
have been relatively few incidences involving its catastrophic release into the environment.
There have been several occasions of leaking of underground storage tanks containing ethanol
fuel blends, some for very long periods. These have involved E-10 type fuels which are not the
focus of this report.
Most of the high-concentration ethanol is moved from production plants to blending terminals by
rail. Consequently, the majority of the event data is from rail incidents, several of which will be
discussed in detail in Appendix A. The other well-documented sources of ethanol impact to the
environment have been the result of fire incidents at distilleries. Two very significant events
occurred in Kentucky in 1996 and 2000. There have been few marine incidents. Some of the
more significant incidents that have occurred involving ethanol are summarized in Table 3-1.
More detail is presented in Appendix A.
TABLE 3-1 ETHANOL SPILL INCIDENT SUMMARIES

Description Volume Comments
Railroad Incidents
2006-New Brighton, PA Approximately 600,000 gallons Fire allowed to burn itself out over a few
either burned or released with days
Derailment of 23 30,000 gallon railcars an estimated 60,000 gallons Three cars were in the river, but were not
containing denatured ethanol along a into Beaver River compromised
bridge crossing the Beaver River Beaver River is large and fast-flowing no
detrimental impacts noted
Removal of limited impacted soil and ballast
performed
2007-Painesville, OH 150,000 gallons either spilled Fires controlled and allowed to burn
or burned Presence of other more flammable materials
Derailment of 30 cars including five caused fire-fighters to use copious amounts
30,000 gallon cars containing of water
denatured ethanol. Additional Two streams impacted. 500K gallons of
involved cars of phthalic anhydride, water/chemicals removed from one,
bio-diesel, and butane aerators used in the other
Visibly impacted soils excavated
2008 Luther, OK Up to 210,000 gallons of Fire allowed to burn itself out
ethanol/crude oil Limited visible impact, site not near water
Derailment of seven 30K cars
containing ethanol and crude oil.
2009-Knoxville, TN 6000 gallons spilled Cars flipped but did not explode or burn
Estimated 6000 gallons missing from two
Derailment of five 30K gallon cars with leaking cars when up righted
ethanol Approximately 1000 gallons collected from
ground surface
Occurred in paved area with little soil and no
surface water nearby

TABLE 3-1 ETHANOL SPILL INCIDENT SUMMARIES (continued)

Description Volume Comments
2009-Rockford, IL Estimated 360,000 gallons One motorist killed and nine injured
burned, 75,000 gallons spilled Massive fire required evacuation of 600
Derailment of fourteen 30K gallon cars homes
of denatured ethanol. Fire allowed to burn for 24-hours
About 1400 tons soil and 57,000 gallons
ethanol removed from site
Fish kill observed in Rock River, but has not
been definitely related to spill
Sampling of air, soil, surface water,
groundwater, private wells, and fish showed
no significant impacts to air, water, or soil;
ethanol and acetaldehyde detected in fish
2010 – Bryan, OH 80,000 gallons spilled No fire resulted
Impact to waterway
Derailment of 37 cars, some of which Monitored using dissolved oxygen and
contained ethanol biochemical oxygen demand
Restoration of dissolved oxygen in surface
water took several months
2011-Arcadia, OH Estimated 680,000 gallons Massive fire allowed to burn for several days
burned or spilled Foam used inside tankers prior to pumping
Derailment and burning of thirty-one them off
30K gallon cars of denatured ethanol. A ethanol/water entered a nearby creek and
total of 23 cars involved in fire and/or field drainage system
compromised Over 800,000 gallons of fuel/water mix
removed, with collection ongoing
Distillery Events
1996-Bardstown, KY 5.6MM gallons of 107-112 High winds created massive fire that was
proof (54-56% alcohol) controlled and allowed to burn out
Seven bourbon storage/aging bourbon burned or spilled Spilled liquids pooled and burned, burn
warehouses and thirteen distillery footprint was within paved area
structures No impact to surface water
2000-Lawrenceburg, KY 980,000 gallons of 107-112 Building located above Kentucky River, fire
proof bourbon allowed to burn out
One bourbon storage/aging warehouse Liquid travelled down a hill into river below
After 2 days fish kill occurred, became the
largest in KY history
Fisk kill due to depleted dissolve oxygen;
area of “dead water” stretched 7 miles
Barges used to aerate the water for 4 days
until dissolved oxygen levels were restored
Maritime Events
2004-50 miles off VA coast 3.5MM gallons of ethanol on- Explosion on board caused by vapors from
board empty tanks that had previously contained
Tanker ship at sea MTBE
Ship lost 3-dead, 18 crew missing 6-survivors
Ethanol cargo lost, no environmental
damage reported
All environmental damage related to 49K
gallons of fuel oil lost
2010-New York Harbor Cargo tank ruptured while No release to water
taking on 55K barrels of Rupture from over-filling
Tanker ship-ruptured tank ethanol Rupture caused deck collapse

4.0 Fate and Transport Characteristics
This section provides information regarding the fate and transport of ethanol in various
environmental media, including soil, ground water, surface water and air. Information is
provided here in summary form, with further detail included in Appendix B.
Ethanol may be released to the environment as pure (also referred to as neat) ethanol or a blend
with various percentages of gasoline and ethanol (also referred to as an E-blend fuel). Accidents
that occur during large volume transport of ethanol via rail cars and marine tankers or as a result
of structural failure at ethanol bulk storage terminal terminals are possible sources of the release
of neat or denatured ethanol. Tanker truck accidents, splash blending of ethanol with gasoline,
and leaks and spills at retail and non-retail gasoline stations may release moderate to small
volume E-blend fuels into the environment. The release of neat or denatured ethanol into the
environment results in fate and transport issues that can be different than those from an E-blend
release, as shown in Table 4-1.
TABLE 4-1 COMPARISON OF FATE AND TRANSPORT OF NEAT ETHANOL WITH E-BLENDS
Source: NEIWPCC, 2001
Characteristic Neat Ethanol, E95 or Denatured E-Blends (E85 and lower)
Ethanol
Release Type Large volume, surface soil and water spill Moderate to small volume, surface or subsurface
spill
Release Source Rail cars, marine tankers, bulk storage Trucks, retail gas and blending stations
terminals
Transport Surface spreading until reaching surface Nominal surface spreading, followed by soil
Paths water body; soil infiltration and leaching to infiltration and leaching to groundwater
groundwater
Media Soil, groundwater, lakes, wetlands, rivers, Primarily soil and groundwater. Localized impacts
affected harbors, shorelines, and sewers. Explosion to lakes, wetlands, rivers and sewers if located
potential if large volumes flow in confined immediately adjacent to accident site.
spaces such as sewers.
Environmental Rapid biodegradation of ethanol in soil or Rapid biodegradation of ethanol in soil or
fate groundwater. There are multiple variables groundwater, more predictable rates
and uncertainty associated with predicting
degradation and extent of migration after
surface spill.
Co-solvency of Co-solvency not prominent at Ethanol may extend the length of benzene plume
other gasoline uncontaminated locations. When neat in groundwater due to co-solvency of gasoline
ethanol is released into a soil where gasoline components in ethanol and reduced natural
components contamination has already occurred (such as attenuation of benzene
bulk terminals) the mobility of gasoline can
be increased.

Some important fate characteristics of ethanol are described below – migration pathways,
degradation rates, methane generation, and partitioning. This discussion is followed by a
discussion of fate and transport characteristics by environmental medium.
4.1 Ethanol Migration Pathways

TABLE 4-2 FATE OF ETHANOL AFTER MAJOR RELEASE
In evaluating the potential impact of an
Soil •Ethanol is rapidly biodegraded in soil
ethanol release to the environment, it is
essential to take into account the
•Neat ethanol rapidly mixes with
pathways that ethanol could travel water
from the release point. The major •E-blend will mix with water, but in
Surface Water large volume water bodies, ethanol
migration pathways include the will separate from the gasoline.
following: •Ethanol is rapidly biodegraded in
surface water
Infiltration into soil •Ethanol is rapidly biodegraded in

groundwater
Groundwater •Ethanol release may induce the
Transport in groundwater transport of other chemicals such as
benzene
Surface release/runoff to
•Ethanol vapor is denser than air and
streams, fast and slow flowing tends to settle in low areas.
Air •Ethanol vapor disperses rapidly
rivers, lakes, coastal water after release.
areas, outer harbors, open
water, ditches, wetlands and •Ethanol will volatilize and rapidly
biodegrade.
storm/ sanitary sewers •The potential decrease in dissolved
oxygen as a result of ethanol
Storm / sanitary degradation can upset microbial
Dispersion into air sewers functions at wastewater treatment
plants.
Table 4-2 presents a summary of the • The potential flammability hazard
must be addressed when ethanol is
fate of ethanol as it migrates through released to a sanitary or storm
system.
each of these environments. Ethanol
Source: EPA 2009
concentrations are reduced rapidly at
rates that depend upon the migration pathway, as well as the environmental characteristics, such
as temperature, soil type, flow rate, etc. While degradation rates are rapid, there is still a
possibility of rebound if a source is still present.
4.2 Ethanol Degradation Rates

In the atmosphere, it is predicted that ethanol will be oxidized quickly; with half-lives between
0.5 and 5 days. In soil and groundwater, ethanol undergoes rapid biodegradation with a half-life
ranging from 0.1 to 2.1 days, although more recent studies indicate that the half-lives may be

larger (5 to 10 days). In surface water following a pure ethanol spill, ethanol is predicted to
quickly biodegrade with half-lives ranging from 0.25 to 1 day. Due to rapid loss of ethanol
through photo-oxidation in air and biodegradation in soil and water, ethanol is unlikely to
accumulate in the soil, air, surface water, or groundwater. This is consistent with reports of
monitoring results from spill situations (see Section 3.0 and Appendix A). There is a great deal
of uncertainty as to how these estimated rates of ethanol loss (and other literature values) will
apply in realistic field conditions. Therefore, these rates represent generic order-of-magnitude
estimates and may not be applicable for site-specific releases.
4.3 Methane Generation in Soil/Groundwater

Anaerobic biodegradation of ethanol in groundwater results in the production of methane. The
presence of methane in the unsaturated soil in excess of the explosive limits may present an
explosion hazard. Methane vapors can be produced over an extended period of time and persist
in soil gas for a long time, at levels exceeding the lower and upper explosive limits for methane
(3.3% and 19% by volume, respectively). This process is discussed in more detail in Section
4.5.1 and 4.5.2 below and Appendix B.
4.4 Ethanol Partitioning Between Environmental Media

The partitioning of ethanol mass between air, water, and soil media is summarized below. More
detail is presented in Appendix B.
Air/Water Partitioning: Ethanol has a tendency to remain in the aqueous (liquid) state.
Therefore, atmospheric ethanol is likely to partition into water vapor droplets. Ethanol in
surface water and groundwater is likely to remain in the aqueous phase. As a result,
ethanol volatilization from surface water or off-gassing from groundwater are not likely
to be significant mechanisms for ethanol mass loss from water.
Soil/Water Partitioning: Ethanol is not strongly adsorbed to soil particles, and is likely to
migrate at the velocity of the groundwater. Adsorption to aquifer materials in the
subsurface or to sediments in surface water is not likely to affect the fate of ethanol in the
environment.
4.5 Media Fate and Transport Characteristics

4.5.1 Soil
Ethanol and E-blend fuel spilled on land surface will infiltrate the soil, and the ethanol and
gasoline components of the E-blend fuel will slowly infiltrate down through the pores of the soil
until they reach the top of the water table. Ethanol has a higher mobility through the soil as

compared to other gasoline components because it does not preferentially adsorb to the soil
grains.
During the process of infiltration through soil, a fraction of ethanol and gasoline components are
retained in the pores (soil vapor or soil moisture) or adsorbed to soil grains. The fraction that is
not retained in the unsaturated soil will reach groundwater. As discussed above, ethanol tends to
partition to the water phase (soil moisture) in preference to the air in the soil pores or adsorption
to the soil grains. The fraction of ethanol retained in the unsaturated zone depends greatly on the
volume of soil impacted by the release, the water content of the soil, and the rate at which
gasoline infiltrates through the subsurface. The fraction of ethanol that infiltrates to groundwater
goes into solution because of high water solubility of ethanol. The gasoline component of the E-
blend fuel floats on water because it is less dense than water, however these constituents will
also dissolve and migrate downward.
For E-blend spills, the presence of ethanol results in gasoline hydrocarbons being able to enter
smaller pore spaces and drain more easily from unsaturated soils into the groundwater.
Therefore, the presence of ethanol can result in mobilizing existing soil contamination.
As discussed earlier, ethanol has a short half life in soil. Therefore, ethanol present in soil vapor
or soil moisture will rapidly biodegrade. Some volatilization from moist soil surfaces is
expected although the majority of ethanol is expected to be retained in the soil moisture and be
lost through the process of biodegradation. In dry soils, some volatilization is expected to occur
(HSDB, 2011).
Neat ethanol releases at distribution terminals can affect the behavior of previously released fuel
hydrocarbons in the following ways:
Ethanol dissolves and mobilizes light non aqueous phase liquid (LNAPL) that was
previously entrapped in the unsaturated and saturated zones.
Ethanol creates a capillary fringe depression on top of the water table into which all
nearby LNAPL can drain.
As discussed in Section 4.3 and Appendix B, anaerobic biodegradation of ethanol in

groundwater results in the production of methane. Methane generation typically will not occur
until available electron acceptors (i.e., oxygen, nitrate, iron, and sulfate) are consumed.
Laboratory studies indicate that it took 6 to 10 weeks for conditions to be suitable for the
generation of methane. Actual times after a spill until methane is generated will depend on the
presence of oxygen and other electron acceptors, the temperature, the soil type, the presence of

other alcohols or hydrocarbons, the groundwater flow rate, and other site-specific characteristics.
One study of a neat ethanol spill indicated that methane was present in groundwater 15 months
after the spill occurred, and concentrations began to increase dramatically within 3 to 8 months
of that time. From these field observations and the laboratory studies, it can be concluded that
methane generation will generally not start for several months in an environment that is initially
under aerobic conditions. Once methane is present in groundwater, it will volatilize from
groundwater into soil gas. In the field study described above, a methane survey taken 23 months
after the spill showed methane concentrations in soil gas above the LEL at a depth of 4 feet
below the ground surface. This could pose a hazard for construction or monitoring activities in a
spill area, and if the methane in soil gas were to migrate to a confined space, it may lead to an
explosion hazard
After an ethanol spill, the following conditions must be met for an explosion hazard to occur
from methane:
Methane gas generation. Degradation of ethanol to methane is expected to be the

dominant degradation pathway in soil/groundwater. The presence of methane in the
unsaturated soil in excess of the explosive limits may present an explosion hazard;
Methane gas migration. Migration of methane gas from soil and groundwater to
underground utility pipes, drains, conduits or through natural or man-made subsurface
preferential migration pathways; and
Collection in a confined space. Collection of methane gas in a confined space to a

concentration at which it could potentially explode, such as a manhole, a subsurface
space, a utility room in a home, or a basement. For methane, the LEL is 3.3% by volume
and the UEL is 19% by volume. At concentrations below its LEL and above its UEL, a
gas is not considered explosive.
Methane vapors can be produced over an extended period of time and persist in soil gas for a
long time at levels that could pose an explosion hazard.
4.5.2 Groundwater
Like other alcohols, ethanol is hydrophilic (attracted to and soluble in water) whereas standard
gasoline is hydrophobic (repelled by water). Ethanol partitions preferentially into the aqueous
phase. Ethanol is completely miscible in both gasoline and water at all concentrations. The
presence of ethanol, therefore, affects the fate and transport mechanisms of E-blend fuels. In
presence of ethanol, the behaviors of water and gasoline are modified as follows:

Solubility of gasoline hydrocarbons in water increase;

Solubility of water in gasoline increases; and
Interfacial tension between the water and the gasoline phases is reduced.
The release of ethanol can impact groundwater after infiltrating through the soil. An ethanol
plume in groundwater may result, depending upon TABLE 4-3 EFFECT OF ETHANOL ON
the volume of ethanol spilled on the surface, the GASOLINE FATE AND TRANSPORT IN
GROUNDWATER
thickness of the unsaturated soil column (depth to
groundwater), and the conductivity of the soil. •Inhibits the
degradation of more
Once ethanol reaches the groundwater, it will toxic components in
Depletion of
dissolve and disperse rapidly. oxygen and gasoline (e.g. BTEX)
nutrients • May make the
dissolved BTEX
Ethanol tends to dissolve completely into the plume longer
groundwater and move with the groundwater in
the direction of groundwater flow. In case of E-
•Causes gasoline
blend fuels, the soluble components of gasoline Surface components to
Tension Effect spread laterally
that include benzene, toluene, ethylbenzene and
xylenes (BTEX) will partially dissolve, while
ethanol will dissolve completely. Unlike the
gasoline components, ethanol does not adsorb to • Makes other
Co-solvency gasoline
the saturated soil and therefore moves with constituents more
groundwater faster than the BTEX components. soluble
The BTEX components of E-blend fuels adsorb to

Source: HSDB, 2011
soil particles and later desorb to become
dissolved again in the groundwater, resulting in these gasoline constituents traveling at a slower
rate than groundwater and ethanol. The less soluble constituents of E-blend fuels will migrate
with the undissolved hydrocarbon pool.
In general, the impacts of neat ethanol with respect to the contamination of groundwater are less
severe compared to E-blend fuels. When neat ethanol is released into the groundwater it can be
degraded rapidly by microorganisms until the necessary electron acceptors are depleted, unless
the ethanol volume and concentrations are so high that they restrict microbial activity. On the
other hand, an E-blend gasoline release to groundwater enhances the groundwater transport of
benzene, toluene, ethylbenzene and xylenes (BTEX) in gasoline, especially benzene. The
environmental effects of ethanol on the gasoline components of E-blends are summarized in
Table 4-3.

The rapid biodegradation of ethanol first depletes the oxygen content of groundwater and then
the anaerobic electron acceptors (e.g., nitrate, sulfate), and therefore could potentially reduce the
rate of biodegradation of the BTEX constituents. The presence of ethanol in E-blend fuels can
cause the BTEX compounds of gasoline to travel farther than a standard gasoline blend without
ethanol. Some recent studies contradict this and suggest that ethanol may actually enhance the
rate of benzene biodegradation, thereby reducing benzene plume length and persistence.
The rapid biodegradation of ethanol has a side effect on the groundwater transport. Ethanol acts
as an energy source and stimulates the growth of aerobic and anaerobic microorganisms in
groundwater. This may in turn result in the growth of biofilms on aquifer material, mineral
precipitation and the generation of nitrogen and methane gases, processes which alter the
hydraulic properties of the aquifer such as reduction in porosity and hydraulic conductivities.
The rapid biodegradation of ethanol may also lead to a significant accumulation of volatile fatty
acids which are potential degradation products of ethanol and that could decrease the pH to
levels that inhibit further bioremediation. The rapid consumption of oxygen by ethanol means
the groundwater will become anaerobic quickly. Anaerobic biodegradation of BTEX and
ethanol typically occurs much more slowly than aerobic biodegradation, although the rates of
anaerobic biodegradation of ethanol are still fast enough (in days) that ethanol is not expected to
persist for a long duration. Empirical data from a case study of an ethanol spill at a Pacific
Northwest terminal (presented in Appendix B) indicates that for most spills the ethanol in
groundwater is expected to be degraded and not be of concern in a year or two. In comparison,
BTEX constituents have been measured in groundwater for several years and sometimes even
decades after a gasoline spill.
The enhanced anaerobic microbial activity caused by the presence of ethanol in groundwater
leads to methanogenesis, which is the production of methane (CH4) and carbon dioxide (CO2) by
biological processes. Details of the chemistry behind the methanogenesis and the volumetric
estimation of methane generation from ethanol are provided in Appendix B. There is potential
for ethanol-induced methane production to restrict groundwater flow and to pose an explosion
hazard, as discussed in Section 4.3.
Empirical data regarding the persistence of ethanol generated methane in soil and groundwater
was collected at a bulk fuel terminal in the Pacific Northwest, where 19,000 gallons of neat
ethanol were accidentally released from an above ground storage tank in 1999. Further details of
the spill and spill monitoring are provided in Appendix B. Over time, the ethanol plume
concentrations declined and high methane concentrations were measured in the area of the
ethanol plume. This empirical data suggests that methane related hazards will extend to the area
occupied by the ethanol plume in groundwater, and will extend to a distance that can be

estimated from the groundwater velocity and the time since the release. The extent of the
groundwater plume will provide the upper bound for the extent of methane impacts, except for
any preferential pathways such as utilities that may provide further spread of the methane in soil
gas.
When neat ethanol is spilled at locations where petroleum contaminated soil and groundwater
plumes already exist (e.g., oil terminals), the ethanol can remobilize the gasoline components
and cause lateral spreading of liquid petroleum and several fold increases in the concentration of
benzene and other constituents of gasoline. This may result in contamination of groundwater
and nearby water supply wells. Ethanol can also facilitate iron reduction and sulfate reduction,
which can have significant impacts on groundwater quality. The potential for contamination of
water wells or degradation of water supply depends on several factors, such as the volumes and
the concentrations of ethanol and gasoline components at the release site, the local
hydrogeological conditions, and the location of the spill relative to the area of groundwater
capture for the water supply well.
4.5.3 Surface Water

Ethanol in surface water can originate from a number of sources:
1. Rainwater (through atmospheric volatilization and deposition) – minimal contributions,

not further considered in this document.
2. Direct discharges from land surface (from accidental spills) – immediate and severe
impacts after spill, serious threat to environment, high concentrations and volumes of
ethanol expected, sudden and severe depletion of dissolved oxygen because of the
biodegradation of ethanol with acute toxic effects potential such as fish kills.
3. Direct discharges from land surface to drainage features or small creeks, which may
discharge to larger surface water bodies – Less severe impacts immediately after spill, but
still may result in severe depletion of oxygen.
4. Marine cargo tanker / barge accidents – short term impacts after the spill, high
concentrations and volumes of ethanol expected intitally, impacts to near-shore coastal
marine environment likely, ethanol is expected to be lost rapidly due to dilution and
dispersion in marine waters. Oxygen depletion may occur in coastal areas with less
flushing.
5. Contaminated groundwater plume migration to surface water – longer term, lower

intensity impacts after a spill, timing and magnitude dependent on the distance of the

surface spill to the surface water body and other factors such as the degree of
biodegradation and natural attenuation during transport in groundwater, the
hydrogeologic settings, the hydrology of the surface water body, and the volume of the
spill.
After a large volume surface spill, neat ethanol or E-blend fuel will flow over pavement and soil
until reaching a point of discharge into storm sewers, wetlands, lakes, and streams. During the
overland flow over soil and pavement, ethanol will partially volatilize into the atmosphere. As
the ethanol flows over soil, some of the ethanol will infiltrate the soil and reach the groundwater,
which may discharge to a surface water body. The remaining ethanol could reach a wetland or a
surface water body directly. Upon reaching a surface water body, either as groundwater
discharge or surface flow, ethanol will rapidly mix with the water and go into solution because
ethanol is completely soluble in water.
Once ethanol reaches fresh water, whether it is a flowing water body such as a stream or a
standing water body such as a lake or wetland, ethanol is not expected to volatilize quickly.
While volatilization from water surfaces does occur, the estimated volatilization half-lives for a
model river and model lake are 3 and 39 days, respectively, which are significantly larger than
the biodegradation rates for ethanol in water (few hours to a day). Ethanol is also not expected
to adsorb to suspended solids and sediment in the surface water bodies. Hydrolysis of ethanol
and photolysis in sunlit surface waters are not expected to reduce ethanol concentrations.
Ethanol is therefore expected to remain in solution in the water while biodegradation is
occurring.
High concentrations of ethanol may occur in the immediate downstream area of a spill with little
biodegradation, especially after a large volume spill into a surface water body. The high
concentrations of ethanol would rapidly deplete the dissolved oxygen content of the fresh water
bodies that have low aeration rates (e.g., lakes, ponds, lakes and large rivers with little
turbulence), leading to the possibility of a fish kill from oxygen stress. As discussed in Section
3.0 and Appendix A, in May 2000, a 500,000 gallon release of Wild Turkey bourbon that
contained 50% ethanol (250,000 gallons) into the Kentucky River caused the worst fish kill in 50
to 60 years. This fish kill was attributed to depletion of dissolved oxygen and not the direct
effects of ethanol.
Biodegradation will begin to reduce ethanol concentration shortly after release as long as the
water is warmer than 10°C (50°F). It is important to note that this temperature is approximately
the same as the threshold for ethanol‟s flammability; at colder temperatures below 10.7°C (51°F)
the vapor pressure of ethanol is outside the flammable range (see Figure 2-2). Therefore, even

though the flammability risk following an ethanol spill is reduced in cold weather, the impacts to
surface water may be greater due to limited biodegradation.
Ethanol has been shown to biodegrade under aerobic and anaerobic conditions. If the
temperature ranges are appropriate, the biodegradation of ethanol in surface water proceeds
rapidly, with half lives ranging from hours to a day. Therefore, in warm waters ethanol is
unlikely to persist for an extended time. In cooler water bodies, ethanol will mix rapidly and
migrate with water without much loss except for dilution. If conditions favorable to
biodegradation are not present, ethanol may persist for several months.
Large volumes of ethanol, up to 2.5 million gallons, may be released into marine waters from the
rupture of a marine tanker or a barge carrying bulk ethanol. Due to the infinite solubility of
ethanol in water, it will tend to distribute near the water surface because it is less dense than
water. Marine ethanol spills pose a threat of being toxic to the ecological receptors in direct
contact with the release and could impact the surface aquatic ecosystem. Ethanol released to the
marine environment is not expected to persist for a long duration because ethanol in the surficial
marine environment will be lost by the processes of dispersion and dilution as well as
biodegradation, resulting in the rapid natural attenuation of the marine ethanol spills. Near-shore
releases of ethanol are of greater concern to the proximity of sensitive receptors and the
possibility of reduced flushing in some locations.
The salinity of the marine water is expected to have minor effects on the fate and transport of the
ethanol. Environmental degradation in salt water may be slower than freshwater. For E-blend
fuels, the higher salinity of marine waters will tend to further reduce the solubility of the gasoline
components, ensuring that the gasoline components continue to float on water and are less
readily available to marine organisms that inhabit the deeper marine environment. In some
marine estuaries, the higher density salt water may form a wedge at the deeper parts of the
estuary. Such a wedge tends to slow the mixing of ethanol and E-blend fuels with the deeper
waters (NRT, 2010).
Another consideration in the fate and transport is the energy level of the surface water body that
receives the spilled ethanol. In flowing or fast water such as rivers, streams, marine environment
with breaking surf, the high mixing energy of the receiving water body will result in rapid
mixing of ethanol with the entire water column. Ethanol concentrations will decrease due to
rapid dilution and also due to the high aeration rates as compared to still water bodies like ponds
and lakes (NRT, 2010)

4.5.4 Air/Vapor
If released to the atmosphere, ethanol disperses rapidly in the vapor phase. Ethanol vapor is
denser than air, and will eventually settle in low lying areas. If there is moisture in the
atmosphere, the atmospheric ethanol is likely to partition into water vapor droplets. Ethanol in
surface water and groundwater is likely to remain in the aqueous phase and degrade at a rate that
is faster than the rate of volatilization. As a result, ethanol volatilization from surface water or
off-gassing from groundwater are not likely to be significant contributors to ethanol in the
atmosphere.
In the atmosphere, the half life of ethanol is similar to that of other alkyl ether oxygenates,
including methyl tertiary-butyl ether (MTBE). Vapor phase ethanol is degraded in the
atmosphere by reaction with photo chemically-produced hydroxyl radicals, and in summer
conditions, half-lives are on the order of days.
Ethanol can impact the air quality and lead to a safety hazard. Some examples are as follows:
Noxious odors may be produced by the generation of butyrate, a metabolite of ethanol

biodegradation;
Ethanol vapor has the potential for formation of explosive mixtures. Ethanol surface
flow into a confined space, such as a storm sewer, may create an explosive situation
when vapors of the ethanol collect in air pockets in the sewer;
Anaerobic biodegradation of ethanol in groundwater produces methane. At higher

concentrations (near 1000 mg/L) ethanol rapidly ferments to methane at a rate near 20 to
60 mg/L per day. Methane leaves the ground water and enters soil gas where it can
present an explosion hazard if it enters a confined space, as discussed previously; and
The methane vapors are produced over an extended period of time and persist in soil gas
for a long time, at levels exceeding the upper explosive limit (19% by volume).
Biodegradation of ethanol and E-blends has the potential to expedite vapor intrusion of BTEX
compounds. The methane originating from the anaerobic degradation of ethanol in groundwater
undergoes aerobic biodegradation in soil pores and consumes the available oxygen from the soil
gas. This oxygen would otherwise be available to degrade benzene and other gasoline
constituents introduced to soil gas from an E-blend spill. The aerobic degradation of benzene is
therefore limited in presence of ethanol. The lack of benzene degradation caused by the
consumption of oxygen by methane results in increased persistence of benzene in soil gas.


5.0 Health Effects and Environmental Risks
5.1 Environmental Risks – Fire and Explosion

Flammability is the greatest hazard for ethanol and E-blend fuels, just like it is for gasoline.
Gasoline has a fairly narrow range of flammability (between 1.4 and 7.6% or 14,000 and 76,000
ppm by volume), while ethanol has a wider range of flammability (3.3 to 19% or 33,000 to
190,000 ppm by volume). Given the concern for flammability, the level determined to be
Immediately Dangerous to Life and Health (IDLH) has been set by NIOSH as 10% of the LEL,
or 3300 ppm.
Ethanol is also completely water soluble unlike gasoline which floats on water. Large amounts
of water are required to dilute ethanol to the point where it no longer supports combustion, as
discussed in Section 2.1. If released as an E-blend fuel into water, gasoline will float on a layer
of an ethanol-water solution, and the resulting ethanol water solution will still be flammable.
While smoke from burning gasoline is thick, black and toxic, pure ethanol burns without visible
smoke and a has a hard-to-see blue flame. In denatured (E-95) form, a slight orange flame and
some smoke may be visible. Because ethanol is flammable, and burns with a virtually invisible
flame, such a fire would be especially hazardous to emergency responders. Anecdotal evidence
from Indy motor races suggests that the invisibility of ethanol flame is a hazard requiring the
maintenance crew to use a corn broom to detect the ethanol flame, unlike gasoline fires that can
be visually detected due to the smoke.
Ethanol and some ethanol blends can conduct electricity; therefore improper grounding and
bonding during transloading operations could lead to electrocution hazards and possibly ignition
of the fuel.
Ethanol vapor has the potential for formation of explosive mixtures. Uncontrolled impingement
of ethanol tank cars after a fire can result in a boiling liquid expanding vapor explosion
(BLEVE). Ethanol has a high upper explosive limit and therefore ethanol will burn, or explode
even in conditions where oxygen is not readily available, such as within tank cars or in sewers
where small airspaces may be present. If released to the soil or groundwater, anaerobic
biodegradation of ethanol will produce methane, which can present an explosion hazard if it
reaches a confined space.

5.2 Potential Exposure Pathways in Spill Situations

The potential human exposure pathways during spill situations depend on the nature of the spill.
In general, given the volatile nature of ethanol and ethanol blends, inhalation exposures are the
most likely for both responders and nearby workers or residents. Skin contact (dermal exposure)
is possible, but unlikely, since responders would be wearing appropriate protective clothing (see
Section 5.5.3). Ingestion exposure is also unlikely, although if the spill reaches surface water,
ethanol will dissolve, as discussed in Section 4.3, and could impact a drinking water source. As
discussed in Section 3.0 and Appendix A, water supply intakes have been shut down, at least
during response actions, during several incidents. In addition, contact could occur as a result of
other uses of surface water, such as swimming or boating, or use for cooling or production water.
Given the greater likelihood of inhalation exposures during spill situations, this section will focus
on health effects related to this route, with limited discussion of other possible routes of
exposure.
5.3 Human Health Effects

This section discusses human health effects of ethanol relevant to spill situations. Most of the
literature on health effects of ethanol relates to the use or abuse of alcoholic beverages. This
information is largely focused on long term exposure by ingestion, and will not be discussed in
detail. This section provides information in summary form, and more detail is presented in
Appendix C. Table 5-1 provides a summary of effect levels for acute and chronic exposure.
5.3.1 Short-Term (Acute) Effects

Acute ingestion of ethanol can cause headache, nausea, vomiting, drowsiness, fatigue, impaired
judgment, lack of coordination, stupor, unconsciousness, and coma. Inhalation can cause eye
and upper respiratory tract irritation, fatigue and headache. Dermal contact can result in
irritation of skin, with prolonged contact leading to dry skin, cracking, peeling, and itching.
Absorption through the skin resulting in other effects is unlikely to be significant.
Ethanol is irritating to eyes and the respiratory system at concentrations of 5,000-10,000 ppm in
air. Headaches and other early signs of intoxication were observed in humans when exposed to
air concentrations of greater than 3000 ppm for 2 hours, although significant neuromotor effects
were not observed in humans exposed to up to 1000 ppm for 6 hours. Similarly, stumbling and
lack of coordination were observed in animals after exposure to 4000-10,000 ppm for 8 hrs.
Inhalation of 10,000-30,000 ppm for extended periods (8 hrs or more) is lethal to rats. Ingestion
of ethanol has caused death in humans, but inhalation of ethanol is unlikely to be lethal.
Rats exposed to E85 at 6130 ppm ethanol and 500 ppm gasoline showed growth effects after 4
weeks of exposure. Recovery was complete by 4 weeks after exposure was stopped. Increased

kidney weight and liver and blood effects were observed primarily with gasoline only exposure.
Combined exposure resulted in an additive effect on growth suppression. Inflammation of the
upper respiratory tract was observed only with combined exposure.
Data suggest that the threshold for acute alcohol effects following ingestion is in the range of
0.1-0.5 g/kg (corresponding to a blood alcohol level of 0.01%-0.05%). Increased motor activity
in rats and increased aggressiveness in monkeys has occurred at these doses. At higher doses,
effects on fine motor control and coordination have been observed. Exposure of rats or mice to
20,000 ppm of ethanol in air
resulted in significant TABLE 5-1 HUMAN HEALTH EFFECTS OF ETHANOL
performance effects, while the ACUTE EFFECTS
lowest dose (12,000 ppm) had
borderline effects. To put these 100 ppm in air Odor threshold
exposures in context, rats 1000 ppm in air No significant neuromotor
exposed to 16,000 ppm resulted effects
in an alcohol blood level of 3000 ppm in air Headaches and early signs
0.05%, a level at which human of intoxication
performance effects are 5000 – 10,000 ppm in air Irritating to eyes and
commonly observed. respiratory system
0.1-0.5 g/kg ingestion (0.01- Threshold for central
5.3.2 Long-Term (Chronic) 0.05% blood alcohol) nervous system effects
Effects CHRONIC EFFECTS
Subchronic and chronic effects 0.2 g/kg/day ingestion Threshold for neurological
associated with alcohol abuse effects in fetuses
are well documented, and are 2 g/kg/day ingestion Liver effects
characterized by progressive
liver dysfunction and cirrhosis 0.5 g/kg/day (50 g/day) Increased incidence of
Alcoholic beverage and cancer of the oral cavity,
with chronic ingestion of 2
ethanol ingestion pharynx, esophagus,
g/kg/day. Inflammatory and colorectum, and female
degenerative changes to the breast
heart have also been observed. 20,000 ppm in air No significant effect on
Neurologic degeneration and fetuses after exposure of
effects on the brain structure female mice and rabbits
have been observed after long during pregnancy
term high level exposure; however no exposure thresholds for severe effects are available.
WHO (2010) concluded that alcoholic beverages and ethanol in alcoholic beverages are
“carcinogenic to humans”, or Group 1. This category is selected when there is sufficient

evidence of carcinogenicity in humans. They concluded that several types of cancer are caused
by alcohol consumption. They also concluded that acetaldehyde, which results from the
metabolism of ethanol, contributes to malignant esophageal tumors. WHO (2010) concluded
that there is sufficient evidence in experimental animals for the carcinogenicity of both ethanol
and acetaldehyde; however, other components of alcoholic beverages may contribute to the
observed carcinogenicity. When ethanol was administered in conjunction with other known
carcinogens, the carcinogenic effect was enhanced.
Some studies in humans and rodents indicate that ethanol induced genetic effects result from
moderate to high levels of ethanol exposure. Rats and mice receiving liquid diets of 5-10%
ethanol for 5 or more weeks showed adverse physical and functional effects on testes. Other
studies showed that consumption of drinking water containing 15% ethanol or inhalation of
20,000 ppm during pregnancy
had no significant effect on
TABLE 5-2 HEALTH PROTECTIVE CONCENTRATIONS
fetuses of mice and rabbits.
AIR
Fetal alcohol syndrome (FAS) 53 ppm (100 mg/m3) California Draft Value for protection of
is well known to result from public health – based on acute irritancy
excess alcohol ingestion effects but protective of chronic effects
Chronic – 7.9 ppm Minnesota Ethanol Sector Specific
during pregnancy. More
(15 mg/m3) Interim Exposure Values, for screening
subtle neurological changes in Acute – 95 ppm purposes at ethanol facilities only –
fetuses have also been (180 mg/m3) based on irritancy
observed. A threshold for DRINKING WATER
these effects has been 1100 mg/L California Draft Value based on the
identified as 0.5 oz per day minimum reporting concentration for
ethanol in food (0.5%)
(about one drink per day or
6500 mg/L NH did not develop drinking water
0.2 g/kg/day). value, but provided value equivalent to
drinking 1 beer (13,000 mg ethanol)
5.3.3 Health Protective 0.4 mg/L NEIWPCC value for comparative
Concentrations purposes, unlikely to increase ethanol
A number of states and in blood over baseline blood
regions have developed concentrations of about 10 mg/L
0.05 mg/L New York state standard for
health-protective oxygenates
concentrations of ethanol in
the environment. These have been developed for various purposes, but none have been
promulgated as standards. These concentrations and their bases are summarized in Table 5-2.

Table 5-2 shows a wide range of concentrations in drinking water. Both the California and New
Hampshire levels are based on exposure by other means that are considered generally acceptable.
The California level is based on a concentration in beverages and food of 0.5%, above which
ethanol must be reported, and an assumption that 0.5 kg of the daily diet contains this amount.
This dose is converted to an equivalent drinking water concentration. Similarly, New Hampshire
derived the level shown in Table 5-2 by developing a drinking water concentration equivalent to
drinking one beer. Neither of these criteria are based on effects data for ethanol. The New York
level is a general level used for oxygenates, and is not specific to ethanol. The NEIWPCC level
is based on a drinking water concentration that is unlikely to result in an increased ethanol
concentration in blood, and incorporates an uncertainty factor to account for sensitive
individuals.
5.4 Environmental Effects

A spill of ethanol or ethanol blend could affect soil and vegetation in the immediate area of the
spill and fire. In addition, if the spill results in a release to the surface water, aquatic organisms
could be affected, as discussed in the following sections.
5.4.1 Aquatic Systems

Ethanol released to a water body could directly affect aquatic organisms. Acute toxicity
indicates that an effect is observed after a very short period of exposure. Mortality is often
measured in the laboratory to various aquatic organisms after short periods of exposure. Such
tests typically result in measures of lethal concentrations in water, such as an LC50, a
concentration that is lethal to 50% of the test population. In some cases, other effects are studied
after acute exposure, such as growth or reproductive effects. Chronic studies involve longer term
exposures, and attempt to identify no observable adverse effect levels.
A large number of studies have been conducted on the effects of ethanol on various species, and
considering different types of effects. NEIWPCC (2001) evaluated the data available at the time
of their report and developed water quality benchmarks for ethanol using EPA Tier II procedures
(EPA, 1995). This approach is intended to derive acute and chronic water quality benchmarks
for aquatic organisms in cases where data is not
sufficient to develop an EPA Water Quality TABLE 5-3 WATER QUALITY BENCHMARKS FOR
ETHANOL
Criteria. They calculated water quality
Acute 564 mg/L
benchmarks using available data for aquatic
invertebrates (daphnia species), rainbow trout, Chronic 63 mg/L
and the fathead minnow as shown in Table 5-3.
Source: NEIWPCC 2001
In order to determine whether additional aquatic

toxicity information has been generated since the time of the NEIWPCC (2001) evaluation, a
search of EPA‟s ECOTOX (EPA, 2011) database was conducted for 2001 to the present. Little
information was found for the species identified above. Olmstead and LeBlanc (2003) did report
that a concentration of 0.5% (5000 mg/L) ethanol had no effect on the production of male
progeny in Daphnia magna over a chronic exposure period of 21 days. Two additional reports
were identified for other species (Chen et al., 2011 and Quinn et al., 2008), but none of these
results would change the benchmarks shown above.
Bioconcentration or bioaccumulation of substances in tissues can also be a concern upon releases

to water. This is the entry and concentration or accumulation of substances in tissues. The
potential for such accumulation is characterized by its octanol/water partition coefficient (Kow),
which is an indication of a substance‟s affinity for fatty tissues. The Kow for ethanol is 0.49
(HSDB, 2011), indicating that it is unlikely to accumulate in fatty tissues. Such accumulation
would also be limited by the expected rapid rate of metabolism.
Oxygen depletion is also a concern with spills to aquatic environments. NEIWPCC (2001)
conducted modeling to evaluate potential oxygen depletion effects upon spills to different
environments. They used the Streeter-Phelps model to estimate the amount of ethanol required
to use up the dissolved oxygen in the stream. This model considers biodegradation and
reaeration rates considering small average and large rivers and assuming an initial dissolved
oxygen concentration of 7 mg/L. Modeling showed that the oxygen demand needed to
biodegrade the benchmark (acute and chronic) levels of ethanol (see Table 5-3) is greater than
the amount of oxygen in the stream. Therefore,
TABLE 5-4 ETHANOL CONCENTRATIONS ABLE
TO DEPLETE STREAM DISSOLVED OXYGEN oxygen depletion in a stream appears to be a
Small Stream 56 mg/L more critical impact than direct toxicity of
ethanol to aquatic organisms. For comparison
Average River 32 mg/L purposes, NEIWPCC (2001) calculated ethanol
Large River
concentrations capable of depleting in stream
13 mg/L
dissolved oxygen, as shown in Table 5-4.
Source: NEIWPCC 2001 These values are based on the assumption of an
initial concentration of dissolved oxygen
concentration of 7 mg/L. However, rivers and streams are considered unimpaired if they have
somewhat lower concentrations. For example, in Massachusetts, 314 CMR 4.05 indicates that
dissolved oxygen shall not be less than 6 mg/L in cold water fisheries and 5 mg/L in warm water
fisheries. If a receiving stream had concentrations lower than 7 mg/L, the concentrations shown
in Table 5-4 would be lower.

NEIWPCC (2001) noted that a lower concentration of ethanol is needed in a larger river to
deplete the dissolved oxygen because the typical reaeration rate of a larger water body is lower
than a smaller water body. They also indicated that if the same volume of ethanol was released
to the three environments, the large water bodies would be less impacted than the smaller ones
due to increased dilution.
This table indicates that complete oxygen depletion is likely to occur at concentrations lower
than those expected to have direct toxicity. In addition, effects on aquatic organisms as a result
of low dissolved oxygen will occur prior to complete oxygen depletion. EPA (1986, 2000) has
set minimum dissolved oxygen values (over a 24 hour period) at 4 mg/L for freshwater cold
water fish and 2.3 mg/L for saltwater aquatic organisms from Cape Cod to Cape Hatteras.
Oxygen depletion was observed in the case of the

Wild Turkey bourbon spill to the Kentucky River,
as discussed in Section 3.0. In this case, oxygen in
the river was almost completely depleted over about
a 6 mile stretch, which migrated downstream,
ultimately affecting over 66 miles of the river and
resulting in massive fish kills.
Source: USCG 2000
5.4.2 Terrestrial Systems

Little information is available on the toxicity of ethanol to wildlife. In order to identify any
available information, an ECOTOX report (EPA, 2011) was run for terrestrial exposures. Most
studies have been done on laboratory or domestic animals, or crops. Many of these studies are
intended to provide insight into mechanisms and effects of alcoholism in humans. For example,
honey bees have been used as model of human intoxication. In order to provide some insight
into the potential toxicity of ethanol to wildlife, some results are summarized in Table 5-5.
In general, exposure to terrestrial organisms is likely to be limited in a spill situation. As

discussed in Section 4.5.1, ethanol in surface soil is likely to volatilize, and migrate to deeper
soils and groundwater. In addition, it is expected to biodegrade rapidly. Therefore, significant
exposure to terrestrial receptors is unlikely to occur. However, localized effects to the soil
microbe and invertebrate community may occur in the spill area.

Sample et al., (1996) derived a TABLE 5-5 ETHANOL EFFECTS ON WILDLIFE (Select
toxicological benchmark for wildlife Results)
based on oral (ingestion) exposure to Douglas fir Applied ethanol concentrations of
Seedlings 10% and greater lethal within a
ethanol. These benchmarks were used
week, effects also observed with 5%
to develop concentrations of ethanol in
and 1% solutions
environmental media that would not be Japanese Ethanol at 2% in drinking water had
hazardous. Due to the lack of Quail significant effects on blood, brain
availability of wildlife data, their weight and growth after 7 day
benchmark was based on reproduction exposure
effects in rats. They derived a Lowest Honey bees Bees fed solutions of ethanol (5%
Observed Adverse Effect Level and greater) showed behavioral
(LOAEL) of 319 mg/kg/day, and effects, and mortality with solutions
of 50% ethanol.
developed a No Observed Adverse
Little brown LD50 of 3.9-4.4 g/kg
Effect Level (NOAEL) of 31.9
bat
mg/kg/day by incorporating a 10 fold Source: USEPA 2011 ECOTOX Report
safety factor. These values were
adjusted for a variety of wildlife species and then benchmarks developed for food, water, and a
combined food and water benchmark for aquatic feeding species. In the absence of empirical
data, these values are useful for providing an insight into concentrations in the environment that
could result in effects on wildlife, as TABLE 5-6 ETHANOL WILDLIFE BENCHMARKS (Based on No
shown in Table 5-6. Observed Effect Levels)
Food 117 to 471 mg/kg (ppm) depending
The concentrations in water shown on species
in Table 5-6 are above Water 137 to 521 mg/L (ppm) depending on
concentrations that are predicted to species
result in oxygen depletion (Table 5- Food and water 123 to 169 mg/L (ppm) depending on
4) or result in chronic effects on combined (for species
aquatic feeding
aquatic organisms (Table 5-3).
species)
Therefore, it appears that ethanol in
Source: Sample et al. 1996
water is a much greater concern for
aquatic organisms than terrestrial organisms. The hazards to wildlife associated with ingestion
of food containing ethanol are likely to be low since it is volatile, and does not accumulate in
fatty tissue.

5.5 Health and Safety Considerations for Responders

5.5.1 Recognizing Product Spilled
Section 2.2 shows the DOT placards used for ethanol and ethanol/gasoline blends. These are the
best ways of identifying the product spilled. E-95 is generally transported from production
facilities to the storage depots by rail. This transport is largely in non-pressurized (general
service) tank cars with a capacity of approximately 30,000 gallons (IFCA, 2008). The DOT
Placard for E95 has a red background and a white flame symbol,
indicating that it is a flammable liquid. It also shows the North
America (NA) code for this substance (1987). Lastly, at the
bottom, it shows the hazard class (3). A flammable liquid (Class 3)
means a liquid having a flash point of not more than 60.5°C
(141°F), or any material in a liquid phase with a flash point at or
above 37.8°C (100°F) that is intentionally heated and offered for
transportation or transported at or above its flash point in a bulk
packaging.
As shown in Section 2.2, a different placard is used for E10. However, this placard is the same
one used for gasoline. This is significant, because E10 requires the use of alcohol resistant foam,
as discussed in Section 7.2, while gasoline does not.
5.5.2 Exposure Limits

The Occupational Safety and Health Administration (OSHA) has established ethanol Permissible
Exposure Limits (PELs) for work place safety (general industry), as shown in Table 5-7. Other
occupational values (the National Institute for Occupational Safety and Health (NIOSH)
Recommended Exposure Limit and the ACGIH Threshold Limit Value) are the same as the
TABLE 5-7 OCCUPATIONAL LIMITS IN AIR
Limit Ethanol Gasoline
OSHA Permissible Exposure 1000 ppm (1900 mg/m3) None, 1 ppm for benzene
Limit (PEL)
NIOSH Immediately 3300 ppm (6237 mg/m3) None, 500 ppm for benzene
Dangerous to Life or Health (10% of the LEL)
(IDLH)
OSHL PEL. PELs are time-weighted average concentrations that must not be exceeded for any 8
hour work shift of a 40 hour week. NIOSH has established a concentration that is deemed to be

Immediately Dangerous to Life or Health (IDLH). In the case of ethanol, this concentration is
10% of the LEL, which is 3.3%. In the case of ethanol, the IDLH is based on the LEL because
acute toxicity data do not indicate that the IDLH should be set at a lower value. In comparison,
there are no occupational limits for gasoline due to its variable composition. Instead, the PEL
and IDLH are shown for benzene, which are substantially lower than those for ethanol.
5.5.3 Protective Clothing

Protective clothing to be worn when responding to an ethanol spill, including E85, consists of
self-contained breathing apparatus (NRT, 2010). According to NRT (2010), structural
firefighters gear will provide limited protection. Contact with skin should be prevented, and
Global (2010) recommends the use of nitrile or neoprene gloves for this purpose.
5.5.4 Other Health and Safety Considerations

NRT (2010) identifies a number of specific health and safety concerns and recommendations
related to spills of fuel grade and E85 ethanol spills. These recommendations are summarized
below:
TABLE 5-8 HEALTH AND SAFETY RECOMMENDATIONS FOR SPILLS OF FUEL

GRADE ETHANOL AND E85
EVACUATION
Large spills Consider initial downwind evacuation
of 300 meters (1000 feet)
Consider initial evacuation of 800
meters (1/2 mile) in all directions due
to potential for fire spread
Large spills with fire (tank, rail car, or tank Consider initial evacuation of 800
truck) meters (1/2 mile) in all directions due
to potential for fire spread
OTHER CONCERNS
Electrical conductivity Good electrical conductor – ground
equipment used in handling
Vapors near engine air Risk of “runaway engines” if vapors
Intakes create a rich fuel mixture
Ethanol entering firefighting water intake Firefighters should avoid drawing raw
hoses water with high concentrations of
ethanol into intake hoses

6.0 Spill Assessment and Delineation
The general spill assessment and delineation process for ethanol and ethanol blend release events
is similar to that utilized for petroleum fuel releases. In fact, the characteristics, relative low
ecological toxicity and non-visible properties of ethanol dictate that any early assessment and
delineation efforts focus primarily upon the more evident and detrimental gasoline components.
Nonetheless, there are readily available methods of detection and screening for ethanol which,
especially in the event of high concentration blend releases, can be utilized to assess the extent of
impact and monitor for ethanol itself. In addition, since the preferred methods are also capable
of simultaneously detecting and determining “typical” gasoline components such as BTEX, these
methods can effectively delineate and assess the impacts of all components in the event of a
release.
6.1 Field Sampling

As stated previously, the spill assessment and investigation process should mimic that utilized
for a petroleum fuel release. This would include screening of ambient air within and outside the
release area for the components of interest; visual determination of impacts including stressed
vegetation, evidence of impacted aquatic biota, and visual detection of sheens from the gasoline
components of blends; statistical determination of appropriate sampling locations and numbers;
collection and screening of environmental samples; and the collection and confirmatory analysis
of samples. Table 6-1 summarizes the sampling objectives and techniques, which are discussed
further below.
The assessment and response phase includes visual observations of impact evidence, screening
of ambient air for component detection, and collection of grab samples from impacted matrices
for both screening and confirmatory analyses. The list below summarizes the types of
observations and/or samples which may be needed to assess the extent and impact of a release.
Details on the actual screening tests and analyses are discussed in Sections 6.2 and 6.3,
respectively.
Visual Observations - look for evidence of sheen from gasoline components, evidence of biota
impacts (dead fish, stressed vegetation, etc.). Ethanol is colorless and water-soluble and cannot
be seen in water. Wet spots on soils or solid surfaces should be investigated and screened for
properties such as flammability to determine if they are spilled product. Pooled liquids and even
surface waters can be quickly screened for flammability and/or ethanol content, as a percentage;
see Section 6.2 for details.

Ambient Air Screening – flammability (LEL) can be used as an indicator of presence/absence

of ethanol and ethanol blends. Real-time screening of air can be conducted for presence of
vapor-phase concentrations of ethanol and ethanol blend components, and, longer term (8-hour)
exposure monitoring can be conducted within and outside spill zone (NIOSH methods).
Collection of Samples from Environmental Media - grab samples can be collected of site
soils, sediments, surface waters, and groundwater, depending upon the extent of release and
exposed media. Since ethanol is rapidly biodegraded, water samples intended for off-site
shipment must be preserved at a pH<2. Soil and sediment samples for confirmatory analysis
must be collected using acceptable VOC sampling and preservation methods.
TABLE 6-1 SAMPLING TECHNIQUES

Objective Matrix Techniques
Visual observation-sheens from denaturing
additives (gasoline), visible fires, pooled
Determine immediate extent of
Surface water, surface soil, large volumes of liquid
spill and impact-including during
paved surfaces Stressed vegetation, dead fish or animals
first responder efforts Quick flammability screen
Hydrometer-water samples only
LEL-flammability
Determine extent and hazard of Indicating tube-target ethanol or benzene
ambient air in spill area and Air- Real-Time Monitoring PID-targets gasoline components (BTEX)
immediate vicinity FT-IR- can differentiate ethanol and gasoline
components (BTEX)
Grab samples for either on-site screening or
Determine vertical and horizontal laboratory analysis.
extent of environmental impacts in Ground and surface water, Water samples to be analyzed for ethanol
site surface water, soils, and soil must be collected and preserved as for VOCs
groundwater Soil samples must be collected using closed-
loop sampling methods
Determine potential off-site 8-hour samples using absorption tube
Air
impacts to nearby air-receptors methods (NIOSH 1400)
6.2 Screening Methods

Although there are a multitude of rapid screening methods for the gasoline components in
ethanol fuel blends, the properties of ethanol make development of rapid detection methods more
of a challenge. Ethanol‟s ionization potential (10.47ev) is close to that of a typical lamp (10.6ev)
found in Photoionization Detectors (PID), resulting in it being a low-response compound to PID
screening instruments (isobutylene Correction Factor (CF) of 10 using a 10.6ev lamp and 3.1
using a 11.7ev lamp). Although it can be easily detected via Flame Ionization Detectors (FID),
the non-specificity of this detector makes it difficult to differentiate ethanol without
chromatographic separation. There is no readily available spot test or immunoassay screen for
ethanol. In addition, its water solubility makes it a poor candidate for the typical field-portable
GC instruments which measure headspace or use purge and trap introduction and cannot tolerate

direct aqueous injections. The available screening methods for ethanol are summarized in Table
6-2, and discussed below:
TABLE 6-2 ETHANOL SPILL SCREENING TECHNIQUES

Method Technique/Detector Detection Limit Comments
Quick Screens for Presence/Absence
Open flame test Exposing small volume of material Presence/Absence Identifies relatively high
to open flame concentration of ethanol
and/or gasoline (still
flammable)
Percent Ethanol Check-water Hydrometer 1-percent Results will be biased low if
only gasoline mixture
Air
Real time monitoring for LEL monitor-calibrated versus 1-percent of LEL Correction Factor (CF)=1.5
flammability methane
Color Tube Air pumped through reactive Ethanol-1000 ppm Need separate tubes for each
sorbent-color change occurs based Benzene-5-40 ppm analyte
upon concentration Ethanol tube requires the
volume of a 1-hr sample to
achieve limits
One-time use
Real-time monitoring w/PID Air pumped into chamber with a Ethanol-50-100 ppm Non-selective
photo-ionization detector- Benzene- 5-20 ppm C F =10 for 10.6ev lamp
calibrated versus isobutylene CF = 3.1 for 11.7ev lamp
Response to gasoline
components (BTEX) greater
than ethanol
Real-time monitoring w/FID Air pumped through chamber, Ethanol-50-100 ppm Non-selective
detected via flame ionization Benzene- 5-20 ppm
Real-time monitoring w/FT-IR Air pumped into chamber where it Ethanol-25 ppm Selective and can screen
is subjected to excitation and the Benzene- 200 ppb simultaneously since bands for
resulting infra-red spectral bands ethanol (3500 cm-1) and BTEX
are detected. FT-IR peaks are (2500-2000 cm-1) are separated
unique to particular compounds Ethanol and BTEX in compound
library
Water
Screen for impact in surface Dissolved oxygen probe 0.5 mg/l dissolved oxygen Can be used to identify impact
water bodies biochemical oxygen demand, to surface water and monitor
chemical oxygen demand per recovery
standard methods
Headspace with GC using Measured volume of sample with Ethanol-5-100 mg/l Ethanol is water-soluble, will
detection by FID, PID, or known headspace is allowed to Benzene- 5-50 ug/l not enter the headspace well-
MS equilibrate and a volume of the resulting in the high limit of
headspace injected for comparison detection
to similarly prepared standards Ethanol is a poor responder to
the PID
Direct injection onto a GC with Known volume injected onto the GC Ethanol-5 mg/l Ethanol is a poor responder to
detection via FID, PID, or and the compounds separated and Benzene-250 ug/l the PID
MS detected. Comparison to standards
Portable GC with Purge & Trap Known volume sparged through a Ethanol-200 ug/l Ethanol is water-soluble, and
system-detection via PID, sorbent media which is then Benzene- 5 ug/l exhibits low purge efficiency
FID, or MS backflushed under rapid heating to resulting in the high limit of
force trapped compounds into the detection
GC. Comparison to standards Ethanol responds poorly to PID

TABLE 6-2 ETHANOL SPILL SCREENING TECHNIQUES (continued)

Soils and Sediments
Headspace with GC using Measured mass of sample is added Ethanol-100 mg/kg Ethanol is water-soluble, will
detection by FID, PID, or to a known volume of water with Benzene- 50-500 ug/kg not enter the headspace well-
MS known headspace and allowed to resulting in the high limit of
equilibrate; headspace injected detection
onto the system for comparison to Ethanol is a poor responder to
similarly prepared standards the PID
Direct injection onto a GC with Measured mass of sample is added Ethanol-1-5 mg/kg None
detection via FID, PID, or to a known volume of water; Benzene-250 ug/kg
MS injected onto the GC and
compounds separated and
detected. Comparison to standards
Portable GC with Purge & Trap Measured mass of sample added to Ethanol-500 ug/kg Ethanol is water-soluble, and
system-detection via known volume of solvent and then Benzene- 50 ug/kg exhibits low purge efficiency
PID,FID, or MS a known volume is placed into a resulting in the high limit of
vessel containing water. The detection
sample/solvent/water volume is Ethanol responds poorly to PID
sparged through a sorbent media
which is then backflushed under
rapid heating to force trapped
compounds into the GC.
Comparison to standards
Screening Presence/Absence-Soils and Waters
One of the simplest ways to ascertain whether or not ethanol and/or blends are present in media
is via a simple open-flame burn test. This can yield valuable information, especially when
performing the visual observation/delineation phase of spill site assessment. There are two basic
means to perform a quick flame test.
Place a very small volume or mass of the material into a shallow container such as a
watch glass or even a small pie tin and wave a lighted match or a propane torch above the
sample; or
Make a small loop in a length of copper wire, dip it into the sample, and then place it into
an open flame.
In either case, if the sample (or wire) burns, sparks, or otherwise supports combustion the spilled
product is present in the test sample.
Gross Screening-Water using a Hydrometer
A quick estimate (percentage) screen for ethanol can be performed via a simple hydrometer test,
like those used in ethanol plants and distilleries. A sample of sufficient size is placed into a
container and the hydrometer floated into it. The percent ethanol can be read as the point on the

hydrometer scale that intersects the liquid meniscus. The reading will be biased low if gasoline
is present. Although the hydrometer is calibrated at 60°F, the actual correction to the reading
varies by less than 1% as temperature falls to 0°F and 6% (adjust higher) at an ambient
temperature of 120°F. Therefore, for purposes of screening for gross concentration the method is
viable without correction. A field SOP, based upon the ASTM Method (1250) is provided in
Appendix D.
Ambient Air Field Screening
Color-indicating tubes are available for ethanol. These will provide rapid single analysis for the
compound. However, the air volume required to meet the stated detection limits requires a 1-
hour collection time at standard input flows, making use of a color indicating tube a poor choice
for real-time data needs. Ethanol is a poor responder to a PID. It does respond to a portable
FID, this detector also responds to other volatile organic compounds, including methane. If real-
time and simultaneous detection of ethanol and gasoline components is necessary, the best
available technology is a portable Fourier Transform Infared (FT-IR) spectrometer, available
from several manufacturers. These instruments are capable of low ppm detection in air, contain
pre-loaded compound libraries which include ethanol, and can simultaneously screen for up to 25
compounds including the major components of gasoline. Detection and quantitation of ethanol is
accomplished by using the response at the wavelength corresponding to the O-H stretch at
approximately 3500 cm-1. The BTEX components are evaluated via the aromatic ring
wavelengths at 2500-2000 cm-1. Thus, the method can provide absolute selectivity and separate
screening data even in low ethanol blend events.
Soil/Sediment and Water Field Screening
Environmental matrix samples can be field-screened using typically available portable gas
chromatographs (GCs). Detection via FID or mass spectrometry (MS) is preferred as ethanol is a
poor responder to a PID. Detection limits will be elevated in most of these systems due to
ethanol‟s solubility in water and its poor purge efficiency. This is because most field portable
GC systems use headspace or purge and trap sample introduction methods and are not designed
for direct liquid injection onto the GC column. Although gasoline components volatilize easily
into sample headspace and are also readily purgeable, ethanol is water soluble, less likely to
quickly enter sample headspace and difficult to purge. These properties result in elevated
detection limits (see Table 6-2) for ethanol compared to benzene, for example. However, even
this elevated detection limit data can be useful in assessing impacts. If a field portable GC
system capable of accepting direct liquid injections is available, detection limits will be similar
to those reached in fixed-based laboratories utilizing published methods, as shown in Table 6-3.

As an alternative to field or laboratory measurements of ethanol, measurements of dissolved

oxygen and biochemical oxygen demand can be used, especially in surface water, to monitor the
impact of ethanol releases over distance and time.
6.3 Analytical Methods

There are several published and well known procedures for analysis of the gasoline components
of ethanol blends. Since ethanol is an industrial chemical and requires monitoring in the work
place, both NIOSH and OSHA published methods for its determination several years ago.
However, while ethanol has been determined in biological matrices for toxicology and
criminology for many years, it was only recently considered as a target in environmental
matrices. Environmental laboratories have determined ethanol primarily by modifying existing
methods; such as SW-8015 or by adding it to mass-spectrometry libraries and target compound
lists used for routine VOC analysis, but the analyte was never listed by EPA as a potential target
analyte within the methods themselves. Recently, EPA developed methods that can more
efficiently extract water-soluble polar organics from environmental matrices and improve
efficiency and detection-limits using GC or GC/MS techniques. Manufacturers are just now
producing commercially available instruments that perform these methods. Available methods
are summarized in Table 6-3, and discussed below.
Air - Both the NIOSH (1400) and OSHA (100) methods rely on collection onto an adsorption
tube, extraction via desorption solvent, and GC-FID quantitation. NIOSH 1400 uses an activated
charcoal collection tube and a dimethyl formamide/carbon disulfide extraction system. The
OSHA method (100) uses an Anosorb™ collection tube and desorption. Commercial
laboratories which perform both analyses are readily available.
Although, air samples may also be collected and analyzed using SUMMA canisters, like other
polar and water-soluble analytes, ethanol tends to “stick” to the canister and valve surfaces under
typical analysis conditions resulting in poor efficiency and elevated detection limits.
Water, Soils, and Sediments - the most prevalent methods for determining ethanol in
environmental matrices utilize direct-injection techniques and GC-FID using wide-bore capillary
columns coated with highly polar stationary phases designed for separation of alcohols.
Laboratories usually refer to these methods as 8015M when citing procedures. Direct injection
methods yield detection-limits in the low ppm range for both waters and soils/sediments.
Laboratories may also analyze samples for ethanol by GC/MS using the purge and trap
techniques (methods 5030A and 5035A). Due to ethanol‟s solubility in water and low purge-
efficiency, detection-limits are in the 100-250 ppb range for waters and soils/sediments.

TABLE 6-3 ANALYTICAL METHODS

Air
NIOSH 1400 Air pumped through charcoal Ethanol-20 ppm None
sorbent tube. Tube is desorbed Benzene-5 ppm
using solvent system and the
compounds in solution
determined by GC-FID
OSHA 100 Air is pumped through a Ethanol-100 ppm None
Anosorb™ 747 sorbent tube. Benzene- 5 ppm
Tube is desorbed using a solvent
system and the compounds in
solution determined by GC-FID
Water
SW-846 Modified Method Direct injection onto a GC-FID Ethanol-25 mg/l None
8015M system Benzene- 500 ug/l
SW-846 5030 with Purge and trap with GC-FID or GC- Ethanol-500 ug/l Ethanol is water soluble
quantitation via MS detection Benzene-0.5 ug/l and has low purge
8015M or 8260 GC-PID for BTEX efficiency
8021 for BTEX
SW-846 5031 Azeotropic distillation with Ethanol-10 ug/l No commercially available
quantitation of the resulting instrument. Expensive and
solution via 8015M or 8260 difficult to find a lab
performing
SW-846 8261 Vacuum distillation (SW-5032) Ethanol-10 ug/l Instrumentation available
with quantitation via GC-MS but only major lab
networks offer analysis
Soils and Sediments
SW-846 Modified Method Measured mass dilution in water, Ethanol-500 ug/kg None
8015M direct injection onto a GC-FID Benzene- 100
Method 8021 system ug/kg
GC-PID for BTEX
SW-846 5035 with Closed-loop purge and trap with Ethanol-50 ug/kg Ethanol is water soluble
quantitation via GC-FID or GC-MS detection Benzene-0.5 ug/kg and has low purge
8015M or 8260 efficiency
SW-846 5031 Azeotropic distillation with Ethanol-5 ug/kg No commercially available
quantitation of the resulting instrument. Expensive and
solution via 8015M or 8260 difficult to find a lab
performing
SW-846 8261 Vacuum distillation (SW-5032) Ethanol-5 ug/kg Instrumentation available
with quantitation via GC-MS but only major lab
networks offer analysis
Newer EPA Methods - during the 1990‟s EPA began looking at ways to improve detection
limits for polar organics such as ethanol. There were two alternative extraction methods
published in SW-846. Method 5031 utilizes azeotropic distillation methods and allows for

analysis of the extracted analytes by GC or GC/MS. Method 5032 uses vacuum distillation and
was also developed for use with either GC or GC/MS quantitation methods. Both methods were
developed by the EPA laboratories and required substantial equipment set-up and in some cases
construction of the required apparatus. These methods were, therefore, slow to be recognized by
the environmental analysis community and manufacturers. To date no commercial company has
produced an instrument for performing Method 5031. Recently, instruments became available to
perform vacuum distillation. EPA in 2007 published Method 8261 which is a vacuum
distillation GC/MS procedure. Ethanol is specifically listed as a potential target analyte in this
method (see Table 6-3).

7.0 Response Options
7.1 General Description

Although ethanol and ethanol blend spills are similar to other fuel release scenarios, the
physical and chemical properties of ethanol add unique challenges and alter remediation
approaches. Ethanol, unlike gasoline, is water soluble and even in blends will enter
solution if exposed to water. This means that in ethanol blend spills there is a potential
for a layered spill profile, gasoline floating on the water surface and ethanol mixing into
the water) requiring two different clean-up strategies. The following sections describe
short term and longer term response priorities. These sections are followed by media-
specific options.
7.1.1 Short Term Response Priorities

The priorities of first responders are life safety, incident stabilization, and property
conservation. It is not the objective of this report to provide guidance as to how to
conduct these activities in the event of an ethanol spill. Rather, it is to provide guidance
as to the potential for long term impacts of various options.
First responders must utilize techniques and products that will counter both the water-
solubility and flammability of ethanol. In many cases, fires result during spill events, and
containment of such fires is often an effective response strategy (contained burn). As
discussed in Section 3.0 and Appendix A, burning in many large spill situations has
greatly reduced the mass of ethanol that reached environmental media. The products of
ethanol combustion are carbon dioxide and water. Under ideal conditions of wind
direction and speed, ground cover, proximity to structures, and other site-specific
elements, the best approach may be to conduct a controlled burn.
While water can be used to cool structures and misting can be used to keep vapors down,
the application of water to an ethanol fire, unless in sufficient volume, does not
substantially decrease the flammability of ethanol. The use of water also results in an
increased potential for migration of ethanol solution to storm and sanitary sewer lines,
groundwater, and surface water, unless it is recovered.
Fire-fighting foams can be effective, but must be alcohol resistant (AR-FFF), or rapid
degradation and loss of the foam blanket can occur. Unless recovery of the foam/ethanol
occurs, the potential for migration to storm and sanitary sewer lines, groundwater and
surface water is still present. The foam and ethanol mixture will result in increased

biochemical oxygen demand /chemical oxygen demand loading to wastewater treatment

facilities or surface water compared to the ethanol alone.
Any efforts by first responders to control or prevent migration of ethanol will have
benefits in reducing future response actions to address groundwater or surface water
impacts. Recovery of ethanol from soil or other surfaces will eliminate a flammability
hazard, and reduce impacts to groundwater and surface water. Physical barriers, such as
booms or plastic-lined earthen dams, can be effective in preventing flow of ethanol to
larger surface water bodies. Booms for such purposes must be designed to absorb water-
soluble materials. Physical barriers are only effective in blocking progress into water
bodies or ditches and afford little control once the ethanol has entered a water body.
7.1.2 Longer Term Response Priorities

Longer term response priorities are focused on preventing migration of ethanol from the
spill site. This can include removal of spilled material, soil removal, damming of creeks
or ditches, aeration, etc. These activities are designed to prevent migration of ethanol to
both groundwater and surface water, as well as eliminating possible flammability and
explosion hazards, as discussed in the following sections.
7.2 Media Specific Options

7.2.1 Soil
Ethanol spills on surface soils present unique challenges to first responders and follow-up
remediation teams. Except under cold winter conditions, ethanol spills pose a significant
flammability hazard. The water solubility of ethanol allows it to rapidly migrate into and
through soils, especially those with higher moisture content. Thus, any response strategy
must be able to quickly eliminate the flammability hazard and suppress the potential
movement of the spill both laterally and through the soil column. Response options for
such spills are summarized in Table 7-1, as well as the conditions required for
implementation and possible issues.
Contained/Controlled Burn
Under ideal conditions of wind direction and speed, ground cover, distance from
structures, and other site-specific elements, the best approach to eliminating the
flammability hazard and minimizing movement of ethanol through soil may be to allow
the product to burn and/or conduct a controlled burn of the spilled product. Unlike
methanol, ethanol does burn with a visible flame, especially when denatured with low
percentages of gasoline. Contained/controlled burns must be conducted with the
oversight, guidance and approval of the local fire officials and appropriate precautions

must be taken to protect areas outside the burn zone and conduct sufficient monitoring to
both protect and satisfy the public. Monitoring should include both chemical and
physical elements; such as particulate matter in smoke.
This method actually leaves little waste and there is no need to dispose of any residuals;
all of the ethanol and/or ethanol blend is thermally destroyed. The risk associated with
this method include unexpected changes in wind direction and/or speed causing the burn
profile to shift, public exposure to the smoke and byproducts, and the overall perception
of an outdoor burn of a chemical spill.
As described in Section 3.0, this method has been used effectively in several ethanol
incidents that have occurred, including the New Brighton, PA and Arcadia, Ohio spills.
However, in both cases, releases to surface water also occurred. In the case of New
Brighton, PA, tank cars entered the river resulting in a direct release of ethanol to surface
water. In the case of Arcadia, OH, however, some of the ethanol released to the surface
did not immediately burn. Evidently pooled product permeated the snow and ice blanket,
entered the underlying soil, and migrated to the field drainage systems resulting in
impacts to the drainage water.
Foam Suppression with Water Flush

In situations where the spill has occurred in close proximity to storm water inlets or catch
basins, the most effective response may be to combine vapor suppression with copious
flushing. Alcohol resistant foam (AR-FFF) must be used or the ethanol will literally
react with and break down the vapor barrier. Although AR-FFF products are
biodegradable, they can have effects on the environment in the short-term (through direct
toxicity or oxygen depletion) and both they and the ethanol itself can be toxic to water
treatment bio-remediation systems in high concentration. In addition, vapor suppression
foams only suppress the ethanol vapor and do not significantly affect concentration.
Dilution in the range of 5-10X with water is necessary to produce foam and ethanol
concentrations that will not affect publicly owned treatment works (POTW) bio-digestion
systems.
Because of the significant volumes of water that the method requires, this process is best
for smaller spills and in soils near POTW intakes. It is also better suited to surfaces such
as gravel, hard-pan soils and clays that will not produce large volumes of wet mud when
flushed with water. Obviously, it is a poor choice in areas near surface water bodies that
could be negatively impacted by the run-off from the flushing process.

TABLE 7-1 RESPONSE OPTIONS FOR SURFACE SOIL SPILLS

Method Conditions Required Issues with Approach
Controlled/contained Wind speed and direction away from Local authorities responsible for public safety
burn of pooled structures Sudden wind shift could threaten other
liquids Open area not near structures or other structures/areas
flammable materials
Foam suppression Near sewer or storm drains that go to Foam and ethanol/fuel blends require dilution
and water flush POTW to keep from affecting POTW
Ability to recover foam/ethanol Foam in surface water can cause oxygen
Works best if soils are hard and won’t depletion, and can be toxic to aquatic species
produce too much mud Ethanol can still affect groundwater unless
Should not be used near surface water recovered
bodies, unless access can be blocked Ethanol/foam mixture can still affect surface
water (biochemical oxygen demand)
Pooled Liquid Temperatures that limit flammability, Must monitor and control work zone for
Removal, Soil ability to wet mist work zone flammability
Excavation and Viable landfill or treatment/disposal If using vacuum methods to remove
Off-site Disposal facility foam/water/ethanol mixtures may need to add
Cost-effective soil volume impact zone dispersant to prevent re-expansion of foam
Excavated soils must be screened for
flammability
Flammable (FP<140F) soils cannot be
transported and must be wetted or otherwise
rendered non-flammable
In-place Mixing and Temperatures that limit flammability Must monitor and control work zone for
Evaporation Ability to wet mist work zone flammability
Large impact areas should be divided into
working grids
Removal and Off-site Disposal
In spills where the product covers large areas of soil and is slow to evaporate, it may be
necessary to physically remove the pooled liquids and impacted soils. Pooled liquids and
even high concentrations in soils can produce enough vapors to become a fire hazard.
They may also impact groundwater and/or surface water. In addition, fire-fighting foam
residuals can have effects on the environment and unless broken down with available
dispersants may re-expand and cause difficulties, especially if a vac truck or Vactor is
used to remove them.
Appropriate safety precautions must be observed. These include continual monitoring of

potential flammability of the work zone and isolation of non-involved personnel. A fine
water mist can be used to both wet/dilute the ethanol and keep vapors down while the
operation is in process. Residual liquids including ethanol/water/foam mixtures can be
removed via vac truck or Vactor if the flammability conditions allow. If large amounts of
foam are present it may be necessary to add dispersants to the mix to prevent re-
expansion during removal. Excavated soils should be screened for flammability, (flash
point tested) for safety and transport purposes. If a non-intrusive excavation method is
used such as a Vactor hydro/air excavator, extreme caution must be observed if free

potentially flammable liquids are present. Disposal options include landfill, bio-
treatment, or low-temperature thermal treatment. However, none of these options is
applicable to soils which are flammable (FP<140°F). Therefore, any soils which have
this potential issue must have their flammability lowered either through natural
evaporation or wetting of the matrix.
In-Place Mixing/Evaporation
For very large impact areas where controlled burning is not possible and off-site disposal
is not feasible, the only option may be to physically mix and manipulate the soils, thus
enhancing the natural volatilization of the ethanol. The objective of this approach is to
safely encourage sufficient volatilization to reduce the concentrations to the point where
the matrix is no longer toxic and natural bio-degradation is supported. Vapor suppression
methods such as water misting should be employed and the work zone must be controlled
and monitored for flammability. In large spills, the work area can be divided into
working grids and each grid screened for residual ethanol through flammability testing;
such as a simple open flame burn test. Soils containing insufficient ethanol to burn will
rapidly biodegrade if left to do so.
7.2.2 Groundwater
If a release of a high ethanol content material impacts the groundwater, the same
properties of ethanol that limit clean-up in surface water bodies apply. Response options
for groundwater impacted by an ethanol or ethanol blend spill are summarized in Table 7-
2. Ethanol will rapidly dissolve and
disperse into groundwater. It may TABLE 7-2 RESPONSE OPTIONS FOR SPILLS
IMPACTING GROUNDWATER
also increase the mobility of any
Method Issues with Approach
gasoline components present in the Water treatment Carbon has limited
blend. Being water soluble and with sand/GAC effectiveness on ethanol
mobile, there are few immediate Will address gasoline
components
response options available. However,
Air sparging Ethanol has limited sparge
bio-degradation will commence efficiency
quickly as the plume concentration is Works well on gasoline
components
reduced. In zones of higher
Bio-augmentation Both ethanol and gasoline
concentrations, groundwater treat- Bio-venting components respond well
ment options are limited to sparging Will not work in high ethanol
and pump and treat methods using concentration systems
Monitored Natural Ethanol is highly and
carbon. These methods have limited Attenuation naturally biodegradable
efficiency due to the high solubility of
ethanol, but they can be used to reduce high concentrations to more treatable levels by

other means. In situ methods other than bio-augmentation are not applicable and the bio-
degradation process is inhibited at high concentration levels.
7.2.3 Surface water

Spills in surface water bodies leave few options. Table 7-3 summarizes the available
options, and possible issues. Ethanol is water-soluble and will quickly migrate through
TABLE 7-3 RESPONSE OPTIONS FOR SURFACE WATER SPILLS

Surface Water Type Approaches Issues
Ditches, Small Creeks, Earthen dams to block outlets to other Ethanol is water soluble and will not be
Streams, and Rivers waters stopped by typical boom or hay bales.
Remove/dispose of ethanol/water Removal effective in ditches and small pools
mixture Water treatment using typical sand/carbon
If dissolved oxygen levels impacted and filter portable systems will have limited effect
biota affected, aerate to replace on ethanol levels, but will reduce BTEX
dissolved oxygen
Large Rivers, Ponds and Deploy boom or construct earthen Limited response options available
Lakes dam(s) to prevent further Notify downstream water intake plants so
infiltration/discharge they may take necessary actions
Gasoline components can be removed by Water treatment using typical sand/carbon
surface boom filter portable systems will have limited effect
Aeration can be used to improve/prevent on ethanol levels, but will reduce BTEX
depleted dissolved oxygen Deployment of aeration equipment for large
rivers, lakes and ponds may take time
Pond aerators can be used for smaller ponds
Freshwater Wetlands Deploy boom or construct earthen Limited response options available, especially
dam(s) to prevent further during high water conditions
infiltration/discharge Water treatment using typical sand/carbon
Gasoline components can be removed by filter portable systems will have limited effect
surface boom. on ethanol levels, but will reduce BTEX
During low-water conditions remove
pooled liquids and/or use controlled burn
methods to prevent migration
Aeration can be used to improve/prevent
depleted dissolved oxygen
Saltwater/Tidal Wetlands Deploy boom or construct earthen Limited response options available -
dam(s) to prevent further infiltration Important to perform as much
Gasoline components can be removed by removal/elimination as possible during low
surface boom. water/tidal conditions.
During low-water conditions remove Water treatment using typical sand/carbon
pooled liquids and/or use controlled burn filter portable systems will have limited effect
methods to prevent reentry into marine on ethanol levels, but will reduce BTEX
habitat
Aeration can be used to improve
depleted dissolved oxygen
Marine-inner harbor Gasoline components can be managed by Limited response options available and
surface boom. mostly target BTEX components of gasoline
Mixing and aeration can be used to
improve dispersion and dissolved oxygen
Marine-outer harbor Deeper water and varied currents make Very limited options focused entirely on non-
dissolved oxygen replacement difficult ethanol components
Open ocean No viable means of removing or Response focuses on gasoline components
counteracting ethanol effects Ethanol allowed to run its course

the matrix. Being water soluble and quickly biodegraded, reduction in dissolved oxygen
can result in fish kills. Such effects will continue until sufficient dilution has occurred to
reduce toxicity. Response options depend upon the types of surface water structures
impacted and are discussed in the next several sub-sections.
Ditches
If the spill is confined to a ditch with slow-moving water, the best response is to dam the
ditch down-stream of the site or just up-stream of any threatened water body. Earthen
dams can be effective in preventing migration
Impacts to Stream to surface water. In cases where flow cannot
Painesville, Ohio be prevented, rip-rap can be used in the
Source: Ohio EPA 2007
construction of earthen dams to increase
turbulence and aeration. Typical emergency
response dams such as those made of hay
bales will not stop movement of the ethanol
since it is water-soluble. Booming is
ineffective for the same reason.
Once the impact zone is confined and defined,

the ethanol can be left to naturally evaporate
and degrade. If faster removal is required,
options include sparging (via aeration) or
active water treatment with discharge.
Pond aerators can be placed within the ditch to perform the sparging. Active water
treatment consisting of typical skid-mounted sand/carbon systems will remove both the
ethanol and gasoline components, although removal of ethanol will be limited.
Below is shown a simple aeration system implemented at the Bryan Ohio spill. The liner
Aeration of Stream, Bryan,
is used to prevent infiltration to
Ohio groundwater. Aeration is used over
Source: Ohio EPA short stretch of the stream to increase
oxygen content.
Small Streams and Rivers

If spills occur into moving water systems
ethanol‟s solubility will limit response
2011 options. The only recourse is to get
downstream of the spill and block its

progress or to simply allow it to run its course until dilution eliminates impacts. Aeration
can be used to reduce or restore oxygen depletion. Any blocks/dams must be constructed
to block or significantly impede water or dissolved ethanol will not be controlled.
Large Rivers
Aside from keeping spills from entering larger rivers by blocking progress through
smaller streams and tributaries, there is little that can be done if material enters or is
released into a large river. Any downstream municipal plants must be notified of the spill
so that they may shut-off intakes and avoid reduction of loss of biological activity in their
wastewater treatment processes. Down flow industrial facilities which are using the
source for process water should also be notified in case ethanol could react negatively
with their process. In extreme cases, treat and release systems may be required upstream
of water plants to protect them from harmful concentrations of ethanol. In some cases,
aeration may be used to prevent or improve anoxic conditions resulting from the
biodegradation of ethanol. This was used in the case of the Wild Turkey Distillery
release to the Kentucky River, although only after a significant fish kill occurred. In may
be difficult to use such techniques to prevent such effects due to difficulties with the
deployment of such equipment in a sufficiently timely way.
Aeration of Kentucky River after Fish Kill, Source: U.S. Coast Guard 5/24/2000
Ponds and Lakes

When spills occur into ponds and lakes, response options for the ethanol component are
limited at best. Since ethanol is water soluble it will rapidly disperse into the water body

and follow any underwater currents. If the spill occurs into a smaller body such as a farm
or residential pond, techniques such as aeration can be deployed to reduce concentrations
and oxygen depletion. Active pump and treat systems can also be employed. In larger
water bodies these methods would have limited influence and aside from preventing
additional release from the spill source there is little that can be done aside from allowing
the ethanol to dilute to a non-toxic level so that natural degradation can begin. As
discussed above, aeration techniques can be used, but the timeliness of such techniques is
critical.
7.2.4 Wetlands
Spills occurring in wetland environments pose unique challenges. Response options will
depend upon factors such as size and depth of the wetland/marsh, proximity to larger
open water, and in the case of tidal marshes, the tide stage and resulting water levels.
Ethanol impacts fresh and salt water in the same way and will rapidly dissolve into both,
as well as into brackish waters in estuaries and tidal rivers. Thus, options are once again
constrained by the rapid dispersion of ethanol and its solubility in the water.
Freshwater Marsh/Wetland
Response to spills in freshwater marsh/wetland areas depends upon factors such as the
size and depth of the impacted area. Spills in small shallow marshes are most likely to
result in high toxicity conditions as the dilution effects are greatly reduced. In these
cases, aeration, using typical pond aerators can help reduce ethanol concentrations and
avoid oxygen depletion. Although ethanol is soluble in water and actually forms an
azeotrope, it can be sparged from the water. The low efficiency will allow for aeration to
be utilized without fear of creating a flammable environment within the vicinity of the
marsh. This method can even work in larger/deeper marshes if the number of aerators
necessary is practical.
Salt water and Tidal Marshes

Spills which occur in these environments allow for varying response options depending
upon factors such as size of the marsh, depth, proximity to larger water and current tidal
condition. For releases which occur in larger marshes at high water times. Response to
the ethanol component is very limited and will most likely be simply to allow the spill to
disperse into the larger water and dilute.
If a spill happens during low-water conditions there are more options including those
similar to response and clean-up of soil spills. If the low-tide marsh condition leaves
pockets of water or a low flow surrounded by wet exposed ground, the ethanol will not

completely disperse providing opportunity to remove it and potential for dangers

associated with its flammability. Failure to adequately remove accessible ethanol during
the low-water condition will simply allow it to dilute and impact more water once tidal
levels return. Thus, it is imperative to address the spill while tidal conditions leave it
exposed. Methods in this case can include pumping water/ethanol mixture from isolated
pockets; applying sorbents designed to pick up water soluble liquids over exposed areas,
and controlled burning of the material.
7.2.5 Marine Areas

Ethanol and blends spilled into salt-water environments will behave in essentially the
same manner as in fresh-water incidents. Ethanol is still highly water soluble in salt-water
and it can also consume dissolved oxygen very quickly. Even in marine environments
BTEX components of the denaturing additive will separate and must be dealt with
differently. Options are very limited and decrease with the size of the water body and its
proximity to open ocean.
Inner Harbor
A release which occurs in the calmer and less current influenced waters of an inner
harbor allows a more targeted response. As in fresh-water systems, any gasoline
components will float and can be controlled with booms and removed by skimming if
required. The ethanol will enter solution rapidly and also consume dissolved oxygen as it
either assimilates into the water or follows whatever currents are present. Since removal
of the alcohol from a large water body is almost impossible, the only options available
include 1) letting the material dissolve and disperse and 2) supplementing dissolved
oxygen by means of barge mounted air compressors and lengths of perforated pipe. This
proved effective and restored dissolved oxygen values to habitable levels in the Kentucky
River several years ago following a massive bourbon spill.
Outer Harbor
A spill which occurs in the outer harbor areas will be more difficult to respond to,
especially in dealing with the ethanol component. Outer harbor zones are deeper and
contain stronger currents. Recovery of the BTEX component if the material was
denatured with gasoline can be accomplished via booms and skimming. The ethanol will
quickly dissipate in currents and is virtually impossible to control. Addition of dissolved
oxygen is difficult as the “dead zone”, if present, will be guided by currents and may
even be confined to certain depths within the thermocline.

Open Ocean
There are no real response options in the open ocean. The deeper waters, stronger
currents and larger waves will serve to quickly dilute the material and make any sort of
recovery or dissolved oxygen supplementation virtually impossible. Any response efforts
should be focused on the gasoline components, if present, and any fuel oil released from
the craft involved.


8.0 References
Section 1.0
Dinneen, Bob. 2011. 2011 State of the Ethanol Industry. President and Chief Executive
Officer, Renewable Fuels Association, National Ethanol Conference, Phoenix, Arizona.
February 21, 2011.
Renewable Fuels Association (RFA). 2011. Industry Statistics. Found at:

http://www.ethanolrfa.org/pages/statistics
Rudolph, Erich. 2009. Improvements in Safe Rail Transportation of Ethanol and Lessons
Learned. DOT Federal Railroad Administration (FRA). Presented at Biofuels Training Meeting,
Gettysburg, Pennsylvania. September 15, 2009.
U. S. Department of Agriculture. 2007. Ethanol Transportation Backgrounder. Agricultural

Marketing Service, September. Found at:
http://www.ams.usda.gov/AMSv1.0/getfile?dDocName=STELPRDC5063605
Section 2.0
Global. 2010. Material Safety Data Sheet, Denatured Fuel Grade Ethanol. Revision 9/17/2010
Hazardous Substance Data Bank (HSDB). 2011. National Library of Medicine Online Data
Base. Accessed January 2011. http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB
International Fire Chiefs Association. (IFCA). 2008. Responding to Ethanol Incidents. Course
Manual. Module 2. Chemical and Physical Characteristics of Ethanol and Hydrocarbon Fuels.
National Fire Protection Association (NFPA). 2002. Fire Protection Guide to Hazardous
Materials. 13th Edition. Pages 325-357.
Speedway. 2004. Material Safety Data Sheet for E85. Revision Date 1/30/2004.
Section 3.0 (and Appendix A)
Boulevard Distillers and Importers, Inc. Wild Turkey Bourbon Spill Kentucky River, May 2000
Dissolved Oxygen Impact Analysis. PowerPoint™ presentation provided by MassDEP

Bevill, Kris, Clean-up begins after ethanol train derailment, February 7, 2011, Ethanol Producer
Magazine, at EthanolProducer.com, found at http://ethanolproducer.com/articles/7464/clean-up-
begins-after-ethanol-train-derailment
Brown, Joy, „Huge Fireballs’ light sky after train derails, burns, February 7, 2011, The Courier,
The Findlay Publishing Company, Findlay, Ohio, TheCourier.com, found at
http://www.thecourier.com/templates/print.asp?d=020711_story1,2011,Feb,07&c=n
Evans, Murray, Train explodes in fireball, after derailment in Oklahoma, Associated Press
article, August 23, 2008, located at WSLS, Tulsa, OK web-site found at
http://www2.wsls.com/member-center/share-this/print/?content=ar399631
Jacobs, Don, Cleanup of 6000 gallons of ethanol at train derailment under way, September 16,
2009, Knoxville News Sentinel, web-site knoxnews.com found at
http://www.knoxnews.com/news/2009/sep/16/cleanup-6000-gallons-ethanol-train-derailment-
under-way
Maughan, Linsey, „It looked like a big mushroom bomb’, February 7, 2011, The Courier, The
Findlay Publishing Company, Findlay, Ohio, TheCourier.com, found at
http://www.thecourier.com/templates/print.asp?d=020711_story2,2011,Feb,07&c=n
National Transportation Safety Board (NTSB). 2008. Derailment of Norfolk Southern Railway
Company Train 68QB119 with Release of Hazardous Materials and Fire, New Brighton,
Pennsylvania, October 20, 2006. Railroad Accident Report NTSB/RAR-08/02. Washington,
DC.
Norfolk Southern Train Derailment, October 20, 2006, PowerPoint™ presentation provided by
MassDEP
Ohio Environmental Protection Agency. 2007. Report of the Painesville, Ohio train derailment.
Incident # 0710-43-3825. Found at:
http://www.epa.ohio.gov/portals/30/ersis/er/docs/derailNE.pdf
One Dead, Nine Injured in Ethanol Train Explosion, June 22, 2009, Environment News Service,
at http://www.ens-newswire.com/ens/jun2009/2009-06-22-092.asp
Riecher, Anton, Whiskey River Encore, May 2000, International Firefighting World magazine,
found at http://www.fireworld.com/ifw_articales/encore_00.php

Ship’s tank overloaded with ethanol ruptures in New York Harbor, Professional Mariner
magazine, located on the web-site at
http://www.professionalmariner.com/ME2/dirmod.asp?sid=&nm=&type=news&mod=News&mid=9A02E3B
96F2A415ABC72CB5F516B4C10&tier=3&nid=EABF8C7F37CF4A91A3BB36EB54205FE7
US Coast Guard (USCG). 2005. Investigation into the Explosion and Sinking of the Chemical
Tanker BOW MARINER in the Atlantic Ocean on February 28, 2004 with Loss of Life and
Pollution, USCG report, December 14, 2005
US Coast Guard (USCG). 2010. Understanding ethyl alcohol. Proceedings Spring 2010.
Chemical of the Quarter. Located at:
http://www.uscg.mil/proceedings/spring2010/articles/28_Saburn_ChemicalOfTheQuarter.pdf
US Environmental Protection Agency (EPA). 2009a. EPA Update: Rockford Freight Train
Derailment and Rock River Fish Kill. Press Release. 6/26/09
US Environmental Protection Agency (EPA). 2009b. Train Derailment Emergency Response.

Chicago Central & Pacific (CC&P), Railroad Line, Mile Post 80.1, Rockford, Winnebago
County, Illinois. Presentation.
Section 4.0 (and Appendix B)
Adair, C., Wilson, J.T. 2010. Anaerobic Biodegradation of Biofuels (Ethanol, Biodiesel, n-
Propanol, n-Butanol, and iso-Butanol) in Aquifer Sediment, 22nd National Tanks Conference,
Boston, MA, September 20-22
American Petroleum Institute (API). 2003. Bulletin No. 20, Answers to Frequently Asked
Questions About Ethanol Impacts to Groundwater, prepared by Tim Buscheck, Chevron Texaco
Energy Technology Company
Agency for Toxic Substances and Disease Registry (ASTDR). 2001. Landfill Gas Primer – An
Overview for Environmental Health Professionals.
Buscheck, T. E., K.O‟Reilly, G. Koschal, and G. O‟Regan. 2001. Ethanol in Groundwater at a

Pacific Northwest Terminal in Biodegradation of MTBE, Alcohols and Ethers. Battelle Press.
Deeb, R.A., J. O. Sharp, A. Stocking, S. McDonald, K. A. West, M. Laugier, P. J. J. Alvarez, M.

C. Kavanaugh, and L. Alvarez-Cohen. 2002. Impact of Ethanol on Benzene Plume Lengths:
Microbial and Modeling Studies. Journal of Environmental Engineering, 128:9 (868)

Gomez, D.E. and P. J. J. Alvarez. 2009. Modeling the Natural Attenuation of Benzene in
Groundwater Impacted by Ethanol-Blended Fuels: Effect of Ethanol Content on the Lifespan and
Maximum Length of Benzene Plumes. Water Resources Research, Vol. 45.
Howard, P.H., R.S. Boethling, W.F. Jarvis, W.M. Meylan and E.M. Michalenko. 1991. The
Handbook of Environmental Degradation Rates. Lewis Publishers, Boca Raton, Florida
Jewell, K., J.T. Wilson and J. Skender. 2010. Monitoring Production of Methane From Spills of
Gasoline at UST Release Sites, 22nd National Tanks Conference, Boston, MA, September 20-22
Lawrence Livermore National Laboratory (LLNL), University of California, Livermore. 1999.

Health and Environmental Assessment of the Use of Ethanol as a Fuel Oxygenate, Report to the
California Environmental Policy Council in Response to Executive Order D-5-99, December
McDowell C.J., S.E. Powers. 2003. Mechanisms affecting the infiltration and distribution of
ethanol-blended gasoline in the vadose zone, Environ Sci. Technol., 2003, May 1, 37(9)
Malcolm Pirnie, Inc. 1998. Evaluation of the Fate and Transport of Ethanol in the Environment.
Report prepared for American Methanol Institute, Washington, DC. Report No.3522-001
National Response Team. 2010. Quick Reference Guide: Fuel Grade Ethanol Spills (including
E85).
New England Interstate Water Pollution Control Commission (NEIWPCC). 2001. Health,
Environmental, and Economic Impacts of Adding Ethanol to Gasoline in the Northeast States,
volume 3, Water Resources and Associated Health Impacts
Powers, S.E., C.S. Hunt, S.E. Heermann, H.X. Corseuil, D. Rice, and P.J.J. Alvarez. 2001. The
Transport and Fate of Ethanol and BTEX in Groundwater Contaminated by Gasohol. CRC
Critical Reviews
Schaefer, C.E., Y. Xiaomin, P. Oliver, D. T. Tsao, S. H. Streger, R. J. Steffan. 2010. Aerobic

Biodegradation of Iso-butanol and Ethanol and their Relative Effects on BTEX Biodegradation
in Aquifer Materials. Chemosphere volume 81:1104–1110

Schaefer, C.E., Y. Xiaomin, P. Oliver, D. T. Tsao, S. H. Streger, R. J. Steffan. 2010. Anaerobic

Biodegradation of Iso-butanol and Ethanol and their Relative Effects on BTEX Biodegradation
in Aquifer Materials. Chemosphere volume 81: 1111–1117
Tousignant, L.P. and E. Evrard. 2009. Environmental Monitoring and Rehabilitation Following
a Denatured Ethanol Train Tanker Car Spill. Presented at 2009 Railroad Environmental
Conference. October 27-29, 2009.
U.S. EPA. 2008. FOOTPRINT- A Screening Model for Estimating the Area of a Plume
Produced from Gasoline Containing Ethanol. EPA/600/R-08/058
U.S. EPA. 2009. Biofuels and Emerging Issues for Emergency Responders: An Introduction to
Basic Response Guides and Case Study Examples from Biofuel Spills. Power Point Presentation
by Jeff Kimble, OSC, Region 5
Wilson, J.T. and C. Adair. 2007. Some Environmental Consequences of a Release of Ethanol to
Ground Water, in the 14th International Petroleum Environmental Conference, Houston, TX.
Wood, A., Bouchard, D., Brusseau, M. and Rao, P. 1990. Cosolvent effects on sorption and
mobility of organic contaminants in soils. Chemosphere 21(4-5):575-587
Zogorski, J. S., A. Morduchowitz, A. L. Baehr, B. J. Bauman. D. L. Conrad, R. T. Drew, N. I.

Korte, W. W. Lapham, J. F. Pankow and E. R. Washington. 1996. Report prepared for
Interagency Oxygenated Fuel Assessment. Coordinated by Office of Science and Technology
Policy, Executive Office of the President, Washington, DC
Section 5.0 (and Appendix C)
Armstrong, S.R. 1999. Ethanol: Brief Report on its Use in Gasoline. Cambridge
Environmental, Inc. Sponsored by the Renewable Fuels Association.
Baan, R., K. Straif, Y. Grosse, B. Secretan, F. El Ghissassi, V. Bouvard, A. Altieri, and V.

Cogliano. 2007. Carcinogenicity of alcoholic beverages. On behalf of the WHO International
Agency for Research on Cancer Monograph Working Group. The Lancet Oncology, Vol. 8,
Issue 4, Pages 292-293.
Bingham, E.; B. Cohrssen; C.H. Powell. 2001. Patty's Toxicology Volumes 1-9 5th ed. John
Wiley & Sons. New York, N.Y. p. V6 p.393 in HSDB (2011) (peer reviewed)
Brecher, R. 2005. Ethanol. Hazardous Materials Magazine. August.

Cakmak, I., C.I. Abramson, W. Seven-Cakmak, P. Nentchev, and H. Wells. 2009. Observations
of Ethanol Exposure on the Queen Honey Bee Apis mellivera anatoliaca (Preliminary Note).
Bulletin of Insectology. 62(1)99-101.
Chen, T., Y. Wang, and Y. Wu. 2011. Developmental exposures to ethanol or

dimethylsulfoxide at low concentrations alter locomotor activity in larval zebrafish: Implications
for behavioral toxicity bioassays. Aquatic Toxicology 102:162-166.
Chu, I., R. Poon, V. Valli, A. Yagminas, W.J. Bowers, R. Seegal, and R. Vincent. 2005. Effects
of an Ethanol-Gasoline Mixture: Results of a 4-Week Study in Rats. Journal of Applied
Toxicology. 25(3):193-199. Abstract only.
Cosmetic Ingredient Review Expert Panel (CIREP). 2008. Final Report of the Safety
Assessment of Alcohol, Denat., including SD Alcohol 3-1, SD Alcohol 30, SD Alcohol 39, SD
Alcohol 39-B, SD Alcohol 39-C, SD Alcohol 40, SD Alcohol 40-B, and SD Alcohol 40-C, and
the denaturants, Quassin, Brucine Sulfate/Brucine, and Denatonium Benzoate. Int J Toxcol. 27:
Suppl 1:1-43. Abstract only
Global. 2010. Material Safety Data Sheet, Denatured Fuel Grade Ethanol. Revision 9/17/2010
Hardman, J.G., L.E. Limbird, A.G. Gilman. Goodman and Gilman's The Pharmacological Basis
of Therapeutics. 10th ed. New York, NY: McGraw-Hill, 2001., p. 430 in HSDB (2011) (peer
reviewed)
Health Effects Institute (HEI). 1996. The potential Health Effects of Oxygenates Added to
Gasoline, A Review of the Current Literature. A Special Report of the Institute‟s Oxygenates
Evaluation Committee. April.
Manual.
International Fire Chiefs Association. (IFCA). 2009. Course Manual. Module 2: Chemical
and Physical Characteristics of Ethanol and Hydrocarbon Fuels.
Joseph, G, and R.G. Kelsey. 2000. Physiology and Growth of Douglas-fir Seedlings Treated
with Ethanol Solutions. Plant Science (Limerick) 50(2):191-199. Abstract Only.

Jacobson, J. L., S.W. Jacobson, and R.J Sokol. 1996. Increased Vulnerability to Alcohol-
Related Birth Defects in the Offspring of Mothers Over 30. Alcoholism: Clinical and
Experimental Research. 20(2): 359-363. Abstract only.
Maze, I.S., G.A. Wright, and J.A. Mustard. 2006. Acute Ethanol Ingestion Produces Dose-
dependent Effects on Motor Behavior in the Honey Bee (Apis mellifera). J Insect Physiol.
52(11-12):1243-1253.
Minnesota Department of Health (MDH). 2005. Guidance for Air, Ethanol Sector Specific
Interim Exposure Values. July 26.
Moore, Kristy. 2009. Production, Transportation, Handling and Logistics of Ethanol and
Biofuels. Renewable Fuels Association Presented at Biofuels Response Training, Gettysburg
Pennsylvania, September 15, 2009.
Nadeau, V., D. Lamoureaux, A. Beuter, M. Charbonneau, and R. Tardif. 2003. Neuromotor

Effects of Acute Ethanol Inhalation Exposure in Humans: A Preliminary Study. J. Occup.
Health 45:215-222.
National Institute of Occupational Safety and Health (NIOSH). 1995. Documentation for
Immediately Dangerous to Life or Health Concentrations (IDLHs). Accessed online 1/31/11 at
http://www.cdc.gov/niosh/idlh/64175.html
National Institute of Occupational Safety and Health (NIOSH). 2010. Pocket Guide. Accessed
online 1/31/2011 at http://www.cdc.gov/niosh/npg/
National Response Team (NRT). 2010. Quick Reference Guide: Fuel Grade Ethanol Spills
(Including E85). Final. Rev #00.
National Toxicology Program (NTP). 2005. Report on Carcinogens, Eleventh Edition. U.S.
Department of Health and Human Services, Public Health Service, January 31. 2005.
Nelson, B.K., W.S. Brightwell, D.R. Mackenzie, A. Khan, J.R. Burg, W.W. Weigel, and P.T.
Goad. Teratological Assessment of Methanol and Ethanol at High Inhalation Levels in Rats.
Fundamental and Applied Toxicology. 5:727-736.
Environmental, and Economic Impacts of Adding Ethanol to Gasoline in the Northeast States.
Volume 3, Water Resources and Associated Health Impacts. July, 2001.

New Hampshire Department of Environmental Services (NHDES). 2009. Gasoline Oxygenates

Additives: Health Information Summary. ARD-EHP-32.
Office of Environmental Health Hazard Assessment (OEHHA). 1999. Ethanol. Appendix to

Health and Environmental Assessment of the Use of Ethanol as a Fuel Oxygenate. Report to the
California Environmental Policy Council in Response to Executive Order D-5-99. December.
Pastino, GM., B. Asgharian, K. Roberts, MS Medinsky, JA Bond. 1997. A comparison of

physiologically based pharmacokinetic model predictions and experimental data for inhaled
ethanol in male and female B6C3F1 mice, F344 rats, and humans. Toxicol Appl Pharmacol.
Jul;145(1):147-57 (abstract and as cited in OEHHA (1999).
Quinn, B., F. Gag , and C. Blaise. 2008. An investigation into the acute and chronic toxicity
of eleven pharmatceuticals (and their solvents) found in wastewater effluent o the cnidarians,
Hydra attenuata. Science of the Total Environment. 389:306-314.
Rudner, Glen. 2009. Ethanol/Ethanol Blends Emergency Response Safety Issues. Virginia
DEM. Presented at Biofuels Response Training, Gettysburg Pennsylvania, September 15, 2009.
Rudolph, Erich. 2009. Improvements in Safe Rail Transportation of Ethanol and Lessons
Learned. DOT, Federal Railroad Administration. Presented at Biofuels Response Training,
Gettysburg Pennsylvania, September 15, 2009.
Sample, B. E, D. M. Opresko, and G.W. Suter II. 1996. Toxicological Benchmarks for Wildlife:
1996 Revision. Prepared for U.S. Department of Energy, Office of Environmental Management.
Risk Assessment Program, Health Sciences Research Division, Oak Ridge, TN. ES/ER/TM-
86/R3. June.
Speedway. 2004. Material Safety Data Sheet for E85. Revision Date 1/30/2004.
U. S. Department of Transportation. 2008. Advisory Guidance: Emergency Response Involving

Ethanol and Gasoline Fuel Mixtures, Pipeline and Hazardous Materials Safety Administration.
September 19, 2008.
U.S Environmental Protection Agency (USEPA). 2011. ECOTOX Database. Online database,
accessed 2/7/2011. http://cfpub.epa.gov/ecotox/
U.S Environmental Protection Agency (USEPA). 2009. Biofuels and Emerging Issues for
Emergency Responders: An Introduction to Basic Response Guides and Case Study Examples
from Biofuel Spills. Power Point Presentation by Jeff Kimble, OSC, Region 5

U.S Environmental Protection Agency (USEPA). 2000. Ambient aquatic life water quality
criteria for Dissolved Oxygen (Saltwater). Cape Cod to Cape Hatteras. EPA-882-R-00-012.
November.
U.S. Environmental Protection Agency (USEPA). 1997. Exposure Factors Handbook, Volume
1. EPA/600/P-95/002Fa. August.
U.S. Environmental Protection Agency (USEPA). 1995. Final Water Quality Guidance for the
Great Lakes System. Federal Register. Volume 60, Number 56. March 23, 1995.
U.S. Environmental Protection Agency (USEPA). 1986. Quality Criteria for Water. EPA
440/5-86-001. Office of Water. May 1.
World Health Organization (WHO). 2010. IARC Monographs on the Evaluation of

Carcinogenic Risks to Humans. Volume 96, Alcohol Consumption and Ethyl Carbamate.
International Agency for Research on Cancer. Lyon, France.
Section 6
LEL Correlation Factors Table, Industrial Scientific Corporation, found at

htpp://www.indisci.com/training_details.aspx?id=1564
Method 1400, Alcohols I, Issue 2, August 1994, NIOSH Manual Of Analytical Methods
(NMAM), 4th ed., DHHS (NIOSH) Publication No. 94-113 (August, 1994), located from the
NIOSH web-site
Organic Method #100, OSHA Sampling and Analytical Methods Manual, Organic Methods
Evaluation Branch, OSHA Salt Lake City Technical Center, 1996, located from the OSHA web-
site
Technical Note TN-106, RAE Systems Inc.
Test Methods for Evaluating Solid Waste, Physical/Chemical Methods, Office of Solid Waste
and Emergency Response, USEPA, November 1986, as updated:
Method 5030B, Purge and Trap for Aqueous Samples, Revision 2, December 1996
Method 5031, Volatile Nonpurgeable, Water Soluble Compounds by Azeoptropic

Distillation, Revision 0, December 1996

Method 5032, Volatile Organic Compounds by Vacuum Distillation, Revision 0,

December 1996
Method 5035A, Closed System Purge and Trap and Extraction for Volatile Organic
Compounds in Soil and Waste Samples, Revision 1, July 2002
Method 8261, Volatile Organic Compounds by Vacuum Distillation in Combination with

Gas-chromatography/Mass-spectrometry (VD/GC/MS), Revision 0, February 2007
Section 7
Manual. Module 6: Ethanol-Blended Fuel Emergencies
Lawrence Livermore National Laboratory, University of California, Livermore. 1999. Health and
Environmental Assessment of the Use of Ethanol as a Fuel Oxygenate, Report to the California
Environmental Policy Council in Response to Executive Order D-5-99, December
Environmental, and Economic Impacts of Adding Ethanol to Gasoline in the Northeast States.
Volume 3, Water Resources and Associated Health Impacts. July, 2001.
Ohio Environmental Protection Agency. 2007. Report of the Painesville, Ohio train derailment.
Incident # 0710-43-3825. Found at:
http://www.epa.ohio.gov/portals/30/ersis/er/docs/derailNE.pdf

Appendix A
Case Studies
A1. INTRODUCTION
Although ethanol has been produced and transported in large volumes for several decades there
have been relatively few incidences involving its catastrophic release into the environment.
There have been several occasions of underground storage tanks containing ethanol fuel blends
leaking, some for very long periods. These have involved E-10 type fuels which are not the
focus of this report.
Most of the high-concentration ethanol is moved from production plants to blending terminals by
rail. In fact, the majority of the event data is from rail incidents, several of which will be
discussed in detail. The other well-documented sources of ethanol impact to the environment
have been the result of fire incidents at distilleries. Two very significant events occurred in
Kentucky in 1996 and 2000. This section summarizes incidents that have occurred involving
ethanol. In many cases, the information presented lacks detail due to the very limited
information available.
A2. RAILROAD INCIDENTS
Recently, with the rise of many more corn to ethanol plants across the Midwest Corn Belt, rail
road incidents involving ethanol have begun to occur. Trains can carry upwards of eighty 30,000
gallon capacity tank cars. Even so, considering the amount of ethanol which travels over the
nation‟s rails, there have been only a few major incidents and the environmental impacts have
been limited in the majority of these, primarily due to the resulting fires consuming most of the
material.
New Brighton, PA
On October 20, 2006 an eastbound Norfolk Southern train derailed consisting of eighty 30K
gallon tank cars of 95% ethanol denatured with gasoline. The incident occurred at
approximately 10:30 pm and while the train was traversing the bridge over the Beaver River just
west of the city of New Brighton. A total of twenty-three (23) tank cars derailed. Three cars
ended up in the river and the other twenty were scattered along the bank and the rails at the
eastern end of the bridge with approximately 17 being compromised.
There were fortunately no deaths or injuries. The resulting explosion and fire warranted the
evacuation of all persons within a several block radius, which amounted to approximately fifty
people since the incident occurred in a largely commercial section of town. The fire was
controlled and then allowed to burn itself out. This action consumed the bulk of the material and
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP A-1

limited release to the soil and water. The three cars which actually entered the river were not
punctured and the product did not leak from them in any significant quantity.
The fire consumed most of the product and although an estimated 60,000 gallons may have
entered the river there was little impact on the environment noted. The Beaver River is a large
and fast flowing (18,000 cfs at the time) system and no fish kill or any other impact was noted.
Trace levels of ethanol and gasoline components were detected downstream of the site. The
nearest public drinking water supply intake was located 11 miles downriver and was not
impacted from the spill.
From NTSB (2008)
Painesville, Ohio
On October 10, 2007 approximately 30 cars of a CSX train derailed outside Painesville, OH. Of
the thirty cars that left the tracks, five
Painesville Ohio Spill, From City of were tankers containing denatured
Painesville Fire Department ethanol. The other cars contained bio-
diesel, phthalic anhydride, and butane.
Several of the ethanol cars exploded and
burned. Fire fighters used copious
amounts of water to cool the butane car
and the resulting run-off carried spilled
ethanol into a nearby stream.
The fire burned for three days. The

stream was dammed and pumped to

remove approximately 500,000 gallons of impacted water for disposal. When it became evident
that ethanol had impacted a second stream it was aerated to minimize the loss of dissolved
oxygen. Samples were collected from the streams and the nearest outlet stream. In addition,
water quality checks were performed on a regular basis at locations along both impacted streams
and their outlets. Visibly impacted soils from the area of the derailed cars were removed and
samples collected.
No long-term or adverse effects were noted following the actions taken.
Luther, Oklahoma
In August 2008 eight cars of 110-unit train derailed in central Oklahoma, outside the small rural
community of Luther, OK. Seven of the cars were tank cars containing denatured ethanol or
crude oil. The resulting explosions and fire forced evacuation of all persons within a 1-mile
radius of the incident. There were no injuries or deaths. The fire was allowed to burn itself out
and there was minimal environmental impact.
Rockford, Illinois
On June 19, 2009 14 tank cars of denatured ethanol derailed while traversing a crossing near the
city of Rockford, IL. Twelve of the tanker cars caught fire, and one motorist was killed and nine
others injured from the resulting explosion and fire. Approximately 600 homes were evacuated
and the fire was allowed to burn itself out, which took approximately 24-hours. Approximately
360,000 gallons of ethanol were consumed in the fire, and 55,000 to 75,000 gallons released in
soil and unnamed creek. The unnamed creek is a tributary to the Kishwaukee River, which
drains into the Rock River.
Approximately 1400 tons of soil were removed from the site, and runoff water was controlled. A
nearby drinking water supply was also sampled, with no ethanol detected. Air monitoring was
conducted at the site and surrounding community from June 21 through July 2, and no elevated
volatile organic compound concentrations were identified.
On June 20, a fish kill was observed on the Rock River over a 50 mile area. This area is about
35 miles downstream of the spill location, and has not definitively been related to the spill.
Surface water sampling was initiated on June 21 in the unnamed creek, and the Kishwaukee and
Rock Rivers, but ethanol was not detected (EPA 2009). Dissolved oxygen levels were
determined to be normal, although the time of sampling was not specified.
Soil borings and monitoring wells were installed and sampled at the site. In addition, several
private wells in the area were sampled. The results for all soil and water samples were either
non-detect or below applicable screening criteria (EPA (2009b). However, the analyses may

have been limited to BTEX and Total Petroleum Hydrocarbons (TPH) – Gasoline Range
Organics (GRO). Fish tissue samples were also analyzed, and both ethanol and acetaldehyde
were detected (EPA 2009b).
Knoxville, Tennessee
On September 15, 2009 five tank cars hauling ethanol overturned in Knoxville, TN. The
derailment occurred while the train was slowing to off-load and as a result no fire resulted.
Approximately 6000 gallons of ethanol are believed to have been released from the two cars that
were compromised. Approximately 1000 gallons were recovered from visible pools once the
cars were up-righted.
Arcadia, Ohio
On February 6, 2011 at approximately 2:15 am, a Norfolk Southern train with 62 tank cars all
loaded with denatured ethanol (95%) derailed approximately one and a half miles outside the
village of Arcadia, OH. Thirty-four of the cars derailed and two immediately exploded and
burned. Thirty-two others became involved due to the heat. Two cars were intact and later
transferred to semi tankers and reloaded on train cars to be delivered. Local volunteer fire-
fighting crews concentrated on the safety of nearby residents, preventing access to the area.
Numerous fire departments staged in Arcadia in the event it was determined that protection of a
nearby Farmers Co-op was needed.
First-responder actions concentrated on Arcadia Spill
evacuation of approximately 20 houses Source: OhioEPA
EPADEPA
and maintaining a secure perimeter.
The fires were essentially allowed to
burn, involving other cars within the
crash pile for several hours. Once the
major fires had subsided sufficiently to
permit site entry, railroad salvage
workers began to separate uninvolved
cars.
Fire-fighters shuttled water to the scene

using 7 tankers, and supplied a
continuous source of water to the environmental and railroad salvage crews. The environmental
and railroad salvage crews foamed the inside of the cars to extinguish the fire and applied
cooling waters to the exterior of the cars before they were emptied by vac trucks which were off
loaded to frac tanks until the material could be shipped off site. Once the cars were cooled that
were removed from the accident zone. It is estimated that 80% of the foam was contained within

the tank cars. Salvage and product removal operations continued for several days with the last
burning car extinguishing by late Monday evening. The tracks were replaced and re-opened by
Tuesday afternoon. An estimated 780,000 gallons of denatured ethanol were either burned or
spilled in the incident. Relevant response approaches and observations are summarized below:
During the response, air-monitoring was conducted primarily for BTEX using portable
PID systems. Ethanol was not directly monitored other than through LEL readings.
Product and cooling water spilled onto the track area, onto two tiled farm fields bisected
by the tracks and into a small bar ditch located below the tracks and a storm catch basin
directly under the derailment site. Cooling water potentially mixed with denatured
ethanol also entered a storm drain located at the Co-op. Both the storm water drain and
creek empty into the South Branch of the Portage River.
The creek was first dammed approximately half a mile from the derailment to protect this
resource and to allow recovery operations to proceed along the creek. Due to the weather
conditions, the creek was frozen which caused the ethanol to migrate downstream under
the ice. A second dam was place approximately a mile from the derailment and ahead of
the migrating ethanol. At the ethanol migrated downstream it melted the surface ice and
open pools were seen along the creek. The liquid was vacuumed from the creek in three
locations and transferred into fractionation tanks for off-site disposal. Vacuuming
continued for several days until the melt and rains made it impossible. By that time
aeration systems had been place in the creek at three locations and activated carbon was
en route to be staged near the dams. The dams remain in place and aeration of the creek
is continuing at the time of this report. Pools of water onsite continue to be collected due
to high levels of ethanol.
No visible fish kill was noted. Soil remediation actions did not commence until all of the
cars were removed from the tracks and are continuing at the time of this report. These
consist of removal of visibly impacted areas and post removal sampling.
Preliminary analysis showed there to be approximately 10 mg/l of benzene in the

drainage water, which is 2000 times the Ohio drinking water standard of 5 ug/l. Ohio
EPA directed that collection and testing continue until the drainage water meets the 5 ug/l
benzene limit. Those actions were continuing at the time of this report.

State and Federal environmental agencies directed sampling for BTEX and ethanol in
soils. Benzene was determined to be the site action-level driver, as there is no clean-up
level for ethanol defined in Ohio regulations. Ethanol concentrations were determined
for informational purposes only. In the
creek and South Branch of the Portage
Arcadia Spill
Source: OhioEPA River samples were collected and analyzed
for BTEX, ethanol, and water quality
parameters including biochemical oxygen
demand, chemical oxygen demand, and
dissolved oxygen. Residents‟ groundwater
wells were also sampled for ethanol and
BTEX. No groundwater samples indicated
impacts.
A3. DISTILLERY INCIDENTS
Aside from incidents in transport of fuel ethanol, large volumes of ethanol have entered the
environment as a result of distillery fires. Two incidents in Kentucky were found. The first in
1996 occurred at the Heaven‟s Hill‟s Distillery in Bardstown, KY. In the case of this fire the
location of the buildings, distance from a water body, and intensity of the fire limited the
environmental impact. This particular fire occurred during a very windy day (55 mph winds)
and as such, a total of seven storage/aging buildings, each holding 900,000 gallons of bourbon
and thirteen other buildings were destroyed. However, the intensity of the flames and the terrain
caused more pooling and burning of the liquids and limited damage outside the fire zones. The
second incident, at the Wild Turkey Distillery in Lawrenceburg, KY did not result in the same
limited impact to the environment.
Wild Turkey Distillery-Warehouse K Fire.

On the afternoon of May 7, 2000 workers at a nearby water treatment plant noticed flames
coming from a bourbon storage/aging building known as Warehouse K. Warehouse K was
situated at the end of a long line of similar buildings and on the edge of the distillery property
overlooking the Kentucky River. It was constructed of slat board siding and a tin roof and stored
approximately 17,300 53-gallon barrels of 107-112 proof bourbon whiskey. It was also designed
to collapse onto itself in the event of fire which it did. By the time fire-fighters arrived, the
building was totally involved and the crews concentrated on protection of nearby structures and
worker safety, essentially allowing Warehouse K to burn its self out. Upon arrival, fire-fighters
noted that a flow of burning bourbon was traveling down a wooded hill and into the river below.

They concentrated on protecting the other distillery structures and controlling any spot fires in
the woods, but did not block the flow of burning alcohol.
Once it was discovered that alcohol was indeed entering the river, at a point upstream of the city
of Lawrenceburg‟s drinking water plant intake, the plant was shut down to keep the alcohol from
entering the treatment process. Fire-fighters then used shuttle tankers filled in the river to bring
cooling/protection water to the fight. The fire burned and cooling/protection activities continued
through the night. The city water plant was back on line within 24-hours.
Initial assessment from the state environmental agency was that the incident had resulted in
limited impact to the environment and that possibly 20-percent of the alcohol had actually
entered the river. State officials figured that this volume (approximately 200,000 gallons) would
have limited impact on a large river system such as the Kentucky River. A couple of days later,
the morning of May 11th, the city of Frankfurt, located 14-miles downstream from the site
reported a sweet smell in the river and a massive fish kill. Other reports soon followed in what
would be the largest chemical spill induced fish kill in the history of the state. At its peak the
area of “dead water” stretched five to six miles in length and traveled approximately five-miles
per hour downstream.
Officials were surprised that the movement of the material through the various locks and dams
did not serve to eliminate the alcohol and aerate the water. On May 18th, when it became
obvious that the zone of dead water was not subsiding, EPA began to oxygenate the dead water
area as it reached the confluence of the Ohio River. They did this by using six barges equipped
with air-compressors connected to lengths of perforated pipe. Aeration continued until dissolved
oxygen levels reached at least 5 ppm, and ended on the 25th of May.
A4. Marine Incidents
The Coast Guard monitors ethanol spill statistics. They reported (USCG 2010) that there have
been only two ethanol spills over the last six years while loading or discharging, and both were
less than five gallons. They also report that waterfront facilities have averaged one spill a year,
but only one of these was over 100 gallons.
Below are the descriptions of two documented incidents from marine transport of ethanol and
ethanol blends. One occurred in the open ocean (not included in statistics above), and the other
during on-loading activities in port. In both instances no response actions were targeted to the
ethanol itself.

Bow Mariner Incident

On February 28, 2004 a chemical tanker Bow Mariner, exploded and sank approximately 50
miles off the coast of Virginia. At the time she was carrying 3.5MM gallons of ethanol in 10 full
cargo tanks. The USCG investigation (USCG 2005) determined that the explosion was actually
due to the empty tanks, which had previously contained another volatile and flammable gasoline
additive, MTBE, had not been inerted after off-loading, and were opened while at sea. The
explosion caused massive rupturing of the entire cargo deck and the ship sank in approximately
two hours. Six crewmen were rescued, three bodies recovered and eighteen crewmen lost and
never recovered. Although environmental response actions were required, they focused entirely
on the fuel oil that was released from the ship‟s tanks. In fact, ethanol was considered non-
regulated and not addressed in any way during the response.
Harbor On-loading Incident

On January 11, 2010 a chemical tanker, Sichem Defiance, was on-loading a cargo of 55,000
barrels of ethanol while in port at New York Harbor. Operators failed to properly monitor the
on-loading process and over-filled one of the ship‟s cargo tanks to the point of rupture. The
rupture collapsed a portion of the upper deck, but did not release material into the harbor.

Appendix B
Fate and Transport Literature Review
B1. INTRODUCTION
This appendix provides a review of the fate and transport of ethanol in soil, ground water,
surface water and the atmosphere. The information provided here is presented in summary form
in Section 4. This review uses information from numerous sources, including peer-reviewed
literature, industry publications, and agency presentations.
B2. NEAT VERSUS E-BLEND SPILLS
The New England Interstate Water Pollution Control Commission (NEIWPCC, 2001) report
summarizes the fate and transport issues associated with a release of neat ethanol into the
environment and compares them with the issues related to ethanol blends. A spill that releases
large volumes of neat or denatured ethanol into the environment, such as an accident involving a
unit train or a marine tanker carrying ethanol, or an accident at a bulk ethanol storage facility,
would result in a large surface spill migrating rapidly over the land surface. This spill would
eventually reach a surface water body such as a pond, stream, river or the ocean; or it may
infiltrate into the soil and reach the groundwater. In comparison, E-blend releases, such as E10
or E85, are expected to be smaller in volume, as these releases often occur during splash
blending of ethanol with gasoline, tanker truck accidents, or at retail gasoline stations. Unlike
gasoline spills, the sampling and analysis of ethanol following E-blend releases have been
limited. Some studies have indicated that the presence of ethanol in gasoline can inhibit BTEX
(benzene, ethyl benzene, toluene, and xylenes) biodegradation in groundwater systems, resulting
in enhanced BTEX plumes (Powers et al., 2001; Deeb et al., 2002). In contrast, other studies
have suggested that the presence of ethanol in gasoline can reduce the persistence of benzene in
E-blend releases due to increased biomass growth facilitated by the ethanol (Gomez and Alvarez,
2009).
B3. GENERAL DISCUSSION OF IMPORTANT FATE PROCCESSES
This section describes some of the important fate processes that affect ethanol in the
environment, including biodegradation, partitioning and methane production. The following
sections (4.0 through 7.0), discuss fate and transport processes by medium.
B3-1 Ethanol Biodegradation

Howard et al. (1991) and NEIWPCC (2001) indicate that ethanol undergoes biodegradation at a
rapid rate in the atmosphere, soil, surface water and groundwater if there are sufficient levels of
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP B-1

electron acceptors and nutrients available to degrade the ethanol. Degradation rates of ethanol
are higher than gasoline, with half lives ranging from hours to days (Malcolm Pirnie, 1998;
HSDB, 2011). Due to the rapid loss of ethanol through photo-oxidation in air and
biodegradation in soil and water, ethanol is unlikely to accumulate in the soil, air, surface water,
or groundwater. Degradation rates have been estimated using field and laboratory studies;
however, there is a great deal of uncertainty as to how these estimated rates of ethanol loss will
apply in realistic field conditions. Therefore, rates discussed below are considered to represent
order-of-magnitude estimates and may not be applicable for site-specific releases.
Under aerobic conditions, biodegradation of ethanol in fresh and salt water with filtered sewage
seed resulted in 5-day theoretical biochemical oxygen demand values ranging from 37% to 86%,
at concentrations of 3 to 10 mg/L (HSDB 2011). In a microcosm using sandy aquifer material
and groundwater, a half life for ethanol with a starting concentration of 100 mg/L, was reported
to be 3 days in samples prepared with 20 mg/L of benzene, toluene or o-xylene under aerobic
conditions (HSDB 2011). Using the same microcosm setup, but under anaerobic conditions, the
half-life was reported as 1.5 days (denitrifying conditions, and 5 days (iron-reducing conditions).
Further discussion of biodegradation is provided by medium in later sections of this Appendix.
B3-2 Partitioning of Ethanol Between Environmental Media

Malcolm Pirnie (1998) describes the mechanisms that lead to the partitioning of ethanol between
the air, water, and soil media. These mechanisms are summarized in the following sub-sections.
Air/Water Partitioning
The air-to-water partitioning behavior of ethanol is governed by Henry‟s Law and described by
the Henry‟s Law constant, which represents the equilibrium ratio of a contaminant‟s
concentration in the air to its concentration in the water. The value of the dimensionless Henry‟s
Law constant for ethanol is approximately 2.5 x 10-4 at 25o C (Malcolm Pirnie, Inc., 1998). This
relatively low value of the Henry‟s Law constant for ethanol indicates that ethanol has a strong
affinity for the aqueous phase compared to the vapor phase. As a result, ethanol volatilization
from surface water or off-gassing from groundwater are not likely to be significant mechanisms
for ethanol mass loss from water. It is noted, however, that the Henry‟s Law constant is a
function of temperature, and that this constant, and the affinity for ethanol to partition into the
vapor phase, will increase with increasing temperature.

Soil/Water Partitioning
The partitioning of ethanol concentration between the soil and water is described by its soil/water
partition coefficient Kd. Kd values can be estimated by the following:
Kd = Koc foc
where Koc is the partition coefficient for the target species (ethanol) and soil organic carbon, and
foc is the fraction of organic carbon present in the soil. HSDB (2011) reports a Koc for ethanol of
1, resulting in low partitioning of ethanol to most soils. This indicates that ethanol will generally
migrate with groundwater, and adsorption onto soil or sediment are not likely to be significant
fate and transport mechanisms (Wood et al., 1990; Zogorski et al., 1996)..
B3-3 Methane Production

Anaerobic biodegradation of ethanol in groundwater results in the production of methane (API,
2003; Schaefer et al., 2010). The methane may then volatilize from groundwater into soil gas. If
the soil gas were to migrate to a confined space, it may lead to an explosion hazard (Jewell et.
al., 2010)
After an ethanol spill, the following conditions must be met for an explosion hazard to occur
from methane (ASTDR, 2011):
Methane gas generation. At most sites, ethanol degradation is expected to be rapid as

compared to the ability of groundwater flow to flush ethanol away from the spill location.
Methanogenesis will be the dominant degradation pathway and methane will be the
dominant degradation product of ethanol (see discussion below). The resulting methane
can volatilize into the unsaturated soil (Wilson and Adair, 2007).
Methane gas migration. The methane gas must be able to migrate from soil and
groundwater to underground utility pipes, drains, conduits or through natural subsurface
preferential migration pathways present in the geologic media.
Collection in a confined space. The methane gas must collect in a confined space to a
concentration at which it could potentially explode. A confined space might be a
manhole, a subsurface space, a utility room in a home, or a basement. The concentration
level at which gas has the potential to explode is called the explosive limit. The potential
for a gas to explode is determined by its lower explosive limit (LEL) and upper explosive
limit (UEL). The LEL and UEL are measures of the percent of a gas in the air by volume.
However, an explosion hazard may exist if a gas is present in the air between the LEL

and UEL and an ignition source is present. For methane, the LEL is 5% by volume and
the UEL is 15% by volume. At concentrations below its LEL and above its UEL, a gas is
not considered explosive.
The introduction of fuel ethanol to groundwater stimulates anaerobic microbial activity leading
to methanogenesis, which is the production of methane (CH4) and carbon dioxide (CO2) by
biological processes. The chemistry behind the methanogenesis from ethanol is as follows:
CH3CH2OH + H2O →CH3COOH + 2 H2
CH3COOH →CO2+ CH4
For example, 46 mg/L ethanol can produce 16 mg/L methane (Wilson and Adair, 2007). At
higher concentrations (near 1000 mg/L) ethanol rapidly ferments to methane at a rate near 20 to
60 mg/L per day (Jewell, et al., 2010). At an average groundwater temperature of 15°C, and an
atmospheric pressure of 1 atm (atmospheres), 0.73 liters of methane gas will be produced per
gram of ethanol (Powers et al., 2001).
Methane vapors are produced over an extended period of time and persist in soil gas for a long
time, at levels exceeding the lower and upper explosive limits for methane (5% and 15% by
volume, respectively (Wilson and Adair, 2007).
The methane originating from the anaerobic degradation of ethanol in groundwater first
undergoes aerobic biodegradation in soil pores and consumes the available oxygen from the soil
gas (assuming oxygen is initially present). This oxygen would otherwise be available to degrade
benzene and other gasoline constituents introduced to soil gas from an E-blend spill. The aerobic
degradation of benzene is therefore limited in presence of ethanol. One part methane will
consume two parts oxygen. Considering that air is 20% oxygen, the biodegradation of 10%
methane by volume can consume all of the oxygen in soil gas and stop the aerobic
biodegradation of benzene. The lack of benzene degradation caused by the consumption of
oxygen by methane results in increased persistence of benzene in soil gas and poses a fire and
explosion hazard (Jewell et al. 2010).
The production of methane, accumulation and potential for explosion is of concern to emergency
responders following an ethanol spill. Specific issues of concern are addressed below:
Timing of methane generation: The time elapsed after an ethanol release until methane
generation begins, and the rate at which it occurs, will be very site specific. Methane
generation typically will not occur until available electron acceptors (i.e., oxygen, nitrate,
iron, and sulfate) are consumed. Water with high levels of these compounds prior to

ethanol exposure will typically take longer to generate methane. Waters previously
exposed to hydrocarbon or alcohol contaminants might also have higher microbial levels,
thus able to more rapidly consume ethanol and generate methane. In laboratory
experiments (Schaefer et al., 2010), it took about 6 weeks before methane was generated
in anaerobic microcosm experiments. Chen et al. (2008) observed methane generation
after about 10 weeks.
Based on these rates, it appears that there is a lag time of 6 to 10 weeks between the
ethanol spill and generation of methane. The lag time is adequate for an environmental
response to be initiated and actions taken to contain the ethanol spill, recover a large
percentage of the spilled ethanol, provide aeration to the waters if necessary, and thereby
eliminating the source material for methane production. If these actions are taken, the
explosion hazards from methane generation will be minimized.
Conditions for enhancing or inhibiting methane production: Methane is produced by

the anaerobic biodegradation of ethanol in groundwater, through the methanogenic
reactions. Such reactions do not occur in the presence of electron acceptors (i.e., oxygen,
nitrate, iron, and sulfate). In addition, they will not occur in the presence of
concentrations of ethanol that are toxic to microorganisms. Once the conditions are
suitable for methanogenesis, the reaction rate will depend on environmental conditions,
such as temperature.
The general presumption is that at sites with sandy soil, steep topographic gradients (used
as indicator of subsurface hydraulic gradients), and presence of nearby surface water
bodies to which groundwater may discharge, groundwater is likely to be aerobic and
moving rapidly. The potential for methane generation and accumulation of methane in
soil gas is lower in such environments. At sites with flat topography, clay, peat or other
soils with high organic matter, water logged or swampy conditions, it is expected that
groundwater flow is not as rapid and anaerobic conditions favoring the generation of
methane may occur. If the ethanol spill occurs in an area where hydrocarbon or alcohol
contaminants from previous environmental releases may be present, these areas might
also have higher microbial levels, thus able to more rapidly consume ethanol and
generate methane as compared to remote areas with no prior contamination history.
Anaerobic conditions may also already be present in such areas.
Rate of methane production: The rate of methane generation is related to temperature,

and can be conservatively estimated by the ethanol biodegradation rate under
methanogenic conditions. Based on Shaefer et al. (2010) and Deeb et al. (2002), the first

order rate constant for ethanol under methanogenic conditions can range from about 0.08
to 0.3 per day while the first order rate constant for methane is in the 0.16 to 0.6 per day
range. The corresponding half life of ethane ranges from 2.3 days to 8.7 days; which
means that in approximately 2 to 9 days after methanogenic conditions have been
reached, half of the ethanol spilled and introduced to the groundwater will be converted
to methane. The volumetric rate of methane produced depends upon the dissolved
ethanol concentration and the first order rate constant discussed above. There is an upper
limit to ethanol biodegradation, and thus methane generation, as a result of ethanol
toxicity. Some of the methane produced will be transported in groundwater, while the
remainder may escape as soil gas. The accumulation of methane vapors in the subsurface
will likely depend upon the rate at which methane vapor escaping from the water (either
surface or subsurface) can be dissipated. For surface spills, wind and diffusion will likely
prevent any substantial methane accumulation. However, in enclosed areas, in subsurface
environments, or where subsurface soil gas can impact things like basements or utilities,
accumulation can occur. Providing electron acceptors (oxygen, nitrate, sulfate, etc.)
should limit methane generation.
Therefore, while methane will be generated after an ethanol spill, the potential for an
explosion hazard is dependent upon the accumulation of methane gas in a confined space
to a potentially explosive concentration. As discussed previously, the potential for a gas
to explode is determined by its LEL and UEL (5% and 15% by volume), respectively,
measured as the percent of gas in the air by volume. An explosion hazard may exist if a
gas is present in the air between the LEL and UEL and an ignition source is present. For
methane, the LEL is 5% by volume and the UEL is 15% by volume. Powers et al. (2001)
indicate that after an ethanol spill, at an average groundwater temperature of 15°C and an
atmospheric pressure of 1 atm, 0.73 liters of methane gas will be produced per gram of
ethanol. The methane gas is produced over an extended period of time and will persist as
soil gas for a long time, at levels exceeding the LEL and UEL (Wilson and Adair, 2007).
If this soil gas is vented to the atmosphere, an explosion hazard is unlikely to exist;
however, the confinement of the methane in soil gas in subsurface structures like a
manhole, a subsurface space, a utility room in a home, or a basement could lead to an
explosion hazard.
Empirical data from large volume ethanol spills: Empirical data regarding the
persistence of ethanol-generated methane in soil and groundwater was collected at a bulk
fuel terminal in the pacific northwest, where 19,000 gallons of neat ethanol were released
from an above ground storage tank in 1999 (Buscheck et al. 2001). High ethanol
concentrations (exceeding 20,000 ug/L) were measured at distances over 250 feet

downgradient from the spill location. The groundwater velocity in the spill area was
estimated to range from 300 to 400 feet per year. Within three months of the spill, ethanol
concentrations in groundwater of up to about 16,000 mg/L were measured. Groundwater
concentrations declined dramatically, and by July 2001 ethanol was not detected in the
two wells that previously had the highest concentrations.
The degradation of ethanol resulted in strongly anaerobic conditions in groundwater

following the spill. Oxygen, sulfate, and nitrate levels were depleted within the ethanol
plume. Unfortunately, these parameters were not measured until 15 months after the spill
occurred. Dissolved methane concentrations in groundwater at that time ranged from
about 5,000 to 10,000 ug/L, but a year later (June 2001), had increased to over 30,000
ug/L, approximately 27 months after the spill. During the same time frame, ethanol
concentrations in source area groundwater were declining, indicating the progression of
anaerobic degradation of ethanol and the production of methane. A soil gas survey was
conducted in June and July 2001 (27 months after the spill). Methane concentrations in
excess of the upper explosive limit were detected at 4 feet below grade in the areas of the
highest dissolved methane concentrations in groundwater.
Tousignant and Evrard (2009) also reported the results of a spill of approximately 27,000
gallons of denatured ethanol (containing 2% to 5% gasoline) as a result of a rail collision
between Montreal and Ottawa, Canada on May 2, 2005. Impacted surface soil was
removed (12 inches), however, the spill resulted in impacts on groundwater. Surface
application of a quick reacting oxidizer (RegenoxTM) was initiated to reduce ethanol
levels (toxic to bacteria) at the spill location (July 2006). Additional treatment consisted
of surface application of a slow release oxidizer (ORC advancedTM) at the spill location
(September 2006), application of ORC down-gradient of the spill location in
infiltration/interception trenches (November 2006), and ORC injection to groundwater in
the plume area to treat BTEX contamination (August 2008). Concentrations of ethanol in
the source area were as high as 46,000,000 ug/L, but were reduced to non-detect in all
locations by February 2008. BTEX compounds were more persistent, even with the ORC
application, substantiating the longer half lives of BTEX compounds and therefore slower
degradation rates as compared to ethanol. The authors observed methane in groundwater,
but its generation was likely inhibited by the addition of oxidizers. Methane was also
observed in some non impacted wells. The authors attributed this observation to the
degradation of ethanol by-products, but may have been a result of the continued
migration of methane in groundwater.

Extent of methane related hazards: The empirical data from Buscheck et al. 2001
suggests that methane related hazards will extend to the area occupied by the ethanol
plume in groundwater, and will extend to a distance that can be estimated from the
groundwater velocity and the time since the release. The extent of the groundwater
plume will provide the upper bound for the extent of methane impacts, except for any
preferential pathways such as utilities that may provide further spread of the methane in
soil gas. Numerical estimates of the ethanol plume impacts can be made using software
such as FOOTPRINT (EPA, 2008). In general, for most spills, the ethanol in
groundwater is expected to be degraded and not be of concern in a year or two (Wilson
and Adair, 2007).
B4. FATE AND TRANSPORT IN SOIL
As previously discussed, neat ethanol or E-blend fuels can infiltrate into the subsurface. The
liquid will then percolate through the subsurface vadose zone soils, moving through the gas-
filled pore spaces, until it ultimately reached the water table. Due to its affinity to reside in the
water phase, migrating ethanol will partition into soil moisture; this partitioning can slow the
downward migration of ethanol (McDowell and Powers, 2003). Dissolved ethanol present in
soil pore water typically is subject to biodegradation, which can further attenuate the rate of
ethanol migration to the water table.
The Lawrence Livermore National Laboratory (LLNL, 1999) report discusses how the presence
of ethanol in E-blend fuels affects the migration and distribution of gasoline in the unsaturated
zone by reducing the capillary forces and altering the pore structure of some minerals. In the
presence of ethanol, gasoline components can enter smaller pore spaces and drain more easily
from unsaturated zone soils. At bulk terminals and other locations where unsaturated-zone
hydrocarbon contamination may pre-exist, the introduction of ethanol may mobilize the existing
contamination. The depth and the area of hydrocarbon pool on top of the water table may be
altered by the presence of ethanol which reduces the capillary forces and therefore reduces the
height of the capillary fringe.
B5. FATE AND TRANSPORT IN GROUNDWATER
Once ethanol reaches the groundwater, its fate and transport is governed by the groundwater
flow rate and natural attenuation processes such as biodegradation, adsorption, dispersion and the
partitioning of ethanol between soil, water and air. Biodegradation is the primary mechanism for
the loss of ethanol from the groundwater system. The aerobic and anaerobic degradation of

ethanol mechanisms were previously discussed in Section 3.1, while the attenuation caused by
adsorption and partitioning of ethanol among various media was discussed in Section 5.2 of this
Appendix. Although there are non-toxic intermediate byproducts of ethanol degradation such as
acetate and hydrogen gas, the final product of aerobic degradation of ethanol is carbon dioxide,
while ethanol degrades anaerobically to yield methane and carbon dioxide.
Unlike the standard components of gasoline which are hydrophobic, ethanol is hydrophilic. The
LLNL (1999) report and NEIWPCC (2001) identified the following characteristics of ethanol
and E-blend fuel fate and transport in groundwater:
Ethanol degrades rapidly when released to the environment under favorable conditions;
The presence of ethanol in E-blend fuels will affect the dissolved concentrations of
benzene, toluene, ethylbenzene and xylenes (BTEX) in groundwater if the ethanol
concentrations are high;
The presence of ethanol in E-blend fuels will increase the residence time of fuel
hydrocarbons in the groundwater;
The presence of ethanol in groundwater will increase BTEX plume lengths, from 1.1 up
to 2.5 times farther than without ethanol. This is because ethanol alters the processes of
sorption and retardation of gasoline components in groundwater and its biodegradation
reduces the rate of BTEX biodegradation. Some studies (Gomez and Alvarez, 2009)
suggest that ethanol may actually enhance the rate of benzene biodegradation, thereby
reducing benzene plume length and persistence;
If spilled as a neat product, ethanol can remobilize the gasoline components of pre-
existing contaminant plumes and cause lateral spreading of liquid petroleum and 10-fold
increases in the concentration of BTEX; and
The introduction of ethanol may affect aquifer porosity and hydraulic conductivity due to
bio-film growth, mineral precipitation or dissolution, and nitrogen or methane gas
generation.
When ethanol is introduced to groundwater as an E-blend fuel, the behaviors of water and the E-
blend fuels change as follows (LLNL, 1999):
Ethanol partitions preferentially into the aqueous phase;
Solubilities of gasoline hydrocarbons in water increase;

Solubility of water in gasoline increases; and
Interfacial tension between the water and the gasoline phases is reduced.
B6. FATE AND TRANSPORT IN SURFACE WATER
After a large volume surface spill, neat ethanol or E-blend fuel will flow over pavement and soil
until reaching a point of discharge into storm sewers, wetlands, lakes, and streams. During the
overland flow over soil and pavement, ethanol will partially volatilize into the atmosphere. As
the ethanol flows over soil, some of the ethanol will infiltrate the soil and reach the groundwater,
which may discharge to a surface water body. The remaining ethanol could reach a wetland or a
surface water body directly. Upon reaching a surface water body, either as groundwater
discharge or surface flow, ethanol will rapidly mix with the water and go into solution (Malcolm
Pirnie, 1998).
As discussed above, due to the low Koc for ethanol, ethanol in surface water is not expected to
partition onto suspended solids or sediment (HSDB 2011). Also as discussed above,
volatilization from surface water is not expected to be a significant fate and transport
mechanism. HSDB (2011) identified a bioconcentration factor (BCF) for ethanol of 3, indicating
it has a low potential for accumulation in aquatic organisms.
The primary fate and transport mechanism in surface water is expected to be biodegradation.
With concentrations greater 10°C, Malcolm Pirnie (1998) reported half lives ranging from hours
to days.
B7. FATE AND TRANSPORT IN THE ATMOSPHERE
Malcolm Pirnie (1998) reported that the half life of ethanol in the atmosphere is in the order of
days, especially in summer when ethanol undergoes rapid reactions with hydroxyl radicals.

Appendix C
Health Effects Literature Review
C1. INTRODUCTION
This appendix provides a review of health effects of ethanol, which is summarized in Section 5.0
of the report. This review uses abstracts and reviews to the extent possible, as well as original
studies where available. The focus of this review is on inhalation exposures, with a limited
discussion of ingestion exposures. There is a large body of literature on the effects of alcohol
consumption on human health. This is not discussed in detail here, as exposures of this
magnitude and duration would not be expected in a spill situation. This review includes
discussions of uptake and metabolism, acute toxicity, chronic toxicity, teratogenicity,
developmental/reproductive effects, and carcinogenicity.
C2. Uptake and Metabolism
Ethanol is completely absorbed orally, and about 60% is absorbed via inhalation (NHDES 2009).
CIREP (2008) reports that absorption of ethanol occurs through the skin, but doesn‟t affect the
skin barrier, or result in very high internal concentrations. However, they also report that ethanol
can enhance the absorption of other substances through the skin.
Nadeau et al. (2003) reported that absorption of ethanol from the lungs was about 75% upon
exposure to ethanol in air for six hours at 1000 ppm, somewhat higher than that reported by other
authors. They found that ethanol concentrations in expired air reached steady state after three
hours of exposure.
Hardman et al. (2001) reported that most ethanol (90% to 98%) is metabolized primarily in the
liver to acetaldehyde (the rate-limiting step), and subsequently to acetate and ultimately to
carbon dioxide and water. The balance is excreted as unoxidized ethanol in urine, sweat, and
expired air. They reported that the oxidation of ethanol by a 70 kg person occurs at the
approximate rate of 120 mg/kg per hour. Bingham et al. (2001) reported that at an ethanol air
concentration of 8000 ppm and a ventilation rate of 15L/min, the rate of alcohol uptake was
equal to the rate of metabolism. Based on review of the literature, EPA‟s (1997) recommended
ventilation rates for short term exposures of adults range from 7 L/min for adults at rest to 53
L/min for heavy activity. Bingham et al. (2001) concluded that a continuous rise in ethanol
concentrations in blood would not result from exposure to 1000 ppm in air (Bingham et al.
2001). This conclusion is consistent with that reported above by Nadeau et al. (2003).
Acetaldehyde is largely metabolized by aldehyde dehydrogenases (ALDHs) in the liver. ALDH

activity is reduced in the liver of alcoholics. In addition, some individuals, primarily of Asian
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP C-1

descent are deficient in ALDH, making them at higher risk of esophageal cancer (Baan et al.
2007).
C3. ACUTE EXPOSURE
NEIWPCC (2001) identifies an odor threshold for ethanol of 100 ppm in air. Ethanol vapors
cause irritation of mucous membranes of eyes and respiratory tract at concentrations of 5000-
10,000 ppm, although such effects were not observed at concentrations less than 5000 ppm
(Lester and Greenberg, 1951). Stupor and sleepiness have also been observed at these
concentrations (Lester and Greenberg 1951). More severe effects were observed at
concentrations of 16,000 to 21,000 ppm. Headaches and other initial signs of intoxication were
reported in humans exposed to concentrations greater than 3000 ppm for 2 hrs (OEHHA 1999).
Nadeau et al. (2003) evaluated neuromotor effects (reaction time body sway, hand tremor and
rapid alternating movements) in healthy males exposed to 0, 250, 500, and 1000 ppm ethanol in
air for six hours. Ethanol was not detected in blood or alveolar air at exposures up to 500 ppm,
but at 1000 ppm, blood and alveolar air were 0.443 mg/100 ml, and 253.1 ppm, respectively.
Neuromotor tests did not show conclusively significant differences between the exposed and
control conditions.
Narcosis, ataxia and incoordination were observed in animals after exposure to 4000-10,000 ppm
for 8 hrs (Hobbs et al. 1996). Exposure of rats or mice to 20,000 ppm of ethanol resulted in
performance effects, although the lowest dose (12,000 ppm) had marginal effects. The alcohol
blood level of rats exposed to 16,000 ppm was 0.05 % - the point at which decrements in human
performance have been most clearly documented. Inhalation of 10,000-30,000 ppm for eight
hours or more is lethal to rats (HEI 1996). Inhalation of 10,000-30,000 ppm for extended
periods (8 hrs or more) is lethal to rats. Ingestion of ethanol has caused death in humans, but
OEHHA (1999) concluded that a lethal dose by inhalation was unlikely (OEHHA 1999).
Pastino et al. (1997) developed a pharmacokinetic model for ethanol uptake by inhalation in rats
and mice. They concluded that after exposure to 600 ppm ethanol for six hours, maximum blood
ethanol concentrations were less than 10% of the concentration reported as the threshold for
behavioral effects.
NEIWPCC (2001) concluded that overall data from human studies suggest a threshold for acute
neurological effects in blood alcohol range of 0.01-0.05%. Acute ingestion of about 1 g/kg
alcohol approximates 0.1% blood alcohol levels, suggesting a 0.1 to 0.5 g/kg as the lowest
human observable adverse effect level (LOAEL) for acute ethanol neurotoxicty in humans.

Gleason et al (1969) summarized the following effects associated with blood alcohol levels:
0.05-0.15% - decreased inhibitions, incoordination, slow reaction time, blurred vision;

0.15-0.3% definite visual impairment, slurred speech, hypoglycemia, and staggering;
>0.3% marked incoordination, stupor, hypoglycemia, convulsions, coma, and death; and
0.18-0.6% - lethal blood alcohol concentrations.
Effects on laboratory animals appear to occur at similar ethanol doses, and with similar
symptoms. Ethanol doses of 0.1-0.5 g/kg resulted in increased motor activity in rats and
increased aggressiveness in monkeys. At higher doses, incoordination was observed (HEI 1996).
Acute lethal doses in dogs range from 3-10 g/kg, with death resulting in respiratory failure and
death within 12 hrs (Reese and Kimbrough 1993). The oral LD50 for adult rats (lethal dose to
50% of the population) ranges from 11.5 to 17.8 g/kg, while younger rats were more sensitive
(LD50 of 6.2 g/kg) (OEHHA 2000).
C4. CHRONIC EXPOSURE
C4-1 Subchronic and Chronic Effects

Most of the literature on chronic exposure of ethanol is related to alcohol abuse. OEHHA 1999
reported that chronic exposure to ethanol results in adverse effects on the liver in animals and
humans. Symptoms include fat accumulation and inflammation progressing to focal necrosis
and fibrosis. Oral doses initiating these effects were 8-15 g/kg/day in rats and dogs. In humans,
alcoholic hepatitis and cirrhosis have been observed with chronic ingestion of 2 g/kg/day (HEI
1996). Toxic effects on the heart, such as inflammatory and degenerative changes have also
been observed (NEIWPCC 2001). Severe effects on the heart, central nervous system, and liver
have been reported after long term high level exposures, although no thresholds for such severe
effects are available (NEIWPCC 2001).
NEIWPCC (2001) reported the results of several researchers that identified effects of chronic
exposure (generally oral) to ethanol on blood cellularity and function, particularly white blood
cells (Malik and Wickramasinghe, 1986 and Marietta et al. 1998), although the effect of these
changes on immune function is unclear. NEIWPCC (2001) indicated that the dose response data
is limited in such studies, and it is unclear whether such effects are relevant to low environmental
exposures.
One study (Chu et al. 2005) considered the effects of inhalation exposure of rats to ethanol and
gasoline separately, as well as combined. They exposed rats to 6130 ppm ethanol, 500 ppm

gasoline, and 85% ethanol gas (6130 ppm ethanol and 500 ppm gasoline) for 6 hours per day,
five days per week for four weeks. They found that female rats treated with the mixture showed
growth suppression, which was reversed after four weeks in filtered air. They also observed
increased kidney weight and liver effects, including increased liver weight and enzyme activity,
with the most significant effects associated with gasoline exposure. Combined exposure resulted
in additive effects on growth suppression. While other researchers have identified inflammation
of the upper respiratory tract with acute ethanol exposures of this magnitude, Chu et al. (2005)
observed this effect only with combined exposure suggesting irritating effect when combined.
They concluded that inhalation of ethanol and gasoline at the concentrations tested resulted in
mild, reversible, biochemical hematological and histological effects, with some indications of
interactions when combined.
C4-2 Reproductive and Developmental Effects

Nelson et al. (1985) administered ethanol to rats at 20,000, 16,000, 10,000, and 0 ppm in air for 7
hrs/day on Days 1-19 of gestation. Maternal weight gain and feed intake decreased during the
first week of exposure at 20,000 ppm, and dams were completed narcotized at the conclusion of
exposure. They reported no definite increase in malformations at any level of ethanol exposure,
although incidence at the highest exposure level was “borderline” significant. They evaluated
skeletal, visceral, and external malformations. They concluded that at maternally toxic
concentrations (20,000 ppm), ethanol was only possibly teratogenic, and lower concentrations
were not teratogenic.
NEIWPCC (2001) indicated that there are some studies in humans and rodents that support
ethanol induced genetic effects resulting from moderate to high levels of ethanol exposure
(Froines et al, 1998). Findings have related ethanol exposure to chromosomal abnormalities in
miscarried pregnancies and sperm, and dominant lethal mutations in mice and rats. They
suggested that the mechanism may involve exposure to acetaldehyde as well as ethanol. (Froines
et al. 1998) also reports that a variety of studies have shown that exposure of prepubertal rats and
mice are exposed to ethanol can result in delays development of male reproductive tract,
although dose response data are insufficient to identify specific effects.
OEHHA (1999) reported that rats and mice on liquid diets of 5-10% ethanol for 5 or more weeks
showed adverse effects on the testes. They also identified that some studies show effects on the
fetus, including growth retardation, malformations, and death in rats and mice fed diets
comprised of 15-35% ethanol (by calories). However, other studies showed no effects on mice
and rabbits given drinking water containing 15% ethanol.

Human fetal alcohol syndrome is a well known result of alcohol abuse during pregnancy
(OEHHA 1999). Effects observed include retardation of growth and development, physical
malformations, and behavioral and cognitive problems. In addition, more subtle neurological
changes in fetuses have been observed, such as performance on neuropsychological tests,
hyperactivity, and lowered intellectual capacity (HEI 1996). HEI (1996) suggested a threshold
for fetal alcohol effects of 0.5 oz per day (about one drink per day or 0.2 g/kg/day) for most
neurological endpoints, based on the work of Jacobson et al. (1996). They also concluded that
this threshold is supported by animal data. Neuromotor effects were observed in monkeys at 1-3
g/kg/d, and some effects occurred at maternal doses of 0.25 g/kg/day (HEI 1996).
C4-3 Cancer
In 2007, the International Agency for Research on Cancer (IARC) reassessed the carcinogenicity
of alcoholic beverages. The results of their evaluation are provided in WHO (2010), and
summarized in Baan et al. (2007). The conclusion of this evaluation was that alcoholic
beverages and ethanol in alcoholic beverages are “carcinogenic to humans”, or Group 1. This
category is selected when there is sufficient evidence of carcinogenicity in humans. They
concluded that “occurrence of malignant tumours of the oral cavity, pharynx, oesophagus, liver,
colorectum, and female breast is causally related to alcohol consumption”. They also concluded
that acetaldehyde resulting from the metabolism of ethanol contributes to malignant esophageal
tumors.
WHO (2010) also concluded that there is sufficient evidence in experimental animals for the
carcinogenicity of both ethanol and acetaldehyde. Their overall conclusions regarding the
carcinogenicity of ethanol are based on epidemiological data indicating that cancer effects are
not dependant on the type of alcoholic beverage, the information indicating ethanol causes
cancer in experimental animals is sufficient, and the evidence that acetaldehyde contributes to
the incidence of esophageal tumors. WHO (2010) provides an extensive discussion of possible
mechanisms for ethanol-induced carcinogenicity, and concludes that the mechanisms are
complex and not well characterized. They also indicated that the identification of ethanol as a
carcinogenic component of alcoholic beverages does not preclude the possibility of other
components contributing to carcinogenicity. Baan et al (2007) reported that in most studies
where ethanol was administered in conjunction with a known carcinogen, the carcinogenic effect
was enhanced.
An earlier evaluation of the carcinogenicity of ethanol (NTP 2005) also lists consumption of
alcoholic beverages as known to be a human carcinogen based on sufficient evidence of
carcinogenicity in human studies. They found consumption of alcoholic beverages as causally
related to cancers of the mouth, pharynx, larynx, and esophagus. They also concluded that

animal studies indicated that the ethanol component may not solely be responsible for cancer
incidence resulting from alcohol consumption.
C4-4 Relevance of Chronic Exposure Levels to Environmental Exposures

Spill events of ethanol generally last for a relatively short time frame (days), as described in
Section 3.0 and Appendix A. The only possibility of long term or chronic exposures is from
drinking water exposures, which may result from groundwater or surface water releases.
However, biodegradation is expected to reduce concentrations in these media relatively rapidly.
As a result, the potential for exposures of a magnitude and duration that could result in chronic
effects, such as fetal alcohol syndrome and cancer, is unlikely in spill situations.

Appendix D
Draft SOP
Field Hydrometer Gross Measurement of Ethanol and/or
Denatured Ethanol
NOTE: THIS DRAFT SOP WAS DEVELOPED FROM ASTM METHOD 1250. IT HAS NOT BEEN TESTED
FOR USE IN THE FIELD WITH DENATURED ETHANOL.
D1. INTRODUCTION
Hydrometers have been used for many applications to determine the specific gravity of materials,
including ethanol. It is used by ATF to quickly identify the approximate concentration of
ethanol.
The use of hydrometers with temperature correction for ethanol and water can provide a
concentration of ethanol and water with good approximation, as long as the liquid is a mixture of
ethanol and water. When other materials are also in solution, the resulting specific gravity and
therefore the reading from the hydrometer will result in a reduced level of accuracy. When
ethanol has been denatured, this will be the case.
It is expected that the use of a hydrometer in the field for a release situation, will provide a gross
measurement of the concentration of ethanol, dependent on the level of other contaminants in the
liquid.
D2. EQUIPMENT AND SUPPLIES
Depending on the chosen method, use:
A proof hydrometer with a range from 0 to 200 proof (0-100%) and hydrometer jar.
A thermometer with a temperature range of 0oF to 110oF
Filter paper, funnel and 500 ml. flask.
Recordkeeping and Documentation Supplies:
Field logbook (w/ waterproof paper is recommended) or field forms
Indelible pens
Calibration and Use
SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP D-1

D3. HYDROMETER METHOD CALIBRATION
For purposes of having a reference material, a known high proof liquid should be used to
calibrate the use of the hydrometer and thermometer using the following steps:
Rinse the hydrometer jar with the reference liquid.
Fill the jar with a liquid volume that will allow the hydrometer to freely float the
hydrometer without overflowing when the hydrometer is placed in the liquid.
Place the hydrometer in the liquid, letting the hydrometer settle it‟s movement in the
liquid. Record the raw reading as shown in Figure 2.
After the hydrometer reading has been recorded, remove and place the thermometer in
the liquid.
Take the temperature reading of the liquid allowing time for the temperature reading to
equilibrate. Record the temperature.
The reading is typically adjusted for temperature, but for this gross reading, this
adjustment is not necessary.
This result should be within 5 proof (2.5%) of the labeled proof of the liquid (not considering the
presence of other contaminants).
D4. GENERAL PROCEDURE INFORMATION
The hydrometers used are graduated to read the proof of aqueous alcoholic solutions at 60
degrees Fahrenheit; thus, they read, 0 for water, 100 for proof spirits, and 200 for absolute
alcohol. Because of temperature-density relationships and the selection of 60 degrees Fahrenheit
for reporting proof, the hydrometer readings will be less than the true percent of proof at
temperatures below 60 degrees Fahrenheit and greater than the true percent of proof at
temperatures above 60 degrees Fahrenheit. However, the differences are relatively small and not
necessary for a gross screening.
D4-1 Field sample method

Follow the same steps as in the calibration however, if the raw sample contains visible
particulate, filtering of the sample is recommended. Use the filter paper, funnel and flask to

catch the filtered liquid. Then proceed to the steps for calibration to estimate the proof of the
liquid.
Figure 1 Figure 2
D4-2 General Concerns for Hydrometer Method

Care should be exercised to obtain accurate hydrometer and thermometer readings. In order to
accomplish this result, the following precautions should be observed. Bulk liquids should be
thoroughly agitated so that the test samples will be representative of the entire quantity. The
hydrometers should be kept clean and free of any oily substance. Immediately before readings
are taken, the glass cylinder containing the thermometer should be rinsed several times with the
liquid which is to be gauged so as to bring both the cylinder and the thermometer to the
temperature of the spirits (if time permits, it is desirable to bring both the spirits and the
instruments to room temperature). If the outer surface of the cylinder becomes wet, it should be
wiped dry to avoid the cooling effect of rapid evaporation. During the readings the cylinder
should be protected from drafts or other conditions which might affect its temperature. The
hands should not be placed on the cylinder in such a manner as to warm the liquid contained
therein. The hydrometer should be inserted in the liquid and the hydrometer bulb raised and
lowered 5 or 6 times to obtain an even temperature distribution over its surface.
When the ethanol has been denatured there will be a skewing of the resultant proof reading (if
still in solution) because the denaturant has a different density. In the case of gasoline, the
specific gravity is lower than ethanol or water, therefore the apparent proof reading will be

higher than it actually is. Because of this, realize that the proof reading could be as much as 10%
lower than the reading given on a proof hydrometer.
D4-3 Preventive Maintenance:
To ensure proper readings, it is important to keep the hydrometer and thermometer in a case after
cleaning both after each use.
Any debris left on the hydrometer will result with incorrect readings. Check the condition of the
hydrometer and thermometer before each use to ensure there is not brakes in the glass. If there
are any cracks, the hydrometer of thermometer must be replaced.
D4-4 Documentation
Record all field-testing measurement data, to include the following:
Project name
Date and time of measurement or test (including time zone, if applicable)
Source and location of the measurement or test sample (e.g., monitoring well
identification number, outfall number, station number or other description)
Latitude and longitude of sampling source location (if required)
Measurement or test sample value
Temperature of sample
Initials or name of analyst performing the measurement.

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LARGE VOLUME ETHANOL SPILLS – ENVIRONMENTAL

IMPACTS AND RESPONSE OPTIONS

Shaw’s Environmental and Infrastructure Group

List of Tables ___________________________________________________

List of Figures __________________________________________________

Figure 2-1 Flashpoint as a Function of Water Content _______________________________________ 2-1

Appendix A Case Studies

In general, ethanol in the environment degrades rapidly. Biodegradation is rapid in soil,

depleted as a result of aerobic degradation, anaerobic biodegradation of ethanol in groundwater

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-2

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-3

As a result of the above observations, the following recommendations can be made:

Ethanol pools or impacts to soils should be identified as quickly as possible to prevent

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-4

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-5

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP E-6

1.2 Scope of Document

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 1-1

TABLE 1-1 ETHANOL AND BLENDS AND THEIR USES

Ethanol Blend Composition Use

E85 85% ethanol, 15 % gasoline Used in flex-fuel vehicles (< 2% ethanol

E10 10% ethanol, 90% gasoline 70 % of nation’s gasoline (98% ethanol

This document provides the following information:

Physical and chemical characteristics of ethanol and blends (Section 2.0);

Summary of case studies of incidents involving ethanol (Section 3.0);

Fate and transport characteristics of ethanol and blends (Section 4.0);

Summary and recommendations (Section 8.0).

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 1-2

2.0 Physical and Chemical Characteristics of Ethanol/Gasoline Blends

The flammability of ethanol is affected by Source: HSDB 2011

100 Flammable Liquid the lowest temperature at which heating

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 2-1

TABLE 2-2 COMPARISON OF PROPERTIES FOR ETHANOL/GASOLINE BLENDS

PROPERTY ETHANOL E95 E85 E10 Gasoline

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 2-2

2.2 DOT Placards

Gasohol, NA 1203; Gasoline, UN 1203 (E1-E10)

Ethanol and gasoline mixture, UN 3475 (E11-E99)

Denatured Alcohol, NA 1987 (E95-E99)

Ethanol or Ethyl alcohol, UN1170 (E100)

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 2-3

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 2-4

3.0 Summary of Case Studies

TABLE 3-1 ETHANOL SPILL INCIDENT SUMMARIES

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 3-1

TABLE 3-1 ETHANOL SPILL INCIDENT SUMMARIES (continued)

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 3-2

4.0 Fate and Transport Characteristics

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 4-1

4.1 Ethanol Migration Pathways

Infiltration into soil •Ethanol is rapidly biodegraded in

4.2 Ethanol Degradation Rates

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 4-2

4.3 Methane Generation in Soil/Groundwater

4.4 Ethanol Partitioning Between Environmental Media

4.5 Media Fate and Transport Characteristics

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 4-3

As discussed in Section 4.3 and Appendix B, anaerobic biodegradation of ethanol in

SHAW’S ENVIRONMENTAL & INFRASTRUCTURE GROUP 4-4

Methane gas generation. Degradation of ethanol to methane is expected to be the