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    UNDERGROUND COAL GASIFICATION

    HISTORY,ENVIRONMENTAL ISSUES,AND THE PROPOSED PROJECT AT BELUGA,ALASKA

    Kendra L. Zamzow, Ph.D.

    Center for Science in Public Participation

    March 2010

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    Table of Contents

    CIRI's proposed project ................................................................................................................................. 4

    Natural Gas and Coal Gas .............................................................................................................................. 5

    How UCG works ............................................................................................................................................ 7

    Getting coal to burn .................................................................................................................................. 7

    Operational parameters............................................................................................................................ 9

    Deep and Thick .................................................................................................................................... 10

    Temperature ....................................................................................................................................... 11

    Water .................................................................................................................................................. 11

    Faults and fractures ............................................................................................................................ 11

    Historical Perspective.................................................................................................................................. 12

    Regional experiences .............................................................................................................................. 12

    Former Soviet Union ........................................................................................................................... 12United States ....................................................................................................................................... 12

    Europe ................................................................................................................................................. 13

    Other countries ................................................................................................................................... 13

    Key test sites ........................................................................................................................................... 14

    Hoe Creek ............................................................................................................................................ 14

    Centralia, WA ...................................................................................................................................... 15

    Rocky Mountain I ................................................................................................................................ 15

    El Tremedal ......................................................................................................................................... 16

    Chinchilla ............................................................................................................................................. 16

    Environmental Impacts ............................................................................................................................... 17Structural Integrity of Host Rock ............................................................................................................. 19

    Formation of contaminants .................................................................................................................... 19

    Migration of contaminants ..................................................................................................................... 20

    CO2 .............................................................................................................................................................. 21

    Life cycle greenhouse gas emissions ....................................................................................................... 21

    Carbon capture ....................................................................................................................................... 24

    Carbon sequestration ............................................................................................................................. 25

    Summary ..................................................................................................................................................... 27

    Bibliography ................................................................................................................................................ 29

    Appendix A: UCG reactions and Syngas Reactions ..................................................................................... 31Appendix B: Natural Gas Processing ........................................................................................................... 32

    Appendix C: UCG sites worldwide ............................................................................................................... 33

    Appendix D: Water Analysis at Contaminated UCG Sites .......................................................................... 39

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    Figures

    Figure 1. Location of proposed UCG project, Beluga, AK.4

    Figure 2. CRIP process of gasification.8

    Figure 3. Depth and thickness of coal seams by global region..9

    Figure 4. Faulted and dipping seams11Figure 5. UCG at Chinchilla, Australia...15

    Figure 6. Comparison of life cycle greenhouse gas emissions by fuel type.22

    Tables

    Table 1. Composition of Natural Gas, Syngas, and UCG gas...5

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    In November 2009, Cook Inlet Region, Inc. (CIRI), an Alaskan Native regional

    corporation, filed for exploration permits to examine the potential to fuel a 100 MW power plant

    using "underground coal gasification" (UCG) technology. This paper explores the history of

    UCG technology globally, including environmental impacts during historical trials, how those

    impacts might be mitigated, and risk of environmental impacts at the Beluga, Alaska project.

    CIRI's proposed project

    Information on CIRI's proposed project is limited since the project is only at the

    conception and permitting states. The property is located in a remote location on the west side of

    Cook Inlet, just north of the Beluga River, on CIRI lands (Figure 1). The site is 5-10 miles from

    the current 385 MW Chugach Electric Plant, located at Beluga, which utilizes natural gas from

    nearby offshore platforms to provide electricity. The CIRI project proposes a 100 MW

    combined cycle power plant run on the syngas that would be the product of 'gasifying' coal in the

    ground.1 Although no maps have been produced to indicate where the power plant would be

    located, it would almost certainly be adjacent to the targeted coal fields.

    1CIRI presentation to the Alaska State House Resources, Senate Resources, and Senate Energy committees,

    October 9, 2009

    Figure 1. Location of proposed UCG project, Beluga, AK.

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    Natural Gas and Coal Gas

    Natural gas, as extracted from production wells, is mostly methane (CH4) with a high

    heating value (>1000 BTU/ft3). The composition depends on how the natural gas was formed. Ifit is biogenic (produced by living organisms) it is nearly pure methane. Thermogenic natural gas

    (produced by the breakdown of organic matter) is methane with contaminants (small

    hydrocarbons, water, sulfur, and CO2) and must be processed before it can be used (Table 1).2

    The hydrocarbons can be separated and sold while the other constituents are corrosive.3,4Cook

    Inlet gas is primarily biogenic, and North Slope natural gas is thermogenic.5 At the Beluga

    Power Plant, seven gas turbines and one steam turbine together produce 385 MW of electricity,

    the primary source of electricity to Anchorage. In the combustion process, methane is burned

    and water, CO2, and oxidized sulfur and nitrogen products are the primary waste products.

    "Syngas", or synthetic gas, is the term that refers to a carbon monoxide-hydrogen gas

    mixture. It can be made from coal, natural gas, or biomass. "UCG gas" is used in this paper to

    refer to gas produced from burning coal underground, although some literature also refers to this

    as "syngas". Both are primarily carbon monoxide (CO) and hydrogen gas (H2), but the processes

    of making them are different (Appendix A). To make coal-derived syngas above ground, coal is

    put under heat (>700 oC) and pressure to make carbon monoxide and hydrogen gas. Hydrogen or

    the building blocks for chemical products like methanol are the products. To make electricity,

    the CO and H2are reacted with steam to form CO2and more hydrogen. Hydrogen is combusted

    to produce power. Water, CO2, and oxidized sulfur and nitrogen products are the waste products.

    Syngas plants are relatively common, with over 150 in operation.

    6

    The UCG process burns coal under heat (10001600 oC) and pressure with steam while

    the coal is still underground. UCG gas as it comes out of the product well is carbon dioxide

    (CO2) and hydrogen gas (H2), with more methane and less CO than syngas, and lower in sulfur,

    tars, mercury, and other metals which are left underground in the residual ash after the burn.

    The actual proportions of each component will vary depending on how the burn is operated:

    Thickness of coal seam. Thin coal seams (< 2 m) produce a gas that is mostly CO2, with

    little H2, CO, and methane. This is a low quality gas, and may not be economic. Thicker

    2http://www.naturalgas.org/naturalgas/processing_ng.asp

    3http://housemajority.org/coms/hres/gas_report_chapter1.pdf;

    http://www.naturalgas.org/naturalgas/processing_ng.asp4

    http://housemajority.org/coms/hres/gas_report_chapter1.pdf;

    http://www.naturalgas.org/naturalgas/processing_ng.asp5

    Clayton, G. 1980; Goldsmith and Szymoniak 2009; http://housemajority.org/coms/hres/gas_report_chapter1.pdf6

    Simbeck, 2002, in Burton et al 2006.

    http://www.naturalgas.org/naturalgas/processing_ng.asphttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://www.naturalgas.org/naturalgas/processing_ng.asphttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://www.naturalgas.org/naturalgas/processing_ng.asphttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://www.naturalgas.org/naturalgas/processing_ng.asphttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://www.naturalgas.org/naturalgas/processing_ng.asphttp://housemajority.org/coms/hres/gas_report_chapter1.pdfhttp://www.naturalgas.org/naturalgas/processing_ng.asp
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    seams don't change the amount of CO2, CO or methane, but produce a lot more H2. This

    is useful for generating hydrogen or a CO/H2syngas.

    Depth of coal seam. Burning deep seams where the pressure is greater creates more

    methane and less CO and H2, and therefore a higher quality gas.

    Temperature. High temperature reactions produce more methane,, but temperatures that

    are too high reduce the quality of the gas

    Water. Changing the amount of water changes the amount of methane and hydrogen.

    Oxygen. Injecting air to start the burn instead of oxygen increases the nitrogen content of

    the gas, lowering the gas quality.

    The product gas will also contain sulfur, nitrogen, and volatile trace metal species. Like

    thermogenic natural gas, it needs to be 'cleaned' to remove hydrogen sulfide and other

    contaminants (Appendix B). UCG produces either hydrogen or a methane-hydrogen mixture for

    combustion after clean-up. If a methane-hydrogen mixture is combusted, CO2will be the

    primary air emission. If hydrogen is combusted, water will be the primary emission, but CO2

    will be produced as part of the process of making hydrogen. Hydrogen may also have other

    industrial uses, or may be used for hydrogen fuel cells and other parts of the emerging hydrogen

    economy. Similarly, chemical reactions can begin with UCG gas to make methane, methanol,

    fertilizer, and other products.

    Table 1. Composition of Natural Gas, Syngas, and UCG gas. Natural gas and UCG gas composition is as it occurs

    at the well-head, not after cleanup. UCG gas composition will vary depending on the purpose the gas is to be used for.

    and the conditions under which it is generated. The table is a compilation from the following sources: Shafirovich andVarma 2009, Goldsmith and Szymoniak 2009, Friedmann 2007, Bakker 2004, Claypool 1980, and the following

    websites: http://www.naturalgas.org/naturalgas/processing_ng.asp,

    http://www.naturalgas.org/overview/background.asp, http://www.uniongas.com/aboutus/aboutng/composition.asp,

    http://www.fluent.com/about/news/newsletters/04v13i2/s8.htm

    Natural Gas Syngas UCG gas

    Methane (CH4) 70-90% 1-2% 5-14%

    Hydrogen (H2) 24%-30% 25-40%

    Carbon dioxide (CO2) 0-12% 4%-15% 25-40%

    Carbon monoxide (CO) 35-65% 5-20%

    Hydrogen Sulfide (H2S) 0-5% 1% 2-8%

    Nitrogen (N2) 0-5% 1% ?

    http://www.naturalgas.org/naturalgas/processing_ng.asphttp://www.naturalgas.org/naturalgas/processing_ng.asphttp://www.naturalgas.org/overview/background.asphttp://www.naturalgas.org/overview/background.asphttp://www.uniongas.com/aboutus/aboutng/composition.asphttp://www.uniongas.com/aboutus/aboutng/composition.asphttp://www.fluent.com/about/news/newsletters/04v13i2/s8.htmhttp://www.fluent.com/about/news/newsletters/04v13i2/s8.htmhttp://www.fluent.com/about/news/newsletters/04v13i2/s8.htmhttp://www.uniongas.com/aboutus/aboutng/composition.asphttp://www.naturalgas.org/overview/background.asphttp://www.naturalgas.org/naturalgas/processing_ng.asp
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    Water (H2O) saturated 15-25% 33%

    Producing electricity by burning these different gases will generate different

    environmental footprints. For instance, syngas requires mining and transporting coal; natural gas

    production requires deep, often offshore wells; while UCG gas may require deep wells but hasvery little above ground disturbance. Similarly each has a different potential to pollute water or

    air, and different greenhouse gas types and amounts.

    How UCG works

    The basic concept is to drill two wells into a deep coal seam and burn out the coal

    between them.

    Compressed air or an oxygen/steam mixture is injected through one well, the coal burns

    and releases gases, and the gases come out of the ground at the second well, called the

    production well. The burn creates a cavity or "combustion chamber", and the process works best

    with deep seams of low-quality coal, exactly the material that is difficult to traditionally mine

    economically. Water flowing into the cavity is not pumped out, but is used as part of the burn

    reaction. Because of the cost of transporting the gas, power plants would likely be sited adjacent

    to the coal field.

    Pilot projects have been conducted since the 1940's, and particularly in the 1970's and

    1980's in the US and the 1990's in Europe and China. Trials focused on how to get the coal to

    burn, how to control the burn, maximizing efficiency, and minimizing environmental

    contamination.

    Getting coal to burn

    The first difficulty in the early trials was getting the coal to burn. Although there are

    numerous instances of uncontrollable underground coal fires around the world, the fires are

    dependent on oxygen reaching the coal. Deep coal seams several hundred feet underground are

    saturated with water and isolated from oxygen, and attempts to simply set the seam on fire

    fizzled. In researching science journals, federal documents, and company literature this author

    was unable to find any instances of uncontrolled coal fires during UCG.

    Eventually two techniques proved to be successful.

    Inject air at the injection well. The ignition source is placed at the production

    well to "draw" the fire towards the high oxygen area in a process called "reverse

    combustion", burning a path through the seam.

    Drill a simple vertical well as the production well. The injection well begins

    vertical then bends to become a horizontal tunnel through the coal seam towards

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    the production well. A "controlled retractable injection point" (CRIP) is a point

    where coiled tubing burns through the horizontal tunnel borehole casing; oxygen

    and steam are forced through the point to ignite the coal. This is initially placed

    near the juncture of the injection and production wells. The coal burns for a

    while, forming a cavity as hot gases move up and outward, but it eventually

    fizzles. When the burn is done, the point is retracted and ignition is started again

    at a point in the horizontal tunnel closer to the injection well. In this way the

    burning coal front proceeds in a controlled manner (Figure 2). The CRIP

    technique allows for several production wells for each injection well, reducing the

    overall footprint.

    A proprietary technology developed by Ergo Energy was successfully used in the

    30-month long Chinchilla Australia project. However, the specifics of the

    technology are not known.

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    In general, the CRIP process and the Ergo technology have worked better than hydraulic

    fracturing and reverse combustion in controlling the UCG process.7

    Operational parameters

    Constraints such as depth, thickness, dipping of the coal seam and temperature, pressure,

    oxygen, and water in the burn cavity all play a role in gas quality, economics, and potential

    environmental impacts.

    7Hydraulic fracturing is a technique of fracturing the coal seam between the two wells to encourage gas flow; this

    did not work, as gases spread out and did not flow consistently in the desired direction.

    Overburde

    Coa

    Inject oxygen

    and steamGas

    Old burned out

    cavity with

    New injection

    point, new burn

    burned out injection well

    heat and hot gases

    pyrolyis products line

    water influx

    Figure 2. CRIP process of gasification. The movable injection point begins the burn near the production

    well. When the first burn expires, a second burn is initiated closer to the injection well. This procedurecontinues until the seam is burned out. Adapted from Burton et al 2006.

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    Deep and Thick

    Trials have determined that UCG should be conducted on deep, thick coal beds. This

    provides a better quality gas and reduces the risk of groundwater pollution or surface subsidence.

    The pressure in the burn cavity affects how well the reaction will proceed, thecomposition of product gas, and how the surrounding rock will be altered. Burns conducted at

    depth (200 m to over 1000 m) where the pressure is greater produce better quality gas with more

    methane. This has been proven in the field: using oxygen injection, gas produced at 4 bars of

    pressure contained 5%

    methane (and 21% CO

    and 38% hydrogen) while

    gas produced at 5.3 bars

    contained 13% methane

    (and 13% CO and 25%

    hydrogen.8

    Theremainder of gases in both

    cases was carbon dioxide

    and hydrogen sulfide. The

    difference affected the

    heat content of the gas,

    with 8.7 and 10.9 MJ/m3

    produced respectively.

    Deep seams also

    cause the economics of airversus oxygen injection to

    change. Injecting air

    requires compressing nitrogen and injecting oxygen requires an oxygen separation plant both

    are expensive. Oxygen injection becomes economically favorable for deeper coal seams as the

    cost of making oxygen becomes less expensive than additional compressors for injecting air. 9

    Thick seams allow gas production with fewer wells. Seams that are too thin (less than 2

    m) allow heat to escape into surrounding rock too easily, and the resulting product gas is of poor

    quality.10

    Some UCG development companies suggest seams should be at least 10 m thick,11

    while others believe seams as thin as 0.5 m can be used; this is likely biased by the depth ofavailable coal (Figure 3).

    8Kreinin in Shafirovich et al 2008; Shafirovich and Varma 2009

    9 Boysen et al 1998; Burton et al 2006

    10 Bowen and Irwin 2008

    11Shafirovich et al 2008

    Figure 3. Depth and thickness of coal seams by global region. The US tends

    to have thick seams of coal near the ground surface, while Europe tends to have

    thin, deep seams of coal. Thick seams produce better quality gas, but deep seams

    are more likely to isolate contaminants and reduce the risk of subsidence. FromBurton et al 2006.

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    Figure 4. Faulted and dipping

    seams. (Left) Drilling faulted

    seams. (Below) Gasification of

    steeply dipping seams.

    Temperature

    Temperatures that are too low allow tars to form and can cause the pathway between

    wells to plug, but if too high reduce the efficiency of the gasification process and the heat value

    of the final gas.

    Water

    Although coal contains water and combustion cavities are expected to have water flux

    into them, too much water will reduce the methane content in the gas, reducing the heating value.

    For this reason, if UCG is being used to provide electricity it is preferable to use coal with low

    moisture with no overlying aquifer within 25 times the height of the seam.12 This also reduces

    the risk of groundwater contamination, particularly groundwater that might reach surface water

    or enter drinking water wells.

    Faults and fractures

    Coal seams may dip up and down, or a fault may cause the seam to be discontinuous,

    suddenly stopping at one depth and starting again at another. To adjust for fault discontinuities,

    drilling equipment has the capacity to contain "eyes" that "see" the geologic structure ahead of

    the drill bit; the drill can then be adjusted as necessary (Figure 4).

    To use the technology on steeply dipping coal seams, combustion occurs at the deep end

    and the coal above "gravity feeds" down into the fire, with production gases working their way

    upward (Figure 4) and coal tar flows down away from the burn. Testing on dipping seams has

    been conducted at Rawlins, WY and in Russia (Juschno-Abinsk).

    12Sury et al 2004, in Shafirovich et al 2008

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    Historical Perspective

    This section lays out some the general history of underground coal gasification in

    different countries, and describes some key sites in detail. A list of all gasification sites is

    available in Appendix C.

    Regional exper iences

    Former Soviet Union

    The technology for burning coal into gas while it was still in the ground began in the

    1930's in the USSR, and by the 1950's the USSR was producing about 300 MW of electricity

    with this gas.13

    About 200 pilots were conducted in the USSR and, after 1991, in Russia,

    Ukraine, and Uzbekistan. One station (Yuzhno-Abinsk, Kuznetsk Basin, Russia) produced gas

    for 14 boilers from 1955 1996, finally closing as equipment failed during the post-Soviet era.

    Another plant built in the 1950's in Uzbekistan is still operating. Most closed as cheap natural

    gas came on-line. During the trials in the former Soviet Union, it was learned that injecting

    oxygen rather than air produced gas with higher heat value, that transporting the gas any distance

    is often uneconomical, and that high temperatures (540-760 oC) cause rocks to swell.14

    Environmental modeling was also developed.

    United States

    In the US, initial tests began in Alabama in the 1940's and 1950's. Testing was

    revitalized during the years of high oil prices, with 31 tests conducted 1973-1989, mostly by the

    Department of Energy (DOE). They were short-term projects, with a total of only 50,000 tons of

    coal gasified. It was during this period that the CRIP technology was developed by Lawrence

    Livermore National Labs (LLNL). Most trials attempted to answer specific questions about

    managing the burn, shutdown and startup, gas consistency and quality, and groundwater impacts.

    New projects are scheduled to begin in Wyoming: in July 2007, British Petroleum (BP), LLNL,

    13Shafirovich et al 2008; Shafirovich and Varma 2009

    14Den'gina et al 1994, in Shafirovich et al 2008

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    and a UCG developer signed an agreement for a pilot in the Powder River Basin of Wyoming

    that would incorporate carbon capture and sequestration (CCS) with UCG.15

    Europe

    In the European Union, a series of experiments was conducted 1982-1999, primarily inBelgium, France, and Spain. These trials tested methods to get coal to ignite, move gas to the

    production well, and determined that coal burning could be conducted in deep coal seams.

    Repeated testing of reverse combustion and hydraulic fracturing to direct gas to the production

    wells failed. Not until directional drilling and oxygen injection were attempted at the El

    Tremedal site in Spain were researches able to link wells productively.

    All were short-term tests primarily designed to learn more about the technology. No

    electricity is currently generated from UCG in Europe, although more trials are planned. A

    consortium of countries led by Poland has started a pilot to test the feasibility of using UCG as a

    cornerstone of developing a hydrogen economy and the feasibility of integrating it withgeothermal heat exchange and CCS.

    16 The UK is examining the feasibility of conducting UCG

    in a coal seam that lies under the Firth of Forth in Scotland; the gas would be used in conjunction

    with fuel cells to make electricity. This would be the first UCG project beneath ocean water.

    Other countries

    In Australia, one of the most successful pilots was conducted. The Chinchilla project ran

    from 1999-2003 and demonstrated that UCG could be controlled, including shutdown and re-

    start. During the 4-year period, 35,000 tons of coal from a seam 140 m deep was gasified with

    no environmental problems. Today two major pilot projects are in development, and severalother smaller projects. Pilots include a planned 400 MW combined cycle gas turbine (CCGT)

    power plant and a 100-day pilot to test a module-based system to produce 20 MW per module,17

    with the goal of developing a commercial CCGT plant. In October 2008, a coal gas-to-liquids

    fuel production facility was started.18

    Canada has not had any historical UCG projects, but two projects are moving forward in

    Alberta to use UCG for power, fuel, and hydrogen and sequester CO2using enhanced oil

    recovery (EOR).19

    The steam from UCG may be used in tar sands oil recovery.20

    The

    proponents of these projects, Laurus Energy, may become a partner in the CIRI Beluga project.21

    15Shafirovich and Varma 2009

    16Rogut 2008

    17Shafirovich et al 2008

    18Friedmann et al 2009

    19ibid

    20Maev 2008; Shafirovich and Varma 2009

    21Bluemink 2009

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    A test project in New Zealand in 1994 only lasted 13 days. The information available

    says the area was "tectonically active with coal deposits faulted and folded, providing a geologic

    challenge" but does not explicitly detail the issues, except to say that they did not achieve good

    gasification.22South Africa started a pilot UCG project in January 2007 with the intent to use it

    for both power and coal gas-to-liquid fuel. The small amount of UCG gas would be used to co-

    fire turbines at a large natural gas facility. The co-firing was successful 2007-2008, but it is

    unclear if a scale-up occurred after that. China has had 16 UCG trials since the 1980's. One

    project currently operating in XinWen uses six UCG reactors to provide gas for cooking and

    heating, while one in Shanxi uses the gas to produce ammonia and hydrogen. A $100 million

    pilot commercial project has started in Inner Mongolia next to a coal mine. Other plants are used

    to produce fertilizer. More trials are planned, including feasibility of UCG for hydrogen and

    methanol production.23

    Key test sites24

    Hoe Creek

    The Hoe Creek site in Wyoming was operated from 1976-1979. The coal seam was 10 m

    thick, lying 40-50 m below ground, with a shallow layer (5 m thick) of siltstone and clay

    separating it from an upper coal seam; overburden above that was primarily silt, sand, and

    sandstone. The sand and coal seams were the primary aquifers. Three experiments (Hoe Creek

    I, II, and III) were conducted and heavily monitored to examine the burn process, gas

    composition, cavity formation, and geotechnical data.

    The primary research at this time was in getting gas to move to the production well. At

    Hoe Creek I, explosives were used to fracture the coal bed and air was injected for 11 days. Thetest was not very successful, with about 7% of the gas lost to the overburden. At Hoe Creek II,

    three separate trials of 2-43 days used reverse combustion with air or oxygen. Water entering the

    burn cavity lowered gas quality, so the pressure was increased to keep water out. However, this

    forced much of the gas out of the cavity away from the production well, and about 20% of the

    gas was lost. Hoe Creek III used directional drilling and reverse combustion over a 47 day test.

    Unfortunately the burn at the lower coal seam target moved into the upper coal seam, a mere 10

    m above, and again nearly 20% of the gas was lost. Eventually subsidence occurred at both Hoe

    Creek II and III.

    Twelve monitoring wells were sampled before, during, and for up to two years aftergasification.

    25Groundwater contamination occurred within seven days of the start of

    gasification. The pressure used in the cavity to try to push water out also pushed out soluble

    22Shafirovich and Varma 2009

    23ibid

    24These compilations are derived from Burton et al 2008, except where noted

    25This section from Campbell et al 1979

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    volatile organics (such as phenols) and other contaminants (like cyanide) into the aquifer above.

    The problem was exacerbated by surface subsidence, which occurred due to the shallow depth of

    the seam and the lack of structural integrity in overlying rock. Toxic organics in residual ash

    dissolved in inflowing water and moved into all three aquifers. Due to the extensive monitoring

    well system and groundwater analysis, the contamination was picked up and monitored.

    Analysis was done for 250 different organic and inorganic compounds, and 70 were detected

    (Appendix D). Testing up to two years after the burns found all contaminants were within 30 m

    of the burn zone, and concentrations decreased very rapidly with distance; many probably sorbed

    to overburden and residual coal layers.

    However, by 1993, the DOE found that contaminants remained in an aquifer 55 m below

    the surface, and had migrated off of the original BLM-owned property the testing was conducted

    on. Contaminants included phenol and benzene (known carcinogens) and other organics known

    to cause kidney and nerve damage; all were small, highly soluble molecules that do not sorb well

    to soils. In 1998, DOE installed 64 air-sparging wells to remediate the site, and another 50 were

    installed in 1999. A variety of remediation technologies were in use as of 2006.

    Much of what we know now came out of this test, and later tests based on these findings.

    This was the first successful use of oxygen/steam injection and a movable injection point. What

    was learned from the subsidence and groundwater contamination became part of the basis for

    site-based risk assessment by today's standards, the site would have been considered as having

    high environmental risk due to the shallow depth of the coal and proximity to aquifers.

    Centralia, WA

    Between 1981 and 1982, the CRIP system was further tested at Centralia, WA for 4 andfor 30 day burns. Different oxygen/steam ratios as well as a propane-silane (SiO4) combination

    were used to ignite the burns, and drilling configurations and slants were tried to examine

    changes in syngas quality. The variations did not change gas quality much. This trial was the

    first real test of the CRIP system, and also tested whether models could predict how cavities

    would grow. Cavity shape and size models were validated by quarrying out the actual burn

    cavities. Quarrying also allowed researchers to examine the products left in the cavitydried

    coal, char, and ash. No subsidence was predicted, and none was observed.

    Rocky Mountain I

    The Rocky Mountain I test in Wyoming November 1987-February 1988 was considered

    the most successful US test to date. The project focused on siting the project to prevent

    groundwater contamination. Significant effort went into pre- and post-burn water, temperature,

    and mineral analysis to determine how the burn changed the underground make-up of the rock

    and water chemistry. The coal seam was 10 m thick and 130 m below ground. The successful

    directional drilling and CRIP processes tested in Centralia were used continuously for several

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    months.26 Negative pressure was used to ensure that water flowed into, not out of, the burn

    cavity, and water that filled the cavity post-burn was pumped to the surface and treated to

    remove underground contamination from dissolution of ash and pyrolysis products, both to

    ensure that no contaminated water remained underground, and also to cool the cavity quickly to

    reduce steam, which can crack the rock above and induce fractures, and reduce transfer of hot

    gases to surrounding rock. No environmental contamination was found by the 19 groundwater

    monitoring wells.

    Research indicated that the heat in rocks surrounding the burn cavity does not dissipate

    quickly, and rocks can still be 4-12oC hotter than normal two years after a burn. Similarly,

    groundwater temperatures did not always rise until several months after gasification ended.27

    The rise in temperature in wells was entered into models to calculate the temperature along

    production lines. Within 1 m of the well, rocks could be 750-1000oC, nearly as high as

    temperatures in the burn zone. This is potentially high enough to cause the rock around the gas

    lines to change and affect the cement-rock seals and could lead to gas leaks. Temperatures

    decreased rapidly with distance from the line: as modeled they would have been 100 oC four

    meters away and within 16 m they were only 4.5 oC higher than background.

    Although the testing was successful and the operators intended to go into commercial

    production of ammonia, the Rocky Mountain UCG site was shut down when cheap oil became

    available.

    El Tremedal

    The El Tremedal site was a joint project of Spain, the UK, and Belgium located in Spain

    and operated 1992-1999. Directional drilling and oxygen injection were used. The tests wereconducted to determine if gasification could be done on deep seams (550 m) while maintaining

    negative cavity pressure to prevent groundwater contamination. A methane explosion damaged

    the injection well and stopped the project, but no environmental contamination was detected by

    the several monitoring wells.28

    Chinchilla29

    The Chinchilla project emerged from testing in the 1980's at the University of

    Newcastle, Australia. It was conducted over 30 months from December 26 1999-April 2003

    using the proprietary Ergo technology and consisted of 9 injection/production wells surroundedby 19 monitoring wells (Figure 5). The coal was 140 m deep and 10 m thick. The test was

    conducted under low temperatures (300 oC) and reverse combustion with air/water injection

    26Clean Air Task Force 2009

    27Gosnald 1998

    28Friedmann et al 2009

    29Information from Shafirovich et al 2008 and from Burton et al 2006

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    (rather than the CRIP technology) was successfully used between vertical wells. Up to 675 tons

    of coal per day was gasified, with 75% total energy recovery. No groundwater or surface water

    contamination was detected, nor was there any subsidence. A gas-to-liquids plant was

    constructed in 2008 at the site, with the intent of using UCG product gas.

    What made this project important was that it validated the concept of keeping the cavityat a pressure less than the surrounding rock to allow groundwater to flow into the cavity and

    keep volatiles from being pushed out; essentially a successful scale-up of the testing done at

    Rocky Mountain.

    Environmental Impacts

    The primary concerns are the potential for uncontrollable fire, sinkholes (subsidence),

    groundwater contamination, and air emissions, including increased greenhouse gases.

    Essentially, the risks can be broken down into: will contaminants dissolve, how much CO2canbe captured and sequestered without leakage, and will any contaminants reach anything

    important?

    Although a literature review has not revealed any instances of uncontrolled fires,

    most projects have been conducted for only a short period of time and little

    information is available regarding the New Zealand pilot in a tectonically

    Figure 5. UCG at Chinchilla, Australia. From Hattingh, L. 2008. Underground Coal Gasification.

    Sasol.

    http://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%

    20GASIFICATION%20%20-%20Lian%20Hattingh.pdf

    http://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%20GASIFICATION%20%20-%20Lian%20Hattingh.pdfhttp://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%20GASIFICATION%20%20-%20Lian%20Hattingh.pdfhttp://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%20GASIFICATION%20%20-%20Lian%20Hattingh.pdfhttp://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%20GASIFICATION%20%20-%20Lian%20Hattingh.pdfhttp://www.sacea.org.za/SeminarsSymposium/Seminar22Aug2008/UNDERGROUND%20COAL%20GASIFICATION%20%20-%20Lian%20Hattingh.pdf
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    complicated area. Current recommendations are that there should be no major

    faulting within 45 m of the proposed gasifier.30 The potential for new faults to

    develop and provide a route for air to reach the coal seam will need to be assessed in

    Beluga.

    Subsidence and groundwater contamination have been issues in past projects whereshallow coal seams were burned; the recommendation now is to use coal seams

    greater than 200 m deep with an impermeable, structurally sound layer above the

    seam and no potable aquifers nearby or within 25 times the height of the coal seam.

    CIRI proposes to use a seam 198 m deep. If an impermeable overburden layer is

    present it also helps prevents product gas from flowing into the surrounding rock,

    improving the quantity of gas retrieved. However, it should be noted that a

    structurally sound layer does not eliminate the risk of subsidence. Any rock

    overlying a burned out cavity could develop fractures.

    About half the mercury, arsenic, sulfur, tars, and particulates produced from burningcoal remain underground. While this reduces air emissions, it is a potential concern

    for groundwater contamination.

    Groundwater can become contaminated with volatile, soluble organics like benzene

    and phenols.31

    Site-specific geologic and hydrologic assessment will need to assess

    whether the aquifers in the area are fresh or saltwater, the potential for connection

    between the coal seam and aquifers, and the potential for the aquifers to reach surface

    water. A connection to surface or tidal water is a serious risk, in that benzene at

    levels safe for humans can cause genetic damage in salmon exposed to it

    consistently.32

    High temperatures in production wells could cause well casings to crack and release

    hot gas;33

    if the well passes through an aquifer this could be a route for

    contamination.

    To gasify coal above ground, the coal must be mined, transport, and put under great

    pressure and heat before it can fuel turbines. The environmental impacts include all the impacts

    of mining (water contamination, methane release, potential subsidence for underground mining,

    human health impacts for miners) as well as air pollution from combustion (CO2, mercury, sulfur

    and nitrogen oxides). By gasifying the coal below ground, many of the mining impacts areeliminated, and groundwater and air pollution become the primary risks.

    30Surey et al 2004, in Burton et al 2006

    31Campbell et al 1979

    32Carls et al 2008

    33Gosnald 1998

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    Structural I ntegri ty of H ost Rock

    Coal will be surrounded by "host rock". In the nearby Chuitna coal fields near the Chuit

    River (less than 100 m deep), the host rock is primarily permeable sandstone saturated in water.

    If the same geologic forces that created this set of conditions also created the coal and host rock

    at the Beluga coal fields (200 m deep), they could also be overlain by a permeable sandstoneaquifer.34 This would increase the risk of a UCG burn contaminating an aquifer, and would be

    important unless the aquifer were saline.

    Tectonic activity can create faults and fractures that allow UCG gas to escape, allow

    water to move in unexpected directions, and provide a route for contaminant transport.35 Not

    only do any current faults need to be assessed, but the potential for high temperature activity to

    cause stresses and fractures and provide new pathways, collapse of the burn cavity, or subsidence

    needs to be assessed.

    Subsidence occurs when coal is removed, leaving a void under the surface. Subsidencedoes not always occur; it was minimal in pilot tests in Centralia, WA and Chinchilla, Australia.

    However, these were pilot projects, and it is not known what would happen in a commercial

    situation where large quantities of coal are removed. Given the remote location, the primary risk

    is the potential to create pathways for contaminants rather than direct risk to habitation.

    Formation of contaminants

    The high temperatures of the burn cause volatile hydrocarbons and some trace metals to

    become gases and carbon in coal and carbonate rocks to release carbon dioxide. These generally

    partition into either the production gas or end up in the residual ash that stays in the cavity after

    the burn is complete. If there is a route to an aquifer, highly soluble off-gassed volatiles like

    phenol can cause persistent water contamination, as can material in ash. Organic compounds

    such as tars, benzene, toluene, phenols, and polycyclic aromatic hydrocarbons (PAH's) will be

    created as heat dries and burns coal. The rocks themselves will change: carbonate rocks will

    release calcium and CO2; mafic rocks will release iron and magnesium, and so forth. Metals

    from rocks will volatilize and move out with production gas, remain in residual ash, and may

    move into pore spaces of surrounding rock. A lining of burn products can be generated around

    the burn cavity.

    There are two periods to consider: during the burn and after the burn. During the burn,

    contaminants are most likely to volatilize and move out with product gases. After the burn,

    contaminants are most likely to become soluble in water and migrate out of the burn cavity as

    normal hydrologic flow re-establishes.

    34Burton et al 2006 Section 5.3.1.2

    35Creedy and Garner 2004, in Burton et al 2006; Gregg 1977 in Burton et al 2006

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    Migration of contaminants

    Very high temperatures (greater than 1000 oC) cause rocks to crack and burn and solid

    metals become gases; also water becomes less dense and less viscous so it moves more easily

    allowing easier transport of contaminants. High temperatures in the production well, carrying the

    gas product, may be high enough to crack the well casing and allow gases to escape

    gases thatcan contain metals and toxic organics. The production of contaminants and their movement is

    entirely different from any other industry, and prediction needs to rely strongly on results from

    pilot tests. Whether contaminants become a risk depends on whether they are able to reach water

    being used by aquatic life or people.

    Just as steam and oxygen, temperature and pressure affect the quality of the UCG product

    gas, they also affect what happens to the unintended byproducts. Burns will be operated at very

    high temperatures in order to shift the reaction to produce methane, and the higher the

    temperature the less byproduct. However, higher temperatures also increase the solubility of

    organics, allowing them to move further in water. High temperatures can thermally drive waterup through the burn cavity roofing, cause cracks or collapse of the burn cavity that allow water to

    migrate out, and cause organics to become soluble in water.36

    Deep UCG projects will need to

    be run at higher pressures to keep the burn going, risking outflow of water from the cavity, but

    are more likely to be far from potable aquifers. High pressure and the buoyant gas forces can

    combine to overcome the pressure surrounding the cavity, resulting in vaporized material

    moving out of the cavity and condensing in the outer rock. If the burn is advancing in that

    direction, the process may repeat.37

    As material is pushed away from the hot cavity, it condenses, absorbs, adsorbs, or in

    other ways reacts to precipitate away from the cavity. Organics and ammonia may sorb to coalor surrounding clay. This material may be encountered as groundwater re-establishes its natural

    flow post-burn.

    After the burn, the normal hydrologic flow will fill the underground chamber and

    dissolve the ash left behind. When it encounters the precipitated or sorbed material outside the

    burn cavity, different reactions may occur. Some material may dissolve; some will be detoxified

    if the groundwater is high in oxygenfor instance, ammonia will become the non-toxic nitrate

    and some may be broken down by aerobic bacteria. The migration of contaminants may be

    irrelevant if the coal was capped by an impermeable layer or no potable aquifer is at risk.

    However, some of the contaminants are toxic to fish, if they are able to reach fish-bearing

    waters: ammonia, high concentrations of calcium or other cations, high concentrations of total

    dissolved solids (TDS commonly mostly sulfate), and low but persistent concentrations of

    36Under room temperature conditions, many organics are not soluble in water, which is why oil forms a sheen on

    water instead of dissolving.37

    Burton et al 2006

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    PAH's. One method of mitigation to prevent harm to drinking water or aquatic life is to pump

    and treat water as it enters the burn chamber until all toxic compounds are below safe levels, as

    was done at Rocky Mountain I. One author has suggested that UCG sites should be at least 1.6

    km from rivers and lakes, and 0.8 km from major faults to prevent groundwater contamination

    conditions that may be difficult to meet at Beluga.38

    CO2

    Carbon dioxide is the defining pollutant of our age endangering entire populations of

    people, plants, and animals through its role in global warming and ocean acidification. Models

    developed by international consensus through the IPCC are proving to have underestimated the

    rise in global temperatures. Feedbacks such as reduced ice cover at the poles (less reflection of

    sunlight, more absorption), release of methane from warming Arctic tundra,39and positive

    biological feedback mechanisms such as vast stretches of dying trees in the Pacific Northwest

    (due to increases in beetle kills because winter temperatures no longer kill the beetles) and no

    longer removing CO2may account for the unexpectedly rapid temperature increase. Ocean pH is

    dropping, Arctic ice is melting, and permafrost is thawing at rates much faster than predicted,

    and there has been increased drought in Australia, the US, Africa, and the Middle East; increased

    flooding; eroding beaches in Hawaii and villages in Alaska; and more. The measured physical

    observations indicating the fast rate of global warming, the human face of it, and the likely fiscal

    impacts on individual gas emitters make it an imperative to consider greenhouse gas emissions in

    any large scale project.

    L ife cycle greenhouse gas emissions

    Carbon dioxide will be produced from the UCG process as the raw gas exits the

    production well and also when methane is combusted in the power plant if a methane/hydrogen

    mixture is used. All carbon products become CO2during combustionif the product gas

    entering the power plant contains CO2, CO, and methane, all of these will exit the stack as CO2.

    If CO2and CO are removed during a "cleanup" or carbon capture process, only the methane will

    be converted to CO2in the stack.

    Although no studies could be found that analyzed the life cycle greenhouse gas emissions

    of syngas made through the UCG process, analysis has been done comparing coal, syngas,

    natural gas, and liquefied natural gas both with and without mitigation technologies (Figure 6).

    40

    The study notes that natural gas is one of the largest sources of greenhouse gas emissions in the

    38Bowen, BH. A review and future of UCG. Powerpoint.

    http://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-

    08.pdf39

    Methane is a greenhouse gas more than 20 times as potent as CO240

    Jaramillo et al 2007

    http://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-08.pdfhttp://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-08.pdfhttp://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-08.pdfhttp://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-08.pdfhttp://www.purdue.edu/discoverypark/energy/events/cctr_meetings_dec_2008/presentations/Bowen-12-11-08.pdf
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    US when processing, transmission, and combustion are included, producing about 800 lbs of

    CO2-equivalents per MWh, or an estimated 250 lbs if CCS could be incorporated. But this is

    less than traditional pulverized coal plants, which produce about 1800 lbs of CO 2-equivalents per

    MWh, or an estimated 400 lbs if CCS could be utilized. UCG product gas is likely to be similar

    to natural gas in the combustion, processing, and transmission components, although it will

    require extra release of CO2for air compression or making oxygen; it will be significantly lower

    than traditional above-ground gasification CO2releases in that no coal mining, processing, or

    transportation are required, nor is energy required for the gasification process as in above-ground

    facilities.

    While UCG combined with carbon capture is likely to produce much lower greenhouse

    gas emissions than a traditional natural gas plant, it is not a zero-emissions technology. In 2001,

    the Beluga plant supplied 300,000 MWh of electricity.41 If UCG with CCS fueled a similar

    amount of electricity, it would generate at least 375,000 tons of CO2-equivalent annually if the

    estimates of about 250 lbs of CO2per MWh are correct.

    41ISER 2003

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    electricity is estimated to be 35-70% higher for a natural gas combined cycle plant, such as is

    used at Beluga, if CO2capture is installed.43 Pre-combustion technology itself (Selexol) costs

    about $25/ton CO2captured.44

    Carbon sequestration

    The locations where CO2is removed from natural gas are in the southern US, where

    pipelines transport the CO2to declining oil fields. Geologic sequestration has been discussed

    and theorized, but rarely implemented. The only commercial-sized long term sequestration of

    CO2outside of enhanced oil recovery is at the Sleipner, Norway natural gas production platform,

    where CO2has been injected into saline aquifers 1000 m beneath the ocean floor since 1996.

    This project has been driven by Norway's high carbon tax, $55/ton CO2in 1991 (the equivalent

    of over $100,000 per day for Sleipner). Drilling the injection well and installing a compressor

    added $100 million to the project; adding scrubbers to remove CO2and monitoring equipment

    were additional expenses.

    While Sleipner has been successful, not all projects have gone smoothly.

    Norway's Snohvit natural gas platform has had significant technological problems

    with storing CO2. The CO2freezes at temperatures required to make LNG,

    blocking the LNG transport pipe. The plant was shut down twice in 2008 and

    again in 2009.45

    Pilot projects that injected CO2into rock formations to make solid carbonate

    rocks instead caused carbonic acid to form, and the acid dissolved the rock cavity

    intended to contain it. The process stopped when neutralizing rock was

    encountered.46

    Injecting CO2into basalt rock to make mineral carbonates failed

    when the rock swelled and plugged the underground pore spaces.47

    CO2captured at a power plant in Wisconsin (as a demonstration project) did not

    store the CO2because the geology under the plant was not favorable.48

    Currently there has not been enough test-drilling to determine if the geology at the

    Beluga coal fields would support sequestration. CIRI has suggested injecting the CO2into

    declining natural gas or oil fields, but currently no producers have showed interest in the idea. A

    report from the National Energy Technology Lab suggests that sequestration can only be done as

    43Thambimuthu 2005 in Burton et al 2006

    44Burton et al 2006

    45Hurst 2008 andhttp://www.pr-inside.com/golar-lng-q2-2009-results-r1456514.htm

    46Kharaka et al 2006

    47Sturmer et al 2007

    48http://www.scientificamerican.com/article.cfm?id=first-look-at-carbon-capture-and-storage

    http://www.pr-inside.com/golar-lng-q2-2009-results-r1456514.htmhttp://www.pr-inside.com/golar-lng-q2-2009-results-r1456514.htmhttp://www.pr-inside.com/golar-lng-q2-2009-results-r1456514.htmhttp://www.scientificamerican.com/article.cfm?id=first-look-at-carbon-capture-and-storagehttp://www.scientificamerican.com/article.cfm?id=first-look-at-carbon-capture-and-storagehttp://www.scientificamerican.com/article.cfm?id=first-look-at-carbon-capture-and-storagehttp://www.pr-inside.com/golar-lng-q2-2009-results-r1456514.htm
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    EOR or as saline aquifer injections in the Beluga area, and that both are likely to be cost-

    prohibitive.49

    CIRI has discussed geologic sequestration of CO2,50

    although they have not shown how

    this would be economically feasible. It is likely that storing the CO2in depleted underground

    burn chambers will be considered; it is possible the capacity will be available, and injecting CO2

    into residual coal causes swelling that would plug fractures and migrating CO2would tend to

    adsorb to coal and not move far.

    However, at Beluga the burn cavities are only expected to be 200 m below the surface,

    and CO2storage should be at least 800-1000 m below the surface to maintain CO2in a dense

    supercritical state. Nevertheless, the CO2is still likely to be less dense than water, and will be

    "buoyed" up to the top of a caprock layer, making it important for the caprock to remain

    impermeable in perpetuity.51 This may be particularly important in a seismically active area

    such as Beluga.

    The heat and steam may cause the rock around the cavity to be quite different

    than pre-burn, potentially initiating cracks, fractures, and section collapses.

    Volatile organics (benzene, etc) left behind in the cavity dissolve easily in CO2

    and will be carried upwards by CO2if the rock above the cavity is permeable.

    CO2forms carbonic acid as it dissolves in water and may form sulfuric acid on

    contact with coal and ash. These acids lower the pH of groundwater and

    potentially allow metals in surrounding rock to dissolve and migrate in a plume

    along the groundwater pathway.

    The act of injecting CO2will also create changes in temperature, pressure, pH, rock-water

    chemistry, and gas-water chemistry. If injected too quickly after a burn, the CO2could boil,

    increasing the pressure in the cavity. If injected with too much pressure, the water that has filled

    the cavity and dissolved volatile organics and ash material could be flushed out or fractures

    could be created. CO2that dissolves decreases water pH, and CO2that does not dissolve can

    push up on the cavity, putting pressure on it.

    Should CO2migrate up and out of the geologic storage location, it is likely to kill plants

    and ground-dwelling animals at the discharge location. Slow, non-catastrophic natural leaks of

    49Chaney and van Bibber 2006 Chapter 2

    50CIRI's Coal Development plans presentation to the Alaska Bar Association Environmental Law/Natural Resource

    Law Section Nov 9 200951

    Keith et al 2005

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    CO2continue to kill forests in the Sierra Mountains in California, and very large discharges from

    natural sources have in the past asphyxiated plants, humans, and animals.52

    This means that it is not feasible to safely remove product gas then use the same wells to

    pump CO2back down into the burned out coal seams at the proposed Beluga project. At the very

    least, injection wells will need to be drilled much further down, and the geology will need to be

    favorable both for safe UCG reactions at the proposed 200 m coal seam level and the 800+ m

    CO2storage level. The seismic analysis during the feasibility period of the project will be

    critical to determine whether there is a risk of air entering the coal seam during the burn, and

    further analysis post-burn may be required to determine the risk of CO2leaks from deep storage

    locations if earthquakes open new faults.

    In the feasibility studies for the UCG project, the true feasibility and costs of carbon

    capture from both the product well gas and the power plant need to be presented, along with the

    feasibility, costs, and risks of geologic storage.

    Summary

    The CIRI Beluga UCG project proposes to take components of two emerging

    technologies and join them together. This will require scrutiny of both components. The UCG

    component has been conducted successfully in pilot scale tests around the world; the one long-

    term plant in existence (Angren, Uzbekistan) does not have environmental information readily

    available. The operators will need to satisfy both the requirements of producing high quality gas

    and the requirements of maintaining environmental integrity. Given the proximity of the

    proposed project to the Beluga River, Cook Inlet tidelands, and the Castle Mountain Fault, it is

    particularly important to examine the hydrogeologic and geophysical details to ensure

    Geologic conditions that preventing subsidence

    o At least 200 m below ground

    o Structural integrity of host rock

    o Geophysical modeling of temperature/pressure stresses on fractures

    Siting to prevent contaminant migration

    o Impermeable caprock

    o a distance at least 25 times the depth of the coal seam between the seam and

    aquifer

    o a minimum of 1.6 km from rivers and lakes

    o a minimum of 0.8 km from major faults

    52Wilson et al 2003

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    o seams should be thick and widely separatedto prevent burn-through between

    seams

    In addition to the conditions that must be satisfied for coal gasification, conditions also must

    allow for carbon capture and sequestration. No UCG projects currently capture and sequester

    carbon. Separating CO2and transporting it to an appropriate declining oil field will require extrafinancing and negotiations with Cook Inlet oil and gas companies. If the CO2is to be injected

    back into the coal fields, injection wells at least 800 m deepfar deeper than the 200 m deep

    target coal seamwill need to be drilled and the geologic conditions at that depth will need to be

    sufficient to entrain the CO2for thousands of years.

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    Gosnald, WD. 1998.Postgasification thermal regime of the Rocky Mountain I underground coal gasification test

    site. Gas Research Institute and US Department of Energy. Washington, DC.

    http://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/Beluga%20Coal%20Gasif%20Feasibility%20Study9_15_06.pdfhttp://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/Beluga%20Coal%20Gasif%20Feasibility%20Study9_15_06.pdfhttp://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/Beluga%20Coal%20Gasif%20Feasibility%20Study9_15_06.pdfhttp://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/Beluga%20Coal%20Gasif%20Feasibility%20Study9_15_06.pdfhttp://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/Beluga%20Coal%20Gasif%20Feasibility%20Study9_15_06.pdf
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    Gregg, DW. 1977.Ground subsidence resulting from underground coal gasification. Lawrence Livermore National

    Laboratories. UCRL-52255. Livermore, CA.

    Hurst, S. 2008. Snohvit CO2 storage underway. Petroleum News Vol 13 (21). May 25.

    Institute of Social and Economic Research. 2003.Alaska electric power statistics 1960-2001. University of Alaska

    Anchorage for Alaska Energy Authority. Anchorage, AK.

    Jaramillo, P, WM Griffin, and HS Matthews. 2007. Comparative life-cycle air emissions of coal, domestic natural

    gas, LNG and SNG for electricity generation.Environ Sci and Technol 41:6290-6296.

    Keith, DW, JA Giardina, MG Morgan, and EJ Wilson. 2005. Regulating the underground injection of CO2. Environ

    Sci and Technol, pp. 499A-507A.

    Kharaka, YK, DR Cole, SD Hovorka, WD Gunter, KG Knauss, and BM Freifield. 2006. Gas-water interactions in Frio

    Formation following CO2injection: implications for the storage of greenhouse gases in sedimentary basins.

    Geology 34 (7): 577-580.

    Maev, S. 2008. Development of a UCG based project in Canada. Twenty-fifth annual international Pittsburgh coalconference. Paper 32-6. Pittsburgh, PA.

    Rogut, J. 2008. Hydrogen Oriented Underground Coal Gasification.Twenty-Fifth Annual International Pittsburgh

    Coal Conference. Paper 20-3. Pittsburgh, PA

    Shafirovich, E and A Varma. 2009. UCG: a brief review of current status. Ind Eng Chem Res Vol 48: 7865-7875.

    Shafirovich, E, M Mastalarz, J Rupp and A Varma. 2008.Potential for UCG in Indiana: Phase I report to the Indiana

    Center for Coal Technology Research. Purdue University, Indiana.

    Simbeck, D. 2002. Carbon separation and capture from energy systems: the forms and costs of separation and

    capture. Complements to Kyoto: technologies for controlling CO2emissions. National Academy of Engineering.Washington, DC.

    Sturmer, DM, DD LaPointe, JG Price, and RH Hess. 2007. Assessment of the potential for carbon dioxide

    sequestration by reactions with rocks in Nevada. Nevada Bureau of Mines and Geology Report 52. University of

    Nevada, Reno.

    Thambimuthu, K et al. 2005.IPCC special report on carbon dioxide capture and storage, Chapter 3. International

    Panel on Climate Change, 2005.

    Walter, K. 2007. Fire in the Hole. Sci Tech Rev, pp. 12-18.

    Wilson, EJ, TL Johnson, and DW Keith. 2003. Regulating the ultimate sink: managing the risks of geologic CO2storage. Env Sci Technol 37: 3476-3483.

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    Appendix A: UCG reactions and Syngas Reactions

    The table below lists the primary reactions found in producing syngas (SNG) or UCG product gas (UCG). The most important

    reaction for both is Step 1, the actual transformation of coal into gases. Other reactions either provide the heat to drive the desired

    reaction (burning coal) or are reactions to produce a desired product (methane, etc). Adapted from Burton et al 2006, Table 4-1.

    Step Reaction Name Chemical reaction Chemical equation UCG SNG Notes

    1

    Gasification

    reaction (Water-

    Gas Shift reaction)

    Carbon + waterhydrogen and carbon monoxide

    C + H2OH2+ CO x x

    main reaction; makeshydrogen for combustion

    requires heat from steps

    5,6

    2 Shift conversionCarbon monoxide + waterhydrogen and carbon dioxide

    CO + H2OH2+ CO2 x xreact CO to make more

    hydrogen

    3 MethanationCarbon monoxide and hydrogenmethane and water

    CO + 3 H2CH4+ H2Oside

    reaction

    increase methane conten

    of gas; to make hydrogen

    from natural gas, reverse

    the reactions

    4Hydrogenating

    gasification

    Carbon + hydrogenmethane

    C + 2H2CH4side

    reaction

    increase methane conten

    of gas

    5

    Partial oxidation

    (incomplete

    combustion of coal)

    Carbon + oxygen

    carbon monoxide

    C + O2CO xreleases heat to drive ste

    1

    6

    Oxidation

    (complete

    combustion of coal)

    Carbon + oxygencarbon dioxide

    C + O2CO2 x xreleases heat to drive ste

    1

    7 Boudouard reactionCarbon + carbon dioxidecarbon monoxide

    C + CO22COside

    reaction

    requires heat, provides CO

    for steps 2,3

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    Appendix B: Natural Gas Processing

    fromhttp://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdf

    http://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdfhttp://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdfhttp://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdfhttp://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdf
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    Appendix C: UCG sites worldwide

    (all tables are from Burton et al 2006)

    International experiments, not including the US or the Former Soviet Union

    Dates

    Place (Test

    Name)

    Dur -

    ation

    (days)

    Coal

    Gas-

    ified

    (tons)

    Feed

    gas

    Coal

    Seam

    Depth

    (m)

    Auspices/

    Comments Original Reference

    1982-1985

    Thulin,Belgium

    12 4

    air;mixof N2,O2,CO2

    860

    Institut pour leDevelopment dela GazeificationSouterraine,Belgium

    Chandelle, V, 1986, OverviewAbout Thulin Field Test,Proceedings of the TwelfthAnnual Underground CoalGasification Symposium,DOE/FE/60922-H1.

    1983-1984

    Initially atBruay enArtois, andlater at LaHauteDeule,France

    75

    0.3 1stphase

    1.5next

    phase

    N2,O2,CO2

    880

    Groupe d'Etudede laGazeificationSouterraine,France(Production wellplugged byparticulates andtar, terminatingthe tests)

    Gadelle, C., et al., 1985, Statusof French UCG Field Test at LaHaute Deule, Proceedings ofthe Eleventh AnnualUnderground Coal GasificationSymposium, DOE/METC-85/6028 (DE85013720).

    1992-1999

    Province ofTeruel, NESpain (ElTremedal)

    550

    Spain, UK,

    Belgium,Supported by theEuropeanCommission,used CRIP

    www.coal-ucg.com/currentdevelopments2.html

    1980-present

    China, 16separatetrails *

    UCG centre atChina Univ. ofMining andTechnology,Beijing.

    1990 -present

    Chinchilla,

    Queensland,Australia

    1994Huntley,NewZealand

    with US technicalassistance

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    Experiments in the Former Soviet Union

    Dates

    Place (Test

    Name)

    Dur -

    ation

    (days)

    Coal Gas-

    ified (tons)

    Coal

    seam

    Thickness

    (m)

    Coal

    Seam

    Depth

    (m)

    Auspices/

    Comments

    Original

    Reference

    1959-1976Shatsk, MoscowBasin (ShatskayaUCG 1)

    17 262,0302 to 4,

    average1.9

    30 to60,avg40

    Flat bed

    Olness,Dolores, "TheShatskaya UCGStation",UCRL-53229,1981

    1941-1946

    Tula, MoscowBasin(PodmoskovnayaUCG 1)

    5

    Phase 2 wassmall-scalecommercialoperation; flat bed

    Olness,Dolores, "ThePodmoskovnayaUCG Station",UCRL-53144,1981

    1946-1963

    Tula, MoscowBasin(PodmoskovnayaUCG 2)

    171,647,800

    (from 1950to 1960)

    1 to 5 50

    Phase 1 R&D;110 boreholesdrilled, 61 links(1588 m) usingcounter-currentcombustion; flatbed; shut down1963, partly dueto coalexhaustion;production peaked

    at 2 billion m3/yr(0.85 million tons)

    Olness,Dolores, "ThePodmoskovnayaUCG Station",UCRL-53144,1981

    productionstopped in1977

    Donets coalbasin(Lisichansk)

    831,604(from 1950to 1960)

    Steeply dippingbeds; shut downin 1964, partiallydue to coal sourceexhaustion

    Stephens et al.,"UndergroundCoal Gasification:Status andProposedProgram",UCRL-53572,1984; Olness, DUCRL-50026-80-1

    Siberia (Yuzhno-Abinsk)

    1,735,112

    (sporadicdata oroperation,from 1955 to1977)

    Steeply dippingbeds

    Stephens et al.,"UndergroundCoal Gasification:

    Status andProposedProgram",UCRL-53572,1984; Olness, DUCRL-50026-80-1

    1955 topresent

    Tashkent,Uzbekistan(Angren)

    50 1,040,060 24 250Flat bed; stilloperating

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    Experiments in the US

    Dates

    Place (Test

    Name)

    Dur-

    ation

    (days)

    Coal

    Gasi-

    fied

    (tons)

    Feed

    Gas

    Coal

    Seam

    Depth

    (m) Auspices Original Reference

    1947 -1960

    Gorgas,Alabama, US

    US Bureau ofMines

    Stephens, D.R., R. W.Hill, and I. Y. Borg,1985, Underground CoalGasificationReview. LawrenceLivermore NationalLaboratory, Livermore,CA UCRL-92068.

    1976

    Hoe Creek,Wyoming,USA (HoeCreek I)

    11 123 air LLNL/USDOE

    Stephens, D.R., R. W.Hill, and I. Y. Borg,

    1985, Underground CoalGasificationReview. LawrenceLivermore NationalLaboratory, Livermore,CA UCRL-92068.

    Wang, F.T., Mead, S.W.and Stuermer, D.H.,1982c, Mechanisms forgroundwatercontamination by UCGpreliminaryconclusions from the

    Hoe Creek study,Proceedingsof the EighthUnderground CoalConversion Symposium.

    1977

    Hoe Creek,Wyoming,

    USA (HoeCreek IIair-1)

    13 286 air LLNL/USDOE

    1977

    Hoe Creek,Wyoming,USA (HoeCreek II-O2)

    2 47Oxy-gen

    LLNL/USDOE

    1977

    Hoe Creek,Wyoming,USA (HoeCreek II-air -2)

    43 1155 air LLNL/USDOE

    1979Hoe Creek,Wyoming,USA (HoeCreek III-air)

    7 256 air LLNL/USDOE

    1979

    Hoe Creek,Wyoming,USA (HoeCreek III-O2)

    47 3251Oxy-gen/

    steamLLNL/USDOE

    1981-1982

    Centralia,Washington(Centralia-LBK-O2)

    20 140Oxy-gen/

    steam

    LLNL/GasResearchInstitute/USDOE

    Stephens, D.R., R. W.Hill, and I. Y. Borg,1985, Underground CoalGasificationReview. LawrenceLivermore NationalLaboratory, Livermore,CA UCRL-92068.

    1981-1982

    Centralia,Washington(CentraliaLBK-air)

    Un-known

    Un-known

    airLLNL/GasResearchInstitute/USDOE

    1983

    Centralia,Washington(CentraliaCRIP-O2)

    28 2000Oxy-gen/

    steam

    LLNL/GasResearcInstitute/USDOE

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    Experiments in the US, continued

    Dates

    Place (Test

    Name)

    Dur-

    ation

    (days)

    Coal

    Gasified

    (tons)

    Feed

    Gas

    Coal

    Seam

    Depth

    (m) Auspices

    Original

    Reference

    1973-1974

    Hanna, Wyoming(LETC-1)

    168 2720 airLaramie EnergyTechnologyCenter/USDOE

    Stephens, D.R., R.

    W. Hill, and I. Y.Borg, 1985,Underground CoalGasificationReview. LawrenceLivermore

    NationalLaboratory,Livermore, CAUCRL-92068.

    1975Hanna, Wyoming(LETC-II-1A)

    37 962Laramie EnergyTechnologyCenter/USDOE

    1975Hanna, Wyoming(LETC-II-1B)

    38 780Laramie EnergyTechnologyCenter/USDOE

    1976Hanna, Wyoming(LETC-II-II)

    26 2201Laramie EnergyTechnologyCenter/USDOE

    1976Hanna, Wyoming(LETC-II-III)

    39 3414Laramie EnergyTechnologyCenter/USDOE

    1977Hanna, Wyoming(LETC-III)

    38 2663Laramie EnergyTechnologyCenter/USDOE

    1978Hanna, Wyoming(LETC-IV-A(a))

    7 294Laramie EnergyTechnologyCenter/USDOE

    1978Hanna, Wyoming

    LETC-IV-A(b)48 3184

    Laramie EnergyTechnologyCenter/USDOE

    1977Hanna, Wyoming(LETC-III)

    38 2663Laramie EnergyTechnologyCenter/USDOE

    1978Hanna, Wyoming(LETC-IV-A(a))

    7 294Laramie EnergyTechnologyCenter/USDOE

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    Experiments in the US, continued

    Dates

    Place (Test

    Name)

    Dur-

    ation

    (days)

    Coal

    Gasified

    (tons)

    Feed

    Gas

    Coal

    Seam

    Depth

    (m) Auspices

    Original

    Reference

    1977Hanna,Wyoming(LETC-III)

    38 2,663Laramie EnergyTechnologyCenter/USDOE

    Stephens, D.R.,R. W. Hill, andI. Y. Borg,1985,UndergroundCoalGasificationReview.LawrenceLivermore

    NationalLaboratory,Livermore, CAUCRL-92068.

    1978Hanna,Wyoming(LETC-IV-A(a))

    7 294Laramie EnergyTechnologyCenter/USDOE

    1978Hanna,WyomingLETC-IV-A(b)

    48 3,184Laramie EnergyTechnologyCenter/USDOE

    1979Hanna,Wyoming

    LETC-IV-B(a)

    7 468Laramie EnergyTechnology

    Center/USDOE

    1979Hanna,Wyoming (LTC-IV-B(b))

    16 663Laramie EnergyTechnologyCenter/USDOE

    1979Princetown, W.Virginia(METC-1)

    17 234Morgantown EnergyTechnologyCenter/USDOE

    1979

    Rawlins, CarbonCounty,Wyoming(GRD-I-air)

    30 1,207 airGulf Research andDevelopmentCompany/USDOE

    1979

    Rawlins, CarbonCounty,Wyoming(GRD-I-O2)

    5 125Oxy-gen

    Gulf Research andDevelopmentCompany/USDOE

    1979

    Rawlins, CarbonCounty,Wyoming(GRD-I-O2)

    5 125Oxy-gen

    Gulf Research andDevelopmentCompany/USDOE

    1981

    Rawlins, CarbonCounty,Wyoming(GRD-II-O2)

    66 8,550Oxy-gen

    Gulf Research andDevelopmentCompany/USDOE

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    Experiments in the US, continued

    Dates

    Place (Test

    Name)

    Duration

    (days)

    Coal

    Gasified

    (tons) Feed Gas

    Coal

    Seam

    Depth

    (m) Auspices

    Original

    Reference

    1976Fairfield,Texas (BRI-I)

    26Basic Resources,Inc. (privatelyfunded)

    Stephens, D.R.,R. W. Hill, and I.Y. Borg, 1985,Underground

    Coal GasificationReview.LawrenceLivermore

    NationalLaboratory,Livermore, CAUCRL-92068.

    1978-1979

    TennesseeColony, Texas(BRI-IIa)

    197 4500 airBasic Resources,Inc. (privatelyfunded)

    1978-1979

    TennesseeColony, Texas(BRI-IIb)

    10 212 OxygenBasic Resources,Inc. (privatelyfunded)

    1978

    RenoJunction,Wyoming

    (ARCO-I)

    60 3600Atlantic RichfieldCompany

    (privately funded)

    1977CollegeStation, Texas(TAM-I)

    1 2

    Texas A&MUniversityIndustrialConsortium(privately funded)

    1979BastropCounty, Texas(TAM-II)

    2 Unknown

    Texas A&MUniversityIndustrialConsortium(privately funded)

    1980

    Bastrop

    County, Texas(TAM-III)

    Un-known Unknown

    Texas A&MUniversity

    IndustrialConsortium(privately funded)

    1987-1988

    Hanna,Wyoming(Rocky Mt.)(RM1-ELW)(extended linkwell)

    40 4,100 Oxygen/steam 10Gas ResearchInstitute andMETC (USDOE)

    GRI ReportGRI-90/008;Thorsness, C.B.,and Britten, J.A.,1989, LawrenceLivermore

    NationalLaboratoryUndergroundCoal GasificationProject: Final

    Report.LawrenceLivermore

    NationalLaboratory,Livermore, CA.UCRL-21853.

    1987-1988

    Hanna,

    Wyoming(Rocky Mt.)(CRIP-ELW)

    93 11,400 Oxygen/steam 10Gas ResearchInstitute andMETC (USDOE)

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    Appendix D: Water Analysis at Contaminated UCG Sites

    Groundwater Quality UCG Hoe Creek I, from Campbell et al 1979

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    Water analysis in the burn cavity before and after a UCG burn at a small Texas site, from

    Humenick, MJ and CF Mattox. 1977. Groundwater pollutants from underground coal

    gasification. Wat Research 12: 463-469