Showing posts with label Coal Gasification. Show all posts
Showing posts with label Coal Gasification. Show all posts

Environmental Effects of Coal Gasification

Environmental Effects of Coal Gasification: From its original development until the wide-scale adoption of natural gas, more than 50,000 manufactured gas plants were in existence in the United States alone. The process of manufacturing gas usually produced a number of by-products that contaminated the soil and groundwater in and around the manufacturing plant, so many former town gas plants are a serious environmental concern, and cleanup and remediation costs are often high. Manufactured gas plants (MGPs) were typically sited near or adjacent to waterways that were used to transport in coal and for the discharge of wastewater contaminated with tar, ammonia and/or drip oils, as well as outright waste tars and tar-water emulsions.

In the earliest days of MGP operations, coal tar was considered a waste and often disposed into the environment in and around the plant locations. While uses for coal tar developed by the late-19th century, the market for tar varied and plants that could not sell tar at a given time could store tar for future use, attempt to burn it as fuel for the boilers, or dump the tar as waste. Commonly, waste tars were disposed of in old gas holders, adits or even mine shafts (if present). Over time, the waste tars degrade with phenols, benzene (and other mono-aromatics – BTEX) and polycyclic aromatic hydrocarbons released as pollutant plumes that can escape into the surrounding environment. Other wastes included "blue billy", which is a ferroferricyanide compound—the blue colour is from Prussian blue, which was commercially used as a dye. Blue billy is typically a granular material and was sometimes sold locally with the strap line "guaranteed weed free drives". The presence of blue billy can give gas works waste a characteristic musty/bitter almonds or marzipan smell which is associated with cyanide gas.

The shift to the CWG process initially resulted in a reduced output of water gas tar as compared to the volume of coal tars. The advent of automobiles reduced the availability of naphtha for carburetion oil, as that fraction was desirable as motor fuel. MGPs that shifted to heavier grades of oil often experienced problems with the production of tar-water emulsions, which were difficult, time consuming, and costly to break. (The cause of tar-water emulsions is complex and was related to several factors, including free carbon in the carburetion oil and the substitution of bituminous coal as a feedstock instead of coke.) The production of large volumes of tar-water emulsions quickly filled up available storage capacity at MGPs and plant management often dumped the emulsions in pits, from which they may or may not have been later reclaimed. Even if the emulsions were reclaimed, the environmental damage from placing tars in unlined pits remained. The dumping of emulsions (and other tarry residues such as tar sludges, tank bottoms, and off-spec tars) into the soil and waters around MGPs is a significant factor in the pollution found at FMGPs today.

Commonly associated with former manufactured gas plants (known as "FMGPs" in environmental remediation) are contaminants including:

  • BTEX
    • Diffused out from deposits of coal/gas tars
    • Leaks of carburetting oil/light oil
    • Leaks from drip pots, that collected condensible hydrocarbons from the gas
  • Coal tar waste/sludge
    • Typically found in sumps of gas holders/decanting ponds.
    • Coal tar sludge has no resale value and so was always dumped.
  • Volatile organic compounds
  • Polycyclic aromatic hydrocarbons (PAHs)
    • Present in coal tar, gas tar, and pitch at significant concentrations.
  • Heavy metals
    • Leaded solder for gas mains, lead piping, coal ashes.
  • Cyanide
    • Purifier waste has large amounts of complex ferrocyanides in it.
  • Lampblack
    • Only found where crude oil was used as gasification feedstock.
  • Tar emulsions

Coal tar and coal tar sludges are frequently denser than water and are present in the environment as a dense non-aqueous phase liquid.

In the UK, former gasworks have commonly been developed over for residential and other uses (including the Millennium Dome), being seen as prime developable land in the confines of city boundaries. Situations such as these are now lead to problems associated with planning and the Contaminated Land Regime and have recently been debated in the House of Commons.

The more modern coal gasification processes (circa 1970 to 2006) also have environmental problems requiring various available technologies for mitigation.

UCG Environmental and Social Impacts

Underground Coal Gasification Environmental and Social Impacts

Eliminating mining eliminates mine safety issues. Compared to traditional coal mining and processing the underground coal gasification eliminates surface damage and solid waste discharge, and reduces sulfur dioxide (SO2) and nitrogen oxide (NOx) emissions. For comparison, the ash content of UCG syngas is estimated to be approximately 10 mg/m³ compared to smoke from traditional coal burning where ash content may be up to 70 mg/m³. However, UCG operations cannot be controlled as precisely as surface gasifiers. Variable include the rate of water influx, the distribution of reactants in the gasification zone, and the growth rate of the cavity. These can only be estimated from temperature measurements, and analyzing product gas quality and quantity.

Subsidence is a common issue with all forms of extractive industry. While UCG leaves the ash behind in the cavity, the depth of the void left after UCG is typically more than other methods of coal extraction.

Underground combustion produces NOx and SO2 and lowers emissions, including acid rain. The process has advantages for geologic carbon storage. Combining UCG with CCS technology allows re-injecting some of the CO2 on-site into the highly permeable rock created during the burning process, i.e. where the coal used to be. Contaminants such as ammonia and hydrogen sulfide can be removed from product gas at a relatively low cost.

Aquifer contamination is a potential environmental concerns. Organic and often toxic materials (such as phenol) remain in the underground chamber after gasification and therefore are likely to leach into ground water, absent appropriate site selection. Phenol leachate is the most significant environmental hazard due to its high water solubility and high reactiveness to gasification. Livermore conducted a burn at Hoe Creek, Wyoming, producing operating pressure in the burn cavity greater than the surrounding rock, forcing contaminants (including the carcinogen benzene) into potable groundwater. However, some research has shown that the persistence of such substances in the water is short and that ground water recovers within two years

Underground Coal Gasification

Underground coal gasification (UCG) is an industrial process, which converts coal into product gas. UCG is an in-situ gasification process carried out in non-mined coal seams using injection of oxidants, and bringing the product gas to surface through production wells drilled from the surface. The product gas could to be used as a chemical feedstock or as fuel for power generation. The technique can be applied to resources that are otherwise unprofitable or technically complicated to extract by traditional mining methods and it also offers an alternative to conventional coal mining methods for some resources.

Process of Underground Coal Gasification

Underground coal gasification converts coal to gas while still in the coal seam (in-situ). Gas is produced and extracted through wells drilled into the unmined coal–seam. Injection wells are used to supply the oxidants (air, oxygen, or steam) to ignite and fuel the underground combustion process. Separate production wells are used to bring the product gas to surface. The high pressure combustion is conducted at temperature of 700–900 °C (1290–1650 °F), but it may reach up to 1,500 °C (2,730 °F). The process decomposes coal and generates carbon dioxide (CO2), hydrogen (ḥ), carbon monoxide (CO) and small quantities of methane (CH4) and hydrogen sulfide(H2S). As the coal face burns and the immediate area is depleted, the oxidants injected are controlled by the operator.

As coal varies considerably in its resistance to flow, depending on its age, composition and geological history, the natural permeability of the coal to transport the gas is generally not adequate. For high pressure break-up of the coal, hydro-fracturing, electric-linkage, and reverse combustion may be used in varying degrees.

Two methods are commercially available. One uses vertical wells and a method of reverse combustion to open internal pathways in the coal. The process was used in the Soviet Union and was later modified by Ergo Exergy. It was tested in Chinchilla site in 1998–2003. Livermore developed another method that creates dedicated inseam boreholes, using drilling and completion technology adapted from oil and gas production. It has a movable injection point known as CRIP (controlled retraction injection point) and generally uses oxygen or enriched air for gasification.

According to the Commonwealth Scientific and Industrial Research Organisation the following coal seam characteristics are most suitable for the underground coal gasification:

  • Depth of 100–600 metres (330–2,000 ft)
  • Thickness more than 5 metres (16 ft)
  • Ash content less than 60%
  • Minimal discontinuities
  • No nearby aquifers (to avoid polluting supplies of drinking water).


Coal Gasification

Coal gasification is the process of producing coal gas, a type of syngas–a mixture of carbon monoxide (CO) and hydrogen (H2) gas–from coal. Carbon monoxide, which is a combustible gas, was traditionally used as a source of energy for municipal lighting and heat before the advent of industrial-scale production of natural gas, while the hydrogen obtained from gasification can be used for various purposes such as making ammonia, powering a hydrogen economy, or upgrading fossil fuels. Alternatively, the coal gas (also known as "town gas") can be converted into transportation fuels such as gasoline and diesel through additional treatment via the Fischer-Tropsch process. This latter purpose of coal gasification has been implemented by nations that have abundant sources of coal but little to no petroleum reserves, as well as by nations seeking to decrease their dependence on foreign sources of petroleum.

During gasification, the coal is blown through with oxygen and steam (water vapor) while also being heated (and in some cases pressurized). If the coal is heated by external heat sources the process is called "allothermal", while "autothermal" process assumes heating of the coal via exothermal chemical reactions occurring inside the gasifier itself. It is essential that the oxidizer supplied is insufficient for complete oxidizing (combustion) of the fuel. During the reactions mentioned, oxygen and water molecules oxidize the coal and produce a gaseous mixture of carbon dioxide (CO2), carbon monoxide (CO), water vapour (H2O), and molecular hydrogen (H2). (Some by-products like tar, phenols, etc. are also possible end products, depending on the specific gasification technology utilized.) This process has been conducted in-situ within natural coal seams (referred to as underground coal gasification) and in coal refineries. The desired end product is usually syngas (i.e., a combination of H2 + CO), but the produced coal gas may also be further refined to produce additional quantities of H2:

3C (i.e., coal) + O2 + H2O → H2 + 3CO

If the refiner wants to produce alkanes (i.e., hydrocarbons present in natural gas, gasoline, and diesel fuel), the coal gas is collected at this state and routed to a Fischer-Tropsch reactor. If, however, hydrogen is the desired end-product, the coal gas (primarily the CO product) undergoes the water gas shift reaction where more hydrogen is produced by additional reaction with water vapor:

CO + H2O → CO2 + H2

Although other technologies for coal gasification currently exist, all employ, in general, the same chemical processes. For low-grade coals (i.e., "brown coals") which contain significant amounts of water, there are technologies in which no steam is required during the reaction, with coal (carbon) and oxygen being the only reactants. As well, some coal gasification technologies do not require high pressures. Some utilize pulverized coal as fuel while others work with relatively large fractions of coal. Gasification technologies also vary in the way the blowing is supplied.

"Direct blowing" assumes the coal and the oxidizer being supplied towards each other from the opposite sides of the reactor channel. In this case the oxidizer passes through coke and (more likely) ashes to the reaction zone where it interacts with coal. The hot gas produced then passes fresh fuel and heats it while absorbing some products of thermal destruction of the fuel, such as tars and phenols. Thus, the gas requires significant refining before being used in the Fischer-Tropsch reaction. Products of the refinement are highly toxic and require special facilities for their utilization. As a result, the plant utilizing the described technologies has to be very large to be economically efficient. One of such plants called SASOL is situated in the Republic of South Africa (RSA). It was built due to embargo applied to the country preventing it from importing oil and natural gas. RSA is rich in its own brown coal and was able to arrange the use of the well known high pressure "Lurgi" gasification process developed in Germany in the first half of 20-th century.

"Reversed blowing" (as compared to the previous type described which was invented first) assumes the coal and the oxidizer being supplied from the same side of the reactor. In this case there is no chemical interaction between coal and oxidizer before the reaction zone. The gas produced in the reaction zone passes solid products of gasification (coke and ashes), and CO2 and H2O contained in the gas are additionally chemically restored to CO and H2. As compared to the "direct blowing" technology, no toxic by-products are present in the gas: those are disabled in the reaction zone. This type of gasification has been developed in the first half of 20-th century, along with the "direct blowing", but the rate of gas production in it is significantly lower than that in "direct blowing" and there were no further efforts of developing the "reversed blowing" processes until 1980-s when a Soviet research facility KATEKNIIUgol' (R&D Institute for developing Kansk-Achinsk coal field) began R&D activities to produce the technology now known as "TERMOKOKS-S" process. The reason for reviving the interest to this type of gasification process is that it is ecologically clean and able to produce two types of useful products (simultaneously or separately): gas (either combustible or syngas) and middle-temperature coke. The former may be used as a fuel for gas boilers and diesel-generators or as syngas for producing gasoline, etc., the latter - as a technological fuel in metallurgy, as a chemical absorbent or as raw material for household fuel briquettes. Combustion of the product gas in gas boilers is ecologically cleaner than combustion of initial coal. Thus, a plant utilizing gasification technology with the "reversed blowing" is able to produce two valuable products of which one has relatively zero production cost since the latter is covered by competitive market price of the other. As the Soviet Union and its KATEKNIIUgol' ceased to exist, the technology was adopted by the individual scientists who originally developed it and is now being further researched in Russia and commercially distributed worldwide. Industrial plants utilizing it are now known to function in Ulaan-Baatar (Mongolia) and Krasnoyarsk (Russia).