Coal

From Wikipedia, the free encyclopedia

Coal (IPA: /ˈkəʊl/) is a fossil fuel formed in swamp ecosystems where plant remains were saved by water and mud from oxidization and biodegradation. Coal is a readily combustible black or brownish-black rock. It is a sedimentary rock, but the harder forms, such as anthracite coal, can be regarded as metamorphic rocks because of later exposure to elevated temperature and pressure. It is composed primarily of carbon along with assorted other elements, including sulfur. It is the largest single source of fuel for the generation of electricity world-wide, as well as the largest source of carbon dioxide emissions, which have been implicated as the primary cause of global warming. Coal is extracted from the ground by coal mining, either underground mining or open-pit mining (surface mining).

Outcrop coal was used in Britain during the Bronze Age (2-3000 years BCE), where it has been detected as forming part of the composition of funeral pyres.^[1] It was also commonly used in the early period of the Roman occupation. Evidence of trade in coal (dated to about 200 CE) has been found at the inland port of Heronbridge, near Chester, and in the Fenlands of East Anglia, where coal from the Midlands was transported via the Car Dyke for use in drying grain.^[2] Coal cinders have been found in the hearths of villas and military forts, particularly in Northumberland, dated to around 400 CE. In the west of England contemporary writers described the wonder of a permanent brazier of coal on the altar of Minerva at Aquae Sulis (modern day Bath) although in fact easily-accessible surface coal from what is now the Somerset coalfield was in common use in quite lowly dwellings locally.^[3]

However, there is no evidence that the product was of great importance in Britain before the High Middle Ages, after about 1000 CE. Mineral coal came to be referred to as "seacoal," probably because it came to many places in eastern England, including London, by sea. This is accepted as the more likely explanation for the name than that it was found on beaches, having fallen from the exposed coal seams above or washed out of underwater coal seam outcrops. These easily accessible sources had largely become exhausted (or could not meet the growing demand) by the 13th century, when underground mining from shafts or adits was developed.^[1] In London there is still a Seacoal Lane (off the north side of Ludgate Hill) where the coal merchants used to conduct their business. An alternative name was "pitcoal," because it came from mines.

Contents 1 Etymology and folklore 2 Composition 3 Origin of coal 4 Types of coal 5 Uses 5.1 Coal as fuel 5.2 Coking and use of coke 5.2.1 Gasification 5.2.2 Liquefaction 6 Harmful effects 6.1 Coal mining 6.2 Coal burning 7 Energy density 8 Relative Carbon Cost 9 Coal fires 10 World coal reserves 11 Major Coal Exporters 12 See also 13 External links 14 References 15 Notes

[edit] Etymology and folklore

The term originates from the Anglo-Saxon word col "charcoal" and is related to a common Germanic root of otherwise unclear origins.

It is associated with the astrological sign Capricorn and is carried by thieves to protect them from detection and to help them to escape when pursued. It is an element of a popular ritual associated with New Year's Eve. To dream of burning coals is a symbol of disappointment, trouble, affliction, and loss, unless they are burning brightly, when the symbol gives promise of uplifting and advancement.

In some countries, misbehaving children are traditionally threatened with receiving lumps of coal instead of gifts in their Christmas stockings.

In Scotland coal is brought to a household as a symbolic gift in the Hogmanay ritual of first-footing.

[edit] Composition

Carbon forms more than 50 percent by weight and more than 70 percent by volume of coal (this includes inherent moisture). This is dependent on coal rank, with higher rank coals containing less hydrogen, oxygen and nitrogen, until 95% purity of carbon is achieved at Anthracite rank and above. Graphite formed from coal is the end-product of the thermal and diagenetic conversion of plant matter (50% by volume of water) into pure carbon.

Coal usually contains a considerable amount of incidental moisture, which is the water trapped within the coal in between the coal particles. Coals are usually mined wet and may be stored wet to prevent spontaneous combustion, so the carbon content of coal is quoted as both a 'as mined' and on a 'moisture free' basis.

Lignite and other low-rank coals still contain a considerable amount of water and other volatile components trapped within the particles of the coal, known as its macerals. This is present either within the coal particles, or as hydrogen and oxygen atoms within the molecules. This is because coal is converted from carbohydrate material such as cellulose, into carbon, which is an incremental process (see below). Therefore coal carbon contents also depend heavily on the degree to which this cellulose component is preserved in the coal.

Other constituents of coals include mineral matter, usually as silicate minerals such as clays, illite, kaolinite and so forth, as well as carbonate minerals like siderite, calcite and aragonite. Iron sulfide minerals such as pyrite are common constituents of coals. Sulfate minerals are also found, as is some form of salt, trace amounts of metals, notably iron, uranium, cadmium, and (rarely) gold.

Methane gas is another component of coal, produced from methanogenesis. Methane in coal is dangerous, as it can cause coal seam explosions, especially in underground mines, and may cause the coal to spontaneously combust. It is, however, a valuable by-product of some coal mining, serving as a significant source of natural gas.

Coal composition is determined by specific coal assay techniques, and is performed to quantify the physical, chemical and mechanical behaviour of the coal, including whether it is a good candidate for coking coal.

Some of the macerals of coal are:-

• vitrinite: fossil woody tissue, likely often charcoal from forest fires in the coal forests
• fusinite: made from peat made from cortical tissue
• exinite: fossil spore casings and plant cuticles
• resinite: fossil resin and wax
• alginite: fossil algal material

[edit] Origin of coal

Coal is formed from plant remains that have been compacted, hardened, chemically altered, and metamorphosed by heat and pressure over geologic time.

Coal was formed in swamp ecosystems which persisted in lowland sedimentary basins similar, for instance, to the peat swamps of Borneo today. These swamp environments were formed during slow subsidence of passive continental margins, and most seem to have formed adjacent to estuarine and marine sediments suggesting that they may have been in tidal delta environments. They are often called the "coal forests".

When plants die in these peat swamp environments, their biomass is deposited in anaerobic aquatic environments where low oxygen levels prevent their complete decay by bacteria and oxidation. For masses of undecayed organic matter to be preserved and to form economically valuable coal the environment must remain steady for prolonged periods of time, and the waters feeding these peat swamps must remain essentially free of sediment. This requires minimal erosion in the uplands of the rivers which feed the coal swamps, and efficient trapping of the sediments.

Eventually, and usually due to the initial onset of orogeny or other tectonic events, the coal forming environment ceases. In the majority of cases this is abrupt, with the majority of coal seams having a knife-sharp upper contact with the overlying sediments. This suggests that the onset of further sedimentation quickly destroys the peat swamp ecosystem and replaces it with meandering stream and river environments during ongoing subsidence.

Burial by sedimentary loading on top of the peat swamp converts the organic matter to coal by the following processes;

• compaction, due to loading of the sediments on the coal which flattens the organic matter
• removal of the water held within the peat in between the plant fragments
• with ongoing compaction, removal of water from the inter-cellular structure of fossilised plants
• with heat and compaction, removal of molecular water
• methanogenesis; similar to treating wood in a pressure cooker, methane is produced, which removes hydrogen and some carbon, and some further oxygen (as water)
• dehydrogenation, which removes hydroxyl groups from the cellulose and other plant molecules, resulting in the production of hydrogen-reduced coals

Generally, to form a coal seam 1 metre thick, between 10 and 30 metres of peat is required. Peat has a moisture content of up to 90%, so loss of water is of prime importance in the conversion of peat into lignite, the lowest rank of coal. Lignite is then converted by dehydrogenation and methanogenesis to sub-bituminous coal. Further dehydrogenation reactions, removing progressively more methane and higher hydrocarbon gases such as ethane, propane, etcetera, create bituminous coal and, when this process is complete at sub-metamorphic conditions, anthracite and graphite are formed.

Evidence of the types of plants that contributed to carbonaceous deposits can occasionally be found in the shale and sandstone sediments that overlie coal deposits and within the coal. Fossil evidence is best preserved in lignites and sub-bituminous coals, though fossils in anthracite are not too rare. To date only three fossils have been found in graphite seams created from coal.

The greatest coal-forming time in geologic history was during the Carboniferous era (280 to 345 million years ago). Further large deposits of coal are found in the Permian, with lesser but still significant Triassic and Jurassic deposits, and minor Cretaceous and younger deposits of lignite. In the modern European lowlands of Holland and Germany considerable thicknesses of peat have accumulated, testifying to the ubiquity of the coal-forming process.

In Europe, Asia, and North America, the Carboniferous coal was formed from tropical swamp forests, which are sometimes called the "coal swamps". Southern hemisphere Carboniferous coal was formed from the Glossopteris flora, which grew on cold periglacial tundra when the South Pole was a long way inland in Gondwanaland.

[edit] Types of coal

As geological processes apply pressure to peat over time, it is transformed successively into:

• Lignite - also referred to as brown coal, is the lowest rank of coal and used almost exclusively as fuel for steam-electric power generation. Jet is a compact form of lignite that is sometimes polished and has been used as an ornamental stone since the Iron Age.
• Sub-bituminous coal - whose properties range from those of lignite to those of bituminous coal and are used primarily as fuel for steam-electric power generation.
• Bituminous coal - a dense coal, usually black, sometimes dark brown, often with well-defined bands of bright and dull material, used primarily as fuel in steam-electric power generation, with substantial quantities also used for heat and power applications in manufacturing and to make coke.
• Anthracite - the highest rank; a harder, glossy, black coal used primarily for residential and commercial space heating.
• Graphite - technically the highest rank, but difficult to ignite and is not so commonly used for ignition.

[edit] Uses

[edit] Coal as fuel

See also Clean coal and Fossil fuel power plant

Coal is primarily used as a solid fuel to produce electricity and heat through combustion. World coal consumption is about 5,800 million short tons (5.3 petagrams) annually, of which about 75% is used for the production of electricity. The region including the People's Republic of China and India uses about 1,700 million long tons (1.5 Pg) annually, forecast to exceed 3,000 million short tons (2.7 Pg) in 2025.^[4] The USA consumes about 1,100 million short tons (1.0 Pg) of coal each year, using 90% of it for generation of electricity. Coal is the fastest growing energy source in the world, with coal use increasing by 25% for the three-year period ending in December 2004 (BP Statistical Energy Review, June 2005).

When coal is used for electricity generation, it is usually pulverized and then burned in a furnace with a boiler. The furnace heat converts boiler water to steam, which is then used to spin turbines which turn generators and create electricity. The thermodynamic efficiency of this process has been improved over time. "Standard" steam turbines have topped out with some of the most advanced reaching about 35% thermodynamic efficiency for the entire process, which means 65% of the coal energy is rejected as waste heat into the surrounding environment. Old coal power plants, especially "grandfathered" plants, are significantly less efficient and reject higher levels of waste heat. The emergence of the supercritical turbine concept envisions running a boiler at extremely high temperatures and pressures with projected efficiencies of 46%, with further theorized increases in temperature and pressure perhaps resulting in even higher efficiencies^[5] Approximately 40% of the world electricity production uses coal. The total known deposits recoverable by current technologies, including highly polluting, low energy content types of coal (i.e., lignite, bituminous), might be sufficient for 300 years' use at current consumption levels, although maximal production could be reached within decades (see World Coal Reserves, below).

A more energy-efficient way of using coal for electricity production would be via solid-oxide fuel cells or molten-carbonate fuel cells (or any oxygen ion transport based fuel cells that do not discriminate between fuels, as long as they consume oxygen), which would be able to get 60%–85% combined efficiency (direct electricity + waste heat steam turbine). Currently these fuel cell technologies can only process gaseous fuels, and they are also sensitive to sulfur poisoning, issues which would first have to be worked out before large scale commercial success is possible with coal. As far as gaseous fuels go, one idea is pulverized coal in a gas carrier, such as nitrogen. Another option is coal gasification with water, which may lower fuel cell voltage by introducing oxygen to the fuel side of the electrolyte, but may also greatly simplify carbon sequestration.

[edit] Coking and use of coke

Main article: Coke (fuel)

Coke is a solid carbonaceous residue derived from low-ash, low-sulfur bituminous coal from which the volatile constituents are driven off by baking in an oven without oxygen at temperatures as high as 1,000 °C (1,832 °F) so that the fixed carbon and residual ash are fused together. Coke is used as a fuel and as a reducing agent in smelting iron ore in a blast furnace. Coke from coal is grey, hard, and porous and has a heating value of 24.8 million Btu/ton (29.6 MJ/kg). Byproducts of this conversion of coal to coke include coal tar, ammonia, light oils, and "coal-gas".

Petroleum coke is the solid residue obtained in oil refining, which resembles coke but contains too many impurities to be useful in metallurgical applications.

[edit] Gasification

High prices of oil and natural gas are leading to increased interest in "BTU Conversion" technologies such as gasification, methanation and liquification.

Coal gasification breaks down the coal into its components, usually by subjecting it to high temperature and pressure, using steam and measured amounts of oxygen. This leads to the production of syngas, a mixture mainly consisting of carbon monoxide (CO) and hydrogen (H₂).

In the past, coal was converted to make coal gas, which was piped to customers to burn for illumination, heating, and cooking. At present, the safer natural gas is used instead. South Africa still uses gasification of coal for much of its petrochemical needs.

The Synthetic Fuels Corporation was a U.S. government-funded corporation established in 1980 to create a market for alternatives to imported fossil fuels (such as coal gasification). The corporation was abolished in 1985.

Gasification is also a possibility for future energy use, as the produced syngas can be cleaned-up relatively easily leading to cleaner burning than burning coal directly (the conventional way). The cleanliness of the cleaned-up syngas is comparable to natural gas enabling to burn it in a more efficient gas turbine rather than in a boiler used to drive a steam turbine. Syngas produced by gasification can be CO-shifted meaning that the combustible CO in the syngas is transferred into carbon dioxide (CO₂) using water as a reactant. The CO-shift reaction also produces an amount of combustible hydrogen (H₂) equal to the amount of CO converted into CO₂. The CO₂ concentrations (or rather CO₂ partial pressures) obtained by using coal gasification followed by a CO-shift reaction are much higher than in case of direct combustion of coal in air (which is mostly nitrogen). These higher concentrations of carbon dioxide make carbon capture and storage much more economical than it otherwise would be.

[edit] Liquefaction

Coal can also be converted into liquid fuels like gasoline or diesel by several different processes. The Fischer-Tropsch process of indirect synthesis of liquid hydrocarbons was used in Nazi Germany for many years and is today used by Sasol in South Africa — in both cases because those regimes were politically isolated and unable to purchase crude oil on the open market. Coal would be gasified to make syngas (a balanced purified mixture of CO and H₂ gas) and the syngas condensed using Fischer-Tropsch catalysts to make light hydrocarbons which are further processed into gasoline and diesel. Syngas can also be converted to methanol, which can be used as a fuel, fuel additive, or further processed into gasoline via the Mobil M-gas process.

A direct liquefaction process Bergius process (liquefaction by hydrogenation) is also available but has not been used outside Germany, where such processes were operated both during World War I and World War II. SASOL in South Africa has experimented with direct hydrogenation. Several other direct liquefaction processes have been developed, among these being the SRC-I and SRC-II (Solvent Refined Coal) processes developed by Gulf Oil and implemented as pilot plants in the United States in the 1960s and 1970s.^[6]

Another direct hydrogenation process was explored by the NUS Corporation in 1976 and patented by Wilburn C. Schroeder. The process involved dried, pulverized coal mixed with roughly 1wt% molybdenum catalysis. Hydrogenation occurred by use of high temperature and pressure synthesis gas produced in a separate gasifier. The process ultimately yielded a synthetic crude product, Naptha, a limited amount of C₃/C₄ gas, light-medium weight liquids (C₅-C₁₀) suitable for use as fuels, small amounts of NH₃ and significant amounts of CO₂.^[7]

Yet another process to manufacture liquid hydrocarbons from coal is low temperature carbonization (LTC). Coal is coked at temperatures between 450 and 700 °C compared to 800 to 1000 °C for metallurgical coke. These temperatures optimize the production of coal tars richer in lighter hydrocarbons than normal coal tar. The coal tar is then further processed into fuels. The Karrick process was developed by Lewis C. Karrick, an oil shale technologist at the U.S. Bureau of Mines in the 1920s.^[8]

All of these liquid fuel production methods release carbon dioxide (CO₂) in the conversion process, far more than is released in the extraction and refinement of liquid fuel production from petroleum. If these methods were adopted to replace declining petroleum supplies, carbon dioxide emissions would be greatly increased on a global scale. For future liquefaction projects, Carbon dioxide sequestration is proposed to avoid releasing it into the atmosphere, though no pilot projects have confirmed the feasibility of this approach on a wide scale. As CO₂ is one of the process streams, sequestration is easier than from flue gases produced in combustion of coal with air, where CO₂ is diluted by nitrogen and other gases. Sequestration will, however, add to the cost.

Coal liquefaction is one of the backstop technologies that could potentially limit escalation of oil prices and mitigate the effects of transportation energy shortage under peak oil. This is contingent on liquefaction production capacity becoming large enough to satiate the very large and growing demand for petroleum. Estimates of the cost of producing liquid fuels from coal suggest that domestic U.S. production of fuel from coal becomes cost-competitive with oil priced at around 35 USD per barrel,^[9] (break-even cost). This price, while above historical averages, is well below current oil prices. This makes coal a viable financial alternative to oil for the time being, although production is not great enough to make synfuels viable on a large scale.^[10]

Among commercially mature technologies, advantage for indirect coal liquefaction over direct coal liquefaction are reported by Williams and Larson (2003). Estimates are reported for sites in China where break-even cost for coal liquefaction may be in the range between 25 to 35 USD/barrel of oil.

[edit] Harmful effects

[edit] Coal mining

Coal mining causes a number of harmful effects. When coal surfaces are exposed, pyrite (iron sulfide), also known as "fool's gold", comes in contact with water and air and forms sulfuric acid. As water drains from the mine, the acid moves into the waterways, and as long as rain falls on the mine tailings the sulfuric acid production continues, whether the mine is still operating or not. If the coal is strip mined, the entire exposed seam leaches sulfuric acid, leaving the infertile subsoil on the surface and begins to pollute streams by acidifying and killing fish, plants, and aquatic animals who are sensitive to drastic pH shifts.

By the late 1930s, it was estimated that American coal mines produced about 2.5 million tons of sulfuric acid annually. In the Ohio River Basin, where twelve hundred operating coal mines drained an estimated annual 1.5 million tons of sulfuric acid into the waters in the 1960s and thousands of abandoned coal mines leached acid as well. In Pennsylvania alone, mine drainage had blighted 2,000 stream miles by 1967.

[edit] Coal burning

Combustion of coal, like any other fossil fuel, produces carbon dioxide (CO₂) and nitrogen oxides (NO_x) along with varying amounts of sulfur dioxide (SO₂) depending on where it was mined. Sulfur dioxide reacts with oxygen to form sulfur trioxide (SO₃), which then reacts with water to form sulfuric acid (see Acid anhydride for more information). The sulfuric acid is returned to the Earth as acid rain.

Emissions from coal-fired power plants represent the largest source of carbon dioxide emissions, which have been implicated as the primary cause of global warming. Coal mining and abandoned mines also emit methane, another cause of global warming. Since the carbon content of coal is much higher than oil, burning coal is a more serious threat to the stability of the global climate, as this carbon forms CO₂ when burned. Many other pollutants are present in coal power station emissions, as solid coal is more difficult to clean than oil, which is refined before use. A study commissioned by environmental groups claims that coal power plant emissions are responsible for tens of thousands of premature deaths annually in the United States alone.^[11] Modern power plants utilize a variety of techniques to limit the harmfulness of their waste products and improve the efficiency of burning, though these techniques are not subject to standard testing or regulation in the U.S. and are not widely implemented in some countries, as they add to the capital cost of the power plant. To eliminate CO₂ emissions from coal plants, carbon capture and storage has been proposed but has yet to be commercially used.

Coal and coal waste products including fly ash, bottom ash, boiler slag, and flue gas desulferization contain many heavy metals, including arsenic, lead, mercury, nickel, vanadium, beryllium, cadmium, barium, chromium, copper, molybdenum, zinc, selenium and radium, which are dangerous if released into the environment. Coal also contains low levels of uranium, thorium, and other naturally-occurring radioactive isotopes whose release into the environment may lead to radioactive contamination.^[12][13] While these substances are trace impurities, enough coal is burned that significant amounts of these substances are released, resulting in more radioactive waste than nuclear power plants.^[14]

Due to its scientifically accepted connection with climate change [1], the world's reliance on coal as an energy source, and health concerns in areas with poor air pollution controls, The Economist recently labeled the burning of coal "Environmental Enemy No. 1."^[15]

[edit] Energy density

The energy density of coal is roughly 24 Megajoules per kilogram.^[16] It is perhaps more useful to put this into another unit of energy, kilowatt-hours. This is the unit that electricity is most commonly sold in. In that case, the energy density of coal is 6.67 kW-h/kg.

One can put this information to use to figure out how much coal is needed to power things. For example, running one 100 Watt computer for one year requires this much electricity:

100 W × 24 h × 365 {days in a year} = 876000 W-h = 876 kW-h

A typical Thermodynamic efficiency of coal power plants is about 30%. Of the 6.67 kW-h of energy per kilogram of coal, about 30% of that can successfully be turned into electricity - the rest is waste heat. Coal power plants obtain approximately 2.0 kW-h per kg of burned coal.

Plugging in this information one finds how much coal must be burned to power a typical computer for one year:

.

It takes 967 pounds of coal to power a computer for one full year.^[17]

[edit] Relative Carbon Cost

Because coal is at least 50% carbon (by mass), then 1 kg of coal contains at least 0.5 kg of carbon, which is where 1 mol is equal to N_A (Avogadro Number) particles. This combines with oxygen in the atmosphere during combustion, producing carbon dioxide, with an atomic weight of (12 + 16 × 2 = mass(CO₂) = 44 kg/kmol). of CO₂ is produced from the present in every kilogram of coal, which once trapped in CO₂ weighs approximately .

This fact can be used to put a carbon-cost of energy on the use of coal power. Since the useful energy output of coal is about 30% of the 6.67 kW-h/kg(coal), we can say about 2 kW-h/kg(coal) of energy is produced. Since 1 kg coal roughly translates as 1.83 kg of CO₂, we can say that using electricity from coal produces CO₂ at a rate of about 0.915 kg(CO₂) / kW-h, or about 0.254 kg(CO₂) / MJ.

[edit] Coal fires

There are hundreds of coal fires burning around the world.^[18] Those burning underground can be difficult to locate and many cannot be extinguished. Fires can cause the ground above to subside, combustion gases are dangerous to life, and breaking out to the surface can initiate surface wildfires. See also Mine fire.

Coal seams can be set on fire by spontaneous combustion or contact with a mine fire or surface fire. A grass fire in a coal area can set dozens of coal seams on fire.^[19][20] Coal fires in China burn 120 million tons of coal a year, emitting 360 million metric tons of carbon dioxide. This amounts to 2-3% of the annual worldwide production of CO₂ from fossil fuels, or as much as emitted from all of the cars and light trucks in the United States.^[21][22]

In Centralia, Pennsylvania (a borough located in the Coal Region of the United States) an exposed vein of coal ignited in 1962 due to a trash fire in the borough landfill, located in an abandoned anthracite strip mine pit. Attempts to extinguish the fire were unsuccessful, and it continues to burn underground to this day.

The reddish siltstone rock that caps many ridges and buttes in the Powder River Basin (Wyoming), and in western North Dakota is called porcelanite, which also may resemble the coal burning waste "clinker" or volcanic "scoria."^[23] Clinker is rock that has been fused by the natural burning of coal. In the case of the Powder River Basin approximately 27 to 54 billion metric tons of coal burned within the past three million years.^[24] Wild coal fires in the area were reported by the Lewis and Clark Expedition as well as explorers and settlers in the area.^[25]

The Australian Burning Mountain was originally believed to be a volcano, but the smoke and ash comes from a coal fire which may have been burning for over 5,500 years.^[26]

[edit] World coal reserves

In 1996 it was estimated that there was around one exagram (1 × 10¹⁵ kg or 1 trillion tonnes) of total coal reserves accessible using current mining technology, approximately half of it being hard coal. The energy value of all the world's coal is 290 zettajoules.^[27] At the current global consumption of 15 terawatt,^[28] there is enough coal to provide the entire planet with all of its energy for 600 years.

British Petroleum, in its annual report 2006, estimated at 2005 end, there were 909,064 million tons of proven coal reserves worldwide, or 155 years reserve to production ratio. This figure only includes reserves classified as 'proven', exploration drilling programs by mining companies, particularly in under-explored areas, are continually providing new reserves. In many cases, companies are aware of coal deposits that have not been sufficiently drilled to qualify as 'proven.' There is, therefore, much more recoverable coal in the world than indicated by proven reserve figures.

The United States Department of Energy uses estimates of coal reserves in the region of 1,081,279 million short tons, which is about 4,786 BBOE (billion barrels of oil equivalent) .^[29] The amount of coal burned during 2001 was calculated as 2.337 GTOE (gigatonnes of oil equivalent), which is about 46 million barrels of oil equivalent per day .^[30] Were consumption to continue at that rate those reserves would last about 285 years. As a comparison natural gas provided 51 million barrels (oil equivalent), and oil 76 million barrels, per day during 2001.

Of the 3 fossil fuels coal has the most widely distributed reserves, and coal is mined in over 100 countries, and on all continents except Antarctica. The largest reserves are found in the USA, Russia, Australia, China, India and South Africa.

Proved recoverable coal reserves at end-1999 (million tonnes)[2]

Country	Bituminous (including anthracite)	Sub- bituminous	Lignite	TOTAL
United States of America	115891	101021	33082	249994
Russian Federation	49088	97472	10450	157010
China	62200	33700	18600	114500
India	82396		2000	84396
Australia	42550	1840	37700	82090
Germany	23000		43000	66000
South Africa	49520			49520
Ukraine	16274	15946	1933	34153
Kazakhstan	31000		3000	34000
Poland	20300		1860	22160
Serbia, Montenegro	64	1460	14732	16256
Brazil		11929		11929
Colombia	6267	381		6648
Canada	3471	871	2236	6578
Czech Republic	2114	3414	150	5678
Indonesia	790	1430	3150	5370
Botswana	4300			4300
Uzbekistan	1000		3000	4000
Turkey	278	761	2650	3689
Greece			2874	2874
Bulgaria	13	233	2465	2711
Pakistan		2265		2265
Iran (Islamic Rep.)	1710			1710
United Kingdom	1000		500	1500
Romania	1	35	1421	1457
Thailand			1268	1268
Mexico	860	300	51	1211
Chile	31	1150		1181
Hungary		80	1017	1097
Peru	960		100	1060
Kyrgyzstan			812	812
Japan	773			773
Spain	200	400	60	660
Korea (Democratic People's Rep.)	300	300		600
New Zealand	33	206	333	572
Zimbabwe	502			502
Netherlands	497			497
Venezuela	479			479
Argentina		430		430
Philippines		232	100	332
Slovenia		40	235	275
Mozambique	212			212
Swaziland	208			208
Tanzania	200			200
Nigeria	21	169		190
Greenland		183		183
Slovakia			172	172
Vietnam	150			150
Congo (Democratic Rep.)	88			88
Korea (Republic)	78			78
Niger	70			70
Afghanistan	66			66
Algeria	40			40
Croatia	6		33	39
Portugal	3		33	36
France	22		14	36
Italy		27	7	34
Austria			25	25
Ecuador			24	24
Egypt (Arab Rep.)		22		22
Ireland	14			14
Zambia	10			10
Malaysia	4			4
Central African Republic			3	3
Myanmar (Burma)	2			2
Malawi		2		2
New Caledonia	2			2
Nepal	2			2
Bolivia	1			1
Norway		1		1
Taiwan	1			1
Sweden		1		1
TOTAL	519062	276301	189090	984453

[edit] Major Coal Exporters

Exports of Coal by Country and year (million tonnes)[3]

Country	2003	2004
Australia	238.1	247.6
United States	43.0	48.0
South Africa	78.7	74.9
Former Soviet Union	41.0	55.7
Poland	16.4	16.3
Canada	27.7	28.8
China	103.4	95.5
South America	57.8	65.9
Indonesia	107.8	131.4
Total	713.9	764.0

[edit] See also

• Energy: world resources and consumption
• Charcoal
• Clean coal
• Coal assay
• Coal dust
• Coal Measure (stratigraphic unit)
• Coal mining
• Coal mining debate
• Coal-tar
• World Coal Institute
• Energy value of coal
• Fluidized bed combustion
• Future energy development
• Granular material
• Australian Coal Alliance
• History of coal mining
• List of environment topics
• Major coal producing regions
• World energy resources and consumption

[edit] External links

• World Coal Institute
• Coal: Facts & Figures
• MSNBC report on coal pollution health effects in the United States
• Clean coal technologies
  • Advanced methods of using coal (Japanese Coal Energy Center)
• USDOE Hydrogen from Coal Research
• Coal Preparation, Journal of
• Wyoming Coal from the University of Wyoming
• Coal - origin, purification and consumption
• History of coal seams and the practice of coal mining in North Staffordshire, UK

[edit] References

• (2005) The Face of Decline: The Pennsylvania Anthracite Region in the Twentieth Century. Cornell University Press. ISBN 0-8014-8473-1. 
• Rottenberg, Dan (2003). In the Kingdom of Coal; An American Family and the Rock That Changed the World. Routledge. ISBN 0-415-93522-9. 
• Robert H. Williams and Eric D. Larson (December 2003). "A comparison of direct and indirect liquefaction technologies for making fluid fuels from coal" (PDF). Energy for Sustainable Development VII: 103-129. 
• Outwater, Alice (1996). Water: A Natural History. New York, NY: Basic Books. ISBN 0-465-03780-1. 
• Smith, Duane A. (May 1993). Mining America: The Industry and the Environment, 1800-1980 (in English). Lawrence, KS: University Press of Kansas, 210. ISBN 0870813064. 

[edit] Notes

1. ^ ^{a b} Britannica 2004: Coal mining: ancient use of outcropping coal.
2. ^ Salway, Peter (2001): A History of Roman Britain. Oxford University Press.
3. ^ Forbes, R J (1966): Studies in Ancient Technology. Brill Academic Publishers, Boston.
4. ^ International Energy Outlook. Retrieved on September 9, 2005.
5. ^ [http://www.powergeneration.siemens.com/download/pool/PGE2005_BalancingEconomics.pdf Balancing economics and environmental friendliness - the challenge for supercritical coal-fired power plants with highest steam parameters in the future] (PDF). Retrieved on 2006-10-23.
6. ^ Cleaner Coal Technology Programme (October 1999). "Technology Status Report 010: Coal Liquefaction". Department of Trade and Industry (UK). Retrieved on November 23.
7. ^ Phillip A. Lowe, Wilburn C. Schroeder, Anthony L. Liccardi (1976). "Technical Economies, Synfuels and Coal Energy Symposium, Solid-Phase Catalytic Coal Liquefaction Process". The American Society of Mechanical Engineers.
8. ^ http://www.rexresearch.com/karrick/karric~1.htm. Retrieved on September 9, 2005.
9. ^ Diesel Fuel News: Ultra-clean fuels from coal liquefaction: China about to launch big projects - Brief Article. Retrieved on September 9, 2005.
10. ^ Welcome to Coal People Magazine. Retrieved on September 9, 2005.
11. ^ Deadly power plants? Study fuels debate. Retrieved on September 4, 2006.
12. ^ Coal Combustion. Retrieved on September 9, 2005.
13. ^ Radioactive Elements in Coal and Fly Ash, USGS Factsheet 163-97. Retrieved on September 9, 2005.
14. ^ Coal Combustion: Nuclear Resource or Danger. Retrieved on October 16, 2006.
15. ^ Environmental enemy No. 1. Retrieved on September 4, 2006.
16. ^ Fisher, Juliya. Energy Density of Coal. The Physics Factbook. Retrieved on 2006-08-25.
17. ^ A similar result, using a lightbulb instead, see
    How much coal is required to run a 100-watt light bulb 24 hours a day for a year?. Howstuffworks. Retrieved on 2006-08-25.
18. ^ Sino German Coal fire project. Retrieved on September 9, 2005.
19. ^ Committee on Resources-Index. Retrieved on September 9, 2005.
20. ^ http://www.fire.blm.gov/textdocuments/6-27-03.pdf. Retrieved on September 9, 2005.
21. ^ EHP 110-5, 2002: Forum. Retrieved on September 9, 2005.
22. ^ Overview about ITC's activities in China. Retrieved on September 9, 2005.
23. ^ North Dakota's Clinker. Retrieved on September 9, 2005.
24. ^ BLM-Environmental Education- The High Plains. Retrieved on September 9, 2005.
25. ^ http://www.wsgs.uwyo.edu/Coal/CR01-1.pdf. Retrieved on September 9, 2005.
26. ^ Burning Mountain Nature Reserve. Retrieved on September 9, 2005.
27. ^ Sustainable Energy" 2005 page 303 The MIT Press by Jefferson W. Tester et al. ISBN 0-262-20153-4
28. ^ BP2006 energy report, and US EIA 2006 overview
29. ^ International Energy Annual 2003: Reserves. Retrieved on September 9, 2005.
30. ^ IEA Publications Bookshop. Retrieved on September 9, 2005.