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Coal (from the Old English term col, which has meant "mineral of fossilized carbon" since the 13th century) is a combustible black or brownish-black sedimentary rock usually occurring in rock strata in layers or veins called coal beds or coal seams. The harder forms, such as anthracite coal, can be regarded as metamorphic rock because of later exposure to elevated temperature and pressure. Coal is composed primarily of carbon along with variable quantities of other elements, chiefly hydrogen, sulfur, oxygen, and nitrogen.
Throughout history, coal has been used as an energy resource, primarily burned for the production of electricity and/or heat, and is also used for industrial purposes, such as refining metals. A fossil fuel, coal forms when dead plant matter is converted into peat, which in turn is converted into lignite, then sub-bituminous coal, after that bituminous coal, and lastly anthracite. This involves biological and geological processes that take place over a long period. The Energy Information Administration estimates coal reserves at 948×109 short tons (860 Gt). One estimate for resources is 18 000 Gt.
Coal is the largest source of energy for the generation of electricity worldwide, as well as one of the largest worldwide anthropogenic sources of carbon dioxide releases. In 1999, world gross carbon dioxide emissions from coal usage were 8,666 million tonnes of carbon dioxide. In 2011, world gross emissions from coal usage were 14,416 million tonnes. Coal-fired electric power generation emits around 2,000 pounds of carbon dioxide for every megawatt-hour generated, which is almost double the approximately 1100 pounds of carbon dioxide released by a natural gas-fired electric plant per megawatt-hour generated. Because of this higher carbon efficiency of natural gas generation, as the market in the United States has changed to reduce coal and increase natural gas generation, carbon dioxide emissions have fallen. Those measured in the first quarter of 2012 were the lowest of any recorded for the first quarter of any year since 1992. In 2013, the head of the UN climate agency advised that most of the world's coal reserves should be left in the ground to avoid catastrophic global warming.
Coal is extracted from the ground by coal mining, either underground by shaft mining, or at ground level by open pit mining extraction. Since 1983 the world top coal producer has been China. In 2011 China produced 3,520 million tonnes of coal – 49.5% of 7,695 million tonnes world coal production. In 2011 other large producers were United States (993 million tonnes), India (589), European Union (576) and Australia (416). In 2010 the largest exporters were Australia with 328 million tonnes (27.1% of world coal export) and Indonesia with 316 million tonnes (26.1%), while the largest importers were Japan with 207 million tonnes (17.5% of world coal import), China with 195 million tonnes (16.6%) and South Korea with 126 million tonnes (10.7%).
At various times in the geologic past, the Earth had dense forests in low-lying wetland areas. Due to natural processes such as flooding, these forests were buried underneath soil. As more and more soil deposited over them, they were compressed. The temperature also rose as they sank deeper and deeper. As the process continued the plant matter was protected from biodegradation and oxidation, usually by mud or acidic water. This trapped the carbon in immense peat bogs that were eventually covered and deeply buried by sediments. Under high pressure and high temperature, dead vegetation was slowly converted to coal. As coal contains mainly carbon, the conversion of dead vegetation into coal is called carbonization.
The wide, shallow seas of the Carboniferous Period provided ideal conditions for coal formation, although coal is known from most geological periods. The exception is the coal gap in the Permian–Triassic extinction event, where coal is rare. Coal is known from Precambrian strata, which predate land plants — this coal is presumed to have originated from residues of algae.
The classification of coal is generally based on the content of volatiles. However, the exact classification varies between countries. According to the German classification, coal is classified as follows:
|German Classification||English Designation||Volatiles %||C Carbon %||H Hydrogen %||O Oxygen %||S Sulfur %||Heat content kJ/kg|
|Braunkohle||Lignite (brown coal)||45–65||60–75||6.0–5.8||34-17||0.5-3||<28,470|
|Gasflammkohle||Gas flame coal||35-40||82-85||5.8-5.6||9.8-7.3||~1||<33,910|
|Note, the percentages are percent by mass of the indicated elements|
The middle six grades in the table represent a progressive transition from the English-language sub-bituminous to bituminous coal, while the last class is an approximate equivalent to anthracite, but more inclusive (US anthracite has < 6% volatiles).
Hilt's law is a geological term that states that, in a small area, the deeper the coal, the higher its rank (grade). The law holds true if the thermal gradient is entirely vertical, but metamorphism may cause lateral changes of rank, irrespective of depth.
|Mercury (Hg)||0.10±0.01 ppm|
|Arsenic (As)||1.4 – 71 ppm|
|Selenium (Se)||3 ppm|
Coal from the Fushun mine in northeastern China was used to smelt copper as early as 1000 BCE. Marco Polo, the Italian who traveled to China in the 13th century, described coal as "black stones ... which burn like logs", and said coal was so plentiful, people could take three hot baths a week. In Europe, the earliest reference to the use of coal as fuel is from the geological treatise On stones (Lap. 16) by the Greek scientist Theophrastus (circa 371–287 BC):
Among the materials that are dug because they are useful, those known as anthrakes [coals] are made of earth, and, once set on fire, they burn like charcoal. They are found in Liguria ... and in Elis as one approaches Olympia by the mountain road; and they are used by those who work in metals.—Theophrastus, On Stones (16) translation
Outcrop coal was used in Britain during the Bronze Age (3000–2000 BC), where it has been detected as forming part of the composition of funeral pyres. In Roman Britain, with the exception of two modern fields, "the Romans were exploiting coals in all the major coalfields in England and Wales by the end of the second century AD". Evidence of trade in coal (dated to about AD 200) has been found at the Roman settlement at 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. Coal cinders have been found in the hearths of villas and Roman forts, particularly in Northumberland, dated to around AD 400. 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 became the Somerset coalfield was in common use in quite lowly dwellings locally. Evidence of coal's use for iron-working in the city during the Roman period has been found. In Eschweiler, Rhineland, deposits of bituminous coal were used by the Romans for the smelting of iron ore.
No evidence exists of the product being of great importance in Britain before the High Middle Ages, after about AD 1000. Mineral coal came to be referred to as "seacoal" in the 13th century; the wharf where the material arrived in London was known as Seacoal Lane, so identified in a charter of King Henry III granted in 1253. Initially, the name was given because much coal was found on the shore, having fallen from the exposed coal seams on cliffs above or washed out of underwater coal outcrops, but by the time of Henry VIII, it was understood to derive from the way it was carried to London by sea. In 1257–59, coal from Newcastle upon Tyne was shipped to London for the smiths and lime-burners building Westminster Abbey. Seacoal Lane and Newcastle Lane, where coal was unloaded at wharves along the River Fleet, are still in existence. (See Industrial processes below for modern uses of the term.)
These easily accessible sources had largely become exhausted (or could not meet the growing demand) by the 13th century, when underground extraction by shaft mining or adits was developed. The alternative name was "pitcoal", because it came from mines. It was, however, the development of the Industrial Revolution that led to the large-scale use of coal, as the steam engine took over from the water wheel. In 1700, five-sixths of the world's coal was mined in Britain. Britain would have run out of suitable sites for watermills by the 1830s if coal had not been available as a source of energy. In 1947, there were some 750,000 miners in Britain, but by 2004, this had shrunk to some 5,000 miners working in around 20 collieries.
Coal is primarily used as a solid fuel to produce electricity and heat through combustion. World coal consumption was about 7.25 billion tonnes in 2010 (7.99 billion short tons) and is expected to increase 48% to 9.05 billion tonnes (9.98 billion short tons) by 2030. China produced 3.47 billion tonnes (3.83 billion short tons) in 2011. India produced about 578 million tonnes (637.1 million short tons) in 2011. 68.7% of China's electricity comes from coal. The USA consumed about 13% of the world total in 2010, i.e. 951 million tonnes (1.05 billion short tons), using 93% of it for generation of electricity. 46% of total power generated in the USA was done using coal.
When coal is used for electricity generation, it is usually pulverized and then combusted (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; some older coal-fired power stations have thermal efficiencies in the vicinity of 25% whereas the newest supercritical and "ultra-supercritical" steam cycle turbines, operating at temperatures over 600 °C and pressures over 27 MPa (over 3900 psi), can practically achieve thermal efficiencies in excess of 45% (LHV basis) using anthracite fuel, or around 43% (LHV basis) even when using lower-grade lignite fuel. Further thermal efficiency improvements are also achievable by improved pre-drying (especially relevant with high-moisture fuel such as lignite or biomass) and cooling technologies.
An alternative approach of using coal for electricity generation with improved efficiency is the integrated gasification combined cycle (IGCC) power plant. Instead of pulverizing the coal and burning it directly as fuel in the steam-generating boiler, the coal can be first gasified (see coal gasification) to create syngas, which is burned in a gas turbine to produce electricity (just like natural gas is burned in a turbine). Hot exhaust gases from the turbine are used to raise steam in a heat recovery steam generator which powers a supplemental steam turbine. Thermal efficiencies of current IGCC power plants range from 39-42% (HHV basis) or ~42-45% (LHV basis) for bituminous coal and assuming utilization of mainstream gasification technologies (Shell, GE Gasifier, CB&I). IGCC power plants outperform conventional pulverized coal-fueled plants in terms of pollutant emissions, and allow for relatively easy carbon capture.
At least 40% of the world's electricity comes from coal, and in 2012, about one-third of the United States' electricity came from coal, down from approximately 49% in 2008. As of 2012 in the United States, use of coal to generate electricity was declining, as plentiful supplies of natural gas obtained by hydraulic fracturing of tight shale formations became available at low prices.
In Denmark, a net electric efficiency of > 47% has been obtained at the coal-fired Nordjyllandsværket CHP Plant and an overall plant efficiency of up to 91% with cogeneration of electricity and district heating. The multifuel-fired Avedøreværket CHP Plant just outside Copenhagen can achieve a net electric efficiency as high as 49%. The overall plant efficiency with cogeneration of electricity and district heating can reach as much as 94%.
An alternative form of coal combustion is as coal-water slurry fuel (CWS), which was developed in the Soviet Union. CWS significantly reduces emissions, improving the heating value of coal. Other ways to use coal are combined heat and power cogeneration and an MHD topping cycle.
The total known deposits recoverable by current technologies, including highly polluting, low-energy content types of coal (i.e., lignite, bituminous), is sufficient for many years.[quantify] However, consumption is increasing and maximal production could be reached within decades (see world coal reserves, below). On the other hand much may have to be left in the ground to avoid climate change.
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 the fixed carbon and residual ash are fused together. Metallurgical coke is used as a fuel and as a reducing agent in smelting iron ore in a blast furnace. The result is pig iron, and is too rich in dissolved carbon, so it must be treated further to make steel. The coking coal should be low in sulfur and phosphorus, so they do not migrate to the metal.
The coke must be strong enough to resist the weight of overburden in the blast furnace, which is why coking coal is so important in making steel using the conventional route. However, the alternative route is direct reduced iron, where any carbonaceous fuel can be used to make sponge or pelletised iron. Coke from coal is grey, hard, and porous and has a heating value of 24.8 million Btu/ton (29.6 MJ/kg). Some cokemaking processes produce valuable byproducts, including coal tar, ammonia, light oils, and coal gas.
Coal gasification can be used to produce syngas, a mixture of carbon monoxide (CO) and hydrogen (H2) gas. Often syngas is used to fire gas turbines to produce electricity, but the versatility of syngas also allows it to be converted into transportation fuels, such as gasoline and diesel, through the Fischer-Tropsch process; alternatively, syngas can be converted into methanol, which can be blended into fuel directly or converted to gasoline via the methanol to gasoline process. Gasification combined with Fischer-Tropsch technology is currently used by the Sasol chemical company of South Africa to make motor vehicle fuels from coal and natural gas. Alternatively, the hydrogen obtained from gasification can be used for various purposes, such as powering a hydrogen economy, making ammonia, or upgrading fossil fuels.
During gasification, the coal is mixed with oxygen and steam while also being heated and pressurized. During the reaction, oxygen and water molecules oxidize the coal into carbon monoxide (CO), while also releasing hydrogen gas (H2). This process has been conducted in both underground coal mines and in the production of town gas.
If the refiner wants to produce gasoline, the syngas is collected at this state and routed into a Fischer-Tropsch reaction. If hydrogen is the desired end-product, however, the syngas is fed into the water gas shift reaction, where more hydrogen is liberated.
In the past, coal was converted to make coal gas (town gas), which was piped to customers to burn for illumination, heating, and cooking.
Coal can also be converted into synthetic fuels equivalent to gasoline or diesel by several different direct processes (which do not intrinsically require gasification or indirect conversion). In the direct liquefaction processes, the coal is either hydrogenated or carbonized. Hydrogenation processes are the Bergius process, the SRC-I and SRC-II (Solvent Refined Coal) processes, the NUS Corporation hydrogenation process and several other single-stage and two-stage processes. In the process of low-temperature carbonization, coal is coked at temperatures between 360 and 750 °C (680 and 1,380 °F). 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. An overview of coal liquefaction and its future potential is available.
Coal liquefaction methods involve carbon dioxide (CO
2) emissions in the conversion process. If coal liquefaction is done without employing either carbon capture and storage (CCS) technologies or biomass blending, the result is lifecycle greenhouse gas footprints that are generally greater than those released in the extraction and refinement of liquid fuel production from crude oil. If CCS technologies are employed, reductions of 5–12% can be achieved in Coal to Liquid (CTL) plants and up to a 75% reduction is achievable when co-gasifying coal with commercially demonstrated levels of biomass (30% biomass by weight) in coal/biomass-to-liquids plants. For future synthetic fuel projects, carbon dioxide sequestration is proposed to avoid releasing CO
2 into the atmosphere. Sequestration adds to the cost of production.
Refined coal is the product of a coal-upgrading technology that removes moisture and certain pollutants from lower-rank coals such as sub-bituminous and lignite (brown) coals. It is one form of several precombustion treatments and processes for coal that alter coal's characteristics before it is burned. The goals of precombustion coal technologies are to increase efficiency and reduce emissions when the coal is burned. Depending on the situation, precombustion technology can be used in place of or as a supplement to postcombustion technologies to control emissions from coal-fueled boilers.
Finely ground bituminous coal, known in this application as sea coal, is a constituent of foundry sand. While the molten metal is in the mould, the coal burns slowly, releasing reducing gases at pressure, and so preventing the metal from penetrating the pores of the sand. It is also contained in 'mould wash', a paste or liquid with the same function applied to the mould before casting. Sea coal can be mixed with the clay lining (the "bod") used for the bottom of a cupola furnace. When heated, the coal decomposes and the bod becomes slightly friable, easing the process of breaking open holes for tapping the molten metal.
Coal is an important feedstock in production of a wide range of chemical fertilizers and other chemical products. The main route to these products is coal gasification to produce syngas. Primary chemicals that are produced directly from the syngas include methanol, hydrogen and carbon monoxide, which are the chemical building blocks from which a whole spectrum of derivative chemicals are manufactured, including olefins, acetic acid, formaldehyde, ammonia, urea and others. The versatility of syngas as a precursor to primary chemicals and high-value derivative products provides the option of using relatively inexpensive coal to produce a wide range of valuable commodities.
Historically, production of chemicals from coal has been used since the 1950s and has become established in the market. According to the 2010 Worldwide Gasification Database, a survey of current and planned gasifiers, from 2004 to 2007 chemical production increased its gasification product share from 37% to 45%. From 2008 to 2010, 22% of new gasifier additions were to be for chemical production.
Because the slate of chemical products that can be made via coal gasification can in general also use feedstocks derived from natural gas and petroleum, the chemical industry tends to use whatever feedstocks are most cost-effective. Therefore, interest in using coal tends to increase for higher oil and natural gas prices and during periods of high global economic growth that may strain oil and gas production. Also, production of chemicals from coal is of much higher interest in countries like South Africa, China, India and the United States where there are abundant coal resources. The abundance of coal combined with lack of natural gas resources in China is strong inducement for the coal to chemicals industry pursued there. In the United States, the best example of the industry is Eastman Chemical Company which has been successfully operating a coal-to-chemicals plant at its Kingsport, Tennessee, site since 1983. Similarly, Sasol has built and operated coal-to-chemicals facilities in South Africa.
Coal to chemical processes do require substantial quantities of water. As of 2013 much of the coal to chemical production was in the People's Republic of China where environmental regulation and water management was weak.
It is also customary and considered lucky in Scotland and the North of England to give coal as a gift on New Year's Day. This occurs as part of First-Footing and represents warmth for the year to come.
In North America, Central Appalachian coal futures contracts are currently traded on the New York Mercantile Exchange (trading symbol QL). The trading unit is 1,550 short tons (1,410 t) per contract, and is quoted in U.S. dollars and cents per ton. Since coal is the principal fuel for generating electricity in the United States, coal futures contracts provide coal producers and the electric power industry an important tool for hedging and risk management.
In addition to the NYMEX contract, the IntercontinentalExchange (ICE) has European (Rotterdam) and South African (Richards Bay) coal futures available for trading. The trading unit for these contracts is 5,000 tonnes (5,500 short tons), and are also quoted in U.S. dollars and cents per ton.
The price of coal increased from around $30.00 per short ton in 2000 to around $150.00 per short ton as of September 2008. As of October 2008, the price per short ton had declined to $111.50. Prices further declined to $71.25 as of October 2010. In early 2015, it was trading near $56/ton.
Coal (by liquefaction technology) is one of the backstop resources that could limit escalation of oil prices and mitigate the effects of transportation energy shortage that will occur 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 per barrel, with the $35 being the break-even cost. With oil prices as low as around $40 per barrel in the U.S. as of December 2008, liquid coal lost some of its economic allure in the U.S., but will probably be re-vitalized, similar to oil sand projects, with an oil price around $70 per barrel.
In China, due to an increasing need for liquid energy in the transportation sector, coal liquefaction projects were given high priority even during periods of oil prices below $40 per barrel. This is probably because China prefers not to be dependent on foreign oil, instead utilizing its enormous domestic coal reserves. As oil prices were increasing during the first half of 2009, the coal liquefaction projects in China were again boosted, and these projects are profitable with an oil barrel price of $40.
China is the largest producer of coal in the world. It is the world's largest energy consumer, and relies on coal to supply 69% of its energy needs. An estimated 5 million people worked in China's coal-mining industry in 2007.
The energy density of coal, i.e. its heating value, is roughly 24 megajoules per kilogram (approximately 6.7 kilowatt-hours per kg). For a coal power plant with a 40% efficiency, it takes an estimated 325 kg (717 lb) of coal to power a 100 W lightbulb for one year.
As of 2006, the average efficiency of electricity-generating power stations was 31%; in 2002, coal represented about 23% of total global energy supply, an equivalent of 3.4 billion tonnes of coal, of which 2.8 billion tonnes were used for electricity generation.
The US Energy Information Agency's 1999 report on CO2 emissions for energy generation quotes an emission factor of 0.963 kg CO2/kWh for coal power, compared to 0.881 kg CO2/kWh (oil), or 0.569 kg CO2/kWh (natural gas).
Thousands of coal fires are burning around the world. Those burning underground can be difficult to locate and many cannot be extinguished. Fires can cause the ground above to subside, their combustion gases are dangerous to life, and breaking out to the surface can initiate surface wildfires. Coal seams can be set on fire by spontaneous combustion or contact with a mine fire or surface fire. Lightning strikes are an important source of ignition. The coal continues to burn slowly back into the seam until oxygen (air) can no longer reach the flame front. A grass fire in a coal area can set dozens of coal seams on fire. Coal fires in China burn an estimated 120 million tons of coal a year, emitting 360 million metric tons of CO2, amounting to 2–3% of the annual worldwide production of CO2 from fossil fuels. In Centralia, Pennsylvania (a borough located in the Coal Region of the United States), an exposed vein of anthracite 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 Australian Burning Mountain was originally believed to be a volcano, but the smoke and ash comes from a coal fire that has been burning for some 6,000 years.
At Kuh i Malik in Yagnob Valley, Tajikistan, coal deposits have been burning for thousands of years, creating vast underground labyrinths full of unique minerals, some of them very beautiful. Local people once used this method[clarification needed] to mine ammoniac. This place has been well-known since the time of Herodotus, but European geographers misinterpreted the Ancient Greek descriptions as the evidence of active volcanism in Turkestan (up to the 19th century, when the Russian army invaded the area).
The reddish siltstone rock that caps many ridges and buttes in the Powder River Basin in Wyoming and in western North Dakota is called porcelanite, which resembles the coal burning waste "clinker" or volcanic "scoria". Clinker is rock that has been fused by the natural burning of coal. In the Powder River Basin approximately 27 to 54 billion tons of coal burned within the past three million years. Wild coal fires in the area were reported by the Lewis and Clark Expedition as well as explorers and settlers in the area.
In 2006, China was the top producer of coal with 38% share followed by the United States and India, according to the British Geological Survey. As of 2012 coal production in the United States was falling at the rate of 7% annually with many power plants using coal shut down or converted to natural gas; however, some of the reduced domestic demand was taken up by increased exports with five coal export terminals being proposed in the Pacific Northwest to export coal from the Powder River Basin to China and other Asian markets; however, as of 2013, environmental opposition was increasing. High-sulfur coal mined in Illinois which was unsaleable in the United States found a ready market in Asia as exports reached 13 million tons in 2012.
The 948 billion short tons of recoverable coal reserves estimated by the Energy Information Administration are equal to about 4,196 BBOE (billion barrels of oil equivalent). The amount of coal burned during 2007 was estimated at 7.075 billion short tons, or 133.179 quadrillion BTU's. This is an average of 18.8 million BTU per short ton. In terms of heat content, this is about 57,000,000 barrels (9,100,000 m3) of oil equivalent per day. By comparison in 2007, natural gas provided 51,000,000 barrels (8,100,000 m3) of oil equivalent per day, while oil provided 85,800,000 barrels (13,640,000 m3) per day.
British Petroleum, in its 2007 report, estimated at 2006 end that there were 147 years reserves-to-production ratio based on proven coal reserves worldwide. 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". However, some nations haven't updated their information and assume reserves remain at the same levels even with withdrawals.
Of the three fossil fuels, coal has the most widely distributed reserves; coal is mined in over 100 countries, and on all continents except Antarctica. The largest reserves are found in the United States, Russia, China, Australia and India. Note the table below.
|Country||Anthracite & Bituminous||SubBituminous||Lignite||Total||Percentage of World Total|
|Bosnia and Herzegovina||484||0||2,369||2,853||0.3|
The reserve life is an estimate based only on current production levels and proved reserves level for the countries shown, and makes no assumptions of future production or even current production trends. Countries with annual production higher than 100 million tonnes are shown. For comparison, data for the European Union is also shown. Shares are based on data expressed in tonnes oil equivalent.
|Country||2003||2004||2005||2006||2007||2008||2009||2010||2011||Share||Reserve Life (years)|
Countries with annual consumption higher than 20 million tonnes are shown.
Countries with annual gross export higher than 10 million tonnes are shown. In terms of net export the largest exporters are still Australia (328.1 millions tonnes), Indonesia (316.2) and Russia (100.2).
Countries with annual gross import higher than 20 million tonnes are shown. In terms of net import the largest importers are still Japan (206.0 millions tonnes), China (172.4) and South Korea (125.8).
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