in the earths crust, which has been formed by the partial decay of plant materials accumulated millions of years ago and further altered by the action of heat and pressure.
COAL DEFINITION IN SITU THEORY DRIFT THEORY (Flood /Tsunami type wave velocity 800 km/h) 300 million of years/earth is 4.6 billion years old 15-20 m OF PLANT MATERIAL= 1 m OF COAL SEAM In INDIA 30 m seam of coal has been found THEORIES OF COAL FORMATION 450-600 m of plant material might have accumulated at that place. (Taipei 101:509 m tallest building in world) COAL FORMATION COALIFICATION
COAL % C C H O Heating value (MJ/kg) Cellulose Wood Peat Lignite Brown coal Bituminous coal Anthracite Graphite 44.5 50.0 59.9 61.8 69.5 78.7 91.0 100 100 100 100 100 100 100 100 100 13.9 12.0 10.0 7.8 7.9 6.0 4.7 0.0 111 88 57 54 36 21 5.2 0.0 - 19.77 18.66 20-25 27.20 32.10 32.56 32.91 COAL RANKS 1. Peat: starting point of coal formation does not come in the category of coal Carbon: 62-64%; Oxygen:35-30% 2. Lignites: mark the transition of peat to coal Carbon: 60-75% ; Oxygen: 30-20% Colour: black, brown, earthy Disintegrate very easily Briquetting is done Neyveli Lignite Corporation, Chennai Tamilnadu possesses largest reserves in India Electricity generation: 2490 MW COAL RANKS contd 3. Bituminous coals Sub-bituminous Between lignites and bituminous Carbon: 75-83% ; Oxygen: 20-10% No caking power Bituminous: black and banded Industrial and domestic usage Carbon: 75-90%: Oxygen:10-5% Semi-bituminous Between bituminous and anthracite Metallurgical coke formation Carbon: 90-93%; Oxygen:4-1% COAL RANKS contd 4. Anthracites Highest rank of coal Extreme of metamorphosis from the original plant material Carbon: 93+%: Oxygen: 2-1% Caking power zero Unusual coals Cannels: found rarely; high hydrogen content: burn with smoke and bright flame; does not fall in any category. Torbanites: fine grained coal, named after Torbane Hill of Scotland, rich in paraffin oil. Country Million tonnes % of world production China 2380 39.75 USA 1053.6 17.59 India 447.3 7.47 Australia 373.8 6.24 South Africa 256.9 4.29 Canada 62.9 1.05 United Kingdom 18.6 0.31 Pakistan 4.3 0.07 Japan 1.3 0.02 Total of the world 5,986.90 100 WORLD PRODUCTION OF COAL IN YEAR 2006
WORLD TOP TEN COAL PRODUCING AND CONSUMING COUNTRIES 1 quadrillion=1000 trillion 1 Btu=1.055 kJ Type of coal TOTAL RESERVE PROVED RESERVE INDICATED RESERVE INFERRED RESERVE COKING 32 17 13 2 NON- COKING 223 81 105 36 TOTAL 255 98 118 38
COAL RESERVES OF INDIA Source: MoC Years to consume this coal with present rate: 600 (As on 1.1.2007 in billion tonnes) State Proved Indicated Inferred Total % of total Jharkhand 36881 31094 6339 74314 29.11 Orissa 17464 30239 14296 61999 24.29 Chhattisgarh 10182 26826 4443 41451 16.24 West Bengal 11454 11810 5071 28335 11.10 Madhya Pradesh 7584 9259 2934 19777 7.75 Andhra Pradesh 8475 6328 2658 17461 6.84 Maharashtra 4856 2822 1992 9670 3.79 Uttar Pradesh 766 296 0 1062 0.42 Meghalaya 118 41 301 460 0.18 Assam 315 27 34 376 0.15 Bihar 0 0 160 160 0.06 Arunachal Pdesh 31 40 19 90 0.04 Sikkim 0 55 18 73 0.03 Nagaland 3 1 15 19 0.01 Total 98129 118838 38280 255247 100 COAL RESOURCES OF STATES IN MILLION TONNES Jan 1, 2007 Coking coal (carbon: 81-91%) Non-coking coal GRADING OF INDIAN COAL Grade Industry Ash % I steel <15 II steel 15-18 I washery 18-21 II washery 21-24 III washery 24-28 IV washery 28-35 Grades of coking coal High ash content (up to 50%) Lower heating/calorific value Inferior quality but suitable for power gen. GRADING OF INDIAN COAL Grade UHV, kcal/kg Ash % A >6200 <13.56 B 5600-6200 13.56-17.91 C 4940-5600 17.91-22.69 D 4200-4940 22.69-28.06 E 3360-4200 28.06-34.14 F 2400-3360 34.14-41.10 G 1300-2400 41.10-49.07 Based on 6 % moisture content Grades of non-coking coal Nationalization in 1971 Coal companies are paying the royalty to states This varies from Rs 90-250/tonne The rate is dependent of coal grade Rates are 16 August 2002 onwards ROYALTY TO STATES IMPORT OF COAL Coking and non-coking coals being imported Year Coking Non-coking Total 1991/92 5.27 0.66 5.93 1996/97 10.62 2.56 13.18 2000/01 11.06 9.87 19.70 2003/04 12.99 8.69 21.68 2005/06 16.89 21.70 38.59 2006/07 22.00 23.00 45.00 In million tonnes Proximate analysis Ultimate analysis Heating/calorific value
ANALYSIS OF COAL 1. Moisture content: 105 -110 o C 2. Volatiles: 92515 o C for 7 min time (with lid) 3. Fixed carbon: by difference 4. Ash: 80015 o C (without lid) PROXIMATE ANALYSIS IS:1350-I (1984) REPORTING: AS RECEIVED BASIS, MOISTURE FREE BASIS/DRY BASIS OR DRY ASH FREE BASIS A sample of finely ground coal of mass 0.9945 g was placed in a crucible of 8.5506 g in an oven, maintained at 105 o C for 4.0 ks. The sample was then removed, cooled in a dessicator and reweighed; the procedure being repeated until a constant total mass of 9.5340 g was attained. A second sample, of mass 1.0120 g in a crucible of mass 8.5685 g was heated with a lid in a furnace at 920 o C for 420 s. On cooling and reweighing, the total mass was 9.1921g. This sample was then heated without a lid in the same furnace maintained at 725 o C until a constant total mass of 8.6255 g was attained. Calculate the proximate analysis of the sample and express the results on as sampled and dry, ash-free basis. EXAMPLE OF PA MOISTURE mass of sample = 0.9945 g mass of dry coal = (9.5340-8.5506) = 0.9834 g mass of moisture = (0.9945-0.9834) = 0.0111 g % moisture = 0.0111 100/0.9945 = 1.11 % EXAMPLE OF PA contd.. ASH mass of sample = 1.0120 g mass of ash = (8.6255 - 8.5685) = 0.0560 g % ash = 0.0560 100/1.0120 = 5.53 % VOLATILE MATTER mass of sample = 1.0120 g mass of volatile matter + moisture = (9.1921-8.5685) = 0.6236 g % = 0.6236 x 100/1.0120 = 61.60
VOLATILE MATTER = 61.60-1.11 = 60.49% EXAMPLE OF PA contd.. FIXED CARBON % FC = 100 - % VM - % ash - % moisture = 100 - 60.49 - 5.53 - 1.11 = 32.87% Proximate analysis as received basis Moisture : 1.11% Ash : 5.53% Fixed carbon :32.87% Volatile matter :60.49%
EXAMPLE OF PA contd.. 1. Carbon 2. Hydrogen 3. Oxygen 4. Sulfur :0.5-2.50 % 5. Nitrogen :1.0-2.25 % 6. Phosphorus :0.1%;Blast Furnace: <0.01 % 7. Chlorine ULTIMATE ANALYSIS IS:1350- IV (1974) Mercury: A big problem from NTPC plants (up to 0.3mg/kg) 1. Calculated from proximate analysis 2. Calculated from ultimate analysis 3. Experimental determination HEATING VALUE 1. Gross/High heating value 2. Useful/low heating value Hydrogen Water (gas/vapor or liquid phase) Carbon Carbon Dioxide (gas phase) Latent heat of vaporization of water: 2.26 MJ/kg 1. Calculated from proximate analysis HEATING VALUE TAYLOR AND PATTERSON RELATIONSHIP HV=4.19 (82FC+ a VM) kJ/kg Where FC and VM are on dry ash free basis and a is an empirical constant which depends on the VM content of coal.
VM 5 10 15 20 25 30 35 38 40 a 145 130 117 109 103 98 94 85 80 2. Calculated from ultimate analysis HEATING VALUE DULONG FORMULA HV=338.2C+1442.8(H-O/8)+94.2S kJ/kg Where C, H, O and S are the % of these elements on dry ash free basis. 3. Experimental determination: Bomb calorimeter HEATING VALUE IS:1350-II (1970) solid /liquid samples can be analyzed 1 g air dried sample is burnt in a bomb in oxygen atmosphere rise in temperature gives the heat liberated and heating value is determined after doing the corrections for resistance wire and thread.
microprocessor based bomb calorimeters are now available BOMB OF CALORIEMETER VARIOUS COMPONENTS OF BOMB CALORIMETERIC EQUIPMENT ROUTES OF GENERATION OF HEAT AND POWER FROM COAL 1. Direct use as thermal energy in heating processes, furnaces and domestic heating by open fires 2. Transfer of the heat to a thermal fluid and application of the latter for heating and power i.e., steam for heating in process industry, central heating and electricity generation by steam turbines 3. Gas turbine route to electricity generation 4. Conversion to gas/liquid fuels and subsequent usage in IC engines/turbines (gas/steam) ROUTE I Domestic cooking/tea stalls/dhabas Space heating Lime and brick kilns Ceramic industry Generation of steam in a boiler Space heating by transferring heat of steam to air Process industry : Cogeneration is employed Utility services : steam turbines used ROUTE II GOVERNMENT ALLOWED ELECTRICITY GENERATION BY PRIVATE DEVELOPERS Tariffing Wheeling Banking SUPERCRITICAL BOILERS: A RECENT CONCEPT Critical pressure: 218 bar; Critical temperature: 374 o C Mark Benson; in 1922 Patent was granted 22 MPa pressure ; = 1-T 1 /T 2 ROUTE II contd.. Coal Boiler Steam turbine Heat exchanger Condensate Coal Hot air for space heating Alternator Electricity to process plant/grid Process plant Steam Steam
Cogeneration Steam turbine Alternator Electricity to grid Condensate Steam Steam Air ROUTE III Pulverizer Gas turbine Heat exchanger Coal Compressor Electricity to grid Alternator Preheated air Combustion chamber Air Vent Turbine exhaust ROUTE III (cleaner option) Gasifier and gas cleaning unit Gas turbine Heat exchanger Coal Compressor Electricity to grid Alternator Preheated air Combustion chamber Air Vent Turbine exhaust ROUTE IV (Pyrolysis / Gasification) 1. Partial Gasification or Pyrolysis /coking /carbonization / destructive distillation (heating in the absence of air) Solid Liquid Gas 2. Complete gasification with air/oxygen Gas PYROLYSIS
Coke (solid fuel) maximum; classical domestic smokeless fuel production Gas and liquid fractions low
Liquid fraction for chemicals recovery/liquid fuel
Coke for metallurgical furnaces; gas yield high; liquid low Low temperature carbonization 500-700 o C High temperature carbonization >900 o C Medium temperature carbonization 700-900 o C PYROLYSIS Pyrolyser Coal Condenser Water in Water out Gas for IC engines/ Gas turbines/ thermal applications Coke Liquid fraction Gas for heating of pyrolyser Flue gas Pretreatment unit Coal tar Liquid fuels Chemicals GASIFICATION ROUTE IV BERGIUS PROCESS 1. Bergius process Friedrich Karl Rudolf Bergius in 1913, Germany Nobel Prize in 1931 Worked with Haber World war II 56,000 bbl per day production Hydrogenation of vegetable oils 2. Fischer-Tropsch process Franz Fischer and Hans Tropsch in 1926, Germany Coal is hydrogen starved/hydrogen needs to be added to make it liquid (directly or indirectly) BERGIUS PROCESS Pulverizer Coal pasting unit Hydrogen Coal Fractionating column Bergius Reactor Heavy fraction HCs T=400-500 o C P= 20 -70 MPa Catalyst=Tin Conver.=97% F-T PROCESS Gasification unit Syn gas Cleaning Coal Fractionating column F-T Reactor HCs T=150-250 o C P= 1 -25 MPa Syn gas Catalysts : Iron or cobalt based Large number of patents worldwide F-T PROCESS (COMMERCIAL PLANTS) South Africa Oil and Gas Company 1950 established Oldest plant proving the F-T process viability Presently engaged in Qatar, Iran and Nigeria in similar projects F-T PROCESS (COMMERCIAL PLANTS) F-T PROCESS(COMMERCIAL PLANTS) F-T PROCESS Players in this area of Gas To Liquid (GTL) 1. GE 2. Exxon 3. Shell 4. BP 5. Chevron 6. Sasol With crude touching the $145+ these two technologies would be economically viable now UNDERGROUND/ IN SITU COAL GASIFICATION A process applied to the non-mined coal seams Injection and production wells are drilled End gas mix depends on type of coal seam Air/ oxygen can be used for gasification Syn gas can be used for power generation in combined cycle Syn gas can be converted to chemicals/fuel by F-T process UNDERGROUND/ IN SITU COAL GASIFICATION Source: World Coal Institute COAL COMBUSTION AND ENVIORNMENT Global warming Green house gases: water vapor, carbon dioxide, methane, nitrous oxide, CFCs, SF 6 (circuit breakers, high DE constant) SF 6 is 22, 200 more potential than CO 2 Carbon dioxide gas: main culprit from fossil fuels; not from biomass Intergovernmental Panel on Climate Change (IPCC) Nobel Peace Prize 2007 : R. K. Pauchari and Al Gore Reduction in Carbon Dioxide emissions G8 meeting in Japan in July 2008
COAL COMBUSTION AND ENVIORNMENT Carbon Dioxide Emissions and Carbon Dioxide Concentrations (1751-2004) Present CO 2 level:483 PPM COAL COMBUSTION AND ENVIORNMENT Global Carbon Cycle (Billion Metric Tons Carbon) COAL COMBUSTION AND ENVIORNMENT U.S. Anthropogenic Greenhouse Gas Emissions by Gas, 2006 (Million Metric Tons of Carbon Dioxide Equivalent) CARBON DIOXIDE CAPTURE AND SEQUESTRATION Sequestration 1. Gaseous storage in various deep geological formations (including saline formations and exhausted gas fields) 2. Liquid storage in the ocean 3. Solid storage by reaction of carbon dioxide with metal oxides to produce stable carbonates Capture Proven technology being used in process industries and power plants
BUT THE COST IS DECIDING FACTOR ULTIMATE SOLUTIONS