• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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    • 专利摘要:
    An improvement in a process for producing hydrocarbons which boil in the gasoline or diesel fuel range from coal where the coal is reduced to a particle size below 2 mm, mixed with oil to form a pumpable pulp which is contacted with hydrogen in a hydrogenation zone resulting in a liquid fraction and a high melting residue fraction is disclosed. The invention resides in removing the high melting residue to a gasifying vessel to which is introduced granular coal of particle size of 3-50 mm. To the gasifying vessel is added a gasifying agent, e.g., water vapor alone or in admixture with oxygen which flows in countercurrent to the direction of the granular coal. As a result of the process, a gasification product is obtained comprising hydrogen and carbon monoxide.
    公开号:SU812186A3
    申请号:SU782646409
    申请日:1978-08-09
    公开日:1981-03-07
    发明作者:Айзенлор Карл-Хайнц；Гэнсслен Ханс
    申请人:Металлгезельшафт Аг (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to methods for producing hydrocarbons from coal and can be used in the coal chemical industry.
    Known methods for producing hydrocarbons from coal by catalytic hydrogenation of source coal, followed by separation of the hydrogenation products [1] and [2].
    Closest to the invention is a method for producing hydrocarbons from coal by hydrogenation of the source coal, followed by separation of the hydrogenation products (h].,
    The process is carried out in the presence of a catalyst or without it, at 350 450 ° C, a hydrogen pressure of 100-350 atm, a ratio of solvent and coal 1: 2 - 10: 1.
    As a solvent, a distillation residue of vacuum distillate is used. crude oil with a boiling point of 260 ° С.
    The products obtained are separated with (production of hydrocarbons and a tarry residue.
    The aim of the invention is to increase the yield of target products.
    This goal is achieved by the proposed method for producing hydrocarbons from coal 1 by hydrogenating the initial coal, then separating the hydrogenation products to produce hydrocarbons and a tarry residue, mixing the residue with coal having a grain size of 3-50 mm, and gasifying the mixture in a fixed bed under pressure of 10-100 atm in countercurrent gasifying agents.
    Preferably, the resinous residue is granulated before mixing with coal to obtain granules of 3-50 mm in size.
    Hydrogenation of coal is carried out at 300-500 ^ 0, a pressure of 100-400 atm in the presence of or without catalyst introduced from the outside.
    Products resulting in- result-. gasification can be processed in various ways.
    The possibility of varying the method is illustrated using the drawing.
    In the zone 1 of preparation (enrichment) of coal through line 2, pre-crushed coal with a grain size of less than 2 mm is loaded, oil fractions with so-called bales are fed through line 3. 250-450 ° C. In the preparation zone 1, the power of the conveying device 28 is supplied to the coal gasification zone 29 under pressure, where granular coal with a grain size of 3-50 mm is fed through line 30. Gasification is carried out in a fixed bed, "through which gasification agents are passed from below from below in countercurrent flow. Water vapor supplied through line 31 and oxygen fed through line 3.2 are used as gasification agents. Along with these gasifying agents you can use! also С0 а , In the zone of coal gasification the technological process is carried out at a pressure of 10-100, mainly 15-50 at.
    The lines 33 from the coal gasification zone divert the zone containing the catalyst used in the hydrogenation zone 5. The resulting crude gas ....... .. ^ with a temperature of 300-800 ° C is removed by pressure, mainly at 50-200C, 20 from the coal gasification zone via line 34 and sent to the cooling zone 35, in which coarse washing is also carried out using circulating condensate. ' Excess condensate is fed through line 36 to the resin separation aeon 37, since the condensate contains resin and oil. The cooled gas of line 38 is fed into the fine purification zone 39, where sulfur compounds are removed from the gas and in order to bring the gas to the required degree of purity for synthesis.
    further grinding of coal and intensive mixing with oil fractions. A catalyst is fed through line 4 to the preparation zone, 2-10% by weight, relative to the starting coal. From preparation zone 1, a coal pulp is sent to hydrogenation zone 5.
    .,. Hydrogen is fed via line 6 to hydrogenation zone 5. ''
    The product of the hydrogenation zone 5 po.
    (lines 7 are sent to separation zone 8, where liquid and vapor phases are separated at 400-450 ° C. Liquefied hydrocarbons are separated from the gas stream by fractionated condensation. Residual gas is taken off via pipeline 9. Some condensable components in the zone Separations are separated by distillation (distillation). The fraction with a boiling point of 30-250 ^ 0 with a normal line 10 is sent to a hydrotreatment unit 11, where hydrogen is fed through a line 12, and the coal hydrotreatment unit catalyzes coal serivaniem.
    In line 13, gasoline used as a motor fuel is diverted. To increase the octane number, gasoline can be supplied in whole or in part via line 14 to aromatization zone 15 .. The resulting product is taken along line 16. From the separation zone 8, a high-boiling fraction of st. bale. at least 230 ^ 0 at normal pressure and direct it to the hydrocracking unit 18,. where hydrogen is fed from line 19 * Hydrocracking is preferably carried out using catalysts. The hydrocracking product is sent to distillation zone 20 (distillation). The heavier fraction is diverted to ϊιό of line 21 and used as diesel fuel. The lighter fraction along line 22 is directed to aromatization zone 15.
    The pulp fed into zone 5 of hydrogenation contains 30-60% solids.
    The pressure in the hydrogenation zone is 100-400, mainly 120-350 at, temperature 300-500, mainly 4О0 ~ 475 ° С.
    ♦ Hot sludge is removed from zone .8. separation along line 23. It contains unreacted coal, high-fatty oils, and catalyst material if used for hydration. The sludge is fed into the vacuum distillation zone 24. The obtained niekokipalny fraction on line 25 serves on the installation 18 of hydrocracking. High melting resin containing resin. and solids, the residue along line 26 is sent to granulation zone 27. Granular residue with 10
    Depending on the gas composition before or after conversion Fine purification can be controlled and CO content = I th in the gas (not shown). Gas from the fine zone, consisting mainly of CO, and sc 4 , is sent. along line 40 to the synthesis zone 41 40 according to the Fischer-Tropsch method.
    The process in this zone is carried out at a pressure of 5-30 bar, a Temperature of 150-350 ° C, mainly in the presence of catalysts. the catalysts may contain As active components, for example, cobalt, manganese or iron. Typically, a fixed catalyst bed is used. The conversion reaction proceeds isothermally and adiabatically * The primary product of synthesis by heat exchange and cooling is isolated from the gas stream and sent to line separation device 43 via line 42, gasoline is taken off line 44, and diesel fuel is fed through line 44e 45. The high-boiling residue is taken off via line 46 and directed to paraffin cleavage zone 47, where hydrogen is supplied via line 48. The resulting gasoline is discharged 60 through line 49, diesel fuel through line 50. It is advisable to further clean these products to remove oxygen-containing compounds (not shown in the drawing). Residual gases from aeons of synthesis 41 by the method
    Fischer-Tropsch is taken off line 51 and used for its intended purpose.
    Resin distillation products from the hydrogenation zone 5 can be fed into the resin separation zone 37 through line 52. The fractions obtained from this can be reused in the process. So, for example, heavy resin containing solids and boiling distillates and condensates boiling at temperatures above 250 ° C are sent to line 3 and from there to preparation (enrichment) zone 1. a fraction with a range of gasoline boiling points can be sent to a hydrotreating unit · 11, and higher boiling condensates or distillates, with the exception of solids containing condensates or residual oils, can be sent to a hydrocracking unit 18, the heaviest dust-containing fraction can be 'but recycle to coal gasification zone 29.
    Example 1. Used. Coal contains about 4.65 weight,% ash and about 2.78 wt.% Water. Pure coal without water and ash has the following), wt.%: 80,44
    4.76
    12.37
    1.27
    1.17.
    below is the relative chemical composition • S n o
    N s
    All of the following are sown to clean coal. 1000 tons of PURE coal with a grain size of less than 2 mm are mixed with ύ 1500 tons of a fraction of hydrogenation hydrogen having t. Bales. 250 33 450 ° C in zone 1 in the preparation of pulp. In the preparation zone 1, subsequent grinding of coal to grains less than 500 microns in size and not less than 50% with grains less than 100 microns in size is carried out. With the same grain sizes, 20 tons of ferruginous sludge from the bauxite enrichment site is fed into the preparation zone 1 as a catalyst. The sludge consists mainly of iron oxide hydrate. The pulp from coal, oil and catalyst is fed into the hydrogenation zone and at the same time it is compressed to 350 bar and heated to a reaction temperature of 460 ° C. The pulp is heated in the presence of hydrogen, which in the amount of 65 tons is supplied as fresh gas via a pipeline <6 a zone 5 hydrogenation. In the hydrogenation zone, 5555 t of Hj, 10 t chemically binds together with non-condensing low boiling hydrocarbons from separation zone 8 as residual. gas is discharged via line 9. This residual gas also contains CO, 0 ¾ g HjjS and NHj. In the first stage, the separation at 450 ° C and an operating pressure in the hydrogenation zone 350 bar semi-> chayut slurry in an amount of 480 t, koto-: ing consists of non-evaporable 65 carbon hydrogens, unreacted coal / ash and catalyst. After a stepwise decrease in pressure, the sludge is subjected to vacuum distillation (distillation) in zone 24. This gives 260 tons of distillate and 220 tons of high-melting resinous residue, which consists of 25 tons of ash, 50 tons of unreacted coal, 20 tons of catalyst and 100 tons of carbon compounds. yes, hydrogen, oxygen, sulfur, and azo. The distillate is sent along line 3 directly to preparation zone 1.
    In the separation zone 8, after cooling, 1740 tons of liquid products are released: TOV, which are subjected to further separation by distillation 15 '.
    At the same time, 1240 tons of heavy oil released through pipeline 3 are also fed into preparation zone 1. Then, during distillation, 530 tons of liquid products with an upper boiling point of 440 ° C are isolated, which are fed partially to the hydrotreating unit 11 and partially to the hydrocracking unit 18. High-melting residue from the distillation zone 24 under vacuum, which has a so pl. above 100 ° C, served in the zone 27 granulation. In the granulation zone, the melt is pumped through nozzles with a diameter of about 10 mm into a water bath and is thus formed into bundles, which are then crushed into granules 5-10 mm long. Wet granulate is mixed with granular (with a grain size of 3-50 mm) coal in the ratio of 220 tons of granulate to 897 tons of coal (in terms of clean coal) and fed into pressure gasification zone 29, from which 125 tons of ash are removed in pieces contain .20 tons of hydrogenation catalyst. This amount of catalyst is considered lost. When the crude gas is cooled from the hydrogenation zone, 77 tons of tar and oil are condensed under pressure. The fraction containing heavy resin, along line 3 is also served in zone 1 of the preparation, environments; the distillate from the separation zone 37 is directed to a hydrocracking unit 18. A low boiling fraction is fed to the hydrotreating unit 11. The resulting fine gas purification of gas gasoline in an amount of 43 tons is also processed at the hydrotreatment unit 11. The resulting hydrotreating product, together with the gasoline obtained in the hydrocracking unit, is aromatized in the aromatization zone, while hydrogen is formed in the aromatization zone. From the zone of coal hydrogenation and processing of products emitted during gasification (without synthesis according to the Fischer-Tropsch method), 284 tons of automobile gasoline and 314 tons of diesel fuel are obtained. Residual hectares formed in zones and installations 5, 8, 11, 18 and 20
    Ί they are freed from CO ^, desulfurized and, together with the desulfurized residual gas from the aromatization zone 15, at temperature and pressure · decompose into components. The recovered hydrogen is returned to the process. Methane and ethane are used to produce hydrogen in a known manner. Propane can be discharged as a liquefied gas, and butane serves to control the pressure. a pair of gasoline received.
    The last zone 39 Hepa, sintee-SEA consists essentially of CO and H together with a small amount of methane.
    In the synthesis zone, according to the Fischer-Tropsch method, in the presence of a multistage fixed bed of an iron catalyst-synthe-gae catalyst at temperatures of about 220 ° C and a pressure of 30 atm it is converted to hydrocarbons. The degree of conversion (conversion) is 20 90% in terms of CO and H ^. The reaction product is isolated from the gas stream by condensation by cooling to room temperature. By cooling to a temperature of 25 below 0 ° C., ligroin is isolated at a working synthesis pressure. In the separation device, the gasoline fraction of diesel fuel is distilled from the capacitors. Both products are lightly cleaned before being diverted as motor fuels in order to increase the octane number and remove oxygen-containing components.
    From the separation device 43 __, the distillation residue is sent to paraffin cleavage zone 47, where, in the presence of hydrogen, catalytic decomposition takes place to produce mainly diesel fuel and gasoline. In total, after processing in the synthesis zone according to the Fischer-Tropsch method, 142 tons of motor gasoline and 72 tons of diesel fuel are obtained.
    Residual gases are cooled and decomposed.
    The mixture of the components of the synthesis gas, C0 2 and H 2 is returned to the synthesis aeon 41, methane / and ethane are reformed, the fraction after hydrogenation of jq olefins is removed as a liquefied gas. The C l fraction is added to the resulting gasoline.
    "in. the hydrogenation zone and the Fischer-Tropsch synthesis zone together from 1897 tons of clean coal receive · 426 tons of gasoline and 386 tons of diesel fuel. In addition, 110 tons of propane are discharged in the form of liquefied gas. This yield corresponds to a thermal efficiency of 60 actions of 65% without taking into account the coal needed to create energy and without including 'by-products' of sulfur, ammonia and C 4 alcohols - synthesis eons according to the Fischer-Tropsch method. 65
    Example 2. The process is carried out as in example 1.
    1000 tons of pure coal are hydrogenated. However, 1794 tons of pure coal and 220 tons of high-melting residue are charged into the gasification zone. Thus, an additional 64 tons of resin are sent to a hydrocracking unit 12 and 16 tons of gasoline to a hydrotreating unit 11. Due to this, the output from the hydrogenation zone of motor gasoline and diesel fuel increases, respectively, to 284 tons and 384 tons.
    The yield of the primary product from the synthesis zone by the Fischer-Tropsch method is almost doubled compared to Example 1. In zone 47 of paraffin cleavage, lower temperatures are maintained, thereby increasing the yield of liquid products. Receive 178 tons of gasoline and 217 tons of diesel fuel. The propane yield rises to 150 tons. Due to the increased yield of products from the synthesis zone according to the Fischer-Tropsch method, the amount of residual gas increases accordingly. Since the hydrogen consumption for hydrogenation varies insignificantly, the excess residual gas can be used for energy production, for example, as a long-distance gas supply gas or for a gas turbine.
    Example 3. The process is carried out as in example 1, however, the synthesis according to the Fischer-Tropsch method is not included in the technological scheme. As explained in example 1, for the hydrogenation of 1000 tons of pure coal requires 70-75 tons of hydrogen. Part of this hydrogen is obtained from 60 tons of methane formed during hydrogenation. With the help of the well-known steam reforming and ^ »- this methane, a gas rich in hydrogen is obtained. 220 tons of high-melting residue and 200 tons of granular coal are supplied to aeon · 29 of gasification. After purification and conversion (conversion), gas with a content of at least 95 vol.% H ^ is obtained from the gasification zone gas after purification and conversion (conversion). It can be used in the hydrogenation process. Gas condensate Gasification eons are directed to resin separation aeon 37. In this case, 43 tons of resin are separated and sent to a hydrocracking unit 18. In addition, 23 tons of gas benein are formed, which are sent to the hydrotreatment unit 11. The result of the process is' 264 tons of gasoline and 284 tons of diesel fuel.
    权利要求:
    Claims (3)
    [1]
    This invention relates to methods for producing hydrocarbons from coal and can be used in coal chemical applications. Siodoids for the production of hydrocarbons from coal are known by catalytic hydrogenation of the original coal with an after-ampoule separation of the products of yards and iroa fl and 2. The most brightening of the invention is a method for producing hydrocarbons from coal by hydrogenating the original coal followed by separating the hydrogenation products of 1h. The process is carried out in the presence of talizator or without it, at 356450 ° C, hydrogen pressure of 100-350 atm, the ratio of solvent and coal 1: 2 - 10: 1. As a solvent, the bottom residue is used by vacuum distillation of crude oil with the initial boiling point. The resulting products are separated to produce hydrocarbons and a gummy residue. The aim of the invention is to increase the yield of the target products. The goal is achieved by the proposed method of producing hydrocarbons from coal by hydrogenating the original coal, subsequent separation of hydrogenation products to obtain hydrocarbons and tarry residue, mixing the residue with coal having a grain size of 3-50 mm, and gasifying the mixture in a fixed bed under a pressure of 10-100 at in countercurrent gasification agents. It is desirable to granulate the gummy residue before mixing with coal to obtain granules of 3-50 mm in size. Hydrogenation of coal is carried out at SrO-500 ° C, a pressure of 100-400 atm in the presence or absence of a catalyst introduced from outside. The products obtained by a result. those gasifications can be recycled in various ways. The possibility of varying the method is explained by the drawing. Pre-crushed coal with a grain size of less than 2 mm is loaded into line 1 of preparation (enrichment) of coal via line 2, and oil fractions with so-called bales are transferred via line 3. 250-450 0. In zone 1 of the preparation, the coal is further crushed and interactively mixed with the oil fractions. On line 4 in the preparation area serves the catalyst, 2-1.0 weight, 1W relative to the original coal. From zone 1 of preparation. Pulp from coal is directed to hydrogenation zone. 5..,. Along the line b hydrogen is fed to the hydrogenation zone 5. . . The product of the hydrogenation zone is 5 per. Tinium 7 is directed to the jS section where neither at 400-450s does the separation of liquid and vapor phase occur. By means of fractionation condensation, liquefied hydrocarbons are separated from the gas stream. The residual gas is withdrawn through line 9. Which is the densitating component of the zone; 8 separations are separated by distillation (distillation). Fraction with t. Kip. BW-250 s at normal pressure, mainly when the line 10 is directed to the unit 11 Hydrotreating, where the line 12 serves hydrogen. At the hydrotreatment unit, catalytic conversion of coal is carried out together with desulfurization. Gasoline, used as motor fuel, is discharged through line 13. Gasoline can be supplied in whole or in part through line 14 to the aromatization zone 15 to hang the octane number. The resulting product is taken along line 16. From zone 8, the line 17 is discharged Vyokokok fraction of Art. kip not less than 2 at normal pressure and press it onto the mouth of the plant, 18 hydrocracking where water supply is fed via line 19. It is desirable to conduct hydrocracking using catalysts. The hydrocracking product is sent to distillation zone 20 (distillation). The heavier fraction is withdrawn along line 21 and used as diesel fuel. The lighter fraction in line 22 is directed to the rearm zone 15. The pulp fed to the hydrogenation zone 5 contains 30-60% solids. The pressure in the hydrogenation zone is 100-400, preferably 120-350 atm, the temperature is 300-500, preferably 400-475 C. Hot sludge is removed from zone 8 separation along line 23. It contains un-reacted coal, high-grade oil and catalyst material when used; for hydrogenation. The slurry is fed to the vacuum distillation zone 24. The resulting effluent fraction via line 25 is fed to hydrocracking unit 18. The high melting resin-containing resin and solids along line 26 are directed to granule area 27. The granulated residue is conveyed by means of a conveyor device 28 to coal gasification zone 29 under pressure, where granular coal with a grain size of 3-50 mm is supplied via line 30. The gasification is carried out in a fixed bed, through which gasification agents are passed from below in a countercurrent. Water vapor I of the supplied software line 31, and oxygen, nojaiiEtSiaeMEaK through line 3.2, are used as gasifying agents. Along with these gasifying agents, you can also use GO. In the gasification zone of the coal, the technological orotropy is at a pressure of 15–5–0 atm. According to the 33 KZ LINE of the gasification zone, the coal was diverted to the zone containing the hydrogen permeation zone Q5 and Qjop. Obz azuyadnys untreated pelvis; t: y and aturry 300-VOb ° C are taken out of the zone of gadifitsyy coal via line 34 and aa is equal to 50 (t. cooling zone 35, in which the coarse is also carried out. "Filling with condensate condensate. Liuin 36 supplies pitch to eon 37 offices as the condensate contains Resin and oil. The cooled gas 6 of LIVIA 38 is fed to zone 39 tons of cleaning, where the sulfur compounds and NH are removed from the gas to bring the gas to 10% of the 5GTV1 for syntheses. ,.., The air composition and the gas composition before and after fine cleaning with a condenser. Make a gas with a gas, e gas (not shown on drawing ©), Gas ya / fine zone, iBi rnaBflSM composed from FROM, N. i.Sn, NBV: avl $ 051: on line 40 to zone 41 (Zainfea according to the Fischer-tropsha method. The procession in this zone is carried out at a pressure of 5-36, an extension of 150-350 s, and it can be carried out in the presence of catamatron | rv Catalizaforn. As a rule, nvaodaihi B1 catalyst layer is used. The reaction is converted isothermal &amp; adiabatically. The primary product of the synthesis of the heat-coil and cooling is transferred from the gas plant and sent via line 42 to the radar unit 43. Senenn is diverted through line 44, and diesel fuel is withdrawn through line 44. High boiling point residue is withdrawn through line 46 and sent to paraffin cleavage in Erk 47, where line 48 supplies hydrogen. Gasoline is diverted to 49, D15Zelnov fuel via line 50. These products should be further refined to remove oxygen-containing compounds (not shown). The residual gases from the Fischer-Tropsch zone 41 synthesis are withdrawn via line 51 and used for their intended purpose. Resin transfer products from the hydrogenation zone 5 can be fed to the resin separation zone 37 via line 52. The resulting fractionline can be reused in the process. For example, solids containing solid resin and distillates boiling at a temperature above 25 0 ° C are sent to line 3 and from Tyj a to preparation zone 1 (enrichment). The fraction with a boiling range of gasoline can be sent to unit 11 for hydraulic sources, and higher boiling condensates or distants, with the exception of those containing hard solids or residual condensates, can be directed to the most heavy, heavy dust by setting 18 hydrocracking. the fraction can be recycled to coal gasification zone 29. Etc. and me 1. Activity. Coal contains about 4, 5 Å of EOLA and about 2.76 wt.% of water. Pure urol without water and ash has the following; OW x 1 by composition, wt.% J: C 80.44:. .V H 4.76 O 12.37 N 1.27; , L. vs:, 1.17 ..., .... All the data below refer to pure coal, 1000 tons of pure coal with a grain size of less than 2 mm are mixed, e 1500 tons of the Madf fraction, and hydrogenation having a bale. $ 2, in zone 1 of the preparation in the pulp, in zone 1, the coal is subjected to crushing to a grain of e less than 500 microns and not less than 50% with a grain size: less than 100 microns. With the same grain sizes, 20 tons of ferrous sludge are fed to the preparation zone 1 as a catalyst at a bauxite processing site. The sludge consists mainly of iron oxide hydroxide. The pulp from coal, oil and catalyst is fed to the hydrogenation zone and at the same time it is combined to 350 bar and heated to a reaction temperature of 46 ° H :, the pulp is heated in the presence of hydrogen, which in the amount of 65 tons in the form of this gas is fed through pipeline 6 to the zone 5 hydrogenations, in the hydrogenation zone, chemically bound 55 tons of N, 10 tons of N, together with non-condensable low-boiling hydrocarbons from zone 8. the separation as residual gas is withdrawn through conduit 9. Etsk residual gas contains, in addition, CO, CQj,, and MHj. In the first stage of separation, at 450 s and the working pressure of the scientific research institute in the hydrogenation zone of 350 bar, 480 tons of sludge is obtained, which consists of non-evaporating hydrocarbons, unreacted coal, ash and catalyst. After a stepwise decrease in pressure, the ishes are subjected to distillation (distillation) under vacuum in zone 24. This produces 260 tons of distillate and 220 tons of high-melting resinous residue, which consists of 25 tons of ash, 50 tons of unreacted carbon, 20 tons of catalyst and 100 tons of compounds carbon, hydrogen, oxygen, sulfur and azoTa, Distillate is sent along line 3 i directly to zone 1 of the preparation. In the separation zone 8 after cooling, the day is allocated 1,740 tons of liquid products, which are subjected to further separation by distillation. At the same time, 1240 tons of heavy crude oil through pipeline 3 is also fed to zone 1 of the preparation. Then, during distillation, 530 tons of liquid products with an upper boiling point of 440-G are separated, which are supplied partially to the hydrotreating unit 11 and partially to the hydrocracking unit 18. The high melting residue from the distillation zone 24 under vacuum, which is m.p. above 100 ° C, is fed to granulation zone 27. In the granulation zone, the Hari melt etaut through nozzles about 10 mm in diameter into a water bath and is thus formed into strands, which are then shot into granules 5-10 mm long. Wet granulate is mixed with granular (with a granule size of 3-50 mm) coal in the ratio of 220 tons of granules to 897 tons of coal (in terms of pure coal) and is fed to the gasification zone 29 under pressure, from which 125 tons of ash are removed in the form chunks that contain .20 tons of hydrogenation catalyst. This amount of catalyst is considered lost. Upon cooling, the crude gas from the hydrogenation zone under pressure condenses 77 tons of tar and oil. The fraction containing the heavy resin is also fed via line 3 to preparation zone 1, and the research institute distills the short-circuit distillate of separation zone 37 to the hydrocracking unit 18. The low boiling fraction is fed to the hydrotreating unit 11. The gas gasoline produced in the amount of 43 tons is also treated in the hydrotunnage unit 11. The hydrorefine product obtained with this, together with gasoline obtained at the installation, is subjected to hydrocracking, is subjected to aromatization in the aromatization zone 15, while hydrogen is formed in the aromatization zone. 284 tons of motor gasoline and 314 tons of diesel fuel are obtained from the coal hydrogenation zone and the processing of products released during gasification (without Fisher-Tropsch synthesis). The residual gas is freed from Sat ,, desulfurized and, together with two sulfated ostag exact gas from the aromatization zone 15 at a temperature and under pressure, is decomposed into the components, the endowed hydrogen is returned to process. Methane and ethane serve to produce hydrogen in a known manner. Propane can be discharged as a liquefied gas, and butane serves to control the pressure. The vapor of gas produced. The past 39 fine purification zone. The synthesis gas consists practically of CO and H / j, along with a small amount of methane. In the Fischer-Tropsch synthesis zone, in the presence of a multi-stage fixed bed of an iron catalyst, synthesis gas is converted to hydrocarbons at terarate pax around and pressure of 30 af. The degree of conversion (conversion) is 90% in terms of CO and Hj. The reaction product from the gas stream is condensed by cooling to room temperature. By cooling to a temperature below 0 ° C at the working pressure of the synthesis, ligroin is isolated. In the separator unit, the gasoline fraction of diesel fuel is distilled from the condensers. Both products, before they are discharged as motor fuels, are subjected to easy purification in order to increase the octane number and remove the oxygen-containing components. From the separation device (43), the distillation residue is sent to the zone of paraffin 4 4 cleavage, where, in the presence of hydrogen, catalytic decomposition takes place, producing mainly diesel fuel and gasoline. In general, after processing in the synthesis zone by the Fischer-Tropsch method, 142 tons of motor gasoline and 72 tons of diesel fuel are obtained. Residual gases are subjected to cooling and decomposition. The mixture of the components of synthesis gas, CO and H, j is returned to zone 41 of the synthetic, methane / and ethane is subjected to reforming, the fraction C after the hydrogenation of olefins is removed in the form of liquefied gas. Fraction C is added to the resulting gasoline. sB. in the hydrogenation zone and the synthesis zone by the Fischer-Tropsch method, out of 1,897 tons of pure coal, 426 tons of motor gasoline and 386 diesel fuel are obtained. In addition, 110 tons of propane are discharged as liquefied gas. This yield corresponds to a thermal efficiency ratio of 65% without taking into account the coal required for energy production and without the inclusion of sulfur byproducts J, ammonia and alcohol C in the Fischer-Troshi synthesis zone. Example 2. The process is carried out as in Example 1. A loop of pure coal is subjected to hydrogenation. However, 1794 tons of pure coal and 220 tons of high-melting residue are loaded into the gasification zone. Thus, an additional 64 tons of resin are sent to hydrocracking unit 12 and 16 tons of gasoline to unit 11 for hydrotreatment. The moisture output from the hydrogenation zone of motor gasoline and diesel fuel increases, corresponding to BeifHo, to 284 tons and 384 tons,. The yield of the primary product from the Fischer-Tropsch synthesis zone is almost doubled in comparison with Example 1. In the paraffin cleavage zone 47, lower temperatures are maintained, thereby increasing the yield of liquid products. Get 178 tons of gasoline and 217 tons of diesel fuel. The yield of propane rises to 150 tons. Due to the increased output of products from the synthesis zone by the Fisher-Tro1V method, the amount of residual gas increases accordingly. Since the hydrogen consumption for hydrogenation varies only slightly, the excess residual gas can be used to produce energy, for example, as a gas for long-distance gas supply for a gas turbine. Example 3. The process is carried out as in Example 1, however, Fischer-Tropsch synthesis is not included in the flow chart. As explained in Example 1, 70-75 tons of hydrogen are required to hydrogenate 1000 tons of clean coal. Part of this hydrogen is obtained from forming Eoc with hydrogenation in the amount of 60 tons of methane. With psschoshch famous steam reforming th th methane polupigot. rich wyudog native gas. Zone 29 gaeif Kats111 serves 220 tons of high-granular residue and 200 tons of granular coal. Ne gas of the gasification zone after purification and cooling (conversion) produces a gas with a content of at least 95 vol.% H, through low-temperature decomposition. It can be used in the progress of hydrogenation. The gas condensate of the gasification zone is directed to the resin separation zone 37. At the same time, the 43 h resin section, which is sent to the Kpoi hydrocracking unit 18 u | In addition, 23 tons of gas turbine gas are produced, which are sent to the hydrotreating unit 11. As a result of the process, 264 tons of motor gasoline and 284 tons of diesel fuel are obtained. . . Claims 1. A method of producing hydrocarbons from coal by hydrogenating raw coal in the presence of crude oil at elevated temperature and pressure, then separating the hydrogenation products to produce hydrocarbons and resinous residue, with the increase of the yield of the target objects, the resinous residue is mixed: “with coal having a granule size of 3–50 mm, and subjected to gasification under pressure of 10–100 atm in a countercurrent {gasification agents.
    [2]
    2. The method according to p. 1, m and m jm and also with the fact that / resinous wasps; | H | 1 Trk before being mixed with coal, granulate with obtaining granules of 3-50 mm in size.
    [3]
    3. A method according to claim 1, characterized in that the hydrogenation of the carbon is carried out at 300-500 ° C, a pressure of 100-400 at.
    Sources of information taken into account in the examination
    1. US Patent No. 3,745,108, cl. 208-10, published. 1973.
    2. US patent 3769198, cl. 208-10, published. 1973.
    3. US patent 3849287,
    , cl. 208-8, published. 1974 (prototype).
    "3
    F F UU
    eight
    42
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    同族专利:
    公开号 | 公开日
    US4260472A|1981-04-07|
    DE2735829A1|1979-02-22|
    AU519923B2|1982-01-07|
    AU3869978A|1980-02-14|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE19772735829|DE2735829A1|1977-08-09|1977-08-09|METHOD FOR PRODUCING HYDROCARBONS FROM COAL|
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