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Improvements in or relating to the manufacture of valuable oils and/or gases from coal by a hydrogenation process

机译:通过加氢工艺从煤炭生产有价值的油和/或气的改进或与之有关的改进

摘要

Hydrocarbon oils and gases are obtained from coal by subjecting the coal to extraction with an organic solvent or solvent mixture, removing the solvent from the extracted fraction and replacing it by a second solvent capable of holding the extracted material in solution or suspension, and subjecting the composition so formed to hydrogenation. When a gaseous final product is desired, the hydrogenation product is subjected to thermal decomposition at temperatures between 700--900 DEG C. As first solvents, hydrocarbons or other neutral solvents may be used, e.g. tetrahydronaphthalene, decahydronaphthalene, or hydrocarbons boiling above 250 DEG C., e.g. phenanthrene, hydrogenated phenanthrenes and anthracenes, benzylnaphthalenes, diphenylbenzene and tetra-amylene; or phenols, e.g. tar acids, p p-benzyl-phenol, or 1-(a -hydroxy-benzyl) naphthalene; or basic compounds, e.g. pyridine, quinoline, quinaldine, acridine, benzyl quinolines, hydrogenated acridines and other hydrogenated heterocyclic bases. Preferably, a neutral solvent is used with a phenol or basic solvent. Extraction temperatures of 200--400 DEG C. are employed, the temperature being raised in stages. As second solvent, a cheap substance not substantially altered in the hydrogenation stage is preferred, e.g. mixtures of hydrocarbon oils produced by the hydrogenation of coal extracts, low temperature tars or tetradecahydroanthracene, tetradecahydrophenanthrene, tricyclohexyl or dicyclohexylmethane, tricyclo or dicyclohexyl ethane or dodecahydrodiphenyl. The second solvent is added after the first has been removed by distillation or when the second solvent has a higher boiling point it may be added direct to the extract and the first solvent then distilled off. The extract is then mixed with a solution or suspension of a catalyst, e.g. nickel, molybdic acid, phosphoric acid, ammonium molybdate, tungstate, or phosphate, tin oxalate or hydroxide. The molybdenum catalysts are preferably heated in air to 500 DEG C. before use. The hydrogenation is carried out at 200--600 DEG C. and preferably under low pressure due to that produced by a small amount of hydrogen and the vapour pressure of the solvent. The oils obtained may be used as fuel oils or may be subjected to further hydrogenation to produce lighter oils. The oils are converted into olefines by heating their vapours in a turbulent stream to 700--900 DEG C. while at temperatures above 1000 DEG C. acetylene is obtained. The olefines may be recovered by absorption in charcoal or sulphuric acid. Powdered bituminous coal is extracted under a pressure of 50--70 atmos. with a mixture comprising 85 parts hydrogenated naphthalene and 15 parts quinoline, the temperature being raised at intervals from 260--350 DEG C. The solution is separated from the residue and after desulphurization with alkali is mixed with an oil of boiling range 290--380 DEG C., obtained by hydrogenation, and a previously heated molybdenum catalyst. The first solvent is separated by distillation and the remaining mixture hydrogenated at 450--500 DEG C. under 80 atmos. pressure. The oils produced are again hydrogenated under similar conditions and the products are vaporized and led through narrow tubes heated to 900 DEG C. A gas is obtained containing considerable proportions of olefines particularly ethylene and propylene.ALSO:Hydrocarbon oils and gases are obtained from coal by subjecting the coal to extraction with an organic solvent or solvent mixture, removing the solvent from the extracted fraction and replacing it by a second solvent capable of holding the extracted material in solution or suspension, and subjecting the composition so formed to hydrogenation. When a gaseous final product is desired the hydrogenation product is subjected to thermal decomposition at temperatures between 700--900 DEG C. As first solvents hydrocarbons or other neutral solvents may be used, e.g. tetrahydronaphthalene, decahydronaphthalene, or hydrocarbons boiling above 250 DEG C., e.g. phenanthrene, hydrogenated phenanthrenes and anthracenes, benzylnaphthalenes, diphenyl-benzene and tetraamylene; or phenols e.g. tar acids, p-benzylphenol, or 1-(b -hydroxy-benzyl) naphthalene; or basic compounds e.g. pyridine, quinoline, quinaldine, acridine, benzyl quinolines, hydrogenated acridines and other hydrogenated heterocyclic bases. Preferably a neutral solvent is used with a phenol or basic solvent. Extraction temperatures of 200--400 DEG C. are employed the temperature being raised in stages. As second solvent a cheap substance not substantially altered in the hydrogenation stage is preferred, e.g. mixtures of hydrocarbon oils produced by hydrogenation of a coal extract, low temperature tars or tetradecahydroanthracene, tetradecahydrophenanthrene, tri- or dicyclohexylmethane, tri- or di-cyclohexyl ethane or dodecahydrodiphenyl. The second solvent is added after the first has been removed by distillation or when the second solvent has a higher boiling point it may be added direct to the extract and the first solvent then distilled off. The extract is then mixed with a solution or suspension of a catalyst e.g. nickel, molybdic acid, phosphoric acid, ammonium molybdate, tungstate or phosphate, tin oxalate or hydroxide. The molybdenum catalysts are preferably heated in air to 500 DEG C. before use. The hydrogenation is carried out at 200--600 DEG C. and preferably under low pressure due to that produced by a small amount of hydrogen and the vapour pressure of the solvent. The oils obtained may be used as fuel oils or may be subjected to further hydrogenation to produce lighter oils. The oils are converted into olefines by heating their vapours in a turbulent stream to 700--900 DEG C. while at temperatures above 1000 DEG C. acetylene is obtained. The olefines may be recovered by absorption in charcoal or sulphuric acid. Powdered bituminous coal is extracted under a pressure of 50--70 atmos. with a mixture comprising 85 parts hydrogenated naphthalene and 15 parts quinoline the temperature being raised at intervals from 260--350 DEG C. The solution is separated from the residue and is mixed with an oil of boiling range 290--380 DEG C. obtained by hydrogenation and a previously heated molybdenum catalyst. The first solvent is separated by distillation and the remaining mixture hydrogenated at 450--500 C. under 80 atmos. pressure. The oils produced are again hydrogenated under similar conditions and the products are vaporized and led through narrow tubes heated to 900 DEG C. A gas is obtained containing considerable proportions of olefines particularly ethylene and propylene. According to the second Provisional Specification decalin, tetralin, dihydroanthracene, ketones, and organic bases boiling above 250 DEG C. may also be used as solvents to extract the coal.
机译:通过用有机溶剂或溶剂混合物对煤进行萃取,从萃取的馏分中除去溶剂,并用能够将萃取的物质保持在溶液或悬浮液中的第二种溶剂进行替代,并对煤进行处理,从而从煤中获得烃类油和气。如此形成加氢的组合物。当需要气态最终产物时,将氢化产物在700-900℃的温度下进行热分解。作为第一溶剂,可以使用烃或其他中性溶剂,例如烃。四氢萘,十氢萘或沸点高于250℃的烃,例如菲,氢化菲和蒽,苄基萘,二苯苯和四戊基;或酚类,例如焦油酸,对对苄基苯酚或1-(α-羟基苄基)萘;或碱性化合物,例如吡啶,喹啉,奎尼丁,a啶,苄基喹啉,氢化a啶和其他氢化杂环碱。优选地,中性溶剂与酚或碱性溶剂一起使用。提取温度为200--400℃,分阶段提高温度。作为第二溶剂,优选在氢化步骤中基本不改变的廉价物质,例如,碳酸氢钠。由煤提取物,低温焦油或十四氢化蒽,十四氢菲,三环己基或二环己基甲烷,三环或二环己基乙烷或十二氢二苯乙烷加氢制得的烃油混合物。在通过蒸馏除去第一种溶剂之后,或者当第二种溶剂具有较高沸点时,可以将第二种溶剂直接添加到萃取液中,然后蒸馏掉第一种溶剂。然后将提取物与催化剂的溶液或悬浮液混合,例如催化剂的溶液。镍,钼酸,磷酸,钼酸铵,钨酸盐或磷酸盐,草酸锡或氢氧化物。钼催化剂在使用前最好在空气中加热到500℃。氢化是在200--600℃下进行的,最好是在低压下进行,因为氢化是由少量的氢气和溶剂的蒸气压产生的。所获得的油可以用作燃料油,或者可以进行进一步的氢化以产生较轻的油。通过在湍流中将其蒸气加热至700--900℃,同时在高于1000℃的温度下加热,将油转化为烯烃。获得了乙炔。可以通过吸收木炭或硫酸来回收烯烃。在50--70个大气压的压力下提取粉状烟煤。用由85份氢化萘和15份喹啉组成的混合物,将温度从260--350℃间隔升高。将溶液与残留物分离,并在用碱脱硫后与沸程290-通过氢化获得的380℃,和预先加热的钼催化剂。通过蒸馏分离出第一溶剂,剩余的混合物在80个大气压下于450--500℃氢化。压力。产生的油再次在相似的条件下进行氢化,然后将产品蒸发并通过加热到900℃的细管引导。得到的气体含有相当比例的烯烃,尤其是乙烯和丙烯。用有机溶剂或溶剂混合物对煤进行萃取,从萃取的馏分中除去溶剂,并用能够将萃取的物质保持在溶液或悬浮液中的第二种溶剂代替,然后使形成的组合物进行氢化。当需要气态最终产物时,将氢化产物在700-900℃的温度下进行热分解。作为第一溶剂,可以使用烃或其他中性溶剂,例如烃。四氢萘,十氢萘或沸点高于250℃的烃,例如菲,氢化菲和蒽,苄基萘,二苯-苯和四am基;或酚类焦油酸,对苄基苯酚或1-(b-羟基苄基)萘;或碱性化合物,例如吡啶,喹啉,奎尼丁,a啶,苄基喹啉,氢化a啶和其他氢化杂环碱。优选地,中性溶剂与苯酚或碱性溶剂一起使用。提取温度为200--400℃,分阶段升高温度。作为第二溶剂,优选在氢化步骤中基本不改变的廉价物质,例如,碳酸氢钠。煤提取物加氢制得的烃油混合物,低温焦油或十四碳蒽,十四氢菲,三或二环己基甲烷,三或二环己基乙烷或十二氢二苯基。在通过蒸馏除去第一种溶剂之后,或者当第二种溶剂具有较高沸点时,可以将第二种溶剂直接添加到萃取液中,然后蒸馏掉第一种溶剂。然后将提取物与催化剂的溶液或悬浮液混合,例如催化剂的溶液。镍,钼酸,磷酸,钼酸铵,钨酸盐或磷酸盐,草酸锡或氢氧化物。钼催化剂在使用前最好在空气中加热到500℃。氢化是在200--600℃下进行的,最好是在低压下进行,因为氢化是由少量的氢气和溶剂的蒸气压产生的。所获得的油可以用作燃料油,或者可以进行进一步的氢化以产生较轻的油。通过在湍流中将其蒸气加热至700--900℃,同时在高于1000℃的温度下加热,将油转化为烯烃。获得了乙炔。可以通过吸收木炭或硫酸来回收烯烃。在50--70个大气压的压力下提取粉状烟煤。用包含85份氢化萘和15份喹啉的混合物以每隔260--350℃的间隔升高温度。将溶液与残留物分离,并与沸程290--380℃的油混合。通过氢化和预先加热的钼催化剂。通过蒸馏分离第一溶剂,并将剩余的混合物在80个大气压下在450--500℃下氢化。压力。所产生的油在相似的条件下再次被氢化,产物被蒸发并通过加热到900℃的细管。得到的气体含有相当比例的烯烃,特别是乙烯和丙烯。根据第二临时规范,十氢化萘,四氢化萘,二氢蒽,酮和沸点高于250℃的有机碱也可用作溶剂来提取煤。

著录项

  • 公开/公告号GB478720A

    专利类型

  • 公开/公告日1938-01-24

    原文格式PDF

  • 申请/专利权人 HENRY DREYFUS;

    申请/专利号GB19370014961

  • 发明设计人

    申请日1936-07-23

  • 分类号C10G1/00;

  • 国家 GB

  • 入库时间 2022-08-24 05:22:20

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