首页> 外国专利> A procedure for liquid phase dehydrohalogenation of 1,2,3-tetracloropropan to obtain 1,2,3-tricloropropene. (Machine-translation by Google Translate, not legally binding)

A procedure for liquid phase dehydrohalogenation of 1,2,3-tetracloropropan to obtain 1,2,3-tricloropropene. (Machine-translation by Google Translate, not legally binding)

机译:1,2,3-四氯丙烷液相脱卤化氢制得1,2,3-三氯丙烯的方法。 (通过Google翻译进行机器翻译,没有法律约束力)

摘要

A procedure for the liquid phase dehydrogenation of 1,2,2,3-tetrachloropropane to obtain 1,2,3-trichloropropene, comprising: (A) introducing a stream comprising 1,2,3-trichloropropane into a chlorinator in liquid phase; (B) chlorinate the feed stream so that from about 20 to about 60 weight percent of the gilt effluent remains unreacted 1,2,3-trichloropropane; (C) passing the effluent from the dorador to a fractionation column; (D) fractionating said dorado effluent into a 1,2,3-trichloropropane fraction, a 1,2,2,3-tetra-chloropropane fraction, a 1,1,2,3-tetrachloropropane fraction, a fraction of 1,1,1,2,3- and 1,1,2,2,3-pentachloropropanes and a fraction of 1,1,2,3,3-pentachloropropane and heavy ends; (E) (1) recirculate the 1,2,3-trichloropropane fraction to the gild; (2) separating the 1,2,2,3-tetrachloropropane fraction; (3) (a) passing the 1,1,2,3-tetrachloropropane fraction from the fractionation column to a caustic dehydrochlorinator; (b) dehydrochloride 1,1,2,3-tetrachloropropane; (c) passing the effluent from the dehydrochlorinator, which includes mixed trichloropropenes, to a second liquid phase gilder; (d) add chlorine to the carbon/carbon double bond of the trichloropropenes contained in the dehydrochlorinator effluent; (e) pause the effluent from the second browner to a second caustic dehydrochlorinator; (4) passing the fraction of 1,1,1,2,3- and 1,1,2,2,3-pentachloropropanes from the fractionation column to the second caustic dehydrochlorinator; (f) dehydrochlorinating the effluent from the second dorado and the fraction of 1,1,1,2,3- and 1,1,2,2,3-pentachloropropanes from the fractionation column; (g) passing the effluent from the second dehydrochlorinator, comprising mixed mixed tetrachloropropenes, to an isomerizer filled with siliceous granules having a polar surface; and (H) isomerizing 2,3,3,3-tetrachloropropene to 1,1,2,3-tetrachloropropene, by heating the effluent from the second dehydrochlorinator in contact with the siliceous granules, at a temperature of approximately 150ºC to approximately 200ºC, during from about 0.4 to about 2 hours. (Machine-translation by Google Translate, not legally binding)
机译:一种将1,2,2,3-四氯丙烷进行液相脱氢以获得1,2,3-三氯丙烯的方法,该方法包括:(A)将包含1,2,3-三氯丙烷的物流引入液相的氯化器中; (B)对进料流进行氯化,以使约20至约60重量%的后备母猪流出物保持未反应的1,2,3-三氯丙烷; (C)将废水从多拉多尔输送到分馏塔; (D)将所述多拉多流出物分馏成1,2,3-三氯丙烷馏分,1,2,2,3-四氯丙烷馏分,1,1,2,3-四氯丙烷馏分,1,1馏分,1,2,3-和1,1,2,2,3-五氯丙烷和一部分1,2,3,3-五氯丙烷和重质末端; (E)(1)将1,2,3-三氯丙烷馏分再循环至镀金层; (2)分离1,2,2,3-四氯丙烷馏分; (3)(a)将1,1,2,3-四氯丙烷馏分从分馏塔送入苛性碱脱氯化氢器中; (b)脱盐酸盐1,1,2,3-四氯丙烷; (c)将包括混合三氯丙烯在内的脱氯化器的废水送入第二液相镀金机; (d)将氯加到脱氯化氢器流出物中所含三氯丙烯的碳/碳双键上; (e)暂停从第二个褐变器到第二个苛性脱盐器的废水; (4)将1,1,1,2,3-和1,1,2,2,3-五氯丙烷的馏分从分馏塔送入第二苛性脱氯化器; (f)将来自第二多拉多的流出物和来自分馏塔的1,1,1,2,3-和1,1,2,2,3-五氯丙烷的馏分脱氯化氢; (g)将来自第二脱氯化器的,包括混合的混合四氯丙烯的流出物送入填充有极性表面硅质颗粒的异构器中; (H)通过在与硅质颗粒接触的状态下,将第二脱氯化器的出水加热到大约150ºC至大约200ºC,将2,3,3,3-四氯丙烯异构化为1,1,2,3-四氯丙烯,在约0.4至约2小时内。 (通过Google翻译进行机器翻译,没有法律约束力)

著录项

  • 公开/公告号ES415834A1

    专利类型

  • 公开/公告日1976-05-16

    原文格式PDF

  • 申请/专利权人 MONSANTO COMPANY;

    申请/专利号ES19730415834

  • 发明设计人

    申请日1973-06-12

  • 分类号C07C;

  • 国家 ES

  • 入库时间 2022-08-23 02:29:44

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