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    • 4. 发明授权
    • Equipment and method for producing polyhydroxycarboxylic acid
    • 多羟基羧酸的制备方法和设备
    • US08153754B2
    • 2012-04-10
    • US12544477
    • 2009-08-20
    • Masayuki KamikawaToshiaki MatsuoNaruyasu OkamotoKenichiro OkaTakeyuki Kondo
    • Masayuki KamikawaToshiaki MatsuoNaruyasu OkamotoKenichiro OkaTakeyuki Kondo
    • C08G63/08B01D53/00B01J19/18
    • C08G63/785B01J4/002B01J19/24B01J2219/00006B01J2219/00777B01J2219/185C08G63/06Y02P20/582
    • An equipment for producing polyhydroxycarboxylic acid, includes a ring-opening polymerization apparatus, a liquid phase devolatilizing apparatus, and a drying apparatus, wherein an indirect heat exchanger is connected to a vent gas discharge path of the liquid phase devolatilizing apparatus. The indirect heat exchanger captures a dispersed in-process substance containing hydroxycarboxylic acid cyclic dimers and transfers the substance to the ring-opening polymerization apparatus; a wet condenser and a hot well are connected to a vent gas discharge path of the indirect heat exchanger and that of the drying apparatus, respectively. The wet condenser captures a dispersed in process substance containing the cyclic dimers with the use of a refrigerant containing hydroxycarboxylic acid corresponding to the cyclic dimers and transfers the substance to the hot well; the hot well causes hydrolysis of the cyclic dimers for generation of hydroxycarboxylic acid; the generated hydroxycarboxylic acid is mixed with a refrigerant and the mixture is circulated to the wet condenser; and hydroxycarboxylic acid is highly concentrated via circulation between the wet condenser and the hot well and then discharged.
    • 用于制备聚羟基羧酸的设备包括开环聚合设备,液相脱挥发酵设备和干燥设备,其中间接热交换器连接到液相脱挥发设备的通气气体排放路径。 间接热交换器捕获含有羟基羧酸环二聚体的分散的在线物质并将物质转移到开环聚合装置中; 湿式冷凝器和热井分别连接到间接热交换器和干燥装置的排放气体排出路径。 湿式冷凝器使用含有对应于环状二聚体的羟基羧酸的制冷剂捕获含有环状二聚体的分散过程物质,并将物质转移到热井中; 热阱引起环状二聚体的水解产生羟基羧酸; 将所生成的羟基羧酸与制冷剂混合,并将混合物循环至湿式冷凝器; 并且羟基羧酸通过湿式冷凝器和热井之间的循环高度浓缩,然后排出。
    • 6. 发明授权
    • Polylactide manufacturing apparatus and method for manufacturing polylactide
    • 聚丙交酯制造装置和聚丙交酯的制造方法
    • US08106150B2
    • 2012-01-31
    • US12453912
    • 2009-05-27
    • Kenichiro OkaToshiaki MatsuoMasayuki KamikawaNaruyasu Okamoto
    • Kenichiro OkaToshiaki MatsuoMasayuki KamikawaNaruyasu Okamoto
    • C08G63/08B01D53/78B01J19/18
    • C08G63/08B01J19/1818B01J2219/00006
    • In a process of manufacturing polylactide, synthesis of high-quality polymers is achieved with a sufficient degree of vacuum secured. Provided is an apparatus for manufacturing polylactide which includes the steps of preparing lactide through oligomerization of lactic acid and depolymerization of the resulting oligomers, effecting ring-opening polymerization of the lactide, and removing unreacted lactide. The apparatus comprises an exhausting gas treatment device for reducing pressure in the step of removing unreacted lactide. The exhausting gas treatment device includes boilers (81-83) for generating water vapor; a pressure-reducing section having stages each including an ejector (71-73) driven with the water vapor, a condenser (61-63) connected downstream of the ejector, and a hot well tank (41-43) connected to the condenser; and a main condenser 60 and a main hot well tank 40 connected to the main condenser that are disposed on a pipe line through which a gas of the unreacted lactide is suctioned into the pressure-reducing section. The gas of the unreacted lactide is washed away in the main condenser using a liquid containing lactic acid as a main component that has been collected in the main hot well tank.
    • 在制备聚丙交酯的过程中,通过确保足够的真空度实现高质量聚合物的合成。 提供了一种制备聚丙交酯的装置,包括通过乳酸低聚制备丙交酯并使所得低聚物解聚,进行丙交酯的开环聚合和除去未反应的丙交酯的步骤。 该装置包括用于在去除未反应的丙交酯的步骤中降低压力的排气处理装置。 排气处理装置包括用于产生水蒸汽的锅炉(81-83) 减压部,其具有各自包括由水蒸气驱动的喷射器(71-73)的台阶,连接在喷射器下游的冷凝器(61-63)和连接到冷凝器的热井箱(41-43); 以及主冷凝器60和连接到主冷凝器的主热水箱40,所述主冷凝器60设置在管道上,未反应的丙交酯的气体被吸入减压部。 未反应的丙交酯的气体在主冷凝器中使用含有乳酸作为主要成分的液体在主要热水槽中被收集。
    • 7. 发明授权
    • Method for synthesizing acrolein
    • 丙烯醛合成方法
    • US08450531B2
    • 2013-05-28
    • US12979459
    • 2010-12-28
    • Takeyuki KondoMasayuki KamikawaKenichiro OkaToshiaki MatsuoMasashi TantoYasunari SaseHiroyuki ItoTomofumi ShiraishiTsutomu KawamuraNaruyasu Okamoto
    • Takeyuki KondoMasayuki KamikawaKenichiro OkaToshiaki MatsuoMasashi TantoYasunari SaseHiroyuki ItoTomofumi ShiraishiTsutomu KawamuraNaruyasu Okamoto
    • C07C45/64C07D307/46C07H1/00
    • C07D307/48B01F5/0057B01F5/0615B01F5/0682B01F5/0688C07C45/52Y02P20/544C07C47/22
    • An object of the present invention is to provide a method for commercially manufacturing acrolein in a large flow rate by making supercritical water and an acid interact with glycerin, wherein by efficiently mixing high-concentration glycerin and supercritical water with each other, the method is made capable of making the synthesis stably proceed with a high yield while the occlusion and abrasion of the pipes and devices due to the generation of by-products are being suppressed. The method for synthesizing acrolein of the present invention is a method for synthesizing acrolein by making supercritical water and an acid interact with glycerin, the method using a reaction apparatus including: a cylindrical mixing flow path for mixing a fluid including glycerin and a fluid including supercritical water with each other; a first inlet flow path, disposed offset from the central axis of the mixing flow path, for making the fluid including glycerin flow into the mixing flow path; and a second inlet flow path, disposed offset from the central axis of the mixing flow path, for making the fluid including supercritical water flow into the mixing flow path, wherein the first inlet flow path and the second inlet flow path are each provided in a plurality of numbers in such a way that the first inlet flow paths and the second inlet flow paths are alternately arranged so as to encircle the central axis of the mixing flow path.
    • 本发明的目的是提供一种通过使超临界水和酸与甘油相互作用而大量流动丙烯醛的方法,其中通过将高浓度甘油和超临界水相互有效地混合,制备方法 能够以高产率稳定地进行合成,同时由于副产物的产生而引起的管道和装置的堵塞和磨损被抑制。 本发明的丙烯醛的合成方法是通过使超临界水和酸与甘油相互作用来合成丙烯醛的方法,使用反应装置的方法包括:将含有甘油的液体和包含超临界流体的流体混合的圆筒状混合流路 水相互; 第一入口流动路径,设置为偏离混合流动路径的中心轴线,用于使包含甘油的流体流入混合流动路径; 以及第二入口流动路径,其设置成偏离混合流动路径的中心轴线,用于使包括超临界水流的流体流入混合流动路径,其中第一入口流动路径和第二入口流动路径分别设置在 多个数字,使得第一入口流动路径和第二入口流动路径交替地布置成环绕混合流动路径的中心轴线。
    • 8. 发明申请
    • REACTION PROCESS UTILIZING CRITICAL
    • 反应过程利用关键
    • US20110319667A1
    • 2011-12-29
    • US13148760
    • 2010-02-05
    • Takeyuki KondoHiroyuki ItoNaruyasu OkamotoYasunari SaseToshiaki MatsuoKenichiro OkaMasayuki Kamikawa
    • Takeyuki KondoHiroyuki ItoNaruyasu OkamotoYasunari SaseToshiaki MatsuoKenichiro OkaMasayuki Kamikawa
    • C07C45/00B01J19/00
    • B01J3/008B01J2219/00006B01J2219/00168C07C45/52Y02P20/544C07C47/22
    • In order to perform organic synthesis process through action with supercritical water and acid stably while suppressing a trouble caused by a by-product, a method and an apparatus are provided, including the following steps. Water is supplied to high-pressure pumps (110) and (210) from water headers (101) and (201), and a pressure-reducing valve (324) is regulated to increase the pressure to 35 MPa. Temperatures of preheaters (120) and (220) and a heater (310) are increased until the reaction solution is at a temperature of 400° C. Acid (sulfuric acid) and an organic compound raw material (glycerin) are supplied from an acid header (203) and a raw-material header (203′) for action with the supercritical water to obtain a reaction solution. The obtained reaction solution is cooled to 100 to 200° C. by first cooling (420) and a solid component included in the reaction solution is separated for removal from the reaction solution by a filter (320), and then the reaction solution is cooled to a temperature of about 100° C. or lower by second cooling (620) and pressure thereof is reduced (324). Further, the reaction solution is cooled by third cooling (720) and then a synthesized product (acrolein) is captured.
    • 为了通过超临界水和酸稳定地进行有机合成工艺,同时抑制由副产物引起的故障,提供了包括以下步骤的方法和装置。 从集水管(101)和(201)向高压泵(110)和(210)供水,调节减压阀(324)以将压力增加至35MPa。 增加预热器(120)和(220)和加热器(310)的温度,直到反应溶液处于400℃的温度。酸(硫酸)和有机化合物原料(甘油)由酸 标题(203)和原料头(203'),用于与超临界水作用以获得反应溶液。 将得到的反应溶液通过第一次冷却(420)冷却至100〜200℃,分离包含在反应溶液中的固体成分,通过过滤器(320)从反应溶液中除去,然后将反应溶液冷却 通过第二冷却(620)至约100℃或更低的温度,并且其压力降低(324)。 此外,将反应溶液通过第三次冷却(720)冷却,然后捕获合成产物(丙烯醛)。
    • 9. 发明申请
    • METHOD FOR SYNTHESIZING ACROLEIN
    • 用于合成ACROLEIN的方法
    • US20110160447A1
    • 2011-06-30
    • US12979459
    • 2010-12-28
    • Takeyuki KONDOMasayuki KamikawaKenichiro OkaToshiaki MatsuoMasashi TantoYasunari SaseHiroyuki ItoTomofumi ShiraishiTsutomu KawamuraNaruyasu Okamoto
    • Takeyuki KONDOMasayuki KamikawaKenichiro OkaToshiaki MatsuoMasashi TantoYasunari SaseHiroyuki ItoTomofumi ShiraishiTsutomu KawamuraNaruyasu Okamoto
    • C08B37/00C07C45/61C07D307/34
    • C07D307/48B01F5/0057B01F5/0615B01F5/0682B01F5/0688C07C45/52Y02P20/544C07C47/22
    • An object of the present invention is to provide a method for commercially manufacturing acrolein in a large flow rate by making supercritical water and an acid interact with glycerin, wherein by efficiently mixing high-concentration glycerin and supercritical water with each other, the method is made capable of making the synthesis stably proceed with a high yield while the occlusion and abrasion of the pipes and devices due to the generation of by-products are being suppressed. The method for synthesizing acrolein of the present invention is a method for synthesizing acrolein by making supercritical water and an acid interact with glycerin, the method using a reaction apparatus including: a cylindrical mixing flow path for mixing a fluid including glycerin and a fluid including supercritical water with each other; a first inlet flow path, disposed offset from the central axis of the mixing flow path, for making the fluid including glycerin flow into the mixing flow path; and a second inlet flow path, disposed offset from the central axis of the mixing flow path, for making the fluid including supercritical water flow into the mixing flow path, wherein the first inlet flow path and the second inlet flow path are each provided in a plurality of numbers in such a way that the first inlet flow paths and the second inlet flow paths are alternately arranged so as to encircle the central axis of the mixing flow path.
    • 本发明的目的是提供一种通过使超临界水和酸与甘油相互作用而大量流动丙烯醛的方法,其中通过将高浓度甘油和超临界水相互有效地混合,制备方法 能够以高产率稳定地进行合成,同时由于副产物的产生而引起的管道和装置的堵塞和磨损被抑制。 本发明的丙烯醛的合成方法是通过使超临界水和酸与甘油相互作用来合成丙烯醛的方法,使用反应装置的方法包括:将含有甘油的液体和包含超临界流体的流体混合的圆筒状混合流路 水相互; 第一入口流动路径,设置为偏离混合流动路径的中心轴线,用于使包含甘油的流体流入混合流动路径; 以及第二入口流动路径,其设置成偏离混合流动路径的中心轴线,用于使包括超临界水流的流体流入混合流动路径,其中第一入口流动路径和第二入口流动路径分别设置在 多个数字,使得第一入口流动路径和第二入口流动路径交替地布置成环绕混合流动路径的中心轴线。
    • 10. 发明授权
    • Reaction process utilizing critical water
    • 使用临界水的反应过程
    • US08558035B2
    • 2013-10-15
    • US13148760
    • 2010-02-05
    • Takeyuki KondoHiroyuki ItoNaruyasu OkamotoYasunari SaseToshiaki MatsuoKenichiro OkaMasayuki Kamikawa
    • Takeyuki KondoHiroyuki ItoNaruyasu OkamotoYasunari SaseToshiaki MatsuoKenichiro OkaMasayuki Kamikawa
    • C07C45/52B01J19/00
    • B01J3/008B01J2219/00006B01J2219/00168C07C45/52Y02P20/544C07C47/22
    • In order to perform organic synthesis process through action with supercritical water and acid stably while suppressing a trouble caused by a by-product, a method and an apparatus are provided, including the following steps. Water is supplied to high-pressure pumps (110) and (210) from water headers (101) and (201), and a pressure-reducing valve (324) is regulated to increase the pressure to 35 MPa. Temperatures of preheaters (120) and (220) and a heater (310) are increased until the reaction solution is at a temperature of 400° C. Acid (sulfuric acid) and an organic compound raw material (glycerin) are supplied from an acid header (203) and a raw-material header (203′) for action with the supercritical water to obtain a reaction solution. The obtained reaction solution is cooled to 100 to 200° C. by first cooling (420) and a solid component included in the reaction solution is separated for removal from the reaction solution by a filter (320), and then the reaction solution is cooled to a temperature of about 100° C. or lower by second cooling (620) and pressure thereof is reduced (324). Further, the reaction solution is cooled by third cooling (720) and then a synthesized product (acrolein) is captured.
    • 为了通过超临界水和酸稳定地进行有机合成工艺,同时抑制由副产物引起的故障,提供了包括以下步骤的方法和装置。 从集水管(101)和(201)向高压泵(110)和(210)供水,调节减压阀(324)以将压力增加至35MPa。 增加预热器(120)和(220)和加热器(310)的温度,直到反应溶液处于400℃的温度。酸(硫酸)和有机化合物原料(甘油)由酸 标题(203)和原料头(203'),用于与超临界水作用以获得反应溶液。 将得到的反应溶液通过第一次冷却(420)冷却至100〜200℃,分离包含在反应溶液中的固体成分,通过过滤器(320)从反应溶液中除去,然后将反应溶液冷却 通过第二冷却(620)至约100℃或更低的温度,并且其压力降低(324)。 此外,将反应溶液通过第三次冷却(720)冷却,然后捕获合成产物(丙烯醛)。