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    • 7. 发明申请
    • PROCESS FOR PREPARING POLYAMIDES
    • 制备聚氨酯的方法
    • US20120245308A1
    • 2012-09-27
    • US13514364
    • 2010-12-03
    • Faissal-Ali El-ToufailiPhilippe DesboisAndreas WollnySven LawrenzChristian Schmidt
    • Faissal-Ali El-ToufailiPhilippe DesboisAndreas WollnySven LawrenzChristian Schmidt
    • C08G69/28C08G69/26
    • C08G69/265C08G69/28
    • The present invention relates to a process for preparing a polyamide based on dicarboxylic acids and diamines, comprising the following stages: A) providing an aqueous monomer mixture composed of dicarboxylic acids and diamines, where the molar ratio of dicarboxylic acids to diamines is adjusted such that, at the outlet of stage C), there is a molar deficiency of dicarboxylic acids or diamines of 1 to 10 mol%, based on the respective other component, B) transferring the aqueous mixture from stage A) into a continuous evaporator reactor in which diamines and dicarboxylic acids are converted at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, C) transferring the mixture from stage B) into a separator which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar with removal of gaseous components, D) transferring the mixture from stage C) together with diamine or dicarboxylic acid in an amount suitable for compensation for the molar deficiency into a tubular reactor which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, for a residence time in the range from 10 seconds to 30 minutes, E) transferring the mixture from stage D) into an extruder which is operated at a temperature in the range from 150 to 400° C. for a residence time in the range from 10 seconds to 30 minutes with removal of gaseous components through venting orifices.
    • 本发明涉及一种制备基于二羧酸和二胺的聚酰胺的方法,包括以下步骤:A)提供由二羧酸和二胺组成的含水单体混合物,其中二羧酸与二胺的摩尔比被调整为使得 ,在阶段C)的出口处,基于各自的其它组分,存在摩尔不足的二羧酸或二胺的1至10摩尔%,B)将水性混合物从阶段A)转移到连续的蒸发器反应器中,其中 二胺和二羧酸在100至370℃的温度和1至50巴的压力范围内转化,C)将混合物从阶段B)转移到分离器中,该分离器在 范围为100至370℃,压力为1至50巴,除去气态组分,D)将混合物与阶段C)一起转移至二胺或二羧酸的量 适合于将摩尔不足补偿到在100至370℃的温度和1至50巴的压力范围内操作的管式反应器中,停留时间在10秒至 30分钟,E)将混合物从阶段D)转移到挤出机中,该挤出机在150-400℃的温度下操作,停留时间在10秒至30分钟之间,同时除去气体成分 通风孔。
    • 9. 发明授权
    • Process for preparing polyamides
    • 制备聚酰胺的方法
    • US09315626B2
    • 2016-04-19
    • US13514364
    • 2010-12-03
    • Faissal-Ali El-ToufailiPhilippe DesboisAndreas WollnySven LawrenzChristian Schmidt
    • Faissal-Ali El-ToufailiPhilippe DesboisAndreas WollnySven LawrenzChristian Schmidt
    • C08G69/24C08G69/26C08G69/28
    • C08G69/265C08G69/28
    • The present invention relates to a process for preparing a polyamide based on dicarboxylic acids and diamines, comprising the following stages: A) providing an aqueous monomer mixture composed of dicarboxylic acids and diamines, where the molar ratio of dicarboxylic acids to diamines is adjusted such that, at the outlet of stage C), there is a molar deficiency of dicarboxylic acids or diamines of 1 to 10 mol %, based on the respective other component, B) transferring the aqueous mixture from stage A) into a continuous evaporator reactor in which diamines and dicarboxylic acids are converted at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, C) transferring the mixture from stage B) into a separator which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar with removal of gaseous components, D) transferring the mixture from stage C) together with diamine or dicarboxylic acid in an amount suitable for compensation for the molar deficiency into a tubular reactor which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, for a residence time in the range from 10 seconds to 30 minutes, E) transferring the mixture from stage D) into an extruder which is operated at a temperature in the range from 150 to 400° C. for a residence time in the range from 10 seconds to 30 minutes with removal of gaseous components through venting orifices.
    • 本发明涉及一种制备基于二羧酸和二胺的聚酰胺的方法,其包括以下步骤:A)提供由二羧酸和二胺组成的含水单体混合物,其中二羧酸与二胺的摩尔比被调整为使得 ,在阶段C)的出口处,基于各自的其它组分,存在摩尔不足的二羧酸或二胺的1至10摩尔%,B)将水性混合物从阶段A)转移到连续的蒸发器反应器中,其中 二胺和二羧酸在100至370℃的温度和1至50巴的压力范围内转化,C)将混合物从阶段B)转移到分离器中,该分离器在 范围为100至370℃,压力范围为1至50巴,除去气态组分,D)将混合物从阶段C)与二胺或二羧酸一起转移 t适用于将摩尔不足补偿为在100至370℃的温度和1至50巴的压力范围内操作的管式反应器中,停留时间为10秒 至30分钟,E)将混合物从阶段D)转移到挤出机中,该挤出机在150-400℃的温度下操作,停留时间为10秒至30分钟,同时除去气体组分 通过通风口。
    • 10. 发明申请
    • Metod For The Continuous Production Of Thermoplastically-Processable Polyurethane Elastomers
    • 用于连续生产热塑性加工性聚氨酯弹性体的方法
    • US20080139776A1
    • 2008-06-12
    • US11815221
    • 2006-01-31
    • Gunter ScholzMarian MoursSven LawrenzHorst PapenfussChristoph BahrRudiger Krech
    • Gunter ScholzMarian MoursSven LawrenzHorst PapenfussChristoph BahrRudiger Krech
    • C08G18/00
    • C08G18/222B29C35/02B29C47/0004B29C47/0021B29C47/34B29C47/40B29C47/50B29C47/786B29C47/827B29C47/862B29K2021/00B29K2075/00B29K2105/0014C08G18/0895C08G18/664C08G18/6674
    • Process for continuous production of thermoplastically processable polyurethane elastomers with improved homogeneity, by metering a polyisocyanate (A), a proportion of from 1 to 80 equivalent %, based on the isocyanate group content of the polyisocyanate (A), of a compound (B) having an average of at least 1.8 and at most 3.0 hydrogen atoms having Zerewitinoff activity, with an average molar mass of from 450 g/mol to 5000 g/mol, a proportion of from 12 to 99 equivalent %, based on the isocyanate group content of the polyisocyanate (A), of a chain extender (C) having an average of at least 1.8 and at most 3.0 hydrogen atoms having Zerewitinoff activity per molecule, with an average molar mass of from 60 g/mol to 400 g/mol, from 0 to 30% by weight, based on the total amount of the polyurethane elastomer, of catalysts and further auxiliaries and additives (D), the molar NCO:OH ratio of polyisocyanate (A) to the entirety composed of the compound (B), of the chain extender (C), and of the further auxiliaries and additives (D) being from 0.9:1 to 1.2:1 into a self-cleaning twin-screw extruder which is operated at high shear rates, and then bringing the mixture from the self-cleaning twin-screw extruder into a further apparatus in order to complete the reaction, which comprises setting shear rates above 6000 s−1 and residence times in the range from 1 to 20 s in the self-cleaning twin-screw extruder.
    • 基于多异氰酸酯(A)的异氰酸酯基含量的化合物(B),通过计量多异氰酸酯(A),1至80当量%的比例,连续生产具有改进的均匀性的热塑性可加工聚氨酯弹性体的方法, 平均摩尔质量为450g / mol至5000g / mol,平均摩尔质量为12至99当量%,基于异氰酸酯基含量 的多异氰酸酯(A),平均摩尔质量为60g / mol至400g / mol的平均值至少为1.8且至多3.0个氢原子的扩链剂(C)具有每分子Zerewitinoff活性, 0至30重量%,基于聚氨酯弹性体的总量,催化剂和其它助剂和添加剂(D),多异氰酸酯(A)与由化合物(B)组成的整体的NCO:HOH摩尔比为 ,扩链剂(C)和f 进一步的助剂和添加剂(D)为0.9:1至1.2:1,进入以高剪切速率操作的自清洁双螺杆挤出机,然后将来自自清洁双螺杆挤出机的混合物进一步 装置,以完成反应,其包括在自清洁双螺杆挤出机中将剪切速率设定在6000s -1以上并且在1至20s范围内的停留时间。