首页> 外国专利> METHOD OF PRODUCING N-2-ETHYLHEXYL-N'-PHENYL-N-PHENYLENEDIAMINE AND SEPARATING COMMERCIAL GRADE 2-ETHYLHEXANOIC ACID FROM WASTES FROM PRODUCTION OF N-2-ETHYHEXYL-N'-PHENYL-N-PHENYLENEDIAMINE

METHOD OF PRODUCING N-2-ETHYLHEXYL-N'-PHENYL-N-PHENYLENEDIAMINE AND SEPARATING COMMERCIAL GRADE 2-ETHYLHEXANOIC ACID FROM WASTES FROM PRODUCTION OF N-2-ETHYHEXYL-N'-PHENYL-N-PHENYLENEDIAMINE

机译:制备N-2-乙基己基-N'-苯基-N-苯二乙胺并从生产N-2-乙基己基-N'-苯基-N-苯二胺的废料中分离出商业级2-乙基己酸的方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to an improved method of producing N-2-ethylhexyl-N'-phenyl n-phenylenediamine, which can be used as an antioxidant for polymers and separation of commercial 2-ethylhexanoic acid from wastes from production of N-2-ethylhexyl-N'-phenyl n-phenylenediamine, which is achieved through alkylation of n-aminodiphenylamine with 2-ethylhexanol at temperature ranging from 170 to 235°C with distillation of azeotropic alcohol with water, returning condensed hot alcohol to the reaction zone, separation of the desired product from the organic layer after aqueous extraction of the reaction mass. The alkylating agent used is an alcohol solution of potassium alcoholate, which is added continuously in uniform portions to molten n-aminodiphenylamine, preheated to temperature ranging from 210 to 230°C. Distillation of azeotropic alcohol with water is done using a fractional column in which temperature is kept between 90 and 110°C; the aqueous layer remaining after separation of the organic layer is treated with hydrochloric, sulphuric or phosphoric acid until pH between 2 and 4, the obtained mixture is divided into layers and 2-ethylhexanoic acid is extracted from the organic layer through vacuum distillation.;EFFECT: cutting on alkylation time, increased amine conversion, reduced specific consumption of alcohol, specific energy consumption, higher quality of desired product and obtaining end product from waste products.;5 cl, 8 ex, 1 tbl
机译:发明领域本发明涉及一种改进的生产N-2-乙基己基-N'-苯基正苯二胺的方法,其可以用作聚合物的抗氧化剂以及从生产废料中分离出商业2-乙基己酸的方法。 N-2-乙基己基-N'-苯基正苯二胺的制备,这是通过将正氨基醇与2-乙基己醇在170至235°C的温度下与2-乙基己醇烷基化,并与水共沸的乙醇进行蒸馏,然后将冷凝的热醇还原为在反应区中,水萃取反应物料后,将所需产物与有机层分离。所用的烷基化剂是醇钾的醇溶液,将其均匀地连续地连续加入到预热至210至230℃的熔融n-氨基二苯胺中。使用温度保持在90到110°C之间的分馏塔将水与共沸酒精蒸馏;将分离出有机层后剩余的水层用盐酸,硫酸或磷酸处理直至pH为2至4,将所得混合物分成几层,并通过真空蒸馏从有机层中提取2-乙基己酸。 :减少烷基化时间,提高胺转化率,减少酒精的单位消耗,降低单位能耗,提高所需产品的质量,并从废品中获得最终产品。; 5 cl,8 ex,1 tbl

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