首页 | 本学科首页   官方微博 | 高级检索  
     

己二酸二甲酯加氢制1,6-己二醇催化剂工业侧线研究
引用本文:顾国耀,徐晓清,陈仕萍,涂云宝,刘霞,刘东东. 己二酸二甲酯加氢制1,6-己二醇催化剂工业侧线研究[J]. 工业催化, 2018, 26(6): 64-68. DOI: 10.3969/j.issn.1008-1143.2018.06.013
作者姓名:顾国耀  徐晓清  陈仕萍  涂云宝  刘霞  刘东东
作者单位:1.中国石油化工股份有限公司上海石油化工研究院,上海201208;2.中国石化集团重庆川维化工有限公司,重庆401254
摘    要:采用共沉淀法制备新型Cu基己二酸二甲酯加氢制1,6-己二醇催化剂,在工业侧线试验装置上,考察入口温度、反应压力、氢酯物质的量比和液相空速等工艺条件的影响,完成1 000 h稳定性试验。结果表明,在入口温度210℃、反应压力≥5.0 MPa、空速(0.1~0.2)h~(-1)和氢酯物质的量比≥170条件下,己二酸二甲酯转化率大于99%,1,6-己二醇选择性97%,催化剂性能稳定,显示了良好的工业应用前景。

关 键 词:精细化学工程  Cu基催化剂  己二酸二甲酯  1  6-己二醇  工业侧线  

Industrial side-line test of catalyst for dimethyl adipate hydrogenation to 1,6-Hexanediol
Gu Guoyao,Xu Xiaoqing,Chen Shiping,Tu Yunbao,Liu Xia,Liu Dongdong. Industrial side-line test of catalyst for dimethyl adipate hydrogenation to 1,6-Hexanediol[J]. Industrial Catalysis, 2018, 26(6): 64-68. DOI: 10.3969/j.issn.1008-1143.2018.06.013
Authors:Gu Guoyao  Xu Xiaoqing  Chen Shiping  Tu Yunbao  Liu Xia  Liu Dongdong
Affiliation:1.Shanghai Research Institute of Petrochemical Technology,SINOPEC,Shanghai 201208,China;2.Chongqing SVW Chemical Co., Ltd.,SINOPEC,Chongqing 401254,China
Abstract:New Cu-based catalyst for hydrogenation of dimethyl adipate to 1,6-hexanediol was prepared by co-precipitation method.Effects of inlet temperature,reaction pressure,mole ratio of H2 to ester and liquid phase space velocity on catalytic performance were examined on industrial side-line plant for dimethyl adipate hydrogenation.Meanwhile,stability test was carried for 1 000 h.The results showed that dimethyl adipate conversion was higher than 99% and 1,6-HDO selectivity was 97%,respectively,under the operation conditions of inlet temperature 210 ℃,reaction pressure≥5.0 MPa,liquid phase space velocity (0.1~0.2) h-1 and mole ratio of H2/ester≥170.The catalyst posed good stability and showed predictable industrial application prospect.
Keywords:fine chemical engineering  copper-based catalyst  dimethyl adipate  1  6-hexanediol  industrial side-line  
本文献已被 CNKI 等数据库收录!
点击此处可从《工业催化》浏览原始摘要信息
点击此处可从《工业催化》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号