首页 | 本学科首页   官方微博 | 高级检索  
     检索      

固体酸催化剂在醇解聚对苯二甲酸乙二醇酯反应中的催化性能
引用本文:李增喜,刘彦轻,王慧,张香平,闫瑞一.固体酸催化剂在醇解聚对苯二甲酸乙二醇酯反应中的催化性能[J].天津大学学报(自然科学与工程技术版),2009,42(10):891-896.
作者姓名:李增喜  刘彦轻  王慧  张香平  闫瑞一
作者单位:李增喜,刘彦轻,王慧(中国科学院研究生院化学与化学工程学院,北京,100049;中国科学院过程工程研究所,北京,100190);张香平,闫瑞一(中国科学院过程工程研究所,北京,100190) 
基金项目:国家高技术研究发展(863)计划资助项目 
摘    要:采用浸渍法制备了SO4^2-/ZnO和S^4^2-/TiO2固体酸催化剂,用XRD、SEM等对催化剂的晶型结构和表面形貌进行了表征,并考察了它们降解聚对苯二甲酸二乙二醇酯制备对苯二甲酸二乙二醇酯的催化性能.实验结果表明,焙烧温度对SO4^2-/ZnO的催化活性影响不大,而对SO4^2-/TiO2的催化活性影响明显,随焙烧温度的升高,其催化活性出现先上升后下降的趋势反应时间、反应温度、催化剂浓度等工艺条件对两种催化剂活性的影响趋势是一致的.

关 键 词:固体酸  催化剂  表征  醇解  聚对苯二甲酸乙二醇酯

Catalytic Property of Solid Acid Catalyst in Glycolysis of Polyethylene Terephthalate
Institution:LI Zeng-xi, LIU Yan-qing, WANG Hui, ZHANG Xiang-ping, YAN Rui-yi (1. School of Chemistry and Chemical Engineering ,Graduate University of the Chinese Academy of Sciences, Beijing 100049,China; 2. Institute of Process Engineering ,Chinese Academy of Sciences ,Beijing 100190 ,China)
Abstract:Solid acid catalysts SO4^2-/ZnO and SO4^2-/TIO2 were prepared with wetness impregnation method,and calcined at different temperatures. The structural properties of these samples were investigated using XRD and SEM. The catalytic activity was tested by the depolymerization of polyethylene terephthalate (PET) with ethylene glycol (EG). The experimental results indicate that the calcination temperature has little influence on the catalytic activity of SO4^2- /ZnO ,but has much influ- ence on the catalytic activity of SO4^2-/TiO2. As the calcination temperature increases ,the catalytic activity of SO4^2-/TiO2 first rises and then drops with the best'catalytic activity reached at 340 ℃. The two solid acid catalysts show the same tendency in the conversion of PET and the yield of bis-2-hydroxyethy terephthalate (BHET) under the influence of different parameters, such as the reaction time ,the reaction temperature and the catalyst concentration.
Keywords:solidacid  catalyst  characterization  glycolysis  polyethyleneterephthalate
本文献已被 维普 万方数据 等数据库收录!
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