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

不同催化剂对苯酚H_2O_2羟基化反应的比较
引用本文:徐明涛,赵亮亮,朱艳婧,童莺,陈庆渺,杨柏林,王康斌,杨元法.不同催化剂对苯酚H_2O_2羟基化反应的比较[J].应用化学,2010,27(12):1419-1423.
作者姓名:徐明涛  赵亮亮  朱艳婧  童莺  陈庆渺  杨柏林  王康斌  杨元法
作者单位:(1.浙江师范大学物理化学研究所,浙江省固体表面反应化学重点实验室 金华 321004; 2.浙江仙琚制药股份有限公司 仙居)
基金项目:浙江省大学生科研创新团队资助项目
摘    要:用苯酚、双氧水经羟基化反应合成邻、对苯二酚,在Fe2O3为催化剂的反应系统中,反应诱导期长,且反应剧烈;当以杂多酸盐或Fe/ZrO2为催化剂时,诱导期消失,且羟基化反应平稳。反应的诱导期可能是由铁的氧化物转化为活性物种Fe3+和Fe2+的过程引起的;在杂多酸盐或Fe/ZrO2催化剂的反应体系中,羟基化反应可能发生在催化剂表面而使反应变得缓慢平稳,反应诱导期消失。

关 键 词:苯酚羟基化  Fe2O3  诱导期  杂多酸盐  ·OH自由基  
收稿时间:2010-01-18
修稿时间:2010-04-11

Comparasion of Different Catalysts on Phenol Hydroxylation
XU Ming-Tao,ZHAO Liang-Liang,ZHU Yan-Jing,TONG Ying,CHEN Qing-Niao,YANG Bai-Lin,WANG Kang-Bin,YANG Yuan-Fa.Comparasion of Different Catalysts on Phenol Hydroxylation[J].Chinese Journal of Applied Chemistry,2010,27(12):1419-1423.
Authors:XU Ming-Tao  ZHAO Liang-Liang  ZHU Yan-Jing  TONG Ying  CHEN Qing-Niao  YANG Bai-Lin  WANG Kang-Bin  YANG Yuan-Fa
Institution:(1.Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces,Institute of Physical Chemistry,Zhejiang Normal University,Jinhua 321004; 2.Zhejiang Xianju Pharmaceutical Co. Ltd.,Xianju)
Abstract:Fe2O3, heteropoly salt and Fe/ZrO2 exhibited high catalytic activity toward phenol hydroxylation using H2O2 as oxidant. A rapid hydroxylation of phenol was observed after an induction period in the hydroxylation of phenol catalyzed by Fe2O3; however, a slow hydroxylation of phenol was observed and the induction period disappeared in the same system catalyzed by heteropoly salt or Fe/ZrO2. The results suggest that, first, an induction period in hydroxylation of phenol is related to the formation of active species Fe3+ and Fe2+ from Fe2O3; and second, the slow hydroxylation is related to the surface catalysis reaction on heteropoly salt or Fe/ZrO2, leading to the disappearance of the induction period.
Keywords:phenol hydroxylation  Fe2O3  induction period  heteropoly acidic salt  ·OH free radical
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《应用化学》浏览原始摘要信息
点击此处可从《应用化学》下载免费的PDF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