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磷钨酸-尿素/四氧化三铁磁性氧化脱硫催化剂反应性能
引用本文:宋鹏月,朱江,于博浩,王旭阳,杨娇,李禹蒙,李传鹏,杨晓宇,陈立东,姜春杰.磷钨酸-尿素/四氧化三铁磁性氧化脱硫催化剂反应性能[J].应用化学,2015,32(3):317-321.
作者姓名:宋鹏月  朱江  于博浩  王旭阳  杨娇  李禹蒙  李传鹏  杨晓宇  陈立东  姜春杰
基金项目:国家自然科学基金(21171082);辽宁省博士科研启动基金项目(2013106)
摘    要:制备了铁磁性Fe3O4基质,并引入磷钨酸尿素复合物制备了有机硫化物氧化催化剂(HPW-Urea/Fe3O4),并通过IR、XRD、Raman和TG等技术手段测定了磁性催化剂的物理化学和热学性质。 研究结果表明,在Fe3O4上引入HPW-Urea后,磷钨酸尿素复合物以Keggin结构存在于载体Fe3O4上,且和载体之间是化学键作用。 在以有机硫化物乙硫醇的正己烷溶液的H2O2氧化反应中,磷钨酸尿素复合物的引入提高了磁性Fe3O4对乙硫醇的氧化活性,并探讨了尿素在活性改善中的作用。

关 键 词:磷钨酸  四氧化三铁  乙硫醇  尿素  过氧化氢  
收稿时间:2014-07-03

Performance of Phosphotungstic Acid-Urea/Ferroferric Oxide Magnetic Oxidative Desulfurization Catalyst
SONG Pengyue,ZHU Jiang,YU Bohao,WANG Xuyang,YANG Jiao,LI Yumeng,LI Chuanpeng,YANG Xiaoyu,CHEN Lidong,JIANG Chunjie.Performance of Phosphotungstic Acid-Urea/Ferroferric Oxide Magnetic Oxidative Desulfurization Catalyst[J].Chinese Journal of Applied Chemistry,2015,32(3):317-321.
Authors:SONG Pengyue  ZHU Jiang  YU Bohao  WANG Xuyang  YANG Jiao  LI Yumeng  LI Chuanpeng  YANG Xiaoyu  CHEN Lidong  JIANG Chunjie
Institution:Faculty of Chemistry and Chemical Engineering,Institute of Chemistry for Functionalized Materials,Liaoning Normal University,Dalian,Liaoning 110629,China;Analysis and Testing Center,Beihua University,Jilin,Jilin 132013,China;PetroChina Dalian Petrochemical Company,Dalian,Liaoning 116032,China
Abstract:Oxidation catalysts of organic sulfide were synthesized by the ferromagnetic Fe3O4 matrix and phosphotungstic acid urea complexes(PAUC). The properties of products were characterized by IR, XRD, Raman and TG. With introduction of oxidation catalysts of organic sulfide, it is found that PAUC exists on Fe3O4 support in a Keggin structure and there is a chemical bond effect between them. If the H2O2 oxidation of ethanethiol proceeds in n-hexane, the oxidation activity of ethanethiol over ferromagnetic Fe3O4 matrix is increased in the presence of the PAUC. The effect of urea on activity has been discussed.
Keywords:phosphotungstic acid  magnetic iron oxide  ethanethiol  urea  hydrogen peroxide
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