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配位还原制备膦酸功能化Pd/C催化剂及其应用
引用本文:闫晓红,葛霞,张琳,齐丽娟,刘洋,魏少华,朱晓舒,唐亚文.配位还原制备膦酸功能化Pd/C催化剂及其应用[J].高等学校化学学报,2017,38(9):1619.
作者姓名:闫晓红  葛霞  张琳  齐丽娟  刘洋  魏少华  朱晓舒  唐亚文
作者单位:江苏省新型动力电池重点实验室, 江苏省生物医药功能材料协同创新中心, 南京师范大学化学与材料科学学院, 南京 210023
基金项目:国家自然科学基金(批准号:21376122;21576139)资助. Supported by the National Natural Science Foundation of China
摘    要:采用活性炭为载体,乙二胺四亚甲基膦酸(EDTMPA)作为配位剂和稳定剂,氯化钯(PdCl2)为前驱体,硼氢化钠(NaBH4)为还原剂,通过一步还原制备得到膦酸功能化的超细高分散Pd/C催化剂.透射电子显微镜(TEM)及X射线衍射(XRD)分析结果表明,制得的Pd/C催化剂中Pd粒子的平均粒径为2.7 nm,分散度为37.1%,高于同类型商业化催化剂.制得的催化剂对罗丹明(RhB)和对硝基苯酚(4-NP)的催化加氢反应的活化能分别为27.18和16.79 kJ/mol,明显低于商业化Pd/C催化剂(57.12和55.71 kJ/mol).

关 键 词:Pd/C催化剂  乙二胺四亚甲基膦酸  配合物  催化加氢  
收稿时间:2017-02-18

Preparation of Phosphoric Acid-functionalized Pd/C Catalyst by Coordination Reduction and Its Application
YAN Xiaohong,GE Xia,ZHANG Lin,QI Lijuan,LIU Yang,WEI Shaohua,ZHU Xiaoshu,TANG Yawen.Preparation of Phosphoric Acid-functionalized Pd/C Catalyst by Coordination Reduction and Its Application[J].Chemical Research In Chinese Universities,2017,38(9):1619.
Authors:YAN Xiaohong  GE Xia  ZHANG Lin  QI Lijuan  LIU Yang  WEI Shaohua  ZHU Xiaoshu  TANG Yawen
Institution:Jiangsu Key Laboratory of New Power Batteries, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China
Abstract:We presented a one-step reduction approach to the synthesis of highly dispersed and ultrafine phos-phonate functionalized Pd nanoparticles supported by carbon(Pd/C) using XC-72 as the catalyst support, ethylenediamine tetramethylene phosphonic acid( EDTMPA) as both coordination agent and stabilizer, palla-dium chloride(PdCl2) as the precursor and sodium borohydride(NaBH4) as the reducing agent, respectively. Transmission electron microscopy ( TEM ) and X-ray diffraction ( XRD ) analysis results indicated that the average particle size and the dispersion degree in the Pd/C catalysts are 2. 7 nm and 37. 1%, respectively, much higher than those of the commercial catalysts. The activation energy of catalytic hydrogenation for rhoda-mine(RhB) and p-nitrophenol(4-NP) for the obtained catalyst are calculated to be 27. 1 and 16. 9 kJ/mol, respectively, obviously lower than those in the commercial Pd/C catalyst(57. 2 and 55. 7 kJ/mol).
Keywords:Pd/C catalyst  Ethylenediamine tetramethylene phosphonic acid( EDTMPA)  Complex  Catalyt-ic degradation
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