中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
An efficient approach to modify the catalyst activity for the hydrogenation of nitrobenzene

文献类型:期刊论文

作者Mo, WM; Wan, BS; Liao, SJ
刊名chinese chemical letters
出版日期2001-09-01
卷号12期号:9页码:817-820
关键词bimetallic catalyst synergic effect catalytic hydrogenation palladium
英文摘要the addition of a suitable amount of pph3 to pdcl2 or pdcl2(phcn)(2) in situ can considerably increase the catalytic activity in the hydrogenation of nitrobenzene, while the catalytic activities of pdcl2 (reduced)+pph3, pdcl2(pph3)(2) and pd(pph3)(4) are very poor. the poisoning of catalyst by mercury indicates that the catalytically active species are composed of pd(0) colloidal particles. transmission electron micrographs show that the size of nanometric pd(0) particles of pdcl2 with pph3 added in situ is smaller than that of phcl2(pph3) or pdcl2 (reduced)+pph3. a synergic effect of bimetallic catalysts such as pdcl2+npph(3)+nicl2 (n= 0.5, 1) and pdcl2(phcn)(2)+pph3+fecl3 gives rise to a further increase in the catalytic activity.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, multidisciplinary
研究领域[WOS]chemistry
关键词[WOS]bimetallic catalyst ; oxidative carbonylation
收录类别SCI
原文出处true
语种英语
WOS记录号WOS:000170947200022
公开日期2010-11-30
源URL[http://159.226.238.44/handle/321008/91937]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
2.Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
推荐引用方式
GB/T 7714
Mo, WM,Wan, BS,Liao, SJ. An efficient approach to modify the catalyst activity for the hydrogenation of nitrobenzene[J]. chinese chemical letters,2001,12(9):817-820.
APA Mo, WM,Wan, BS,&Liao, SJ.(2001).An efficient approach to modify the catalyst activity for the hydrogenation of nitrobenzene.chinese chemical letters,12(9),817-820.
MLA Mo, WM,et al."An efficient approach to modify the catalyst activity for the hydrogenation of nitrobenzene".chinese chemical letters 12.9(2001):817-820.

入库方式: OAI收割

来源:大连化学物理研究所

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