中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Catalytic co-oxidation of CO and H-2 over FeOx-supported Pd catalyst at low temperatures

文献类型:期刊论文

作者Liu LQ(刘乐全); Qiao BT(乔波涛); He YD(何昱徳); Zhou F(周锋); Yang BQ(杨本群); Deng YQ(邓友全)
刊名Journal of Catalysis
出版日期2012
卷号294页码:29-36
关键词Co-oxidation CO oxidation H-2 oxidation Palladium FeOx support Pd/Al2O3 Particle size effect Vacancy Active oxygen CO titration
ISSN号0021-9517
通讯作者邓友全
英文摘要Co-oxidation of CO and H2 or oxidation of H2 in the presence of CO was first achieved at low temperatures(0–20 ℃) over single-component catalysts (Pd/FeOx) at a space velocity of 15,000 ml g-1cat h-1. A systematical study of FeOx- and Al2O3-supported Pd catalysts is carried out by means of STEM, TEM, XRD, XPS, Mössbauer spectra, and time-resolved CO titration. Highly dispersed Pd nanoparticles with size 1–1.8 nm over 5.4 wt% Pd/FeOx are confirmed by HAADF-STEM and HRTEM. Time-resolved CO titration, Mössbauer spectra, and XRD and XPS results suggest FeOx support supplying active oxygen is involved in the oxidations. Particle size effect and oxygen supply from FeOx support are speculated to be the main reasons for the excellent performance of Pd/FeOx in co-oxidation of CO and H2 or oxidation of H2 in the presence of CO.
学科主题物理化学与绿色催化
收录类别SCI
资助信息the National Sciences Foundation of China (No. 20773146)
语种英语
WOS记录号WOS:000309314500003
公开日期2013-08-28
源URL[http://210.77.64.217/handle/362003/3690]  
专题兰州化学物理研究所_绿色化学研究发展中心
作者单位Chinese Acad Sci, Lanzhou Inst Chem Phys, Ctr Green Chem & Catalysis, Lanzhou 730000, Peoples R China
推荐引用方式
GB/T 7714
Liu LQ,Qiao BT,He YD,et al. Catalytic co-oxidation of CO and H-2 over FeOx-supported Pd catalyst at low temperatures[J]. Journal of Catalysis,2012,294:29-36.
APA Liu LQ,Qiao BT,He YD,Zhou F,Yang BQ,&Deng YQ.(2012).Catalytic co-oxidation of CO and H-2 over FeOx-supported Pd catalyst at low temperatures.Journal of Catalysis,294,29-36.
MLA Liu LQ,et al."Catalytic co-oxidation of CO and H-2 over FeOx-supported Pd catalyst at low temperatures".Journal of Catalysis 294(2012):29-36.

入库方式: OAI收割

来源:兰州化学物理研究所

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