Deactivation of a au/ceo2-co3o4 catalyst during co preferential oxidation in h-2-rich stream
文献类型：期刊论文
| 作者 | Wang, Hui1,2; Zhu, Huaqing1; Qin, Zhangfeng1; Liang, Feixue1,2; Wang, Guofu1; Wang, Jianguo1 |
| 刊名 | Journal of catalysis
 |
| 出版日期 | 2009-06-10 |
| 卷号 | 264期号:2页码:154-162 |
| 关键词 | Co preferential oxidation Co oxidation Au/ceo2-co3o4 Deactivation |
| ISSN号 | 0021-9517 |
| DOI | 10.1016/j.jcat.2009.04.003 |
| 通讯作者 | Wang, jianguo(iccjgw@sxicc.ac.cn) |
| 英文摘要 | The origins of the deactivation of a au/ceo2-co3o4 catalyst during co preferential oxidation (prox) are investigated in detail by means of high-resolution transmission electron microscopy (hrtem), x-ray diffraction (xrd), x-ray photoelectron spectroscopy (xps), temperature-programmed reduction of hydrogen (h-2-tpr), temperature-programmed oxidation of oxygen (o-2-tpo), and diffuse reflectance infrared fourier transform spectroscopy (drifts). a possible mechanism involving -ooh intermediate is proposed and used to explain the deactivation in the long-term stability test of co prox. the aggregation or sintering of the au particles is excluded from the origins of deactivation by hrtem and xrd. the deactivation of the catalyst is mainly due to an intrinsic transformation in the chemical state of the gold species and the support oxides in the au/ceo2-co3o4 catalyst. the xps, xrd, and h2-tpr results demonstrate the reduction of ionic au to metallic au and of cobalt oxide to cobaltous compound. the changes of the chemical states imply a structure reordering of the catalyst surface, which will suppress the supplement of active oxygen and the formation of -ooh species, inhibit the co oxidation reaction, and lead to the deactivation of the catalyst. the accumulation of carbonates and h2o on the deactivated catalyst is revealed by xps, drifts, o-2-tpo, and a regeneration test. they are responsible for the complete deactivation of the catalyst. the hydration of the catalyst surface may play a more important role than the formation of carbonates in the deactivation of the catalyst. (c) 2009 elsevier inc. all rights reserved. |
| WOS关键词 | WATER-GAS SHIFT ; SUPPORTED GOLD NANOPARTICLES ; CARBON-MONOXIDE OXIDATION ; LOW-TEMPERATURE ; AU/TIO2 CATALYST ; SELECTIVE OXIDATION ; CERIA CATALYSTS ; H-2 ; HYDROGEN ; MECHANISM |
| WOS研究方向 | Chemistry ; Engineering |
| WOS类目 | Chemistry, Physical ; Engineering, Chemical |
| 语种 | 英语 |
| WOS记录号 | WOS:000267061800007 |
| 出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
| URI标识 | http://www.irgrid.ac.cn/handle/1471x/2399656 |
| 专题 | 中国科学院大学 |
| 通讯作者 | Wang, Jianguo |
| 作者单位 | 1.Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China 2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China |
| 推荐引用方式 GB/T 7714 | Wang, Hui,Zhu, Huaqing,Qin, Zhangfeng,et al. Deactivation of a au/ceo2-co3o4 catalyst during co preferential oxidation in h-2-rich stream[J]. Journal of catalysis,2009,264(2):154-162. |
| APA | Wang, Hui,Zhu, Huaqing,Qin, Zhangfeng,Liang, Feixue,Wang, Guofu,&Wang, Jianguo.(2009).Deactivation of a au/ceo2-co3o4 catalyst during co preferential oxidation in h-2-rich stream.Journal of catalysis,264(2),154-162. |
| MLA | Wang, Hui,et al."Deactivation of a au/ceo2-co3o4 catalyst during co preferential oxidation in h-2-rich stream".Journal of catalysis 264.2(2009):154-162. |
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来源：中国科学院大学
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