Promotion effect of support calcination on ethanol production from CO hydrogenation over Rh/Fe/Al2O3 catalysts | |
Chen, Weimiao1; Ding, Yunjie1,2; Song, Xiangeng1,3; Wang, Tao1; Luo, Hongyuan1 | |
刊名 | applied catalysis a-general |
2011-11-04 | |
卷号 | 407期号:1-2页码:231-237 |
关键词 | Rhodium Alumina Iron Carbon monoxide hydrogenation Calcination temperature Ethanol |
英文摘要 | a series of rh/fe/al2o3 catalysts, in which the al2o3 supports were calcined at different temperatures, were prepared by a sequential impregnation method. the catalysts were tested by co hydrogenation and characterized by n-2 adsorption-desorption, x-ray diffraction (xrd), co pulse chemisorption, temperature programmed surface reaction (tpsr) and temperature programmed reduction (tpr) techniques. the activity of ethanol formation was the highest when the catalyst support was calcined at 800 degrees c, while that of methanol formation increased continuously with the calcination temperature of the support. according to the commonly accepted mechanism of c-2-oxygenates formation, co conversion followed three separate pathways after co dissociation, and our results suggested that the activity towards co insertion and dissociation increased gradually with the calcination temperature, but began to decrease at 900 degrees c. on the other hand, direct hydrogenation of co to methanol was still increasing at 900 degrees c. these observations were in agreement with tpsr results. dispersion of the rh or fe species was not impaired, and even improved, with the declining of the surface area of the support due to high temperature calcination. tpr results revealed that rh-fe interaction was strengthened after calcination, due to a lowering in surface hydroxyl reactivity of the support and an increase of the rh-fe interface area. as a result, the amount of rh-fe-o sites for co dissociation and insertion increased with the calcination temperature, giving rise to the increase in ethanol formation activity. however, an over-strong rh-fe interaction would be resulted when the catalyst support was calcined at 900 degrees c, and this would cause more fe species to be reduced, which would then cover the rh sites. consequently. co uptake as well as dissociation and insertion of co would decrease, leading to more co molecules being hydrogenated directly to methanol, thus causing a decrease in the selectivity of ethanol formation. (c) 2011 elsevier b.v. all rights reserved. |
WOS标题词 | science & technology ; physical sciences ; life sciences & biomedicine |
类目[WOS] | chemistry, physical ; environmental sciences |
研究领域[WOS] | chemistry ; environmental sciences & ecology |
关键词[WOS] | rhodium catalysts ; fischer-tropsch ; carbon-monoxide ; rh catalysts ; c-2-oxygenates synthesis ; syngas conversion ; synthesis gas ; h-2/co ratio ; oxide ; iron |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000297234400028 |
公开日期 | 2015-11-17 |
内容类型 | 期刊论文 |
源URL | [http://159.226.238.44/handle/321008/142508] |
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 Natl Lab Clean Energy, Dalian 116023, Peoples R China 2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China 3.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China |
推荐引用方式 GB/T 7714 | Chen, Weimiao,Ding, Yunjie,Song, Xiangeng,et al. Promotion effect of support calcination on ethanol production from CO hydrogenation over Rh/Fe/Al2O3 catalysts[J]. applied catalysis a-general,2011,407(1-2):231-237. |
APA | Chen, Weimiao,Ding, Yunjie,Song, Xiangeng,Wang, Tao,&Luo, Hongyuan.(2011).Promotion effect of support calcination on ethanol production from CO hydrogenation over Rh/Fe/Al2O3 catalysts.applied catalysis a-general,407(1-2),231-237. |
MLA | Chen, Weimiao,et al."Promotion effect of support calcination on ethanol production from CO hydrogenation over Rh/Fe/Al2O3 catalysts".applied catalysis a-general 407.1-2(2011):231-237. |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论