Isobutane dehydrogenation over the mesoporous Cr2O3/Al2O3 catalysts synthesized from a metal-organic framework MIL-101
文献类型:期刊论文
作者 | Zhao HH(赵华华)1,2![]() ![]() ![]() ![]() ![]() |
刊名 | Applied Catalysis A: General
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出版日期 | 2013 |
卷号 | 456页码:188-196 |
关键词 | Chromia/alumina Isobutane dehydrogenation Mesoporous Metal-organic framework MIL-101 |
ISSN号 | 0926-860X |
通讯作者 | 丑凌军 |
英文摘要 | The reactivity of isobutane dehydrogenation over a series of non-ordered mesoporous chromia/alumina (Cr2O3/Al2O3) catalysts with large specific surface area (149.4–381.6 m2 g−1) and high pore volume (0.77–1.24 cm3 g−1), synthesized using a metal-organic framework MIL-101 as a molecular host and chromium precursor, aluminium isopropoxide (Al(i-OC3H7)3) as the aluminium precursor, were studied in detail. The chromium species were highly dispersed over the catalyst with chromia loading up to 10 wt.%. The specific surface area of the catalyst decreased, whereas the amount of surface Cr3+ species and the mole ratio of Cr3+ and Cr6+ species (Cr3+/Cr6+) increased with the increasing chromia loadings (5–25 wt.%) and calcination temperature (500–900 ℃), respectively. The addition of potassium to the catalyst system greatly promoted isobutene selectivity and catalyst stability. The catalyst with 1.5 wt.% K2O and 10 wt.% Cr2O3 loadings calcined at 800 ℃ was found to exhibit the highest isobutane conversion 60.1% with the isobutene selectivity up to 93.2% among all the catalysts. The maintainable catalytic reactivity demonstrated the high stability of the catalyst in ten dehydrogenation-regeneration cycles. Moreover, it was proposed that the Cr3+ species was mainly the active site and catalytic selectivity was depended on the surface Cr3+/Cr6+ value over the catalyst. The catalyst presented much more stable dehydrogenation activity compared with the conventional catalyst. Consequently, this study presents a feasible way to facile synthesis of the mesoporous MOF-derived Cr2O3/Al2O3 catalysts with high stability and good catalytic reactivity over isobutane dehydrogenation. |
学科主题 | 物理化学与绿色催化 |
收录类别 | SCI |
资助信息 | the State Key Laboratory for Oxo Synthesis and Selective Oxidation of China;Suzhou Science and Technology Bureau of Applied Foundation Research Project (SYG201219) |
语种 | 英语 |
WOS记录号 | WOS:000319637400022 |
公开日期 | 2013-12-04 |
源URL | [http://210.77.64.217/handle/362003/4414] ![]() |
专题 | 兰州化学物理研究所_OSSO国家重点实验室 |
通讯作者 | Chou LJ(丑凌军) |
作者单位 | 1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 3.Suzhou Inst Nanotech & Nanobion, Suzhou 215123, Peoples R China |
推荐引用方式 GB/T 7714 | Zhao HH,Song HL,Xu LL,et al. Isobutane dehydrogenation over the mesoporous Cr2O3/Al2O3 catalysts synthesized from a metal-organic framework MIL-101[J]. Applied Catalysis A: General,2013,456:188-196. |
APA | Zhao HH,Song HL,Xu LL,Chou LJ,&丑凌军.(2013).Isobutane dehydrogenation over the mesoporous Cr2O3/Al2O3 catalysts synthesized from a metal-organic framework MIL-101.Applied Catalysis A: General,456,188-196. |
MLA | Zhao HH,et al."Isobutane dehydrogenation over the mesoporous Cr2O3/Al2O3 catalysts synthesized from a metal-organic framework MIL-101".Applied Catalysis A: General 456(2013):188-196. |
入库方式: OAI收割
来源:兰州化学物理研究所
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