CrOx/Ce1?xZrxO2 for chemical looping propane oxidative dehydrogenation: The redox interaction between CrOx and the support

被引:6
|
作者
Chen, Xinyi [1 ]
Tian, Xin [2 ]
Zheng, Chaohe [1 ]
Zhao, Haibo [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, State Key Lab Coal Combust, Wuhan 430074, Peoples R China
[2] Wuhan Univ, Sch Power & Mech Engn, Wuhan 430072, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Oxidative dehydrogenation; Chemical looping; Reodx catalyst; Supported Cr; Oxide support; LIGHT ALKANES; CATALYSTS; ALUMINA; OXYGEN; ISOBUTANE; KINETICS;
D O I
10.1016/j.ces.2023.118697
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Propane dehydrogenation is an attractive alternative for propylene production to petroleum-based routes. However, overcoming deactivation and toxicity of catalysts in propane direct dehydrogenation (PDH), and over oxidation in oxidative dehydrogenation (ODHP) remain challenging. Here, a chromium-based catalyst supported on a Ce-Zr solid solution is constructed for chemical looping oxida-tive propane dehydrogenation (CL-ODHP). A dual modulation of oxygen species by Zr doping was unrav-eled by characterizations and DFT calculation: the oxygen of surface CrOx was constrained while the oxygen mobility of the Ce-Zr support was promoted. Based on these properties, the interaction between surface CrOx and the support further enables an oxygen "donor-acceptor", which potentially functions as in situ activation and regeneration of redox CrOx species as well as blockage of non-selective oxygen released from the Ce-Zr support. The optimized material (7.5Cr/Ce0.8Zr0.2O2) achieves propane conversion up to 50% and propylene yield of 31% at 600 degrees C, and has the lowest Cr content among previously reported Cr-based catalysts that have comparable performance. These results provide insights for the design of highly active and selective redox catalysts for chemical looping as a reaction engineering strategy for the upgrading of propane dehydrogenation processes.(c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:10
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