脱氢
选择性
催化作用
丙烷
纳米棒
化学
纳米片
组合化学
光化学
化学工程
有机化学
材料科学
纳米技术
工程类
作者
Zhi‐Ping Zhao,Zhixia Wang,Yanbing Tong,Jinru Sun,Ming Ke,Weiyu Song
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-27
卷期号:13 (5): 807-807
被引量:8
标识
DOI:10.3390/catal13050807
摘要
The search for inexpensive, environmentally friendly, and highly effective catalysts to activate C-H bonds in propane dehydrogenation (PDH) reactions is still a major challenge. Co-based catalysts have gained significant attention in recent years due to their excellent ability to activate C-H bonds and their high selectivity towards olefins, despite being a non-noble and environmentally unfriendly metal. However, further improvements are necessary for practical utilization, particularly in terms of activity and anti-carbon deposition capacity. In this study, we synthesized Al2O3 nanorods with abundant pentacoordinated Al3+ (Al3+penta) sites. The supported Co on the Al2O3 nanorod (Co/Al2O3-NR) exhibited higher selectivity (>96% propylene selectivity) and stability (deactivation rate 0.15 h−1) compared to Co supported on an Al2O3 nanosheet with fewer pentacoordinated Al3+ sites. Various characterizations confirmed that Co(II) mainly exists as CoAl2O4 rather than Co3O4 in the form of Co/Al2O3-NR, which inhibits the reduction of Co(II) to Co0 and accordingly improves catalyst stability.
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