Al2O3 Nanorod with Rich Pentacoordinate Al3+ Sites Stabilizing Co2+ for Propane Dehydrogenation

Author:

Zhao Zhiping1,Wang Zhixia1,Tong Yanbing1,Sun Jinru1,Ke Ming1,Song Weiyu1

Affiliation:

1. State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249, China

Abstract

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.

Funder

National Natural Science Foundation of China

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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