Unravelling the Anomalous Coking Resistance over Boron Nitride- Supported Ni Catalysts for Dry Reforming of Methane

被引:17
作者
Deng, Jiang [1 ]
Gao, Min [2 ,3 ]
Hasegawa, Jun-ya [3 ]
Zhang, Xiaoyu [1 ]
Wang, Aiyong [1 ]
Chen, Aling [1 ]
Zhang, Dengsong [1 ]
机构
[1] Shanghai Univ, Coll Sci, Int Joint Lab Catalyt Chem, Shanghai 200444, Peoples R China
[2] Hokkaido Univ, Inst Chem React Design & Discovery WPI ICReDD, Sapporo 0010021, Japan
[3] Hokkaido Univ, Inst Catalysis, Sapporo 0010021, Japan
来源
CCS CHEMISTRY | 2023年 / 5卷 / 09期
基金
中国国家自然科学基金;
关键词
dry reforming of methane; coking resistance; meth-ane conversion; DEHYDROGENATION; CO2;
D O I
10.31635/ccschem.022.202202342
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal oxides have been used as the supports for heterogeneous catalysis for many years, but they still suffer from coking in some high-temperature applications. The main reasons for coking are the uncontrollable dissociation of C-H and the overbalance between carbon deposition and removal. Herein, we find a boron nitride (BN)-immobilized Ni catalyst shows unprecedented coking resistance in dry reforming of methane via the incomplete decomposition of methane. Unlike the Ni-based catalysts supported by traditional metal oxides, BN-supported Ni accelerates the first C-H dissociation while inhibiting the breaking of the final C-H bond; hence, the suppression of the complete decomposition of methane thoroughly addresses the coking issue. This work reveals the fundamental reason for the coking resistance over BN-supported Ni catalysts is selective activation of the C-H bond, which can provide an inspiring idea for other applications.
引用
收藏
页码:2111 / 2124
页数:14
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