Deciphering transient carbon footprint for methane dry reforming over Ni@S-1 nanosheet zeolite catalyst

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作者
Zhang, Quanqi [1 ,2 ]
Jiang, Zhonghua [1 ,2 ]
Zhang, Yimin [1 ,2 ]
Xu, Xinyu [1 ,2 ]
Yang, Ye [3 ]
Qin, Yucai [3 ]
Song, Lijuan [3 ]
Mei, Yi [1 ,2 ]
Zu, Yun [1 ,2 ]
机构
[1] Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming,650500, China
[2] Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical Engineering and New Phosphorus Materials, Kunming,650500, China
[3] Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning Petrochemical University, Fushun,113001, China
基金
中国国家自然科学基金;
关键词
D O I
10.1016/j.apcatb.2024.124722
中图分类号
学科分类号
摘要
Carbon deposition, an inevitable product operated at high temperatures, is a headache-inducing obstacle to enhance catalyst stability for methane dry reforming (MDR). Herein, we have ingeniously designed sintering-resistant Ni@S-1 nanosheet zeolites to purposefully induce common linear and non-linear deactivation of catalysts during MDR reaction for deciphering carbon footprint. Multiple evidences unveiled that transient carbon, composed of multi-phenyl-rings via rapidly rearrangement of CHx* fragments, was a crucial vane for catalyst deactivation. Accordingly, we proposed a dynamic equilibrium theory for the generation and elimination of transient carbon. Achieving this balance was dependent of the matching degree between Ni0 nanoparticles and NiOx(OH)y, which both separately originated from the evolutions of 1:1 and 2:1 Ni phyllosilicates controlled by nanosheet thickness. Delightfully, synthetic Ni@S-1–60nm catalyst with an optimal ratio of Ni0/NiOx(OH)y contributed higher MDR activity and durability. These findings derived a new MDR reaction pathway and afforded value-filled information for developing high carbon-resistant MDR catalysts. © 2024 Elsevier B.V.
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