催化作用
烧结
钴
焦炭
镍
材料科学
甲烷
脱氢
化学工程
沸石
纳米颗粒
金属
无机化学
冶金
化学
纳米技术
有机化学
工程类
作者
Qiuyan Zhu,Yifeng Liu,Xuedi Qin,Бо Лю,Zhouhong Ren,Xin Tao,Chengtao Wang,Hai Wang,Lina Li,Xi Liu,Liwei Chen,Liang Wang,Feng‐Shou Xiao
标识
DOI:10.1016/j.ces.2023.119030
摘要
Dry reforming of methane (DRM) displays a crucial role in CO2 fixation, but the current catalysts suffer from deactivation from thermodynamically oriented coking and metal sintering. Herein, we reported a catalyst by fixing the cobalt–nickel nanoparticles within the zeolite crystals (CoNi@zeolite), where the SiOx-O-Mδ+ (M = Ni or Co) linkage enhanced the reduction resistance of Co and Ni species compared with the generally supported catalysts, efficiently hindering the deep dehydrogenation of methane, which is well known as a reaction channel for coke formation. In addition, the rigid and thermally stable zeolite framework stabilized the cobalt–nickel nanoparticles to avoid their sintering during the reaction. As a result, the CoNi@zeolite catalyst exhibited a long reaction lifetime and great regenerability in a test for 980 h with reaction gas flow at 1200 L per unit mass of metal species per hour, outperforming conventionally supported metal catalysts. This work enables a proof-of-the-concept design of durable catalysts by zeolite fixation for the reactions in strongly reductive atmospheres.
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