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
二氧化碳重整
无机化学
冶金
化学
合成气
纳米技术
有机化学
工程类
作者
Qiuyan Zhu,Yifeng Liu,Xuedi Qin,Lu Liu,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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