甲烷
催化作用
二氧化碳重整
期限(时间)
甲烷转化炉
化学工程
化学
环境科学
材料科学
合成气
蒸汽重整
有机化学
制氢
工程类
物理
量子力学
作者
Haehyun Min,Yongkyu Ju,Yaying Ji,Do Yeong Kim,Young Jin Kim,Sung Bong Kang
标识
DOI:10.1016/j.cej.2024.151520
摘要
Dry reforming of methane (DRM) is a fascinating catalysis to convert greenhouse gases into valuable syngas; however, the catalyst deactivation due to coking and sintering has posed a significant obstacle to practical use. Here, we introduce a novel synthetic approach for creating Ni nanoclusters (∼2 nm) embedded inside silica (NiES), without using any catalytic metal promoters. Compared to conventional Ni-SiO₂ catalysts, the NiES catalyst could fully utilize unique Ni-O-Si bonding within a bimodal silica matrix. This leads to exceptional reactivity and long-term stability for DRM without noticeable deactivation over 500 h of operations. Notably, characterizations revealed that Ni nanoclusters maintained their particle size even after this extended operation, significantly contributing to their resistance against carbon coking. These Ni clusters appeared to efficiently promote CH4 decomposition, while the continuously regenerated OH groups from dissociative adsorption of CO2 assisted in oxidizing carbon species. This study will substantially contribute to the swift implementation of the catalytic DRM process.
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