沸石
催化作用
甲烷
材料科学
空间速度
二氧化碳重整
分子
化学工程
粒子(生态学)
有机化学
选择性
化学
合成气
海洋学
地质学
工程类
作者
Han Chun-lan,Xiaoxiao Zhu,Xinping Wang
标识
DOI:10.1142/s1793604723400258
摘要
This paper reports a highly active and stable Ni@silicalite-1 catalyst for dry reforming of methane. In the reaction conducted at 800[Formula: see text]C, CH 4 /CO 2 =1/1 and GHSV=100,000 mL⋅ g[Formula: see text] h[Formula: see text] for 100 h, the Ni@silicalite-1 delivered CH 4 conversions of 93% without deactivation. This superior property of the catalyst comes from the special structure that large amounts of Ni (13.7 wt.%) are embedded in the silicalite-1 zeolite crystals as small particles ([Formula: see text]4.7 nm), with the zeolite channels transferring molecules while with the zeolite framework resisting the Ni particle migration.
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