甲醇
催化作用
钼
聚甲醛
沸石
化学
选择性
氧化还原
化学工程
无机化学
材料科学
有机化学
聚合物
工程类
作者
Xiaqing Wang,Xiujuan Gao,Faen Song,Xiaoxing Wang,Guozhuang Cao,Junfeng Zhang,Yizhuo Han,Qingde Zhang
标识
DOI:10.1021/acscatal.3c04941
摘要
Direct oxidation of methanol to polyoxymethylene dimethyl ethers (PODEn) with longer C–O chains faces a challenge due to difficult matching of active sites. Herein, a core–shell catalyst composed of an iron molybdenum core and a zeolite shell has been designed, successfully realizing methanol oxidation to PODEn. The PODE2–6 selectivity reaches 41.0% at 85.6% methanol conversion over the FeMo@HZSM-5 catalyst. Combined with the designed experiments and characterizations, the special core–shell structure and the synergy between acid sites with different strengths and redox sites are the pivotal factors for promoting the chain growth of the C–O bond.
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