脱氢
催化作用
二胺
乙醇
化学
有机化学
化学工程
工程类
作者
Jin Guo,Jifeng Pang,Ming Yin,Lele Feng,Shimin Liu,Pengfei Wu,Mingyuan Zheng
标识
DOI:10.1002/cctc.202400269
摘要
Abstract Encapsulation of metal particles into zeolites is an attractive strategy for stabilizing metal species. Nevertheless, most metal cations tend to precipitate under basic and hydrothermal conditions without the use of effective anchoring agents. Herein, low‐cost diamines of ethylenediamine and propanediamine were selected as effective chelators, which stabilized the Cu species under basic conditions and then anchored them into the framework of MFI (silicate‐1) during the hydrothermal process. The obtained Cu@MFI−R catalyst showed >96 % ethanol conversion and 98 % acetaldehyde selectivity in the 300 h time on stream, demonstrating superior advantages over the impregnation method prepared Cu/MFI catalysts. Characterization of Cu@MFI−R catalysts revealed that Cu nanoparticles were fixed in the framework of MFI, producing abundant Cu + species for ethanol conversion. Additionally, the spatial confinement effects inhibited Cu + reduction and aggregations, affording a high catalyst stability. Differently, over Cu/MFI catalysts, the unconfined Cu + species were prone to be reduced into Cu 0 during the reaction, resulting in the Cu particles aggregation and activity depression.
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