钙长石
沸石
成核
化学工程
吸附
苯酚
分子
化学
离子
相(物质)
材料科学
纳米技术
无机化学
组合化学
催化作用
有机化学
工程类
作者
Yanpeng Chen,Rongshu Zhu,Guanyu Chen,Minghu Zhao,J. Min,Rongming Cai,Jinqiang Gao,Mei Hong,Shihe Yang
标识
DOI:10.1016/j.cej.2024.154727
摘要
Synthesis of small-pore chabazite (CHA) zeolites in the absence of organic structure-directing agents (OSDA) has been proven difficult. A judicious mixed cation approach recently reported could expand the design space of CHA formation. In a seemingly opposite direction, we herein report an anion tuning approach for controlling the zeolite polymorphism in an OSDA-free system that effectively promotes hierarchical CHA formation in a competitive growth with MER. Phenoxide media, utilizing mild in-situ nucleophilic etching in cooperation with zeolite framework growth, allow beneficial kinetic control to facilitate CHA nucleation. Operando analyses reveal the crucial role of stabilized dimeric aluminate species as a key intermediate for CHA phase selection. The phenol-mediated CHA zeolites exhibit almost perfect 9 molecules per unit cell CO2 uptake capacity and no CH4 adsorption. This work offers an anion tuning strategy for controlling zeolite polymorphism as a supplement to the current phase-selection toolbox that utilizes mixed inorganic cations.
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