咪唑酯
沸石咪唑盐骨架
催化作用
煅烧
选择性
化学工程
水溶液
化学
降级(电信)
热液循环
环境友好型
水热合成
水解
材料科学
金属有机骨架
无机化学
有机化学
吸附
工程类
生物
电信
计算机科学
生态学
作者
Fraz Saeed Butt,Muddasar Safdar,Allana Lewis,Nurul A. Mazlan,Norbert Radacsi,Xianfeng Fan,Harvey Arellano‐García,Yi Huang
标识
DOI:10.1016/j.mtadv.2023.100448
摘要
Zeolitic Imidazolate Framework-67 (ZIF-67) has been used in a variety of applications including catalysis, separations, and energy storage. However, the weak hydrostability of ZIF-67, due to structural hydrolysis and degradation, dramatically limits their applicability after aqueous exposure. In this work, cosolvent-stabilized superhydrophobic, highly hydrostable ZIF-67 was synthesized at room temperature using a facile, one-pot hydrothermal synthesis route, and the effect of cosolvent concentration on ZIF-67 crystal structure properties and hydrostability was studied systematically. The underlying mechanism for the cosolvent-supported hydrostability improvement was also proposed. Furthermore, the influence of hydrotreatment on the resultant ZIF-67s' catalytic performance was studied in the 'Sabatier reaction' for CO2 to synthetic natural gas (CH4) conversion. The ZIF-67-derived calcined catalysts obtained from the hydrotreated samples of the cosolvent-stabilized ZIF-67 exhibited no prominent loss in catalytic performance and showed better CO2 conversion, higher CH4 selectivity, and less CO production, in comparison to the conventional ZIF-67 samples. Notably, the use of a lower ligand-to-metal ratio (∼8) in the current synthesis significantly reduced the overall chemical consumption, achieving highly economically and environmentally friendly manufacturing of exceptionally hydrostable ZIF-67.
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