Metal-organic frameworks MOF-808-X as highly efficient catalysts for direct synthesis of dimethyl carbonate from CO2 and methanol

微型多孔材料 碳酸二甲酯 催化作用 金属有机骨架 甲醇 化学 无机化学 摩尔比 比表面积 化学工程 材料科学 物理化学 有机化学 吸附 工程类
作者
Keng Xuan,Yanfeng Pu,Li Feng,Jianxun Luo,Ning Zhao,Fang Xiao
出处
期刊:Chinese Journal of Catalysis [China Science Publishing & Media Ltd.]
卷期号:40 (4): 553-566 被引量:67
标识
DOI:10.1016/s1872-2067(19)63291-2
摘要

A series of metal-organic frameworks MOF-808-X (6-connected) were synthesized by regulating the ZrOCl2·8H2O/1,3,5-benzenetricarboxylic acid (BTC) molar ratio (X) and tested for the direct synthesis of dimethyl carbonate (DMC) from CO2 and CH3OH with 1,1,1-trimethoxymethane (TMM) as a dehydrating agent. The effect of the ZrOCl2·8H2O/BTC molar ratio on the physicochemical properties and catalytic performance of MOF-808-X was investigated. Results showed that a proper ZrOCl2·8H2O/BTC molar ratio during MOF-808-X synthesis was fairly important to reduce the redundant BTC or zirconium clusters trapped in the micropores of MOF-808-X. MOF-808-4, with almost no redundant BTC or zirconium clusters trapped in the micropores, exhibited the largest surface area, micropore size, and the number of acidic-basic sites, and consequently showed the best activity among all MOF-808-X, with the highest DMC yield of 21.5% under the optimal reaction conditions. Moreover, benefiting from the larger micropore size, MOF-808-4 outperformed our previously reported UiO-66-24 (12-connected), which had even more acidic-basic sites and larger surface area than MOF-808-4, mainly because the larger micropore size of MOF-808-4 provided higher accessibility for the reactant to the active sites located in the micropores. Furthermore, a possible reaction mechanism over MOF-808-4 was proposed based on the in situ FT-IR results. The effects of different reaction parameters on DMC formation and the reusability of MOF-808-X were also studied.
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