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CuCl2 immobilized on amino-functionalized MCM-41 and MCM-48 as efficient heterogeneous catalysts for dimethyl carbonate synthesis by vapor-phase oxidative carbonylation of methanol

机译:固定在氨基官能化MCM-41和MCM-48上的CuCl2是通过甲醇气相氧化羰基化合成碳酸二甲酯的有效多相催化剂

摘要

Pure silica mesoporous molecular sieves MCM-41 and MCM-48 organofunctionalized with 3-aminopropyltrimethoxysilane and N-[(3-trimethoxysilyl) propyl] ethylene-diamine, respectively, were served as supports to immobilize CuCl2 with conventional impregnation method. The supported copper catalysts showed a considerable enhancement in the reaction rate in heterogeneous vapor-phase oxidative carbonylation of methanol to produce dimethyl carbonate in comparison with that obtained by CuCl2-supported nonfunctionalized mesoporous silicas under identical conditions. The electronic donation of the amino groups, the accessibility and dischargeability of reactants in the regular mesopores probably account for the good catalytic performance as evidenced by the characteristic studies with XRD, BET, FTIR, TG- DTA, and XPS.
机译:分别用3-氨基丙基三甲氧基硅烷和N-[(3-三甲氧基甲硅烷基)丙基]乙二胺进行有机官能化的纯二氧化硅介孔分子筛MCM-41和MCM-48用作载体,用常规浸渍方法固定CuCl2。与在相同条件下由CuCl 2负载的非官能化介孔二氧化硅得到的催化剂相比,负载的铜催化剂在甲醇的非均相气相氧化羰基化反应中生成碳酸二甲酯的反应速率显着提高。 XRD,BET,FTIR,TG-DTA和XPS的特性研究证明,氨基的电子给体,规则介孔中反应物的可及性和排出性可能是良好的催化性能。

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