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首页> 外文期刊>Journal of Catalysis >Immobilization of (n-Bu_4N)_4W_10O_32 on Mesoporous MCM-41 and Amorphous Silicas for Photocatalytic Oxidation of Cycloalkanes with Molecular Oxygen
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Immobilization of (n-Bu_4N)_4W_10O_32 on Mesoporous MCM-41 and Amorphous Silicas for Photocatalytic Oxidation of Cycloalkanes with Molecular Oxygen

机译:(n-Bu_4N)_4W_10O_32固定在介孔MCM-41和无定形二氧化硅上用于分子氧光催化氧化环烷烃

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摘要

Heterogenization of (n-Bu_4N)_4W_10O_32 on amorphous and MCM-41 silicas by impregnation is a suitable method to prepare efficient and stable catalysts able to oxidize unactivated C-H bonds to the corresponding alcohols and ketones with molecular oxygen and near ultraviolet light. The thus-prepared catalysts were characterized by spectroscopic and N_2 adsorption-desorption experiments. A better dispersion of decatungstate was achieved with MCM-41, which also has the higher surface area. Results obtained in the model photooxidation of cyclohexane and cycclododecane confirm that the decatungstate heterogenized on the more ordered MCM-41 silica promotes the process with higher chemoselectivity (cyclohexanone/cyclohexanol molar ratio = 2.6). The photocatalytic efficiency of (n-Bu_4N)_4W_10O_32 is not reduced after heterogenization; moreover, decautungstate immobilized on amorphous silica oxidizes cyclododecane with a markedly higher efficiency than in the homogeneous phase. The supported photocatalysts can be used at least three times without any loss of activity.
机译:通过浸渍在无定形和MCM-41二氧化硅上进行(n-Bu_4N)_4W_10O_32的异质化是制备有效和稳定的催化剂的合适方法,该催化剂能够利用分子氧和近紫外线将未活化的C-H键氧化为相应的醇和酮。通过光谱学和N_2吸附-脱附实验表征了如此制备的催化剂。 MCM-41可以更好地分散去离子钨酸盐,MCM-41的表面积也更大。在环己烷和环十二烷的光氧化模型中获得的结果证实,在更有序的MCM-41二氧化硅上杂化的十碳酸盐能以更高的化学选择性(环己酮/环己醇摩尔比= 2.6)促进该过程。异质化后,(n-Bu_4N)_4W_10O_32的光催化效率不会降低;此外,固定在无定形二氧化硅上的十水合十价钨酸盐比均匀相中的氧化效率高得多。负载的光催化剂可以使用至少3次而没有任何活性损失。

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