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Selective hydrogenation of aromatic carboxylic acids over basic N-doped mesoporous carbon supported palladium catalysts

机译:碱性N掺杂介孔碳负载钯催化剂上芳香族羧酸的选择性加氢

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摘要

Mesoporous carbon nitride (MCN) has been prepared through a simple polymerization reaction between ethylenediamine (EDA) and carbon tetrachloride (CTC) by a nano hard-templating approach. The obtained MCN possesses high surface area (166.3 m(2)/g), average pore size of 9.2 nm and high N content (up to 18.5 wt%). The negative charge and the basicity on MCN surface are originated from its rich carbon nitride heterocycles, which notably improves the surface hydrophilicity and the adsorption of acidic molecules. Furthermore, MCN can be adopted as the proper support for highly dispersed Pd NPs with well-controlled size distribution. Compared with microporous N-doped active carbon with low N-content, the MCN-supported Pd catalyst shows an enhanced activity in water phase for the selective ring hydrogenation of benzoic acid, benzamide and phenol, in which 11.3 times higher activity in comparison to undoped catalyst is achieved. Wide characterizations reveal that big pore size, selective adsorption for acid substrate and strong interaction between N and Pd may lead to the high activity of Pd/MCN. (C) 2016 Elsevier B.V. All rights reserved.
机译:介孔碳氮化物(MCN)是通过乙二胺(EDA)与四氯化碳(CTC)之间的简单聚合反应,采用纳米硬模板法制备的。所获得的MCN具有高表面积(166.3 m(2)/ g),平均孔径为9.2 nm和高N含量(最高18.5 wt%)。 MCN表面的负电荷和碱性来自其丰富的氮化碳杂环,从而显着提高了表面亲水性和酸性分子的吸附性。此外,MCN可以用作高度分散的Pd NP的适当支持,且尺寸分布可控。与低N含量的微孔N掺杂活性炭相比,MCN负载的Pd催化剂在水相中对苯甲酸,苯甲酰胺和苯酚的选择性环加氢显示出增强的活性,与未掺杂的相比,其活性高11.3倍实现催化剂。广泛的特征表明,大孔径,对酸性底物的选择性吸附以及N和Pd之间的强相互作用可能导致Pd / MCN的高活性。 (C)2016 Elsevier B.V.保留所有权利。

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