多壁碳纳米管和氧化石墨烯添加剂对三维金属催化剂对1-苯乙醇氧化活性的影响

IF 5.062
Ana Paula C. Ribeiro , Emmanuele Fontolan , Elisabete C.B.A. Alegria , Maximilian N. Kopylovich , Roberta Bertani , Armando J.L. Pombeiro
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引用次数: 13

摘要

采用球磨法制备了三维金属(Cu, Fe, Co, V)复合催化剂,用于1-苯乙醇在无溶剂微波催化下以过氧化叔丁基(TBHP)为氧化剂转化为苯乙酮。研究了多壁碳纳米管(CNTs)和氧化石墨烯(GO)添加剂对催化剂催化活性的影响。通过球磨将CNTs或GO与金属盐(CoCl2)、氧化物(CuO、Fe2O3、V2O5)或二元体系(Fe2O3-CoCl2、CoCl2-V2O5、CuO-Fe2O3)混合。对于基于cocl2的催化体系,添加少量(0.1-5%)的CNTs或GO可显著提高催化活性,例如,在相同的催化条件下,添加1%的CNTs添加剂可将产率从28%提高到77%。其中,CoCl2-5%CNTs复合材料的活性最高,产率为85%,1 h后TON为43。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The influence of multiwalled carbon nanotubes and graphene oxide additives on the catalytic activity of 3d metal catalysts towards 1-phenylethanol oxidation

The influence of multiwalled carbon nanotubes and graphene oxide additives on the catalytic activity of 3d metal catalysts towards 1-phenylethanol oxidation

3d metal (Cu, Fe, Co, V) containing composite catalysts for the solvent-free microwave-assisted transformation of 1-phenylethanol to acetophenone with tert-butyl hydroperoxide (TBHP) as oxidant were prepared by ball milling. The influence of multiwalled carbon nanotubes (CNTs) and graphene oxide (GO) additives on the catalytic activity of the catalysts was studied. CNTs or GO were mixed by ball milling with the metal salts (CoCl2), oxides (CuO, Fe2O3, V2O5) or binary systems (Fe2O3-CoCl2, CoCl2-V2O5, CuO-Fe2O3). For CoCl2-based catalytic systems, addition of small amounts (0.1–5%) of CNTs or GO leads to significant improvement in catalytic activity, e.g. 1% of the CNTs additive allows to rise yields from 28 to 77%, under the same catalytic conditions. The CoCl2-5%CNTs composite is the most active among the studied ones with 85% yield and TON of 43 after 1 h.

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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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