二维碳化钒(V2CTx) MXene负载的NiIn金属间化合物用于肉桂醛选择性加氢制肉桂醇

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Yunqian Wang, Haixiang Shi, Liuyun Chen, Tongming Su, Xuan Luo, Xinling Xie, Hongbing Ji, Zuzeng Qin
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引用次数: 0

摘要

在V2CTx MXene上构建了九金属间化合物,用于肉桂醛(CAL)选择性加氢成肉桂醇(COL)。Ni4In/V2CTx对CAL的转化率为93.6%,对COL的选择性为77.4%。Ni4In/V2CTx的COL收率远高于Ni4In、Ni/V2CTx和Ni4In/Al2O3。此外,V2CTx载体是NiIn金属间化合物形成的关键,能有效抑制金属Ni的氧化。NiIn金属颗粒均匀分布在V2CTx表面,增加了金属与载体的相互作用。缺电子金属Ni和In抑制了C=C键的氢化。此外,In的引入提供了更丰富和更强的Lewis酸位点,有利于C=O键的吸附,从而提高了COL的选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
2D vanadium carbide (V2CTx) MXene supported NiIn intermetallic compounds for the selective hydrogenation of cinnamaldehyde to cinnamyl alcohol

NiIn intermetallic compounds are constructed over V2CTx MXene for the selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL). Ni4In/V2CTx demonstrated a conversion rate of 93.6% for CAL, with a high selectivity of 77.4% for COL. The COL yield of Ni4In/V2CTx is much greater than that of Ni4In, Ni/V2CTx, and Ni4In/Al2O3. Moreover, the V2CTx support is the key to the formation of NiIn intermetallic compounds, which effectively inhibit the oxidation of metallic Ni. NiIn metal particles are uniformly distributed on the surface of V2CTx, increasing the metal‒support interaction. Electron-deficient metallic Ni and In inhibit the hydrogenation of the C=C bond. Furthermore, the introduction of In provides more abundant and stronger Lewis acid sites, facilitating the adsorption of C=O bonds and thereby enhancing the selectivity for COL.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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