Construction of N-Doped Carbon-Modified Ni/SiO2 Catalyst Promoting Cinnamaldehyde Selective Hydrogenation

被引:8
作者
Ren, Yongwang [1 ]
Xu, Huizhong [2 ]
Han, Beibei [3 ]
Xu, Jing [4 ]
机构
[1] Zhejiang Ocean Univ, Sch Naval Architecture & Maritime, Zhoushan 316022, Peoples R China
[2] SGS CSTC Stand Tech Serv Co Ltd, Shanghai 201205, Peoples R China
[3] Zhejiang Tianyuan Fabr Co Ltd, Wenling 317513, Peoples R China
[4] Zhejiang Ocean Univ, Natl Engn Res Ctr Marine Aquaculture, Zhoushan 316022, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 10期
关键词
Ni catalyst; N-doped carbon; electronic effect; cinnamaldehyde hydrogenation; ALPHA; BETA-UNSATURATED ALDEHYDES; NITROGEN; NICKEL;
D O I
10.3390/molecules28104136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
At present, the selective hydrogenation of alpha, beta-unsaturated aldehydes remains a challenge due to competition between unsaturated functional groups (C=C and C=O). In this study, N-doped carbon deposited on silica-supported nickel Mott-Schottky type catalysts (Ni/SiO2@NxC) was prepared for the selective hydrogenation of cinnamaldehyde (CAL) by using the respective hydrothermal method and high-temperature carbonization method. The prepared optimal Ni/SiO2@N7C catalyst achieved 98.9% conversion and 83.1% selectivity for 3-phenylpropionaldehyde (HCAL) in the selective hydrogenation reaction of CAL. By constructing the Mott-Schottky effect, the electron transfer from metallic Ni to N-doped carbon at their contact interface was promoted, and the electron transfer was demonstrated by XPS and UPS. Experimental results indicated that by modulating the electron density of metallic Ni, the catalytic hydrogenation of C=C bonds was preferentially performed to obtain higher HCAL selectivity. Meanwhile, this work also provides an effective way to design electronically adjustable type catalysts for more selective hydrogenation reactions.
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页数:14
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