HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Graduate School of Engineering / Faculty of Engineering >
Peer-reviewed Journal Articles, etc >

Pd and PdZn supported on ZnO as catalysts for the hydrogenation of cinnamaldehyde to hydrocinnamyl alcohol

This item is licensed under:Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International

Files in This Item:
Mitani-Revised manuscript.pdf761.77 kBPDFView/Open
Please use this identifier to cite or link to this item:

Title: Pd and PdZn supported on ZnO as catalysts for the hydrogenation of cinnamaldehyde to hydrocinnamyl alcohol
Authors: Fujita, Shin-ichiro Browse this author →KAKEN DB
Mitani, Haruka Browse this author
Zhang, Chao Browse this author
Li, Kai Browse this author
Zhao, Fengyu Browse this author
Arai, Masahiko Browse this author
Keywords: PdZn alloy
alpha, beta-Unsaturated aldehyde
Selectivity control
Substrate-product interaction
Issue Date: Dec-2017
Publisher: Elsevier
Journal Title: Molecular Catalysis
Volume: 442
Start Page: 12
End Page: 19
Publisher DOI: 10.1016/j.mcat.2017.08.018
Abstract: Liquid phase selective hydrogenation of cinnamaldehyde (CAL) was investigated over ZnO-supported Pd and PdZn catalysts different in the Pd loading. The former monometallic catalyst was less selective to the formation of cinnamyl alcohol (COL) irrespective of the Pd loading (5 and 30 wt.-% Pd). When the Pd loading was small (5 wt.-%), PdZn catalyst (PdZn-5) indicated similar catalytic actions. However, PdZn catalyst containing Pd in a larger content of 30 wt.-% (PdZn-30) showed different results: the COL selectivity was about 20% at low conversion but it increased with CAL conversion, reaching to >50% at a conversion of 60%. The COL selectivity was likely to change depending on the concentration of a product of hydrocinnamaldehyde (HCAL). The coadsorption of HCAL should control the orientation of CAL molecules adsorbed on the PdZn-30 catalyst. This may assist the adsorption of CAL via its aldehyde group on the surface of catalyst, resulting in an increase in the COL selectivity. Unique catalysis of PdZn-30 may result from structural features of the surface of its large PdZn particles, which are different from those of PdZn-5 having smaller PdZn particles. (C) 2017 Elsevier B.V. All rights reserved.
Rights: © 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license
Type: article (author version)
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 藤田 進一郎

Export metadata:

OAI-PMH ( junii2 , jpcoar_1.0 )

MathJax is now OFF:


 - Hokkaido University