Selective hydrogenation of furfural to furfuryl alcohol over Pd/TiH2 catalyst

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2021-05-01 DOI:10.1016/j.mcat.2021.111599
Zhuangqing Wang , Xinchao Wang , Chao Zhang , Masahiko Arai , Leilei Zhou , Fengyu Zhao
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引用次数: 16

Abstract

In this work, the selective hydrogenation of furfural to furfuryl alcohol has been studied over Pd/TiH2 catalysts. The catalytic performances of several catalysts with different Pd loading (0.2–3% in weight) were discussed, among which a higher selectivity to furfuryl alcohol was obtained over 0.5Pd/TiH2 and it gave rise to a 73% furfural alcohol selectivity at complete conversion at 60 °C. The physicochemical properties of catalysts were well characterized by TEM, XRD, XPS, Raman, TPR and TPD, as well as in-situ DRIFT for the adsorption of the reactant. The size and the electronic state of Pd particles, and the surface defects of catalysts presented significant influence on the catalytic performance. The furfural is preferentially adsorbed with its C=O bond on the boundary of Pd particle and TiH2 support, leading to the high selectivity to furfuryl alcohol.

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Pd/TiH2催化糠醛选择性加氢制糠醇
在Pd/TiH2催化剂上,研究了糠醛选择性加氢制糠醇的反应。讨论了几种不同Pd负载(重量0.2 ~ 3%)的催化剂的催化性能,其中在0.5Pd/TiH2条件下对糠醛的选择性较高,60℃完全转化时糠醛的选择性为73%。通过TEM、XRD、XPS、Raman、TPR、TPD以及对反应物吸附的原位漂移等手段对催化剂的理化性质进行了表征。钯粒子的大小、电子态以及催化剂表面缺陷对催化性能有显著影响。糠醛的C=O键优先吸附在Pd粒子和TiH2载体的边界上,对糠醇具有较高的选择性。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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