Promoting role of bismuth and antimony on Pt catalysts for the selective oxidation of glycerol to dihydroxyacetone

被引:114
|
作者
Ning, Xiaomei [1 ]
Li, Yuhang [1 ]
Yu, Hao [1 ]
Peng, Feng [1 ]
Wang, Hongjuan [1 ]
Yang, Yanhui [2 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
基金
中国国家自然科学基金;
关键词
Platinum; Bismuth; Glycerol oxidation; 1,3-Dihydroxyacetone; Leaching; Geometrical effect; LIQUID-PHASE OXIDATION; AEROBIC OXIDATION; PLATINUM CATALYSTS; ALCOHOL OXIDATION; ELECTROOXIDATION; BI; ALLOY; NANOPARTICLES; ENHANCEMENT; ADSORPTION;
D O I
10.1016/j.jcat.2015.12.020
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The group 15 metals, bismuth and antimony, play important roles in promoting noble-metal-catalyzed oxidation reactions toward high value-added chemicals. Herein, we report that the selective oxidation of glycerol to 1,3-dihydroxyacetone (DHA) catalyzed by Pt supported on N-doped carbon nanotubes (Pt/NCNT) can be significantly promoted in the presence of Bi or Sb in reaction solution. This catalyst system showed not only comparable even better performance to the Pt/NCNT with pre-loaded Bi, but also the greatly simplified catalyst preparation. It was found that the Bi-promoted Pt/NCNT underwent dynamic surface reconstruction through leaching and adsorption of Bi adatoms, due to the formation of glyceric acid. By characterizing the adsorption of Bi on Pt catalyst with high-resolution transmission electron microscopy, CO-stripping, horizontal attenuated total reflection infrared spectroscopy and X-ray photoelectron spectroscopy, it has been ascertained that Bi preferentially deposits on the step sites of Pt, and then blocks the terrace sites to promote the Pt catalyst mainly through a geometrical effect, which facilitates the activation and transformation of the secondary hydroxyl group of glycerol through the chelation between substrate and Pt-Bi sites. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 104
页数:10
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