High selective oxidation of 5-hydroxymethyl furfural to 5-hydroxymethyl-2-furan carboxylic acid using Ag-TiO2

被引:18
|
作者
Xie, Tao [1 ]
Yue, Shitong [1 ]
Su, Ting [2 ]
Song, Mingqi [1 ]
Xu, Wenjie [1 ]
Xiao, Yaxi [1 ]
Yang, Zhenglong [1 ]
Len, Christophe [3 ,4 ]
Zhao, Deyang [1 ]
机构
[1] Ludong Univ, Sch Chem & Mat Sci, Yantai 264025, Peoples R China
[2] Yantai Univ, Green Chem Ctr, Coll Chem & Chem Engn, Yantai 264005, Peoples R China
[3] PSL Res Univ, Chim ParisTech, CNRS, Inst Chem Life & Hlth Sci, 11 Rue Pierre & Marie Curie, F-75005 Paris, France
[4] Univ Technol Compiegne, F-60200 Compiegne, France
基金
中国国家自然科学基金;
关键词
HMF; Selective oxidation; HMFCA; Ag-TiO2; AEROBIC OXIDATION; 2,5-FURANDICARBOXYLIC ACID; CATALYTIC-OXIDATION; PERFORMANCE; TIO2; HETEROSTRUCTURES; INSIGHTS; CELLS;
D O I
10.1016/j.mcat.2022.112353
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
Production of 5-hydroxymethyl-2-furan carboxylic acid (HMFCA) from 5-hydroxymethylfurfural (HMF) selective oxidation using Ag-TiO2 were investigated under oxygen atmosphere. The novel catalyst was prepared by a simple sol-gel method, different characterizations were performed, which included N-2 adsorption and desorption measurements, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), NH3/CO2 temperature-programmed desorption (NH3/CO2-TPD), scanning electron microscope (SEM), and high revolution transmission electron microscope (HR-TEM). Reaction parameters, such as temperature, base content, oxygen pressure, catalyst loading and reaction time were investigated. 99% HMF conversion, 96% HMFCA yield, and 97% HMFCA selectivity obtained under optimum condition (25 mg Ag-TiO2, 4 eq. Na2CO3, 1 MPa O-2, 80 degrees C, 32 h). Catalyst stability experiment revealed negligible deactivation (90% HMF conversion and 85% HMFCA yield in fourth time). The appropriate proportion of acidic/basic sites, large surface areas, and strong synergistic interaction between Ag+, metallic Ag and TiO2 for oxygen activation attributed to high catalytic activation.
引用
收藏
页数:9
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