Kinetic modeling on oxidation of arabinose to arabinonic acid in base-free medium over synergistic PtCu/TiO2 catalyst

被引:1
|
作者
Miao, Wen [1 ]
Geng, Ang [1 ]
Lai, Linyi [1 ]
Li, Xiran [1 ]
Wang, Xin [1 ]
Liu, Mengyuan [1 ]
Wang, Zhenyang [1 ]
Zhang, Dongpei [1 ]
Wang, Yuangao [1 ]
Wang, Dongchao [2 ]
Li, Shuang [2 ]
Jin, Xin [1 ]
Yang, Chaohe [1 ]
机构
[1] China Univ Petr, Coll Chem & Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China
[2] Chambroad Holding Grp, Bingzhou 256500, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Arabinose; Oxidation; Catalysts; Kinetics; SOLVOTHERMAL SYNTHESIS; GLUCOSE-OXIDATION; GOLD CATALYSTS; BIOMASS; NANOPARTICLES; OXYGEN; CHEMICALS; ROUTES; TRANSFORMATION; GLYCEROL;
D O I
10.1016/j.ces.2023.119557
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Arabinonic acid (AA) is an essential building block for the food and pharmaceutical industries. However, green and atomically efficient synthesis of AA remains a grand challenge, as most previous reports have been focused on the alkaline-promoted oxidation of arabinose. In this work, we firstly reported lumped kinetic modeling of the oxidation of arabinose to AA in base-free medium, with detailed reaction networks involved in the C-H and C-C cleavage reactions. It is found that the bimetallic PtCu/TiO2 catalyst displays strong synergism due to electronic coupling at metal-support interface, leading to an almost two-fold enhancement in catalytic activity in comparison with monometallic Pt/TiO2 catalyst. According to detailed analysis on reaction network and kinetic modeling, the presence of Cu mainly contributes to formulating additional active sites for the oxidation and C-C cleavage reactions. The quantitative assessment for conversion of arabinose could provide useful information for modeling and process development for various other important sugars.
引用
收藏
页数:13
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