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Green oxidative esterification of furfural over nano-Au supported on highly basic anion exchange resin beads  ( SCI-EXPANDED收录 EI收录)   被引量:4

文献类型:期刊文献

英文题名:Green oxidative esterification of furfural over nano-Au supported on highly basic anion exchange resin beads

作者:Wan, Cong[1];Cen, Shuangshuang[1];Chai, Xinyan[1];Tao, Feifei[1];Li, Lei[1];Yao, Xiandong[1];Xiao, Huiquan[1];Wang, Lijun[1]

机构:[1]Shaoxing Univ, Sch Chem & Chem Engn, Shaoxing 312000, Peoples R China

年份:2023

卷号:549

外文期刊名:MOLECULAR CATALYSIS

收录:SCI-EXPANDED(收录号:WOS:001099224000001)、、EI(收录号:20233614692279)、Scopus(收录号:2-s2.0-85169816104)、WOS

基金:Acknowledgements This work was funded by Natural Science Foundation of Zhejiang Province (Grant No. Y20B070011) , Scientific Research Project of Shaoxing University (Grant No. 2019LG1010) and Science and Tech-nology Innovation Activity Plan (New Talent Plan) Project for college students in Zhejiang province (Grant No. 2023R465011) .

语种:英文

外文关键词:Furfural; Heterogeneous catalysis; Oxidative esterification; Au; Solid base

外文摘要:Au nanoparticles with an average diameter of 3.7 nm supported on the macroporous anion exchange resin beads with cationic -CH2N+Me3 functional groups and OH(-)as counter anions were first prepared, for catalyzing the oxidative esterification of biomass-derived furfural in methanol using green O-2 as an oxidant. The main product methyl furoate with a high yield of 98% was obtained at 130 degrees C for 2 h in the absence of soluble alkali additives. The catalyst beads possessed a particle size range of 560 similar to 700 mu m inherited from the shaped support, enabling the separation of catalyst and liquid reaction medium by a simple decantation method. Catalyst poisoning experiments demonstrated Au activated superoxide radical O-2(-) and the basic OH- stored in the anion exchange resin are the decisive active components for the oxidative esterification, and the main product methyl furoate with a yield of 20% and a high selectivity of 96% was obtained under N-2 atmosphere revealed the reaction in this catalytic system followed an oxidative dehydrogenation route. In all catalytic cases except for the catalyst poisoning experiments and the cases of low catalyst dosages, the by-product acetal was almost completely suppressed, probably attributed to the presence of the alkaline OH- in the anion exchange resin of the catalyst.

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