Co decorated low Pt loading nanoparticles over TiO2 catalyst for selective hydrogenation of furfural

被引:12
|
作者
Liang, Changhui [1 ,2 ]
Li, Huixiang [1 ]
Peng, Mao [3 ]
Zhang, Xiaoqiang [1 ]
Jiang, Qike [1 ]
Cui, Jin [1 ]
Ding, Yunjie [1 ]
Zhang, Z. Conrad [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, 457 Zhongshan Rd, Dalian 116023, Liaoning, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
Zero-valent Pt atom precursor; PtCo bimetallic catalyst; Selective activation; Furfural hydrogenation; Furfuryl alcohol; COPPER CHROMITE CATALYSTS; BIMETALLIC CATALYSTS; BIOMASS; ALCOHOL; CONVERSION; GREEN; FUELS; HYDRODEOXYGENATION; REDUCTION; STABILITY;
D O I
10.1016/j.apcata.2022.118766
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
Selective hydrogenation of carbonyl groups in biobased chemicals to alcohols is crucial to the economics of broadly sustainable product portfolios. Furfuryl alcohol (FOL), the most prominent chemical of hemicellulose, has been produced by furfural (FAL) hydrogenation over heterogeneous catalysts. In this work, we show the outstanding activity, selectivity, and stability of supported bimetallic PtCo nanoparticle (np) synthesized from a pre-made stock solution of zero valent atomic Pt precursor and Co-2(CO)8. With only 0.5 wt% Pt on TiO2, the np-PtCo/TiO2 catalyst exhibits TOF of 14,023 h-1 at 30 ? with > 99.9% FOL selectivity. The stability of the np-PtCo/TiO2 catalyst is verified by the steady performance in reuses at both moderate and full conversions. The oxyphilic Co delta+ in the PtCo nanoparticles induces nucleophilic chemisorption of-C--O, resulting in deeply polarized -C--O bond. DFT calculated FAL adsorption energies on np-Pt and np-PtCo are -0.22 eV and -0.74 eV, respectively.
引用
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页数:11
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