Calcium decorated Copper@Nitrogen-Doped carbon towards highly selective hydrogenation of biomass derived furfural

被引:1
作者
Zhang, Jun [1 ,2 ,3 ]
Xiao, Yaoxin [1 ,2 ,3 ,4 ]
Shan, Rui [1 ,2 ,3 ,5 ]
Yuan, Haoran [1 ,2 ,3 ,4 ]
Chen, Yong [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
[2] CAS Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
[3] Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China
[4] South China Agr Univ, Inst Biomass Engn, Guangzhou 510642, Peoples R China
[5] Shuye Environm Technol Co Ltd, Shantou 515800, Peoples R China
基金
中国国家自然科学基金;
关键词
Furfural; Hydrogenation; Tetrahydrofurfuryl alcohol; Nitrogen-doped carbon; Basic site; CATALYTIC-HYDROGENATION; REDUCTION; NANOPARTICLES; CONVERSION; ALCOHOL; CO; ADSORPTION;
D O I
10.1016/j.fuel.2023.130829
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In the present research, calcium decorated copper@nitrogen-doped carbon (marked as Cu1Cax@CN) derived from biomass was constructed for highly selective hydrogenation of bio-based furfural (FFR), which remarkably favored furan ring hydrogenation for tetrahydrofurfuryl alcohol (THFA) formation via regulating the hydrogenation path. Remarkably, the in-situ generated basic sites from N- and Ca-containing species were beneficial to the good metal dispersion as well as the chemical activation of aldehyde and C = C groups, thus favoring the FFRto-THFA transformation. The optimal basic density-to-copper mass ratio in a range of 3.0 similar to 4.0 was attained, in consideration of THFA generation. The as-prepared Cu1Ca0.87@CN catalyst could afford full FFR conversion as well as 75.6 % THFA yield under 3 MPa H-2 atmosphere, which also exhibited excellent stability and could be recycled four times without any deactivation. In addition, the basic sites in the as-prepared Cu1Cax@CN samples were capable of activating both the C = O and C = C bonds, and the activation of C = O bond took precedence over that of C=C bond, especially in the case of relative low temperatures. Plausible reaction mechanism for FFR-to-THFA transformation under the synergistic effect of active Cu-0 center and basic sites was proposed in detail.
引用
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页数:12
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