Catalytic performance of zinc-supported copper and nickel catalysts in the glycerol hydrogenolysis

被引:5
作者
RJChimento [1 ]
BCMiranda [2 ]
DRuiz [1 ]
FGispertGuirado [3 ]
FMedina [4 ]
JLlorca [5 ]
JBOSantos [6 ]
机构
[1] Physical Chemistry Department,Faculty of Chemical Sciences,University of Concepcion
[2] Chemical Engineering School,Universidad de Costa Rica
[3] Scientific Resources Service,Universitat Rovira i Virgili
[4] Department of Chemical Engineering,Universitat Rovira i Virgili
[5] Department of Chemical Engineering,Barcelona Research Center in Multiscale Science and Engineering,Institute of Energy Technologies,Universitat Politècnica de Catalunya,EEBE
[6] Department of Chemical Engineering,Universidade Federal de S?o Carlos (UFSCAR)
关键词
Glycerol; Hydrogenolysis; Dehydration; Hydroxyacetone; Copper; Nickel; Catalyst;
D O I
暂无
中图分类号
TQ221.11 []; O643.36 [催化剂];
学科分类号
0817 ; 081705 ;
摘要
Gas-phase catalytic conversion of glycerol to value added chemicals was investigated over zinc-supported copper and nickel catalysts.The addition of aluminum in the support was also investigated in glycerol conversion and the results indicate an increase in the acidity and adsorption capacity for both copper and nickel catalysts.HRTEM and XRD analysis revealed Ni Zn alloy formation in the Ni/ZnO catalyst.The XRD patterns of the prepared Zn Al mixed oxide catalysts show the presence of Gahanite phase(ZnAl2O4).In addition,H2 chemisorption and TPR results suggest a strong metal-support interactions(SMSI)effect between Ni and Zn O particles.Bare supports Zn O and ZnAl(Zn/Al=0.5) were investigated in the glycerol conversion and they did not present activity.Copper supported on ZnO and ZnAl mixed oxide(Zn/Al=0.5)was active towards hydroxyacetone formation.Nickel was active in the hydrogenolysis of glycerol both for C–C and C–O bonds cleavage of glycerol producing CH4.Strong metal-support interactions(SMSI)between Ni and ZnO has a remarkable suppression effect on the methanation activity during the glycerol conversion.
引用
收藏
页码:185 / 194
页数:10
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