The hydrogenation of levulinic acid to γ-valerolactone over Cu-ZrO2 catalysts prepared by a pH-gradient methodology

被引:35
作者
Orlowski, Igor [1 ]
Douthwaite, Mark [1 ]
Iqbal, Sarwat [1 ,2 ]
Hayward, James S. [1 ]
Davies, Thomas E. [1 ]
Bartley, Jonathan K. [1 ]
Miedziak, Peter J. [1 ,3 ]
Hirayama, Jun [1 ,4 ]
Morgan, David J. [1 ]
Willock, David J. [1 ]
Hutchings, Graham J. [1 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff Catalysis Inst, Main Bldg,Pk Pl, Cardiff CF10 3AT, S Glam, Wales
[2] Univ Lincoln, Sch Chem, Joseph Bank Labs, Beevor St, Lincoln LN6 7DL, England
[3] Univ South Wales, Sch Appl Sci, Pontypridd CF37 4AT, M Glam, Wales
[4] Hokkaido Univ, Inst Catalysis, Sapporo, Hokkaido 0010021, Japan
来源
JOURNAL OF ENERGY CHEMISTRY | 2019年 / 36卷
关键词
Cu-ZrO2; Hydrogenation; Levulinic acid; gamma-Valerolactone; SELECTIVE PRODUCTION; BIOMASS; COPPER; LIQUID; WATER; 1,4-PENTANEDIOL; FEASIBILITY; CONVERSION; CHEMICALS;
D O I
10.1016/j.jechem.2019.01.015
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel pH gradient methodology was used to synthesise a series of Cu-ZrO2 catalysts containing different quantities of Cu and Zr. All of the catalysts were highly selective to the desired product, gamma-valerolactone, and are considerably more stable than Cu-ZrO2 catalysts prepared by other co-precipitation methods for this reaction. Characterisation and further investigation of these catalysts by XRD, BET, SEM and XPS provided insight into the nature of the catalytic active site and the physicochemical properties that lead to catalyst stability. We consider the active site to be the interface between Cu/CuOx and ZrOx and that lattice Cu species assist with the dispersion of surface Cu through the promotion of a strong metal support interaction. This enhanced understanding of the active site and roles of lattice and surface Cu will assist with future catalyst design. As such, we conclude that the activity of Cu-ZrO2 catalysts in this reaction is dictated by the quantity of Cu-Zr interface sites. (C) 2019 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:15 / 24
页数:10
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