Selective hydrogenation of furfural using a membrane reactor

被引:43
|
作者
Delima, Roxanna S. [1 ,2 ]
Stankovic, Mia D. [3 ]
MacLeod, Benjamin P. [2 ,3 ]
Fink, Arthur G. [3 ]
Rooney, Michael B. [3 ]
Huang, Aoxue [3 ]
Jansonius, Ryan P. [3 ]
Dvorak, David J. [2 ]
Berlinguette, Curtis P. [1 ,2 ,3 ,4 ]
机构
[1] Univ British Columbia, Dept Chem & Biol Engn, 2360 East Mall, Vancouver, BC V6Y 1Z3, Canada
[2] Univ British Columbia, Stewart Blusson Quantum Matter Inst, 2355 East Mall, Vancouver, BC V6T 1Z4, Canada
[3] Univ British Columbia, Dept Chem, 2036 Main Hall, Vancouver, BC V6T 1Z1, Canada
[4] Canadian Inst Adv Res CIFAR, MaRS Ctr, West Tower,661 Univ Ave, Toronto, ON M5G 1M1, Canada
关键词
ELECTROCATALYTIC HYDROGENATION; ELECTRODE; HYDROGENOLYSIS; CONVERSION; PATHWAYS; ALCOHOL; ENERGY;
D O I
10.1039/d1ee02818a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic palladium membrane reactors (ePMRs) use electricity and water to drive hydrogenation reactions without forming H-2 gas. In these reactors, a hydrogen-permeable palladium foil physically separates electrochemical proton generation in aqueous media from chemical hydrogenation in organic media. We report herein the use of the ePMR to electrolytically hydrogenate furfural, an important biomass derivative. This system was proven to convert furfural into furfuryl alcohol and tetrahydrofurfuryl alcohol with 84% and 98% selectivities, respectively. To reach these high selectivities, we designed and built an ePMR for high-throughput testing. Using this apparatus, we tested how different solvents, catalysts, and applied currents impacted furfural hydrogenation. We found that bulky solvents with weak nucleophilicities suppressed the formation of side products. Notably, these types of solvents are not compatible with standard electrochemical hydrogenation architectures where electrolysis and hydrogenation occur in the same reaction chamber. This work highlights the utility of the ePMR for selective furfural hydrogenation without H-2 gas, and presents a possible pathway for helping to decarbonize the hydrogenation industry.
引用
收藏
页码:215 / 224
页数:10
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