Kinetics of the Homogeneous and Heterogeneous Coupling of Furfural with Biomass-Derived Alcohols

被引:3
|
作者
Goulas, Konstantinos A. [1 ,2 ]
Gokhale, Amit A. [1 ,3 ]
机构
[1] Univ Calif Berkeley, Energy Biosci Inst, Berkeley, CA 94720 USA
[2] Univ Delaware, Catalysis Ctr Energy Innovat, Newark, DE 19711 USA
[3] BASF Corp, Iselin, NJ 08830 USA
关键词
aldol reaction; biomass; isotope effects; dehydrogenation; kinetics; CATALYTIC TRANSFER HYDROGENATION; CONTROLLED RADICAL POLYMERIZATION; PONNDORF-VERLEY REDUCTION; FUEL RANGE CYCLOALKANES; HIGH-QUALITY DIESEL; MIXED OXIDES; CONDENSATION; HYDRODEOXYGENATION; HYDROTALCITE; KETONES;
D O I
10.1002/cctc.201701866
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
The tandem dehydrogenation and aldol condensation of butanol with furfural was investigated over homogeneous and heterogeneous catalysts using kinetics and isotope effects. In the homogeneous system, Ni(dppe)Cl-2 catalyzes the transfer dehydrogenation of butanol to the furfural, whereas the aldol condensation of butyraldehyde and furfural takes place over the basic K2CO3 cocatalyst. In the heterogeneous system, a transition-metal-free mixed Mg-Al oxide, both the transfer hydrogenation and aldol condensation take place over the basic sites of the catalyst, and the rate-determining step is the alpha-hydride transfer from the butanol to the furfural.
引用
收藏
页码:2387 / 2393
页数:7
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