Heterogeneous Catalytic Transfer Hydrogenation as an Effective Pathway in Biomass Upgrading

被引:703
作者
Gilkey, Matthew J. [1 ]
Xu, Bingjun [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Catalysis Ctr Energy Innovat, Newark, DE 19716 USA
关键词
catalytic transfer hydrogenation; hydrogen donor; hydride transfer; hydrodeoxygenation; biomass; lignocellulose; PONNDORF-VERLEY REDUCTION; LEWIS-ACID ZEOLITES; PHASE GLYCEROL HYDROGENOLYSIS; SN-BETA ZEOLITE; GAMMA-VALEROLACTONE; FORMIC-ACID; LEVULINIC ACID; GLUCOSE ISOMERIZATION; REACTION-MECHANISM; PROPYLENE-GLYCOL;
D O I
10.1021/acscatal.5b02171
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
Reducing oxygen content in biomass-derived feedstocks via hydrodeoxygenation (HDO) is a key step in their upgrading to fuels and valuable chemicals. Organic molecules, e.g., alcohols and formic acid, can donate hydrogen to reduce the substrate in a process called catalytic transfer hydrogenation (CTH). Although it is practiced far less frequently than molecular hydrogen-based HDO processes, CTH has been proven to be an efficient and selective strategy in biomass upgrading in the last two decades. In this paper, we present a selective review of recent progress made in the upgrade of biomass-derived feedstocks through heterogeneous CTH, with a focus on the mechanistic interpretation. Hydrogenation and cleavage of C=O and C-O bonds, respectively, are the two main categories of reactions discussed, owing to their importance in the HDO of biomass-derived feedstocks. On acid base catalysts, Lewis acid base pair sites, rather than a single acid or base site, mediate hydrogenation of carbonyl groups with alcohols as the hydrogen donor. While acid base catalysts typically only catalyze the hydrogenation of carbonyl groups with alcohols as the hydrogen donor, metal-based catalysts are able to mediate both hydrogenation and hydrogenolysis reactions with either alcohols or formic acid. Several model reactions involving platform chemicals in biomass upgrading, e.g., 5-hydroxymethylfurfural, levulinic acid, and glycerol, are used in the discussion to illustrate general trends. Because alcohols are typically both the hydrogen donor and the solvent, the donor and solvent effects are intertwined. Therefore, solvent effects are discussed primarily in the context of sugar isomerization and reactions with formic acid as the hydrogen donor, in which the solvent and hydrogen donor are two separate species. Current challenges and opportunities of future research to develop CTH into a competitive and complementary strategy of the conventional molecular-hydrogen-based processes are also discussed.
引用
收藏
页码:1420 / 1436
页数:17
相关论文
共 146 条
[1]   Analysis of Kinetics and Reaction Pathways in the Aqueous-Phase Hydrogenation of Levulinic Acid To Form γ-Valerolactone over Ru/C [J].
Abdelrahman, Omar Ali ;
Heyden, Andreas ;
Bond, Jesse Q. .
ACS CATALYSIS, 2014, 4 (04) :1171-1181
[2]   Solvent-free γ-valerolactone hydrogenation to 2-methyltetrahydrofuran catalysed by Ru/C: a reaction network analysis [J].
Al-Shaal, Mohammad G. ;
Dzierbinski, Adam ;
Palkovits, Regina .
GREEN CHEMISTRY, 2014, 16 (03) :1358-1364
[3]   Pd/C catalyzed conversion of levulinic acid to γ-valerolactone using alcohol as a hydrogen donor under microwave conditions [J].
Amarasekara, Ananda S. ;
Hasan, Muhammad A. .
CATALYSIS COMMUNICATIONS, 2015, 60 :5-7
[4]   One-pot conversion of furfural to useful bio-products in the presence of a Sn,Al-containing zeolite beta catalyst prepared via post-synthesis routes [J].
Antunes, Margarida M. ;
Lima, Sergio ;
Neves, Patricia ;
Magalhaes, Ana L. ;
Fazio, Enza ;
Fernandes, Auguste ;
Neri, Fortunato ;
Silva, Carlos M. ;
Rocha, Silvia M. ;
Eiro, Maria F. Rib ;
Pillinger, Martyn ;
Urakawa, Atsushi ;
Valente, Anabela A. .
JOURNAL OF CATALYSIS, 2015, 329 :522-537
[5]   Catalytic hydrogen transfer from 2-propanol to cyclohexanone over basic Mg-Al oxides [J].
Aramendía, MA ;
Borau, V ;
Jiménez, U ;
Marinas, JA ;
Ruiz, JR ;
Urbano, FJ .
APPLIED CATALYSIS A-GENERAL, 2003, 255 (02) :301-308
[6]   Liquid-phase heterogeneous catalytic transfer hydrogenation of citral on basic catalysts [J].
Aramendía, MA ;
Borau, V ;
Jiménez, C ;
Marinas, JM ;
Ruiz, JR ;
Urbano, FJ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2001, 171 (1-2) :153-158
[7]   Activity of basic catalysts in the Meerwein-Ponndorf-Verley reaction of benzaldehyde with ethanol [J].
Aramendía, MA ;
Borau, V ;
Jiménez, C ;
Marinas, JM ;
Ruiz, JR ;
Urbano, FJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 238 (02) :385-389
[8]   Theoretical Study of 1,2-Hydride Shift Associated with the Isomerization of Glyceraldehyde to Dihydroxy Acetone by Lewis Acid Active Site Models [J].
Assary, Rajeev S. ;
Curtiss, Larry A. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2011, 115 (31) :8754-8760
[9]   On the role of the atmosphere in the catalytic glycerol transformation over iridium-based catalysts [J].
Auneau, Florian ;
Noel, Sebastien ;
Aubert, Guillaume ;
Besson, Michele ;
Djakovitch, Laurent ;
Pinel, Catherine .
CATALYSIS COMMUNICATIONS, 2011, 16 (01) :144-149
[10]   Aqueous phase hydrogenolysis of glycerol to bio-propylene glycol over Pt-Sn catalysts [J].
Barbelli, Maria L. ;
Santori, Gerardo F. ;
Nichio, Nora N. .
BIORESOURCE TECHNOLOGY, 2012, 111 :500-503