TY - JOUR
T1 - Oxidative Conversion of Glucose to Formic Acid as a Renewable Hydrogen Source Using an Abundant Solid Base Catalyst
AU - Takagaki, Atsushi
AU - Obata, Wataru
AU - Ishihara, Tatsumi
N1 - Funding Information:
This work was supported by a Grand‐in‐Aid for Science Research (B) (No. 18H01785) of JSPS, Japan.
Publisher Copyright:
© 2021 The Authors. Published by Wiley-VCH GmbH
PY - 2021/10
Y1 - 2021/10
N2 - Formic acid is one of the most desirable liquid hydrogen carriers. The selective production of formic acid from monosaccharides in water under mild reaction conditions using solid catalysts was investigated. Calcium oxide, an abundant solid base catalyst available from seashell or limestone by thermal decomposition, was found to be the most active of the simple oxides tested, with formic acid yields of 50 % and 66 % from glucose and xylose, respectively, in 1.4 % H2O2 aqueous solution at 343 K for 30 min. The main reaction pathway is a sequential formation of formic acid from glucose by C−C bond cleavage involving aldehyde groups in the acyclic form. The reaction also involves base-catalyzed aldose-ketose isomerization and retroaldol reaction, resulting in the formation of fructose and trioses including glyceraldehyde and dihydroxyacetone. These intermediates were further decomposed into formic acid or glycolic acid. The catalytic activity remained unchanged for further reuse by a simple post-calcination.
AB - Formic acid is one of the most desirable liquid hydrogen carriers. The selective production of formic acid from monosaccharides in water under mild reaction conditions using solid catalysts was investigated. Calcium oxide, an abundant solid base catalyst available from seashell or limestone by thermal decomposition, was found to be the most active of the simple oxides tested, with formic acid yields of 50 % and 66 % from glucose and xylose, respectively, in 1.4 % H2O2 aqueous solution at 343 K for 30 min. The main reaction pathway is a sequential formation of formic acid from glucose by C−C bond cleavage involving aldehyde groups in the acyclic form. The reaction also involves base-catalyzed aldose-ketose isomerization and retroaldol reaction, resulting in the formation of fructose and trioses including glyceraldehyde and dihydroxyacetone. These intermediates were further decomposed into formic acid or glycolic acid. The catalytic activity remained unchanged for further reuse by a simple post-calcination.
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U2 - 10.1002/open.202100074
DO - 10.1002/open.202100074
M3 - Article
C2 - 34236148
AN - SCOPUS:85109383257
SN - 2191-1363
VL - 10
SP - 954
EP - 959
JO - ChemistryOpen
JF - ChemistryOpen
IS - 10
ER -