TY - JOUR
T1 - Simultaneously converting carbonate/bicarbonate and biomass to value-added carboxylic acid salts by aqueous-phase hydrogen transfer
AU - Su, Ji
AU - Yang, Lisha
AU - Yang, Xiaokun
AU - Lu, Mi
AU - Luo, Bing
AU - Lin, Hongfei
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2015/1/5
Y1 - 2015/1/5
N2 - A novel approach to coproduce value-added carboxylic acids has been developed via a 'one-pot' aqueous-phase hydrogen transfer (APHT) process, in which hydrogen in biomass molecules is transferred to carbonate/bicarbonate ions over supported noble metal nanocatalysts. In mild hydrothermal media, a variety of biomass derived alcohols or polyols have been efficiently converted to carboxylic acids, while simultaneously, formates have been obtained from the reduction of carbonates/bicarbonate salts without using external H2. In an APHT process at the optimized reaction conditions, a high yield of lactate, ∼55%, was achieved using glycerol as the hydrogen donor, and simultaneously, ∼30% of formate was produced by the reduction of sodium bicarbonates over the Pd on a carbon catalyst. The catalyst was stable after three-time consecutive reuse without regeneration, and the possible APHT reaction mechanism was proposed.
AB - A novel approach to coproduce value-added carboxylic acids has been developed via a 'one-pot' aqueous-phase hydrogen transfer (APHT) process, in which hydrogen in biomass molecules is transferred to carbonate/bicarbonate ions over supported noble metal nanocatalysts. In mild hydrothermal media, a variety of biomass derived alcohols or polyols have been efficiently converted to carboxylic acids, while simultaneously, formates have been obtained from the reduction of carbonates/bicarbonate salts without using external H2. In an APHT process at the optimized reaction conditions, a high yield of lactate, ∼55%, was achieved using glycerol as the hydrogen donor, and simultaneously, ∼30% of formate was produced by the reduction of sodium bicarbonates over the Pd on a carbon catalyst. The catalyst was stable after three-time consecutive reuse without regeneration, and the possible APHT reaction mechanism was proposed.
KW - Aqueous-phase hydrogen transfer
KW - bicarbonate hydrogenation
KW - biomass dehydrogenation
KW - carboxylic acids
KW - palladium catalyst
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U2 - 10.1021/sc5007158
DO - 10.1021/sc5007158
M3 - Article
AN - SCOPUS:84920281062
SN - 2168-0485
VL - 3
SP - 195
EP - 203
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 1
ER -