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Coupling Glucose Dehydrogenation with CO 2 Hydrogenation by Hydrogen Transfer in Aqueous Media at Room Temperature
Author(s) -
Ding Guodong,
Su Ji,
Zhang Cheng,
Tang Kan,
Yang Lisha,
Lin Hongfei
Publication year - 2018
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201800570
Subject(s) - dehydrogenation , formate , ammonium formate , chemistry , catalysis , transfer hydrogenation , yield (engineering) , aqueous solution , inorganic chemistry , hydrogen , sodium formate , photochemistry , organic chemistry , formic acid , materials science , ruthenium , metallurgy
Conversion of CO 2 into value‐added chemicals and fuels provides a direct solution to reduce excessive CO 2 in the atmosphere. Herein, a novel catalytic reaction system is presented by coupling the dehydrogenation of glucose with the hydrogenation of a CO 2 ‐derived salt, ammonium carbonate, in an ethanol–water mixture. For the first time, the hydrogenation of CO 2 to formate by glucose has been achieved under ambient conditions. Under the optimal reaction conditions, the highest yield of formate reached approximately 46 %. We find that the apparent pH value in the ethanol–water mixture plays a central role in determining the performance of the hydrogen‐transfer reaction. Based on the 13 C NMR and ESI–MS results, a possible pathway of the coupled glucose dehydrogenation and CO 2 hydrogenation reactions was proposed.

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