The
electrochemical hydrogenation and hydrogenolysis (ECH) of furfural
(FF) on a copper electrocatalyst has been investigated to produce
biofuels and fine chemicals in an H-type batch reactor at room temperature.
We report a systematic study of ECH of FF to gain a better understanding
of the relationships between products and reaction conditions: current
density, electrolyte, and cosolvent ratio in acidic solutions. The
acidity of electrolytes had the most significant impact on the product
distribution. Mildly acidic electrolytes mainly produced furfuryl
alcohol (FA), while strongly acidic electrolytes produced both 2-methyl
furan (MF) and FA. Also, the yield of products depended on the current
density and reaction time when equivalent charge was transferred to
the reaction. However, the mole balance accounting for FF, MF, and
FA was not higher than 70% in any reaction condition when the theoretical
amount of electrons for complete MF production from FF (e–/FF = 4) was transferred to the system. The investigation of nonelectrochemical
homogeneous side reactions suggested that the low mole balance in
a mildly acidic electrolyte may be from the charge transfer promoted
side reactions on the copper electrode. On the other hand, it was
shown that the low mole balance in strongly acidic electrolytes was
due to homogeneous side reactions.