TY - JOUR
T1 - Photoelectrocatalytic oxidation of phenol by UV-assisted electrogenerated Ce(IV) in aqueous solution
AU - Liu, Yi Hung
AU - Huang, Wei Jin
AU - Wang, Chih Ta
N1 - Publisher Copyright:
© 2019 Taiwan Institute of Chemical Engineers
PY - 2019/9
Y1 - 2019/9
N2 - A UV (UV-C, 254 nm)-assisted Ce(IV) mediated electrochemical oxidation (MEO) system is developed to treat phenol-containing water. For comparison, an individual Ce(IV)-MEO system without UV and a UV photocatalytic oxidation system without applying an electrical current are also evaluated. The operation conditions of electrical current, nitric acid concentration, stirring speed, and electrode area ratio of anode to cathode for Ce(IV) electrogeneration are optimized in terms of percent yield of Ce(IV) and energy consumption. According to the kinetic model of the Ce(IV)/Ce(III) redox reaction, the forward rate constant of Ce(III) oxidation is twice as high as that of the reverse reaction. For the wastewater treatment, Ce(IV)-MEO and photocatalytic oxidation systems both show good capability for degrading phenol in an acidic environment rather than the direct electrochemical oxidation (DEO) system. Importantly, the UV-assisted MEO system exhibits excellent removal efficiency (RE) of phenol (up to 98%) in only 40 min because of the synergistic effect of the electrocatalytic and photocatalytic systems, which individually exhibit REs of <80%. Moreover, phenol degradation in the photoelectrocatalytic oxidation system follows pseudo-first order kinetics with a rate constant of 0.083 min−1.
AB - A UV (UV-C, 254 nm)-assisted Ce(IV) mediated electrochemical oxidation (MEO) system is developed to treat phenol-containing water. For comparison, an individual Ce(IV)-MEO system without UV and a UV photocatalytic oxidation system without applying an electrical current are also evaluated. The operation conditions of electrical current, nitric acid concentration, stirring speed, and electrode area ratio of anode to cathode for Ce(IV) electrogeneration are optimized in terms of percent yield of Ce(IV) and energy consumption. According to the kinetic model of the Ce(IV)/Ce(III) redox reaction, the forward rate constant of Ce(III) oxidation is twice as high as that of the reverse reaction. For the wastewater treatment, Ce(IV)-MEO and photocatalytic oxidation systems both show good capability for degrading phenol in an acidic environment rather than the direct electrochemical oxidation (DEO) system. Importantly, the UV-assisted MEO system exhibits excellent removal efficiency (RE) of phenol (up to 98%) in only 40 min because of the synergistic effect of the electrocatalytic and photocatalytic systems, which individually exhibit REs of <80%. Moreover, phenol degradation in the photoelectrocatalytic oxidation system follows pseudo-first order kinetics with a rate constant of 0.083 min−1.
KW - Cerium
KW - Degradation
KW - Mediated electrochemical oxidation
KW - Phenol
KW - Photoelectrocatalysis
KW - Wastewater treatment
UR - http://www.scopus.com/inward/record.url?scp=85067899341&partnerID=8YFLogxK
U2 - 10.1016/j.jtice.2019.06.003
DO - 10.1016/j.jtice.2019.06.003
M3 - 期刊論文
AN - SCOPUS:85067899341
SN - 1876-1070
VL - 102
SP - 218
EP - 224
JO - Journal of the Taiwan Institute of Chemical Engineers
JF - Journal of the Taiwan Institute of Chemical Engineers
ER -