TY - JOUR
T1 - Blue LED light-driven photoelectrocatalytic removal of naproxen from water
T2 - Kinetics and primary by-products
AU - Changanaqui, Katherina
AU - Alarcón, Hugo
AU - Brillas, Enric
AU - Sirés, Ignasi
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/6/15
Y1 - 2020/6/15
N2 - Here, we demonstrate the viability of a ZnO/TiO2/Ag2Se thin-film composite synthesized on FTO to degrade the drug naproxen in aqueous solutions by visible-light photoelectrocatalysis (PEC). The experiments were made with 100 mL of solutions containing 5 mg L−1 drug and 50 mM Na2SO4 at natural pH, using a cell equipped with a Pt wire as cathode and the composite as photoanode exposed to a 36 W blue LED lamp. Total degradation was achieved after 210 min of electrolysis at anodic potential of +1.0 V/Ag|AgCl. This resulted from the oxidative action of hydroxyl radicals formed via direct anodic water discharge and through mediated water oxidation by photogenerated holes. The degradation rate decreased at higher naproxen concentration, but the treatment efficiency became higher due the deceleration of the parasitic reactions involving hydroxyl radicals. In chloride medium, the photoanode showed a large ability to produce active chlorine, which contributed to the oxidation of the target molecule. LC-QToF-MS analysis of treated solutions revealed the generation of four primary naphthalenic by-products, from which the initial degradation route of naproxen is proposed.
AB - Here, we demonstrate the viability of a ZnO/TiO2/Ag2Se thin-film composite synthesized on FTO to degrade the drug naproxen in aqueous solutions by visible-light photoelectrocatalysis (PEC). The experiments were made with 100 mL of solutions containing 5 mg L−1 drug and 50 mM Na2SO4 at natural pH, using a cell equipped with a Pt wire as cathode and the composite as photoanode exposed to a 36 W blue LED lamp. Total degradation was achieved after 210 min of electrolysis at anodic potential of +1.0 V/Ag|AgCl. This resulted from the oxidative action of hydroxyl radicals formed via direct anodic water discharge and through mediated water oxidation by photogenerated holes. The degradation rate decreased at higher naproxen concentration, but the treatment efficiency became higher due the deceleration of the parasitic reactions involving hydroxyl radicals. In chloride medium, the photoanode showed a large ability to produce active chlorine, which contributed to the oxidation of the target molecule. LC-QToF-MS analysis of treated solutions revealed the generation of four primary naphthalenic by-products, from which the initial degradation route of naproxen is proposed.
KW - Blue LED light
KW - Oxidation by-products
KW - Pharmaceutical residue
KW - Photoelectrocatalysis
KW - Water treatment
UR - http://www.scopus.com/inward/record.url?scp=85084174741&partnerID=8YFLogxK
U2 - 10.1016/j.jelechem.2020.114192
DO - 10.1016/j.jelechem.2020.114192
M3 - Artículo (Contribución a Revista)
AN - SCOPUS:85084174741
SN - 1572-6657
VL - 867
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
M1 - 114192
ER -