TY - JOUR
T1 - In Situ-Generated Reactive Oxygen Species in Precharged Titania and Tungsten Trioxide Composite Catalyst Membrane Filters
T2 - Application to As(III) Oxidation in the Absence of Irradiation
AU - Park, Jiyeon
AU - Lim, Jonghun
AU - Park, Yiseul
AU - Han, Dong Suk
AU - Shon, Ho Kyong
AU - Hoffmann, Michael R.
AU - Park, Hyunwoong
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/8/4
Y1 - 2020/8/4
N2 - This study demonstrates that in situ-generated reactive oxygen species (ROSs) in prephotocharged TiO2 and WO3 (TW) composite particle-embedded inorganic membrane filters oxidize arsenite (As(III)) into arsenate (As(V)) without any auxiliary chemical oxidants under ambient conditions in the dark. TW membrane filters have been charged with UV or simulated sunlight and subsequently transferred to a once-through flow-type system. The charged TW filters can transfer the stored electrons to dissolved O2, producing ROSs that mediate As(III) oxidation in the dark. Dramatic inhibition of As(V) production with O2 removal or addition of ROS quenchers indicates an ROS-mediated As(III) oxidation mechanism. Electron paramagnetic spectroscopic analysis has confirmed the formation of the HO2â¢/O2â¢- pair in the dark. The WO3 fraction in the TW filter significantly influences the performance of the As(III) oxidation, while As(V) production is enhanced with increasing charging time and solution pH. The As(III) oxidation is terminated when the singly charged TW filter is fully discharged; however, recharging of TW recovers the catalytic activity for As(III) oxidation. The proposed oxidation process using charged TW membrane filters is practical and environmentally benign for the continuous treatment of As(III)-contaminated water during periods of unavailability of sunlight.
AB - This study demonstrates that in situ-generated reactive oxygen species (ROSs) in prephotocharged TiO2 and WO3 (TW) composite particle-embedded inorganic membrane filters oxidize arsenite (As(III)) into arsenate (As(V)) without any auxiliary chemical oxidants under ambient conditions in the dark. TW membrane filters have been charged with UV or simulated sunlight and subsequently transferred to a once-through flow-type system. The charged TW filters can transfer the stored electrons to dissolved O2, producing ROSs that mediate As(III) oxidation in the dark. Dramatic inhibition of As(V) production with O2 removal or addition of ROS quenchers indicates an ROS-mediated As(III) oxidation mechanism. Electron paramagnetic spectroscopic analysis has confirmed the formation of the HO2â¢/O2â¢- pair in the dark. The WO3 fraction in the TW filter significantly influences the performance of the As(III) oxidation, while As(V) production is enhanced with increasing charging time and solution pH. The As(III) oxidation is terminated when the singly charged TW filter is fully discharged; however, recharging of TW recovers the catalytic activity for As(III) oxidation. The proposed oxidation process using charged TW membrane filters is practical and environmentally benign for the continuous treatment of As(III)-contaminated water during periods of unavailability of sunlight.
UR - http://www.scopus.com/inward/record.url?scp=85088981224&partnerID=8YFLogxK
U2 - 10.1021/acs.est.0c01550
DO - 10.1021/acs.est.0c01550
M3 - Article
C2 - 32543843
AN - SCOPUS:85088981224
SN - 0013-936X
VL - 54
SP - 9601
EP - 9608
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 15
ER -