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Synergistic combination of bandgap-modified carbon nitride and WO3 for visible light-induced oxidation of arsenite accelerated by in-situ Fenton reaction SCIE SCOPUS

Title
Synergistic combination of bandgap-modified carbon nitride and WO3 for visible light-induced oxidation of arsenite accelerated by in-situ Fenton reaction
Authors
Moon, Gun-heeKim, SujeongCho, Young-JinLim, JonghunKim, Dong-hyoChoi, Wonyong
Date Issued
2017-12
Publisher
ELSEVIER SCIENCE BV
Abstract
Photocatalytic oxidation of arsenite (As(III)) to arsenate (As(V)) using non-toxic semiconductor materials has been considered as an environmentally-benign pretreatment process of arsenic contaminated waters, but poor visible light activity hinders the practical applications utilizing solar light. In this study, we designed a ternary photocatalytic system consisting of modified carbon nitride (mCN), WO3, and Fe3+ for efficient oxidation of As(III) which was done by using in-situ generated H2O2 as a Fenton reagent under visible light (lambda > 420 nm). While superoxide anion and H2O2 were effectively produced via the reduction of dissolved O-2 by mCN, WO3 regenerated Fe2+ from Fe3+, which activated in-situ generated H2O2 for Fenton process. The overall photocatalytic oxidation activity of As(III) was optimized at a specific mixing ratio of catalysts (mCN:WO3 = 60:40) where there is an optimal balance between the conduction band electron transfer to dissolved O-2 (to produce H2O2 on mCN) and the competing electron transfer to Fe3+ (to regenerate Fe2+ on WO3). The ternary combination enabled the simultaneous participation of superoxide anions, hydroxyl radicals, and holes to complete the oxidation of 500 mu M As(III) within 90 min with 1.0 g/L catalyst and 70 mu M Fe3+ and that of 10 mu M As(III) within 60 min with a tenth amount of catalyst (0.1 g/L) and Fe3+ (7 mu M) under visible light without requiring noble metal catalysts and chemical additives. The process consists of earth abundant elements only (C, N, O, W, and Fe) and operates with utilizing visible light photons and dissolved O-2 only, which is eco-friendly and cost effective. (C) 2017 Elsevier B.V. All rights reserved.
Keywords
PHOTOCATALYTIC OXIDATION; HYDROGEN-PEROXIDE; TIO2; MECHANISM; REMOVAL; WATER; ELECTRON; AS(III); OXYGEN; H2O2
URI
https://oasis.postech.ac.kr/handle/2014.oak/50766
DOI
10.1016/j.apcatb.2017.07.021
ISSN
0926-3373
Article Type
Article
Citation
APPLIED CATALYSIS B-ENVIRONMENTAL, vol. 218, page. 819 - 824, 2017-12
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최원용CHOI, WONYONG
Div of Environmental Science & Enginrg
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