Efficient Oxidative Debromination of Decabromodiphenyl Ether by TiO2-Mediated Photocatalysis in Aqueous Environment

Huang, A; Wang, Nan; Lei, M; Zhu, L; Zhang, Y; Lin, Z; Yin, D; Tang, H

HERO ID

1590696

Reference Type

Journal Article

Year

2013

Language

English

PMID

23199337

HERO ID 1590696
In Press No
Year 2013
Title Efficient Oxidative Debromination of Decabromodiphenyl Ether by TiO2-Mediated Photocatalysis in Aqueous Environment
Authors Huang, A; Wang, Nan; Lei, M; Zhu, L; Zhang, Y; Lin, Z; Yin, D; Tang, H
Journal Environmental Science & Technology
Volume 47
Issue 1
Page Numbers 518-525
Abstract Direct evidence was first demonstrated for the oxidative degradation of decabromodiphenyl ether (BDE209) in aqueous TiO(2) dispersions under UV irradiation (λ > 340 nm). BDE209 was hardly debrominated over TiO(2) in UV-irradiated acetonitrile dispersions, but the addition of water into the dispersions greatly enhanced its photocatalytic oxidative debromination. The debromination efficiency of BDE209 as high as 95.6% was achieved in aqueous TiO(2) dispersions after 12 h of UV irradiation. The photocatalytic oxidation of BDE209 resulted in generation of aromatic ring-opening intermediates such as brominated dienoic acids, which were further degraded by prolonging UV irradiation time. The photocatalytic oxidative debromination of BDE209 was further confirmed by the observation that the BDE209 degradation in water-acetonitrile mixtures with different water contents was positively correlated with the formation of •OH radicals, but not photogenerated electrons. The use of water not only avoided the scavenging of reactive radicals by organic solvent but also enhanced the adsorption of BDE209 on the surface of TiO(2), both of which favor the contact of BDE209 with photogenerated holes and •OH species. The confirmation of efficient oxidative degradation and debromination of BDE209 is very important for finding new ways to remove polybrominated diphenyl ethers from the environment.
Doi 10.1021/es302935e
Pmid 23199337
Wosid WOS:000313220300066
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000313220300066
Is Public Yes
Language Text English