TY - JOUR
T1 - Bromine Radical (Br•and Br2•-) Reactivity with Dissolved Organic Matter and Brominated Organic Byproduct Formation
AU - Lei, Yu
AU - Lei, Xin
AU - Westerhoff, Paul
AU - Tong, Xingyu
AU - Ren, Jianing
AU - Zhou, Yangjian
AU - Cheng, Shuangshuang
AU - Ouyang, Gangfeng
AU - Yang, Xin
N1 - Funding Information:
The authors would like to acknowledge the financial support from the National Natural Science Foundation of China (21876210 and 22176225), the National Science Foundation of the United States (CBET-1804229), and the China Postdoctoral Science Foundation (2020M683055). Laurel Passantino provided technical editing.
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/4/19
Y1 - 2022/4/19
N2 - Dissolved organic matter (DOM) is a major scavenger of bromine radicals (e.g., Br•and Br2•-) in sunlit surface waters and during oxidative processes used in water treatment. However, the literature lacks quantitative measurements of reaction rate constants between bromine radicals and DOM and lacks information on the extent to which these reactions form brominated organic byproducts. Based on transient kinetic analysis with different fractions and sources of DOM, we determined reaction rate constants for DOM with Br•ranging from <5.0 × 107to (4.2 ± 1.3) × 108MC-1s-1, which are comparable with those of HO•but higher than those with Br2•-(k = (9.0 ± 2.0) × 104to (12.4 ± 2.1) × 105MC-1s-1). Br•and Br2•-attack the aromatic and antioxidant moieties of DOM via the electron transfer mechanism, resulting in Br-release with minimal substitution of bromine into DOM. For example, the total organic bromine was less than 0.25 μM (as Br) at environmentally relevant bromine radicals' exposures of ∼10-9M·s. The results give robust evidence that the scavenging of bromine radicals by DOM is a crucial step to prevent inorganic bromine radical chemistry from producing free bromine (HOBr/OBr-) and subsequent brominated byproducts.
AB - Dissolved organic matter (DOM) is a major scavenger of bromine radicals (e.g., Br•and Br2•-) in sunlit surface waters and during oxidative processes used in water treatment. However, the literature lacks quantitative measurements of reaction rate constants between bromine radicals and DOM and lacks information on the extent to which these reactions form brominated organic byproducts. Based on transient kinetic analysis with different fractions and sources of DOM, we determined reaction rate constants for DOM with Br•ranging from <5.0 × 107to (4.2 ± 1.3) × 108MC-1s-1, which are comparable with those of HO•but higher than those with Br2•-(k = (9.0 ± 2.0) × 104to (12.4 ± 2.1) × 105MC-1s-1). Br•and Br2•-attack the aromatic and antioxidant moieties of DOM via the electron transfer mechanism, resulting in Br-release with minimal substitution of bromine into DOM. For example, the total organic bromine was less than 0.25 μM (as Br) at environmentally relevant bromine radicals' exposures of ∼10-9M·s. The results give robust evidence that the scavenging of bromine radicals by DOM is a crucial step to prevent inorganic bromine radical chemistry from producing free bromine (HOBr/OBr-) and subsequent brominated byproducts.
KW - advanced oxidation processes (AOPs)
KW - bromine radicals
KW - dissolved organic matter (DOM)
KW - halogenated byproducts
KW - kinetics
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U2 - 10.1021/acs.est.2c00549
DO - 10.1021/acs.est.2c00549
M3 - Article
C2 - 35349263
AN - SCOPUS:85127833510
SN - 0013-936X
VL - 56
SP - 5189
EP - 5199
JO - Environmental Science & Technology
JF - Environmental Science & Technology
IS - 8
ER -