Formation of halonitromethanes from benzylamine during UV/chlorination: Impact factors, toxicity alteration, and pathways

被引:1
作者
Xue, Qi [1 ]
Deng, Lin [1 ]
Tang, Qian [1 ]
Wang, Tao [1 ]
Luo, Wei [1 ]
机构
[1] Southeast Univ, Dept Municipal Engn, Nanjing 211189, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Halonitromethanes; UV/chlorination; Benzylamine; Impact factors; Toxicity alteration; Formation pathways; DISINFECTION-BY-PRODUCTS; FREE-RADICAL CHEMISTRY; CHLORINE TREATMENT; RATE CONSTANTS; DBPS FORMATION; UV TREATMENT; AMINO-ACIDS; WATER; DEGRADATION; MECHANISMS;
D O I
10.1007/s11356-024-32132-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Halonitromethanes (HNMs), a representative nitrogen-containing disinfection byproduct, have gained significant concerns due to their higher cytotoxicity and genotoxicity. UV/chlorination is considered a promising alternative disinfection technology for chlorination. This study aimed to investigate the HNMs formation from benzylamine (BZA) during UV/chlorination. The experimental results revealed that the yields of HNMs initially raised to a peak then dropped over time. Higher chlorine dosage and BZA concentration promoted the formation of HNMs, whereas alkaline pH inhibited their formation. The presence of bromine ion (Br-) not only converted chlorinated-HNMs (Cl-HNMs) to brominated (chlorinated)-HNMs Br (Cl)-HNMs) and brominated-HNMs (Br-HNMs) but also enhanced the total concentration of HNMs. Besides, the calculated cytotoxicity index (CTI) and genotoxicity index (GTI) of HNMs were elevated by 68.97% and 60.66% as Br- concentration raised from 2 to 6 mu M. The possible formation pathways of HNMs from BZA were proposed based on the intermediates identified by a gas chromatography/mass spectrometry (GC/MS). In addition, the formation rules of HNMs in actual water verified the results in deionized water during UV/chlorination. The results of this study provide basic data and a theoretical basis for the formation and control of HNMs, which is conducive to applying UV/chlorination.
引用
收藏
页码:16667 / 16684
页数:18
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