Effects of Combined UV and Chlorine Treatment on the Formation of Trichloronitromethane from Amine Precursors

被引:99
作者
Deng, Lin [1 ,2 ]
Huang, Ching-Hua [2 ]
Wang, Yung-Li [2 ]
机构
[1] Southeast Univ, Dept Municipal Engn, Nanjing 210096, Jiangsu, Peoples R China
[2] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
关键词
DISINFECTION BY-PRODUCTS; N-NITROSODIMETHYLAMINE; AQUEOUS CHLORINE; DRINKING-WATER; ULTRAVIOLET WAVELENGTHS; CHLOROPICRIN FORMATION; ADVANCED OXIDATION; REACTION-KINETICS; NITROGEN ORIGINS; ORGANIC NITROGEN;
D O I
10.1021/es404116n
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The objective of this study was to investigate the effects of combined low-pressure ultraviolet (LPUV) irradiation and free chlorination on the formation of trichloronitromethane (TCNM) byproduct from amine precursors, including a commonly used polyamine coagulant aid (poly(epichlorohydrin dimethylamine)) and simple alkylamines dimethylamine (DMA) and methylamine (MA). Results showed that TCNM formation can increase up to 15 fold by combined UV/chlorine under disinfection to advanced oxidation conditions. The enhancement effect is influenced by UV irradiance, chlorine dose, and water pH. Extended reaction time leads to the decay of TCNM by direct photolysis. The combined UV/chlorine conditions significantly promoted degradation of polyamine to generate intermediates, including DMA and MA, which are better TCNM precursors than polyamine, and also facilitated transformation of these amine precursors to TCNM. Under combined UV/chlorine, polyamine degradation was likely promoted by radical oxidation, photodecay of chlorinated polyamine, and chlorine oxidation/substitution. Promoted TCNM formation from primary amine MA was primarily due to radicals' involvement. Promoted TCNM formation from secondary amine DMA likely involved a combination of radical oxidation, photoenhanced chlorination reactions, and other unknown mechanisms. Insights obtained in this study are useful for reducing TCNM formation during water treatment when both UV and chlorine will be encountered.
引用
收藏
页码:2697 / 2705
页数:9
相关论文
共 51 条
[1]   Kinetic study of the reactions of chlorine atoms and Cl2•- radical anions in aqueous solutions.: 1.: Reaction with benzene [J].
Alegre, ML ;
Geronés, M ;
Rosso, JA ;
Bertolotti, SG ;
Braun, AM ;
Mártire, DO ;
Gonzalez, MC .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (14) :3117-3125
[2]   Precursors of nitrogenous disinfection by-products in drinking water-A critical review and analysis [J].
Bond, Tom ;
Templeton, Michael R. ;
Graham, Nigel .
JOURNAL OF HAZARDOUS MATERIALS, 2012, 235 :1-16
[3]   Occurrence and control of nitrogenous disinfection by-products in drinking water - A review [J].
Bond, Tom ;
Huang, Jin ;
Templeton, Michael R. ;
Graham, Nigel .
WATER RESEARCH, 2011, 45 (15) :4341-4354
[4]   RADIATION-CHEMISTRY AND PHOTOCHEMISTRY OF OXYCHLORINE IONS .2. PHOTODECOMPOSITION OF AQUEOUS-SOLUTIONS OF HYPOCHLORITE IONS [J].
BUXTON, GV ;
SUBHANI, MS .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1972, 68 :958-&
[5]   Free radical chemistry of disinfection byproducts. 2. Rate constants and degradation mechanisms of trichloronitromethane (chloropicrin) [J].
Cole, S. Kirkham ;
Cooper, William J. ;
Fox, Robert V. ;
Gardinali, Piero R. ;
Mezyk, Stephen P. ;
Mincher, Bruce J. ;
O'Shea, Kevin E. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (03) :863-869
[6]   Interactions of fluoroquinolone antibacterial agents with aqueous chlorine: Reaction kinetics, mechanisms, and transformation pathways [J].
Dodd, MC ;
Shah, AD ;
Von Gunten, U ;
Huang, CH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (18) :7065-7076
[7]   UV disinfection implementation status in US water treatment plants [J].
Dotson, Aaron O. ;
Rodriguez, Caitlin E. ;
Linden, Karl G. .
JOURNAL AMERICAN WATER WORKS ASSOCIATION, 2012, 104 (05) :77-78
[8]   Kinetics and mechanisms of pH-dependent degradation of halonitromethanes by UV photolysis [J].
Fang, Jing-Yun ;
Ling, Li ;
Shang, Chii .
WATER RESEARCH, 2013, 47 (03) :1257-1266
[9]  
Feng YG, 2007, J ENVIRON ENG SCI, V6, P277, DOI [10.1139/S06-052, 10.1139/s06-052]
[10]   GENERATION AND REACTIONS OF THE CHLORINE ATOM IN AQUEOUS-SOLUTION [J].
GILBERT, BC ;
STELL, JK ;
PEET, WJ ;
RADFORD, KJ .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1988, 84 :3319-3330