Effects of typical water components on the UV254 photodegradation kinetics of haloacetic acids in water

被引:20
作者
Bu, Yinan [1 ]
Wang, Liwei [1 ]
Chen, Baiyang [1 ]
Niu, Ruilan [1 ]
Chen, Yi [1 ]
机构
[1] Harbin Inst Technol, Shenzhen Key Lab Organ Pollut Prevent & Control, Shenzhen Engn Lab Microalgal Bioenergy, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Haloaceticacid; UV photolysis; Point-of-use; UV254n; Influencing factors; DISINFECTION BY-PRODUCTS; DRINKING-WATER; AQUEOUS-SOLUTION; SWIMMING POOL; UV-RADIATION; REMOVAL; DEGRADATION; OXIDATION; REDUCTION; GENOTOXICITY;
D O I
10.1016/j.seppur.2018.02.045
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study investigated a range of typical water components and parameters, including pH, carbonate, bicarbonate, halides, nitrate, dissolved organic matter (DOM), free chlorine, and initial concentration, on the photodegradadon kinetics of seven different haloacetic acids (HAM) with different halogen substitutions. The results show that the photolysis rates can generally be enhanced by additions of free chlorine and iodide yet decelerated by increases of DOM and bromide. In contrast, pH and feeding HAA concentration did not affect the photodegradadon of HAM significantly over pH ranges from 6 to 11 or doses from 0.05 to 50 mg/L. One exception existed that hydroxide, bicarbonate, and carbonate apparently inhibited the photolysis kinetics of monochloroacetic acid, suggesting that indirect photolysis via hydroxyl radical was partially responsible for this compound. As for the combined influences of water matrix, the photolysis rates of HAM dosed into tap, lake, and ocean waters were lower than those dosed into ultrapure water by on average 21-38%, indicating that most components in these real waters tended to suppress the photolysis. The study therefore demonstrates the complexity of DBP removal using a UV system, and such results may help assessment of the real potential of UV photolysis for HAA control in water.
引用
收藏
页码:255 / 265
页数:11
相关论文
共 72 条
[1]   Photolytic dehalogenation of disinfection byproducts in water by natural sunlight irradiation [J].
Abusallout, Ibrahim ;
Hua, Guanghui .
CHEMOSPHERE, 2016, 159 :184-192
[2]   Formation and fate of chlorination by-products in reverse osmosis desalination systems [J].
Agus, Eva ;
Sedlak, David L. .
WATER RESEARCH, 2010, 44 (05) :1616-1626
[3]  
[Anonymous], 2010, ULTRAVIOLET LIGHT WA
[4]   Pilot study of the removal of THMs, HAAs and DOC from drinking water by GAC adsorption [J].
Babi, K. G. ;
Koumenides, K. M. ;
Nikolaou, A. D. ;
Makri, C. A. ;
Tzoumerkas, F. K. ;
Lekkas, T. D. .
DESALINATION, 2007, 210 (1-3) :215-224
[5]   Impact of biomass on the stability of HAAs and THMs in a simulated distribution system [J].
Baribeau, H ;
Krasner, SW ;
Chinn, R ;
Singer, PC .
JOURNAL AMERICAN WATER WORKS ASSOCIATION, 2005, 97 (02) :69-81
[6]   OXIDATION OF POLYNUCLEAR AROMATIC-HYDROCARBONS IN WATER .2. UV-RADIATION AND OZONATION IN THE PRESENCE OF UV-RADIATION [J].
BELTRAN, FJ ;
OVEJERO, G ;
GARCIAARAYA, JF ;
RIVAS, J .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (05) :1607-1615
[7]   Treatment of disinfection by-product precursors [J].
Bond, T. ;
Goslan, E. H. ;
Parsons, S. A. ;
Jefferson, B. .
ENVIRONMENTAL TECHNOLOGY, 2011, 32 (01) :1-25
[8]   Haloacetic Acids in Swimming Pools: Swimmer and Worker Exposure [J].
Cardador, M. J. ;
Gallego, M. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2011, 45 (13) :5783-5790
[9]   Modulation of the cytotoxicity and genotoxicity of the drinking water disinfection byproduct iodoacetic acid by suppressors of oxidative stress [J].
Cemeli, E ;
Wagner, ED ;
Anderson, D ;
Richardson, SD ;
Plewa, MJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (06) :1878-1883
[10]   Predicting disinfection by-product formation potential in water [J].
Chen, Baiyang ;
Westerhoff, Paul .
WATER RESEARCH, 2010, 44 (13) :3755-3762