[1] ROOK J. Formation of haloform during chlorination of natural water [J]. Water Treatment and Examination, 1972, 21: 259.
[2] HU J, SONG H, ADDISON J W, et al. Halonitromethane formation potentials in drinking waters [J]. Water Research, 2010, 44(1): 105-114. doi: 10.1016/j.watres.2009.09.006
[3] JEONG C H, POSTIGO C, RICHARDSON S D, et al. Occurrence and comparative toxicity of haloacetaldehyde disinfection byproducts in drinking water [J]. Environmental Science & Technology, 2015, 49(23): 13749-13759.
[4] WAGNER E D, PLEWA M J. CHO cell cytotoxicity and genotoxicity analyses of disinfection by-products: An updated review [J]. Journal of Environmental Sciences, 2017, 58: 64-76. doi: 10.1016/j.jes.2017.04.021
[5] XIA Y, LIN Y L, XU B, et al. Iodinated trihalomethane formation during chloramination of iodate-containing waters in the presence of zero valent iron [J]. Water Research, 2017, 124: 219-226. doi: 10.1016/j.watres.2017.07.059
[6] ZHANG H F, YANG M. Characterization of brominated disinfection byproducts formed during chloramination of fulvic acid in the presence of bromide [J]. Science of the Total Environment, 2018, 627: 118-124. doi: 10.1016/j.scitotenv.2018.01.215
[7] LI X F, MITCH W A. Drinking water disinfection byproducts (DBPs) and human health effects: Multidisciplinary challenges and opportunities [J]. Environmental Science & Technology, 2018, 52(4): 1681-1689.
[8] PLEWA M J, WAGNER E D, RICHARDSON S D, et al. Chemical and biological characterization of newly discovered iodoacid drinking water disinfection byproducts [J]. Environmental Science & Technology, 2004, 38(18): 4713-4722.
[9] MUELLNER M G, WAGNER E D, McCALLA K, et al. Haloacetonitriles vs. regulated haloacetic acids: Are nitrogen-containing DBPs more toxic? [J]. Environmental Science & Technology, 2007, 41(2): 645-651.
[10] WHITEHEAD D C. The distribution and transformations of iodine in the environment [J]. Environment International, 1984, 10(4): 321-339. doi: 10.1016/0160-4120(84)90139-9
[11] SIDDIQUI M S, AMY G L, RICE R G. Bromate ion formation: A critical review [J]. Journal - American Water Works Association, 1995, 87(10): 58-70. doi: 10.1002/j.1551-8833.1995.tb06435.x
[12] MAGAZINOVIC R S, NICHOLSON B C, MULCAHY D E, et al. Bromide levels in natural waters: Its relationship to levels of both chloride and total dissolved solids and the implications for water treatment [J]. Chemosphere, 2004, 57(4): 329-335. doi: 10.1016/j.chemosphere.2004.04.056
[13] WANG N, ZHANG G, XIONG R X, et al. Synchronous moderate oxidation and adsorption on the surface of γ-MnO2 for efficient iodide removal from water [J]. Environmental Science & Technology, 2022, 56(13): 9417-9427.
[14] WANG Y, CUI Y S, CHEN C, et al. Stopping the supply of iodized salt alone is not enough to make iodine nutrition suitable for children in higher water iodine areas: A cross-sectional study in Northern China [J]. Ecotoxicology and Environmental Safety, 2020, 188: 109930. doi: 10.1016/j.ecoenv.2019.109930
[15] ZHA X S, LIU Y, LIU X, et al. Effects of bromide and iodide ions on the formation of disinfection by-products during ozonation and subsequent chlorination of water containing biological source matters [J]. Environmental Science and Pollution Research, 2014, 21(4): 2714-2723. doi: 10.1007/s11356-013-2176-x
[16] ZHANG Y, ZHANG N, ZHAO P, et al. Characteristics of molecular weight distribution of dissolved organic matter in bromide-containing water and disinfection by-product formation properties during treatment processes [J]. Journal of Environmental Sciences, 2018, 65: 179-189. doi: 10.1016/j.jes.2017.03.013
[17] KRISTIANA I, LIEW D, HENDERSON R K, et al. Formation and control of nitrogenous DBPs from Western Australian source waters: Investigating the impacts of high nitrogen and bromide concentrations [J]. Journal of Environmental Sciences, 2017, 58: 102-115. doi: 10.1016/j.jes.2017.06.028
[18] 高乃云, 赵璐, 楚文海. 饮用水中典型含氮消毒副产物卤乙腈的质量浓度分布 [J]. 同济大学学报(自然科学版), 2012, 40(2): 251-255. doi: 10.3969/j.issn.0253-374x.2012.02.016 GAO N Y, ZHAO L, CHU W H. Concentration distribution of typical nitrogenous disinfection by-products HANs in drinking water [J]. Journal of Tongji University (Natural Science), 2012, 40(2): 251-255(in Chinese). doi: 10.3969/j.issn.0253-374x.2012.02.016
[19] ZHAI H Y, CHENG S Z, ZHANG L Y, et al. Formation characteristics of disinfection byproducts from four different algal organic matter during chlorination and chloramination[J]. Chemosphere, 2022, 308(Pt 1): 136171.
[20] 付顺, 孙越. 碘代消毒副产物在净水工艺中的生成机制与控制措施 [J]. 环境化学, 2016, 35(6): 1153-1163. doi: 10.7524/j.issn.0254-6108.2016.06.2015111203 FU S, SUN Y. Formation mechanism and control measures of iodinated disinfection by-products in drinking water process [J]. Environmental Chemistry, 2016, 35(6): 1153-1163(in Chinese). doi: 10.7524/j.issn.0254-6108.2016.06.2015111203
[21] LI X, RAO N R H, LINGE K L, et al. Formation of algal-derived nitrogenous disinfection by-products during chlorination and chloramination [J]. Water Research, 2020, 183: 116047. doi: 10.1016/j.watres.2020.116047
[22] WANG X X, LIU B M, LU M F, et al. Characterization of algal organic matter as precursors for carbonaceous and nitrogenous disinfection byproducts formation: Comparison with natural organic matter [J]. Journal of Environmental Management, 2021, 282: 111951. doi: 10.1016/j.jenvman.2021.111951
[23] HONG H C, MAZUMDER A, WONG M H, et al. Yield of trihalomethanes and haloacetic acids upon chlorinating algal cells, and its prediction via algal cellular biochemical composition [J]. Water Research, 2008, 42(20): 4941-4948. doi: 10.1016/j.watres.2008.09.019
[24] WEI Y Y, LIU Y, MA L M, et al. Speciation and formation of iodinated trihalomethane from microbially derived organic matter during the biological treatment of micro-polluted source water [J]. Chemosphere, 2013, 92(11): 1529-1535. doi: 10.1016/j.chemosphere.2013.04.019
[25] YANG Y, KOMAKI Y, KIMURA S Y, et al. Toxic impact of bromide and iodide on drinking water disinfected with chlorine or chloramines [J]. Environmental Science & Technology, 2014, 48(20): 12362-12369.
[26] YE Z, LIU W J, SUN W J, et al. Role of ammonia on haloacetonitriles and halonitromethanes formation during Ultraviolet irradiation followed by chlorination/chloramination [J]. Chemical Engineering Journal, 2018, 337: 275-281. doi: 10.1016/j.cej.2017.12.073
[27] CARTER R A A, LIEW D S, WEST N, et al. Simultaneous analysis of haloacetonitriles, haloacetamides and halonitromethanes in chlorinated waters by gas chromatography-mass spectrometry [J]. Chemosphere, 2019, 220: 314-323. doi: 10.1016/j.chemosphere.2018.12.069
[28] 顾允轩, 仇付国, 刘子奇, 等. 水中溴代消毒副产物的生成综述 [J]. 环境化学, 2022, 41(6): 1934-1946. doi: 10.7524/j.issn.0254-6108.2021021801 GU Y X, QIU F G, LIU Z Q, et al. Brominated disinfection by-products formation in water: A review [J]. Environmental Chemistry, 2022, 41(6): 1934-1946(in Chinese). doi: 10.7524/j.issn.0254-6108.2021021801
[29] ALLARD S, HU W, le MENN J B, et al. Method development for quantification of bromochloramine using membrane introduction mass spectrometry [J]. Environmental Science & Technology, 2018, 52(14): 7805-7812.
[30] ALLARD S, CADEE K, TUNG R, et al. Impact of brominated amines on monochloramine stability during in-line and pre-formed chloramination assessed by kinetic modelling [J]. Science of the Total Environment, 2018, 618: 1431-1439. doi: 10.1016/j.scitotenv.2017.09.281
[31] BOND T, TEMPLETON M R, GRAHAM N. Precursors of nitrogenous disinfection by-products in drinking water: A critical review and analysis [J]. Journal of Hazardous Materials, 2012, 235/236: 1-16. doi: 10.1016/j.jhazmat.2012.07.017
[32] HONG H C, QIAN L Y, XIAO Z Q, et al. Effect of nitrite on the formation of halonitromethanes during chlorination of organic matter from different origin [J]. Journal of Hydrology, 2015, 531: 802-809. doi: 10.1016/j.jhydrol.2015.10.046
[33] LIU Y S, LIU K Q, PLEWA M J, et al. Formation of regulated and unregulated disinfection byproducts during chlorination and chloramination: Roles of dissolved organic matter type, bromide, and iodide [J]. Journal of Environmental Sciences, 2022, 117: 151-160. doi: 10.1016/j.jes.2022.04.014
[34] YANG X, SHEN Q Q, GUO W H, et al. Precursors and nitrogen origins of trichloronitromethane and dichloroacetonitrile during chlorination/chloramination [J]. Chemosphere, 2012, 88(1): 25-32. doi: 10.1016/j.chemosphere.2012.02.035
[35] NIHEMAITI M, le ROUX J, HOPPE-JONES C, et al. Formation of haloacetonitriles, haloacetamides, and nitrogenous heterocyclic byproducts by chloramination of phenolic compounds [J]. Environmental Science & Technology, 2017, 51(1): 655-663.