[1] ZHANG H, IHARA M O, NAKADA N, et al. Biological activity-based prioritization of pharmaceuticals in wastewater for environmental monitoring: G protein-coupled receptor inhibitors [J]. Environmental Science & Technology, 2020, 54(3): 1720-1729.
[2] MEYER M F, POWERS S M, HAMPTON S E. An evidence synthesis of pharmaceuticals and personal care products (PPCPs) in the environment: Imbalances among compounds, sewage treatment techniques, and ecosystem types [J]. Environmental Science & Technology, 2019, 53(22): 12961-12973.
[3] WANG Y F, JING B H, WANG F L, et al. Mechanism Insight into enhanced photodegradation of pharmaceuticals and personal care products in natural water matrix over crystalline graphitic carbon nitrides [J]. Water Research, 2020, 180: 115925. doi: 10.1016/j.watres.2020.115925
[4] CHO K, AN B M, SO S, et al. Simultaneous control of algal micropollutants based on ball-milled powdered activated carbon in combination with permanganate oxidation and coagulation [J]. Water Research, 2020, 185: 116263. doi: 10.1016/j.watres.2020.116263
[5] LIU B, ZHU T T, LIU W K, et al. Ultrafiltration pre-oxidation by boron-doped diamond anode for algae-laden water treatment: Membrane fouling mitigation, interface characteristics and cake layer organic release [J]. Water Research, 2020, 187: 116435. doi: 10.1016/j.watres.2020.116435
[6] LIN S Y, YU X, FANG J Y, et al. Influences of the micropollutant erythromycin on cyanobacteria treatment with potassium permanganate [J]. Water Research, 2020, 177: 115786. doi: 10.1016/j.watres.2020.115786
[7] YANG Y, BANERJEE G, BRUDVIG G W, et al. Oxidation of organic compounds in water by unactivated peroxymonosulfate [J]. Environmental Science & Technology, 2018, 52(10): 5911-5919.
[8] LEE J, von GUNTEN U, KIM J H. Persulfate-based advanced oxidation: Critical assessment of opportunities and roadblocks [J]. Environmental Science & Technology, 2020, 54(6): 3064-3081.
[9] GUO Y Q, LIANG H, BAI L M, et al. Application of heat-activated peroxydisulfate pre-oxidation for degrading contaminants and mitigating ultrafiltration membrane fouling in the natural surface water treatment [J]. Water Research, 2020, 179: 115905. doi: 10.1016/j.watres.2020.115905
[10] 谢鹏超, 岳思阳, 邹景, 等. 四种预氧化方式对AOC及消毒副产物影响的对比 [J]. 中国给水排水, 2015, 31(7): 6-9. doi: 10.19853/j.zgjsps.1000-4602.2015.07.002 XIE P C, YUE S Y, ZOU J, et al. Comparison of effects of four different preoxidation processes on formation of assimilable organic carbon and disinfection by-products [J]. China Water & Wastewater, 2015, 31(7): 6-9(in Chinese). doi: 10.19853/j.zgjsps.1000-4602.2015.07.002
[11] QI J, LAN H C, MIAO S Y, et al. KMnO4-Fe(II) pretreatment to enhance Microcystis aeruginosa removal by aluminum coagulation: Does it work after long distance transportation? [J]. Water Research, 2016, 88: 127-134. doi: 10.1016/j.watres.2015.10.004
[12] XIE P C, CHEN Y Q, MA J, et al. A mini review of preoxidation to improve coagulation [J]. Chemosphere, 2016, 155: 550-563. doi: 10.1016/j.chemosphere.2016.04.003
[13] LI X Y, PI Y H, WU L Q, et al. Facilitation of the visible light-induced Fenton-like excitation of H2O2 via heterojunction of g-C3N4/NH2-Iron terephthalate metal-organic framework for MB degradation [J]. Applied Catalysis B:Environmental, 2017, 202: 653-663. doi: 10.1016/j.apcatb.2016.09.073
[14] SUN Q, LIU M, LI K Y, et al. Synthesis of Fe/M (M = Mn, Co, Ni) bimetallic metal organic frameworks and their catalytic activity for phenol degradation under mild conditions [J]. Inorganic Chemistry Frontiers, 2017, 4(1): 144-153. doi: 10.1039/C6QI00441E
[15] ANIPSITAKIS G P, DIONYSIOU D D. Radical generation by the interaction of transition metals with common oxidants [J]. Environmental Science & Technology, 2004, 38(13): 3705-3712.
[16] GUAN Y H, MA J, LI X C, et al. Influence of pH on the formation of sulfate and hydroxyl radicals in the UV/peroxymonosulfate system [J]. Environmental Science & Technology, 2011, 45(21): 9308-9314.
[17] WEN G, WANG S B, WANG T, et al. Inhibition of bromate formation in the O3/PMS process by adding low dosage of carbon materials: Efficiency and mechanism [J]. Chemical Engineering Journal, 2020, 402: 126207. doi: 10.1016/j.cej.2020.126207
[18] CHEN T T, YU Z Y, XU T, et al. Formation and degradation mechanisms of CX3R-type oxidation by-products during cobalt catalyzed peroxymonosulfate oxidation: The roles of Co3+ and SO4·- [J]. Journal of Hazardous Materials, 2021, 405: 124243. doi: 10.1016/j.jhazmat.2020.124243
[19] CHEN T T, DONG S K, GUO X P, et al. Dissolved organic carbon removal and CX3R-type byproduct formation during the peroxymonosulfate pre-oxidation followed by coagulation [J]. Chemical Engineering Journal, 2021, 421: 129654. doi: 10.1016/j.cej.2021.129654
[20] 李忠禹, 彭健伟, 文怡心, 等. 饮用水含氮与含碳消毒副产物的生成潜能及其毒性 [J]. 环境科学学报, 2021, 41(9): 3401-3407. doi: 10.13671/j.hjkxxb.2020.0485 LI Z Y, PENG J W, WEN Y X, et al. Formation potential and estimated toxicity of nitrogenous and carbonaceous disinfection byproducts in drinking water [J]. Acta Scientiae Circumstantiae, 2021, 41(9): 3401-3407(in Chinese). doi: 10.13671/j.hjkxxb.2020.0485
[21] 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
[22] LIU J Q, ZHANG X R. Comparative toxicity of new halophenolic DBPs in chlorinated saline wastewater effluents against a marine alga: Halophenolic DBPs are generally more toxic than haloaliphatic ones [J]. Water Research, 2014, 65: 64-72. doi: 10.1016/j.watres.2014.07.024
[23] 洪涵璐, 赵伟, 尹金宝. 饮用水消毒副产物基因毒性与致癌性研究进展 [J]. 环境监控与预警, 2020, 12(5): 36-48. HONG H L, ZHAO W, YIN J B. A review on the genotoxicity and carcinogenicity of disinfection by-products in drinking water [J]. Environmental Monitoring and Forewarning, 2020, 12(5): 36-48(in Chinese).
[24] YAO D C, CHU W H, BOND T, et al. Impact of ClO2 pre-oxidation on the formation of CX3R-type DBPs from tyrosine-based amino acid precursors during chlorination and chloramination [J]. Chemosphere, 2018, 196: 25-34. doi: 10.1016/j.chemosphere.2017.12.143
[25] SHAH A D, MITCH W A. Halonitroalkanes, halonitriles, haloamides, and N-nitrosamines: A critical review of nitrogenous disinfection byproduct formation pathways [J]. Environmental Science & Technology, 2012, 46(1): 119-131.
[26] RAM N M. A review of the significance and formation of chlorinated N-organic compounds in water supplies including preliminary studies on the chlorination of alanine, tryptophan, tyrosine, cytosine, and syringic acid [J]. Environment International, 1985, 11(5): 441-451. doi: 10.1016/0160-4120(85)90227-2
[27] DING S K, CHU W H, BOND T, et al. Formation and estimated toxicity of trihalomethanes, haloacetonitriles, and haloacetamides from the chlor(am)ination of acetaminophen [J]. Journal of Hazardous Materials, 2018, 341: 112-119. doi: 10.1016/j.jhazmat.2017.07.049
[28] WACŁAWEK S, LUTZE H V, GRÜBEL K, et al. Chemistry of persulfates in water and wastewater treatment: A review [J]. Chemical Engineering Journal, 2017, 330: 44-62. doi: 10.1016/j.cej.2017.07.132
[29] CHEN T T, WANG R, ZHANG A H, et al. Peroxymonosulfate/chloride disinfection versus sodium hypochlorite disinfection in terms of the formation and estimated cytotoxicity of CX3R-type disinfection by-products under the same dose of free chlorine [J]. Chemical Engineering Journal, 2020, 391: 123557. doi: 10.1016/j.cej.2019.123557
[30] HOU S D, LING L, DIONYSIOU D D, et al. Chlorate formation mechanism in the presence of sulfate radical, chloride, bromide and natural organic matter [J]. Environmental Science & Technology, 2018, 52(11): 6317-6325.
[31] LIANG L, SINGER P C. Factors influencing the formation and relative distribution of haloacetic acids and trihalomethanes in drinking water [J]. Environmental Science & Technology, 2003, 37(13): 2920-2928.
[32] CHU W H, GAO N Y, DENG Y. Formation of haloacetamides during chlorination of dissolved organic nitrogen aspartic acid [J]. Journal of Hazardous Materials, 2010, 173(1/2/3): 82-86.
[33] YU Y, RECKHOW D A. Kinetic analysis of haloacetonitrile stability in drinking waters [J]. Environmental Science & Technology, 2015, 49(18): 11028-11036.
[34] LI Z B, CHEN Z, XIANG Y Y, et al. Bromate formation in bromide-containing water through the cobalt-mediated activation of peroxymonosulfate [J]. Water Research, 2015, 83: 132-140. doi: 10.1016/j.watres.2015.06.019
[35] DEBORDE M, von GUNTEN U. Reactions of chlorine with inorganic and organic compounds during water treatment−Kinetics and mechanisms: A critical review [J]. Water Research, 2008, 42(1/2): 13-51.
[36] GLEZER V, HARRIS B, TAL N, et al. Hydrolysis of haloacetonitriles: Linear free energy relationship, kinetics and products [J]. Water Research, 1999, 33(8): 1938-1948. doi: 10.1016/S0043-1354(98)00361-3
[37] PLEWA M J, MUELLNER M G, RICHARDSON S D, et al. Occurrence, synthesis, and mammalian cell cytotoxicity and genotoxicity of haloacetamides: An emerging class of nitrogenous drinking water disinfection byproducts [J]. Environmental Science & Technology, 2008, 42(3): 955-961.