[1] A.C. de Groot, J.W. Weyland, Kathon CG:A review, J. Am. Acad. Dermatol. 18(2)(1988)350-358. [2] X.Z. Li, Z.M. Li, Z.H. Xing, Z.M. Song, B. Ye, Z.M. Wang, Q.Y. Wu, UV-LED/P25-based photocatalysis for effective degradation of isothiazolone biocide, Front. Environ. Sci. Eng. 15(5)(2020)1-12. [3] M. Critchley, R. Bentham, The efficacy of biocides and other chemical additives in cooling water systems in the control of amoebae, J. Appl. Microbiol. 106(3)(2009)784-789. [4] P.J. Frosch, A. Lahti, M. Hannuksela, K.E. Andersen, J.D. Wilkinson, S. Shaw, J.M. Lachapelle, Chloromethylisothiazolone/methylisothiazolone (CMI/MI) use test with a shampoo on patch-test-positive subjects results of a multicentre double-blind crossover trial, Contact Dermat. 32(4)(1995)210-217. [5] R. Matissek, Analysis of preservatives in cosmetics-methylisothiazolones, Chromatographia 28(1-2)(1989)34-38. [6] A. Li, Q.Y. Wu, G.P. Tian, H.Y. Hu, Effective degradation of methylisothiazolone biocide using ozone:Kinetics, mechanisms, and decreases in toxicity, J. Environ. Manag. 183(2016)1064-1071. [7] G.A. Kahrilas, J. Blotevogel, P.S. Stewart, T. Borch, Biocides in hydraulic fracturing fluids:A critical review of their usage, mobility, degradation, and toxicity, Environ. Sci. Technol. 49(1)(2015)16-32. [8] U.E. Bollmann, C. Tang, E. Eriksson, K. Jönsson, J. Vollertsen, K. Bester, Biocides in urban wastewater treatment plant influent at dry and wet weather:Concentrations, mass flows and possible sources, Water Res. 60(2014)64-74. [9] A.M. Amat, A. Arques, M.F. López-Pérez, M. Nacher, S. Palacios, Effect of methylisothiazolinone on biological treatment:Efficiency of SBRs and bioindicative studies, Environ. Eng. Sci. 32(6)(2015)479-485. [10] J.B. Carbajo, J.A. Perdigón-Melón, A.L. Petre, R. Rosal, P. Letón, E. García-Calvo, Personal care product preservatives:Risk assessment and mixture toxicities with an industrial wastewater, Water Res. 72(2015)174-185. [11] M. Poberžnik, M. Bauman, M. Roš, A. Lobnik, Reduction of biocide-polluted wastewater using O3 and H2O2/O3 oxidation processes, Ozone 33(1)(2011)31-36. [12] S.F. Krzeminski, C.K. Brackett, J.D. Fisher, Fate of microbicidal 3-isothiazolone compounds in the environment. Modes and rates of dissipation, J. Agric. Food Chem. 23(6)(1975)1060-1068. [13] F.A. Guardiola, A. Cuesta, J. Meseguer, M.A. Esteban, Risks of using antifouling biocides in aquaculture, Int. J. Mol. Sci. 13(2)(2012)1541-1560. [14] S. Kresmann, A.H.R. Arokia, C. Koch, B. Sures, Ecotoxicological potential of the biocides terbutryn, octhilinone and methylisothiazolinone:Underestimated risk from biocidal pathways?, Sci Total Environ. 625(2018)900-908. [15] K. He, J. Huang, C.F. Lagenaur, E. Aizenman, Methylisothiazolinone, A neurotoxic biocide, disrupts the association of src family tyrosine kinases with focal adhesion kinase in developing cortical neurons, J. Pharmacol. Exp. Ther. 317(3)(2006)1320-1329. [16] F. Tang, H.Y. Hu, Q.Y. Wu, X. Tang, Y.X. Sun, X.L. Shi, J.J. Huang, Effects of chemical agent injections on genotoxicity of wastewater in a microfiltrationreverse osmosis membrane process for wastewater reuse, J. Hazard. Mater. 260(2013)231-237. [17] N. Chatterjee, H. Lee, J. Kim, D. Kim, S. Lee, J. Choi, Critical window of exposure of CMIT/MIT with respect to developmental effects on zebrafish embryos:Multi-level endpoint and proteomics analysis, Environ.. Pollut. 268(2021)115784. [18] R. Urwin, M. Wilkinson, Methylchloroisothiazolinone and methylisothiazolinone contact allergy:A new 'epidemic', Contact Dermat. 68(4)(2013)253-255. [19] V.Q. Do, Y.S. Seo, J.M. Park, J. Yu, M.T.H. Duong, J. Nakai, S.K. Kim, H.C. Ahn, M.Y. Lee, A mixture of chloromethylisothiazolinone and methylisothiazolinone impairs rat vascular smooth muscle by depleting thiols and thereby elevating cytosolic ZN2+and generating reactive oxygen species, Arch. Toxicol. 95(2)(2021)541-556. [20] J. Arning, M. Matzke, S. Stolte, F. Nehen, U. Bottin-Weber, A. Böschen, S. Abdulkarim, B. Jastorff, J. Ranke, Analyzing cytotoxic effects of selected isothiazol-3-one biocides using the toxic ratio concept and structure-activity relationship considerations, Chem. Res. Toxicol. 22(12)(2009)1954-1961. [21] C.L. Winder, I.S.I. Al-Adham, S.M.A. Abdel Malek, T.E.J. Buultjens, A.J. Horrocks, P.J. Collier, Outer membrane protein shifts in biocide-resistant Pseudomonas aeruginosa PAO1, J. Appl. Microbiol. 89(2)(2000)289-295. [22] D. Feng, A. Soric, O. Boutin, Treatment technologies and degradation pathways of glyphosate:A critical review, Sci. Total Environ. 742(2020)140559. [23] S.L. Morris, R.C. Walsh, J.N. Hansen, Identification and characterization of some bacterial membrane sulfhydryl groups which are targets of bacteriostatic and antibiotic action, J. Biol. Chem. 259(21)(1984)13590-13594. [24] M.A. Diehl, J.S. Chapman, Association of the biocide 5-chloro-2-methylisothiazol-3-one with Pseudomonas aeruginosa and Pseudomonas fluorescens, Int. Biodeterior. Biodegrad. 44(4)(1999)191-199. [25] P.J. Collier, A.J. Ramsey, P. Austin, P. Gilbert, Growth inhibitory and biocidal activity of some isothiazolone biocides, J. Appl. Bacteriol. 69(4)(1990)569-577. [26] D.B. Miklos, C. Remy, M. Jekel, K.G. Linden, J.E. Drewes, U. Hübner, Evaluation of advanced oxidation processes for water and wastewater treatment-A critical review, Water Res. 139(2018)118-131. [27] Q. Yang, Y.H. Ma, F. Chen, F.B. Yao, J. Sun, S.N. Wang, K.X. Yi, L.H. Hou, X.M. Li, D.B. Wang, Recent advances in photo-activated sulfate radical-advanced oxidation process (SR-AOP) for refractory organic pollutants removal in water, Chem. Eng. J. 378(2019)122149. [28] T. Wang, Q.Y. Wu, W. Wang, A. Li, H.Y. Hu, Degradation of methylisothiazolinone by UV/chlorine advanced oxidation process, C. Journal, E. Engineering. 11(01)(2017)2126.(in Chinese) [29] V. Kandavelu, H. Kastien, K.R. Thampi, Photocatalytic degradation of isothiazolin-3-ones in water and emulsion paints containing nanocrystalline TiO2 and ZnO catalysts, Appl. Catal. B 48(2)(2004)101-111. [30] C.Q. Tan, N.Y. Gao, Y. Deng, Y.J. Zhang, M.H. Sui, J. Deng, S.Q. Zhou, Degradation of antipyrine by UV, UV/H2O2 and UV/PS, J. Hazard. Mater. 260(2013)1008-1016. [31] Y. Du, W.L. Wang, D.Y. Zhang, T.H. Zhou, M.Y. Lee, Q.Y. Wu, H.Y. Hu, Z.M. He, T. Y. Huang, Degradation of non-oxidizing biocide benzalkonium chloride and bulk dissolved organic matter in reverse osmosis concentrate by UV/chlorine oxidation, J. Hazard. Mater. 396(2020)122669. [32] C.C. Lin, H.Y. Lin, L.J. Hsu, Degradation of ofloxacin using UV/H2O2 process in a large photoreactor, Sep. Purif. Technol. 168(2016)57-61. [33] A. Lopez, A. Bozzi, G. Mascolo, J. Kiwi, Kinetic investigation on UV and UV/H2O2 degradations of pharmaceutical intermediates in aqueous solution, J. Photochem. Photobiol. A 156(1-3)(2003)121-126. [34] X.D. Xin, S.H. Sun, A.R. Zhou, M.Q. Wang, Y. Song, Q.H. Zhao, R.B. Jia, Sulfadimethoxine photodegradation in UV-C/H2O2 system:Reaction kinetics, degradation pathways, and toxicity, J. Water Process. Eng. 36(2020)101293. [35] C.Y. Lu, J. Wang, D.L. Cao, F. Guo, X.L. Hao, D. Li, W.L. Shi, Synthesis of magnetically recyclable g-C3N4/NiFe2O4 S-scheme heterojunction photocatalyst with promoted visible-light-response photo-Fenton degradation of tetracycline, Mater. Res. Bull. 158(2023)112064. [36] W.L. Shi, W. Sun, Y.N. Liu, K. Zhang, H.R. Sun, X. Lin, Y.Z. Hong, F. Guo, A selfsufficient photo-Fenton system with coupling in situ production H2O2 of ultrathin porous g-C3N4 nanosheets and amorphous FeOOH quantum dots, J. Hazard. Mater. 436(2022)129141. [37] W.L. Shi, L.J. Wang, J. Wang, H.R. Sun, Y.X. Shi, F. Guo, C.Y. Lu, Magnetically retrievable CdS/reduced graphene oxide/ZnFe2O4 ternary nanocomposite for self-generated H2O2 towards photo-Fenton removal of tetracycline under visible light irradiation, Sep. Purif. Technol. 292(2022)120987. [38] Y.C. Liu, X.G. Ji, J.J. Yang, W. Tang, Y.L. Zhu, Y. Wang, Y.X. Zhang, Y. Zhang, J.M. Duan, W. Li, Degradation of the typical herbicide atrazine by UV/persulfate:Kinetics and mechanisms, Environ. Sci. Pollut. Res. 29(29)(2022)43928-43941. [39] N.T. Hoang, V.T. Nguyen, N.D. Minh Tuan, T.D. Manh, P.C. Le, D. Van Tac, F.M. Mwazighe, Degradation of dyes by UV/Persulfate and comparison with other UV-based advanced oxidation processes:Kinetics and role of radicals, Chemosphere 298(2022)134197. [40] K. Kocaman, U. Yetis, F.B. Dilek, Investigating the effect of solids retention time on pesticides removal in an activated sludge process, Sustain. Chem. Pharm. 29(2022)100784. [41] O. Legrini, E. Oliveros, A.M. Braun, Photochemical processes for water treatment, Chem. Rev. 93(2)(1993)671-698. [42] M. Lojo-López, J.A. Andrades, A. Egea-Corbacho, M.D. Coello, J.M. Quiroga, Degradation of simazine by photolysis of hydrogen peroxide Fenton and photo-Fenton under darkness, sunlight and UV light, J. Water Process. Eng. 42(2021)102115. [43] S.K. Cai, S.R. Zhang, G.Q. Wang, J.Z. Cui, C.Z. Gao, Degradation of a fluorescent tracer-PTSA in circulating cooling water:Kinetics, pathways, and degradation efficiency of a polycyclic aromatic hydrocarbon derivative, J. Water Process. Eng. 41(2021)102036. [44] R.O. Rahn, Potassium iodide as a chemical actinometer for 254 nm radiation:Use of lodate as an electron scavenger, Photochem. Photobiol. 66(4)(1997)450-455. [45] J.C. Crittenden, S.M. Hu, D.W. Hand, S.A. Green, A kinetic model for H2O2/UV process in a completely mixed batch reactor, Water Res. 33(10)(1999)2315-2328. [46] Z.H. Zuo, Z.L. Cai, Y. Katsumura, N. Chitose, Y. Muroya, Reinvestigation of the acid-base equilibrium of the (bi) carbonate radical and pH dependence of its reactivity with inorganic reactants, Radiat. Phys. Chem. 55(1)(1999)15-23. [47] J.R. Bolton, K.G. Bircher, W. Tumas, C.A. Tolman, Figures-of-merit for the technical development and application of advanced oxidation technologies for both electric- and solar-driven systems (IUPAC Technical Report), Pure Appl. Chem. 73(4)(2001)627-637. [48] A. Safarzadeh-Amiri, J.R. Bolton, S.R. Cater, Ferrioxalate-mediated photodegradation of organic pollutants in contaminated water, Water Res. 31(4)(1997)787-798. [49] O. Guideline, F.O.R. Testing, O.F. OECD Guideline for the Testing of Chemicals, Adopted by the Council on 17 th July 1992,(1992)1-62. [50] S.K. Cai, S.R. Zhang, C.Z. Gao, Z.F. Cheng, Degradation of fluorescent dyeSolvent Green 7(HPTS) in wastewater by advanced oxidation process, Water Sci. Technol. 82(11)(2020)2525-2535. [51] N. Daneshvar, M.A. Behnajady, M.K. Ali Mohammadi, M.S. Seyed Dorraji, UV/H2O2 treatment of Rhodamine B in aqueous solution:Influence of operational parameters and kinetic modeling, Desalination 230(1-3)(2008)16-26. [52] T. Jasemizad, L. Bromberg, L.P. Padhye, The fate of aqueous betrixaban during adsorption, photolysis, and advanced oxidation:Removal, kinetics, and reaction mechanisms, J. Water Process Eng. 44(2021)102430. [53] J.Z. Cui, S.K. Cai, S.R. Zhang, G.Q. Wang, C.Z. Gao, Degradation of a nonoxidizing biocide in circulating cooling water using UV/persulfate:Kinetics, pathways, and cytotoxicity, Chemosphere 289(2022)133064. [54] Y.M. Lee, G. Lee, K.D. Zoh, Benzophenone-3 degradation via UV/H2O2 and UV/persulfate reactions, J. Hazard. Mater. 403(2021)123591. [55] G.V. Buxton, C.L. Greenstock, W.P. Helman, A.B. Ross, Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (OH/O-in aqueous solution, J. Phys. Chem. Ref. Data 17(2)(1988)513-886. [56] E. Atinault, V. De Waele, U. Schmidhammer, M. Fattahi, M. Mostafavi, Scavenging of es- and OH radicals in concentrated HCl and NaCl aqueous solutions, Chem. Phys. Lett. 460(4-6)(2008)461-465. [57] M.A. Behnajady, B. Vahid, N. Modirshahla, M. Shokri, Evaluation of electrical energy per order (EEO) with kinetic modeling on the removal of malachite green by US/UV/H2O2 process, Desalination 249(1)(2009)99-103. |