References

1. M.A. González-Curbelo, B. Socas-Rodríguez, M. Herrero, A.V. Herrera-Herrera, J. Hernández-Borges, Dissipation kinetics of organophosphorus pesticides in milled toasted maize and wheat flour (gofio) during storage, Food Chem., 229 (2017) 854–859.
2. W.-J. Li, Y. Li, D. Ning, Q. Liu, L. Chang, W.-J. Ruan, An Fe(II) metal–organic framework as a visible responsive photo-Fenton catalyst for the degradation of organophosphates, New J. Chem., 42 (2018) 29–33.
3. R. Pamanji, B. Yashwanth, M.S. Bethu, S. Leelavathi, K. Ravinder, J. Venkateswara Rao, Toxicity effects of profenofos on embryonic and larval development of Zebrafish (Danio rerio), Environ. Toxicol. Pharmacol., 39 (2015) 887–897.
4. P.V. Toan, Z. Sebesvari, M. Bläsing, I. Rosendahl, F.G. Renaud, Pesticide management and their residues in sediments and surface and drinking water in the Mekong Delta, Vietnam, Sci. Total Environ., 452–453 (2013) 28–39.
5. X.T. Lu, C. Yu, Enantiomer-specific profenofos-induced cytotoxicity and DNA damage mediated by oxidative stress in rat adrenal pheochromocytoma (PC12) cells, J. Appl. Toxicol., 34 (2014) 166–175.
6. R.O. Sule, L. Condon, A.V. Gomes, A common feature of pesticides: oxidative stress-the role of oxidative stress in pesticide-induced toxicity, Oxid. Med. Cell. Longevity, 2022 (2022) 5563759, doi: 10.1155/2022/5563759.
7. A.M. Parker, Y. Lester, E.K. Spangler, U. von Gunten, K.G. Linden, UV/H₂O₂ advanced oxidation for abatement of organophosphorous pesticides and the effects on various toxicity screening assays, Chemosphere, 182 (2017) 477–482.
8. X. Li, D. Zhang, Z. Liu, Y. Xu, D. Wang, Synthesis, characterization of a ternary Cu(II) Schiff base complex with degradation activity of organophosphorus pesticides, Inorg. Chim. Acta, 471 (2018) 280–289.
9. C. Zamy, P. Mazellier, B. Legube, Phototransformation of selected organophosphorus pesticides in dilute aqueous solutions, Water Res., 38 (2004) 2305–2314.
10. C. Fang, X. Zhang, X. Lou, Y. Shi, Y. Tang, D. Huang, J. Liu, Y. Guo, Insights into effect of chloride ion on the degradation of 4-bromo-2-chlorophenol by sulphate radical-based oxidation process, Int. J. Environ. Anal. Chem., (2022), doi: 10.1080/03067319.2022.2060091.
11. D. Angthararuk, M. Harir, P. Schmitt-Kopplin, S. Sutthivaiyakit, A. Kettrup, P. Sutthivaiyakit, Degradation products of profenofos as identified by high-field FTICR mass spectrometry: isotopic fine structure approach, J. Environ. Sci. Health., Part B, 52 (2017) 10–22.
12. M. Menager, J.S. Pilichowski, M. Sarakha, Reaction pathways for the photodegradation of the organophosphorus cyanophos in aqueous solutions, Photochem. Photobiol., 86 (2010) 247–254.
13. Y. Chen, Y. Xiong, Z. Wang, Y. Chen, G. Chen, G. Liu, UV/ferrate(VI) oxidation of profenofos: efficiency and mechanism, Desal. Water Treat., 55 (2015) 506–513.
14. C.P. James, E. Germain, S. Judd, Micropollutant removal by advanced oxidation of microfiltered secondary effluent for water reuse, Sep. Purif. Technol., 127 (2014) 77–83.
15. F.L. Rosario-Ortiz, E.C. Wert, S.A. Snyder, Evaluation of UV/H₂O₂ treatment for the oxidation of pharmaceuticals in wastewater, Water Res., 44 (2010) 1440–1448.
16. N.M. Costa, V.M. Silva, G. Damaceno, R.M.F. Sousa, E.M. Richter, A.E.H. Machado, A.G. Trovó, Integrating coagulationflocculation and UV-C or H₂O₂/UV-C as alternatives for pre- or complete treatment of biodiesel effluents, J. Environ. Manage., 203 (2017) 229–236.
17. M.M. Amin, B. Jaberian, B. Bina, M. Sadani, R. Hadian, G. Bonyadinejad, M.M.A. Moazzam, 2009. Advanced oxidation of the endosulfan and profenofos in aqueous solution using UV/H₂O₂ process, Environ. Asia, 7 (2014) 57–64.
18. M.I. Badawy, M.Y. Ghaly, T.A. Gad-Allah, Advanced oxidation processes for the removal of organophosphorus pesticides from wastewater, Desalination, 194 (2006) 166–175.
19. E.N. Evgenidou, I.K. Konstantinou, D.A. Lambropoulou, Occurrence and removal of transformation products of PPCPs and illicit drugs in wastewaters: a review, Sci. Total Environ., 505 (2015) 905–926.
20. N. Hermes, K.S. Jewell, A. Wick, T.A. Ternes, Quantification of more than 150 micropollutants including transformation products in aqueous samples by liquid chromatographytandem mass spectrometry using scheduled multiple reaction monitoring, J. Chromatogr. A, 1531 (2018) 64–73.
21. T. Cáceres, M. Megharaj, R. Naidu, Toxicity of fenamiphos and its metabolites to the cladoceran Daphnia carinata: the influence of microbial degradation in natural waters, Chemosphere, 66 (2007) 1264–1269.
22. S. Benfeito, T. Silva, J. Garrido, P.B. Andrade, M.J. Sottomayor, F. Borges, E. Manuela Garrido, Effects of chlorophenoxy herbicides and their main transformation products on DNA damage and acetylcholinesterase activity, BioMed Res. Int., 2014 (2014) 709036, doi: 10.1155/2014/709036.
23. C. Matsubara, N. Kawamoto, K. Takamura, Oxo[5, 10, 15, 20-tetra(4-pyridyl)porphyrinato]titanium(IV): an ultra-high sensitivity spectrophotometric reagent for hydrogen peroxide, Analyst, 117 (1992) 1781–1784.
24. H.T. Madsen, E.G. Søgaard, J. Muff, Study of degradation intermediates formed during electrochemical oxidation of pesticide residue 2,6-dichlorobenzamide (BAM) in chloride medium at boron doped diamond (BDD) and platinum anodes, Chemosphere, 120 (2015) 756–763.
25. J.C. Crittenden, S. Hu, D.W. Hand, S.A. Green, A kinetic model for H₂O₂/UV process in a completely mixed batch reactor, Water Res., 33 (1999) 2315–2328.
26. N.A. Mishchuk, L.L. Lysenko, O.V. Zayats, Investigation of the kinetics of catalytic decomposition of hydrogen peroxide depending on the solution phase state, J. Water Chem. Technol., 31 (2009) 71–80.
27. R.O. Ramos, M.V.C. Albuquerque, W.S. Lopes, J.T. Sousa, V.D. Leite, Degradation of indigo carmine
    by photo-Fenton, Fenton, H₂O₂/UV-C and direct UV-C: comparison of pathways, products and kinetics, J. Water Process Eng., 37 (2020) 101535, doi: 10.1016/j.jwpe.2020.101535.
28. E. Azizi, M. Fazlzadeh, M. Ghayebzadeh, L. Hemati, M. Beikmohammadi, H.R. Ghaffari, K. Sharafi, Application of advanced oxidation process (H₂O₂/UV) for removal of organic materials from pharmaceutical industry effluent, Environ. Prot. Eng., 43 (2017) 183–192.
29. Y.S. Lay, Oxidation of 1,2-Dibromo-3-chloropropane in Groundwater Using Advanced Oxidation Processes, Ph.D. Dissertation, University of California, Los Angeles, 1989.
30. N.M. Costa, V.M. Silva, G. Damaceno, R.M.F. Sousa, E.M. Richter, A.E.H. Machado, A.G. Trovó, Integrating coagulationflocculation and UV-C or H₂O₂/UV-C as alternatives for pre- or complete treatment of biodiesel effluents, J. Environ. Manage., 203 (2017) 229–236.
31. P.A. Soares, R. Souza, J. Soler, T.F.C.V. Silva, S.M.A. Guelli, U. Souza, R.A.R. Boaventura, V.J.P. Vilar, Remediation of a synthetic textile wastewater from polyester-cotton dyeing combining biological and photochemical oxidation processes, Sep. Purif. Technol., 172 (2017) 450–462.
32. P. Avetta, A. Pensato, M. Minella, M. Malandrino, V. Maurino, C. Minero, K. Hanna, D. Vione, Activation of persulfate by irradiated magnetite implications for the degradation of phenol under heterogeneous photo-Fenton-like conditions, Environ. Sci. Technol., 49 (2015) 1043–1050.
33. Q. Li, N. Gao, Y. Deng, X. Ma, W. Chu, Factors affecting UV/H₂O₂ oxidation of 17α-ethynyestradiol in water. Clean–Soil, Air, Water, 41 (2013) 143–147.
34. C. Luo, J. Ma, J. Jiang, Y. Liu, Y. Song, Y. Yang, Y. Guan, D. Wu, Simulation and comparative study on the oxidation kinetics of atrazine by UV/H₂O₂, UV/HSO₅^– and UV/S₂O₈^2–, Water Res., 80 (2015) 99–108.
35. P.C. St. John, Y. Guan, Y. Kim, S. Kim, R.S. Paton, Prediction of organic homolytic bond dissociation enthalpies at near chemical accuracy with sub-second computational cost, Nat. Commun., 11 (2020) 2328, doi: 10.1038/s41467-020-16201-z.
36. C. Zamy, P. Mazellier, B. Legube, Phototransformation of selected organophosphorus pesticides in dilute aqueous solutions, Water Res., 38 (2004) 2305–2314.
37. M.L. Chacón-Patiño, C. Blanco-Tirado, J.P. Hinestroza, M.Y. Combariza, Biocomposite of nanostructured MnO₂ and fique fibers for efficient dye degradation, Green Chem., 15 (2013) 2920–2928.