Formation and Decomposition of New Iodinated Halobenzoquinones during Chloramination in Drinking Water

Previously four chlorinated and brominated halo-benzoquinones were reported as new disinfection byproducts (DBPs) in drinking water, which have drawn great concern due to their high toxicity. In this study, three new iodinated halobenzoquinones, including 2-chloro-6-iodo-1,4-benzoquinone (2,6-CIBQ), 2-bromo-6-iodo-1,4-benzoquinone (2,6-BIBQ), and 2,6-diiodo-1,4-benzoquinone (2,6-DIBQ), were detected and identified in drinking water for the first time. Their cytotoxicity was evaluated, and their formation under various conditions was examined. Since they were not stable during chloramination, their further decomposition during chloramination was also explored. The results indicated that the concentrations of 2,6-CIBQ, 2,6-BIBQ, and 2,6-DIBQ in drinking water were in the ranges of 0.7-1.3, 1.8-8.0, and 0.4-15.9 ng/L, respectively. Compared with 2,6-dibromo-1,4-benzoquinone, the iodinated halobenzoquinones were generally more cytotoxic. The formation of 2,6-DIBQ during chloramination was significantly affected by the iodide concentration, pH, and natural organic matter. The five tested iodinated halobenzoquinones decomposed during chloramination following pseudo-first-order decay, with the decomposition rate constants in the rank order of 2,6-CIBQ > 2,6-BIBQ > 2,6-DIBQ > 2,3-diiodo-1,4-benzoquinone >2-iodo-1,4-benzoquinone. Nine polar halogenated intermediates as well as ten aliphatic halogenated DBPs were detected as the decomposition products of 2,6-DIBQ during chloramination, based on which the decomposition pathways of 2,6-DIBQ during chloramination were proposed and verified.