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Effects of pre-oxidation by ozone, permanganate and ferrate on generation and toxicities of disinfection byproducts

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Abstract

When organic compounds are pre-oxidized before coagulation, the disinfection byproducts are usually generated in the following chlorination process in drinking water treatment. In this study, the effects of pre-oxidation on carbon removal and generation of disinfection byproducts were investigated by using common oxidants of ozone, permanganate and ferrate. It was demonstrated that turbidities were reduced by 35%, 37.5% and 38.3%, and dissolved organic carbon was reduced by 18.8%, 26.5% and 20.8%, respectively, with the pre-oxidation of ozone, permanganate and ferrate under optimal dosage but inorganic carbon was not affected. Turbidity, dissolved organic carbon and dissolved organic matter showed an initial decrease and then increase pattern with increase in ozone and permanganate concentrations, but a different continuously decreasing pattern was demonstrated by ferrate. The results indicated that pre-oxidation of organic compounds was incomplete and may include steps of colloid destabilization, cell lysis and partial mineralization. The removal rates of total disinfection byproducts under optimal concentrations were 31.69%, 45.36% and 39.35%, respectively. Eleven disinfection byproducts were identified and quantified, and the major species were chloroform, trichloroacetaldehyde and dichloroacetonitrile, which were either generated directly from organic compounds or converted from other species of disinfection byproducts. The highest LC50 of disinfection byproducts were dibromo- and bromochloro- acetonitriles, indicating the cytotoxicity was mostly contributed by the nitrogen-containing disinfection byproducts, which combined accounted for 79.6% to 83.4% of the total toxicity.

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Abbreviations

BCAN:

Bromochloroacetonitriles

BSF:

Bromine substitution factor

CHO:

Chinese hamster ovary

CH:

Chloral hydrate

DBAN:

Dibromoacetonitriles

DBPs:

Disinfection byproducts

DBPFPs:

Disinfection by product formation potentials

DCAN:

Dichloroacetonitriles

DHAAs:

Diheloaceticacids

DHANs:

Dihaloacetonitrile

DOC:

Dissolved organic carbon

DOM:

Dissolved organic matter

ECD:

Electron capture detector

EDCs:

Endocrine disruptor compound

EOMs:

Emerging organic matters

FIs:

Fluorescence intensities

GC:

Gas chromatograph

HAAs:

Haloaceticacids

HANs:

Haloacetonitriles

HKs:

Halidketones

IC:

Inorganic carbon

IOM:

Intracellular organic matter

LC50:

Lethal concentration

PAC:

Polyaluminum chloride

PCE:

Tetrachloroethylene

PFC:

Poly ferric chloride

SMP:

Soluble microbial products

TCA:

Trichloroacetaldehyde

TCM:

Chloroform

TCN:

Trichloronitromethane

TCP:

1,1,1-Trichloropropanone

tDBP:

Total disinfection byproducts

THAAs:

Triheloaceticacids

THMs:

Trihalidemethanes

Tl:

Thallium

TOCs:

Total organic compounds

UV:

Ultraviolet light

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Acknowledgements

Our work was supported by the National Natural Science Foundation of China [Grant numbers No. 51778267], the National Water Pollution Control and Treatment Science and Technology Major Project [Grant numbers No. 2012ZX07408001], the Jilin Province Science and Technology Department Project [Grant numbers No. 20190201113JC], the Jilin Provincial Department of Ecology and Environment Project [Grant numbers No.2019-15].

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Correspondence to Y. Lin.

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The authors have no relevant financial or non-financial interests to disclose. The authors have no conflicts of interest to declare that are relevant to the content of this article. All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest or non-financial interest in the subject matter or materials discussed in this manuscript. The authors have no financial or proprietary interests in any material discussed in this article.

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Editorial responsibility: Samareh Mirkia.

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Lin, Y., Lou, Y., Li, A. et al. Effects of pre-oxidation by ozone, permanganate and ferrate on generation and toxicities of disinfection byproducts. Int. J. Environ. Sci. Technol. 19, 5969–5984 (2022). https://doi.org/10.1007/s13762-021-03526-5

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  • DOI: https://doi.org/10.1007/s13762-021-03526-5

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