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Effect of photochemical advanced oxidation processes on the formation potential of emerging disinfection by-products in groundwater from part of the Pannonian Basin
Author(s) -
Jelena Molnar Jazić,
Jasmina Agbaba,
Aleksandra Tubić,
Malcolm Watson,
Tajana Simetić,
Dejan Krčmar,
Božo Dalmacija
Publication year - 2018
Publication title -
water science and technology water supply
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.318
H-Index - 39
eISSN - 1607-0798
pISSN - 1606-9749
DOI - 10.2166/ws.2018.196
Subject(s) - chemistry , ozone , bromide , environmental chemistry , photochemistry , hydroxyl radical , nuclear chemistry , antioxidant , inorganic chemistry , biochemistry , organic chemistry
This study evaluates the effect of photochemical advanced oxidation processes (AOPs) (O3/UV, H2O2/UV and O3/H2O2/UV) on the formation potential (FP) of emerging disinfection by-products including nitrogenous by-products (N-DBPs) and haloketones (HKs) in groundwater from part of the Pannonian Basin (AP Vojvodina, Republic of Serbia). Among the N-DBPs, the haloacetonitrile (HAN) precursor contents were 9.83 ± 0.59 μg/L while precursors of halonitromethanes, particularly trichloronitromethane (TCNM) were not detected. Similarly, precursors of HKs as carbonaceous DBPs were also not detected in raw water. Ozonation alone and the H2O2/UV process with a lower UV dose maximally decomposed HAN precursors (about 70%) while during O3-based AOPs, HANFP varied significantly. Application of UV photolysis and H2O2/UV processes with increasing UV dose doubled the HANFP. Ozone alone, O3/UV and H2O2/UV slightly increased HK formation potential, particularly 1,1-dichloro-2-propanone FP (0.93 ± 0.21 to 2.01 ± 0.37 μg/L). None of the investigated treatments influenced the formation of TCNM precursors. The effect of the applied treatments on bromide incorporation was most evident for HANs.

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