4.8 Article

Bromate formation in bromide-containing water through the cobalt-mediated activation of peroxymonosulfate

Journal

WATER RESEARCH
Volume 83, Issue -, Pages 132-140

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2015.06.019

Keywords

Bromate; Oxidation by-products; Advanced oxidation processes; Sulfate radicals; Transition metals; Water treatment

Funding

  1. Hong Kong's Research Grants Council [618312]
  2. National Natural Science Foundation of China [51378515, 51108117]
  3. Fundamental Research Funds for the Central Universities [131gjc11]

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Bromate formation in bromide-containing water through the cobalt (Co)-mediated activation of peroxymonosulfate (PMS) was investigated. Increasing the PMS dosage and the cobalt dosage increased the formation of bromate and bromate yields of up to 100% were recorded under the test conditions. The bromate yield increased to a maximum as the pH rose from 2.7 to 6 before decreasing by over 90% as the pH rose further from 6 to above 9. The bromate formation is a two-step process involving free bromine as a key intermediate and bromate as the final product. In the first step, apart from the known oxidation of bromide to free bromine and of free bromine to bromate by sulfate radicals (SO4 center dot-), Co(sIII) produced from the oxidation of Co(II) by PMS and SO4 center dot- also oxidizes bromide to free bromine. The contribution of Co(III) to the bromate formation was verified with the addition of methanol and EDTA, a radical scavenger and a Co(III) ligand, respectively. In the presence of methanol, free bromine formation increased with increasing Co(II) dosage but no bromate was detected, indicating that Co(III) oxidized bromide to form free bromine but not bromate. In the presence of both EDTA an(d) methanol, no free bromine or bromate was detected, as Co(III) was stabilized by EDTA to form the Co(III)EDTA(-) complex, which could not oxidize bromide. Mathematical simulation further suggested that Co(III) outweighed SO4 center dot- to oxidize bromide to free bromine. On the other hand, SO4 center dot- is essential for the oxidation of free bromine to bromate in the second step. In real water, the presence of NOM significantly decreased the bromate formation but caused the brominated organic DBP formation with high quantity. This is the first study to demonstrate the significant bromate formation in the Co/PMS system and the substantial contribution of Co(III) to the formation. (C) 2015 Elsevier Ltd. All rights reserved.

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