4.7 Article

Insights on free radical oxidation and in-situ coagulation in PMS/Fe(II) process for the removal of algogenic organic matter precursors

期刊

CHEMICAL ENGINEERING JOURNAL
卷 446, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136986

关键词

Sulfate radical; Natural organic matter; Oxidation; Coagulation; Disinfection byproducts

资金

  1. Ministry of Science and Technology of Taiwan [MOST 108-2221-E-009-075-MY3]

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This study examines a novel hybrid oxidation-coagulation PMS/Fe(II) process for effective removal of algogenic organic matter (AOM)-derived disinfection byproduct (DBP) precursors. The results show that under neutral pH conditions, PMS/Fe(II) is able to significantly remove dissolved organic carbon (DOC) and AOM-fluorescent components, as well as effectively degrade AOM-derived DBPs. This research fills the knowledge gap in the study of PMS/Fe(II) and highlights its potential as an alternative for sustainable water treatment.
Algogenic organic matter (AOM) is unwelcome in raw water as it is a major precursor of carcinogenic disinfection byproducts (DBPs). Unfortunately, conventional coagulation is ineffective against AOM, raising the need for a better alternative for AOM and AOM-derived-DBP removal. This study examined the effectiveness and underlying mechanisms of a novel hybrid oxidation-coagulation PMS/Fe(II) process for effective removal of AOM-DBP precursors. Under optimal conditions, only PMS/Fe(II) or combined PMS/Fe(II) with Al/Fe coagulation removed significant amounts of dissolved organic carbon (DOC) (45-52%) and 50-65% AOM-fluorescent components. These values were much better than conventional Al/Fe coagulations (e.g. 15-19% DOC and < 40% fluorescent components at [Fe3+] = [Al3+] = 100 mu M, pH 5.5-6). AOM-derived DBPs were thus significantly eliminated (> 80% of total DBP levels) after PMS/Fe(II) related processes, which markedly outperformed Al/Fe coagulations (of only 20-30%). PMS/Fe(II) presented its strongest oxidative ability at pH 4 (with [SO4 center dot(-)] = 2.16 x 10(-12 )and [center dot OH] = 1.26 x 10(-12) M), rather than at pH 7 or 9. Acidic conditions rapidly increased oxidized carbon contents (e.g. %ketone + %carbonyl increased from 10% to 25%) in AOM structure after PMS/Fe(II) treatment. By contrast, pH 7 and 9 were the favorable conditions for in-situ coagulation with faster floc aggregation and growth rates than pH 4. Regardless, PMS/Fe(II) process performed best in effectively removing AOM-DBP precursor only under neutral pH of 6-7 by gaining the synergistic benefits of free radical oxidation and in-situ coagulation. Our findings are a significant contribution to filling the knowledge gap in the study of PMS/ Fe(II) and highlight the possibilities of this novel hybrid process as an alternative to conventional coagulation for sustainable water treatment.

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