4.5 Article

Performance of A Combination Process of UV/H2O2/Micro-Aeration for Oxidation of Dichloroacetic Acid in Drinking Water

期刊

CLEAN-SOIL AIR WATER
卷 37, 期 3, 页码 233-238

出版社

WILEY
DOI: 10.1002/clen.200900002

关键词

Drinking water; Dichloroacetic acid; UV/H2O2/micro-aeration process; Hydroxyl radical; Reaction kinetics; Cost analysis

资金

  1. national 11th Five-year Plan' science and technology support [2006BAJ08B06, 2007BAC26B03, 2006BAJ08B02]
  2. Shanghai Science & Technology Commission Key Scientific & Technological project [072312001]

向作者/读者索取更多资源

The decomposition of dichloroacetic acid (DCAA) in water using a UV/H2O2/micro-aeration process was investigated in this paper. DCAA cannot be removed by UV radiation, H2O2 oxidation or micro-aeration alone, while UV/H2O2/micro-aeration combination processes have proved effective and can degrade this compound completely. With initial concentrations of about 110 mu g/L, more than 95.1% of DCAA can be removed in 180 min under UV intensity of 1048.7 mu W/cm(2), H2O2 dosage of 30 mg/L and micro-aeration flow rate of 2 L/min. However, more than 30 mu g/L of DCAA was left after 180 min by UV/H2O2 combination process without micro-aeration with the same UV intensity and H2O2 dosage. The effects of applied UV radiation intensity, H2O2 dose, initial DCAA concentration and pH on the degradation of DCAA have been examined in this study. Degradation mechanisms of DCAA with hydroxyl radical oxidation have been discussed. The removal irate of DCAA was sensitive to operational parameters. There was a linear relationship between rate constant k and UV intensity and initial H2O2 concentration, which indicated that a higher removal capacity can be achieved by improvement of both factors. A newly found nitrogenous disinfection by-product (N-DBP)-DCAcAm, which has the potential to form DCAA, was easier to remove than DCAA by UV/H2O2 and UV/H2O2/micro-aeration processes. Finally, a preliminary cost comparison revealed that the UV/H2O2/micro-aeration process was more cost-effective than the UV/H2O2 process in the removal of DCAA from drinking water.

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