4.7 Article

Formation of halogenated disinfection by-products in cobalt-catalyzed peroxymonosulfate oxidation processes in the presence of halides

期刊

CHEMOSPHERE
卷 154, 期 -, 页码 613-619

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2016.04.025

关键词

Sulfate radical; Peroxymonosulfate; Bromide; Chloride; Disinfection by-products

资金

  1. Natural Science Foundation of China [51578294]
  2. Fundamental Research Funds for the Central Universities [KYZ201407]
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institute

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Sulfate radicals (SO4 center dot-) generated by activation of peroxymonosulfate (PMS) and persulfate (PS) are highly oxidative and applied to degrade various organic pollutants. This research was designed to investigate formation of halogenated by-products in Co2+ activated PMS process in the presence of halides and natural organic matter (NOM). It was revealed that no halogenated by-products were detected in the presence of Cl- while 189 mu g/L bromoform and 100.7 mu g/L dibromoacetic acid (DBAA) were found after 120 h when 2 mg/L NOM, 0.1 mM Br-, 1.0 mM PMS, and 5 mu L Co2+ were present initially. These products are known as disinfection by-products (DBPs) since they are formed in water disinfection processes. Formation of DBPs was even more significant in the absence of Co2+. The data indicate that both PMS and SO4 center dot- can transform Br- to reactive bromine species which react with NOM to form halogenated by-products. Less DBP formation in Co2+-PMS systems was due to the further destruction of DBPs by SO4 center dot-. More DBPs species including chlorinated ones were detected in the presence of both Cl- and Br-. However, more brominated species produced than chlorinate ones generally. The total DBP yield decreased with the increase of Cl- content when total halides kept constant. This is one of the few studies that demonstrate the formation of halogenated DBPs in Co2+/PMS reaction systems, which should be taken into consideration in the application of SO4 center dot- based oxidation technologies. (C) 2016 Elsevier Ltd. All rights reserved.

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