4.2 Article

Identification of Oxidation Intermediates in Humic Acid Oxidation

Journal

OZONE-SCIENCE & ENGINEERING
Volume 40, Issue 2, Pages 93-104

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/01919512.2017.1392845

Keywords

Ozone; DBPs; Humic Acid; Intermediates; Ozone-UV; UV

Funding

  1. National Water Pollution Control and Major Projects of Science and Technology Management, China [2012ZX07403001]

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The effects of using ultraviolet irradiation (UV), ozone (O-3) and the combined O-3-UV advanced oxidation process (AOP) on humic acid (HA), which is regarded as the main disinfection by-products (DBPs) precursor, have been evaluated and compared. In particular, aromatic acids, short-chain aldehydes and carboxylic acids were measured. The purpose of this study was to determine the different classes and yields of oxidation intermediates, compare O-3, UV and O-3-UV for HA removal, as well as investigate the effects of O-3, irradiation time, UV intensity on the mineralization of HA. Based on that, the knowledge gap of DBPs generation was made up. The results showed that by UV irradiation and O-3 oxidation, HA broke down into smaller molecules that were more hydrophilic, namely formaldehyde, acetaldehyde, propaldehyde, butyraldehyde, glyoxal, methyl-glyoxal, formic, acetic, fumaric, benzoic, phthalic, protocatechuic and 3-hydroxybenzoic acids. Meanwhile, unsaturated conjugated double bonds in the structure of HA were destroyed, which lead to UV254 a slight decrease. Due to the synergistic effect of O-3-UV, DOC and UV254 significantly decreased and remained stable after the reaction of 10min, indicating that O-3-UV system had stronger potential of mineralization and lower nonselectivity. Besides, the kinds and concentration levels of the intermediates were obviously reduced with light intensity increasing. Hydroxyl radical ((OH)-O-.) could mineralize some organics that could not be mineralized by O-3.

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