Performance of microbubble ozonation on treated tropical peat water: Effects on THM4 and HAA5 precursor formation
Muammar Qadafi1, Suprihanto Notodarmojo2, Yuniati Zevi2
1Environmental Engineering Program, Institut Teknologi Bandung, Jalan Ganesha No. 10, Bandung, 40132, Indonesia.
Abstract:
The hydrophobicity properties of dissolved organic matter (DOM) found in tropical peat water has an impact on the formation of carcinogenic DBPs such as trihalomethanes-4 (THM4) and haloacetic acids-5 (HAA5). This study was conducted to determine the effect of microbubble ozonation on changes in DOM fraction and its effect on the formation of THM4 and HAA5. Alum coagulation and activated carbon adsorption were carried out to reduce the DOM concentration before microbubble ozonation. Microbubble ozonation was carried out at acidic (pH 5.5), neutral (pH 7) and alkaline (pH 8.5) conditions to determine the effect of pH. Coagulation and adsorption of activated carbon were successful in reducing the presence of the hydrophobic acid fraction (HPOA) in peat water completely, but the transphilic (TPH), charged hydrophilic (HPIC) and neutral hydrophilic (HPIN) fractions remained in the water. Microbubble ozonation succeeded in decreasing the presence of TPH fraction but increased the formation of HPIC and HPIN. The degradation of the TPH fraction resulted in reduced formation of chlorinated THM4 and HAA5 (C-THM4 and C-HAA5). On the other hand, the formation of HPIC and HPIN fractions increased the formation of brominated THM4 and HAA5 (B-THM4 and B-HAA5) after the final chlorination process.
More Related Videos
09:38Single-throughput Complementary High-resolution Analytical Techniques for Characterizing Complex Natural Organic Matter Mixtures
Published on: January 7, 2019
09:49Use of a Battery of Chemical and Ecotoxicological Methods for the Assessment of the Efficacy of Wastewater Treatment Processes to Remove Estrogenic Potency
Published on: September 11, 2016
Related Concept Videos
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Hydroboration-Oxidation of Alkenes
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
