| Literature DB >> 25433979 |
Brooke K Mayer1, Erin Daugherty2, Morteza Abbaszadegan2.
Abstract
Advanced oxidation processes (AOPs) are gaining traction as they offer mineralization potential rather than transferring contaminants between media. However, AOPs operated with limited energy and/or chemical inputs can exacerbate disinfection byproduct (DBP) formation, even as precursors such as dissolved organic carbon, UV254, and specific UV absorbance (SUVA) decrease. This study examined the relationship between DBP precursors and formation using TiO2 photocatalysis experiments, external AOP and non-AOP data, and predictive DBP models. The top-performing indicator, SUVA, generally correlated positively with trihalomethanes and haloacetic acids, but limited-energy photocatalysis yielded contrasting negative correlations. The accuracy of predicted DBP values from models based on bulk parameters was generally poor, regardless of use and extent of AOP treatment and type of source water. Though performance improved for scenarios bounded by conditions used in model development, only 0.5% of the model/dataset pairings satisfied all measured parameter boundary conditions, thereby introducing skepticism toward model usefulness. Study findings suggest that caution should be employed when using bulk indicators and/or models as a metric for AOP mitigation of DBP formation potential, particularly for limited-energy/chemical inputs.Entities:
Keywords: Advanced oxidation; Disinfection byproduct; Haloacetic acid; Model; Titanium dioxide photocatalysis; Trihalomethane
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Year: 2014 PMID: 25433979 DOI: 10.1016/j.chemosphere.2014.10.070
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086