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Heterogeneous catalytic ozonation (HCO) is a promising advanced oxidation process (AOP) that can effectively degrade recalcitrant organic pollutants. While research efforts have been mainly devoted to the development of different catalysts to enhance the process efficiency, more studies are needed to investigate and address the other challenge faced by AOPs, i.e. generation of harmful byproducts. Bromate is the major inorganic byproduct of concern when ozone is involved. While most studies have reported less bromate formation in HCO than ozonation alone, the effects of catalysts depend on their interaction with O 3 and the dominant bromate formation pathway (direct O 3 oxidation vs. indirect ˙OH oxidation) in the system. Production of H 2 O 2 and cyclic redox reactions on the catalyst surface can also reduce different Br species leading to a lower bromate yield. Generation of organic byproducts (OBPs; e.g. aldehydes, keto-acids, carboxylic acids) in HCO depends on the reactivity of precursors ( e.g. dissolved organic matter/DOM) and OBPs with O 3 /˙OH, interactions between DOM/OBPs and catalysts, characteristics of DOM, and O 3 dose. HCO generally increased the removal of dissolved organic carbon (DOC) and the biodegradability of the bulk organics. HCO treatment may also decrease the formation potential of some disinfection byproducts (DBPs) such as trihalomethanes (THMs) and haloacetic acids (HAAs) but may increase the brominated species of the DBPs and also the formation potential of haloacetonitrile (HAN) under certain conditions. This review discusses the current status of studies on both organic and inorganic byproduct formation in HCO as well as transformation of bulk organics and the effects on DBP formation in the downstream disinfection process, and further provides recommendations for future research and development. A standardized experimental protocol and rigorous experimental design is important to deepen our understanding and gain insights on the byproduct formation in HCO from different studies collectively.
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Sulfite-activated ferrate for water reuse applications
Ferrate is a promising, emerging water treatment technology. However, there has been limited research on the application of ferrate in a water reuse paradigm. Recent literature has shown that ferrate oxidation of target contaminants could be improved by “activation” with the addition of reductants or acid. This study examined the impact of sulfite-activated ferrate in laboratory water matrix and spiked municipal wastewater effluents with the goal of transforming organic contaminants of concern (e.g., 1,4-dioxane) and inactivating pathogenic organisms. Additionally, the formation of brominated disinfection byproducts by activated ferrate were examined and a proposed reaction pathway for byproduct formation is presented. In particular, the relative importance of reaction intermediates is discussed. This represents the first activated ferrate study to examine 1,4-dioxane transformation, disinfection, and brominated byproduct formation. Results presented show that the sub-stoichiometric ([Sulfite]:[Ferrate] = 0.5) activated ferrate treatment approach can oxidize recalcitrant contaminants by >50%, achieve >4-log inactivation of pathogens, and have relatively limited generation of brominated byproducts. However, stoichiometrically excessive ([Sulfite]:[Ferrate] = 4.0) activation showed decreased performance with decreased disinfection and increased risk of by-product formation. In general, our results indicate that sub-stoichiometric sulfite-activated ferrate seems a viable alternative technology for various modes of water reuse treatment.
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- Award ID(s):
- 2046383
- PAR ID:
- 10499045
- Publisher / Repository:
- IWA
- Date Published:
- Journal Name:
- Water Research
- Volume:
- 216
- Issue:
- C
- ISSN:
- 0043-1354
- Page Range / eLocation ID:
- 118317
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1016/j.watres.2022.118317
