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Advanced oxidation process

About: Advanced oxidation process is a research topic. Over the lifetime, 2383 publications have been published within this topic receiving 68600 citations.


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Journal ArticleDOI
TL;DR: Recommendations regarding the use of the EEO concept, including the upscaling of laboratory results, were derived from an extensive analysis of studies reported in the peer-reviewed literature enabling a critical comparison of various established and emerging AOPs based on electrical energy per order (EEO) values.

1,677 citations

Journal ArticleDOI
TL;DR: This Critical Review comparatively examines the activation mechanisms of peroxymonosulfate and peroxydisulfates and the formation pathways of oxidizing species and the impacts of water parameters and constituents such as pH, background organic matter, halide, phosphate, and carbonate on persulfate-driven chemistry.
Abstract: Reports that promote persulfate-based advanced oxidation process (AOP) as a viable alternative to hydrogen peroxide-based processes have been rapidly accumulating in recent water treatment literature. Various strategies to activate peroxide bonds in persulfate precursors have been proposed and the capacity to degrade a wide range of organic pollutants has been demonstrated. Compared to traditional AOPs in which hydroxyl radical serves as the main oxidant, persulfate-based AOPs have been claimed to involve different in situ generated oxidants such as sulfate radical and singlet oxygen as well as nonradical oxidation pathways. However, there exist controversial observations and interpretations around some of these claims, challenging robust scientific progress of this technology toward practical use. This Critical Review comparatively examines the activation mechanisms of peroxymonosulfate and peroxydisulfate and the formation pathways of oxidizing species. Properties of the main oxidizing species are scrutinized and the role of singlet oxygen is debated. In addition, the impacts of water parameters and constituents such as pH, background organic matter, halide, phosphate, and carbonate on persulfate-driven chemistry are discussed. The opportunity for niche applications is also presented, emphasizing the need for parallel efforts to remove currently prevalent knowledge roadblocks.

1,412 citations

Journal ArticleDOI
TL;DR: The advantage of Co/PMS compared to the traditional Fenton Reagent is attributed primarily to the oxidizing strength of the radicals formed, since sulfate radicals are stronger oxidants than hydroxyl and the thermodynamics of the transition-metal-oxidant coupling.
Abstract: A highly efficient advanced oxidation process for the destruction of organic contaminants in water is reported. The technology is based on the cobalt-mediated decomposition of peroxymonosulfate that leads to the formation of very strong oxidizing species (sulfate radicals) in the aqueous phase. The system is a modification of the Fenton Reagent, since an oxidant is coupled with a transition metal in a similar manner. Sulfate radicals were identified with quenching studies using specific alcohols. The study was primarily focused on comparing the cobalt/peroxymonosulfate (Co/PMS) reagent with the traditional Fenton Reagent [Fe(II)/H2O2] in the dark, at the pH range 2.0-9.0 with and without the presence of buffers such as phosphate and carbonate. Three model contaminants that show diversity in structure were tested: 2,4-dichlorophenol, atrazine, and naphthalene. Cobalt/peroxymonosulfate was consistently proven to be more efficient than the Fenton Reagent for the degradation of 2,4-dichlorophenol and atrazine, at all the conditions tested. At high pH values, where the efficiency of the Fenton Reagent was diminished, the reactivity of the Co/PMS system was sustained at high values. When naphthalene was treated with the two oxidizing systems in comparison, the Fenton Reagent demonstrated higher degradation efficiencies than cobalt/peroxymonosulfate at acidic pH, but, at higher pH (neutral), the latter was proven much more effective. The extent of mineralization, as total organic carbon removed,was also monitored, and again the Co/PMS reagent demonstrated higher efficiencies than the Fenton Reagent. Cobalt showed true catalytic activity in the overall process, since extremely low concentrations (in the range of microg/L) were sufficient for the decomposition of the oxidant and thus the radical generation. The advantage of Co/PMS compared to the traditional Fenton Reagent is attributed primarily to the oxidizing strength of the radicals formed, since sulfate radicals are stronger oxidants than hydroxyl and the thermodynamics of the transition-metal-oxidant coupling.

1,390 citations

Journal ArticleDOI
TL;DR: In this paper, the authors present a critical review of novel achievements in the modification of TiO2 photocatalytic systems aimed at achieving complete mineralization of organic dyes and efficient utilization of visible and/or solar light.
Abstract: Organic dyes are one of the largest groups of pollutants released into wastewaters from textile and other industrial processes. Because of potential toxicity of the dyes and their visibility in surface waters, removal and degradation of organic dyes have been a matter of considerable interest. A wide range of methods have been developed, amongst which the heterogeneous photocatalysis involving titanium dioxide (TiO2) appears to be the most promising technology. This paper presents a critical review of novel achievements in the modification of TiO2 photocatalytic systems aimed at: enhanced TiO2 photocatalytic efficiency; complete mineralization of organic dyes; efficient utilization of visible and/or solar light; stability and reproducibility of the modified TiO2; recycle and reuse in real wastewater treatment.

964 citations

Journal ArticleDOI
TL;DR: An overview of the findings from recent studies, which have applied AOPs to degrade pharmaceutical compounds, and a discussion that links various factors of TiO2-mediated photocatalytic treatment to its effectiveness in degrading pharmaceutical residues are included.

781 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202358
2022149
2021265
2020252
2019209
2018184