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Author

Siyang Yue

Other affiliations: Harbin Institute of Technology
Bio: Siyang Yue is an academic researcher from Huazhong University of Science and Technology. The author has contributed to research in topics: Peracetic acid & Chloride. The author has an hindex of 7, co-authored 13 publications receiving 814 citations. Previous affiliations of Siyang Yue include Harbin Institute of Technology.

Papers
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Journal ArticleDOI
TL;DR: The results showed that both 2-MIB and geosmin could be degraded effectively using this process and were likely to be the main radical scavengers in natural waters when using UV/persulfate process to control 2- MIB and Geosmin.

451 citations

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TL;DR: The present study may provide a promising alternative for complete dehalogenation of most HOCs and reductive detoxification of numerous toxicants.
Abstract: Most halogenated organic compounds (HOCs) are toxic and persistent, and their efficient destruction is currently a challenge. Here, we proposed a sulfite/UV (253.7 nm) process to eliminate HOCs. Monochloroacetic acid (MCAA) was selected as the target compound and was degraded rapidly in the sulfite/UV process. The degradation kinetics were accelerated proportionally to the increased sulfite concentration, while the significant enhancement by increasing pH only occurred in a pH range of 6.0–8.7. The degradation proceeded via a reductive dechlorination mechanism induced by hydrated electron (eaq–), and complete dechlorination was readily achieved with almost all the chlorine atoms in MCAA released as chloride ions. Mass balance (C and Cl) studies showed that acetate, succinate, sulfoacetate, and chloride ions were the major products, and a degradation pathway was proposed. The dual roles of pH were not only to regulate the S(IV) species distribution but also to control the interconversion between eaq– and H...

220 citations

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TL;DR: The results suggest that permanganate is a better choice than ozone for controlling algae derived pollutants and disinfection byproducts after preozonation.
Abstract: Aqueous suspensions of Microcystis aeruginosa were preoxidized with either ozone or permanganate and then subjected to chlorination under conditions simulating drinking water purification. The impacts of the two oxidants on the algal cells and on the subsequent production of dissolved organic matter and disinfection byproducts were investigated. Preozonation dramatically increased disinfection byproduct formation during chlorination, especially the formation of haloaldehydes, haloacetonitriles, and halonitromethanes. Preoxidation with permanganate had much less effect on disinfection byproduct formation. Preozonation destroyed algal cell walls and cell membranes to release intracellular organic matter (IOM), and less than 2.0% integrated cells were left after preozonation with the dosage as low as 0.4 mg/L. Preoxidation with permanganate mainly released organic matter adsorbed on the cells' surface without causing any damage to the cells' integrity, so the increase in byproduct formation was much less. More organic nitrogen and lower molecular weight precursors were produced in a dissolved phase after preozonation than permanganate preoxidation, which contributes to the significant increase of disinfection byproducts after preozonation. The results suggest that permanganate is a better choice than ozone for controlling algae derived pollutants and disinfection byproducts.

216 citations

Journal ArticleDOI
Pengchao Xie1, Jun Ma1, Wei Liu1, Jing Zou1, Siyang Yue 
TL;DR: In this article, the authors evaluated the impact of pre-treatment of chlorinated disinfection byproducts (DBPs) on the formation of DBPs during subsequent chlorination of natural organic matter.

96 citations

Journal ArticleDOI
TL;DR: An effective and simple kinetic model is proposed to describe the degradation of organic pollutants in VUV system, by taking the •OH scavenging effects of formed organic intermediates as co-existing organic matter in whole and predicting its degradation kinetics under different conditions.

77 citations


Cited by
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Journal ArticleDOI
TL;DR: Sulfate radical-based advanced oxidation processes (AOPs) have received increasing attention in recent years due to their high capability and adaptability for the degradation of emerging contaminants as mentioned in this paper.

2,267 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

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TL;DR: In this paper, the authors provide an overview of various methods for analysis of persulfate decontamination and their analysis is often prone for interference by other matrix components and hampered by the low stability of peroxydisulfate and peroxymonosulfate in aqueous systems.

1,197 citations

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TL;DR: An extensive review of recently published experimental parameters and results for the destruction of organic compounds via activated persulfate is presented, and focus is placed on emerging methodologies and manipulation of traditional activation techniques.

978 citations

Journal ArticleDOI
TL;DR: Findings have important implications for the development of novel nonradical oxidation processes based on PMS, because 1O2 as a moderately reactive electrophile may suffer less interference from background organic matters compared with nonselective •OH and SO4•-.
Abstract: The reactions between peroxymonosulfate (PMS) and quinones were investigated for the first time in this work, where benzoquinone (BQ) was selected as a model quinone. It was demonstrated that BQ could efficiently activate PMS for the degradation of sulfamethoxazole (SMX; a frequently detected antibiotic in the environments), and the degradation rate increased with solution pH from 7 to 10. Interestingly, quenching studies suggested that neither hydroxyl radical (•OH) nor sulfate radical (SO4•–) was produced therein. Instead, the generation of singlet oxygen (1O2) was proved by using two chemical probes (i.e., 2,2,6,6-tetramethyl-4-piperidinol and 9,10-diphenylanthracene) with the appearance of 1O2 indicative products detected by electron paramagnetic resonance spectrometry and liquid chromatography mass spectrometry, respectively. A catalytic mechanism was proposed involving the formation of a dioxirane intermediate between PMS and BQ and the subsequent decomposition of this intermediate into 1O2. Accordi...

889 citations