Degradation of contaminants of emerging concern by UV/H2O2 for water reuse: Kinetics, mechanisms, and cytotoxicity analysis.

[1]  W. Mitch,et al.  Pilot-scale evaluation of oxidant speciation, 1,4-dioxane degradation and disinfection byproduct formation during UV/hydrogen peroxide, UV/free chlorine and UV/chloramines advanced oxidation process treatment for potable reuse. , 2019, Water research.

[2]  W. Mitch,et al.  Comparison of Toxicity-Weighted Disinfection Byproduct Concentrations in Potable Reuse Waters and Conventional Drinking Waters as a New Approach to Assessing the Quality of Advanced Treatment Train Waters. , 2019, Environmental science & technology.

[3]  Joon-Wun Kang,et al.  The Impact of Natural Variation of OH Radical Demand of Drinking Water Sources on the Optimum Operation of the UV/H2O2 Process. , 2019, Environmental science & technology.

[4]  D. Dionysiou,et al.  Hydrothermal synthesis of photoactive nitrogen- and boron- codoped TiO2 nanoparticles for the treatment of bisphenol A in wastewater: Synthesis, photocatalytic activity, degradation byproducts and reaction pathways , 2019, Applied Catalysis B: Environmental.

[5]  J. Crittenden,et al.  Destruction of phenicol antibiotics using the UV/H2O2 process: Kinetics, byproducts, toxicity evaluation and trichloromethane formation potential , 2018, Chemical Engineering Journal.

[6]  S. Richardson,et al.  Effects of HCO3- on Degradation of Toxic Contaminants of Emerging Concern by UV/NO3. , 2018, Environmental science & technology.

[7]  E. G. Xu,et al.  Cyto- and geno-toxicity of 1,4-dioxane and its transformation products during ultraviolet-driven advanced oxidation processes , 2018 .

[8]  Young-Min Kang,et al.  Effect of nitrate, carbonate/bicarbonate, humic acid, and H2O2 on the kinetics and degradation mechanism of Bisphenol-A during UV photolysis. , 2018, Chemosphere.

[9]  Vincenzo Naddeo,et al.  Photolysis of Mono- and Dichloramines in UV/Hydrogen Peroxide: Effects on 1,4-Dioxane Removal and Relevance in Water Reuse. , 2018, Environmental science & technology.

[10]  V. Sharma,et al.  Degradation of atrazine by ZnxCu1−xFe2O4 nanomaterial-catalyzed sulfite under UV–vis light irradiation: Green strategy to generate SO4− , 2018 .

[11]  M. Satari,et al.  The photochemical decomposition and detoxification of bisphenol A in the VUV/H2O2 process: Degradation, mineralization, and cytotoxicity assessment , 2018 .

[12]  Serena H. Chen,et al.  Comparing the UV/Monochloramine and UV/Free Chlorine Advanced Oxidation Processes (AOPs) to the UV/Hydrogen Peroxide AOP Under Scenarios Relevant to Potable Reuse. , 2017, Environmental science & technology.

[13]  L. Nghiem,et al.  Photolysis and UV/H2O2 of diclofenac, sulfamethoxazole, carbamazepine, and trimethoprim: Identification of their major degradation products by ESI–LC–MS and assessment of the toxicity of reaction mixtures , 2017 .

[14]  Yujiao Long,et al.  Influencing factors and chlorinated byproducts in electrochemical oxidation of bisphenol A with boron-doped diamond anodes , 2017 .

[15]  A. Dhara,et al.  Radical pathways and O2 participation in benzyl alcohol oxidation, and catechol and o-aminophenol oxidase activity studies with novel zinc complexes: an experimental and theoretical investigation , 2016 .

[16]  F. Meng,et al.  Roles of reactive chlorine species in trimethoprim degradation in the UV/chlorine process: Kinetics and transformation pathways. , 2016, Water research.

[17]  M. Gamal El-Din,et al.  Pilot-scale UV/H2O2 advanced oxidation process for municipal reuse water: Assessing micropollutant degradation and estrogenic impacts on goldfish (Carassius auratus L.). , 2016, Water research.

[18]  B. Truffer,et al.  The thorny road to technology legitimation — Institutional work for potable water reuse in California , 2016 .

[19]  S. Gligorovski,et al.  Environmental Implications of Hydroxyl Radicals ((•)OH). , 2015, Chemical reviews.

[20]  R. L. Romero,et al.  Modeling of degradation kinetic and toxicity evaluation of herbicides mixtures in water using the UV/H2O2 process. , 2015, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[21]  M. Guida,et al.  S2O8(2-)/UV-C and H2O2/UV-C treatment of Bisphenol A: assessment of toxicity, estrogenic activity, degradation products and results in real water. , 2015, Chemosphere.

[22]  K. McNeill,et al.  On the use of hydroxyl radical kinetics to assess the number-average molecular weight of dissolved organic matter. , 2014, Environmental science & technology.

[23]  R. Nogueira,et al.  Aquatic toxicity of dyes before and after photo-Fenton treatment. , 2014, Journal of hazardous materials.

[24]  D. Dionysiou,et al.  Degradation mechanism of cyanobacterial toxin cylindrospermopsin by hydroxyl radicals in homogeneous UV/H₂O₂ process. , 2014, Environmental science & technology.

[25]  Rolf Altenburger,et al.  Benchmarking organic micropollutants in wastewater, recycled water and drinking water with in vitro bioassays. , 2014, Environmental science & technology.

[26]  Guiying Li,et al.  Mechanism, kinetics and toxicity assessment of OH-initiated transformation of triclosan in aquatic environments. , 2014, Water research.

[27]  S. Snyder,et al.  An Adaptive, Comprehensive Monitoring Strategy for Chemicals of Emerging Concern (CECs) in California's Aquatic Ecosystems , 2014, Integrated environmental assessment and management.

[28]  B. Wols,et al.  Degradation of 40 selected pharmaceuticals by UV/H2O2. , 2013, Water research.

[29]  R. Murphy,et al.  Mechanism of Formation of the Major Estradiol Product Ions Following Collisional Activation of the Molecular Anion in a Tandem Quadrupole Mass Spectrometer , 2013, Journal of The American Society for Mass Spectrometry.

[30]  W. Arnold,et al.  Experimental and theoretical insights into the involvement of radicals in triclosan phototransformation. , 2013, Environmental science & technology.

[31]  J. Casas,et al.  Triclosan breakdown by Fenton-like oxidation , 2012 .

[32]  D. Dionysiou,et al.  Efficient removal of microcystin-LR by UV-C/H₂O₂ in synthetic and natural water samples. , 2012, Water research.

[33]  L. Eriksson,et al.  Photodegradation mechanism of the common non-steroid anti-inflammatory drug diclofenac and its carbazole photoproduct. , 2009, Physical chemistry chemical physics : PCCP.

[34]  T. Schmidt,et al.  Oxidation of diclofenac with ozone in aqueous solution. , 2008, Environmental science & technology.

[35]  A. Fernández-Alba,et al.  Photo-fenton degradation of diclofenac: identification of main intermediates and degradation pathway. , 2005, Environmental science & technology.

[36]  A. Fernández-Alba,et al.  Evidence of 2,7/2,8-dibenzodichloro-p-dioxin as a photodegradation product of triclosan in water and wastewater samples , 2004 .

[37]  R. Andreozzi,et al.  Advanced oxidation of the pharmaceutical drug diclofenac with UV/H2O2 and ozone. , 2004, Water research.

[38]  W. Arnold,et al.  Photochemical conversion of triclosan to 2,8-dichlorodibenzo-p-dioxin in aqueous solution , 2003 .

[39]  M. Denison,et al.  Recombinant cell bioassays for endocrine disruptors: development of a stably transfected human ovarian cell line for the detection of estrogenic and anti-estrogenic chemicals. , 2000, In vitro & molecular toxicology.

[40]  G. Ossenkoppele,et al.  A tetrazolium-based colorimetric MTT assay to quantitate human monocyte mediated cytotoxicity against leukemic cells from cell lines and patients with acute myeloid leukemia. , 1994, Journal of immunological methods.