Cyanobacteria blooms in source waters have become a worldwide issue for drinking water production. UV-activated persulfate (UV/PS) technology was firstly applied to remove cultivated Microcystis aeruginosa (M. aeruginosa) in bench scale. The presence of persulfate significantly enhanced both cytoclasis and algal organic matter mineralization compared with UV-C inactivation alone. Around 98.2% of algal cells were removed after UV/PS process treatment for 2 h at a dosage of PS being 1500 mg/L (approximately 6 mM). Both sulfate and hydroxyl radicals were proven to contribute to the removal of algae and the loss of cell integrity. The cultivated M. aeruginosa in death growth phase were found to be more vulnerable to UV/PS treatment than those growing in log phase, thus a significant lower dosage of PS is needed to achieve the desired removal efficiency. This study suggested a novel application of UV/PS process in the removal of algae in source waters due to the high degradation efficiency of both algal cells and their derived organic matter.@en

The performance of UV-activated persulfate (UV/PS) technology as preoxidation process to enhanceMicrocystis aeruginosa removal by subsequent coagulation-sedimentation was firstly evaluated. Theresults demonstrate that UV/PS preoxidation could successfully promote coagulation of algae cellsthrough the effective neutralization of zeta potential, which was caused by the changes of cell mor-phology, size distribution and surface properties after simultaneous UV irradiation and formed reactivespecies (i.e. SO4•−and HO•) oxidation. Since excessive oxidation would cause cell rupture along withthe release of organics, which could deteriorate coagulation efficiency, optimal PS dose (60 mg/L) andUV dose (375 mJ/cm2) were proposed to exist in this study. The concentrations of extracellular algal∗@en

We report herein the use of ferric iron (Fe 3 + ) and sulfite (SO 3 2 −) to activate persulfate (S 2 O 8 2 −). Decolorization and mineralization of reactive Brilliant Red X-3B (a model azo dye) by an Fe(III)/sulfite/persulfate triple system have been investigated in aqueous solutions. Initial pH and dis- solved oxygen are important factors influencing X-3B decolorization in this system. The rapid decoloriza- tion process occurred in 30 min and about 85% of X-3B was decolorized in this triple system at initial pH 6.0. Moreover, about 66.4% of the TOC was removed through reaction for 36 h. The generation of SO 4 •−and HO •were identified through radical quenching experiments and by electron spin resonance (ESR), which contributed to 61.1% and 28.9% of the oxidation process. Degradation products of X-3B were iden- tified by LC-ESI-MS, and the degradation pathway was proposed. Furthermore, other organic pollutants, such as Orange II, metoprolol, imipramine, naproxen, estradiol, and amitriptyline, could also be efficiently degraded in this triple system. The results of the present work suggest that the Fe(III)/sulfite/persulfate triple system can be used for the rapid decolorization and partial mineralization of dyeing wastewater at near-neutral pH values.@en

A novel advanced oxidation process, combined zero-valent iron and sulfite (Fe0/sulfite) system containing oxygen, was firstly developed to efficiently degrade organic pollutants at weak acidic and neutral conditions by selecting X-3B as a target compound. The removal of X-3B was attributed to the formed reactive radicals, such as SO4 -, SO5 - and HO[rad], in the Fe0/sulfite system, and SO4 - was evidenced as the principal reactive species. The quite low removal efficiency of X-3B (less than 5%) after reaction for 90 min with purging nitrogen gas suggests oxygen to be an essential factor for producing SO4 - in the system. Optimal dosages of Fe0 and sulfite were suggested to be 0.5 mM and 1.0 mM, respectively, in the system as both the two chemicals would scavenge the reactive radicals at overdosing. The presence of 2 mM bicarbonate significantly inhibited the removal of X-3B from 74.1% to 37.5% in the system. Halide ions inhibited the removal of X-3B following a trend that Cl− <Br− <I−. HSO3 −, being effective in complexion of Fe(II) and transferring Fe(III) to Fe(II), is the main species during pHs 4–6, which results in the good reuse of Fe0 and the highest removal efficiency of X-3B at weak acidic condition. Fe0/sulfite system was also evidenced to be effective in the treatment of actual textile effluents along with improving biodegradability, and the removal of nitrobenzene, methylparaben, bisphenol A, imipramine and amitriptyline. Overall, this study provided a cheap and easy operational advanced oxidation process in treatment of aqueous organic pollutants.@en

A novel advanced oxidation process, combined zero-valent iron and sulfite (Fe0/sulfite) system containing oxygen, was firstly developed to efficiently degrade organic pollutants at weak acidic and neutral conditions by selecting X-3B as a target compound. The removal of X-3B was attributed to the formed reactive radicals, such as SO4 -, SO5 - and HO[rad], in the Fe0/sulfite system, and SO4 - was evidenced as the principal reactive species. The quite low removal efficiency of X-3B (less than 5%) after reaction for 90 min with purging nitrogen gas suggests oxygen to be an essential factor for producing SO4 - in the system. Optimal dosages of Fe0 and sulfite were suggested to be 0.5 mM and 1.0 mM, respectively, in the system as both the two chemicals would scavenge the reactive radicals at overdosing. The presence of 2 mM bicarbonate significantly inhibited the removal of X-3B from 74.1% to 37.5% in the system. Halide ions inhibited the removal of X-3B following a trend that Cl− <Br− <I−. HSO3 −, being effective in complexion of Fe(II) and transferring Fe(III) to Fe(II), is the main species during pHs 4–6, which results in the good reuse of Fe0 and the highest removal efficiency of X-3B at weak acidic condition. Fe0/sulfite system was also evidenced to be effective in the treatment of actual textile effluents along with improving biodegradability, and the removal of nitrobenzene, methylparaben, bisphenol A, imipramine and amitriptyline. Overall, this study provided a cheap and easy operational advanced oxidation process in treatment of aqueous organic pollutants.@en