An evaluation of fungal contamination and its relationship with PM levels in public transportation systems.

Transmission of fungi in the air and its impact on health are regarded as important public health issues. Bioaerosols play an important role in causing or exacerbating infectious diseases, acute toxic effects, allergies, and cardiopulmonary symptoms. As many people use the public transportation system daily, it is necessary to determine the type and manner of dispersal and abundance of airborne fungi in public transport places. Three public transportation systems including a bus station, a train station, and an airport in Ahvaz city (Iran) were examined. At each of these stations, the air samples were taken from inside and outside the hall stations, and in-vehicle. A bio-stage Anderson sampler was used by suctioning air and passing it over a Petri dish containing culture medium Sabouraud Dextrose Agar (SDA). Relative humidity (RH, %), temperature (T, ◦C), and mass concentration of particulate matter (PM1, PM2.5, and PM10, µg/m3) at the sampling points were measured. The highest concentration of airborne fungi was observed in the airport. The concentration of fungi in the ambient air was higher than that in the indoor air of halls and in-vehicle. In all sampling points, the ambient predominant airborne fungi were Cladosporium and Alternaria, while the indoor predominant airborne fungi were Cladosporium, Aspergillus, and Penicillium. The indoor to outdoor ratio showed that the fungi were of an external origin. Due to the influence of the ambient air on indoor air, it is recommended to use proper ventilation and enhance the hygiene level of vehicles in public transportation systems to reduce exposure to environmentally pathogenic bioaerosols.

Sequential treatment of landfill leachate by electrocoagulation/aeration, PMS/ZVI/UV and electro-Fenton: Performance, biodegradability and toxicity studies.

This study presents a systematic study on sequential treatment of highly resistant landfill leachate by electrocoagulation (EC)/aeration, sulfate radical advanced oxidation process (SR-AOP) and electro-Fenton (EF). In case of SR-AOP, peroxymonosulfate (PMS) catalyzed by zero valent iron (ZVI) and ultraviolet irradiation (UV) system was developed. Treatment process was optimized in respect to COD removal. Analysis of results revealed that sequential application of EC/aeration, PMS/ZVI/UV, and EF processes provide an extraordinary performance and meet the environmental regulations. The source of iron for EF process was provided from previous process reducing the cost of sequential process. Separately, EC/aeration (inlet COD = 4040 mg/L), PMS/ZVI/UV (inlet COD = 1560 mg/L), and EF (inlet COD = 471 mg/L) removed 61, 69 and 82% of COD respectively. Overall, sequential processes of EC/aeration, PMS/ZVI/UV and EF could remove the COD, TOC and ammonia of the landfill leachate around 98%, 93% and 94%, respectively. The comparison of different sequences of following processes indicated that current configuration (EC/aeration-PMS/ZVI/UV-EF) could meet the discharge standards. Furthermore, humification degree was significantly improved after oxidative processes. Biodegradability study was also performed by means of BOD/COD, average oxidation state (AOS), and Zahn-Wellens test, and the best results associated with these indices were obtained 0.56, 2.37, and over 98%, respectively. Phytotoxicity of leachate was remarkably reduced and the final effluent can be considered as a non-phytotoxic wastewater.

UV-activated persulfates oxidation of anthraquinone dye: Kinetics and ecotoxicological assessment.

Sulfate radical-based advanced oxidation processes (SR-AOPs) are gaining popularity as a feasible alternative for removing recalcitrant pollutants in an aqueous environment. Persulfates, namely peroxydisulfate (PDS) and peroxymonosulfate (PMS) are the most common sulfate radical donors. Persulfates activation by ultraviolet (UV) irradiation is considered feasible due to the high concentration of radicals produced as well as the lack of catalysts leaching. The research focuses on determining the impact of activated PDS and PMS on the degradation of anthraquinone dye, i.e., Acid Blue 129 (AB129). UV-activated PDS and PMS can quickly degrade the AB129 as well as restrict the formation of by-products. This could explain the reduced ecotoxicity levels of the treated water after degradation, using an aquatic plant (Lemna minor) and a crustacean (Daphnia magna). This, on the other hand, can ensure that the sulfate radical-based processes can be an environmentally friendly technology.

Ciprofloxacin degradation by catalytic activation of monopersulfate using Mn-Fe oxides: performance and mineralization.

In this work, Mn2O3/Fe2O3 (MFO) was synthesized and used to activate monopersulfate (MPS) for the degradation of ciprofloxacin (CIP). The effect of several parameters was studied on CIP degradation. Under the optimum conditions (pH = 6.3 (natural pH), MFO = 300 mg/L and MPS = 2 mM), around 92% of CIP was decomposed. Nitrite, phosphate and bicarbonate ions had a strong inhibitory effect on the MFO/MPS process while the effect of chloride and nitrate ions was neutral. The catalytic activity of MFO was also studied by other chemical oxidants such as peroxydisulfate, periodate, hydrogen peroxide, percarbonate and peracetic acid. Scavenging tests showed that the role of sulfate radicals is more than hydroxyl radicals. MFO exhibited high catalytic activity in four recycling with insignificant leaching of Mn and Fe. During CIP oxidation, 45.5% carbon mineralization occurred and antibacterial activity of treated CIP solution was reduced. Finally, MFO/MPS was applied on actual wastewater (hospital effluent) and the results showed that MFO/MPS can be considered as a practical method for the treatment of contaminated water with emerging pollutants.

Heterogeneous photocatalytic activation of electrogenerated chlorine for the production of reactive oxygen and chlorine species: A new approach for Bisphenol A degradation in saline wastewater.

UV-E-chlorination/hematite nanoparticles (UV/E-Cl/HNs) as a heterogeneous photocatalytic activation of electrogenerated chlorine was assessed for the degradation of bisphenol A (BPA) as a new approach based on the generation of reactive chlorine and oxygen species. The prepared sample was characterized using multiple techniques, such as XRD, FTIR, FESEM, EDS, and BET-BJH. An excellent decontamination efficiency of 99.4% was achieved within 40 min of electrolysis under optimum conditions (pH of 5, HNs dosage 100 mg/L, current density of 20 mA/cm2, and NaCl concentration of 50 mM). The HOCl content was reduced more swiftly in the presence of ultraviolet (UV) irradiation and hematite, resulting in the production of oxidative radicals (i.e., •OH, Cl•, and Cl2•-). The scavenging experiments also verified the vital role of these radicals in oxidative treatment. The UV/E-Cl/HNs process is readily supplied with hydroxyl radicals through several mechanisms. Bicarbonate ions showed a noticeable inhibitory impact, whereas nitrate and sulfate anions only slightly affected BPA degradation. The HNs were a recoverable and stable catalyst for six cycles. Furthermore, the ECOSAR program predicted that the UV/E-Cl/HNs can be labeled as an environmental-friendly process. Eventually, reasonable degradation pathways were proposed based on the identified by-products through experimental and theoretical approaches.

Sulfate radicals-based advanced oxidation processes for the degradation of pharmaceuticals and personal care products: A review on relevant activation mechanisms, performance, and perspectives.

Owing to the rapid development of modern industry, a greater number of organic pollutants are discharged into the water matrices. In recent decades, research efforts have focused on developing more effective technologies for the remediation of water containing pharmaceuticals and personal care products (PPCPs). Recently, sulfate radicals-based advanced oxidation processes (SR-AOPs) have been extensively used due to their high oxidizing potential, and effectiveness compared with other AOPs in PPCPs remediation. The present review provides a comprehensive assessment of the different methods such as heat, ultraviolet (UV) light, photo-generated electrons, ultrasound (US), electrochemical, carbon nanomaterials, homogeneous, and heterogeneous catalysts for activating peroxymonosulfate (PMS) and peroxydisulfate (PDS). In addition, possible activation mechanisms from the point of radical and non-radical pathways are discussed. Then, biodegradability enhancement and toxicity reduction are highlighted. Comparison with other AOPs and treatment of PPCPs by the integrated process are evaluated as well. Lastly, conclusions and future perspectives on this research topic are elaborated.

Measurement of polycyclic aromatic hydrocarbons in edible oils and potential health risk to consumers using Monte Carlo simulation, southwest Iran.

Persistent organic pollutants, such as polycyclic aromatic hydrocarbons, are hazardous trace contaminants frequently observed in food ingredients, such as edible oils. This study aimed to measure PAHs in forty brands of edible oils marketed in southwest Iran. Additionally, we characterized the daily intake of MOE and ILCR using Monte Carlo simulation. To analyze the content of PAHs, the liquid-liquid extraction method followed by GC-MS was utilized. The average concentration of PAHs was mostly lower than the maximum value for individual PAH (2 µg/Kg); however, the average concentration of fluorene (3.86 µg/Kg) and benzo(a)anthracene (3.13 µg/Kg) was more than the permitted level. The highest residual concentrations of PAHs were mostly observed in canola and corn oils. The daily intake of BaP and 4-PAH for 95% of consumers was 0.01 ng/kg BW/day and 0.04 ng/kg BW/day, respectively. Also, MOE was more than 10,000 for the percentiles of 5%, 50%, and 95%. The modeled ILCR showed that consumption of oil does not currently pose a cancer risk for Iranian consumers due to PAHs exposure. Concerning potential health risks, consumption of edible oils is safe; however, regular monitoring and assessment are required.

The Relationship Between Dust Sources and Airborne Bacteria in the Southwest of Iran.

The biological agents are carried from deserts and dried lands to long distances by high dust volumes. Their adverse effects can be reduced by specifying and controlling dust sources and their related biological agents. Thus, the current work examined the relationship between the bacteria in air and soil samples by taking samples from the soil surface of two dust sources, as well as from air samples during spring from Khorramshahr and Abadan cities. The dust event is the most influential factor on airborne bacteria. There is an insignificant negative (-0.06), insignificant positive (0.14), and weak positive (0.24) correlation between airborne bacteria and UV radiation, relative humidity, and temperature, respectively. After preparing a 16S ribosomal DNA (rDNA) clone library from the soil and air samples, operational taxonomic unit picking and taxonomic assignment were conducted using QIIME Virtual Box. In the present work, Bacillus was the dominant species. The relationship between dust sources and air samples was determined by principal component analysis. Bacteria in the Hoor-Al-Azim dust source and airborne bacteria on dusty and non-dusty days showed a more significant correlation compared to bacteria in the Shadegan dust source. Source Tracker software was used to estimate the contribution of dust sources. The primary source of dust was associated with the dried areas of Hoor-Al-Azim on the non-dusty and dusty days. Finally, the long transport of airborne bacteria was assessed by moderate resolution imaging spectroradiometer (MODIS) and the back trajectory model of Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) data. The research findings can help decision-makers prioritize dust sources to control the adverse effects of dust.

Bisphenol A degradation by peroxymonosulfate photo-activation coupled with carbon-based cobalt ferrite nanocomposite: Performance, upgrading synergy and mechanistic pathway.

Cobalt ferrite (CoFe2O4, CF) nanoparticles were anchored on the multiwalled carbon nanotube (MWCNT) for synthesis of CF@MWCNT nanocomposite and enhancing the catalytic activity of CF. After well characterization, it was applied as a catalyst towards photo-activation peroxymonosulfate (PMS) for degradation of bisphenol A (BPA). Based on the identified intermediates, a possible degradation pathway was proposed for BPA. CF@MWCNT coupled with PMS and UV (i.e., CF@MWCNT/PMS/UV) exhibited a better performance than homogeneous UV-assisted PMS processes under Fe and Co ions. A significant synergy on the degradation of BPA was observed in the simultaneous application of catalyst, UV light and PMS. Under optimum conditions, the removal efficiencies of 100 and 72.6% were attained respectively for BPA and TOC by CF@MWCNT/PMS/UV within 60 min reaction. These efficiencies were decreased to 88 and 61% after five times use of catalyst, respectively. The leaching of metal ions dissolved from the catalyst was slight during cyclic utilization of catalyst, confirming high stability of CF@MWCNT. In this process, the participation of radical mechanisms was approximately 60%, which SO4•- and HO• species contributed as predominant oxidizing reactive species. It also showed the excellent catalytic performance towards decomposition of persulfate and hydrogen peroxide. Overall, UV-assisted PMS catalyzed by CF@MWCNT exhibited a good catalytic performance and so it can be potentially introduced as a promising method for efficient treatment of water contaminated by BPA.

Assessing the relationship between airborne fungi and potential dust sources using a combined approach.

Dust events impose negative socio-economic, health, and environmental impacts on vulnerable areas and reflect their sources' physiochemical and biological characteristics. This study aimed to assess the impact of two dust sources on the concentration and diversity of airborne fungi in one of the dustiest areas in the world. This study is the first attempt to investigate the relationship between dust sources fungal community and those in airborne dust. Also, the contribution of dust sources to airborne fungi was estimated. Air masses arriving at the study area were assessed using local wind rose and the HYSPLIT model. Sampling was carried out from airborne dust at the Arvand Free Zone as target areas and soil in the dried parts of the Hor al-Azim and Shadegan wetlands as source areas to explore the relationship between fungi in the dust sources and the downwind area. The samples were analyzed in the lab to extract DNA. The internal transcribed spacer (ITS) regions of the rDNA gene were amplified using the primers ITS1F and ITS4, and then PCR products were sent to the lab for sequencing. The raw DNA data were processed using the QIIME virtual box to pick operational taxonomic units and taxonomy assignments. The most common fungi at the genus level were in the order of Penicillium > Aspergillus > Alternaria > Fusarium > Paradendryphiella > Talaromyces. The similarity between air and soil fungal genera was investigated using richness and diversity indices, the phylogenetic tree, and principal component analysis. The results showed that the community structures of ambient fungi in the Hor al-Azim and Shadegan dust sources were more similar to those on dusty days than non-dusty days. The source tracker model was used to quantify the contributions of known dust sources to airborne fungi. The results showed that the main source of airborne fungi was Hor al-Azim on dusty and non-dusty days. This study's results can help managers identify and prioritize dust sources regarding fungal species.

Enhanced degradation of ultra-violet stabilizer Bis(4-hydroxy)benzophenone using oxone catalyzed by hexagonal nanoplate-assembled CoS 3-dimensional cluster.

As UV-light stabilizers, Bis(4-hydroxy)benzophenone (BBP), are extensively consumed to quench radicals from photooxidation, continuous release of BPs into the environment poses serious threats to the ecology in view of their xenohormone toxicities, and BBP shall be eliminated from water to avoid its adverse effect. Since sulfate radical (SR)-based chemical oxidation techniques have been proven as effective procedures for eliminating organic emerging contaminants, this study aims to develop useful SR-based procedures through activating Oxone for degrading BBP in water. In contrast to the conventional Co3O4, cobalt sulfide (CoS) is particularly proposed as an alternative heterogeneous catalyst for activating Oxone to degrade BBP because CoS exhibits more reactive redox characteristics. As structures of catalysts predominantly control their catalytic activities, in this study, a unique nanoplate-assembled CoS (NPCS) 3D cluster is fabricated via a convenient one-step process to serve as a promising heterogeneous catalyst for activating Oxone to degrade BBP. With NPCS = 100 mg/L and Oxone = 200 mg/L, 5 mg/L of BBP can be completely eliminated in 60 min. The catalytic activity of NPCS towards Oxone activation also significantly surpasses the reference material, Co3O4, to enhance degradation of BBP. Ea of BBP degradation by NPCS-activated Oxone is also determined as a relatively low value of 42.7 kJ/mol. The activation mechanism as well as degradation pathway of BBP degradation by NPCS-activated Oxone was investigated and validated through experimental evidences and density functional theory (DFT) calculation to offer valuable insights into degradation behaviors for developing SR-based processes of BBP degradation using CoS catalysts.

Comparative investigation of acetaminophen degradation in aqueous solution by UV/Chlorine and UV/H2O2 processes: Kinetics and toxicity assessment, process feasibility and products identification.

The degradation of acetaminophen (ACM) was comparatively studied by UV/chlorine and UV/H2O2 systems. An apparent reduction in the removal rate was observed above the optimum pH levels of 7.0 and 3.0 in UV/chlorine and UV/H2O2 processes, respectively. The relative contribution of each oxidizing agent in ACM removal using the two advanced oxidation processes (AOPs) was evaluated. Even though hydroxyl radicals, with the contribution percentage of 90.1%, were determined as the primary oxidizing species in ACM removal using the UV/H2O2 process, reactive chlorine species (RCS), with 43.8% of contribution percentage, were also found to play a pivotal role in ACM removal using the UV/chlorine process. For instance, dichlorine radical (Cl2•-) showed an acceptable contribution percentage of 32.2% in the degradation of ACM by the UV/chlorine process. The rate of ACM degradation significantly rose to 99.9% and 75.6%, as higher amounts of oxidants were used in the UV/chlorine and UV/H2O2 processes, respectively, within 25 min. The introduction of HCO3- ions and humic acid remarkably decreased the rate of ACM degradation in both techniques used in this study. The presence of NO3- and Cl- ions did not considerably affect the removal rate in the UV/chlorine process. The acute toxicity analysis revealed that a more pronounced reduction in the ACM solution toxicity could be achieved by the UV/H2O2 process compared to the UV/chlorine process, which should be ascribed to the formation of chlorinated products in the UV/chlorine treatment. Eventually, plausible oxidation pathways were proposed for each process.

Influence of catalyst zeta potential on the activation of persulfate.

The effect of the zeta potential of nano zero-valent iron (nZVI) and carbocatalyst on the activation of persulfate was investigated. The oxidation experiments were performed on three different compounds, with variously modified nZVI and three distinct carbocatalysts. From the obtained results, an evident linear correlation between nanoparticles' zeta potential and reaction rate constants of these three compounds oxidation may be observed. This phenomenon is not mechanism-specific and occurs for the radical and non-radical processes. The present work indicates the critical influence of the surface charge of nZVI and carbocatalysts on the persulfate catalytic activation.

Electrochemical activation of peroxides for treatment of contaminated water with landfill leachate: Efficacy, toxicity and biodegradability evaluation.

Contaminated water with landfill leachate (CWLL) with high salinity and high organic content (total organic carbon (TOC) = 649 mg/L and Chemical Oxygen Demand (COD) = 1175 mg/L) is a toxic and non-biodegradable effluent. The present research aimed to assess the treatment effectiveness of CWLL by electrocoagulation (EC)/oxidant process. The ferrous ions generated during the process were employed as coagulant and catalyst for the activation of different oxidants such as peroxymonosulfate (PMS), peroxydisulfate (PDS), hydrogen peroxide (HP), and percarbonate (PC) to decrease TOC in CWLL. Removal of ammonia, color, phosphorous, and chemical oxygen demand (COD) from CWLL effluent was explored at various processes. EC/HP had the best performance (∼73%) in mineralization of organic pollutants compared to others under the condition of pH 6.8, applied current of 200 mA, oxidant dosage of 6 mM, and time of 80 min. The oxidation priority was to follow this order: EC/HP > EC/PMS > EC/PDS > EC/PC. These processes enhanced the biodegradability of CWLL based on the average oxidation state and biochemical oxygen demand (BOD)/COD ratio. SUVA254 and E2/E3 indices were also investigated on obtained effluents. The phytotoxicity evaluation was carried out based on the germination index, indicating that the electro-activated oxidant was an effective system to reduce the toxicity of polluted waters. EC/HP showed supremacy compared to others in terms of efficiency, cost, and detoxification. Therefore, the electro-activated oxidant system is a good means for removing organic pollutants from real wastewater.

Bamboo-like N-doped carbon nanotube-confined cobalt as an efficient and robust catalyst for activating monopersulfate to degrade bisphenol A.

As bisphenol A (BPA) is an extensively used chemical for manufacturing plastic products, discharge of BPA into the environment has caused serious threats to ecology. Therefore, -based chemical oxidation methods have been employed for eliminating BPA. Because monopersulfate (MNP) has become a popular reagent for obtaining , and Co is the most efficient metal for activating MNP, it is critical to develop heterogeneous Co catalysts for easier implementation and recovery. Herein, a unique Co-based catalyst is proposed by utilizing tubular-structured N-doped carbon substrates, derived dicyandiamide (DCDA), to confine Co nanoparticles (NPs). Through simple pyrolysis of a mixture of Co/DCDA, DCDA would be transformed into N-doped carbon nanotubes (CNT) to wrap the resultant Co NP, and, interestingly, this N-doped CNT would exhibit a special bamboo-like morphology. More importantly, as Co NPs are mono-dispersed and singly-confined in N-doped CNTs, forming CoCNT, CoCNT exhibits significantly higher catalytic activities than Co3O4, for activating MNP to degrade BPA. The enhancement of catalytic activities in CoCNT would be possibly ascribed to the synergistic effects between Co NP and the N-doped CNT which not only acts as the support/protection but also provides active sites. Therefore, CoCNT + MNP could lead to a much lower Ea (i.e., 13.8 kJ/mol) of BPA degradation than the reported Ea values. Besides, CoCNT is still effective for eliminating BPA even in the presence of high-concentration NaCl and surfactants. CoCNT is also reusable over many cycles and retains its catalytic activity with 100% BPA removal, demonstrating that CoCNT is an advantageous and robust catalyst for MNP activation.

Aerobic oxidation of 5-hydroxymethylfurfural into 2,5-diformylfuran using manganese dioxide with different crystal structures: A comparative study.

Aerobic oxidation of 5-Hydroxymethylfurfural (HMF) to 2,5-Diformylfuran (DFF) using O2 gas represents a sustainable approach for valorization of lignocellulosic compounds. As manganese dioxide (MnO2) is validated as a useful oxidation catalyst and many crystalline forms of MnO2 exist, it is critical to explore how the crystalline structures of MnO2 influence their physical/chemical properties, which, in turn, determine catalytic activities of MnO2 crystals for HMF oxidation to DFF. In particular, six MnO2 crystals, α-MnO2, ß-MnO2, γ-MnO2, δ-MnO2, ε-MnO2, and λ-MnO2 are prepared and investigated for their catalytic activities for HMF oxidation to DFF. With different morphologies and crystalline structures, these MnO2 crystals possess very distinct surficial chemistry, redox capabilities, and textural properties, making these MnO2 exhibit different catalytic activities towards HMF conversion. Especially, ß-MnO2 can produce much higher DFF per surface area than other MnO2 crystals. ß-MnO2 could achieve the highest CHMF = 99% and YDFF = 97%, which are much higher than the reported values in literature, possibly because the surficial reactivity of ß-MnO2 appears to be highest in comparison to other MnO2 crystals. Especially, ß-MnO2 could exhibit YDFF > 90% over 5 cycles of reusability test, and maintain its crystalline structure, revealing its advantageous feature for aerobic oxidation of HMF to DFF. Through this study, the relationship between morphology, surface chemistry, and catalytic activity of MnO2 with different crystal forms is elucidated for providing scientific insights into design, application and development of MnO2-based materials for aerobic oxidation of bio-derived molecules to value-added products.

Sonochemical degradation of bisphenol A using persulfate activated by hematite nanoparticles.

In this study, hematite nanoparticles (HNPs) were used as the persulfate (PS) activator for the sonocatalytic degradation of bisphenol A (BPA). The physicochemical properties of the synthesized HNPs were investigated using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The effect of different operational parameters (pH, nanoparticle dosage, persulfate concentration, and ultrasonic power) on catalytic activity were evaluated. The BPA degradation rate was improved when ultrasonic (US) irradiation was used simultaneously with HNPs for activating PS. According to the results, 98.94% of BPA (10 mg/L) was degraded within 15 min of reaction time at 4 mM persulfate and 0.01 g/L HNPs under ultrasonic irradiation of 250 W. The degree of mineralization of BPA was measured using chemical oxygen demand (COD), and 36.98% was achieved under optimum conditions. Quenching tests were done using different scavenger compounds; these showed that both hydroxyl and sulfate radicals were reactive species in BPA degradation. According to the results of reusability tests, the degradation efficiency decreased to 86.34%, indicating that HNPs can be recycled several times. All of the anions tested, but mainly hydrogen phosphate, had an inhibitory effect on BPA degradation. The results showed that the US/HNPs/PS process is effective for the degradation of the organic pollutants.

Acetaminophen degradation by a synergistic peracetic acid/UVC-LED/Fe(II) advanced oxidation process: Kinetic assessment, process feasibility and mechanistic considerations.

Application of peracetic acid (PAA) in Advanced Oxidation Processes (AOPs) has seen an increase in the last few years. In this study, PAA/UVC-LED/transition metal was used to degrade acetaminophen (ACT) in an aqueous solution. Amongst tested transition metals (Fe, Cu, Co, Mn, Ag), Fe(II) demonstrated the highest efficiency. The effect of pH, PAA dosage, initial concentration of ACT and Fe(II) concentration was investigated on ACT removal. More than 95% removal efficiency was obtained in 30 min employing pH = 5.0, PAA 4 mM and 0.5 mM Fe(II) (kapp = 0.0993 min-1). Scavenging experiments highlighted the contribution of oxygen-centered radicals; however, the dominant mechanism is hydroxyl radical-induced, while the superoxide radicals had a negligible role. The effect of anions in water showed that carbonate, (dihydrogen) phosphate and nitrite ions had a strong inhibitory effect, while a neutral effect was observed by sulfate, nitrate and chloride ions. Seven intermediates of ACT oxidation were determined and the ACT degradation pathway by the PAA/UVC-LED/Fe(II) is presented. The efficacy of the PAA/UVC-LED/Fe(II) process was also verified for the degradation of other contaminants of emerging concern and disinfection of fecal indicator microorganisms in real matrix (secondary WW). In conclusion, the studied PAA/UVC-LED/Fe(II) process opens a new perspective as a promising application of advanced oxidation for the degradation of organic pollutants.

Performance of photocatalytic ozonation process for pentachlorophenol (PCP) removal in aqueous solution using graphene-TiO2 nanocomposite (UV/G-TiO2/O3).

The aim of this study was to evaluate the efficiency of photocatalytic ozonation process using graphene-dioxide titanium nanocomposite in removing Pentachlorophenol (PCP) from aqueous solutions. In this study, nanocomposites with graphene to TiO2(G/T) ratios of 1:10 and 1:20 were synthesized by hydrothermal method, and its characteristics were assessed using various analyses, SEM, XRD, FTIR, TEM, BET and TGA. In this process, the effects of parameters including O3 concentration (0.25-1.25 mg/L), nanocomposite concentration (50-500 mg/L), initial PCP concentration (10-100 mg/L), and time (10-60 min), were studied. The results showed that PCP removal efficiency was increased by decreasing solute concentration. Increasing nanocomposite dose to 100 mg/L was led to an increase in efficiency (99.1%), but then a decreasing trend was observed. Increasing the concentration of ozone, up to specific value, also enhanced the efficiency but then had a negative effect on process efficiency. Furthermore, the optimum ratio of the catalyst was determined to be 1:20. The highest efficiency of the process for initial pentachlorophenol concentration of 100 mg/L was obtained 98.82% in optimum conditions (catalyst dose of 100 mg/L and 60 min). It is concluded that the photocatalytic ozonation process using graphene-dioxide titanium nanocomposite had the highest efficiency in removal and mineralization of PCP.

Porous hexagonal nanoplate cobalt oxide derived from a coordination polymer as an effective catalyst for activating Oxone in water.

As cobalt (Co) represents an effective transition metal for activating Oxone to degrade contaminants, tricobalt tetraoxide (Co3O4) is extensively employed as a heterogeneous phase of Co for Oxone activation. Since Co3O4 can be manipulated to exhibit various shapes, 2-dimensional plate-like morphology of Co3O4 can offer large contact surfaces. If the large plate-like surfaces can be even porous, forming porous nanoplate Co3O4 (PNC), such a PNC should be a promising catalyst for Oxone activation. Therefore, a facile but straightforward method is proposed to prepare such a PNC for activating Oxone to degrade pollutants. In particular, a cobaltic coordination polymer with a morphology of hexagonal nanoplate, which is synthesized through coordination between Co2+ and thiocyanuric acid (TCA), is adopted as a precursor. Through calcination, CoTCA could be transformed into hexagonal nanoplate-like Co3O4 with pores to become PNC. This PNC also shows different characteristics from the commercial Co3O4 nanoparticle (NP) in terms of surficial reactivity and textural properties. Thus, PNC exhibits a much higher catalytic activity than the commercial Co3O4 NP towards activation of Oxone to degrade a model contaminant, salicylic acid (SA). Specifically, SA was 100% degraded by PNC activating Oxone within 120 min, and the Ea of SA degradation by PNC-activated Oxone is 70.2 kJ/mol. PNC can also remain stable and effective for SA degradation even in the presence of other anions, and PNC could be reused over multiple cycles without significant loss of catalytic activity. These features validate that PNC is a promising and useful Co-based catalyst for Oxone activation.