- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Photocatalytic removal of phenanthrene and algae by a novel Ca-Ag3PO4 composite under visible light: Reactivity and coexisting effect
摘要： In this study, the feasibility of a novel Ca-Ag3PO4 composite with visible light irradiation for the phenanthrene (PHE) degradation and algae inactivation in artificial seawater was firstly investigated. The experimental findings revealed that Ag3PO4 phase was sucessfully formed on the Ca-based material, and the presence of Ca-based material could effectively keep Ag3PO4 particles stable. An excellent performance on PHE degradation or algae inactivation was observed from Ca-Ag3PO4 composite under visible light irradiation. The degradation of PHE or inactivation of algae not only could be efficiently achieved in the single mode, but also could be successfully achieved in the coexisting mode. Above 96 % of PHE and algae were simultaneously removed within 12 h in the Ca-Ag3PO4/visible light system. It was further observed that the degradation of PHE and/or inactivation of algae increased with the increase of Ca-Ag3PO4 dosage. HO? was the primary radical responsible for PHE degradation, whereas HO? and Ag+ released from Ca-Ag3PO4 mainly contributed to the algae inactivation. A possible mechanism involving the catalytic removal of PHE and algae by Ca-Ag3PO4 under visible light irradiation was proposed. This study provides helpful guide for the simultaneous removal of various pollutants in real seawater.
关键词： Ag3PO4,Algae,Photocatalytic,Advanced oxidation processes (AOPs),Visible light,Phenanthrene (PHE)
更新于2025-09-23 15:23:52
-
Effect of photochemical advanced oxidation processes on the formation potential of emerging disinfection by-products in groundwater from part of the Pannonian Basin
摘要： This study evaluates the effect of photochemical advanced oxidation processes (AOPs) (O3/UV, H2O2/UV and O3/H2O2/UV) on the formation potential (FP) of emerging disinfection by-products including nitrogenous by-products (N-DBPs) and haloketones (HKs) in groundwater from part of the Pannonian Basin (AP Vojvodina, Republic of Serbia). Among the N-DBPs, the haloacetonitrile (HAN) precursor contents were 9.83 ± 0.59 μg/L while precursors of halonitromethanes, particularly trichloronitromethane (TCNM) were not detected. Similarly, precursors of HKs as carbonaceous DBPs were also not detected in raw water. Ozonation alone and H2O2/UV process with a lower UV dose maximally decomposed HAN precursors (about 70%) while during O3 based AOPs, HANFP varied significantly. Application of UV photolysis and H2O2/UV processes with increasing UV dose doubled the HANFP. Ozone alone, O3/UV and H2O2/UV slightly increased HKs formation potential, particularly 1,1-Dichloro-2-propanone FP (0.93 ± 0.21 to 2.01 ± 0.37 μg/L). None of the investigated treatments influenced the formation of TCNM precursors. The effect of the applied treatments on bromide incorporation was the most evident for HANs.
关键词： emerging disinfection by-products,ozone,bromide incorporation,photochemical advanced oxidation processes
更新于2025-09-23 15:23:52
-
Unsubstituted metallophthalocyanine catalysts for the removal of endocrine disrupting compounds using H2O2 as oxidant
摘要： Advanced oxidation processes have become increasingly important to treat non-biodegradable compounds entering environmental waters. In recent decades, water-soluble metallophthalocyanines have been shown to catalyse H2O2-containing oxidation reactions through the production of unique reactive species, nucleophilic metal-peroxo complexes. Few reports in the literature have examined water insoluble metallophthalocyanines (MPc). The oxidative catalytic activity of water insoluble manganese- and iron-phthalocyanine (MnPc, FePc) at pH 7 has been shown through the decolourisation of methylene blue and removal of bisphenol A. These studies expand on this previous study, exploring the catalytic activity of a range of metallophthalocyanines catalysts under both acidic and neutral conditions. FePc, while only active under neutral conditions, was the best performing catalyst. This activity was significantly improved upon by the addition of acetonitrile as a co-solvent, as well as increasing the ratio of H2O2 to catalyst. MnPc was catalytically active at both pH 3 and 7. FePc and MnPc catalysts showed the ability to remove bisphenol A in the presence of dam water. Reaction rates were reduced for bisphenol A removal with FePc as a catalyst but were unchanged in the presence of MnPc. The removal of 17β-estradiol, estrone, and coumestrol was successfully demonstrated, with greater than 96% removal of all tested EDC’s achieved. This is the first reported study showing the removal of the phytoestrogen, coumestrol. Even though considerably lower concentrations of costly catalysts and oxidation reagents were used in our work, the removal extent of EDC’s by the MPc-catalysed oxidation reactions achieved here compares favourably with literature.
关键词： Bisphenol A,Endocrine disrupting compounds,Metallophthalocyanine,Advanced oxidation processes,Coumestrol
更新于2025-09-23 15:22:29
-
Characterization and removal of antibiotic residues by NFC-doped photocatalytic oxidation from domestic and industrial secondary treated wastewaters in Meric-Ergene Basin and reuse assessment for irrigation
摘要： Antibiotics are important contaminants that have become an increasingly big problem due to the discharge of the receiving environment. The presence of these organic based pollutants in influent wastewater can inhibit the biological processes and resist to degradation in wastewater treatment plants. Moreover, the consumption of agricultural products, irrigated with water containing antibiotic residues, leads to major harmful effects to the human body through the food chain. In this study; firstly, a conventional characterization was made in terms of COD, TOC, SS, color and of antibiotic residue characterization of untreated raw (influent) and biologically treated (effluent) water from domestic and industrial wastewater treatment plants located in the Meri?-Ergene Basin. After that, photocatalytic activity test was run under visible light for selected antibiotics (Erythromycin, Ciprofloxacin, Sulphametoxasol) which were detected by HPLC MS/MS in excess amount. Finally, for the photocatalytic oxidation, a new generation NFC (Nitrogen-Floride-Carbon)-doped titanium dioxide photocatalyst, which has never been studied in the literature before, was prepared according to the sol-gel method without using thermal processing. Photocatalysts were characterized by UV–vis DRS reflectance and Laser Raman Spectra measurements. All other analyzes were made according to the standard methods. Considering the conventional characterization results; investigated domestic wastewaters exhibited moderate characteristics while industrial wastewater samples had strong characteristics in terms of COD, TOC and SS pollution in accordance with the literature. By the way, contrary to expectations, antibiotic residue results have proved that the effluent wastewater contains more antibiotics than the influent. This can be explained by the fact that, some antibiotics in domestic wastewaters are probably already trapped in feces and cannot be purified by conventional systems since they are released after biological treatment, as mentioned similar studies in the literature. Moreover, by means of 7 h NFC-doped photocatalytic oxidation under visible light, beside approximately % 62 to %79 COD and 62%–86% TOC removal, %99 to %100 removal of antibiotic residue was provided. According to these results, domestic and industrial secondary treated wastewaters in Meric-Ergene Basin can be advance treated, succesfully, with NFC-doped photocatalyst to remove antibiotic residues besides conventional pollutants. This result show that Meri?-Ergene discharge criteria determined by Forest and Water Ministry of Turkey can be provided with this new type photocatalytic process and healthy reuse of this river for irrigation will be possible.
关键词： Advanced oxidation processes,Domestic/industrial wastewater,Solvent-casting method,UV,Antibiotic,Photocatalyst,NFC-doped TiO2
更新于2025-09-23 15:22:29
-
New Insights on the Photodegradation of Caffeine in the Presence of Bio-Based Substances-Magnetic Iron Oxide Hybrid Nanomaterials
摘要： The exploitation of organic waste as a source of bio-based substances to be used in environmental applications is gaining increasing interest. In the present research, compost-derived bio-based substances (BBS-Cs) were used to prepare hybrid magnetic nanoparticles (HMNPs) to be tested as an auxiliary in advanced oxidation processes. Hybrid magnetic nanoparticles can be indeed recovered at the end of the treatment and re-used in further water purification cycles. The research aimed to give new insights on the photodegradation of caffeine, chosen as marker of anthropogenic pollution in natural waters, and representative of the contaminants of emerging concern (CECs). Hybrid magnetic nanoparticles were synthetized starting from Fe(II) and Fe(III) salts and BBS-C aqueous solution, in alkali medium, via co-precipitation. Hybrid magnetic nanoparticles were characterized via X-ray diffraction (XRD), thermo-gravimetric analysis (TGA) and Fourier transform infrared (FTIR) spectroscopy. The effect of pH, added hydrogen peroxide, and dissolved oxygen on caffeine photodegradation in the presence of HMNPs was assessed. The results allow for the hypothesis that caffeine abatement can be obtained in the presence of HMNPs and hydrogen peroxide through a heterogeneous photo-Fenton mechanism. The role of hydroxyl radicals in the process was assessed examining the effect of a selective hydroxyl radical scavenger on the caffeine degradation kinetic.
关键词： hybrid nanomaterials,photo Fenton,caffeine,advanced oxidation processes,magnetic materials,bio-based substances
更新于2025-09-19 17:15:36
-
Removal of Textile Dye from Aqueous Media Using an Advanced Oxidation Process with UV/H <sub/>2</sub> O <sub/>2</sub>
摘要： This study investigated the treatment of water contaminated with textile dye (Cibacron Red FN-R, reactive red 238) using a UV/H2O2 process. The reaction was influenced by the input concentration of hydrogen peroxide H2O2, pH, temperature, and the concentration of textile dye in the wastewater. Analysis of the experimental results displayed both first order and the second order reactions. The reaction type was found to be of a first order throughout the systems. The removal efficiency of the UV/ H2O2 process at optimal conditions and dosage (H2O2 = 25 mg/L, pH=3, temperature =20 ?C for 50 mg/L dye concentration) were found to be 80.633% , 97.07%, and 99.43% at 60 min, 120 min, and 180 min, respectively with K1 = 0.0293 min-1 and R2=0.9992%. COD removal was also studied for the UV/H2O2 process and found to be 62.5%.
关键词： Hydrogen peroxide,Ozonation process,Destruction of organic and inorganic contaminants,Advanced Oxidation Processes (AOPs),Fenton process,adsorption,coagulation
更新于2025-09-19 17:15:36
-
Intensification of UV-C treatment to remove emerging contaminants by UV-C/H2O2 and UV-C/S2O82?: Susceptibility to photolysis and investigation of acute toxicity
摘要： In this study, the degradation of four emerging contaminants losartan potassium (LP), furosemide (FRSM), caffeine (CAF), and carbendazim (CBZ) under UV-C, UV-C/H2O2, and UV-C/S2O8^2- was investigated. A comparative evaluation of the efficiency of UV-C/H2O2 and UV-C/S2O8^2- in the degradation of these target CECs has not yet been reported. Moreover, target compounds were submitted to UV-C/AOPs individually in pure water and their simultaneous degradation was investigated in real surface water. Evolution of the acute toxicity of each compound during treatment was evaluated using Alivibrio fischeri. Quantum yields were determined for LP (0.011–0.016), FRSM (0.024–0.092), CAF (0.0007–0.0009), and CBZ (0.0016–0.0036) at different pH values. UV-C/H2O2 and UV-C/S2O8^2- achieved more than 98% removal of all compounds within 600 mJ cm^-2, and pseudo-first-order kinetic constants (k′app) for the degradation reactions were up to seven times higher in the presence of these oxidants when compared to k′app values obtained for UV-C photolysis. k′app measured for UV-C/H2O2 were higher than those calculated for UV-C/S2O8^2- except in the case of LP. Acute toxicity analysis suggested the formation of toxic intermediates during the UV-C photolysis of LP and FRSM, and the degradation of LP via UV-C/S2O8^2- also enhanced acute toxicity although electric energy efficiency per order identified UV-C/S2O8^2- as the most efficient process for the removal of this compound. Finally, different transformation products obtained during the degradation of caffeine under the different UV-C AOPs suggested that distinct degradation routes were involved in each treatment tested.
关键词： Contaminants of emerging concern,Advanced oxidation processes,Quantum yield,Persulfate,UV-C process
更新于2025-09-19 17:15:36
-
Co3O4/TiO2 hetero-structure for methyl orange dye degradation
摘要： Advanced oxidation processes based on sulphate radical generated by peroxymonosulphate (PMS) activation is a promising area for environmental remediation. One of the biggest drawbacks of heterogeneous PMS activation is catalyst instability and metal ion leaching. In this study, a simple organic binder mediated route was explored to substitute Ti4t ions into the Co3O4 host lattice structure to create a Co-O-Ti bond to minimise cobalt leaching during methyl orange degradation. The catalyst was characterised by X-ray diffraction, and scanning and transmission electron microscopy. The as-prepared catalysts with Co3O4:TiO2 ratio of 70:30 exhibited minimal leaching (0.9 mg/L) compared to other ratios studied. However, the pristine Co3O4 exhibited highest catalytic activity (rate constant ? 0.41 min(cid:2)1) and leaching (26.7 mg/L) compared to composite material (70:30 Co3O4:TiO2). Interestingly, the morphology of the composite and leaching of Co2t ions were found to be temperature dependent, as an optimum temperature ensured strong Co-O-Ti bond for prevention of Co2t leaching. The classical quenching test was utilised to determine the presence and role of radical species on methyl orange degradation. The fabricated catalyst also exhibited good catalytic activity in degrading mixed dyes and good recyclability, making it a potential candidate for commercial application.
关键词： advanced oxidation processes (AOPs),leaching,TiO2,heterogeneous reaction,Co3O4,PMS
更新于2025-09-10 09:29:36
-
Photodegradation of fluazaindolizine in aqueous solution with graphitic carbon nitride nanosheets under simulated sunlight illumination
摘要： The photodegradation of fluazaindolizine (FZDL) under simulated sunlight irradiation was accelerated by the catalysis of graphitic carbon nitride (g-C3N4). Under optimum conditions, such as 5 mg of amount and dispersion, the photodegradation half-life was dramatically enhanced to 2.7 h. More importantly, the pathway of degradation by g-C3N4 was different from both direct photolysis and the catalysis by titanium oxide, with particular negative ions of m/z 221 and 195, corresponding to the cleavage of sulfamide bond and the ring opening of imidazole, respectively. In addition, hydroxyl and superoxide radicals played important roles in photodegradation. The results enriched not only the study of FZDL photodegradation but also the application of g-C3N4. It also suggested the possibility of the water purification by photodegradation for pesticide removal in real life.
关键词： Advanced oxidation processes,Transformation products,Fluazaindolizine,Mass Spectrometery,Photodegradation,Graphitic carbon nitride
更新于2025-09-10 09:29:36
-
Removal of Carbofuran in aqueous solution by using UV-irradiation/hydrogen peroxide
摘要： Pesticide residues in natural water are one of the biggest environmental problems. carbofuran is an insecticide widely used in agricultural activities and it is easily biodegradable. Although this compound has a relatively short lifetime in soils and its persistence in the environment varies from one to several weeks. For this reason, the elimination of carbofuran residual from contaminated waters using suitable technique is of environmental interest. The aim of this study to investigate the synergetic effect of UV and UV with hydrogen peroxide on the degradation of carbofuran in aqueous solution. 50 mgL-1 aqueous solutions of carbofuran (CBF) were prepared. The solutions were exposed to various UV irradiation times. The irradiation time varied from (15-240 min). Hydrogen peroxide was set at 4.8 mM as a minimum concentration level. To follow the degradation percent, formaldehyde concentration, and to identify the intermediates by-products, GC-MS, IC, and UV-Visible spectrophotometer were used. The pH, total acidity, and dissolved oxygen values were determined before and after treatment with UV irradiation with/without hydrogen peroxide. Depending on the results obtained the mechanism pathway (degradation) was suggested. The complete removal of carbofuran in aqueous solution took place at 180 min in the presence of H2O2.
关键词： advanced oxidation processes (AOP’s),hydrogen peroxide effect,Carbofuran,UV/H2O2
更新于2025-09-10 09:29:36