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Sample records for fenton reagent generation

  1. Industrial detergent wastewater treatment via fenton reagent

    International Nuclear Information System (INIS)

    Mohd Zairie Mohd Yusuff; Mohd Zulkifli Mohamad Noor; Izirwan Izhab

    2010-01-01

    Production of detergent can generates wastewater containing an organic matter with will consume an oxidation demand, surfactants, suspended solids, fat and oil. Besides, sulfate concentration is high in the most detergent plant effluent because of the sulphonation process that has physiological and toxic effects on marine organisms. Therefore, a research must be conducted to find the solution for this problem. The feasibility of Fentons reagent to treat detergent waste was investigated in this study. The sample of detergent wastewater was taken from FPG Oleo chemicals Sdn. Bhd. This experiment studied the effect of temperature towards the feasibility of Fentons reagent process besides the dosage between hydrogen peroxide (H 2 O 2 ) and ferrous ion (Fe 2+ ) in the reagent. While, evaluated efficiency of Fentons reagent in term of chemical oxygen demand (COD), total suspended solid (TSS) and the turbidity reduction within the experimental design. The result found that overall removal was achieved until 96.2 % in term of COD, 98.1 % in term of TSS and 99.6 % in term of turbidity using Fentons reagent process. Besides, also found that this process is optimum at temperature 35 degree Celsius are able to achieve the Standard A of Parameter Limit of Effluent of Standard A and Standard B were outlined by Department of Environment Malaysia (DOE) based on Environment Quality Act 1974. (author)

  2. Treatment of laundrette wastewater using Starbon and Fenton's reagent.

    Science.gov (United States)

    Tony, Maha A; Parker, Helen L; Clark, James H

    2016-09-18

    The use of grey water for a variety of purposes is gaining increased popularity as a means of preserving scarce freshwater resources. In this work, catalytic oxidation over Fenton's reagent and adsorption techniques using Starbon (mesoporous material derived from polysaccharides) has been applied. These novel techniques are used as an alternative to already studied treatments of grey water such as filtration and/or biological processes. In this study, grey water, collected from a commercial laundrette, has been used. Treatment efficiency was determined by changes in the chemical oxygen demand (COD) of the grey water. Experiments using Fenton's reagent at optimum conditions of Fe(3+) = 40 mg L(-1); H2O2 = 400 mg L(-1) and pH 3 were very successful, resulting in a 95% COD removal after 15 min. Treatment with Starbon adsorption was also effective, reaching up to 81% COD removal at pH 3 within 1 h. The combined treatment with Fenton's reagent and Starbon resulted in a 93% COD removal at a significantly reduced concentration of Fenton's reagent compared to the treatment with solo Fenton's reagent. This lower chemical dose has the advantage of reducing costs and lowering sludge generation.

  3. USE OF FENTON'S REAGENT AS A DISINFECTANT

    Science.gov (United States)

    Combined sewage samples obtained from a wastewater treatment facility were disinfected by the Fenton's Reagent of several different compositions. The pre-settled samples contained both suspended solids (SS) and dissolved organic carbon (DOC) at concentrations of 28 and 290 mg/L,...

  4. Fenton's Reagent. Innovative Technology Summary Report

    International Nuclear Information System (INIS)

    None

    1999-01-01

    The Fenton's Reagent DNAPL treatment process is an in situ oxidation method to destroy DNAPLs in groundwater. Residual industrial solvents, primarily Dense Non-Aqueous Phase Liquids (DNAPLs), are currently the most significant barrier to successful completion of most large groundwater and soil cleanup efforts. DNAPL pools and residues slowly dissolve into surrounding groundwater to create large plumes of organic solvent contamination with concentration levels far above regulatory limits

  5. Tunable, Quantitative Fenton-RAFT Polymerization via Metered Reagent Addition.

    Science.gov (United States)

    Nothling, Mitchell D; McKenzie, Thomas G; Reyhani, Amin; Qiao, Greg G

    2018-05-10

    A continuous supply of radical species is a key requirement for activating chain growth and accessing quantitative monomer conversions in reversible addition-fragmentation chain transfer (RAFT) polymerization. In Fenton-RAFT, activation is provided by hydroxyl radicals, whose indiscriminate reactivity and short-lived nature poses a challenge to accessing extended polymerization times and quantitative monomer conversions. Here, an alternative Fenton-RAFT procedure is presented, whereby radical generation can be finely controlled via metered dosing of a component of the Fenton redox reaction (H 2 O 2 ) using an external pumping system. By limiting the instantaneous flux of radicals and ensuring sustained radical generation over tunable time periods, metered reagent addition reduces unwanted radical "wasting" reactions and provides access to consistent quantitative monomer conversions with high chain-end fidelity. Fine tuning of radical concentration during polymerization is achieved simply via adjustment of reagent dose rate, offering significant potential for automation. This modular strategy holds promise for extending traditional RAFT initiation toward more tightly regulated radical concentration profiles and affords excellent prospects for the automation of Fenton-RAFT polymerization. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Oxidative Degradation of Phenol containing Wastewater using Fenton Reagent, Permanganate and Ultraviolet Radiation

    International Nuclear Information System (INIS)

    Abd El-Rahman, N.M.; Talaat, H.A.; Sorour, M.H.

    1999-01-01

    Phenol containing wastewaters are generated by numerous industrial units including integrated steel mills, textile mills, plastic production, etc. The present work is targeted to explore the viable oxidation techniques for degradation of phenolic wastewater. Three modes of treatment have been adopted in this study, namely, sole oxidant mode using Fenton reagent or permanganate, UV-assisted oxidation and two consequent chemical oxidation steps. Results indicated the superiority of fenton reagent over KMnO 4 oxidation in the sole oxidant mode. On the other hand, UV-assisted KMnO 4 oxidation enables almost complete COD reduction. Dual chemical oxidation mode employing KMnO 4 oxidation followed by Fenton reagent is also an efficient oxidative degradation system

  7. Genotoxicity assessment of membrane concentrates of landfill leachate treated with Fenton reagent and UV-Fenton reagent using human hepatoma cell line.

    Science.gov (United States)

    Wang, Guifang; Lu, Gang; Yin, Pinghe; Zhao, Ling; Yu, Qiming Jimmy

    2016-04-15

    Membrane concentrates of landfill leachates contain organic and inorganic contaminants that could be highly toxic and carcinogenic. In this paper, the genotoxicity of membrane concentrates before and after Fenton and UV-Fenton reagent was assessed. The cytotoxicity and genotoxicity was determined by using the methods of methyltetrazolium (MTT), cytokinesis-block micronucleus (CBMN) and comet assay in human hepatoma cells. MTT assay showed a cytotoxicity of 75% after 24h of exposure to the highest tested concentration of untreated concentrates, and no cytotoxocity for UV-Fenton and Fenton treated concentrates. Both CBMN and comet assays showed increased levels of genotoxicity in cells exposed to untreated concentrates, compared to those occurred in cells exposed to UV-Fenton and Fenton reagent treated concentrates. There was no significant difference between negative control and UV-Fenton treated concentrates for micronucleus and comet assay parameters. UV-Fenton and Fenton treatment, especially the former, were effective methods for degradation of bisphenol A and nonylphenol in concentrates. These findings showed UV-Fenton and Fenton reaction were effective methods for treatment of such complex concentrates, UV-Fenton reagent provided toxicological safety of the treated effluent, and the genotoxicity assays were found to be feasible tools for assessment of toxicity risks of complex concentrates. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Textile wastewater reuse after additional treatment by Fenton's reagent.

    Science.gov (United States)

    Ribeiro, Marília Cleto Meirelles; Starling, Maria Clara V M; Leão, Mônica Maria Diniz; de Amorim, Camila Costa

    2017-03-01

    This study verifies textile wastewater reuse treated by the conventional activated sludge process and subjected to further treatment by advanced oxidation processes. Three alternative processes are discussed: Fenton, photo-Fenton, and UV/H 2 O 2 . Evaluation of treatments effects was based on factorial experiment design in which the response variables were the maximum removal of COD and the minimum concentration of residual H 2 O 2 in treated wastewater. Results indicated Fenton's reagent, COD/[H 2 O 2 ]/[Fe 2+ ] mass ratio of 1:2:2, as the best alternative. The selected technique was applied to real wastewater collected from a conventional treatment plant of a textile mill. The quality of the wastewater before and after the additional treatment was monitored in terms of 16 physicochemical parameters defined as suitable for the characterization of waters subjected to industrial textile use. The degradation of the wastewater was also evaluated by determining the distribution of its molecular weight along with the organic matter fractionation by ultrafiltration, measured in terms of COD. Finally, a sample of the wastewater after additional treatment was tested for reuse at pilot scale in order to evaluate the impact on the quality of dyed fabrics. Results show partial compliance of treated wastewater with the physicochemical quality guidelines for reuse. Removal and conversion of high and medium molecular weight substances into low molecular weight substances was observed, as well as the degradation of most of the organic matter originally present in the wastewater. Reuse tests indicated positive results, confirming the applicability of wastewater reuse after the suggested additional treatment. Graphical abstract Textile wastewater samples after additional treatment by Fenton's reagent, photo-Fenton and H 2 O 2 /UV tested in different conditions.

  9. Genotoxicity assessment of membrane concentrates of landfill leachate treated with Fenton reagent and UV-Fenton reagent using human hepatoma cell line

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guifang [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Lu, Gang [Key Laboratory of Water/Soil Toxic Pollutants Control and Bioremediation of Guangdong Higher Education Institutes, Department of Environmental Engineering, Jinan University, Guangzhou 510632 (China); Yin, Pinghe, E-mail: tyinph@jnu.edu.cn [Research Center of Analysis and Test, Jinan University, Guangzhou 510632 (China); Zhao, Ling, E-mail: zhaoling@jnu.edu.cn [Key Laboratory of Water/Soil Toxic Pollutants Control and Bioremediation of Guangdong Higher Education Institutes, Department of Environmental Engineering, Jinan University, Guangzhou 510632 (China); Jimmy Yu, Qiming [Griffith School of Engineering, Griffith University, Nathan Campus, Brisbane, Queensland 4111 (Australia)

    2016-04-15

    Highlights: • Membrane concentrates have a threat to human health and environment. • Untreated membrane concentrates induces cytotoxic and genotoxic to HepG2 cells. • Both methods were effective method for degradation of BPA and NP in concentrates. • Both methods were efficient in reducing genotoxic effects of concentrates. • UV-Fenton reagent had higher removal efficiency and provides toxicological safety. - Abstract: Membrane concentrates of landfill leachates contain organic and inorganic contaminants that could be highly toxic and carcinogenic. In this paper, the genotoxicity of membrane concentrates before and after Fenton and UV-Fenton reagent was assessed. The cytotoxicity and genotoxicity was determined by using the methods of methyltetrazolium (MTT), cytokinesis-block micronucleus (CBMN) and comet assay in human hepatoma cells. MTT assay showed a cytotoxicity of 75% after 24 h of exposure to the highest tested concentration of untreated concentrates, and no cytotoxocity for UV-Fenton and Fenton treated concentrates. Both CBMN and comet assays showed increased levels of genotoxicity in cells exposed to untreated concentrates, compared to those occurred in cells exposed to UV-Fenton and Fenton reagent treated concentrates. There was no significant difference between negative control and UV-Fenton treated concentrates for micronucleus and comet assay parameters. UV-Fenton and Fenton treatment, especially the former, were effective methods for degradation of bisphenol A and nonylphenol in concentrates. These findings showed UV-Fenton and Fenton reaction were effective methods for treatment of such complex concentrates, UV-Fenton reagent provided toxicological safety of the treated effluent, and the genotoxicity assays were found to be feasible tools for assessment of toxicity risks of complex concentrates.

  10. Genotoxicity assessment of membrane concentrates of landfill leachate treated with Fenton reagent and UV-Fenton reagent using human hepatoma cell line

    International Nuclear Information System (INIS)

    Wang, Guifang; Lu, Gang; Yin, Pinghe; Zhao, Ling; Jimmy Yu, Qiming

    2016-01-01

    Highlights: • Membrane concentrates have a threat to human health and environment. • Untreated membrane concentrates induces cytotoxic and genotoxic to HepG2 cells. • Both methods were effective method for degradation of BPA and NP in concentrates. • Both methods were efficient in reducing genotoxic effects of concentrates. • UV-Fenton reagent had higher removal efficiency and provides toxicological safety. - Abstract: Membrane concentrates of landfill leachates contain organic and inorganic contaminants that could be highly toxic and carcinogenic. In this paper, the genotoxicity of membrane concentrates before and after Fenton and UV-Fenton reagent was assessed. The cytotoxicity and genotoxicity was determined by using the methods of methyltetrazolium (MTT), cytokinesis-block micronucleus (CBMN) and comet assay in human hepatoma cells. MTT assay showed a cytotoxicity of 75% after 24 h of exposure to the highest tested concentration of untreated concentrates, and no cytotoxocity for UV-Fenton and Fenton treated concentrates. Both CBMN and comet assays showed increased levels of genotoxicity in cells exposed to untreated concentrates, compared to those occurred in cells exposed to UV-Fenton and Fenton reagent treated concentrates. There was no significant difference between negative control and UV-Fenton treated concentrates for micronucleus and comet assay parameters. UV-Fenton and Fenton treatment, especially the former, were effective methods for degradation of bisphenol A and nonylphenol in concentrates. These findings showed UV-Fenton and Fenton reaction were effective methods for treatment of such complex concentrates, UV-Fenton reagent provided toxicological safety of the treated effluent, and the genotoxicity assays were found to be feasible tools for assessment of toxicity risks of complex concentrates.

  11. POLYNUCLEAR AROMATIC HYDROCARBON (PAH) RELEASE FROM SOIL DURING TREATMENT WITH FENTON'S REAGENT

    Science.gov (United States)

    Fenton's Reagent was used to treat soil from a wood-treating site in southeastern Ohio which had been contaminated with creosote. Slurries, consisting of 10 µg of contaminated soil and 30 mL water were treated with 40 mL of Fenton's Reagent (1:1 of 30% H2O2 ...

  12. Remediation of polluted soils contaminated with Linear Alkyl Benzenes using Fenton's reagent

    Directory of Open Access Journals (Sweden)

    Douglas do Nascimento Silva

    2005-06-01

    Full Text Available Linear Alkyl Benzenes (LABs are used as insulating oil for electric cables. When it happens a spill, LABs they are basically sorbed in the soil, because, these compounds have high hidrophobicity and low vapor pressure. The conventional methods of treatment of soils are not efficient. The Fenton's reaction (reaction between a solution of iron II and hydrogen peroxide it generates hydroxyl radicals, not selective, and capable of oxidize a great variety of organic compounds. A study was conducted to evaluate the viability of use of the Fenton's reagents to promote the remediation of polluted soils with Linear Alkyl Benzenes. A column was especially projected for these experiments, packed with a sandy and other soil loamy. The pH of the soil was not altered. The obtained results demonstrated the technical viability of the process of injection of the Fenton's reagents for the treatment of polluted areas with LABs.Os Linear Alquilbenzenos (LABs são usados como fluido refrigerante de cabos elétricos. Quando ocorre um vazamento, os LABs ficam basicamente adsorvidos no solo, pois, são compostos bastante hidrofóbicos e com baixa pressão de vapor. Os métodos convencionais de tratamento de solos não são eficientes. A reação de Fenton (solução de ferro II e peróxido de hidrogênio gera radicais hidroxila, não seletivos, e capazes de oxidar uma grande variedade de compostos orgânicos, chegando a mineralização dos mesmos. Neste trabalho foi estudada a viabilidade de utilização dos reagentes de Fenton para promover a remediação de solos contaminados com LABs. Utilizou-se uma coluna especialmente projetada para estes experimentos, empacotada com um solo arenoso e outro argiloso. O pH do solo não foi alterado. Os resultados obtidos demonstram a viabilidade técnica do processo de injeção dos reagentes de Fenton para o tratamento de áreas contaminadas com LABs.

  13. Application of Fenton's reagent as a pretreatment step in biological degradation of polyaromatic hydrocarbons

    International Nuclear Information System (INIS)

    Kelley, R.L.; Gauger, W.K.; Srivastava, V.J.

    1991-01-01

    Fenton's reagent (H 2 O 2 and Fe ++ ) has been used for chemical oxidation of numerous organic compounds in water treatment schemes. In this study, the Institute of Gas Technology (IGT) applied Fenton's treatment to polynuclear aromatic hydrocarbons (PAHs) and PAH-contaminated soils. Fenton's treatment was very reactive with PAHs, causing rapid modification of the parental compounds to oxidized products and complete degradation to CO 2 . This treatment was more effective on chemically reactive PAHs, such as benzo(a)pyrene and phenanthrene. Important parameters and conditions for Fenton's treatment of PAHs in solution and soil matrices have been identified. As much as 99% of the PAHs on soil matrices can be removed by treatment with Fenton's reagent

  14. Treatment of landfill leachate by Fenton's reagent in a continuous stirred tank reactor

    International Nuclear Information System (INIS)

    Zhang Hui; Choi, H.J.; Huang, C.-P.

    2006-01-01

    The treatment of landfill leachate by Fenton process was carried out in a continuous stirred tank reactor (CSTR). The effect of operating conditions such as reaction time, hydraulic retention time, pH, H 2 O 2 to Fe(II) molar ratio, Fenton's reagent dosage, initial COD strength, and temperature on the efficacy of Fenton process was investigated. It is demonstrated that Fenton's reagent can effectively degrade leachate organics. Fenton process reached the steady state after three times of hydraulic retention. The oxidation of organic materials in the leachate was pH dependent and the optimal pH was 2.5. The favorable H 2 O 2 to Fe(II) molar ratio was 3, and organic removal increased as dosage increased at the favorable H 2 O 2 to Fe(II) molar ratio. Temperature gave a positive effect on organic removal

  15. Pyrite nanoparticles as a Fenton-like reagent for in situ remediation of organic pollutants

    Directory of Open Access Journals (Sweden)

    Carolina Gil-Lozano

    2014-06-01

    Full Text Available The Fenton reaction is the most widely used advanced oxidation process (AOP for wastewater treatment. This study reports on the use of pyrite nanoparticles and microparticles as Fenton reagents for the oxidative degradation of copper phthalocyanine (CuPc as a representative contaminant. Upon oxidative dissolution in water, pyrite (FeS2 particles can generate H2O2 at their surface while simultaneously promoting recycling of Fe3+ into Fe2+ and vice versa. Pyrite nanoparticles were synthesized by the hot injection method. The use of a high concentration of precursors gave individual nanoparticles (diameter: 20 nm with broader crystallinity at the outer interfaces, providing a greater number of surface defects, which is advantageous for generating H2O2. Batch reactions were run to monitor the kinetics of CuPc degradation in real time and the amount of H2O2. A markedly greater degradation of CuPc was achieved with nanoparticles as compared to microparticles: at low loadings (0.08 mg/L and 20 h reaction time, the former enabled 60% CuPc removal, whereas the latter enabled only 7% removal. These results confirm that the use of low concentrations of synthetic nanoparticles can be a cost effective alternative to conventional Fenton procedures for use in wastewater treatment, avoiding the potential risks caused by the release of heavy metals upon dissolution of natural pyrites.

  16. Degradation of ion spent resin using the Fenton's reagent

    International Nuclear Information System (INIS)

    Araujo, Leandro Goulart de

    2013-01-01

    The most common method for spent radioactive ion exchange resin treatment is its immobilization in cement, which reduces the radionuclides release into the environment. Although this method is efficient, it increases considerably the final volume of the waste due to the low incorporation capacity. The objective of this work was to develop a degradation method of spent resins arising from the nuclear research reactor located at the Nuclear and Energy Research Institute (IPEN-CNEN/SP), using an Advanced Oxidation Process (AOP) with Fenton's reagents. This method would allow a higher incorporation in cement. Three different resins were evaluated: cationic, anionic and a mixture of both resins. The reactions were conducted varying the catalyst concentration (25, 50, 100 and 150 mM), the volume of hydrogen peroxide (320 to 460 mL), and three different temperatures, 50, 60 and 70 deg C. Degradation of about 98% was achieved using a 50 mM catalyst solution and 330 mL of hydrogen peroxide solution. The most efficient temperature was 60 deg C. (author)

  17. Evaluation of the resin oxidation process using Fenton's reagent

    International Nuclear Information System (INIS)

    Araujo, Leandro G.; Goes, Marcos M.; Marumo, Julio T.

    2013-01-01

    The ion exchange resin is considered radioactive waste after its final useful life in nuclear reactors. Usually, this type of waste is treated with the immobilization in cement Portland, in order to form a solid monolithic matrix, reducing the possibility of radionuclides release in to environment. Because of the characteristic of expansion and contraction of the resins in presence of water, its incorporation in the common Portland cement is limited in 10% in direct immobilization, causing high costs in the final product. A pre-treatment would be able to reduce the volume, degrading the resins and increasing the load capacity of this material. This paper is about a method of degradation of ion spent resins from the nuclear research reactor of Nuclear and Energy Research Institute (IPEN/CNEN-SP), Brazil, using the Fenton's reagent. The resin evaluated was a mixture of cationic and anionic resins. The reactions were conducted by varying the concentration of the catalyst (25 to 80 mM), with and without external heat. The time of reaction was two hours. The concentration of 50 mM of catalyst was the most effective in degrading approximately 99%. The resin degradation was confirmed by the presence of CaCO 3 as a white precipitate resulting from the reaction between the Ca(OH) 2 and the CO 2 from the resin degradation. It was possible to degrade the resins without external heating. The calcium carbonates showed no correlation with the residual resin mass. (author)

  18. Degradation of ion spent resin using the Fenton's reagent; Degradacao da resina de troca ionica utilizando o reagente de Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Leandro Goulart de

    2013-07-01

    The most common method for spent radioactive ion exchange resin treatment is its immobilization in cement, which reduces the radionuclides release into the environment. Although this method is efficient, it increases considerably the final volume of the waste due to the low incorporation capacity. The objective of this work was to develop a degradation method of spent resins arising from the nuclear research reactor located at the Nuclear and Energy Research Institute (IPEN-CNEN/SP), using an Advanced Oxidation Process (AOP) with Fenton's reagents. This method would allow a higher incorporation in cement. Three different resins were evaluated: cationic, anionic and a mixture of both resins. The reactions were conducted varying the catalyst concentration (25, 50, 100 and 150 mM), the volume of hydrogen peroxide (320 to 460 mL), and three different temperatures, 50, 60 and 70 deg C. Degradation of about 98% was achieved using a 50 mM catalyst solution and 330 mL of hydrogen peroxide solution. The most efficient temperature was 60 deg C. (author)

  19. Decolorizing textile wastewater with Fenton's reagent electrogenerated with a solar photovoltaic cell.

    Science.gov (United States)

    Figueroa, Sandra; Vázquez, Leticia; Alvarez-Gallegos, A

    2009-02-01

    In this work it is demonstrated that Fenton's reagent can be electroproduced with abundant and cheap feedstock: oxygen saturated wastewater and solar energy. Experiments were carried out in a divided electrochemical flow cell using two electrodes: a three dimensional reticulated vitreous carbon cathode and stainless steel anode. Fenton's reagent is produced by oxygen reduction on the cathode in the presence of 1mM Fe(2+). The influence of electrolyte nature and its concentration and potential difference on the current efficiency, as well as the rate of Fenton's reagent electroproduction is discussed and it is concluded that over this extended range of conditions the current efficiency, for Fenton's reagent production, fell within the range 50-70%. It is possible to electroproduce a stoichiometric amount of Fenton reagent for the oxidation of 0.061mM Reactive Black 5 (in tap water+0.05M Na(2)SO(4), approximately pH 2.8). Similar results were obtained for solutions containing 0.1mM Acid Green 25. Some practical applications in the field of water treatment are included. The energy required for drive electrochemical reaction is supplied to the flow cell by means of a commercial solar panel.

  20. Advanced Treatment of Pesticide-Containing Wastewater Using Fenton Reagent Enhanced by Microwave Electrodeless Ultraviolet

    Directory of Open Access Journals (Sweden)

    Gong Cheng

    2015-01-01

    Full Text Available The photo-Fenton reaction is a promising method to treat organic contaminants in water. In this paper, a Fenton reagent enhanced by microwave electrodeless ultraviolet (MWEUV/Fenton method was proposed for advanced treatment of nonbiodegradable organic substance in pesticide-containing biotreated wastewater. MWEUV lamp was found to be more effective for chemical oxygen demand (COD removal than commercial mercury lamps in the Fenton process. The pseudo-first order kinetic model can well describe COD removal from pesticide-containing wastewater by MWEUV/Fenton, and the apparent rate constant (k was 0.0125 min−1. The optimal conditions for MWEUV/Fenton process were determined as initial pH of 5, Fe2+ dosage of 0.8 mmol/L, and H2O2 dosage of 100 mmol/L. Under the optimal conditions, the reaction exhibited high mineralization degrees of organics, where COD and dissolved organic carbon (DOC concentration decreased from 183.2 mg/L to 36.9 mg/L and 43.5 mg/L to 27.8 mg/L, respectively. Three main pesticides in the wastewater, as Dimethoate, Triazophos, and Malathion, were completely removed by the MWEUV/Fenton process within 120 min. The high degree of pesticides decomposition and mineralization was proved by the detected inorganic anions.

  1. Roles of iron species and pH optimization on sewage sludge conditioning with Fenton's reagent and lime.

    Science.gov (United States)

    Yu, Wenbo; Yang, Jiakuan; Shi, Yafei; Song, Jian; Shi, Yao; Xiao, Jun; Li, Chao; Xu, Xinyu; He, Shu; Liang, Sha; Wu, Xu; Hu, Jingping

    2016-05-15

    Conditioning sewage sludge with Fenton's reagent could effectively improve its dewaterability. However, drawbacks of conditioning with Fenton's reagent are requirement of acidic conditions to prevent iron precipitation and subsequent neutralization with alkaline additive to obtain the pH of the filtrate close to neutrality. In this study, roles of pH were thoroughly investigated in the acidification pretreatment, Fenton reaction, and the final filtrate after conditioning. Through the response surface methodology (RSM), the optimal dosages of H2SO4, Fe(2+), H2O2, and lime acted as a neutralizer were found to be 0 (no acidification), 47.9, 34.3 and 43.2 mg/g DS (dry solids). With those optimal doses, water content of the dewatered sludge cakes could be reduced to 55.8 ± 0.6 wt%, and pH of the final filtrate was 6.6 ± 0.2. Fenton conditioning without initial acidification can simplify the conditioning process and reduce the usage of lime. The Fe(3+) content in the sludge cakes showed a close correlation with the dewaterability of conditioned sludge, i.e., the water content of sludge cakes, SRF (specific resistance to filtration), CST (capillary suction time), bound water content, and specific surface area. It indicated that the coagulation by Fe(3+) species in Fenton reaction could play an important role, compared to traditional Fenton oxidation effect on sludge conditioning. Thus, a two-step mechanism of Fenton oxidation and Fe(III) coagulation was proposed in sewage sludge conditioning. The mechanisms include the following: (1) extracellular polymeric substances (EPS) were firstly degraded into dissolved organics by Fenton oxidation; (2) bound water was converted to free water due to degradation of EPS; (3) the sludge particles were disintegrated into small ones by oxidation; (4) Fe(3+) generated from Fenton reaction acted as a coagulant to agglomerate smaller sludge particles into larger dense particles with less bond water; (5) finally, the dewatered

  2. Mechanism of red mud combined with Fenton's reagent in sewage sludge conditioning.

    Science.gov (United States)

    Zhang, Hao; Yang, Jiakuan; Yu, Wenbo; Luo, Sen; Peng, Li; Shen, Xingxing; Shi, Yafei; Zhang, Shinan; Song, Jian; Ye, Nan; Li, Ye; Yang, Changzhu; Liang, Sha

    2014-08-01

    Red mud was evaluated as an alternative skeleton builder combined with Fenton's reagent in sewage sludge conditioning. The results show that red mud combined with Fenton's reagent showed good conditioning capability with the pH of the filtrate close to neutrality, indicating that red mud acted as a neutralizer as well as a skeleton builder when jointly used with Fenton's reagent. Through response surface methodology (RSM), the optimal dosages of Fe(2+), H2O2 and red mud were proposed as 31.9, 33.7 and 275.1 mg/g DS (dry solids), respectively. The mechanism of the composite conditioner could be illuminated as follows: (1) extracellular polymeric substances (EPS), including loosely bound EPS and tightly bound EPS, were degraded into dissolved organics, e.g., proteins and polysaccharides; (2) bound water was released and converted into free water due to the degradation of EPS; and (3) morphology of the conditioned sludge exhibited a porous structure in contrast with the compact structure of raw sludge, and the addition of red mud formed new mineral phases and a rigid lattice structure in sludge, allowing the outflow of free water. Thus, sludge dewatering performance was effectively improved. The economic assessment for a wastewater treatment plant of 370,000 equivalent inhabitants confirms that using red mud conditioning, combined with Fenton's reagent, leads to a saving of approximately 411,000 USD/y or 50.8 USD/t DS comparing with using lime and ordinary Portland cement combined with Fenton's reagent, and approximately 612,000 USD/y or 75.5 USD/t DS comparing with the traditional treatment. Copyright © 2014 Elsevier Ltd. All rights reserved.

  3. IN-PLACE REGENERATION OF GAC USING FENTON'S REAGENTS

    Science.gov (United States)

    This paper evaluates the feasibility of using Fenton’s reagents for in-place recovery of spent granular activated carbon (GAC). Fenton’s reagents are cycled through spent GAC to degrade sorbed chlorinated hydrocarbons with little loss of carbon capacity. Seven chlorinated compou...

  4. Photo oxidative degradation of azure-B by sono-photo-Fenton and photo-Fenton reagents

    Directory of Open Access Journals (Sweden)

    Prahlad Vaishnave

    2014-12-01

    Full Text Available A model for the decomposition of azure-B by photo-Fenton reagent in the presence of ultrasound in homogeneous aqueous solution has been described. The photochemical decomposition rate of azure-B is markedly increased in the presence of ultrasound. It is a rather inexpensive reagent for wastewater treatment. The effect of different variables like the concentration of ferric ion, concentration of dye, hydrogen peroxide, pH, light intensity etc. on the reaction rate has been observed. The progress of the sono-photochemical degradation was monitored spectrophotometrically. The optimum sono-photochemical degradation conditions were experimentally determined. The results showed that the dye was completely oxidized and degraded into CO2 and H2O. A suitable tentative mechanism for sono-photochemical bleaching of azure-B by sono-photo-Fenton’s reaction has been proposed.

  5. Winery wastewater treatment by a combined process: long term aerated storage and Fenton's reagent.

    Science.gov (United States)

    Lucas, Marco S; Mouta, Maria; Pirra, António; Peres, José A

    2009-01-01

    The degradation of the organic pollutants present in winery wastewater was carried out by the combination of two successive steps: an aerobic biological process followed by a chemical oxidation process using Fenton's reagent. The main goal of this study was to evaluate the temporal characteristics of solids and chemical oxygen demand (COD) present in winery wastewater in a long term aerated storage bioreactor. The performance of different air dosage daily supplied to the biologic reactor, in laboratory and pilot scale, were examined. The long term hydraulic retention time, 11 weeks, contributed remarkably to the reduction of COD (about 90%) and the combination with the Fenton's reagent led to a high overall COD reduction that reached 99.5% when the mass ratio (R = H(2)O(2)/COD) used was equal to 2.5, maintaining constant the molar ratio H(2)O(2)/Fe(2+)=15.

  6. Treatment of textile effluent by chemical (Fenton's Reagent) and biological (sequencing batch reactor) oxidation

    International Nuclear Information System (INIS)

    Rodrigues, Carmen S.D.; Madeira, Luis M.; Boaventura, Rui A.R.

    2009-01-01

    The removal of organic compounds and colour from a synthetic effluent simulating a cotton dyeing wastewater was evaluated by using a combined process of Fenton's Reagent oxidation and biological degradation in a sequencing batch reactor (SBR). The experimental design methodology was first applied to the chemical oxidation process in order to determine the values of temperature, ferrous ion concentration and hydrogen peroxide concentration that maximize dissolved organic carbon (DOC) and colour removals and increase the effluent's biodegradability. Additional studies on the biological oxidation (SBR) of the raw and previously submitted to Fenton's oxidation effluent had been performed during 15 cycles (i.e., up to steady-state conditions), each one with the duration of 11.5 h; Fenton's oxidation was performed either in conditions that maximize the colour removal or the increase in the biodegradability. The obtained results allowed concluding that the combination of the two treatment processes provides much better removals of DOC, BOD 5 and colour than the biological or chemical treatment alone. Moreover, the removal of organic matter in the integrated process is particularly effective when Fenton's pre-oxidation is carried out under conditions that promote the maximum increase in wastewater biodegradability.

  7. Mechanism and Parameter Optimization of Fenton's Reagent Integrated with Surfactant Pretreatment to Improve Sludge Dewaterability.

    Directory of Open Access Journals (Sweden)

    Yi Xing

    Full Text Available Sludge dewatering can effectively reduce the volume and mass of sludge for subsequent treatment and disposal. The work validated the potential of Fenton's reagent combined with dodecyl dimethyl benzyl ammonium chloride (DDBAC in improving sludge dewaterability and proposed the mechanism of joint conditioning. The composite conditioner dosage was optimized using response surface methodology. Results indicated the good conditioning capability of the composite conditioners. The optimum dosages for H2O2, Fe2+, and DDBAC were 44.6, 39.6, and 71.0 mg/g, respectively, at which a sludge cake water content of 59.67% could be achieved. Moreover, a second-order polynomial equation was developed to describe the behavior of joint conditioning. Analysis of the reaction mechanism showed that Fenton oxidation effectively decomposed extracellular polymeric substance (EPS, including loosely bound EPS (LB-EPS and tightly bound EPS (TB-EPS, into dissolved organics, such as proteins and polysaccharides. The process facilitated the conversion of the bound water into free water. Furthermore, DDBAC further released the bound water through solubilization of TB-EPS and LB-EPS after the Fenton reaction. The bound water content of the sludge conditioned with Fenton's reagent decreased from 3.15 to 1.36 g/g and further decreased to 1.08 g/g with the addition of DDBAC. High-performance liquid chromatography analysis verified that the composite conditioning could oxidize and hydrolyze EPS into low-molecular-mass organics (e.g., formic and acetic acid, thereby facilitating the release of bound water.

  8. Fenton reagent and titanium dioxide nanoparticles as antifungal agents to control leaf spot of sugar beet under field conditions

    Directory of Open Access Journals (Sweden)

    Hamza Amany

    2016-07-01

    Full Text Available In this study, foliar sprays of Fenton solutions (Fenton reaction, Fenton-like reaction and Fenton complex, titanium dioxide (TiO2 and the recommended fungicide (chlorothalonil were estimated in the control of sugar beet leaf spot caused by Cercospora beticola under field conditions in two growing seasons. In addition, the impacts of these treatments on some crop characters (leaf dry weight, root fresh weight, soluble solid content, sucrose content and purity of sugar were examined. Biochemical and histological changes in the livers and kidneys of treated rats compared to an untreated control were utilized to assess the toxicity of the examined curative agents. Overall, chlorothalonil and Fenton complex were the most effective treatments for disease suppression in both tested seasons followed by Fenton-like reagent, Fenton’s reagent and TiO2, respectively. Growth and yield characters of treated sugar beet significantly increased in comparison to an untreated control. There were mild or no (biochemical and histological changes in the livers and kidneys of treated rats compared to the control. Fenton solutions and TiO2 may offer a new alternative for leaf spot control in sugar beet.

  9. Optimal Condition of Fenton's Reagent to Enhance the Alcohol Production from Palm Oil Mill Effluent (POME

    Directory of Open Access Journals (Sweden)

    Supawadee Sinnaraprasat

    2011-07-01

    Full Text Available Application of Fenton's reaction for a proper hydrolysis step is an essential and important step in obtaining a higher level of readily biodegradable sugars from palm oil mill effluent (POME for improving the alcohol production by using immobilized Clostridium acetobutylicum. The objective of this research was, therefore, to investigate the optimum condition of Fenton's reaction in terms of COD: H2O2 ratios (w/w and H2O2: Fe2+ ratios (molar ratio used to oxidize carbohydrate and high molecular organic compounds into simple sugars, which are further fermented into alcohol. The experiments were carried out at H2O2: Fe2+ ratios (molar ratios of 5, 10, 20, 30 and 40 and the COD: H2O2 ratios (w/w of 50, 70, 100 and 130 (initial COD about 50,000 mg/L. The total sugar concentrations and organic compounds biodegradability (BOD5/COD ratios were also used for investigating suitable conditions for Fenton's reaction. The concentration of Fenton's reagent at H2O2:Fe2+ and COD:H2O2 ratio of 20 and 130 was identified as the optimum operating condition for the highest simple sugars of about 0.865% and BOD5/COD ratios of 0.539. The alcohol productions were carried out in the continuous stirred tank reactors (CSTR under an anaerobic continuous immobilization system. At a hydraulic retention time of 12 hours and POME pH of 4.8, the maximum total ABE concentration of 495 mg/L and the ABE yield of 0.236 grams of ABE produced/gram of reducing sugars were achieved at the mixed polyvinyl alcohol (PVA and palm oil ash (POA ratio of 10 : 3.

  10. Degradation of ion spent resin using the Fenton's reagent; Degradacao da resina de troca ionica utilizando o reagente de Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Leandro Goulart de

    2013-07-01

    The most common method for spent radioactive ion exchange resin treatment is its immobilization in cement, which reduces the radionuclides release into the environment. Although this method is efficient, it increases considerably the final volume of the waste due to the low incorporation capacity. The objective of this work was to develop a degradation method of spent resins arising from the nuclear research reactor located at the Nuclear and Energy Research Institute (IPEN-CNEN/SP), using an Advanced Oxidation Process (AOP) with Fenton's reagents. This method would allow a higher incorporation in cement. Three different resins were evaluated: cationic, anionic and a mixture of both resins. The reactions were conducted varying the catalyst concentration (25, 50, 100 and 150 mM), the volume of hydrogen peroxide (320 to 460 mL), and three different temperatures, 50, 60 and 70 deg C. Degradation of about 98% was achieved using a 50 mM catalyst solution and 330 mL of hydrogen peroxide solution. The most efficient temperature was 60 deg C. (author)

  11. Effects of Fenton's Reagent on aquifer geochemistry and microbiology at the A/M Area, Savannah River Site

    International Nuclear Information System (INIS)

    Denham, M.

    2000-01-01

    This report details the results of an investigation of Site conditions following a successful 1997 demonstration of in-situ DNAPL destruction by injection of Fenton's Reagent (hydrogen peroxide and ferrous sulfate solution) into DNAPL-bearing zones of an aquifer

  12. The oxidative response and viable reaction mechanism of the textile dyes by fenton reagent

    International Nuclear Information System (INIS)

    Masooda, Q.; Hijira, T.; Sitara, M.; Sehar, M.; Sundus, A.; Mohsin, A.

    2017-01-01

    The mechanism of the degradation of the Reactive Red 239 and Reactive Blue 19 by Fenton reagent was studied by advanced oxidation process in aqueous medium. The spectroscopic technique was adopted for the measurements of dye concentration. Moreover they were determined at 540 nm and 590 nm, respectively. Kinetics of the reaction was studied under the effect of concentration of reactive dyes, concentration of oxidant were followed under pseudo first order condition and found to influence the catalytic mechanism. The pH of the medium, vibrant response of several cations and anions and influence of ionic strength on the reaction kinetics were also monitored. Physical evidences for the degradation and mineralization of the dyes were evaluated by Lime water test, Ring Test and TLC test also confirmed the degradation of dye. Inhibitory effects of dyes were observed by CO3-, HCO3-, HPO42-, Cl-, I- Al3+ and Na+. Thermodynamic activation parameters in the oxidation reaction were studied and mode of mechanism was suggested on the basic of these parameters. This study explored the safe and eco friendly degradation of the textile dyes under Pseudo first order rate constant. It was observed that Fenton assisted degradation of the dyes under controlled conditions was found to be favorable for the treatment of textile wastewater. Moreover compared to other chemical methods it is effective and harmless to the environment. (author)

  13. Remediation of hydrocarbons in crude oil-contaminated soils using Fenton's reagent.

    Science.gov (United States)

    Ojinnaka, Chukwunonye; Osuji, Leo; Achugasim, Ozioma

    2012-11-01

    Sandy soil samples spiked with Bonny light crude oil were subsequently treated with Fenton's reagent at acidic, neutral, and basic pH ranges. Oil extracts from these samples including an untreated one were analyzed 1 week later with a gas chromatograph to provide evidence of hydrocarbon depletion by the oxidant. The reduction of three broad hydrocarbon groups-total petroleum hydrocarbon (TPH); benzene, toluene, ethylbenzene, and xylene (BTEX); and polycyclic aromatic hydrocarbon (PAH) were investigated at various pHs. Hydrocarbon removal was efficient, with treatment at the acidic pH giving the highest removal of about 96% for PAH, 99% for BTEX, and some TPH components experiencing complete disappearance. The four-ringed PAHs were depleted more than their three-ringed counterparts at the studied pH ranges.

  14. Tratamento de água subterrânea contaminada com compostos organoclorados usando ferro elementar e o reagente de Fenton Treatment of groundwater contaminated with chlorinated compounds using elemental iron and Fenton's reagent

    Directory of Open Access Journals (Sweden)

    Tatiana Langbeck de Arruda

    2007-01-01

    Full Text Available The remediation of groundwater containing organochlorine compounds was evaluated using a reductive system with zero-valent iron, and the reductive process coupled with Fenton's reagent. The concentration of the individual target compounds reached up to 400 mg L-1 in the sample. Marked reductions in the chlorinated compounds were observed in the reductive process. The degradation followed pseudo-first-order kinetics in terms of the contaminant and was dependent on the sample contact time with the solid reducing agent. An oxidative test with Fenton's reagent, followed by the reductive assay, showed that tetrachloroethylene was further reduced up to three times the initial concentration. The destruction of chloroform, however, demands an additional treatment.

  15. Degradation of organic dyes by a new heterogeneous Fenton reagent - Fe2GeS4 nanoparticle.

    Science.gov (United States)

    Shi, Xiaoguo; Tian, Ang; You, Junhua; Yang, He; Wang, Yuzheng; Xue, Xiangxin

    2018-07-05

    The heterogeneous Fenton system has become the hotspot in the decontamination field due to its effective degradation performance with a wide pH range. Based on the unstable chemical properties of pyrite, in this article, Fe 2 GeS 4 nanoparticles with better thermodynamic stability were prepared by vacuum sintering and high energy ball milling and its potential as Fenton reagent was investigated for the first time. Three determinants of the heterogeneous Fenton system including the iron source, hydrogen peroxide, pH and the degradation mechanism were investigated. The catalyst dosage of 0.3 g/L, initial H 2 O 2 concentration in the Fenton system of 50 m mol/L and pH of 7 were chosen as the best operational conditions. An almost complete degradation was achieved within 5 min for methylene blue and rhodamine b while 10 min for methyl orange. The total organic carbon removal efficiencies of Fe 2 GeS 4 heterogeneous Fenton system for methylene blue, methyl orange and rhodamine b in 10 min were 56.3%, 66.2% and 74.2%, respectively. It's found that the degradation ability could be attributed to a heterogeneous catalysis occurring at the Fe 2 GeS 4 surface together with a homogeneous catalysis in the aqueous phase by the dissolved iron ions. Copyright © 2018 Elsevier B.V. All rights reserved.

  16. Influence of Fenton's reagent treatment on electrochemical properties of graphite felt for all vanadium redox flow battery

    International Nuclear Information System (INIS)

    Gao, Chao; Wang, NanFang; Peng, Sui; Liu, SuQin; Lei, Ying; Liang, XinXing; Zeng, ShanShan; Zi, HuiFang

    2013-01-01

    Highlights: ► Highly hydroxyl-functionalized graphite felt has been obtained through Fenton's reagent treatment. ► Fenton's reagent treatment involves only one step, works under ambient conditions and will never produce any toxic gas. ► The treated graphite felt exhibits superior electrochemical performance in comparison to the untreated one. -- Abstract: An environmental, economic and highly effective method for carbon fiber hydroxylated-functionalization based on Fenton's reagent treatment is used to improve the electrochemical activity of graphite felt (GF) as the positive electrode in all vanadium redox flow battery (VRFB). The effect of H 2 O 2 content in Fenton's reagent on the structure and electrochemical properties of GF is investigated. The scanning electron microscope (SEM) indicates that the surface of the treated GF is etched increasingly with the content of H 2 O 2 . The Fourier transformation infrared (FTIR) spectroscopy shows that the peak intensity of hydroxyl groups on the treated felt is increased with the H 2 O 2 concentration, which is further verified by X-ray photoelectron spectroscopy (XPS). Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) show that the treated sample exhibits a higher electrochemical activity. A VRFB with the treated GF as electrodes exhibits higher coulombic, voltage and energy efficiency (98.8%, 75.1% and 74.2%) than that with the untreated GF (93.9%, 72.1% and 67.7%) at 60 mA cm −2 , and this method is even superior when compared with the reported methods

  17. Determining the optimal dose of Fenton reagent in a leachate treatment by Fenton-adsorption; Determinacion de la dosis optima de reactivo Fenton en un tratamiento de lixiviados por Fenton-adsorcion

    Energy Technology Data Exchange (ETDEWEB)

    Mendez Novelo, Roger Ivan; Pietrogiovanna Bronca, Jose Alfredo; Santos Ocampo, Beatriz; Sauri Riancho, Maria Rosa; Giacoman Vallejos, German; Castillo Borges, Elba Rene [Universidad Autonoma de Yucatan, Facultad de Ingenieria, Merida, Yucatan (Mexico)]. E-mail: mnovelo@uady.mx

    2010-07-01

    Leachates are formed as a result of the percolation of liquids, through the solid wastes in stabilization process. Their composition is variable and highly toxic; therefore, leachates treatment is a complex task. Due to the high permeability of the soil of the Yucatan Peninsula leachates represent a high risk to health. Fenton type oxidation and adsorption treatment have been tested, and they have showed better results than other types of biological or physicochemical treatment. Fenton process consists in treating the contaminant load with a combination of H{sub 2}O{sub 2} and FeSO{sub 4} under acidic conditions. Experiments were conducted in order to determine if filtration was better than the sedimentation of the sludges. The optimum contact time and the best relations [Fe{sup 2+}]/[H{sub 2}O{sub 2}] and [COD]/[H{sub 2}O{sub 2}] were determined. Subsequently, the oxidized samples were filtered and the adsorption process was tested using two columns in series packed with activated carbon. It was concluded that the sludge generated by the Fenton process was removed more efficiently through filtration than sedimentation. Optimal contact times were 5 min for COD removal, and 1 hour for colour removal; process time was set to one hour in order to protect the activated carbon. The best relations for [Fe{sup 2+}]/[H{sub 2}O{sub 2}] and [COD]/[H{sub 2}O{sub 2}] were 0.6 and 9 respectively. The maximum removal efficiency after the adsorption process was 98.9% for COD and 100% for colour at zero time of the column. A final biodegradability index of 0.24 was reached after the Fenton-adsorption tests. [Spanish] Los lixiviados son el resultado de la percolacion de liquidos a traves de los desechos solidos en proceso de estabilizacion. La complejidad de su tratamiento se debe a que su composicion es altamente toxica y variable. Lo anterior y el suelo altamente permeable de la peninsula de Yucatan, representan un alto peligro a la salud. Se ensayo un tratamiento de oxidacion

  18. Dewaterability of five sewage sludges in Guangzhou conditioned with Fenton's reagent/lime and pilot-scale experiments using ultrahigh pressure filtration system.

    Science.gov (United States)

    Liang, Jialin; Huang, Shaosong; Dai, Yongkang; Li, Lei; Sun, Shuiyu

    2015-11-01

    Sludge conditioning with Fenton's reagent and lime is a valid method for sludge dewatering. This study investigated the influence of different organic matter content sludge on sludge dewatering and discussed the main mechanism of sludge conditioning by combined Fenton's reagent and lime. The results indicated that the specific resistance to filterability (SRF) of sludge was reduced efficiently by approximately 90%, when conditioned with Fenton's reagent and lime. Through single factor experiments, the optimal conditioning combinations were found. In addition, the relationship between VSS% and consumption of the reagents was detected. Furthermore, it was also demonstrated that the SRF and filtrate TOC values had a significant correlation with VSS% of sludge (including raw and conditioned). The main mechanism of sludge dewatering was also investigated. Firstly, it revealed that the dewaterability of sludge was closely correlated to extracellular polymeric substances (EPS) and bound water contents. Secondly, the results of scanning electron microscopy (SEM) stated that sludge particles were to be smaller and thinner after conditioning. And this structure could easily form outflow channels for releasing free water. Additionally, with the ultrahigh pressure filtration system, the water content of sludge cake conditioned with Fenton's reagent and lime could be reduced to below 50%. Moreover, the economic assessment shows that Fenton's reagent and lime combined with ultrahigh pressure filtration system can be an economical and viable technology for sewage sludge dewatering. Finally, three types of sludge were classified: (1) Fast to dewater; (2) Moderately fast to dewater; (3) Slow to dewater sludge. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. Performing in-situ chemical oxidation with Fenton's Reagent at a former gas work in Rotterdam

    Energy Technology Data Exchange (ETDEWEB)

    Plaisier, W.; Pancras, T. [In-situ Technieken BV, Wageningen (Netherlands); Bennen, M.; Bouwhuis, E. [Public Works Rotterdam (Netherlands)

    2003-07-01

    In-Situ Technieken BV is the first company in the Netherlands to apply full-scale in-situ chemical oxidation (ISCO) by means of Fenton's reagent or permanganates. The use of ISCO for soil remediation purposes originated in the USA. After three years of practical experience in the Netherlands it can be stated that ISCO has become a proven technology for source area treatment in the Netherlands as well. We present the results of a pilot ISCO treatment program with Fenton's reagent that was performed at the former gas works facility 'Feyenoord'. The site is one of the largest gas works facilities built in Rotterdam. The former gas production activities have lead to severe pollution of soil and groundwater over an area of approximately 3 hectares. Both laboratory and field observations showed that it would be very difficult to execute an efficient Fenton's reagent ISCO treatment program at this specific site for the following reasons. First of all, the contamination consisting of tar and tar-related compounds is found in an anthropogenic (man-made) soil of 9 meter in thickness. Secondly, high contents of carbonates and organic material were found in the soils, which act as a scavenger for the hydroxyl free radical in a Fenton's reagent ISCO system. The pilot test was performed in two phases with an intermediate period of 2 months. The injection of totally 24 tonnes hydrogen peroxide (50%) was anticipated. Reactions of the reagents in the soil were very strong. The presence of old (forgotten) boreholes and an intensive drainage system, in combination with the aggressive reaction resulted in short-circuiting of reagents to the surface. Out of the proposed 24 tonnes of hydrogen peroxide (50%) only 14.5 tonnes were injected. This would have effect on the amount of contamination oxidized. Nevertheless, the oxidation had a significant effect on the soil contamination. A reduction of approximately 90% for PAH was obtained. Reduction was also

  20. Fenton's reagent as a remediation process in water treatment: application to the degradation of polycyclic aromatic hydrocarbons in waters and sewage sludges; La reaction de fenton comme procede de rehabilitation dans le traitement des eaux: application a la degradation des hydrocarbures aromatiques polycycliques dans les eaux et les boues residuaires

    Energy Technology Data Exchange (ETDEWEB)

    Flotron, V

    2004-05-15

    This study is related to the application of Fenton's reagent to remedy matrices contaminated by polycyclic aromatic hydrocarbons (PAHs). In aqueous solution, the choice of the reagent implementation is important, in order to generate enough radicals to oxidize pollutants. Degradation of the organic compounds is possible, but a large difference in reactivity is observed between 'alternant' and 'non-alternant' PAHs (with a five carbon atoms cycle). Besides, if a few specific precautions are omitted, the PAHs can sorb onto the flask inside surface, and therefore not undergo oxidation. The results on sewage sludges show that under certain conditions (high reagent concentrations), the pollutants can be oxidised although they are adsorbed. Moreover, it appears that the matrix itself plays an important role, as the iron oxides seem to be able to decompose hydrogen peroxide, and thus initiate Fenton reaction. Its application to contaminated soils and sediments is also possible. (author)

  1. Fenton's reagent as a remediation process in water treatment: application to the degradation of polycyclic aromatic hydrocarbons in waters and sewage sludges; La reaction de fenton comme procede de rehabilitation dans le traitement des eaux: application a la degradation des hydrocarbures aromatiques polycycliques dans les eaux et les boues residuaires

    Energy Technology Data Exchange (ETDEWEB)

    Flotron, V.

    2004-05-15

    This study is related to the application of Fenton's reagent to remedy matrices contaminated by polycyclic aromatic hydrocarbons (PAHs). In aqueous solution, the choice of the reagent implementation is important, in order to generate enough radicals to oxidize pollutants. Degradation of the organic compounds is possible, but a large difference in reactivity is observed between 'alternant' and 'non-alternant' PAHs (with a five carbon atoms cycle). Besides, if a few specific precautions are omitted, the PAHs can sorb onto the flask inside surface, and therefore not undergo oxidation. The results on sewage sludges show that under certain conditions (high reagent concentrations), the pollutants can be oxidised although they are adsorbed. Moreover, it appears that the matrix itself plays an important role, as the iron oxides seem to be able to decompose hydrogen peroxide, and thus initiate Fenton reaction. Its application to contaminated soils and sediments is also possible. (author)

  2. Decontamination of soil containing POPs by the combined action of solid Fenton-like reagents and microwaves.

    Science.gov (United States)

    Cravotto, Giancarlo; Di Carlo, Stefano; Ondruschka, Bernd; Tumiatti, Vander; Roggero, Carlo Maria

    2007-10-01

    The effect on halogenated aromatics of solid, non-toxic oxidants such as sodium percarbonate and the urea/hydrogen peroxide complex (Fenton-like reagents) was investigated. A microwaves-assisted, solvent-free method for soil decontamination is presented. It marks a considerable advance in the search of more efficient, environment-friendly procedures for the degradative oxidation of persistent organic pollutants. Residual pollutants in treated soil samples were determined by GC/MS analysis after solvent extraction or direct thermal desorption. Results showed that 4-chloronaphthol, 2,4-dichlorophenoxyacetic acid and p-nonylphenol had been degraded completely, 2,4-dibromophenol to a large extent.

  3. Influence of the apparent molecular size of humic substances on the efficiency of coagulation using Fenton's reagent

    Directory of Open Access Journals (Sweden)

    MARCELO DE JULIO

    2013-06-01

    Full Text Available This work used Fenton's reagent as a coagulating agent in the treatment of water samples with high true colour caused by humic substances (HS extracted from peat. In addition, the effects of the apparent molecular size of HS on coagulation, flocculation and flotation were studied. To that end, four distinct water samples having the same true colour were prepared using HS with different molecular sizes, which were obtained by ultrafiltration fractioning. Through optimisation of coagulant dosage and coagulation pH, as well as posterior construction of coagulation diagrams for each water sample, it was verified that the sample prepared with the smallest apparent molecular size of HS was the most difficult to treat, requiring higher coagulant (Fenton's reagent dosages than samples prepared with larger HS molecular sizes. Furthermore, filtration experiments after dissolved air flotation (DAF were carried out in an attempt to simulate conventional treatment. The most representative results in filtered water were: apparent colour ≤ 3 HU; turbidity Este trabalho empregou o reagente de Fenton como agente coagulante no tratamento de águas contendo cor elevada causada pela introdução de substâncias húmicas extraídas de turfa. Além disto, foi estudado o efeito do tamanho molecular aparente das substâncias húmicas na eficiência da coagulação, floculação e flotação de águas; para isto foram preparadas quatro águas distintas apresentado a mesma cor verdadeira, mas com substâncias húmicas de diferentes tamanhos moleculares, obtidas por fracionamento por ultrafiltração. Por meio da otimização da dosagem de coagulante e respectivo pH de coagulação e posterior construção dos diagramas de coagulação para cada água de estudo, verificou-se que a água preparada com as substâncias húmicas de menor tamanho molecular aparente apresentou maior grau de dificuldade para tratamento, requerendo dosagens de coagulante (reagente de Fenton bem

  4. IN-SITU REGENERATION OF GRANULAR ACTIVATED CARBON (GAC) USING FENTON'S REAGENTS

    Science.gov (United States)

    Fenton-dependent regeneration of granular activated carbon (GAC) initially saturated with one of several chlorinated aliphatic contaminants was studied in batch and continuous-flow reactors. Homogeneous and heterogeneous experiments were designed to investigate the effects of va...

  5. Evaluation of three reagent dosing strategies in a photo-Fenton process for the decolorization of azo dye mixtures

    International Nuclear Information System (INIS)

    Prato-Garcia, D.; Buitrón, Germán

    2012-01-01

    Highlights: ► Dosing strategies for a photo-Fenton process were evaluated. ► The dosing strategy had no effect of on the decolorization. ► The type of strategy influenced SUVA index, toxicity reduction and biodegradability. ► A continuous reagents supply was found to be the most adequate strategy. ► Decolorization as well as a less toxic and biodegradable effluent was produced. - Abstract: Three reagent dosing strategies used in the solar photo-assisted decolorization of a mixture of sulfonated dyes consisting of acid blue 113, acid orange 7 and acid red 151 were evaluated. Results demonstrated that the dosing strategy influenced both reagent consumption and the biodegradability and toxicity of the effluent. In one strategy (E 1 ), the Fenton's reactants were dosed in a punctual mode, while in the other two strategies (E 2 an E 3 ), the reactants were dosed continuously. In the E 2 strategy the reactants were dosed by varying the duration of the injection time. In the E 3 strategy, the reactants were dosed during 60 min at a constant rate, but with different concentrations. All cases showed that feeding the reactor between 40% and 60% of the maximal dose was sufficient to decolorize more than 90% of the mixture of azo dyes. The E 1 strategy was less effective for aromatic content reduction. Conversely, the continuous addition of the reagents (E 2 and E 3 strategies) improved the aromatic content removal. E 3 strategy was substantially more appropriate than E 1 strategy due to improved the effluent quality in two key areas: toxicity and biodegradability.

  6. Electrochemical generation of fentons reagent to treat spent caustic wastewater

    International Nuclear Information System (INIS)

    Hansen, H. K.; Nunez, P.; Rodriguez, N.; Guzman, J.

    2009-01-01

    An important wastewater stream from oil refineries is the spent caustic. Caustic solutions are used as scrubbing agent during the desulphurization process to eliminate sulphur an mercaptans from oil and gasses. Spent caustic is classified as DOO3 (reactive sulphide) hazardous waste under the US Resource Conservation and Recovery Act (RCRA). (Author)

  7. Destruction of Ion-Exchange Resin In Waste From the HFIR, T1 and T2 Tanks Using Fenton's Reagent

    International Nuclear Information System (INIS)

    Taylor, P.A.

    2002-01-01

    The use of Fenton's reagent (hydrogen peroxide and a ferrous iron catalyst) has been tested as a method for destroying ion-exchange resin in radioactive waste from three underground storage tanks at the Oak Ridge National Laboratory. The resin in these wastes must be destroyed before they can be transferred to the Melton Valley Storage Tanks (MVSTs) prior to solidification and disposal at the Waste Isolation Pilot Plant. The reaction with ion-exchange resin requires a dilute acidic solution (pH = 3 to 5) and moderate temperatures (T = 60 to 100 C). Laboratory-scale tests of the process have been successfully completed using both simulants and actual waste samples. The ion-exchange resin is oxidized to carbon dioxide and inorganic salts. The reaction rate is quite slow for temperatures below 70 C but increases almost linearly as the temperature of the slurry increases from 70 to 90 C. Pilot-scale tests have demonstrated the process using larger samples of actual waste slurries. A sample from the High Flux Isotope Reactor (HFIR) tank, containing 500 mL of settled solids (resin and inorganic sludge) in a total volume of 1800 mL, was successfully treated to meet MVST waste acceptance requirements in 9 h of processing time, using 1650 mL of 50 wt% hydrogen peroxide. A composite sample from the T1 and T2 tanks, which contained 1000 mL of settled solids in a total volume of 2000 mL required 8 h of treatment, using 1540 mL of 50 wt% peroxide, to meet waste acceptance requirements. Hydrogen peroxide reaction rates were 0.71 to 0.74 g H 2 O 2 /L/min, with very low (<2000 mg/L) concentrations of peroxide in the slurry. The reaction produces mostly carbon dioxide gas during the early part of the treatment, when organic carbon concentrations in the slurry are high, and then produces increasing amounts of oxygen as the organic carbon concentration drops. Small amounts (<3 vol%) of carbon monoxide are also generated. The off-gas from the pilot-scale tests, which was 81 vol

  8. Optimizing the treatment of landfill leachate by conventional Fenton and photo-Fenton processes

    International Nuclear Information System (INIS)

    Hermosilla, Daphne; Cortijo, Manuel; Huang, Chin Pao

    2009-01-01

    Landfill, a matured and economically appealing technology, is the ultimate approach for the management of municipal solid wastes. However, the inevitable generation of leachate from landfill requires further treatment. Among the various leachate treatment technologies available, advanced oxidation processes (AOPs) are among powerful methods to deal with the refractory organic constituents, and the Fenton reagent has evolved as one promising AOPs for the treatment of leachates. Particularly, the combination of UV-radiation with Fenton's reagent has been reported to be a method that allows both the photo-regeneration of Fe 2+ and photo-decarboxylation of ferric carboxylates. In this study, Fenton and photo-Fenton processes were fine tuned for the treatment of leachates from the Colmenar Viejo (Madrid, Spain) Landfill. Results showed that it is possible to define a set of conditions under which the same COD and TOC removals (approx 70%) could be achieved with both the conventional and photo-Fenton processes. But Fenton process generated an important quantity of iron sludge, which will require further disposal, when performed under optimal COD removal conditions. Furthermore conventional Fenton process was able to achieve slightly over an 80% COD removal from a 'young' leachate, while for 'old' and 'mixed' leachates was close to a 70%. The main advantage showed by the photo-assisted Fenton treatment of landfill leachate was that it consumed 32 times less iron and produced 25 times less sludge volume yielding the same COD removal results than a conventional Fenton treatment.

  9. An oxidative desulfurization method using ultrasound/Fenton's reagent for obtaining low and/or ultra-low sulfur diesel fuel

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Yongchuan; Qi, Yutai [Department of Applied Chemistry, School of Science, Harbin Institute of Technology, Harbin 115001 (China); Zhao, Dezhi [Department of Petroleum Chemical Engineering, Liaoning Shihua University, Fushun 113001 (China); Zhang, Huicheng [Fushun Research Institute of Petroleum and Petrochemicals of SINOPEC Corp., Fushun 113001 (China)

    2008-10-15

    The total development trend in the world is towards continuously lower of sulfur content as a quality standard of diesel fuels. Integrating of an oxidative desulfurization unit with a conventional hydrotreating unit can bring benefits to producing low and/or ultra-low sulfur diesel fuels. Using the hydrotreated Middle East diesel fuel as a feedstock, four processes of the oxidative desulfurization have been studied: a hydrogen peroxide-acetic acid system and a Fenton's reagent system both without/with ultrasound. Results showed that the oxidative desulfurization reaction mechanics fitted apparent first-order kinetics. The addition of Fenton's reagent could enhance the oxidative desulfurization efficiency for diesel fuels and sono-oxidation treatment in combination with Fenton's reagent shows a good synergistic effect. Under our best operating condition for the oxidative desulfurization: temperature 313 K, ultrasonic power 200 W, ultrasonic frequency 28 kHz, Fe{sup 2+}/H{sub 2}O{sub 2} 0.05 mol/mol, pH 2.10 in aqueous phase and reaction time 15 min, the sulfur content in the diesel fuels was decreased from 568.75 {mu}g/g to 9.50 {mu}g/g. (author)

  10. Avaliação de processo oxidativo avançado pelo reagente de Fenton em condições otimizadas no tratamento de lixiviado de aterro sanitário com ênfase em parâmetros coletivos e caracterização do lodo gerado

    Directory of Open Access Journals (Sweden)

    Wagner Guadagnin Moravia

    2011-01-01

    Full Text Available An alternative for landfill leachate treatment are advanced oxidation processes by Fenton's reagent (AOP/Fenton. In this context, the aim of this paper was to evaluate, in a bench scale, the treatability of leachate pós-AOP/Fenton characterizing the supernatant and the sludge generated separately. Observed in optimal conditions, high removal efficiency of COD (76.7%, real color (76.4% and humic substances (50%. Organic compounds were detected in the sludge (2.465 mg COD L-1 and high concentration of iron (1.757 mg L-1 as was expected. Finally, the sludge generated showed low settling hindering their separation by sedimentation (SVI = 321 mL g-1.

  11. Assessment of Fenton's reagent and ozonation as pre-treatments for increasing the biodegradability of aqueous diethanolamine solutions from an oil refinery gas sweetening process.

    Science.gov (United States)

    Durán-Moreno, A; García-González, S A; Gutiérrez-Lara, M R; Rigas, F; Ramírez-Zamora, R M

    2011-02-28

    The aim of this work was to evaluate the efficiency of three chemical oxidation processes for increasing the biodegradability of aqueous diethanolamine solutions (aqueous DEA solutions), to be used as pre-treatments before a biological process. The raw aqueous DEA solution, sourced from a sour gas sweetening plant at a Mexican oil refinery, was first characterized by standardized physico-chemical methods. Then experiments were conducted on diluted aqueous DEA solutions to test the effects of Fenton's reagent, ozone and ozone-hydrogen peroxide on the removal of some physicochemical parameters of these solutions. Lastly, biodegradability tests based on Dissolved Organic Carbon Die Away OECD301-A, were carried out on a dilution of the raw aqueous DEA solution and on the treated aqueous DEA solutions, produced by applying the best experimental conditions determined during the aforementioned oxidation tests. Experimental results showed that for aqueous DEA solutions treated with Fenton's reagent, the best degradation rate (70%) was obtained at pH 2.8, with Fe(2+) and H(2)O(2) at doses of 1000 and 10,000 mg/L respectively. In the ozone process, the best degradation (60%) was observed in aqueous DEA solution (100 mg COD/L), using 100 mg O(3)/L at pH 5. In the ozone-hydrogen peroxide process, no COD or DOC removals were observed. The diluted spent diethanolamine solution showed its greatest increase in biodegradability after a reaction period of 28 days when treated with Fenton's reagent, but after only 15 days in the case of ozonation. Copyright © 2011 Elsevier B.V. All rights reserved.

  12. Treating leachate with advanced oxidation: applying Fenton's reagent; Oxidaciones avanzadas para el tratamiento de lixiviado: aplicacion del Reactivo de Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Maranonn Ruiz, I.; Sancho Seuma, L.

    2003-07-01

    The present study investigates the removal of refractory organics by Advanced Oxidation Process: Fenton's Reaction. A batch test protocol was designed to study the oxidation and coagulation in Fenton Reaction. The batch tests were conducted to determine the optimum conditions for the plant operation such as pH, H{sub 2}O{sub 2} dosage, FeSO{sub 4} dosage and contact time. It was found that the highest removal efficiencies of COD were with the oxidation at acid pH around 3 and the coagulation at basic pH around 8, few minutes of treatment time, the initial concentrations of H{sub 2}O{sub 2} were in the range 68-1550 mg/l and the different dosages of FeSO{sub 4} were in the range 487-3038 mg/l. They were added in determinate proportions to get the highest efficiency of producing OH, DBO{sub 5}/DQO ratio was decreased from 0,3 to 0,1. Therefore Fenton's reaction process is a very effective means for a pretreatment or tertiary treatment of biological methods. (Author) 20 refs.

  13. Nanosized zero-valent iron as Fenton-like reagent for ultrasonic-assisted leaching of zinc from blast furnace sludge

    Energy Technology Data Exchange (ETDEWEB)

    Mikhailov, Ivan, E-mail: ivan.mikhailov@misis.ru [National University of Science and Technology “MISiS”, 4 Leninskiy prospekt, Moscow, 119049 (Russian Federation); Komarov, Sergey [Tohoku University, 6-6-02 Aramaki Aza Aoba, Aoba-ku, Sendai, 980-8576 (Japan); Levina, Vera; Gusev, Alexander; Issi, Jean-Paul; Kuznetsov, Denis [National University of Science and Technology “MISiS”, 4 Leninskiy prospekt, Moscow, 119049 (Russian Federation)

    2017-01-05

    Highlights: • nZVI is used as Fenton-like reagent for activation of Zn leaching from the BFS. • nZVI has positive effect on kinetics of Zn leaching though with some loss of efficiency. • A complex ultrasonic-assisted method for BFS recycling is proposed. - Abstract: Ultrasonic-assisted sulphuric acid leaching combined with a Fenton-like process, utilizing nanoscale zero-valent iron (nZVI), was investigated to enhance the leaching of zinc from the blast furnace sludge (BFS). The leaching of iron (Fe) and zinc (Zn) from the sludge was investigated using Milli-Q water/BFS ratio of 10 and varying the concentration of hydrogen peroxide, sulphuric acid, the temperature, the input energy for ultrasound irradiation, and the presence or absence of nZVI as a Fenton reagent. The results showed that with 1 g/l addition of nZVI and 0.05 M of hydrogen peroxide, the kinetic rate of Zn leaching increased with a maximum dissolution degree of 80.2%, after 5 min treatment. In the absence of nZVI, the maximum dissolution degree of Zn was 99.2%, after 15 min treatment with 0.1 M of hydrogen peroxide. The rate of Zn leaching at several concentrations of hydrogen peroxide is accelerated in the presence of nZVI although a reduction in efficiency was observed. The loss of Fe was no more than 3%. On the basis of these results, the possible route for BFS recycling has been proposed (BFS slurry mixed with sulphuric acid and hydrogen peroxide is recirculated under ultrasonic irradiation then separated).

  14. Comparison of Fenton and sono-Fenton bisphenol A degradation

    International Nuclear Information System (INIS)

    Ioan, Iordache; Wilson, Steven; Lundanes, Elsa; Neculai, Aelenei

    2007-01-01

    Degradation of bisphenol A (BPA) was carried out with the Fenton reagent with and without additional sonochemical treatment. The Fenton and the sono-Fenton decomposition of BPA showed that ultrasound irradiation of wastewater improved the wet oxidation process of 25 mg l -1 BPA solutions. The sonochemical degradation of BPA was monitored using UV absorption and large volume injection packed capillary LC measurements

  15. Optimizing the treatment of landfill leachate by conventional Fenton and photo-Fenton processes

    Energy Technology Data Exchange (ETDEWEB)

    Hermosilla, Daphne, E-mail: dhermosilla@quim.ucm.es [Departamento de Ingenieria Quimica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040 Madrid (Spain); Cortijo, Manuel [U.D. Operaciones Basicas, Departamento de Ingenieria Forestal, E.T.S.I. Montes, Universidad Politecnica de Madrid, Avda. Ramiro de Maeztu s/n, 28040 Madrid (Spain); Huang, Chin Pao [Department of Civil and Environmental Engineering, 352C DuPont Hall, University of Delaware, Newark, DE 19716 (United States)

    2009-05-15

    Landfill, a matured and economically appealing technology, is the ultimate approach for the management of municipal solid wastes. However, the inevitable generation of leachate from landfill requires further treatment. Among the various leachate treatment technologies available, advanced oxidation processes (AOPs) are among powerful methods to deal with the refractory organic constituents, and the Fenton reagent has evolved as one promising AOPs for the treatment of leachates. Particularly, the combination of UV-radiation with Fenton's reagent has been reported to be a method that allows both the photo-regeneration of Fe{sup 2+} and photo-decarboxylation of ferric carboxylates. In this study, Fenton and photo-Fenton processes were fine tuned for the treatment of leachates from the Colmenar Viejo (Madrid, Spain) Landfill. Results showed that it is possible to define a set of conditions under which the same COD and TOC removals (approx 70%) could be achieved with both the conventional and photo-Fenton processes. But Fenton process generated an important quantity of iron sludge, which will require further disposal, when performed under optimal COD removal conditions. Furthermore conventional Fenton process was able to achieve slightly over an 80% COD removal from a 'young' leachate, while for 'old' and 'mixed' leachates was close to a 70%. The main advantage showed by the photo-assisted Fenton treatment of landfill leachate was that it consumed 32 times less iron and produced 25 times less sludge volume yielding the same COD removal results than a conventional Fenton treatment.

  16. Quantifying Fenton reaction pathways driven by self-generated H2O2 on pyrite surfaces

    Science.gov (United States)

    Gil-Lozano, C.; Davila, A. F.; Losa-Adams, E.; Fairén, A. G.; Gago-Duport, L.

    2017-03-01

    Oxidation of pyrite (FeS2) plays a significant role in the redox cycling of iron and sulfur on Earth and is the primary cause of acid mine drainage (AMD). It has been established that this process involves multi-step electron-transfer reactions between surface defects and adsorbed O2 and H2O, releasing sulfoxy species (e.g., S2O32-, SO42-) and ferrous iron (Fe2+) to the solution and also producing intermediate by-products, such as hydrogen peroxide (H2O2) and other reactive oxygen species (ROS), however, our understanding of the kinetics of these transient species is still limited. We investigated the kinetics of H2O2 formation in aqueous suspensions of FeS2 microparticles by monitoring, in real time, the H2O2 and dissolved O2 concentration under oxic and anoxic conditions using amperometric microsensors. Additional spectroscopic and structural analyses were done to track the dependencies between the process of FeS2 dissolution and the degradation of H2O2 through the Fenton reaction. Based on our experimental results, we built a kinetic model which explains the observed trend of H2O2, showing that FeS2 dissolution can act as a natural Fenton reagent, influencing the oxidation of third-party species during the long term evolution of geochemical systems, even in oxygen-limited environments.

  17. The use of Fenton's reagent in treating waste waters from the table olive producing industry; Aplicacion del reactivo de Fenton para la depuracion de las aguas residuales de la industria productora de aceituna de mesa

    Energy Technology Data Exchange (ETDEWEB)

    Beltran de Heredia, J.; Dominguez, J. R.

    2001-07-01

    A study was made of the chemical oxidation by means of Fenton's reagent (H{sub 2}O{sub 2}/Fe''24) on the lye used in pickling black olives. The aim of this process is to eliminate the organic materials from the waste water. It was monitored by tracking several overall reaction parameters such as Chemical Oxygen Demand (COD), total polyphenols, the aromaticity of the sample and the concentration of hydrogen peroxide in the reactor. The elimination rate obtained for the chemical oxygen demand after 90 minutes of reaction varied between 28 and 73% (depending on the conditions of the operation). Polyphenols were reduced by between 26 and 90%, while aromaticity was reduced by between 36 and 94%. In addition, the stechiometric coefficient of the reaction was determined for different operating conditions and was found to range from 0.11 to 1.82 g COD/gH{sub 2}O{sub 2}. An analysis of the results shows that the higher the dose of hydrogen peroxide, the greater the reduction of COD, but also the lower the stechiometric coefficient and, therefore, the less efficient the use made of the hydrogen peroxide. (Author) 19 refs.

  18. Emprego do reagente de fenton como agente coagulante na remoção de substâncias húmicas de água por meio da flotação por ar dissolvido e filtração Fenton's reagent as coagulant agent on removing humic substances from water through dissolved air flotation and filtration

    Directory of Open Access Journals (Sweden)

    Marcelo De Julio

    2006-09-01

    Full Text Available O reagente de Fenton foi empregado como agente coagulante no tratamento de água com cor verdadeira elevada (100 ± 5 uH causada pela introdução de substâncias húmicas extraídas de turfa, empregando-se a flotação por ar dissolvido. Otimizou-se o par de valores dosagem de coagulante x pH de coagulação para posterior construção dos diagramas de coagulação, obtendo-se eficiências de remoção de cor aparente pouco superiores a 60%. Procurou-se simular um tratamento em ciclo completo, realizando-se ensaio de filtração em areia após flotação, obtendo-se efluente de excelente qualidade, apresentando cor aparente, turbidez e absorvância a 253,7 nm remanescentes menores ou iguais a 2 uH, 0,40 uT e 0,009 cm-1, respectivamente, e ferro total residual Fenton's reagent was used as coagulant agent to treat water with high true color (100 ± 5 HU caused by the introduction of humic substances extracted from peat, using dissolved air flotation. The pair value of coagulant dosage x coagulation pH was optimized to posterior construction of coagulation diagrams, reaching apparent color removal efficiency slightly superior to 60%. It was tried to simulate a treatment with complete cycle, carrying out an experiment with sand filtration after flotation, obtaining an effluent with excellent quality, presenting remnant apparent color, turbidity and absorbance of 253.7 nm less or equal to 2 HU, 0.40 TU and 0.009 cm-1, respectively, and residual total iron< 0.005 mg/L and DOC < 0.001 mg/L.

  19. Degradation of Sunset Yellow FCF using copper loaded bentonite and H2O2 as photo-Fenton like reagent

    Directory of Open Access Journals (Sweden)

    Kiran Chanderia

    2017-02-01

    Full Text Available In the present work, photo-Fenton degradation of Sunset Yellow FCF under visible light was carried out by using copper loaded bentonite and hydrogen peroxide. The photocatalyst was prepared by loading copper ions on bentonite by wet impregnation method. The rate of photocatalytic degradation of dye was measured spectrophotometrically by measuring absorbance of the reaction mixture at regular time intervals. The effect of various parameters such as pH, concentration of dye, amount of photocatalyst, amount of H2O2 and light intensity on the reaction rate has also been studied. Characterization of photocatalyst has been done by IR spectroscopy, scanning electron microscopy and X-ray diffraction. The Chemical Oxygen Demand (COD of the reaction mixture has been determined before and after treatment. A tentative mechanism involving ·≡OH radical as an oxidant for degradation of dye has also been proposed. Involvement of ·≡OH radicals as an active oxidizing agent has been confirmed by using isopropanol and butylated hydroxy toluene (BHT as radical scavengers. It has been observed that the rate of reaction is drastically reduced in the presence of these scavengers. The rate of reaction is much retarded by using BHT as compared with isopropanol.

  20. In situ generation of the Ohira-Bestmann Reagent from stable sulfonyl azide

    DEFF Research Database (Denmark)

    Jepsen, Tue Heesgaard; Kristensen, Jesper Langgaard

    2014-01-01

    We report an improved method for in situ generation of the Ohira-Bestmann reagent. Using the recently reported bench stable imidazole-1-sulfonyl azide as diazotransfer reagent, this new method represents a safe and scalable approach for the transformation of aldehydes into terminal alkynes...

  1. VIABILIDADE NO TRATAMENTO DE EFLUENTE INDUSTRIAL ATRAVÉS DA UTILIZAÇÃO DE REAGENTE DE FENTON E FOTOCATÁLISE HETEROGÊNEA (doi:10.5216/reec.V11i1.34861

    Directory of Open Access Journals (Sweden)

    Ravila Pinheiro Valverde

    2016-02-01

    Full Text Available RESUMO: O crescente processo de urbanização e industrialização tem transformado o cenário urbano e consequentemente o meio ambiente, tornando-se necessária a adoção de práticas sustentáveis. O presente trabalho tem por objetivo mostrar uma alternativa de tratamento de efluentes industriais que visa juntamente com os parâmetros das legislações, o tratamento para que possam ser descartados ou reutilizados os efluentes gerados, sem causar nenhum tipo de dano à saúde das pessoas, nem alteração dos demais ecossistemas. O experimento consiste na utilização de Reagente de Fenton onde ocorre uma reação que é formada pela decomposição de H2O2 catalisado por Fe2+ obtendo assim radicais hidroxila e íon hidroxila em meio ácido e a Fotocatalise heterogênea, definido como um processo oxidativo avançado (POA, que é baseado na irradiação de um foto semicondutor, onde se utiliza um fotocatalisador que é ativado por luz solar ou artificial. Neste processo o semicondutor absorve energia dos fótons da radiação ultravioleta, gerando radicais hidroxila (OH• altamente reativos e capazes de mineralizar a matéria orgânica. Uma vez que a matéria orgânica é mineralizada o então efluente tratado poderá ser reutilizado ou descartado no corpo hídrico inicial, tornando o método de tratamento viável e eficaz. ABSTRACT: The growing process of urbanization and industrialization has transformed the urban landscape and consequently the environment, making it necessary to adopt sustainable practices. This paper aims to show an alternative treatment of industrial effluents which aims along with the parameters of the laws, treatment so they can be discarded or reused effluents generated without causing any damage to people's health or change in other ecosystems. The experiment consists of the use of Fenton's Reagent which is a reaction which is formed by the decomposition of H2O2 catalyzed by Fe2+ thereby obtaining hydroxyl and hydroxyl

  2. Oil refinery wastewater treatment using physicochemical, Fenton and Photo-Fenton oxidation processes.

    Science.gov (United States)

    Tony, Maha A; Purcell, Patrick J; Zhao, Yaqian

    2012-01-01

    The objective of this study was to investigate the application of advanced oxidation processes (AOPs) to the treatment of wastewaters contaminated with hydrocarbon oil. Three different oil-contaminated wastewaters were examined and compared: (i) a 'real' hydrocarbon wastewater collected from an oil refinery (Conoco-Phillips Whitegate refinery, County Cork, Ireland); (ii) a 'real' hydrocarbon wastewater collected from a car-wash facility located at a petroleum filling station; and (iii) a 'synthetic' hydrocarbon wastewater generated by emulsifying diesel oil and water. The AOPs investigated were Fe(2+)/H(2)O(2) (Fenton's reagent), Fe(2+)/H(2)O(2)/UV (Photo-Fenton's reagent) which may be used as an alternative to, or in conjunction with, conventional treatment techniques. Laboratory-scale batch and continuous-flow experiments were undertaken. The photo-Fenton parametric concentrations to maximize COD removal were optimized: pH = 3, H(2)O(2) = 400 mg/L, and Fe(2+) = 40 mg/L. In the case of the oil-refinery wastewater, photo-Fenton treatment achieved approximately 50% COD removal and, when preceded by physicochemical treatment, the percentage removal increased to approximately 75%.

  3. Municipal solid waste landfill leachate treatment by fenton, photo-fenton and fenton-like processes: Effect of some variables

    Science.gov (United States)

    2012-01-01

    Advanced oxidation processes like Fenton and photo-Fenton have been effectively applied to oxidize the persistent organic compounds in solid waste leachate and convert them to unharmful materials and products. However, there are limited data about application of Fenton-like process in leachate treatment. Therefore, this study was designed with the objective of treating municipal landfill leachate by Fenton, Fenton-like and photo–Fenton processes to determine the effect of different variables, by setting up a pilot system. The used leachate was collected from a municipal unsanitary landfill in Qaem-Shahr in the north of Iran. Fenton and Fenton-like processes were conducted by Jar-test method. Photo-Fenton process was performed in a glass photo-reactor. In all processes, H2O2 was used as the oxidant. FeSO4.7H2O and FeCl3.6H2O were used as reagents. All parameters were measured based on standard methods. The results showed that the optimum concentration of H2O2 was equal to 5 g/L for the Fenton-like process and 3 g/L for the Fenton and photo-Fenton processes. The optimum ratio of H2O2: Fe+2/Fe+3 were equal to 8:1 in all processes. At optimum conditions, the amount of COD removal was 69.6%, 65.9% and 83.2% in Fenton, Fenton-like and photo–Fenton processes, respectively. In addition, optimum pH were 3, 5 and 3 and the optimum contact time were 150, 90 and 120 minutes, for Fenton, Fenton-like and photo–Fenton processes, respectively. After all processes, the biodegradability (BOD5/COD ratio) of the treated leachate was increased compared to that of the raw leachate and the highest increase in BOD5/COD ratio was observed in the photo-Fenton process. The efficiency of the Fenton-like process was overally less than Fenton and photo-Fenton processes, meanwhile the Fenton-like process was at higher pH and did not show problems. PMID:23369204

  4. Detoxification of Pesticide-Containing Wastewater with FeIII, Activated Carbon and Fenton Reagent and Its Control Using Three Standardized Bacterial Inhibition Tests

    Directory of Open Access Journals (Sweden)

    Eduard Rott

    2017-12-01

    Full Text Available Discharge of toxic industrial wastewaters into biological wastewater treatment plants may result in inhibition of activated sludge bacteria (ASB. In order to find an appropriate method of detoxification, the wastewater of a pesticide-processing plant in Vietnam was treated with three different methods (FeIII, powdered activated carbon (PAC, Fenton (FeII/H2O2 analyzing the detoxification effect with the nitrification inhibition test (NIT, respiration inhibition test (RIT and luminescent bacteria test (LBT. The heterotrophic ASB were much more resistant to the wastewater than the autotrophic nitrificants. The NIT turned out to be more suitable than the RIT since the NIT was less time-consuming and more reliable. In addition, the marine Aliivibrio fischeri were more sensitive than the nitrificants indicating that a lack of inhibition in the very practical and time-efficient LBT correlates with a lack of nitrification inhibition. With 95%, the Fenton method showed the highest efficiency regarding the chemical oxygen demand (COD removal. Although similar COD removal (60–65% was found for both the FeIII and the PAC method, the inhibitory effect of the wastewater was reduced much more strongly with PAC. Both the NIT and the LBT showed that the PAC and Fenton methods led to a similar reduction in the inhibitory effect.

  5. Adaptation of a load-inject valve for a flow injection chemiluminescence system enabling dual-reagent injection enhances understanding of environmental Fenton chemistry

    International Nuclear Information System (INIS)

    Jones, Matthew R.; Nightingale, Philp D.; Turner, Suzanne M.; Liss, Peter S.

    2013-01-01

    Graphical abstract: -- Highlights: •Measurement of multiple components of Fenton chemistry; Fe(II) and H 2 O 2 . •Rapid, quasi-simultaneous analysis enables calculation of environmental kinetics. •Low, nano to pico-molar detection limits with dual analyte analysis. •Able to measure complex matrix samples – organically enriched seawater. •Low cost system with appreciable sensitivity compared to single analyte analysis. -- Abstract: Environmental Fenton chemistry has been poorly constrained within the marine environment at a multi-component level. A simple, unique, reconfiguration of a flow-injection analytical system combined with luminol chemiluminescence allows quasi-simultaneously the measurement, using a single load-inject valve and a single photon multiplier tube, of reduced iron, Fe(II), and hydrogen peroxide. The system enables rapid, every 22 s, measurements with good accuracy at environmentally relevant concentrations, less than 5% relative standard deviations on both a 5 nM Fe(II) standard and a 60 nM hydrogen peroxide standard. Limits of detection were as low as 40 pM Fe(II) and 100 pM hydrogen peroxide. The system showed excellent capability by measuring from within an organic rich seawater the photochemically induced production of Fe(II) and hydrogen peroxide and their subsequent cycling and Fenton like interactions

  6. Pd-catalytic in situ generation of H2O2 from H2 and O2 produced by water electrolysis for the efficient electro-fenton degradation of rhodamine B.

    Science.gov (United States)

    Yuan, Songhu; Fan, Ye; Zhang, Yucheng; Tong, Man; Liao, Peng

    2011-10-01

    A novel electro-Fenton process was developed for wastewater treatment using a modified divided electrolytic system in which H2O2 was generated in situ from electro-generated H2 and O2 in the presence of Pd/C catalyst. Appropriate pH conditions were obtained by the excessive H+ produced at the anode. The performance of the novel process was assessed by Rhodamine B (RhB) degradation in an aqueous solution. Experimental results showed that the accumulation of H2O2 occurred when the pH decreased and time elapsed. The maximum concentration of H2O2 reached 53.1 mg/L within 120 min at pH 2 and a current of 100 mA. Upon the formation of the Fenton reagent by the addition of Fe2+, RhB degraded completely within 30 min at pH 2 with a pseudo first order rate constant of 0.109 ± 0.009 min(-1). An insignificant decline in H2O2 generation and RhB degradation was found after six repetitions. RhB degradation was achieved by the chemisorption of H2O2 on the Pd/C surface, which subsequently decomposed into •OH upon catalysis by Pd0 and Fe2+. The catalytic decomposition of H2O2 to •OH by Fe2+ was more powerful than that by Pd0, which was responsible for the high efficiency of this novel electro-Fenton process.

  7. Degradation of black liquor from bioethanol process using coagulation and Fenton-like methods

    Science.gov (United States)

    Muryanto, Muryanto; Sari, Ajeng Arum; Abimanyu, Haznan

    2017-01-01

    Black liquor is one of the main by-products of the pretreatment process in bioethanol production from oil palm empty fruit bunches. Black liquor wastewater releases black coloured effluent with high chemical oxygen demand (COD) and low dissolved oxygen (DO). It had a distinctive dark coloration, high alkalinity (pH=13), high organic content (COD > 50,000 ppm) and a high solid content (TSS > 5,000 ppm). Lignin destruction can be done by using high oxidation from OH radical system such as advanced oxidation processes (AOPs). Thereafter, the high concentration of COD, color, and TSS can be removed. The general aim of the present investigation was to determine degradation of black liquor wastewater by using a combined coagulation and Fenton-like methods. In this research, we use Poly Aluminum Chloride (PAC) as a coagulant and FeCl3.6H2O and H2O2 for Fenton-like's reagent. The process was conducted in jar test at 200 rpm for 30 minutes and after that slowly mixed for 2 hours and left for sedimentation 24 hours. 50 ml black liquor was added with variation dose of 1-5% PAC, and 10 % Fenton-like reagent. Hydroxyl radical was generated by the Fenton-like's reagent (ratio FeCl3.6H2O : H2O2 was varied). The highest decolorization of black liquor 70 % was obtained under 5% PAC coagulant. The pH of the wastewater was reduced from 13.00 to 8.07 after the addition of the coagulant. The decolorization of original black liquor was approximately 58% through the Fenton-like process. The combination of PAC and Fenton-like reagent has able to enhance the decolorization of black liquor up to 97%.

  8. Comparative study of radical oxidation of DNA and its nucleosides by hydroxyl radicals and ferryl ions generated by the Fenton reaction

    International Nuclear Information System (INIS)

    Mouret, J.F.; Berger, M.; Anselmino, C.; Polverelli, M.; Cadet, J.

    1991-01-01

    A comparative study of the reaction of hydroxyl radicals and Fenton type oxidative species with DNA and 2'-deoxyribonucleosides was investigated. This study was based on the characterization of the diamagnetic products resulting from the chemical transformation of the transient radicals. Emphasis was placed on the radical oxidative reactions of the purine nucleosides. It is interesting to note that oxidative purine radicals can be reduced by reagents such as ascorbic acid or N,N,N',N'-tetramethyl-1, 4-p-phenylenediamine. The observed differences in the nature of the decomposition products resulting from the Fenton reaction are not consistent with the nature of the oxidative species (hydroxyl radicals or ferryl ions) involved, but due to the presence of ferrous sulfate [fr

  9. Zn-Fe-CNTs catalytic in situ generation of H2O2 for Fenton-like degradation of sulfamethoxazole.

    Science.gov (United States)

    Liu, Yong; Fan, Qin; Wang, Jianlong

    2018-01-15

    A novel Fenton-like catalyst (Zn-Fe-CNTs) capable of converting O 2 to H 2 O 2 and further to OH was prepared through infiltration fusion method followed by chemical replacement in argon atmosphere. The catalyst was characterized by SEM, EDS, TEM, XRD and XPS. The reaction between Zn-Fe-CNTs and O 2 in aqueous solution could generate H 2 O 2 in situ, which was further transferred to OH. The Fenton-like degradation of sulfamethoxazole (SMX) using Zn-Fe-CNTs as catalyst was evaluated. The results indicated that Zn-Fe-CNTs had a coral porous structure with a BET area of 51.67m 2 /g, exhibiting excellent adsorption capacity for SMX, which enhanced its degradation. The particles of Zn 0 and Fe 0 /Fe 2 O 3 were observed on the surface of Zn-Fe-CNTs. The mixture of Zn 0 and CNTs could reduce O 2 into H 2 O 2 by micro-electrolysis and Fe 0 /Fe 2 O 3 could catalyze in-situ generation of H 2 O 2 to produce OH through Fenton-like process. When initial pH=1.5, T=25°C, O 2 flow rate=400mL/min, Zn-Fe-CNTs=0.6g/L, SMX=25mg/L and reaction time=10min, the removal efficiency of SMX and TOC was 100% and 51.3%, respectively. The intermediates were detected and the possible pathway of SMX degradation and the mechanism of Zn-Fe-CNTs/O 2 process were tentatively proposed. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Chemical cross-linked polyvinyl alcohol/cellulose nanocrystal composite films with high structural stability by spraying Fenton reagent as initiator.

    Science.gov (United States)

    Song, Meili; Yu, Houyong; Gu, Jiping; Ye, Shounuan; Zhou, Yuwei

    2018-07-01

    Cross-linked polyvinyl alcohol (PVA) composite films with high structural stability were prepared by free radical copolymerization between cellulose nanocrystal (CNC) and maleic anhydride (MAH) modified PVA through spraying Fenton free radical as initiator. The influence of chemical cross-linked and physical network structure on mechanical, thermal and water absorption properties of the composite films were investigated. Compared to PVA and PVA/CNC composite film, significant improvements in the mechanical, thermal and water uptake properties of the cross-linked composite film were found. The tensile strength of the cross-linked composite film was enhanced from 23.1MPa (neat PVA film) and 32.6MPa (PVA/CNC-10%) to 42.5MPa, and the maximum thermal degradation temperature was increased from 266.8°C and 281.2°C to 366.7°C (cross-linked composite film). Besides, the water absorption was reduced from 385.9% and 220.6% to 175.7% for cross-linked composite film. It indicates that compared with physical network structure in PVA/CNC composite film, the multiple cross-linked networks showed excellent thermal stability, resistance of water swelling and structural stability at the same CNC loading level. Thus, the PVA/CNC composite film with the multiple cross-linked network shows greater property reinforcements. Copyright © 2018 Elsevier B.V. All rights reserved.

  11. Improvement of biodegradability of oil wastewater contained PAM by pretreatment with Fenton oxidation

    International Nuclear Information System (INIS)

    Bao, M.; Wang, N.

    2008-01-01

    The use of polymer flooding in enhanced oil recovery operations has resulted in higher levels of polyacrylamide (PAM) found in oil wastewater. PAM is harmful to the environment, particularly the monomer acrylamide that is generated from PAM degradation. In this study, PAM derived from oil wastewater was pretreated by Fenton oxidation. This oxidation method is based on the use of a mixture of H 2 O 2 and iron salts which produce hydroxyl radicals in acidic conditions. The method offers a cost-effective source of hydroxyl radicals, using easy-to-handle reagents. The purpose of this study was to transform PAM to biodegradable intermediums. The optimal conditions for the Fenton reactions were also determined and described. Under optimal conditions, the removal ratios of PAM and chemical oxygen demand (COD) were 83.8 and 77 per cent respectively. It was concluded that Fenton's oxidation is an effective treatment to improved the biodegradability of PAM. 14 refs., 1 tab., 7 figs

  12. Treating leachate by Fenton oxidation

    Directory of Open Access Journals (Sweden)

    Roger Iván Méndez Novelo

    2010-01-01

    Full Text Available Leachates are formed from liquids, mainly rainwater, percolating through solid wastes during stabilisation. Their composition is variable and highly toxic; leachate treatment is therefore a complex task. Leachates represent a high risk to health due to the Yucatan Peninsula’s highly permeable soil. The results are presented from applying the Fenton process to treating leachate from the sanitary Merida landfill, Yucatan, Mexico. The Fenton process consists of treating the contaminant load with an H2O2 and FeSO4 combination in acidic conditions. Optimal reaction time, pH value, Fenton reagent dose, post treatment coagulation – flocculation doses and increased biodegradability index were all determined. Optimal oxidation conditions and doses were 202+ minute contact time, 4 pH, 600 mg/L H2O2 concentration and 1,000 mg/L Fe. Average organic matter removal rate, measured as CODS and TOC, were 78% and 87% respectively. The biodegradability index increased from 0.07 to 0.11 during the Fenton process and up to 0.13 when the Fenton process was followed by coagulation-flocculation.

  13. Microwave-induced electrostatic etching: generation of highly reactive magnesium for application in Grignard reagent formation.

    Science.gov (United States)

    van de Kruijs, Bastiaan H P; Dressen, Mark H C L; Meuldijk, Jan; Vekemans, Jef A J M; Hulshof, Lumbertus A

    2010-04-07

    A detailed study regarding the influence of microwave irradiation on the formation of a series of Grignard reagents in terms of rates and selectivities has revealed that these heterogeneous reactions may display a beneficial microwave effect. The interaction between microwaves and magnesium turnings generates violent electrostatic discharges. These discharges on magnesium lead to melting of the magnesium surface, thus generating highly active magnesium particles. As compared to conventional operation the microwave-induced discharges on the magnesium surface lead to considerably shorter initiation times for the insertion of magnesium in selected substrates (i.e. halothiophenes, halopyridines, octyl halides, and halobenzenes). Thermographic imaging and surface characterization by scanning electron microscopy showed that neither selective heating nor a "specific" microwave effect was causing the reduction in initiation times. This novel and straightforward initiation method eliminates the use of toxic and environmentally adverse initiators. Thus, this initiation method limits the formation of by-products. We clearly demonstrated that microwave irradiation enables fast Grignard reagent formation. Therefore, microwave technology is promising for process intensification of Grignard based coupling reactions.

  14. Advancing Fenton and photo-Fenton water treatment through the catalyst design.

    Science.gov (United States)

    Vorontsov, Alexander V

    2018-04-20

    The review is devoted to modern Fenton, photo-Fenton, as well as Fenton-like and photo-Fenton-like reactions with participation of iron species in liquid phase and as heterogeneous catalysts. Mechanisms of these reactions were considered that include hydroxyl radical and oxoferryl species as the reactive intermediates. The barriers in the way of application of these reactions to wastewater treatment were discussed. The following fundamental problems need further research efforts: inclusion of more mechanism steps and quantum calculations of all rate constants lacking in the literature, checking the outer sphere electron transfer contribution, determination of the causes for the key changes in the homogeneous Fenton reaction mechanism with a change in the reagents concentration. The key advances for Fenton reactions implementation for the water treatment are related to tremendous hydrodynamical effects on the catalytic activity, design of ligands for high rate and completeness of mineralization in short time, and design of highly active heterogeneous catalysts. While both homogeneous and heterogeneous Fenton and photo-Fenton systems are open for further improvements, heterogeneous photo-Fenton systems are most promising for practical applications because of the inherent higher catalyst stability. Modern methods of quantum chemistry are expected to play a continuously increasing role in development of such catalysts. Copyright © 2018 Elsevier B.V. All rights reserved.

  15. In situ generation of the Ohira-Bestmann reagent from stable sulfonyl azide: scalable synthesis of alkynes from aldehydes.

    Science.gov (United States)

    Jepsen, Tue Heesgaard; Kristensen, Jesper Langgaard

    2014-10-03

    We report an improved method for in situ generation of the Ohira-Bestmann reagent. Using the recently reported bench-stable imidazole-1-sulfonyl azide as diazotransfer reagent, this new method represents a scalable and convenient approach for the transformation of aldehydes into terminal alkynes. The method features an easier workup compared to the existing in situ protocol due to increased aqueous solubility of waste products.

  16. Wastewater treatment using hybrid treatment schemes based on cavitation and Fenton chemistry: a review.

    Science.gov (United States)

    Bagal, Manisha V; Gogate, Parag R

    2014-01-01

    Advanced oxidation processes such as cavitation and Fenton chemistry have shown considerable promise for wastewater treatment applications due to the ease of operation and simple reactor design. In this review, hybrid methods based on cavitation coupled with Fenton process for the treatment of wastewater have been discussed. The basics of individual processes (Acoustic cavitation, Hydrodynamic cavitation, Fenton chemistry) have been discussed initially highlighting the need for combined processes. The different types of reactors used for the combined processes have been discussed with some recommendations for large scale operation. The effects of important operating parameters such as solution temperature, initial pH, initial pollutant concentration and Fenton's reagent dosage have been discussed with guidelines for selection of optimum parameters. The optimization of power density is necessary for ultrasonic processes (US) and combined processes (US/Fenton) whereas the inlet pressure needs to be optimized in the case of Hydrodynamic cavitation (HC) based processes. An overview of different pollutants degraded under optimized conditions using HC/Fenton and US/Fenton process with comparison with individual processes have been presented. It has been observed that the main mechanism for the synergy of the combined process depends on the generation of additional hydroxyl radicals and its proper utilization for the degradation of the pollutant, which is strongly dependent on the loading of hydrogen peroxide. Overall, efficient wastewater treatment with high degree of energy efficiency can be achieved using combined process operating under optimized conditions, as compared to the individual process. Copyright © 2013 Elsevier B.V. All rights reserved.

  17. Enzymatic in-situ generation of H2O2 for decolorization of Acid Blue 113 by fenton process

    Directory of Open Access Journals (Sweden)

    Karimi Afzal

    2012-01-01

    Full Text Available Decolorization of Acid Blue 113 in an aqueous medium by bio-Fenton process has been investigated in this research. Enzymatic oxidation of glucose was performed to in-situ generation of H2O2 which was employed to react with Fe2+ for producing hydroxyl radicals. The effect of various parameters include concentrations of 113, glucose, and FeSO4, activity of glucose oxidase (GOx and the effect of pH were assessed. The highest decolorization of AB 113 were achieved at Fe2+ concentration of 0.2 mmol/L, pH =4.0, glucose concentration of 0.018 mol/L, and glucose oxidase activity of 2500 U/L in the constant temperature (23 ±0.1ºC and constant shaking rate (160 r/min, while the concentration of 113 was 40 mg/L. In these conditions, 113 decolorization efficiency after 60 min was obtained about 95%.

  18. Oxidation of microcystin-LR by the Fenton process : Kinetics, degradation intermediates, water quality and toxicity assessment

    NARCIS (Netherlands)

    Park, Jeong-Ann; Yang, Boram; Park, Chanhyuk; Choi, Jae-Woo; van Genuchten, Case M.|info:eu-repo/dai/nl/413489647; Lee, Sang-Hyup

    2017-01-01

    The Fenton process was assessed as a cost-effective technology for the removal of Microcystin-LR (MC-LR) among UV, UV/H2O2, and Fenton process according to efficiency and electrical energy per order (EE/O). The determined practical concentrations of the Fenton reagents were 5 mg/L Fe(II) and 5 mg/L

  19. Fenton's syndrome

    International Nuclear Information System (INIS)

    Rimondi, E.; Albasini, V.

    1989-01-01

    The authors report two recent cases of Fenton's syndrome, a very rare carpal fracture-dislocation. After some anatomophysiopathological considerations and a review of the literature, a wider nosographic frame is proposed in which the entity of the dislocation of the head of capitate bone is not essential. According to both the literature and personal findings, the authors remark that this syndrome is always found in the presence of two morphological variants of the distal radioulnar joint. Finally, the authors stress the importance of a corect diagnosis of this lesion to avoid unnecessary attempts of reduction

  20. Method of Generating Hydrocarbon Reagents from Diesel, Natural Gas and Other Logistical Fuels

    Science.gov (United States)

    Herling, Darrell R [Richland, WA; Aardahl, Chris L [Richland, WA; Rozmiarek, Robert T [Middleton, WI; Rappe, Kenneth G [Richland, WA; Wang, Yong [Richland, WA; Holladay, Jamelyn D [Kennewick, WA

    2008-10-14

    The present invention provides a process for producing reagents for a chemical reaction by introducing a fuel containing hydrocarbons into a flash distillation process wherein the fuel is separated into a first component having a lower average molecular weight and a second component having a higher average molecular weight. The first component is then reformed to produce synthesis gas wherein the synthesis gas is reacted catalytically to produce the desire reagent.

  1. Photo-catalytic degradation of an oil-water emulsion using the photo-fenton treatment process: effects and statistical optimization.

    Science.gov (United States)

    Tony, Maha A; Purcell, P J; Zhao, Y Q; Tayeb, A M; El-Sherbiny, M F

    2009-02-01

    The application of advanced oxidation processes (AOPs) to the treatment of an effluent contaminated with hydrocarbon oils was investigated. The AOPs conducted were Fe2+/H2O2 (Fenton's reagent), Fe2+/H2O2/UV (Photo-Fenton's reagent) and UV-photolysis. These technologies utilize the very strong oxidizing power of hydroxyl radicals to oxidize organic compounds to harmless end products such as CO2 and H2O. A synthetic wastewater generated by emulsifying diesel oil and water was used. This wastewater might simulate, for example, a waste resulting from a hydrocarbon oil spill, onto which detergent was sprayed. The experiments utilising the Photo-Fenton treatment method with an artificial UV source, coupled with Fenton's reagent, suggest that the hydrocarbon oil is readily degradable, but that the emulsifying agent is much more resistant to degradation. The results showed that the COD (chemical oxygen demand) removal rate was affected by the Photo-Fenton parameters (Fe2+, H2O2 concentrations and the initial pH) of the aqueous solution. In addition, the applicability of the treatment method to a 'real' wastewater contaminated with hydrocarbon oil is demonstrated. The 'real' wastewater was sourced at a nearby car-wash facility located at a petroleum filling station and the experimental results demonstrate the effectiveness of the treatment method in this case. A statistical analysis of the experimental data using the Statistical Analysis System (SAS) and the response surface methodology (RSM) based on the experimental design was applied to optimize the Photo-Fenton parameters (concentrations of Fe2+, H2O2 and initial pH) and to maximize the COD removal rate (more than 70%).

  2. A new class of photoactivatable and carbene generating reagents with extremely high specific radioactivity. Synthesis, characterization and applications

    International Nuclear Information System (INIS)

    Weber, T.

    1994-01-01

    The main objective of this work was the development of new photocrosslinking and labeling reagents which show favourable photochemical properties and can be synthesized in an extremely high specific radioactivity. A key compound in the synthesis of these reagents was 2-tributyltin-4-(3-trifluormethyl-3H-diazirin-3-yl)-benzyl alcohol. Esters of this alcohol can be easily radioiodinated at a specific radioactivity of >2000 Ci/mmol under mild conditions. By experiments with a model compound it was shown that 2-iodo-4-(3-trifluormethyl-3H-diazirin-3-yl)-benzyl esters, upon photolysis, generate highly reactive (singlet) carbenes capable of inserting into CH-bonds. Equally important, there is no indication of loss of iodine under the photolysis conditions applied. Therefore two key requirements for photolabeling reagents are fulfilled. Several photoactivatable radioiodinated phospholipids have been synthesized. Their properties have been evaluated by labeling of the the membranes of intact erythrocytes and influenza viruses. Currently these lipids are used to study the interaction of various proteins (shown are experiments with MARCKS) with membranes. Furthermore a new class of actual label transfer crosslinkers (two thiol specific and one amino specific) have been developed. The range of potentialities of these reagents is currently being investigated. Finally a photoactivatable radioiodinated ceramide analogue suitable as a photoaffinity crosslinker has been developed with the goal of identifying the putative receptor of this second messenger-like lipid. Preliminary studies towards this goal are described. We are convinced that the reagents and methods presented in this work are valuable tools, and that they will find widespread use in future cell-biological and biochemical research. (author) figs., tabs., refs

  3. Volumetric Titrations Using Electrolytically Generated Reagents for the Determination of Ascorbic Acid and Iron in Dietary Supplement Tablets: An Undergraduate Laboratory Experiment

    Science.gov (United States)

    Scanlon, Christopher; Gebeyehu, Zewdu; Griffin, Kameron; Dabke, Rajeev B.

    2014-01-01

    An undergraduate laboratory experiment for the volumetric quantitative analysis of ascorbic acid and iron in dietary supplement tablets is presented. Powdered samples of the dietary supplement tablets were volumetrically titrated against electrolytically generated reagents, and the mass of dietary reagent in the tablet was determined from the…

  4. Predição da demanda química de oxigênio em chorume maduro contendo reagente de Fenton, por meio de modelo matemático empírico gerado com planejamento fatorial completo Prediction of chemical oxygen demand in mature landfill leachate doped with Fenton's reagent, using empirical mathematical model obtained by full factorial design

    Directory of Open Access Journals (Sweden)

    André Luís de Castro Peixoto

    2008-01-01

    Full Text Available COD is an important parameter to estimate the concentration of organic contaminants. The closed system technique with the use of K2Cr2O7 is the most important one, however, it has the inconvenience to suffer positive chemical interferences from inorganic compounds such as Fe2+ and H2O2 (not enough reported in the literature. This paper considers a statistical-experimental set capable to validate a empirical mathematical model generated from a 23 experimental design, in the presence of Fe2+ and H2O2. The t test shows that mathematical model has 99,99999% confidence degree and the experimental validation test indicates absolute mean error of 4,70%.

  5. Alkydic resin wastewaters treatment by fenton and photo-Fenton processes

    International Nuclear Information System (INIS)

    Schwingel de Oliveira, Isadora; Viana, Lilian; Verona, Cenira; Fallavena, Vera Lucia Vargas; Azevedo, Carla Maria Nunes; Pires, Marcal

    2007-01-01

    Advanced oxidation processes are an emerging option to treatment of the painting industry effluents. The aim of this study was to compare the effectiveness of the Fenton and photo-Fenton processes in chemical oxygen demand (COD), total organic carbon (TOC) and phenolic compounds removal from wastewaters generated during alkydic resins manufacture. The optimized treatment conditions are the following: pH 3.0, 15.15 x 10 -3 mol L -1 FeSO 4 and 0.30 mol L -1 H 2 O 2 for a reaction time of 6 h. photo-Fenton experiments were carried out in the presence of sunlight or artificial radiation and complementary additions of H 2 O 2 were made for all experiments. The best results were obtained with photo-Fenton process assisted with solar radiation, with reductions of 99.5 and 99.1% of COD and TOC levels, respectively. Fenton and photo-Fenton (with artificial irradiation) processes presented lower but not insignificant removals, within 60-80% reduction for both COD and TOC. In addition, an excellent removal (95%) of total phenols was obtained using photo-Fenton process assisted with artificial irradiation. This study demonstrated that the use of photo-Fenton process on alkydic resins wastewater treatment is very promising especially when solar light is used

  6. Analogies and differences among bacterial and viral disinfection by the photo-Fenton process at neutral pH: a mini review.

    Science.gov (United States)

    Giannakis, Stefanos

    2017-12-19

    Over the last years, the photo-Fenton process has been established as an effective, green alternative to chemical disinfection of waters and wastewaters. Microorganisms' inactivation is the latest success story in the application of this process at near-neutral pH, albeit without clearly elucidated inactivation mechanisms. In this review, the main pathways of the combined photo-Fenton process against the most frequent pathogen models (Escherichia coli for bacteria and MS2 bacteriophage for viruses) are analyzed. Firstly, the action of solar light is described and the specific inactivation mechanisms in bacteria (internal photo-Fenton) and viruses (genome damage) are presented. The contribution of the external pathways due to the potential presence of organic matter in generating reactive oxygen species (ROS) and their effects on microorganism inactivation are discussed. Afterwards, the effects of the gradual addition of Fe and H 2 O 2 are assessed and the differences among bacterial and viral inactivation are highlighted. As a final step, the simultaneous addition of both reagents induces the photo-Fenton in the bulk, focusing on the differences induced by the homogeneous or heterogeneous fraction of the process and the variation among the two respective targets. This work exploits the accumulated evidence on the mechanisms of bacterial inactivation and the scarce ones towards viral targets, aiming to bridge this knowledge gap and make possible the further application of the photo-Fenton process in the field of water/wastewater treatment.

  7. Efficient generation of megakaryocytes from human induced pluripotent stem cells using food and drug administration-approved pharmacological reagents.

    Science.gov (United States)

    Liu, Yanfeng; Wang, Ying; Gao, Yongxing; Forbes, Jessica A; Qayyum, Rehan; Becker, Lewis; Cheng, Linzhao; Wang, Zack Z

    2015-04-01

    Megakaryocytes (MKs) are rare hematopoietic cells in the adult bone marrow and produce platelets that are critical to vascular hemostasis and wound healing. Ex vivo generation of MKs from human induced pluripotent stem cells (hiPSCs) provides a renewable cell source of platelets for treating thrombocytopenic patients and allows a better understanding of MK/platelet biology. The key requirements in this approach include developing a robust and consistent method to produce functional progeny cells, such as MKs from hiPSCs, and minimizing the risk and variation from the animal-derived products in cell cultures. In this study, we developed an efficient system to generate MKs from hiPSCs under a feeder-free and xeno-free condition, in which all animal-derived products were eliminated. Several crucial reagents were evaluated and replaced with Food and Drug Administration-approved pharmacological reagents, including romiplostim (Nplate, a thrombopoietin analog), oprelvekin (recombinant interleukin-11), and Plasbumin (human albumin). We used this method to induce MK generation from hiPSCs derived from 23 individuals in two steps: generation of CD34(+)CD45(+) hematopoietic progenitor cells (HPCs) for 14 days; and generation and expansion of CD41(+)CD42a(+) MKs from HPCs for an additional 5 days. After 19 days, we observed abundant CD41(+)CD42a(+) MKs that also expressed the MK markers CD42b and CD61 and displayed polyploidy (≥16% of derived cells with DNA contents >4N). Transcriptome analysis by RNA sequencing revealed that megakaryocytic-related genes were highly expressed. Additional maturation and investigation of hiPSC-derived MKs should provide insights into MK biology and lead to the generation of large numbers of platelets ex vivo. ©AlphaMed Press.

  8. Drinking water and biofilm disinfection by Fenton-like reaction.

    Science.gov (United States)

    Gosselin, F; Madeira, L M; Juhna, T; Block, J C

    2013-10-01

    A Fenton-like disinfection process was conducted with Fenton's reagent (H2O2) at pH 3 or 5 on autochthonous drinking water biofilms grown on corroded or non-corroded pipe material. The biofilm disinfection by Fenton-like oxidation was limited by the low content of iron and copper in the biomass grown on non-corroded plumbing. It was slightly improved by spiking the distribution system with some additional iron source (soluble iron II or ferrihydrite particles appeared as interesting candidates). However successful in situ disinfection of biofilms was only achieved in fully corroded cast iron pipes using H2O2 and adjusting the pH to 5. These new results provide additional support for the use of Fenton's processes for cleaning drinking water distribution systems contaminated with biological agents or organics. Copyright © 2013 Elsevier Ltd. All rights reserved.

  9. IN-SITU FENTON OXIDATION: A CRITICAL ANALYSIS

    Science.gov (United States)

    In-situ Fenton oxidation (ISFO) is a rapidly emerging technology which involves the injection of hydrogen peroxide (H2O2) and other chemical reagents into the subsurface for the purpose of oxidizing and transforming contaminants. ISFO is being applied at an increasing number of ...

  10. Decontamination of unsymmetrical dimethylhydrazine waste water by hydrodynamic cavitation-induced advanced Fenton process.

    Science.gov (United States)

    Torabi Angaji, Mahmood; Ghiaee, Reza

    2015-03-01

    A pilot scale hydrodynamic cavitation (HC) reactor, using iron metal blades, as the heterogeneous catalyst, with no external source of H₂O₂ was developed for catalytic decontamination of unsymmetrical dimethylhydrazine (UDMH) waste water. In situ generation of Fenton reagents suggested an induced advanced Fenton process (IAFP) to explain the enhancing effect of the used catalyst in the HC process. The effects of the applied catalyst, pH of the initial solution (1.0-9.7), initial UDMH concentration (2-15 mg/l), inlet pressure (5.5-7.8bar), and downstream pressure (2-6 bar), have been investigated. The results showed that the highest cavitation yield can be obtained at pH 3 and initial UDMH concentration of 10mg/l. Also, an increase in the inlet pressure would lead to an increase in the extent of UDMH degradation. In addition, the optimum value of 3 bar was determined for the downstream pressure that resulted to 98.6% degradation of UDMH after 120 min of processing time. Neither n-nitrosodimethylamine (NDMA) nor any other toxic byproduct (/end-product) was observed in the investigated samples. Formic acid and acetic acid, as well as nitromethane, were identified as oxidation by-products. The present work has conclusively established that hydrodynamic cavitation in combination with Fenton's chemistry can be effectively used for the degradation of UDMH. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. Fenton process combined with coagulation for the treatment of black liquor from bioethanol wastewater

    Science.gov (United States)

    Muryanto, Muryanto; Hanifah, Ummu; Amriani, Feni; Ibadurrahman, Ahmad Faiz; Sari, Ajeng Arum

    2017-11-01

    High amounts of black liquor are generated from bioethanol production by using oil palm empty fruit bunches. The black liquor is waste from alkaline pretreatment, it contains high amount of an alkaline solution (NaOH). The black liquor wastewater was highly contaminated with organic materials, and quite toxic for aquatic ecosystems if discharged directly into waters. This study aimed to determine ability of Fenton process combined with coagulation to treat black liquor. The addition 5% of polyaluminium chloride (PAC) could decolorized black liquor, degraded lignin, and produced sludge 70.64%, 68.28%, and 2.76 gram, respectively. Decolorization of black liquor was in line with degradation of black liquor because lignin is the main compound in black liquor. SEM images after addition of PAC of 5% indicated fragmentation of structure. Fenton reagent consist of 0.7 M FeSO4+ 3M H2O2 has able to decolorize black liquor, degrade lignin, and produce sludge 51.67% and 25.44%, and 0.44 gram, respectively. It was concluded that black liquor wastewater from bioethanol can be treated by using Fenton process combined with coagulation. However, these methods still need improvement to obtain the higher degradation rate, and coagulation sludge needs further consideration.

  12. Evaluation of Fenton Oxidation Process Coupled with Biological Treatment for the Removal of Reactive Black 5 from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Pegah Bahmani

    2013-06-01

    Full Text Available Biodegradation of azo dyes is difficult due to their complex structures and low BOD to COD ratios. In the present study, the efficiency of using Fenton’s reagent (H2O2 + Fe2+ as a pretreatment process to enhance microbial transformation of reactive black 5 (RB5 in an aqueous system was evaluated. The RB5 with an initial concentration of 250 mg/L was decolorized up to 90% in 60 h by using a bacterial consortium. Fenton’s reagent at a Fe2+ concentration of 0.5 mM and H2O2 concentration of 2.9 mM (molar ratio, 1:5.8 was most effective for decolorization at pH = 3.0. The extent of RB5 removal by the combined Fenton–biotreatment was about 2 times higher than that of biotreatment alone. The production of some aromatic amines intermediates implied partial mineralization of the RB5 in Fenton treatment alone; in addition, decreasing of GC-MS peaks suggested that dearomatization occurred in Fenton-biological process. Fenton pretreatment seems to be a cost–effective option for the biotreatment of azo dyes, due mainly to the lower doses of chemicals, lower sludge generation, and saving of time. Our results demonstrated positive effects of inoculating bacterial consortium which was capable of dye biodegradation with a Fenton’s pretreatment step as well as the benefits of low time required for the biological process. In addition, the potential of field performance of Fenton-biological process because of using bacterial consortium is an other positive effect of it.

  13. Enhancement of Fenton processes at initial circumneutral pH for the degradation of norfloxacin with Fe@Fe2O3 core-shell nanomaterials.

    Science.gov (United States)

    Liu, Jingyi; Hu, Wenyong; Sun, Maogui; Xiong, Ouyang; Yu, Haibin; Feng, Haopeng; Wu, Xuan; Tang, Lin; Zhou, Yaoyu

    2018-06-13

    The degradation of norfloxacin by Fenton reagent with core-shell Fe@Fe 2 O 3 nanomaterials was studied under neutral conditions in a closed batch system. Norfloxacin was significantly degraded (90%) in the Fenton system with Fe@Fe 2 O 3 in 30 min at the initial pH 7.0, but slightly degraded in Fenton system without Fe@Fe 2 O 3 under the same experimental conditions. The intermediate products were investigated by gas chromatography-mass spectrometry, and the possible Fenton oxidation pathway of norfloxacin in the presence of Fe@Fe 2 O 3 nanowires was proposed. Electron spin resonance spectroscopy was used to identify and characterize the free radicals generated, and the mechanism for norfloxacin degradation was also revealed. Finally, the reusability and the stability of Fe@Fe 2 O 3 nanomaterials were studied using x-ray diffraction and scanning electron microscope, which indicated that Fe@Fe 2 O 3 is a stable catalyst and can be used repetitively in environmental pollution control.

  14. Integration of processes induced air flotation and photo-Fenton for treatment of residual waters contaminated with xylene.

    Science.gov (United States)

    da Silva, Syllos S; Chiavone-Filho, Osvaldo; de Barros Neto, Eduardo L; Nascimento, Claudio A O

    2012-01-15

    Produced water in oil fields is one of the main sources of wastewater generated in the industry. It contains several organic compounds, such as benzene, toluene, ethyl benzene and xylene (BTEX), whose disposal is regulated by law. The aim of this study is to investigate a treatment of produced water integrating two processes, i.e., induced air flotation (IAF) and photo-Fenton. The experiments were conducted in a column flotation and annular lamp reactor for flotation and photodegradation steps, respectively. The first order kinetic constant of IAF for the wastewater studied was determined to be 0.1765 min(-1) for the surfactant EO 7. Degradation efficiencies of organic loading were assessed using factorial planning. Statistical data analysis shows that H(2)O(2) concentration is a determining factor in process efficiency. Degradations above 90% were reached in all cases after 90 min of reaction, attaining 100% mineralization in the optimized concentrations of Fenton reagents. Process integration was adequate with 100% organic load removal in 20 min. The results of the integration of the IAF with the photo-Fenton allowed to meet the effluent limits established by Brazilian legislation for disposal. Copyright © 2011 Elsevier B.V. All rights reserved.

  15. Fenton-like oxidation of 4-chlorophenol using H2O2 in situ generated by Zn-Fe-CNTs composite.

    Science.gov (United States)

    Liu, Yong; Fan, Qing; Liu, Yanlan; Wang, Jianlong

    2018-05-15

    In this paper, a zinc-iron-carbon nanotubes (Zn-Fe-CNTs) composite was prepared, characterized and used to develop a Fenton-like system of Zn-Fe-CNTs/O 2 for the degradation of 4-chlorophenol (4-CP), in which H 2 O 2 was generated in situ from zinc-carbon galvanic cells and oxygen in aqueous solution was activated by iron attached on the surface of CNTs to produce ·OH radicals for the oxidation of 4-CP. The experimental results showed that the particles of Zn and Fe in Zn-Fe-CNTs composite were adhered to the surface of CNTs, which accelerated the electron transfer process. The BET area of Zn-Fe-CNTs composite was 32.9 m 2 /g. The contents of Zn and Fe (% w) in the composite were 44.7% and 4.2%, respectively. The removal efficiency of 4-CP and TOC in Zn-Fe-CNTs/O 2 system was 90.8% and 52.9%, respectively, with the initial pH of 2.0, O 2 flow rate of 800 mL/min, Zn-Fe-CNTs dosage of 1.0 g/L, 4-CP concentration of 50 mg/L and reaction time of 20 min. Based on the analysis of the degradation intermediate products with LC-MS and IC, a possible degradation pathway of 4-CP in Zn-Fe-CNTs/O 2 system was proposed. Copyright © 2018 Elsevier Ltd. All rights reserved.

  16. Influence of generated intermediates’ interaction on heterogeneous Fenton's degradation of an azo dye 1-diazo-2-naphthol-4-sulfonic acid by using sludge based carbon as catalyst

    International Nuclear Information System (INIS)

    Gu, Lin; Huang, Shouqiang; Zhu, Nanwen; Zhang, Daofang; Yuan, Haiping; Lou, Ziyang

    2013-01-01

    Highlights: • End-products have higher tendency to be adsorbed on SC than primarily-formed. • Higher initial H 2 O 2 dosage results in intermediates with strong polarity. • 9 model intermediates differ in their behavior on interactions with catalysts. • Polar surface area dominated their adsorption on SC while K ow acts as a key role on HSC. -- Abstract: Sewage sludge based carbons have recently been used as novel catalyst in heterogeneous Fenton's reactions to degrade azo dye molecules. The carbons, functioning as both catalyst and adsorbent, play an important role in pollutants elimination, especially for those simultaneously generated organic intermediates. Different factors, i.e., H 2 O 2 concentration, may influence the type and properties of those intermediates and may have great impacts on their elimination through the interactions with catalysts’ surface. Thus, techniques including Temperature Programmed Desorption-Mass Spectrometer (TPD-MS), N 2 adsorption isotherm and Scanning Electron Microscope (SEM) were used to probe the ways of the interaction between oxidation products and catalyst by using different initial H 2 O 2 concentrations (10 and 20 mM). The higher Chemical Oxygen Demand (COD) removal with 20 mM H 2 O 2 was found to be related not only to the higher hydroxyl radicals but also the specific interactions between the intermediates and catalyst’ surface. The deep oxidation occurred in the conditions with higher oxidant amount enhances the intermediates’ adsorption on catalyst, thus increasing the COD removal by large margin. Simulated adsorption experiments by using six primarily formed intermediates and three deeply mineralized products on three different catalysts also confirmed the assumption. Results suggested close relations between adsorption capacities and intermediates’ properties such as polar surface area and octanol-water partition coefficient

  17. Removal of phosphonates from industrial wastewater with UV/FeII, Fenton and UV/Fenton treatment.

    Science.gov (United States)

    Rott, Eduard; Minke, Ralf; Bali, Ulusoy; Steinmetz, Heidrun

    2017-10-01

    Phosphonates are an important group of phosphorus-containing compounds due to their increasing industrial use and possible eutrophication potential. This study involves investigations into the methods UV/Fe II , Fenton and UV/Fenton for their removal from a pure water matrix and industrial wastewaters. It could be shown that the degradability of phosphonates by UV/Fe II (6 kWh/m 3 ) in pure water crucially depended on the pH and was higher the less phosphonate groups a phosphonate contains. The UV/Fe II method is recommended in particular for the treatment of concentrates with nitrogen-free phosphonates, only little turbidity and a low content of organic compounds. Using Fenton reagent, the degradation of polyphosphonates was relatively weak in a pure water matrix (Fenton method (6 kWh/m 3 ), those phosphonates with the smallest numbers of phosphonate groups were easier degraded as well at pH 3.5 in a pure water matrix (o-PO 4 3- formation rates of up to 80%). Despite an incomplete transformation of organically bound phosphorus to o-PO 4 3- with Fenton reagent in an organically highly polluted wastewater (max. 15%), an almost total removal of the total P occurred. The most efficient total P elimination rates were achieved in accordance with the following Fenton implementation: reaction → sludge separation (acidic) → neutralization of the supernatant → sludge separation (neutral). Accordingly, a neutralization directly after the reaction phase led to a lower total P removal extent. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Treatment of hazardous waste landfill leachate using Fenton oxidation process

    Science.gov (United States)

    Singa, Pradeep Kumar; Hasnain Isa, Mohamed; Ho, Yeek-Chia; Lim, Jun-Wei

    2018-03-01

    The efficiency of Fenton's oxidation was assessed in this study for hazardous waste landfill leachate treatment. The two major reagents, which are generally employed in Fenton's process are H2O2 as oxidizing agent and Fe2+ as catalyst. Batch experiments were conducted to determine the effect of experimental conditions viz., reaction time, molar ratio, and Fenton reagent dosages, which are significant parameters that influence the degradation efficiencies of Fenton process were examined. It was found that under the favorable experimental conditions, maximum COD removal was 56.49%. The optimum experimental conditions were pH=3, H2O2/Fe2+ molar ratio = 3 and reaction time = 150 minutes. The optimal amount of hydrogen peroxide and iron were 0.12 mol/L and 0.04 mol/L respectively. High dosages of H2O2 and iron resulted in scavenging effects on OH• radicals and lowered degradation efficiency of organic compounds in the hazardous waste landfill leachate.

  19. Peptide Dendrimer/Lipid Hybrid Systems Are Efficient DNA Transfection Reagents: Structure–Activity Relationships Highlight the Role of Charge Distribution Across Dendrimer Generations

    Science.gov (United States)

    2013-01-01

    Efficient DNA delivery into cells is the prerequisite of the genetic manipulation of organisms in molecular and cellular biology as well as, ultimately, in nonviral gene therapy. Current reagents, however, are relatively inefficient, and structure–activity relationships to guide their improvement are hard to come by. We now explore peptide dendrimers as a new type of transfection reagent and provide a quantitative framework for their evaluation. A collection of dendrimers with cationic and hydrophobic amino acid motifs (such as KK, KA, KH, KL, and LL) distributed across three dendrimer generations was synthesized by a solid-phase protocol that provides ready access to dendrimers in milligram quantities. In conjunction with a lipid component (DOTMA/DOPE), the best reagent, G1,2,3-KL ((LysLeu)8(LysLysLeu)4(LysLysLeu)2LysGlySerCys-NH2), improves transfection by 6–10-fold over commercial reagents under their respective optimal conditions. Emerging structure–activity relationships show that dendrimers with cationic and hydrophobic residues distributed in each generation are transfecting most efficiently. The trigenerational dendritic structure has an advantage over a linear analogue worth up to an order of magnitude. The success of placing the decisive cationic charge patterns in inner shells rather than previously on the surface of macromolecules suggests that this class of dendrimers significantly differs from existing transfection reagents. In the future, this platform may be tuned further and coupled to cell-targeting moieties to enhance transfection and cell specificity. PMID:23682947

  20. Constructing Solid-Gas-Interfacial Fenton Reaction over Alkalinized-C3N4 Photocatalyst To Achieve Apparent Quantum Yield of 49% at 420 nm.

    Science.gov (United States)

    Li, Yunxiang; Ouyang, Shuxin; Xu, Hua; Wang, Xin; Bi, Yingpu; Zhang, Yuanfang; Ye, Jinhua

    2016-10-03

    Efficient generation of active oxygen-related radicals plays an essential role in boosting advanced oxidation process. To promote photocatalytic oxidation for gaseous pollutant over g-C 3 N 4 , a solid-gas interfacial Fenton reaction is coupled into alkalinized g-C 3 N 4 -based photocatalyst to effectively convert photocatalytic generation of H 2 O 2 into oxygen-related radicals. This system includes light energy as power, alkalinized g-C 3 N 4 -based photocatalyst as an in situ and robust H 2 O 2 generator, and surface-decorated Fe 3+ as a trigger of H 2 O 2 conversion, which attains highly efficient and universal activity for photodegradation of volatile organic compounds (VOCs). Taking the photooxidation of isopropanol as model reaction, this system achieves a photoactivity of 2-3 orders of magnitude higher than that of pristine g-C 3 N 4 , which corresponds to a high apparent quantum yield of 49% at around 420 nm. In-situ electron spin resonance (ESR) spectroscopy and sacrificial-reagent incorporated photocatalytic characterizations indicate that the notable photoactivity promotion could be ascribed to the collaboration between photocarriers (electrons and holes) and Fenton process to produce abundant and reactive oxygen-related radicals. The strategy of coupling solid-gas interfacial Fenton process into semiconductor-based photocatalysis provides a facile and promising solution to the remediation of air pollution via solar energy.

  1. Integration of processes induced air flotation and photo-Fenton for treatment of residual waters contaminated with xylene

    International Nuclear Information System (INIS)

    Silva, Syllos S. da; Chiavone-Filho, Osvaldo; Barros Neto, Eduardo L. de; Nascimento, Claudio A.O.

    2012-01-01

    Highlights: ► We have studied the treatment of wastewater contaminated with hydrocarbons represented by the xylene, using these processes in an integrated mode: induced air flotation and photo-Fenton. ► We have selected xylene as representative contaminant due to properties of toxicity, solubility in water and vapor pressure. ► The manuscript presents a series of accurate experimental data that can be useful for material and energy optimization purposes in the xylene removal aiming the treatment of oil field produced water. - Abstract: Produced water in oil fields is one of the main sources of wastewater generated in the industry. It contains several organic compounds, such as benzene, toluene, ethyl benzene and xylene (BTEX), whose disposal is regulated by law. The aim of this study is to investigate a treatment of produced water integrating two processes, i.e., induced air flotation (IAF) and photo-Fenton. The experiments were conducted in a column flotation and annular lamp reactor for flotation and photodegradation steps, respectively. The first order kinetic constant of IAF for the wastewater studied was determined to be 0.1765 min −1 for the surfactant EO 7. Degradation efficiencies of organic loading were assessed using factorial planning. Statistical data analysis shows that H 2 O 2 concentration is a determining factor in process efficiency. Degradations above 90% were reached in all cases after 90 min of reaction, attaining 100% mineralization in the optimized concentrations of Fenton reagents. Process integration was adequate with 100% organic load removal in 20 min. The results of the integration of the IAF with the photo-Fenton allowed to meet the effluent limits established by Brazilian legislation for disposal.

  2. Integration of processes induced air flotation and photo-Fenton for treatment of residual waters contaminated with xylene

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Syllos S. da [Departamento Engenharia Quimica, NUPEG, Universidade Federal do Rio Grande do Norte, Campus Universitario, Lagoa Nova, Natal 59066-800, RN (Brazil); Chiavone-Filho, Osvaldo, E-mail: osvaldo@eq.ufrn.br [Departamento Engenharia Quimica, NUPEG, Universidade Federal do Rio Grande do Norte, Campus Universitario, Lagoa Nova, Natal 59066-800, RN (Brazil); Barros Neto, Eduardo L. de [Departamento Engenharia Quimica, NUPEG, Universidade Federal do Rio Grande do Norte, Campus Universitario, Lagoa Nova, Natal 59066-800, RN (Brazil); Nascimento, Claudio A.O. [Departamento de Engenharia Quimica, Escola Politecnica, Universidade de Sao Paulo, Cidade Universitaria, Sao Paulo 05508-900, SP (Brazil)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer We have studied the treatment of wastewater contaminated with hydrocarbons represented by the xylene, using these processes in an integrated mode: induced air flotation and photo-Fenton. Black-Right-Pointing-Pointer We have selected xylene as representative contaminant due to properties of toxicity, solubility in water and vapor pressure. Black-Right-Pointing-Pointer The manuscript presents a series of accurate experimental data that can be useful for material and energy optimization purposes in the xylene removal aiming the treatment of oil field produced water. - Abstract: Produced water in oil fields is one of the main sources of wastewater generated in the industry. It contains several organic compounds, such as benzene, toluene, ethyl benzene and xylene (BTEX), whose disposal is regulated by law. The aim of this study is to investigate a treatment of produced water integrating two processes, i.e., induced air flotation (IAF) and photo-Fenton. The experiments were conducted in a column flotation and annular lamp reactor for flotation and photodegradation steps, respectively. The first order kinetic constant of IAF for the wastewater studied was determined to be 0.1765 min{sup -1} for the surfactant EO 7. Degradation efficiencies of organic loading were assessed using factorial planning. Statistical data analysis shows that H{sub 2}O{sub 2} concentration is a determining factor in process efficiency. Degradations above 90% were reached in all cases after 90 min of reaction, attaining 100% mineralization in the optimized concentrations of Fenton reagents. Process integration was adequate with 100% organic load removal in 20 min. The results of the integration of the IAF with the photo-Fenton allowed to meet the effluent limits established by Brazilian legislation for disposal.

  3. Municipal solid waste landfill leachate treatment by fenton, photo-fenton and fenton-like processes: Effect of some variables

    OpenAIRE

    Zazouli, Mohammad Ali; Yousefi, Zabihollah; Eslami, Akbar; Ardebilian, Maryam Bagheri

    2012-01-01

    Abstract Advanced oxidation processes like Fenton and photo-Fenton have been effectively applied to oxidize the persistent organic compounds in solid waste leachate and convert them to unharmful materials and products. However, there are limited data about application of Fenton-like process in leachate treatment. Therefore, this study was designed with the objective of treating municipal landfill leachate by Fenton, Fenton-like and photo–Fenton processes to determine the effect of different v...

  4. A review on the degradation of organic pollutants in waters by UV photoelectro-Fenton and solar photoelectro-Fenton

    OpenAIRE

    Brillas, Enric

    2014-01-01

    This paper presents a review on emerging electrochemical advanced oxidation processes (EAOPs) such as UV photoelectro-Fenton (PEF) and solar photoelectro-Fenton (SPEF) in which the irradiation of the effluent with UV light and sunlight, respectively, causes a synergistic effect on the degradation process of organic pollutants by the formation of more •OH and/or the photolysis of complexes of Fe(III) with generated carboxylic acids. Fundamentals of these EAOPs are explained to clarify their pe...

  5. Asymmetric Radical Cyclopropanation of Alkenes with In Situ-Generated Donor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis.

    Science.gov (United States)

    Wang, Yong; Wen, Xin; Cui, Xin; Wojtas, Lukasz; Zhang, X Peter

    2017-01-25

    Donor-substituted diazo reagents, generated in situ from sulfonyl hydrazones in the presence of base, can serve as suitable radical precursors for Co(II)-based metalloradical catalysis (MRC). The cobalt(II) complex of D 2 -symmetric chiral porphyrin [Co(3,5-Di t Bu-Xu(2'-Naph)Phyrin)] is an efficient metalloradical catalyst that is capable of activating different N-arylsulfonyl hydrazones for asymmetric radical cyclopropanation of a broad range of alkenes, affording the corresponding cyclopropanes in high yields with effective control of both diastereo- and enantioselectivity. This Co(II)-based metalloradical system represents the first catalytic protocol that can effectively utilize donor-type diazo reagents for asymmetric olefin cyclopropanation.

  6. Tertiary treatment of pulp mill wastewater by solar photo-Fenton

    International Nuclear Information System (INIS)

    Lucas, Marco S.; Peres, José A.; Amor, Carlos; Prieto-Rodríguez, Lucía; Maldonado, Manuel I.; Malato, Sixto

    2012-01-01

    Highlights: ► We firstly report a real pulp mill wastewater treatment by solar photo-Fenton in a CPC reactor. Fenton reagent experiments were tested firstly. ► Solar photo-Fenton presents excellent ability to treat the pulp mill wastewater. ► Experimental conditions were optimised. ► Biodegradability and toxicity tests (respirometry assays and BOD 5 /COD ratio) were performed during the wastewater treatment. ► A way to reduce the economic and environmental impact was evaluated. - Abstract: This work reports on pulp mill wastewater (PMW) tertiary treatment by Fenton (Fe 2+ /H 2 O 2 ) and solar photo-Fenton (Fe 2+ /H 2 O 2 /UV) processes in a pilot plant based on compound parabolic collectors (CPCs). Solar photo-Fenton reaction is much more efficient than the respective dark reaction under identical experimental conditions. It leads to DOC mineralisation, COD and total polyphenols (TP) removal higher than 90%. The solar photo-Fenton experiment with 5 mg Fe L −1 reaches 90% of DOC mineralisation with 31 kJ L −1 of UV energy and 50 mM of H 2 O 2 . The initial non-biodegradability of PMW, as shown by respirometry assays and BOD 5 /COD ratio, can be changed after a solar photo-Fenton treatment. Experiments with 20 and 50 mg Fe L −1 revealed that solar photo-Fenton can reach the same DOC degradation (90%), however, consuming less H 2 O 2 and time. Diluting the initial organic load to 50% also diminishes the dosage of H 2 O 2 and the necessary reaction time to achieve high DOC removals. Accordingly, solar photo-Fenton can be considered an alternative or complementary process to improve the performance of a biologic treatment and, subsequently, achieve legal limits on discharge into natural waters.

  7. Decolorization of Industrial Waste Using Fenton Process and Photo Fenton

    OpenAIRE

    Wardiyati, Siti; Dewi, Sari Hasnah; Fisli, Adel

    2013-01-01

    Industrial waste water decolorization has been done using the method of Fenton and Photo Fenton. The experiment was conducted in order to obtain the optimum process conditions for industrial waste treatment method with Fenton and Photo Fenton. Industrial waste used in this experiment waste of blue batik making process derived from Rara Djograng Batik Yogyakarta. Factors were studied in this research are the effect of the amount of catalyst FeSO4.7H2O, the amount of oxidant H2O2, and the time ...

  8. Regulation of Electrochemically Generated H2O2 in Situ from a Novel CB-PTFE Cathode for Transformation of Chlorine Benzene in Groundwater

    Science.gov (United States)

    Jiang, J.; Zhang, X.; Li, G.

    2014-12-01

    Fenton's reagents (H2O2 and Fe2+ catalyst commonly) have been widely used in soil and groundwater remediation. But the excessive H2O2 decomposition and the pH modification (acidification) problem have been limitations for Fenton based remediation strategies. The Electro-Fenton (E- Fenton) processes has been recently developed to solve the problems, in which Fe2+ or H2O2are generated in situ as continuing source of Fenton's reagents. In this study, a novel CB-PTFE cathode and a Fe cathode were employed to generate H2O2 and Fe2+ in situ simultaneously. The generated reactive oxidizing species, i.e., O2,H2O2 and hydroxyl radical (HO•), oxidized bio-refractory organics to nontoxic matters in groundwater. Automatic pH adjustments are achieved by appropriately arraying the electrodes. Laboratory batch tests and column tests for the E-Fenton oxidation and hybrid electrolysis system were conducted to evaluate the transformation efficiency of chlorine benzene. Results from batch experiments suggested the CB-PTFE cathode was effective for reducing O2 to H2O2. The H2O2 concentration reached 468 mg/L under the condition of pH 3.0 and 30mA/cm2 in 60 minutes, which was 5 and 10 times of that with a graphite and C-felt cathode. The removal efficiency of chlorine benzene reached 80% in 20 minutes. Both chlorine benzene degradation and H2O2 production increased with decreasing solution pH and increasing current density. The results from the columns tests proved that the in situ E-Fenton system is a feasible method for groundwater remediation.

  9. Fenton process-affected transformation of roxarsone in paddy rice soils: Effects on plant growth and arsenic accumulation in rice grain.

    Science.gov (United States)

    Qin, Junhao; Li, Huashou; Lin, Chuxia

    2016-08-01

    Batch and greenhouse experiments were conducted to examine the effects of Fenton process on transformation of roxarsone in soils and its resulting impacts on the growth of and As uptake by a rice plant cultivar. The results show that addition of Fenton reagent markedly accelerated the degradation of roxarsone and produced arsenite, which was otherwise absent in the soil without added Fenton reagent. Methylation of arsenate was also enhanced by Fenton process in the earlier part of the experiment due to abundant supply of arsenate from Roxarsone degradation. Overall, addition of Fenton reagent resulted in the predominant presence of arsenate in the soils. Fenton process significantly improved the growth of rice in the maturity stage of the first crop, The concentration of methylated As species in the rice plant tissues among the different growth stages was highly variable. Addition of Fenton reagent into the soils led to reduced uptake of soil-borne As by the rice plants and this had a significant effect on reducing the accumulation of As in rice grains. The findings have implications for understanding As biogeochemistry in paddy rice field receiving rainwater-borne H2O2 and for development of mitigation strategies to reduce accumulation of As in rice grains. Copyright © 2016 Elsevier Inc. All rights reserved.

  10. E- or Z-Selective synthesis of 4-fluorovinyl-1,2,3-triazoles with fluorinated second-generation Julia-Kocienski reagents.

    Science.gov (United States)

    Kumar, Rakesh; Singh, Govindra; Todaro, Louis J; Yang, Lijia; Zajc, Barbara

    2015-02-07

    A highly modular approach to N-substituted 4-(1-fluorovinyl)triazoles is described. In situ desilylation and Cu-catalyzed ligation reaction of TMS-protected α-fluoropropargyl benzothiazole sulfone with aryl, alkyl, and metallocenyl azides furnished second-generation Julia-Kocienski reagents in good to excellent yields. Condensation reactions of these reagents with aldehydes can be tuned to yield E or Z-alkenes selectively. Under mild conditions with DBU as the base, reactions of aldehydes furnished E-alkenes as the major isomer. On the other hand, in condensation reactions with LHMDS as the base and in appropriate solvents, both aldehydes and ketones reacted to yield fluoroalkenes with Z-selectivity. Stereochemical assignment of E/Z olefins obtained in the reaction of a ketone with two Julia reagents was performed via X-ray crystallographic analysis and comparisons of NMR data. The method allows efficient and ready diversification of the N1-substituent and substituents at the double bond.

  11. Decolorization kinetics of Procion H-exl dyes from textile dyeing using Fenton-like reactions.

    Science.gov (United States)

    Ntampegliotis, K; Riga, A; Karayannis, V; Bontozoglou, V; Papapolymerou, G

    2006-08-10

    The decolorization kinetics of three commercially used Procion H-exl dyes was studied using a Fenton-like reagent. The effect of the major system parameters (pH, concentration of H(2)O(2) and Fe(3+) and initial dye concentration) on the kinetics was determined. For comparison, the effect of the use of UV irradiated Fenton-like reagent and of Fenton reagent on the kinetics was also examined. In addition, mineralization rates and the biodegradability improvement as well as the effect of the addition of Cl(-), CO(3)(2-) or HCO(3)(-) on the decolorization rates was studied. The reactions were carried out in a 300 ml stirred cylindrical reactor with the capability of UV irradiation. The dye half-life time goes through a minimum with respect to the solution pH between 3 and 4. It also exhibits a broad minimum with respect to Fe(3+) and H(2)O(2) at molar ratios of H(2)O(2)/Fe(3+) from about 100 to 10. The addition of CO(3)(2-) and HCO(3)(-) substantially reduces the decolorization rates, while this effect is significantly less pronounced with Cl(-). At an optimum range of parameters, the mineralization rate (TOC reduction) is very slow for the Fenton-like process (TOC decrease from an initial 49.5 to 41.1 mg/l after 30 min and to only 35.2 mg/l after 600 min), but it increases significantly for the photo-Fenton-like process (to TOC values of 39.7 and 11.4 mg/l, respectively). The biodegradability, as expressed by the BOD/COD ratio, increases significantly from an initial value of 0.11-0.55 for the Fenton-like and to 0.72 for the photo-Fenton-like processes.

  12. Degradation of sodium dodecyl sulphate in water using solar driven Fenton-like advanced oxidation processes

    International Nuclear Information System (INIS)

    Bandala, Erick R.; Pelaez, Miguel A.; Salgado, Maria J.; Torres, Luis

    2008-01-01

    Synthetic wastewater samples containing a model surfactant were treated using two different Fenton-like advanced oxidation processes promoted by solar radiation; the photo-Fenton reaction and Co/PMS/UV processes. Comparison between the different experimental conditions was performed by means of the overall surfactant degradation achieved and by obtaining the initial rate in the first 15 min of reaction (IR 15 ). It was found that, for dark Fenton reaction, the maximum surfactant degradation achieved was 14% under low iron and oxidant concentration. Increasing Fenton reagents by one magnitude order, surfactant degradation achieved 63% in 60 min. The use of solar radiation improved the reaction rate by 17% under same conditions and an additional increase of 12.5% was obtained by adjusting initial pH to 2. IR 15 values for dark and irradiated Fenton reactions were 0.143 and 0.154 mmol/min, respectively, for similar reaction conditions and this value increased to 0.189 mmol/min when initial pH was adjusted. The use of the Co/PMS system allow us to determine an increase in the degradation rate, for low reaction conditions (1 mM of transition metal; 4 mM oxidant) similar to those used in dark Fenton reaction. Surfactant degradation increased from 3%, for Fenton reaction, to 44.5% in the case of Co/PMS. When solar irradiation was included in the experiments, under same reaction conditions described earlier, surfactant degradation up to 64% was achieved. By increasing Co/PMS reagent concentration by almost 9 times under irradiated conditions, almost complete (>99%) surfactant degradation was reached in 5 min. Comparing IR 15 values for Co/PMS and Co/PMS/UV, it allow us to observe that the use of solar radiation increased the degradation rate in one magnitude order when compared with dark experiments and further increase of reagent concentration increased reaction rate twice

  13. Interfacial mechanisms of heterogeneous Fenton reactions catalyzed by iron-based materials: A review.

    Science.gov (United States)

    He, Jie; Yang, Xiaofang; Men, Bin; Wang, Dongsheng

    2016-01-01

    The heterogeneous Fenton reaction can generate highly reactive hydroxyl radicals (OH) from reactions between recyclable solid catalysts and H2O2 at acidic or even circumneutral pH. Hence, it can effectively oxidize refractory organics in water or soils and has become a promising environmentally friendly treatment technology. Due to the complex reaction system, the mechanism behind heterogeneous Fenton reactions remains unresolved but fascinating, and is crucial for understanding Fenton chemistry and the development and application of efficient heterogeneous Fenton technologies. Iron-based materials usually possess high catalytic activity, low cost, negligible toxicity and easy recovery, and are a superior type of heterogeneous Fenton catalysts. Therefore, this article reviews the fundamental but important interfacial mechanisms of heterogeneous Fenton reactions catalyzed by iron-based materials. OH, hydroperoxyl radicals/superoxide anions (HO2/O2(-)) and high-valent iron are the three main types of reactive oxygen species (ROS), with different oxidation reactivity and selectivity. Based on the mechanisms of ROS generation, the interfacial mechanisms of heterogeneous Fenton systems can be classified as the homogeneous Fenton mechanism induced by surface-leached iron, the heterogeneous catalysis mechanism, and the heterogeneous reaction-induced homogeneous mechanism. Different heterogeneous Fenton systems catalyzed by characteristic iron-based materials are comprehensively reviewed. Finally, related future research directions are also suggested. Copyright © 2015. Published by Elsevier B.V.

  14. Mature landfill leachate treatment by coagulation/flocculation combined with Fenton and solar photo-Fenton processes.

    Science.gov (United States)

    Amor, Carlos; De Torres-Socías, Estefanía; Peres, José A; Maldonado, Manuel I; Oller, Isabel; Malato, Sixto; Lucas, Marco S

    2015-04-09

    This work reports the treatment of a mature landfill leachate through the application of chemical-based treatment processes in order to achieve the discharge legal limits into natural water courses. Firstly, the effect of coagulation/flocculation with different chemicals was studied, evaluating the role of different initial pH and chemicals concentration. Afterwards, the efficiency of two different advanced oxidation processes for leachate remediation was assessed. Fenton and solar photo-Fenton processes were applied alone and in combination with a coagulation/flocculation pre-treatment. This physicochemical conditioning step, with 2 g L(-1) of FeCl3 · 6H2O at pH 5, allowed removing 63% of COD, 80% of turbidity and 74% of total polyphenols. Combining the coagulation/flocculation pre-treatment with Fenton reagent, it was possible to reach 89% of COD removal in 96 h. Moreover, coagulation/flocculation combined with solar photo-Fenton revealed higher DOC (75%) reductions than single solar photo-Fenton (54%). In the combined treatment (coagulation/flocculation and solar photo-Fenton), it was reached a DOC reduction of 50% after the chemical oxidation, with 110 kJ L(-1) of accumulated UV energy and a H2O2 consumption of 116 mM. Toxicity and biodegradability assays were performed to evaluate possible variations along the oxidation processes. After the combined treatment, the leachate under study presented non-toxicity but biodegradability increased. Copyright © 2014 Elsevier B.V. All rights reserved.

  15. One-pot catalyst preparation : combined detemplating and Fe ionexchange of BEA through Fenton's chemistry

    NARCIS (Netherlands)

    Melián-Cabrera, I.; Kapteijn, F.; Moulijn, J.A.

    2005-01-01

    BEA zeolite has been simultaneously detemplated and Fe-exchanged by treating the parent zeolite with a Fenton's-type reagent (Fe3+ - H2O2) at low temperature. This one-pot process simplifies and speeds up considerably the preparation route. The catalyst shows excellent performance on N2O

  16. APPLICATION OF FENTON’S REAGENT ON REMEDIATION OF POLYCYCLIC AROMATIC HYDROCARBONs (PAHs IN SPIKED SOIL

    Directory of Open Access Journals (Sweden)

    Nursiah La Nafie

    2010-06-01

    Full Text Available Problem associated with Polycyclic Aromatic Hydrocarbons (PAHs contaminated site in environmental media have received increasing attention. To resolve such problems, innovative in situ methods are urgently required. This work investigated the feasibility of using Fenton's Reagent to remediate PAHs in spiked soil. PAHs were spiked into soil to simulate contaminated soil. Fenton's Reagent (H2O2 + Fe2+ and surfactant were very efficient in destruction of PAHs including naphthalene, anthracene, fluoranthene, pyrene, and benzo(apyrene from spiked soil. It was indicated by the fact that more than 96% of PAHs were degraded in the solution and the spiked soil.   Keywords: Environmental, Fenton's Reagent, Polycyclic Aromatic Hydrocarbons, and Spiked soil.

  17. Effects of iron type in Fenton reaction on mineralization and biodegradability enhancement of hazardous organic compounds.

    Science.gov (United States)

    Khan, Eakalak; Wirojanagud, Wanpen; Sermsai, Nawarat

    2009-01-30

    The mineralization and biodegradability increase and their combination of two traditional and two relatively new organic contaminants by Fenton reagents with three different types of iron, Fe(2+), Fe(3+), and Fe(0) were investigated. The traditional contaminants examined were trichloroethene (TCE) and 2,4-dichlorophenol (2,4-DCP) while 1,4-dioxane (1,4-D) and 1,2,3-trichloropropane (TCP) were studied for the relatively new contaminants. The mineralization and biodegradability were represented by dissolved organic carbon (DOC) reduction and the ratio of biodegradable dissolved organic carbon and DOC, respectively. For all four contaminants, Fenton reagent using Fe(2+) was more effective in the DOC reduction than Fenton reagents using Fe(3+) and Fe(0) in most cases. The types of Fe that provided maximum biodegradability increase were not the same for all four compounds, Fe(3+) for TCE, Fe(0) for 2,4-DCP, Fe(2+) for 1,4-D, and Fe(3+) for TCP. When the combination of DOC elimination and biodegradability increase (least refractory fraction) was considered, Fe(2+) was the best choice except for 2,4-DCP which was susceptible to Fe(0) catalyzed Fenton reagent the most. The least refractory fractions remaining after 120 min of reaction were 20-25% for TCE, 2,4-DCP, and TCP and 30-40% for 1,4-D. The iron type in Fenton reaction also affected the type of mineralization kinetics of TCE, 2,4-DCP, and TCP as well as the types of degradation by-products of these contaminants. Some of the by-products found, such as isopropanol and propionic aldehyde, which were produced from Fe(0) catalyzed Fenton degradation of TCP, have not been previously reported.

  18. TREATMENT OF MTBE-CONTAMINATED WATERS WITH FENTON'S REAGENT

    Science.gov (United States)

    Methyl tertiary-butyl ether (MTBE) has been commonly used as a fuel additive because of its many favorable properties that allow it to improve fuel combustion and reduce resulting concentrations of carbon monoxide and unburnt hydrocarbons. Unfortuantely, increased production a...

  19. Iron crystallization in a fluidized-bed Fenton process.

    Science.gov (United States)

    Boonrattanakij, Nonglak; Lu, Ming-Chun; Anotai, Jin

    2011-05-01

    The mechanisms of iron precipitation and crystallization in a fluidized-bed reactor were investigated. Within the typical Fenton's reagent dosage and pH range, ferric ions as a product from ferrous ion oxidation would be supersaturated and would subsequently precipitate out in the form of ferric hydroxide after the initiation of the Fenton reaction. These precipitates would simultaneously crystallize onto solid particles in a fluidized-bed Fenton reactor if the precipitation proceeded toward heterogeneous nucleation. The heterogeneous crystallization rate was controlled by the fluidized material type and the aging/ripening period of the crystallites. Iron crystallization onto the construction sand was faster than onto SiO(2), although the iron removal efficiencies at 180 min, which was principally controlled by iron hydroxide solubility, were comparable. To achieve a high iron removal rate, fluidized materials have to be present at the beginning of the Fenton reaction. Organic intermediates that can form ferro-complexes, particularly volatile fatty acids, can significantly increase ferric ion solubility, hence reducing the crystallization performance. Therefore, the fluidized-bed Fenton process will achieve exceptional performance with respect to both organic pollutant removal and iron removal if it is operated with the goal of complete mineralization. Crystallized iron on the fluidized media could slightly retard the successive crystallization rate; thus, it is necessary to continuously replace a portion of the iron-coated bed with fresh media to maintain iron removal performance. The iron-coated construction sand also had a catalytic property, though was less than those of commercial goethite. Copyright © 2011 Elsevier Ltd. All rights reserved.

  20. Removal of azo dye using Fenton and Fenton-like processes: Evaluation of process factors by Box-Behnken design and ecotoxicity tests.

    Science.gov (United States)

    Fernandes, Neemias Cintra; Brito, Lara Barroso; Costa, Gessyca Gonçalves; Taveira, Stephânia Fleury; Cunha-Filho, Marcílio Sérgio Soares; Oliveira, Gisele Augusto Rodrigues; Marreto, Ricardo Neves

    2018-06-06

    The conventional treatment of textile effluents is usually inefficient in removing azo dyes and can even generate more toxic products than the original dyes. The aim of the present study was to optimize the process factors in the degradation of Disperse Red 343 by Fenton and Fenton-like processes, as well as to investigate the ecotoxicity of the samples treated under optimized conditions. A Box-Behnken design integrated with the desirability function was used to optimize dye degradation, the amount of residual H 2 O 2 [H 2 O 2residual ], and the ecotoxicity of the treated samples (lettuce seed, Artemia salina, and zebrafish in their early-life stages). Dye degradation was affected only by catalyst concentration [Fe] in both the Fenton and Fenton-like processes. In the Fenton reaction, [H 2 O 2residual ] was significantly affected by initial [H 2 O 2 ] and its interaction with [Fe]; however, in the Fenton-like reaction, it was affected by initial [H 2 O 2 ] only. A. salina mortality was affected by different process factors in both processes, which suggests the formation of different toxic products in each process. The desirability function was applied to determine the best process parameters and predict the responses, which were confirmed experimentally. Optimal conditions facilitated the complete degradation of the dye without [H 2 O 2residual ] or toxicity for samples treated with the Fenton-like process, whereas the Fenton process induced significant mortality for A. salina. Results indicate that the Fenton-like process is superior to the Fenton reaction to degrade Disperse Red 343. Copyright © 2018 Elsevier B.V. All rights reserved.

  1. Optimization of radiolytic degradation of sulfadiazine by combining Fenton and gamma irradiation processes

    International Nuclear Information System (INIS)

    Rivas-Ortiz, Iram Barbaro; Cruz-Gonzalez, German; Manduca-Artiles, Michel; Jauregui-Haza, U.J.

    2017-01-01

    Gamma radiation (GR) is a promising technique, among known advanced oxidation processes, degrading water contaminants. Nevertheless, few authors report the degradation of sulfonamides by GR, and limited information exists concerning the use of GR in the case of sulfadiazine (SDZ). The objectives of this work are (1) evaluating GR as an alternative method for treating wastewater contaminated with SDZ and examinating the intensification of GR with oxidants (H 2 O 2 or Fenton reagent). GR was performed with a high-activity 60 Co source. The gamma radiation/Fenton process gave the best result, leading to total SDZ removal and high (74.13%) pollutant mineralization. (author)

  2. Electro-Fenton, UVA photoelectro-Fenton and solar photoelectro-Fenton degradation of the drug ibuprofen in acid aqueous medium using platinum and boron-doped diamond anodes

    International Nuclear Information System (INIS)

    Skoumal, Marcel; Rodriguez, Rosa Maria; Cabot, Pere Lluis; Centellas, Francesc; Garrido, Jose Antonio; Arias, Conchita; Brillas, Enric

    2009-01-01

    The degradation of a 41 mg dm -3 ibuprofen (2-(4-isobutylphenyl)propionic acid) solution of pH 3.0 has been comparatively studied by electrochemical advanced oxidation processes (EAOPs) like electro-Fenton, UVA photoelectro-Fenton and solar photoelectro-Fenton at constant current density. Experiments were performed in a one-compartment cell with a Pt or boron-doped diamond (BDD) anode and an O 2 -diffusion cathode. Heterogeneous hydroxyl radical (·OH) is generated at the anode surface from water oxidation, while homogeneous ·OH is formed from Fenton's reaction between Fe 2+ and H 2 O 2 generated at the cathode, being its production strongly enhanced from photo-Fenton reaction induced by sunlight. Higher mineralization is attained in all methods using BDD instead Pt, because the former produces greater quantity of ·OH enhancing the oxidation of pollutants. The mineralization rate increases under UVA and solar irradiation by the rapid photodecomposition of complexes of Fe(III) with acidic intermediates. The most potent method is solar photoelectro-Fenton with BDD giving 92% mineralization due to the formation of a small proportion of highly persistent final by-products. The effect of Fe 2+ content, pH and current density on photoelectro-Fenton degradation has been studied. The ibuprofen decay always follows a pseudo-first-order kinetics and its destruction rate is limited by current density and UV intensity. Aromatics such as 1-(1-hydroxyethyl)-4-isobutylbenzene, 4-isobutylacetophenone, 4-isobutylphenol and 4-ethylbenzaldehyde, and carboxylic acids such as pyruvic, acetic, formic and oxalic have been identified as oxidation by-products. Oxalic acid is the ultimate by-product and the fast photodecarboxylation of its complexes with Fe(III) under UVA or solar irradiation explains the higher oxidation power of photoelectro-Fenton methods in comparison to electro-Fenton procedures

  3. In Vivo Lighted Fluorescence via Fenton Reaction: Approach for Imaging of Hydrogen Peroxide in Living Systems.

    Science.gov (United States)

    Liu, Changhui; Chen, Weiju; Qing, Zhihe; Zheng, Jing; Xiao, Yue; Yang, Sheng; Wang, Lili; Li, Yinhui; Yang, Ronghua

    2016-04-05

    By virtue of its high sensitivity and rapidity, Fenton reaction has been demonstrated as a powerful tool for in vitro biochemical analysis; however, in vivo applications of Fenton reaction still remain to be exploited. Herein, we report, for the first time, the design, formation and testing of Fenton reaction for in vivo fluorescence imaging of hydrogen peroxide (H2O2). To realize in vivo fluorescence imaging of H2O2 via Fenton reaction, a functional nanosphere, Fc@MSN-FDNA/PTAD, is fabricated from mesoporous silica nanoparticle (MSN), a Fenton reagent of ferrocene (Fc), ROX-labeled DNA (FDNA), and a cationic perylene derivative (PTAD). The ferrocene molecules are locked in the pore entrances of MSN, and exterior of MSN is covalently immobilized with FDNA. As a key part, PTAD acts as not only the gatekeeper of MSN but also the efficient quencher of ROX. H2O2 can permeate into the nanosphere and react with ferrocene to product hydroxyl radical (·OH) via Fenton reaction, which cleaves FDNA to detach ROX from PTAD, thus in turn, lights the ROX fluorescence. Under physiological condition, H2O2 can be determined from 5.0 nM to 1.0 μM with a detection limit of 2.4 nM. Because of the rapid kinetics of Fenton reaction and high specificity for H2O2, the proposed method meets the requirement for real applications. The feasibility of Fc@MSN-FDNA/PTAD for in vivo applications is demonstrated for fluorescence imaging of exogenous and endogenous H2O2 in cells and mice. We expect that this work will not only contribute to the H2O2-releated studies but also open up a new way to exploit in vivo Fenton reaction for biochemical research.

  4. Kaolinite adsorption-regeneration system for dyestuff treatment by Fenton based processes.

    Science.gov (United States)

    Rosales, Emilio; Anasie, Delia; Pazos, Marta; Lazar, Iuliana; Sanromán, M Angeles

    2018-05-01

    The regeneration and reuse of adsorbents is a subject of interest nowadays in order to reduce the pollution and the wastes generated in the adsorption wastewater treatment. In this work, the regeneration of the spent kaolinite by different advanced oxidation processes (Fenton, electro-Fenton and electrokinetic-Fenton) was evaluated. Initially, it was confirmed the ability of a low cost clayey material, kaolinite, for the adsorption of model dye such as Rhodamine B showing Freundlich isotherm fitting. Then, the regeneration and consequent degradation of the pollutant in the adsorbent by Fenton based processes was carried out. The role of different parameters affecting the regeneration process (H 2 O 2 :Fe 2+ ratio, liquid:solid ratio) were evaluated. Working at 100:1 H 2 O 2 :Fe 2+ ratio and 30min near complete dye removal (around 97%) from kaolinite was obtained by Fenton treatment. After that, a two-stage treatment for adsorption-regeneration was evaluated during five treatment cycles demonstrating its viability for regeneration of the adsorbent through dye degradation. Based on the successful application of Fenton technique, the improvement of the treatment by electro-Fenton and electrokinetic-Fenton were studied for different solid:liquid ratios achieving satisfactory regeneration values. Copyright © 2017 Elsevier B.V. All rights reserved.

  5. Simultaneous Removal of Thallium and EDTA by Fenton Process

    Science.gov (United States)

    Xu, Ruibing; Huang, Xuexia; Li, Huosheng; Su, Minhua; Chen, Diyun

    2018-01-01

    The wastewater containing heavy metals and organic pollutants is widely discharged from industries. Because of the coexistence of heavy metals and organic pollutants, the treatment of such wastewater is very difficult. Fenton process is considered to be one of the most effective approaches for the degradation of organic pollutants in aqueous solution due to the strong oxidative ability of hydroxyl radical which generated from the Fenton process. Apart from this, heavy metals are able to be removed during Fenton process owning to the synergic effect of coagulation and precipitation. In this work, pollutants of thallium and EDTA were successfully removed via the Fenton process. A series of single-factor experiments were designed and performed to achieve an optimal reaction conditions for the removal of both thallium and EDTA. Results showed that the removal efficiencies of thallium and TOC could be as high as 96.54% and 70.42%, respectively. The outcomes from our study demonstrate that Fenton process is a promising method for the purification of wastewater containing thallium and EDTA.

  6. A new approach to flow-batch titration. A monosegmented flow titrator with coulometric reagent generation and potentiometric or biamperometric detection.

    Science.gov (United States)

    de Aquino, Emerson Vidal; Rohwedder, Jarbas José Rodrigues; Pasquini, Celio

    2006-11-01

    Monosegmented flow analysis (MSFA) has been used as a flow-batch system to produce a simple, robust, and mechanized titrator that enables true titrations to be performed without the use of standards. This paper also introduces the use of coulometry with monosegmented titration by proposing a versatile flow cell. Coulometric generation of the titrand is attractive for titrations performed in monosegmented systems, because the reagent can be added without increasing the volume of sample injected. Also, biamperomeric and potentiometric detection of titration end-points can increase the versatility of the monosegmented titrator. The cell integrates coulometric generation of the titrand with detection of end-point by potentiometry or biamperometry. The resulting titrator is a flow-batch system in which the liquid monosegment, constrained by the interfaces of the gaseous carrier stream, plays the role of a sample of known volume to be titrated. The system has been used for determination of ascorbic acid, by coulometric generation of I2 with biamperometric detection, and for determination of Fe(II), by coulometric generation of Ce(IV) with potentiometric detection of the end-point, both in feed supplements.

  7. Mineralization of herbicide 3,6-dichloro-2-methoxybenzoic acid in aqueous medium by anodic oxidation, electro-Fenton and photoelectro-Fenton

    International Nuclear Information System (INIS)

    Brillas, Enric; Banos, Miguel Angel; Garrido, Jose Antonio

    2003-01-01

    The mineralization of acidic aqueous solutions with 230 and 115 ppm of herbicide 3,6-dichloro-2-methoxybenzoic acid (dicamba) in 0.05 M Na 2 SO 4 of pH 3.0 has been studied by electro-Fenton and photoelectro-Fenton using a Pt anode and an O 2 -diffusion cathode, where oxidizing hydroxyl radicals are produced from Fenton's reaction between added Fe 2+ and H 2 O 2 generated by the cathode. While electro-Fenton only yields 60-70% mineralization, photoelectro-Fenton allows a fast and complete depollution of herbicide solutions, even at low currents, by the action of UV irradiation. In both treatments, the initial chlorine is rapidly released to the medium as chloride ion. Comparative electrolyses by anodic oxidation in the absence and presence of electrogenerated H 2 O 2 give very poor degradation. The dicamba decay follows a pseudo-first-order reaction, as determined by reverse-phase chromatography. Formic, maleic and oxalic acids have been detected in the electrolyzed solutions by ion-exclusion chromatography. In electro-Fenton, all formic acid is transformed into CO 2 , and maleic acid is completely converted into oxalic acid, remaining stable Fe 3+ -oxalato complexes in the solution. The fast mineralization of such complexes by UV light explains the highest oxidative ability of photoelectro-Fenton

  8. Are clusters important in understanding the mechanisms in atmospheric pressure ionization? Part 1: Reagent ion generation and chemical control of ion populations.

    Science.gov (United States)

    Klee, Sonja; Derpmann, Valerie; Wißdorf, Walter; Klopotowski, Sebastian; Kersten, Hendrik; Brockmann, Klaus J; Benter, Thorsten; Albrecht, Sascha; Bruins, Andries P; Dousty, Faezeh; Kauppila, Tiina J; Kostiainen, Risto; O'Brien, Rob; Robb, Damon B; Syage, Jack A

    2014-08-01

    It is well documented since the early days of the development of atmospheric pressure ionization methods, which operate in the gas phase, that cluster ions are ubiquitous. This holds true for atmospheric pressure chemical ionization, as well as for more recent techniques, such as atmospheric pressure photoionization, direct analysis in real time, and many more. In fact, it is well established that cluster ions are the primary carriers of the net charge generated. Nevertheless, cluster ion chemistry has only been sporadically included in the numerous proposed ionization mechanisms leading to charged target analytes, which are often protonated molecules. This paper series, consisting of two parts, attempts to highlight the role of cluster ion chemistry with regard to the generation of analyte ions. In addition, the impact of the changing reaction matrix and the non-thermal collisions of ions en route from the atmospheric pressure ion source to the high vacuum analyzer region are discussed. This work addresses such issues as extent of protonation versus deuteration, the extent of analyte fragmentation, as well as highly variable ionization efficiencies, among others. In Part 1, the nature of the reagent ion generation is examined, as well as the extent of thermodynamic versus kinetic control of the resulting ion population entering the analyzer region.

  9. Fenton-like chemistry in water: Oxidation catalysis by Fe(III) and H2O2

    NARCIS (Netherlands)

    Ensing, B.; Buda, F.; Baerends, E.J.

    2003-01-01

    The formation of active intermediates from the Fenton-like reagent (a mixture of iron(III) ions and hydrogen peroxide) in aqueous solution has been investigated using static DFT calculations and Car-Parrinello molecular dynamics simulations. We show the spontaneous formation of the iron(III)

  10. Fenton detemplation of ordered (meso)porous materials

    NARCIS (Netherlands)

    Melian-Cabrera, I.; Osman, A. H.; van Eck, E. R. H.; Kentgens, Arno P.M.; Polushkin, E.; Kapteijn, F.; Moulijn, J. A.; Xu, R; Gao, Z; Chen, J; Yan, W

    2007-01-01

    This article describes a new methodology (Fenton detemplation), which consists of removing the template by chemical oxidation and develop the material's porosity. The oxidizing agents are OH radicals, which are generated from H(2)O(2) in the presence of catalytic amounts of Fe cations. This is known

  11. PREDICTING FENTON-DRIVEN DEGRADATION USING CONTAMINANT ANALOG

    Science.gov (United States)

    The reaction of hydrogen peroxide (H2O2) and Fe(II) (Fenton's reaction) generates hydroxyl radicals (OH) that can be used to oxidize contaminants in soils and aquifers. In such environments, insufficient iron, reactions involving H2O2 that do not yield OH, and OH reactions with ...

  12. Handling Pyrophoric Reagents

    Energy Technology Data Exchange (ETDEWEB)

    Alnajjar, Mikhail S.; Haynie, Todd O.

    2009-08-14

    Pyrophoric reagents are extremely hazardous. Special handling techniques are required to prevent contact with air and the resulting fire. This document provides several methods for working with pyrophoric reagents outside of an inert atmosphere.

  13. Using single-chamber microbial fuel cells as renewable power sources of electro-Fenton reactors for organic pollutant treatment

    KAUST Repository

    Zhu, Xiuping; Logan, Bruce E.

    2013-01-01

    accomplish H2O2 generation and Fe2+ release for the Fenton reaction. In tests using phenol, 75±2% of the total organic carbon (TOC) was removed in the electro-Fenton reactor in one cycle (22h), and phenol was completely degraded to simple and readily

  14. Removal of citrate and hypophosphite binary components using Fenton, photo-Fenton and electro-Fenton processes

    Institute of Scientific and Technical Information of China (English)

    Yao-Hui Huang; Hsiao-Ting Su; Li-Way Lin

    2009-01-01

    Both citrate and hypophosphite in aqueous solution were degraded by advanced oxidation processes (Fe2+/H2O2, UV/Fe2+/H2O2, and electrolysis/ Fe2+/H2O2) in this study. Comparison of these techniques in oxidation efficiency was undertaken. It was found that Fenton process could not degrade completely citrate in the presence of hypophosphite since it caused a series inhibition. Therefore, UV light (photo-Fenton) or electron current (electro-Fenton) was applied to improve the degradation efficiency of the Fenton process. Results showed that both photo-Fenton and electro-Fenton processes could overcome the inhibition of hypophosphite, especially the electro-Fenton.

  15. Effect of the ultrasound-Fenton oxidation process with the addition of a chelating agent on the removal of petroleum-based contaminants from soil.

    Science.gov (United States)

    Li, Ying; Li, Fangmin; Li, Fanxiu; Yuan, Fuqian; Wei, Pingfang

    2015-12-01

    The effects of ultrasonic irradiation, the chelating agent modified Fenton reaction, and a combination of ultrasound and the Fenton method in removing petroleum contaminants from a soil were studied. The results showed that the contaminant removal rate of the Fenton treatment combined with an oxalic acid chelating agent was 55.6% higher than that without a chelating agent. The average removal rate of the contaminants using the ultrasound-Fenton treatment was 59.0% higher than that without ultrasonic treatment. A combination of ultrasound and an Fe(2+)/Fe(3+)-oxalate complex-modified Fenton reagent resulted in significantly higher removal rates of n-alkanes (C(n)H(2n+2), n Fenton method. The Fenton reaction and the ultrasound-Fenton treatment can unselectively remove multiple components of residual hydrocarbons and a number of benzene rings in polycyclic aromatic hydrocarbons. The chemistry of the heterocyclic compounds and the position and number of substituents can affect the degradation process.

  16. Tertiary treatment of pulp mill wastewater by solar photo-Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Lucas, Marco S., E-mail: mlucas@utad.pt [Centro de Quimica de Vila Real, Universidade de Tras-os-Montes e Alto Douro, Apartado 1013, 5001-801 Vila Real (Portugal); Peres, Jose A.; Amor, Carlos [Centro de Quimica de Vila Real, Universidade de Tras-os-Montes e Alto Douro, Apartado 1013, 5001-801 Vila Real (Portugal); Prieto-Rodriguez, Lucia; Maldonado, Manuel I.; Malato, Sixto [Plataforma Solar de Almeria (CIEMAT), Carretera de Senes, Km 4, 04200, Tabernas, Almeria (Spain)

    2012-07-30

    Highlights: Black-Right-Pointing-Pointer We firstly report a real pulp mill wastewater treatment by solar photo-Fenton in a CPC reactor. Fenton reagent experiments were tested firstly. Black-Right-Pointing-Pointer Solar photo-Fenton presents excellent ability to treat the pulp mill wastewater. Black-Right-Pointing-Pointer Experimental conditions were optimised. Black-Right-Pointing-Pointer Biodegradability and toxicity tests (respirometry assays and BOD{sub 5}/COD ratio) were performed during the wastewater treatment. Black-Right-Pointing-Pointer A way to reduce the economic and environmental impact was evaluated. - Abstract: This work reports on pulp mill wastewater (PMW) tertiary treatment by Fenton (Fe{sup 2+}/H{sub 2}O{sub 2}) and solar photo-Fenton (Fe{sup 2+}/H{sub 2}O{sub 2}/UV) processes in a pilot plant based on compound parabolic collectors (CPCs). Solar photo-Fenton reaction is much more efficient than the respective dark reaction under identical experimental conditions. It leads to DOC mineralisation, COD and total polyphenols (TP) removal higher than 90%. The solar photo-Fenton experiment with 5 mg Fe L{sup -1} reaches 90% of DOC mineralisation with 31 kJ L{sup -1} of UV energy and 50 mM of H{sub 2}O{sub 2}. The initial non-biodegradability of PMW, as shown by respirometry assays and BOD{sub 5}/COD ratio, can be changed after a solar photo-Fenton treatment. Experiments with 20 and 50 mg Fe L{sup -1} revealed that solar photo-Fenton can reach the same DOC degradation (90%), however, consuming less H{sub 2}O{sub 2} and time. Diluting the initial organic load to 50% also diminishes the dosage of H{sub 2}O{sub 2} and the necessary reaction time to achieve high DOC removals. Accordingly, solar photo-Fenton can be considered an alternative or complementary process to improve the performance of a biologic treatment and, subsequently, achieve legal limits on discharge into natural waters.

  17. In-line electrochemical reagent generation coupled to a flow injection biamperometric system for the determination of sulfite in beverage samples.

    Science.gov (United States)

    de Paula, Nattany T G; Barbosa, Elaine M O; da Silva, Paulo A B; de Souza, Gustavo C S; Nascimento, Valberes B; Lavorante, André F

    2016-07-15

    This work reports an in-line electrochemical reagent generation coupled to a flow injection biamperometric procedure for the determination of SO3(2-). The method was based on a redox reaction between the I3(-) and SO3(2-) ions, after the diffusion of SO2 through a gas diffusion chamber. Under optimum experimental conditions, a linear response ranging from 1.0 to 12.0 mg L(-1) (R=0.9999 and n=7), a detection and quantification limit estimated at 0.26 and 0.86 mg L(-1), respectively, a standard deviation relative of 0.4% (n=10) for a reference solution of 4.0 mg L(-1) SO3(2-) and sampling throughput for 40 determinations per hour were achieved. Addition and recovery tests with juice and wine samples were performed resulting in a range between 92% and 110%. There were no significant differences at a 95% confidence level in the analysis of eight samples when comparing the new method with a reference procedure. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Degradation of carbendazim in water via photo-Fenton in Raceway Pond Reactor: assessment of acute toxicity and transformation products.

    Science.gov (United States)

    da Costa, Elizângela Pinheiro; Bottrel, Sue Ellen C; Starling, Maria Clara V M; Leão, Mônica M D; Amorim, Camila Costa

    2018-05-08

    This study aimed at investigating the degradation of fungicide carbendazim (CBZ) via photo-Fenton reactions in artificially and solar irradiated photoreactors at laboratory scale and in a semi-pilot scale Raceway Pond Reactor (RPR), respectively. Acute toxicity was monitored by assessing the sensibility of bioluminescent bacteria (Aliivibrio fischeri) to samples taken during reactions. In addition, by-products formed during solar photo-Fenton were identified by liquid chromatography coupled to mass spectrometry (UFLC-MS). For tests performed in lab-scale, two artificial irradiation sources were compared (UV λ > 254nm and UV-Vis λ > 320nm ). A complete design of experiments was performed in the semi-pilot scale RPR in order to optimize reaction conditions (Fe 2+ and H 2 O 2 concentrations, and water depth). Efficient degradation of carbendazim (> 96%) and toxicity removal were achieved via artificially irradiated photo-Fenton under both irradiation sources. Control experiments (UV photolysis and UV-Vis peroxidation) were also efficient but led to increased acute toxicity. In addition, H 2 O 2 /UV λ > 254nm required longer reaction time (60 minutes) when compared to the photo-Fenton process (less than 1 min). While Fenton's reagent achieved high CBZ and acute toxicity removal, its efficiency demands higher concentration of reagents in comparison to irradiated processes. Solar photo-Fenton removed carbendazim within 15 min of reaction (96%, 0.75 kJ L -1 ), and monocarbomethoxyguanidine, benzimidazole isocyanate, and 2-aminobenzimidazole were identified as transformation products. Results suggest that both solar photo-Fenton and artificially irradiated systems are promising routes for carbendazim degradation.

  19. Decolorization kinetics of Procion H-exl dyes from textile dyeing using Fenton-like reactions

    Energy Technology Data Exchange (ETDEWEB)

    Ntampegliotis, K. [Department of Physical Sciences, Technological and Educational Institute of Larisa, T.K 411 10 Larisa (Greece); Riga, A. [Department of Physical Sciences, Technological and Educational Institute of Larisa, T.K 411 10 Larisa (Greece); Karayannis, V. [Department of Physical Sciences, Technological and Educational Institute of Larisa, T.K 411 10 Larisa (Greece); Bontozoglou, V. [Department of Mechanical and Industrial Engineering, University of Thessaly, Pedion Areos, T.K 383 34 Volos (Greece); Papapolymerou, G. [Department of Physical Sciences, Technological and Educational Institute of Larisa, T.K 411 10 Larisa (Greece)]. E-mail: papapoly@teilar.gr

    2006-08-10

    The decolorization kinetics of three commercially used Procion H-exl dyes was studied using a Fenton-like reagent. The effect of the major system parameters (pH, concentration of H{sub 2}O{sub 2} and Fe{sup 3+} and initial dye concentration) on the kinetics was determined. For comparison, the effect of the use of UV irradiated Fenton-like reagent and of Fenton reagent on the kinetics was also examined. In addition, mineralization rates and the biodegradability improvement as well as the effect of the addition of Cl{sup -}, CO{sub 3} {sup 2-} or HCO{sub 3} {sup -} on the decolorization rates was studied. The reactions were carried out in a 300 ml stirred cylindrical reactor with the capability of UV irradiation. The dye half-life time goes through a minimum with respect to the solution pH between 3 and 4. It also exhibits a broad minimum with respect to Fe{sup 3+} and H{sub 2}O{sub 2} at molar ratios of H{sub 2}O{sub 2}/Fe{sup 3+} from about 100 to 10. The addition of CO{sub 3} {sup 2-} and HCO{sub 3} {sup -} substantially reduces the decolorization rates, while this effect is significantly less pronounced with Cl{sup -}. At an optimum range of parameters, the mineralization rate (TOC reduction) is very slow for the Fenton-like process (TOC decrease from an initial 49.5 to 41.1 mg/l after 30 min and to only 35.2 mg/l after 600 min), but it increases significantly for the photo-Fenton-like process (to TOC values of 39.7 and 11.4 mg/l, respectively). The biodegradability, as expressed by the BOD/COD ratio, increases significantly from an initial value of 0.11-0.55 for the Fenton-like and to 0.72 for the photo-Fenton-like processes.

  20. Tratamento do lixiviado de aterro de resíduos sólidos urbanos por processo Fenton

    Directory of Open Access Journals (Sweden)

    Victor Wegner Maus

    2009-01-01

    Full Text Available O lixiviado gerado em aterros sanitários pela decomposição dos resíduos sólidos com presença de água de infiltração possuigrande potencial poluidor, devido à elevada concentração de substâncias tóxicas e a sua baixa biodegradabilidade. A coagulaçãoquímica pode ser uma alternativa para o tratamento de efluentes com essas características. O trabalho teve como objetivo avaliar aeficiência do processo Fenton no tratamento de lixiviado gerado em aterros sanitários de resíduos sólidos urbanos. As amostras delixiviado foram coletadas no aterro controlado do município de Santa Maria – RS. No experimento foram testados cincotratamentos com diferentes proporções de reagentes (H2O2 e FeSO4 TH2O2/FeSO4: T0,8, T2,0, T3,0, T4,0 e T6,0. Pelos resultados doexperimento com processo Fenton verifica-se uma eficiência média na remoção da demanda química de oxigênio (DQO de47,9%, na turbidez de 53,0% e na cor de 70,7%. Os valores médios da demanda bioquímica de oxigênio (DBO e dacondutividade elétrica aumentaram em 31,3% e 27,1%, respectivamente. No tratamento T0,8 constatou-se a maior remoção daDQO e o maior aumento da biodegradabilidade. O processo Fenton aplicado no tratamento de lixiviado reduz a DQO e aumenta aDBO, em outras palavras, aumenta a biodegradabilidade do efluente. Esse processo pode ser utilizado como pré-tratamento de umsistema biológico para efluentes de aterros sanitários.Abstract The leachate generated on sanitary landfill bysolid waste decomposition with rainfall water infiltration hashigh potential of pollution, due to high concentration oftoxic substances and low biodegradability. The chemistrycoagulation can be an alternative to treat effluents with thesecharacteristics. The work aimed to evaluate the efficiency ofFenton process in the treatment of leachate landfill fromurban solid waste. The leachate samples were collected fromthe controlled landfill of Santa Maria Council – RS. In theexperiment

  1. Ultrasound coupled with Fenton oxidation pre-treatment of sludge to release organic carbon, nitrogen and phosphorus

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Changxiu [School of Environment, Tsinghua University, Beijing 100084 (China); Jiang, Jianguo, E-mail: jianguoj@mail.tsinghua.edu.cn [School of Environment, Tsinghua University, Beijing 100084 (China); Key Laboratory for Solid Waste Management and Environment Safety, Ministry of Education of China (China); Collaborative Innovation Center for Regional Environmental Quality, Tsinghua University, Beijing (China); Li, De' an [School of Environment, Tsinghua University, Beijing 100084 (China)

    2015-11-01

    We focused on the effects of ultrasound and Fenton reagent in ultrasonic coupling Fenton oxidation (U + F) pre-treatment processes on the disintegration of wastewater treatment plant sludge. The results demonstrated that U + F treatment could significantly increase soluble COD, TOC, total N, proteins, total P and PO{sub 4}{sup 3−} concentrations in sludge supernatant. This method was more effective than ultrasonic (U) or Fenton oxidation (F) treatment alone. U + F treatment increased the soluble COD by 2.1- and 1.4-fold compared with U and F alone, respectively. U + F treatment increased the total N and P by 1.7- and 2.2-fold, respectively, compared with F alone. After U + F treatment, sludge showed a considerably finer particle size and looser microstructure based on scanning electron microscopy, and the highest OH· signal intensity increased from 568.7 by F treatment to 1106.3 using electron spin resonance. This demonstrated that U + F treatment induces disintegration of sludge and release of organic carbon, nitrogen and phosphorus better. - Highlights: • Combined ultrasound–Fenton pre-treatment was proposed for sludge disintegration. • Ultrasound–Fenton significantly increased carbon, nitrogen and phosphorus release. • Higher level of OH· was detected after combined disintegration than Fenton.

  2. Ultrasound coupled with Fenton oxidation pre-treatment of sludge to release organic carbon, nitrogen and phosphorus

    International Nuclear Information System (INIS)

    Gong, Changxiu; Jiang, Jianguo; Li, De'an

    2015-01-01

    We focused on the effects of ultrasound and Fenton reagent in ultrasonic coupling Fenton oxidation (U + F) pre-treatment processes on the disintegration of wastewater treatment plant sludge. The results demonstrated that U + F treatment could significantly increase soluble COD, TOC, total N, proteins, total P and PO 4 3− concentrations in sludge supernatant. This method was more effective than ultrasonic (U) or Fenton oxidation (F) treatment alone. U + F treatment increased the soluble COD by 2.1- and 1.4-fold compared with U and F alone, respectively. U + F treatment increased the total N and P by 1.7- and 2.2-fold, respectively, compared with F alone. After U + F treatment, sludge showed a considerably finer particle size and looser microstructure based on scanning electron microscopy, and the highest OH· signal intensity increased from 568.7 by F treatment to 1106.3 using electron spin resonance. This demonstrated that U + F treatment induces disintegration of sludge and release of organic carbon, nitrogen and phosphorus better. - Highlights: • Combined ultrasound–Fenton pre-treatment was proposed for sludge disintegration. • Ultrasound–Fenton significantly increased carbon, nitrogen and phosphorus release. • Higher level of OH· was detected after combined disintegration than Fenton

  3. Removal of refractory organics in nanofiltration concentrates of municipal solid waste leachate treatment plants by combined Fenton oxidative-coagulation with photo--Fenton processes.

    Science.gov (United States)

    Li, Jiuyi; Zhao, Lei; Qin, Lele; Tian, Xiujun; Wang, Aimin; Zhou, Yanmei; Meng, Liao; Chen, Yong

    2016-03-01

    Removal of the refractory organic matters in leachate brines generated from nanofiltration unit in two full-scale municipal solid waste landfill leachate treatment plants was investigated by Fenton oxidative-coagulation and ultraviolet photo - Fenton processes in this study. Fenton oxidative-coagulation was performed under the condition of an initial pH of 5.0 and low H2O2/Fe(2+) ratios. After precipitate separation, the remaining organic constituents were further oxidized by photo - Fenton process. For both leachate brines with varying pollution strength, more than 90% COD and TOC reductions were achieved at H2O2/Fe(2+) dosages of 35 mM/8 mM and 90 mM/10 mM, respectively. The effluent COD ranged 120-160 mg/L under the optimal operating conditions, and the biodegradability was increased significantly. Fenton oxidative-coagulation was demonstrated to contribute nearly 70% overall removal of organic matters. In the combined processes, the efficiency of hydrogen peroxide varied from 216 to 228%, which may significantly reduce the operating cost of conventional Fenton method. Six phthalic acid esters and thirteen polycyclic aromatic hydrocarbons were found in leachate brines, and, on the average, around 80% phthalic acid esters and 90% polycyclic aromatic hydrocarbons were removed by the combined treatments. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Degradation of ethylparaben under simulated sunlight using photo-Fenton.

    Science.gov (United States)

    Zúñiga-Benítez, Henry; Peñuela, Gustavo A

    2016-01-01

    Ethylparaben (EPB) has been classified by different research groups as a potential endocrine-disrupting chemical, implying that it can potentially interfere with the normal balance of the endocrine system of living beings, which with its presence in different effluents, including drinking water, generates the need to seek methods that allow its removal from different water bodies. Advanced oxidation processes have been employed widely to remove organic compounds from different matrices. In this way, Fenton technology (process based on the reaction between ferrous ions and hydrogen peroxide) has been able to degrade different substrates, but due to the Fe(2+) requirements to carry out the reaction optimally, combination of the conventional Fenton process with visible light radiation (photo-Fenton) is an alternative used in the treatment of pollution due to the presence of chemicals. In this way, the effectiveness of photo-Fenton on EPB degradation was assessed using a face-centered central composite experimental design that allowed assessment of the effects of Fe(2+) and H2O2 initial concentrations on process. In general, results indicated that after 180 min of reaction almost all EPB was eliminated, the dissolved organic carbon in solution was reduced and the sample biodegradability index was increased.

  5. Alternate switching between MFC and MEC for H2O2 synthesis and residual removal in Bioelectro-Fenton system

    DEFF Research Database (Denmark)

    Zhang, Yifeng; Angelidaki, Irini

    2016-01-01

    Sustainable H2O2 supply and elimination of residual H2O2 are two key challenges to the Fenton processes treating recalcitrant contaminants. In this study, an innovative Bioelectro-Fenton system capable of alternate switching between microbial electrolysis cell (MEC) and microbial fuel cell (MFC......) mode of operation was developed to meet the challenges. In the MEC mode, H2O2 was electrochemically produced which reacts with Fenton’s reagent (Fe II) to form hydroxyradical. The residual H2O2 (unused H2O2) is removed as electron acceptor by switching the system to MFC mode. Complete decolorization...

  6. Performance of Fluidized bed Fenton process in Degrading Acid Blue 113

    Science.gov (United States)

    Bello, M. M.; Raman, A. A.

    2017-06-01

    The performance of a fluidized bed Fenton process in degrading Acid Blue 113 (AB 113) was investigated. Fluidized bed Fenton process is a modification of conventional Fenton oxidation, aimed at reducing sludge generation and improving process performance. Response surface methodology was used to study the effects of operational parameter on the color removal from the dye. Dimensionless factors, Dye/Fe2+, H2O2/Fe2+ and pH were used as the independent variables in Box-Behnken Design (BDD). Reduced quadratic model was developed to predict the color removal. The process could remove up to 99 % of the initial color. The most significant factor for color removal was found to be Dye/Fe2+, followed by H2O2/Fe2+. Unlike conventional Fenton, the initial pH of the solution does not have a significant effect on the color removal.

  7. Degradation of phthalate in aqueous solution by advanced oxidation process, photo-fenton

    International Nuclear Information System (INIS)

    Trabelsi, S.; Bellakhal, N.; Oturan, N.; Oturan, M.A.

    2009-01-01

    A photochemical method for degradation of persistent organic pollutants present in liquid effluents from the plastic industry and in the leaching described. This method, called P hoto-Fenton i nvolves the generation of radicals hydroxyl coupling between the Fenton reaction and photochemistry, OH radicals. Thus formed react with very high speeds, organic substances pollutants leading to their oxidation to total mineralization. In this study, we applied the process photo-Fenton treatment Plasticizers, Phthalates. For this, optimization of experimental parameters (namely the relationship between the concentrations of hydrogen peroxide and iron concentration catalyst) was performed. Under optimal conditions and determined the kinetics mineralization of phthalic anhydride by OH was studied. The overall results confirm the effectiveness of photo-Fenton process for the decontamination of liquid effluents responsible for persistent organic pollutants (Pop's).

  8. Application of the photo-fenton process to the mineralization of phthalic anhydride in aqueous medium

    International Nuclear Information System (INIS)

    Trabelsi Souissi, Souhaila; Oturan, N.; Oturan, M. A; Bellakhal, N.

    2009-01-01

    A photochemical method for the oxidation of persistent organic pollutants (POPs) present in liquid effluents of plastic industry is described. This method, called p hoto-Fenton , involves the generation of hydroxyl radicals by coupling the Fenton reaction and photochemistry, .OH radicals thus formed react rapidly with organic pollutants leading to their oxidation until their total mineralization. In this study, we applied the photo-Fenton process for the removal of phthalic anhydride (plasticizer). In this way, an optimization of experimental parameters (namely the ratio R = [H 2 O 2 ]/[Fe 3+ ] and Fe 3+ initial concentration) was performed. Under optimal conditions, the kinetic of mineralization of phthalic anhydride by .OH has been studied. All results confirm the efficiency of photo-Fenton process for the decontamination of liquid effluents loaded with plasticizers.

  9. Involvement of Fenton chemistry in rice straw degradation by the lignocellulolytic bacterium Pantoea ananatis Sd-1.

    Science.gov (United States)

    Ma, Jiangshan; Zhang, Keke; Huang, Mei; Hector, Stanton B; Liu, Bin; Tong, Chunyi; Liu, Qian; Zeng, Jiarui; Gao, Yan; Xu, Ting; Liu, Ying; Liu, Xuanming; Zhu, Yonghua

    2016-01-01

    Lignocellulolytic bacteria have revealed to be a promising source for biofuel production, yet the underlying mechanisms are still worth exploring. Our previous study inferred that the highly efficient lignocellulose degradation by bacterium Pantoea ananatis Sd-1 might involve Fenton chemistry (Fe 2+  + H 2 O 2  + H +  → Fe 3+  + OH· + H 2 O), similar to that of white-rot and brown-rot fungi. The aim of this work is to investigate the existence of this Fenton-based oxidation mechanism in the rice straw degradation process of P. ananatis Sd-1. After 3 days incubation of unpretreated rice straw with P. ananatis Sd-1, the percentage in weight reduction of rice straw as well as its cellulose, hemicellulose, and lignin components reached 46.7, 43.1, 42.9, and 37.9 %, respectively. The addition of different hydroxyl radical scavengers resulted in a significant decline ( P  Fenton reagent treatment. In addition to the increased total iron ion concentration throughout the rice straw decomposition process, the Fe 3+ -reducing capacity of P. ananatis Sd-1 was induced by rice straw and predominantly contributed by aromatic compounds metabolites. The transcript levels of the glucose-methanol-choline oxidoreductase gene related to hydrogen peroxide production were significantly up-regulated (at least P  Fenton-like reactions. Our results confirmed the Fenton chemistry-assisted degradation model in P. ananatis Sd-1. We are among the first to show that a Fenton-based oxidation mechanism exists in a bacteria degradation system, which provides a new perspective for how natural plant biomass is decomposed by bacteria. This degradative system may offer an alternative approach to the fungi system for lignocellulosic biofuels production.

  10. AN ADVANCED OXIDATION PROCESS : FENTON PROCESS

    Directory of Open Access Journals (Sweden)

    Engin GÜRTEKİN

    2008-03-01

    Full Text Available Biological wastewater treatment is not effective treatment method if raw wastewater contains toxic and refractory organics. Advanced oxidation processes are applied before or after biological treatment for the detoxification and reclamation of this kind of wastewaters. The advanced oxidation processes are based on the formation of powerful hydroxyl radicals. Among advanced oxidation processes Fenton process is one of the most promising methods. Because application of Fenton process is simple and cost effective and also reaction occurs in a short time period. Fenton process is applied for many different proposes. In this study, Fenton process was evaluated as an advanced oxidation process in wastewater treatment.

  11. Influence of generated intermediates’ interaction on heterogeneous Fenton's degradation of an azo dye 1-diazo-2-naphthol-4-sulfonic acid by using sludge based carbon as catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Gu, Lin [School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093 (China); School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Huang, Shouqiang [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Zhu, Nanwen, E-mail: nwzhu@sjtu.edu.cn [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Zhang, Daofang, E-mail: Zhangdf-usst@163.com [School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093 (China); Yuan, Haiping; Lou, Ziyang [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2013-12-15

    Highlights: • End-products have higher tendency to be adsorbed on SC than primarily-formed. • Higher initial H{sub 2}O{sub 2} dosage results in intermediates with strong polarity. • 9 model intermediates differ in their behavior on interactions with catalysts. • Polar surface area dominated their adsorption on SC while K{sub ow} acts as a key role on HSC. -- Abstract: Sewage sludge based carbons have recently been used as novel catalyst in heterogeneous Fenton's reactions to degrade azo dye molecules. The carbons, functioning as both catalyst and adsorbent, play an important role in pollutants elimination, especially for those simultaneously generated organic intermediates. Different factors, i.e., H{sub 2}O{sub 2} concentration, may influence the type and properties of those intermediates and may have great impacts on their elimination through the interactions with catalysts’ surface. Thus, techniques including Temperature Programmed Desorption-Mass Spectrometer (TPD-MS), N{sub 2} adsorption isotherm and Scanning Electron Microscope (SEM) were used to probe the ways of the interaction between oxidation products and catalyst by using different initial H{sub 2}O{sub 2} concentrations (10 and 20 mM). The higher Chemical Oxygen Demand (COD) removal with 20 mM H{sub 2}O{sub 2} was found to be related not only to the higher hydroxyl radicals but also the specific interactions between the intermediates and catalyst’ surface. The deep oxidation occurred in the conditions with higher oxidant amount enhances the intermediates’ adsorption on catalyst, thus increasing the COD removal by large margin. Simulated adsorption experiments by using six primarily formed intermediates and three deeply mineralized products on three different catalysts also confirmed the assumption. Results suggested close relations between adsorption capacities and intermediates’ properties such as polar surface area and octanol-water partition coefficient.

  12. Comparison in decoloration efficiency among radiation, ultraviolet ray and Fenton oxidation treatment for aqueous solution of dyes

    International Nuclear Information System (INIS)

    Shimokawa, Toshishige; Sawai, Takeshi

    1984-01-01

    To establish the methods of oxidation and decomposition treatment for dyeing waste water, the processes by radiation, ultraviolet ray and Fenton oxidation were examined comparatively for the decoloration efficiency. The dyes tested were commercially available reactive dyes, RBO-3R, DBR-BB, MBY-6GS and RBB-R. In the radiation process, the dye solution was irradiated with gamma ray of cobalt-60 while blowing air through it. Radiation process and Fenton oxidation were excellent for decoloration. Ultraviolet ray was low in the treatment efficiency, so it is not practical. In the radiation process, the addition of a reagent and the adjustment of pH are not required unlike the case of the Fenton oxidation process. Its continuous operation is also possible, so it is a highly practical means. (Mori, K.)

  13. Electro-Fenton, UVA photoelectro-Fenton and solar photoelectro-Fenton degradation of the drug ibuprofen in acid aqueous medium using platinum and boron-doped diamond anodes

    Energy Technology Data Exchange (ETDEWEB)

    Skoumal, Marcel; Rodriguez, Rosa Maria; Cabot, Pere Lluis; Centellas, Francesc; Garrido, Jose Antonio; Arias, Conchita [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Brillas, Enric [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)], E-mail: brillas@ub.edu

    2009-02-28

    The degradation of a 41 mg dm{sup -3} ibuprofen (2-(4-isobutylphenyl)propionic acid) solution of pH 3.0 has been comparatively studied by electrochemical advanced oxidation processes (EAOPs) like electro-Fenton, UVA photoelectro-Fenton and solar photoelectro-Fenton at constant current density. Experiments were performed in a one-compartment cell with a Pt or boron-doped diamond (BDD) anode and an O{sub 2}-diffusion cathode. Heterogeneous hydroxyl radical ({center_dot}OH) is generated at the anode surface from water oxidation, while homogeneous {center_dot}OH is formed from Fenton's reaction between Fe{sup 2+} and H{sub 2}O{sub 2} generated at the cathode, being its production strongly enhanced from photo-Fenton reaction induced by sunlight. Higher mineralization is attained in all methods using BDD instead Pt, because the former produces greater quantity of {center_dot}OH enhancing the oxidation of pollutants. The mineralization rate increases under UVA and solar irradiation by the rapid photodecomposition of complexes of Fe(III) with acidic intermediates. The most potent method is solar photoelectro-Fenton with BDD giving 92% mineralization due to the formation of a small proportion of highly persistent final by-products. The effect of Fe{sup 2+} content, pH and current density on photoelectro-Fenton degradation has been studied. The ibuprofen decay always follows a pseudo-first-order kinetics and its destruction rate is limited by current density and UV intensity. Aromatics such as 1-(1-hydroxyethyl)-4-isobutylbenzene, 4-isobutylacetophenone, 4-isobutylphenol and 4-ethylbenzaldehyde, and carboxylic acids such as pyruvic, acetic, formic and oxalic have been identified as oxidation by-products. Oxalic acid is the ultimate by-product and the fast photodecarboxylation of its complexes with Fe(III) under UVA or solar irradiation explains the higher oxidation power of photoelectro-Fenton methods in comparison to electro-Fenton procedures.

  14. Heterogeneous Fenton-like discoloration of methyl orange using Fe3O4/MWCNTs as catalyst: kinetics and Fenton-like mechanism

    Science.gov (United States)

    Xu, Huan-Yan; Wang, Yuan; Shi, Tian-Nuo; Zhao, Hang; Tan, Qu; Zhao, Bo-Chao; He, Xiu-Lan; Qi, Shu-Yan

    2018-03-01

    The kinetics and Fenton-like mechanism are two challenging tasks for heterogeneous Fenton-like catalytic oxidation of organic pollutants. In this study, three kinetic models were used for the kinetic studies of Fe3O4/MWCNTs-H2O2 Fenton-like reaction for MO degradation. The results indicated that this reaction followed the first-order kinetic model. The relationship of reaction rate constant and temperature followed the Arrhenius equation. The activation energy and frequency factor of this system were calculated as 8.2 kJ·mol-1 and 2.72 s-1, respectively. The quantifications of Fe ions dissolution and •OH radicals generation confirmed that the homogeneous and heterogeneous catalyses were involved in Fe3O4/MWCNTs-H2O2 Fenton-like reaction. The reaction rate constant was closely related with Fe ions dissolution and •OH radicals generation. Fe3O4/MWCNTs nanocomposites had typical ferromagnetic property and could be easily separated from solution by an external magnet after being used. Furthermore, Fe3O4/MWCNTs nanocomposites exhibited good stability and recyclability. Finally, the Fenton-like mechanisms on homogeneous and heterogeneous catalyses were described.

  15. Degradation of malachite green in aqueous solution by Fenton process.

    Science.gov (United States)

    Hameed, B H; Lee, T W

    2009-05-30

    In this study, advanced oxidation process utilizing Fenton's reagent was investigated for degradation of malachite green (MG). The effects of different reaction parameters such as the initial MG concentration, initial pH, the initial hydrogen peroxide concentration, the initial ferrous concentration and the reaction temperature on the oxidative degradation of MG have been investigated. The optimal reacting conditions were experimentally found to be pH 3.40, initial hydrogen peroxide concentration=0.50mM and initial ferrous concentration=0.10mM for initial MG concentration of 20mg/L at 30 degrees C. Under optimal conditions, 99.25% degradation efficiency of dye in aqueous solution was achieved after 60 min of reaction.

  16. Pretreatment of lignocellulosic biomass using Fenton chemistry

    Science.gov (United States)

    Pretreatment is a necessary step in “biomass to biofuel conversion” due to the recalcitrant nature of lignocellulosic biomass. White-rot fungi utilize peroxidases and hydrogen peroxide (in vivo Fenton chemistry) to degrade lignin. In an attempt to mimic this process, solution phase Fenton chemistry ...

  17. Advanced oxidation of biorefractory organics in aqueous solution together with bioelectricity generation by microbial fuel cells with composite FO/GPEs

    Science.gov (United States)

    Fu, Bao-rong; Shen, Chao; Ren, Jing; Chen, Jia-yi; Zhao, Lin

    2018-03-01

    In this study, ferric oxide loading graphite particle electrodes (FO/GPEs) were prepared as cathode of a three-dimensional electrode MFC-Fenton system. The properties of the composite cathode were examined with higher surface area and more mesopores. FO/GPEs could work as both cathode and Fenton iron reagents, contributing to high oxidation activity and better performance of electricity generation. The application of FO/GPEs MFC-Fenton system on degrading p-nitrophenol presented high catalytic efficiency in a wide range of pH value. The removal of p-nitrophenol and TOC attained to about 85 % within 8 and 64 h at neutral pH, respectively. A neutral FO/GPEs MFC-Fenton oxidation mechanism was also proposed. Specifically, both the surface iron sites and dissolved iron ions catalyzed the decomposition of H2O2. As results, the generated hydroxyl radicals were used for p-nitrophenol degradation and the iron oxide was recycled.

  18. Electrochemical treatment of Acid Red 1 by electro-Fenton and photoelectro-Fenton processes

    Directory of Open Access Journals (Sweden)

    Camilo González-Vargas

    2014-12-01

    Full Text Available Small volumes (100 mL of acidic aqueous solutions with 30-200 mg L-1 TOC of the toxic azo dye Acid Red 1 (AR1 have been comparatively treated by various electrochemical advanced oxidation processes (EAOPs. The electrolytic system consisted of a BDD anode able to produce ·OH and an air-diffusion cathode that generated H2O2, which subsequently reacted with added Fe2+ to yield additional ·OH from Fenton’s reaction. Under optimized conditions (i.e., 1.0 mM Fe2+, 60 mA cm-2, pH 3.0, 35 ºC, the analysis of the initial rates for decolourization and AR1 decay assuming a pseudo-first-order kinetics revealed a much higher rate constant for photoelectro-Fenton (PEF, ~ 2.7x10-3 s-1 compared to electro-Fenton (EF, ~ 0.6x10-3 s-1. Mineralization after 180 min was also greater in the former treatment (90 % vs 63 %. The use of UV radiation in PEF contributed to Fe(III photoreduction as well as to photodecarboxylation of refractory intermediates, yielding a mineralization current efficiency as high as 85% during the treatment of solutions of 200 mg L-1 TOC. Primary reaction intermediates included three aromatic derivatives with the initial naphthalenic structure and four molecules only featuring benzenic rings, which were totally mineralized in PEF. 

  19. Design of a neutral three-dimensional electro-Fenton system with foam nickel as particle electrodes for wastewater treatment

    International Nuclear Information System (INIS)

    Liu, Wei; Ai, Zhihui; Zhang, Lizhi

    2012-01-01

    Highlights: ► Remove RhB by a novel 3D-E-Fenton system using foam nickel as particle electrodes. ► The 3D-E-Fenton system exhibit much higher RhB removal efficiency than the counterpart 3D-E and E-Fenton system. ► Foam nickel as a particle electrode displays good oxygen reduction activity. ► The performance of RhB removal was optimized by some operating parameters and the optimization pH was the neutral. - Abstract: In this work, we demonstrate a novel three-dimensional electro-Fenton system (3D-E-Fenton) for wastewater treatment with foam nickel, activated carbon fiber and Ti/RuO 2 –IrO 2 as the particle electrodes, the cathode, and the anode respectively. This 3D-E-Fenton system could exhibit much higher rhodamine B removal efficiency (99%) than the counterpart three-dimensional electrochemical system (33%) and E-Fenton system (19%) at neutral pH in 30 min. The degradation efficiency enhancement was attributed to much more hydroxyl radicals generated in the 3D-E-Fenton system because foam nickel particle electrodes could activate molecular oxygen to produce ·O 2 − via a single-electron transfer pathway to subsequently generate more H 2 O 2 and hydroxyl radicals. This is the first observation of molecular oxygen activation over the particle electrodes in the three-dimensional electrochemical system. These interesting findings could provide some new insight on the development of high efficient E-Fenton system for wastewater treatment at neutral pH.

  20. Changes of turbidity during the phenol oxidation by photo-Fenton treatment.

    Science.gov (United States)

    Villota, Natalia; Camarero, Luis M; Lomas, Jose M; Perez, Jonatan

    2014-11-01

    Turbidity presented by phenol solutions oxidized with Fenton reagent shows the tendency of a first order intermediate kinetics. Thus, turbidity can be considered a representative parameter of the presence of intermediate oxidation species, which are generated along the decomposition of toxic and reluctant contaminants, such as phenol. Moreover, that parameter presents a linear dependence with the catalyst dosage, but is also determined by the initial contaminant load. When analyzing the oxidation mechanism of phenol, it is found that the maximum turbidity occurs when the treatment is carried out at oxidant to phenol molar ratios R = 4.0. These oxidation conditions correspond to the presence of a reaction mixture mainly composed of dihydroxylated rings, precursors of the muconic acid formation. The oxidation via "para" comprises the formation reactions of charge transfer complexes (quinhydrone), between the para-dihydroxylated intermediates (hydroquinone) and the para-substituted quinones (p-benzoquinone), which are quite unstable and reactive species, quickly decomposed into hydroxyhydroquinones. Working with oxidant ratios up to R = 6.0, the maximum observed value of turbidity in the oxidized solutions is kept almost constant. It is found that, in these conditions, the pyrogallol formation is maximal, what is generated through the degradation of ortho-species (catechol and ortho-benzoquinone) and meta-substituted (resorcinol). Operating with ratios over R = 6.0, these intermediates are decomposed into biodegradable acids, generating lower turbidity in the solution. Then, the residual turbidity is a function of the molar ratio of the ferrous ions vs. moles of oxidant utilized in the essays, that lets to estimate the stoichiometric dosage of catalyst as 20 mg/L at pH = 3.0, whereas operating in stoichiometric conditions, R = 14.0, the residual turbidity of water results almost null.

  1. Degradação de poluentes emergentes por processos Fenton e foto-Fenton

    Directory of Open Access Journals (Sweden)

    Marco A. Benedetti Durigan

    2012-01-01

    Full Text Available A continuous photochemical treatment system was developed for aiming the treatment of aqueous solutions containing relevant micro-pollutants (microcystin-LR, sulfamethoxazole and 17-b estradiol. The continuous photo-Fenton process provided high degradation efficiency. However, contact time between samples and the irradiated region is short relative to total treatment time, indicating that observed changes are predominantly due to the Fenton process. Higher degradation efficiency was observed in systems operated using two treatment cycles, the first involving a batch Fenton process and the second a continuous photo-Fenton treatment.

  2. The Potential of Fe-exchanged Y Zeolite as a Heterogeneous Fenton-type Catalyst for Oxidative Degradation of Reactive Dye in Water

    OpenAIRE

    Aleksić, M.; Koprivanac, N.; Lončarić Božić, A.; Kušić, H.

    2010-01-01

    The study aimed to investigate the potential of Fe-exchanged zeolites of Y-type as a catalyst in heterogeneous Fenton-type processes for the degradation of model organic pollutant, reactive azo dye C.I. Reactive Blue 137, in water. The research work was directed to investigate the influence of process variables, such as FeY catalyst dosage, Fenton reagent ratio, and initial operating pH on the efficiency of the treatment process. The performance of the studied heterogeneous process was compar...

  3. Diagnostic reagent system

    International Nuclear Information System (INIS)

    1976-01-01

    A solid phase reagent for use in radioimmunoassay of antigens and antibodies is described. The reagent is prepared by mixing specific antibody or radiolabeled antigen with polyethylene glycol (4000-6000) and gamma globulin in a buffer at pH 4-10 and lyophilizing, the antigens being thyroxine, triiodothyronine, digoxin and digitoxin (1-1000 μCi 125 I/μg). The buffer consists of a 0.08 molar sodium barbital solution containing 0.1% of ox-serum albumin and 0.35% of 8-anilino-1-naftalene sulfonic acid

  4. PERBANDINGAN EFEKTIFITAS DISINFEKTAN KAPORIT, HIDROGEN PEROKSIDA, DAN PEREAKSI FENTON (H2O2/Fe2+

    Directory of Open Access Journals (Sweden)

    Didik Setiawan

    2013-11-01

    Fenton reagent as disinfectants compared to chlorine. The most effective disinfectant is that having the highest phenol coefficient, and resulting good water quality with pH of 6.5-8.5, high dissolved oxygen (DO, and temperature close to ambient, and cheap. The three materials were tested on Salmonella typhosa and Staphyllococcus aureus and their minimum concentrations that kill the bacteria were compared to that of phenol to determine the phenol coefficients. The results show the phenol coefficients of chlorine, hydrogen peroxide, and Fenton are 4, 6, and 6 respectively. The pH of the water treated by the three disinfectants 10.07-9.2, 9.03-7.33, and 5.97-4.57 respectively. The disinfected waters have DO of 6.63-8.07 mgL-1, 6.93-9.40 mgL-1, and 7.40-8.57 mgL-1 respectively. The temperatures of the water are 28.5-28.3, 28.5-28.03, and 28.47-8.07 oC respectively. Chlorine is the cheapest in price, however, its residue may lead to the formation of the carcinogenic halomethanes in the drinking water, and its phenol coefficient is lower than both hydrogen peroxide and Fenton reagents. The last two disinfectants have the highest phenol coefficient, however, hydrogen peroxide is saver because it does not produce harmful chemicals whereas Fenton reagent results in the formation of residual Iron(III in the water that needs to be treated further.

  5. Effect of seven Indian plant extracts on Fenton reaction-mediated damage to DNA constituents.

    Science.gov (United States)

    Kar, Indrani; Chattopadhyaya, Rajagopal

    2017-11-01

    The influences of substoichiometric amounts of seven plant extracts in the Fenton reaction-mediated damage to deoxynucleosides, deoxynucleoside monophosphates, deoxynucleoside triphosphates, and supercoiled plasmid DNA were studied to rationalize anticancer properties reported in some of these extracts. Extracts from Acacia catechu, Emblica officinalis, Spondias dulcis, Terminalia belerica, Terminalia chebula, as well as gallic acid, epicatechin, chebulagic acid and chebulinic acid enhance the extent of damage in Fenton reactions with all monomeric substrates but protect supercoiled plasmid DNA, compared to standard Fenton reactions. The damage to pyrimidine nucleosides/nucleotides is enhanced by these extracts and compounds to a greater extent than for purine ones in a concentration dependent manner. Dolichos biflorus and Hemidesmus indicus extracts generally do not show this enhancement for the monomeric substrates though they protect plasmid DNA. Compared to standard Fenton reactions for deoxynucleosides with ethanol, the presence of these five plant extracts render ethanol scavenging less effective as the radical is generated in the vicinity of the target. Since substoichiometric amounts of these extracts and the four compounds produce this effect, a catalytic mechanism involving the presence of a ternary complex of the nucleoside/nucleotide substrate, a plant compound and the hydroxyl radical is proposed. Such a mechanism cannot operate for plasmid DNA as the planar rings in the extract compounds cannot stack with the duplex DNA bases. These plant extracts, by enhancing Fenton reaction-mediated damage to deoxynucleoside triphosphates, slow down DNA replication in rapidly dividing cancer cells, thus contributing to their anticancer properties.

  6. Exquisite Enzyme-Fenton Biomimetic Catalysts for Hydroxyl Radical Production by Mimicking an Enzyme Cascade.

    Science.gov (United States)

    Zhang, Qi; Chen, Shuo; Wang, Hua; Yu, Hongtao

    2018-03-14

    Hydrogen peroxide (H 2 O 2 ) is a key reactant in the Fenton process. As a byproduct of enzymatic reaction, H 2 O 2 can be obtained via catalytical oxidation of glucose using glucose oxidase in the presence of O 2 . Another oxidation product (gluconic acid) can suitably adjust the microenvironmental pH contributing to the Fe 3+ /Fe 2+ cycle in the Fenton reaction. Enzymes are extremely efficient at catalyzing a variety of reactions with high catalytic activity, substrate specificity, and yields in living organisms. Inspired by the multiple functions of natural multienzyme systems, an exquisite nanozyme-modified α-FeOOH/porous carbon (PC) biomimetic catalyst constructed by in situ growth of glucose oxidase-mimicking Au nanoparticles and crystallization of adsorbed ferric ions within carboxyl into hierarchically PC is developed as an efficient enzyme-Fenton catalyst. The products (H 2 O 2 , ∼4.07 mmol·L -1 ) of the first enzymatic reaction are immediately used as substrates for the second Fenton-like reaction to generate the valuable • OH (∼96.84 μmol·L -1 ), thus mimicking an enzyme cascade pathway. α-FeOOH nanocrystals, attached by C-O-Fe bondings, are encapsulated into the mesoporous PC frameworks, facilitating the electron transfer between α-FeOOH and the PC support and greatly suppressing iron leaching. This study paves a new avenue for designing biomimetic enzyme-based Fenton catalysts mimicking a natural system for • OH production.

  7. Advanced oxidation of Reactive Blue 181 solution: a comparison between Fenton and Sono-Fenton process.

    Science.gov (United States)

    Basturk, Emine; Karatas, Mustafa

    2014-09-01

    In this work, the decolorization of C.I. Reactive Blue 181 (RB181), an anthraquinone dye, by Ultrasound and Fe(2+) H2O2 processes was investigated. The effects of operating parameters, such as Fe(2+) dosage, H2O2 dosage, pH value, reaction time and temperature were examined. Process optimisation [pH, ferrous ion (Fe(2+)), hydrogen peroxide (H2O2), and reaction time], kinetic studies and their comparison were carried out for both of the processes. The Sono-Fenton process was performed by indirect sonication in an ultrasonic water bath, which was operated at a fixed 35-kHz frequency. The optimum conditions were determined as [Fe(2+)]=30 mg/L, [H2O2]=50 mg/L and pH=3 for the Fenton process and [Fe(2+)]=10 mg/L, [H2O2]=40 mg/L and pH=3 for the Sono-Fenton process. The colour removals were 88% and 93.5% by the Fenton and Sono-Fenton processes, respectively. The highest decolorization was achieved by the Sono-Fenton process because of the production of some oxidising agents as a result of sonication. The paper also discussed kinetic parameters. The decolorization kinetic of RB181 followed pseudo-second-order reaction (Fenton study) and Behnajady kinetics (Sono-Fenton study). Copyright © 2014 Elsevier B.V. All rights reserved.

  8. Chemically modified graphite felt as an efficient cathode in electro-Fenton for p-nitrophenol degradation

    International Nuclear Information System (INIS)

    Zhou, Lei; Zhou, Minghua; Hu, Zhongxin; Bi, Zhaoheng; Serrano, K. Groenen

    2014-01-01

    Highlights: • Chemically modified graphite felt was prepared using ethanol and hydrazine hydrate as reagents. • Carbon nanoparticles with functional groups were deposited on the surface after modification. • The electrochemical activity for ORR and H 2 O 2 generation on the modified electrode was improved. • The cathode modification effictively improved the EF performance for pollutant degradation. - Abstract: A simple method with low-cost chemical reagents ethanol and hydrazine hydrate was used to modify graphite felt as the cathode for electro-Fenton (EF) application, using p-nitrophenol (p-Np) as the model pollutant. Characterized by scanning electron microscope, contact angle, Raman spectrum and X-ray photoelectron spectroscopy, the morphology and surface physicochemical properties after modification were observed considerably changed. After modification, some nanoparticles and oxygen and nitrogen-containing functional groups appeared on the cathode surface, which greatly improved the surface hydrophilic property and the electrocatalytic activity for oxygen reduction reaction. The effects led to the hydrogen peroxide accumulation on the modified cathode markedly increased to 175.8 mg L −1 , while that on the unmodified one was only 67.5 mg L −1 . p-Np of initial 50 mg L −1 could be completely removed by EF using the modified cathode, and the mineralization ratio reached 51.4%, more than 2 times of the pristine one. After 10 cycles, the mineralization ratio of the modified cathode was still above 45%, suggesting that the modification method can provide an effective approach to improve EF performance, and thus benefits to promote its environmental applications

  9. Oxidative degradation of lignin by photochemical and chemical radical generating systems

    International Nuclear Information System (INIS)

    Gold, M.H.; Kutsuki, H.; Morgan, M.A.

    1983-01-01

    Oxidation of specifically radiolabeled 14 C-lignins by UV/H 2 O 2 , Fenton's reagent, photosensitizing riboflavin, UV- and γ-irradiation was examined. In the presence of UV/H 2 O 2 , a hydroxyl radical (radicalOH) generating system, 14 C-methoxy, 2-[ 14 C-sidechain] and 14 C-ring labeled lignin were rapidly and extensively degraded as measured by gel filtration of the reaction products on Sephadex LH-20. This suggested that exposure to radicalOH leads to rapid, nonspecific lignin degradation. Rapid degradation of 14 C-methoxy, 2-[ 14 C-sidechain] and 14 C-ring labeled lignin also occurred in the presence of the radicalOH generating system, Fenton's reagent, confirming the primary role of radicalOH in these reactions. Photosensitizing riboflavin, also capable of effecting transformation of organic compounds via Type I hydrogen radical abstractions, caused extensive oxidative degradation of 14 C-methoxy labeled lignin and significant degradation of 2-[ 14 C-sidechain] and 14 C-ring labeled lignin. In addition, UV- and γ-irradiation caused slower but extensive degradation of the polymers, probably via radical type mechanisms. All of these results indicate that radicalOH as well as organic radical generating systems are effective agents for the purpose of degrading this heterogeneous, optically inactive and random biopolymer. (author)

  10. Citric acid-modified Fenton's reaction for the oxidation of chlorinated ethylenes in soil solution systems.

    Science.gov (United States)

    Seol, Yongkoo; Javandel, Iraj

    2008-06-01

    Fenton's reagent, a solution of hydrogen peroxide and ferrous iron catalyst, is used for an in situ chemical oxidation of organic contaminants. Sulfuric acid is commonly used to create an acidic condition needed for catalytic oxidation. Fenton's reaction often involves pressure buildup and precipitation of reaction products, which can cause safety hazards and diminish efficiency. We selected citric acid, a food-grade substance, as an acidifying agent to evaluate its efficiencies for organic contaminant removal in Fenton's reaction, and examined the impacts of using citric acid on the unwanted reaction products. A series of batch and column experiments were performed with varying H2O2 concentrations to decompose selected chlorinated ethylenes. Either dissolved iron from soil or iron sulfate salt was added to provide the iron catalyst in the batch tests. Batch experiments revealed that both citric and sulfuric acid systems achieved over 90% contaminant removal rates, and the presence of iron catalyst was essential for effective decontamination. Batch tests with citric acid showed no signs of pressure accumulation and solid precipitations, however the results suggested that an excessive usage of H2O2 relative to iron catalysts (Fe2+/H2O2<1/330) would result in lowering the efficiency of contaminant removal by iron chelation in the citric acid system. Column tests confirmed that citric acid could provide suitable acidic conditions to achieve higher than 55% contaminant removal rates.

  11. Study of the degradation performance (TOC, BOD, and toxicity) of bisphenol A by the photo-Fenton process.

    Science.gov (United States)

    Pérez-Moya, M; Kaisto, T; Navarro, M; Del Valle, L J

    2017-03-01

    Degradation of bisphenol A (BPA, 0.5 L, 30 mg L -1 ) was studied by photo-Fenton treatment, while Fenton reagents were variables. The efficiency of the degradation process was evaluated by the reduction of total organic carbon (TOC), the biochemical oxygen demand (BOD), and toxicity. For toxicity analysis, bacterial methods were found infeasible, but the in vitro assay of VERO cells culture was successfully applied. Experiments according to a 2 2 design of experiments (DOE) with star points and three center points for statistical validity allowed selecting those process conditions (Fe(II) and H 2 O 2 load) that maximized the process performance. Photo-Fenton process effectively eliminated BPA and partly degraded its by-products (residual TOC TOC = 92 %) was attained. Toxicity was also detected to 50 % of cellular mortality even at long reaction times. However, 40.25 mg L -1 of H 2 O 2 decreased residual TOC to 70 % while cell mortality decreased down to 25 %. With more H 2 O 2 , the residual TOC decreased down to 15 % but cell mortality remained within the 20-25 % level. Photo-Fenton increased the biodegradability and reduced the toxicity of the studied sample.

  12. Application of solar photo-Fenton toward toxicity removal and textile wastewater reuse.

    Science.gov (United States)

    Starling, Maria Clara V M; Dos Santos, Paulo Henrique Rodrigues; de Souza, Felipe Antônio Ribeiro; Oliveira, Sílvia Corrêa; Leão, Mônica M D; Amorim, Camila C

    2017-05-01

    Solar photo-Fenton represents an innovative and low-cost option for the treatment of recalcitrant industrial wastewater, such as the textile wastewater. Textile wastewater usually shows high acute toxic and variability and may be composed of many different chemical compounds. This study aimed at optimizing and validating solar photo-Fenton treatment of textile wastewater in a semi-pilot compound parabolic collector (CPC) for toxicity removal and wastewater reclamation. In addition, treated wastewater reuse feasibility was investigated through pilot tests. Experimental design performed in this study indicated optimum condition for solar photo-Fenton reaction (20 mg L -1 of Fe 2+ and 500 mg L -1 of H 2 O 2 ; pH 2.8), which achieved 96 % removal of dissolved organic carbon (DOC) and 99 % absorbance removal. A toxicity peak was detected during treatment, suggesting that highly toxic transformation products were formed during reaction. Toxic intermediates were properly removed during solar photo-Fenton (SPF) treatment along with the generation of oxalic acid as an ultimate product of degradation and COS increase. Different samples of real textile wastewater were treated in order to validate optimized treatment condition with regard to wastewater variability. Results showed median organic carbon removal near 90 %. Finally, reuse of treated textile wastewater in both dyeing and washing stages of production was successful. These results confirm that solar photo-Fenton, as a single treatment, enables wastewater reclamation in the textile industry. Graphical abstract Solar photo-Fenton as a revolutionary treatment technology for "closing-the-loop" in the textile industry.

  13. Efficient and Stable Carbon-coated Nickel Foam Cathodes for the Electro-Fenton Process

    International Nuclear Information System (INIS)

    Song, Shuqin; Wu, Mingmei; Liu, Yuhui; Zhu, Qiping; Tsiakaras, Panagiotis; Wang, Yi

    2015-01-01

    Highlights: • Carbon-coated nickel foam (C@NF) was prepared by cycle coating carbon process. • Ni leaching can be effectively controlled at C@NF4 (4 cycle coating times) cathode. • C@NF4 exhibits excellent electro-Fenton performance with desirable stability. • C@NF4 exhibits low energy consumption for DMP degradation. - Abstract: Carbon-coated nickel foam (C@NF) electrodes are prepared via a simple and effective method, hydrothermal-carbonization cycle coating process, characterized by scanning electron microscopy (SEM) with energy dispersive spectrometer (EDS) and employed as the electro-Fenton (E-Fenton) cathode for degrading dimethyl phthalate (DMP) in aqueous solution. For the sake of comparison, nickel foam (NF) electrode and the conventional E-Fenton cathode (graphite gas diffusion electrode (GDE)) are also tested and compared. Experimental results indicate that nickel leaching can be effectively controlled at C@NF4 cathode (4 times cycle coating process), having great significance for promoting the application of NF in E-Fenton system. Moreover, C@NF4 cathode still presents excellent and effective performance on DMP degradation. DMP can be completely degraded within 2 h at −0.5 V and the total organic carbon (TOC) removal reaches as high as 82.1 %, which is almost 3 times as high as that at graphite GDE. Futhermore, the current efficiency for H 2 O 2 generation at C@NF4 is enhanced by 12 times compared to that at NF, and consequently the energy consumption during DMP degradation at C@NF4 is obvious lower than that at both NF cathode and graphite GDE. From the obtained results it can be deduced that C@NF4 is promising to be an attractive alternative E-Fenton cathode for removing organic pollutants in wastewater

  14. Enhanced degradation of paracetamol by UV-C supported photo-Fenton process over Fenton oxidation.

    Science.gov (United States)

    Manu, B; Mahamood, S

    2011-01-01

    For the treatment of paracetamol in water, the UV-C Fenton oxidation process and classic Fenton oxidation have been found to be the most effective. Paracetamol reduction and chemical oxygen demand (COD) removal are measured as the objective functions to be maximized. The experimental conditions of the degradation of paracetamol are optimized by the Fenton process. Influent pH 3, initial H(2)O(2) dosage 60 mg/L, [H(2)O(2)]/[Fe(2+)] ratio 60 : 1 are the optimum conditions observed for 20 mg/L initial paracetamol concentration. At the optimum conditions, for 20 mg/L of initial paracetamol concentration, 82% paracetamol reduction and 68% COD removal by Fenton oxidation, and 91% paracetamol reduction and 82% COD removal by UV-C Fenton process are observed in a 120 min reaction time. By HPLC analysis, 100% removal of paracetamol is observed at the above optimum conditions for the Fenton process in 240 min and for the UV-C photo-Fenton process in 120 min. The methods are effective and they may be used in the paracetamol industry.

  15. Degradation of Procion Red H-E7B reactive dye by coupling a photo-Fenton system with a sequencing batch reactor

    International Nuclear Information System (INIS)

    Garcia-Montano, Julia; Torrades, Francesc; Garcia-Hortal, Jose A.; Domenech, Xavier; Peral, Jose

    2006-01-01

    A bench-scale study combining photo-Fenton reaction with an aerobic sequencing batch reactor (SBR) to degrade a commercial homo-bireactive dye (Procion Red H-E7B, 250 mg l -1 ) was investigated. The photo-Fenton process was applied as a pre-treatment, avoiding complete mineralisation, just to obtain a bio-compatible water able to be treated by means of the SBR in a second step. In this sense, different Fenton reagent concentrations were assessed by following dye solution biodegradability enhancement (BOD 5 /COD), as well as the toxicity (EC 50 ), DOC, colour (Abs 543.5 ) and H 2 O 2 evolution with photo-Fenton irradiation time. Obtained pre-treated solutions were biologically oxidized in a SBR containing non-acclimated activated sludge. Different hydraulic retention time (HRT) in the bioreactor were tested to attain the maximum organic load removal efficiency. Best results were obtained with 60 min of 10 mg l -1 Fe(II) and 125 mg l -1 H 2 O 2 photo-Fenton pre-treatment and 1 day HRT in SBR

  16. Degradation of Procion Red H-E7B reactive dye by coupling a photo-Fenton system with a sequencing batch reactor

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Montano, Julia [Departament de Quimica, Edifici Cn, Universitat Autonoma de Barcelona, E-08193 Bellaterra, Barcelona (Spain); Torrades, Francesc [Departament d' Enginyeria Quimica, ETSEI de Terrassa (UPC), C/Colom, 11, E-08222 Terrassa, Barcelona (Spain); Garcia-Hortal, Jose A. [Departament d' Enginyeria Textil i Paperera, ETSEI de Terrassa (UPC), C/Colom, 11, E-08222 Terrassa, Barcelona (Spain); Domenech, Xavier [Departament de Quimica, Edifici Cn, Universitat Autonoma de Barcelona, E-08193 Bellaterra, Barcelona (Spain); Peral, Jose [Departament de Quimica, Edifici Cn, Universitat Autonoma de Barcelona, E-08193 Bellaterra, Barcelona (Spain)]. E-mail: jose.peral@uab.es

    2006-06-30

    A bench-scale study combining photo-Fenton reaction with an aerobic sequencing batch reactor (SBR) to degrade a commercial homo-bireactive dye (Procion Red H-E7B, 250 mg l{sup -1}) was investigated. The photo-Fenton process was applied as a pre-treatment, avoiding complete mineralisation, just to obtain a bio-compatible water able to be treated by means of the SBR in a second step. In this sense, different Fenton reagent concentrations were assessed by following dye solution biodegradability enhancement (BOD{sub 5}/COD), as well as the toxicity (EC{sub 50}), DOC, colour (Abs{sub 543.5}) and H{sub 2}O{sub 2} evolution with photo-Fenton irradiation time. Obtained pre-treated solutions were biologically oxidized in a SBR containing non-acclimated activated sludge. Different hydraulic retention time (HRT) in the bioreactor were tested to attain the maximum organic load removal efficiency. Best results were obtained with 60 min of 10 mg l{sup -1} Fe(II) and 125 mg l{sup -1} H{sub 2}O{sub 2} photo-Fenton pre-treatment and 1 day HRT in SBR.

  17. Development of a trickle bed reactor of electro-Fenton process for wastewater treatment.

    Science.gov (United States)

    Lei, Yangming; Liu, Hong; Shen, Zhemin; Wang, Wenhua

    2013-10-15

    To avoid electrolyte leakage and gas bubbles in the electro-Fenton (E-Fenton) reactors using a gas diffusion cathode, we developed a trickle bed cathode by coating a layer composed of carbon black and polytetrafluoroethylene (C-PTFE) onto graphite chips instead of carbon cloth. The trickle bed cathode was optimized by single-factor and orthogonal experiments, in which carbon black, PTFE, and a surfactant were considered as the determinant of the performance of graphite chips. In the reactor assembled by the trickle bed cathode, H2O2 was generated with a current of 0.3A and a current efficiency of 60%. This performance was attributed to the fine distribution of electrolyte and air, as well as the effective oxygen transfer from the gas phase to the electrolyte-cathode interface. In terms of H2O2 generation and current efficiency, the developed trickle bed reactor had a performance comparable to that of the conventional E-Fenton reactor using a gas diffusion cathode. Further, 123 mg L(-1) of reactive brilliant red X-3B in aqueous solution was decomposed in the optimized trickle bed reactor as E-Fenton reactor. The decolorization ratio reached 97% within 20 min, and the mineralization reached 87% within 3h. Copyright © 2013 Elsevier B.V. All rights reserved.

  18. Acetaminophen degradation by electro-Fenton and photoelectro-Fenton using a double cathode electrochemical cell

    Energy Technology Data Exchange (ETDEWEB)

    Luna, Mark Daniel G. de [Department of Chemical Engineering, University of the Philippines, 1011 Diliman, Quezon City (Philippines); Environmental Engineering Graduate Program, University of the Philippines, 1011 Diliman, Quezon City (Philippines); Veciana, Mersabel L. [Environmental Engineering Graduate Program, University of the Philippines, 1011 Diliman, Quezon City (Philippines); Su, Chia-Chi [Department of Environmental Resources Management, Chia Nan University of Pharmacy and Science, Tainan 717, Taiwan (China); Lu, Ming-Chun, E-mail: mmclu@mail.chan.edu.tw [Department of Environmental Resources Management, Chia Nan University of Pharmacy and Science, Tainan 717, Taiwan (China)

    2012-05-30

    Highlights: Black-Right-Pointing-Pointer The electro-Fenton reactor using a double cathode electrochemical cell was applied. Black-Right-Pointing-Pointer The initial Fe{sup 2+} concentration was the most significant parameter for the acetaminophen degradation. Black-Right-Pointing-Pointer Thirteen intermediates were identified and a degradation pathway was proposed. - Abstract: Acetaminophen is a widely used drug worldwide and is one of the most frequently detected in bodies of water making it a high priority trace pollutant. This study investigated the applicability of the electro-Fenton and photoelectro-Fenton processes using a double cathode electrochemical cell in the treatment of acetaminophen containing wastewater. The Box-Behnken design was used to determine the effects of initial Fe{sup 2+} and H{sub 2}O{sub 2} concentrations and applied current density. Results showed that all parameters positively affected the degradation efficiency of acetaminophen with the initial Fe{sup 2+} concentration being the most significant parameter for both processes. The acetaminophen removal efficiency for electro-Fenton was 98% and chemical oxygen demand (COD) removal of 43% while a 97% acetaminophen removal and 42% COD removal were observed for the photoelectro-Fenton method operated at optimum conditions. The electro-Fenton process was only able to obtain 19% total organic carbon (TOC) removal while the photoelectro-Fenton process obtained 20%. Due to negligible difference between the treatment efficiencies of the two processes, the electro-Fenton method was proven to be more economically advantageous. The models obtained from the study were applicable to a wide range of acetaminophen concentrations and can be used in scale-ups. Thirteen different types of intermediates were identified and a degradation pathway was proposed.

  19. Acetaminophen degradation by electro-Fenton and photoelectro-Fenton using a double cathode electrochemical cell

    International Nuclear Information System (INIS)

    Luna, Mark Daniel G. de; Veciana, Mersabel L.; Su, Chia-Chi; Lu, Ming-Chun

    2012-01-01

    Highlights: ► The electro-Fenton reactor using a double cathode electrochemical cell was applied. ► The initial Fe 2+ concentration was the most significant parameter for the acetaminophen degradation. ► Thirteen intermediates were identified and a degradation pathway was proposed. - Abstract: Acetaminophen is a widely used drug worldwide and is one of the most frequently detected in bodies of water making it a high priority trace pollutant. This study investigated the applicability of the electro-Fenton and photoelectro-Fenton processes using a double cathode electrochemical cell in the treatment of acetaminophen containing wastewater. The Box–Behnken design was used to determine the effects of initial Fe 2+ and H 2 O 2 concentrations and applied current density. Results showed that all parameters positively affected the degradation efficiency of acetaminophen with the initial Fe 2+ concentration being the most significant parameter for both processes. The acetaminophen removal efficiency for electro-Fenton was 98% and chemical oxygen demand (COD) removal of 43% while a 97% acetaminophen removal and 42% COD removal were observed for the photoelectro-Fenton method operated at optimum conditions. The electro-Fenton process was only able to obtain 19% total organic carbon (TOC) removal while the photoelectro-Fenton process obtained 20%. Due to negligible difference between the treatment efficiencies of the two processes, the electro-Fenton method was proven to be more economically advantageous. The models obtained from the study were applicable to a wide range of acetaminophen concentrations and can be used in scale-ups. Thirteen different types of intermediates were identified and a degradation pathway was proposed.

  20. Stereocontrolled generation of nucleophilic (Z)- or (E)-α-fluoroalkenylchromium reagents via carbon-fluorine bond activation: highly stereoselective synthesis of (E)- or (Z)-β-fluoroallylic alcohols.

    Science.gov (United States)

    Nihei, Takashi; Yokotani, Saya; Ishihara, Takashi; Konno, Tsutomu

    2014-02-14

    Highly nucleophilic (Z)- or (E)-α-fluoroalkenylchromium species could be generated in a stereoselective manner via C-F bond activation of CBrF2-containing molecules, and they reacted smoothly with various aldehydes to give (E)- or (Z)-β-fluoroallylic alcohol derivatives in high yields, respectively.

  1. Comparative study of oxidation of dye-Reactive Black B by different advanced oxidation processes: Fenton, electro-Fenton and photo-Fenton

    International Nuclear Information System (INIS)

    Huang Yaohui; Huang Yifong; Chang Poshun; Chen Chuhyung

    2008-01-01

    This study makes a comparison between photo-Fenton and a novel electro-Fenton called Fered-Fenton to study the mineralization of 10,000 mg/L of dye-Reactive Black B (RBB) aqueous solution, which was chosen as the model dye contaminant. Results indicate that the traditional Fenton process only yields 70% mineralization. This result can be improved by using Fered-Fenton to yield 93% mineralization resulting from the action of ferrous ion regenerated on the cathode. Furthermore, photo-Fenton allows a fast and more complete destruction of dye solutions and as a result of the action of ferrous ion regenerated by UV irradiation yields more than 98% mineralization. In all treatments, the RBB is rapidly decayed to some carboxylic acid intermediates. The major intermediates found are formic acid and oxalic acid. This study finds that formic acid can be completely mineralized by photo-Fenton, but its destruction is problematic using the Fenton method. Oxalic acid is much more difficult to treat than other organic acids. It could get further mineralization with the use of the Fered-Fenton process

  2. Reduction of clarithromycin and sulfamethoxazole-resistant Enterococcus by pilot-scale solar-driven Fenton oxidation.

    Science.gov (United States)

    Karaolia, Popi; Michael, Irene; García-Fernández, Irene; Agüera, Ana; Malato, Sixto; Fernández-Ibáñez, Pilar; Fatta-Kassinos, Despo

    2014-01-15

    The presence of pathogenic antibiotic-resistant bacteria in aquatic environments has become a health threat in the last few years. Their presence has increased due to the presence of antibiotics in wastewater effluents, which are not efficiently removed by conventional wastewater treatments. As a result there is a need to study the possible ways of removal of the mixtures of antibiotics present in wastewater effluents and the antibiotic-resistant bacteria, which may also spread the antibiotic resistance genes to other bacterial populations. In this study the degradation of a mixture of antibiotics i.e. sulfamethoxazole and clarithromycin, the disinfection of total enterococci and the removal of those resistant to: a) sulfamethoxazole, b) clarithromycin and c) to both antibiotics have been examined, along with the toxicity of the whole effluent mixture after treatment to the luminescent aquatic bacterium Vibrio fischeri. Solar Fenton treatment (natural solar driven oxidation) using Fenton reagent doses of 50 mg L(-1) of hydrogen peroxide and 5 mg L(-1) of Fe(3+) in a pilot-scale compound parabolic collector plant was used to examine the disinfection and antibiotic resistance removal efficiency in different aqueous matrices, namely distilled water, simulated and real wastewater effluents. There was a faster complete removal of enterococci and of antibiotics in all aqueous matrices by applying solar Fenton when compared to photolytic treatment of the matrices. Sulfamethoxazole was more efficiently degraded than clarithromycin in all three aqueous matrices (95% removal of sulfamethoxazole and 70% removal of clarithromycin in real wastewater). The antibiotic resistance of enterococci towards both antibiotics exhibited a 5-log reduction with solar Fenton in real wastewater effluent. Also after solar Fenton treatment, there were 10 times more antibiotic-resistant enterococci in the presence of sulfamethoxazole than in the presence of clarithromycin. Finally, the toxicity

  3. Evaluation of ethyl lactate as solvent in Fenton oxidation for the remediation of total petroleum hydrocarbon (TPH)-contaminated soil.

    Science.gov (United States)

    Jalilian Ahmadkalaei, Seyedeh Pegah; Gan, Suyin; Ng, Hoon Kiat; Abdul Talib, Suhaimi

    2017-07-01

    Due to the health and environmental risks posed by the presence of petroleum-contaminated areas around the world, remediation of petroleum-contaminated soil has drawn much attention from researchers. Combining Fenton reaction with a solvent has been proposed as a novel way to remediate contaminated soils. In this study, a green solvent, ethyl lactate (EL), has been used in conjunction with Fenton's reagents for the remediation of diesel-contaminated soil. The main aim of this research is to determine how the addition of EL affects Fenton reaction for the destruction of total petroleum hydrocarbons (TPHs) within the diesel range. Specifically, the effects of different parameters, including liquid phase volume-to-soil weight (L/S) ratio, hydrogen peroxide (H 2 O 2 ) concentration and EL% on the removal efficiency, have been studied in batch experiments. The results showed that an increase in H 2 O 2 resulted in an increase in removal efficiency of TPH from 68.41% at H 2 O 2  = 0.1 M to 90.21% at H 2 O 2  = 2 M. The lowest L/S, i.e. L/S = 1, had the highest TPH removal efficiency of 85.77%. An increase in EL% up to 10% increased the removal efficiency to 96.74% for TPH, and with further increase in EL%, the removal efficiency of TPH decreased to 89.6%. EL with an optimum value of 10% was found to be best for TPH removal in EL-based Fenton reaction. The power law and pseudo-first order equations fitted well to the experimental kinetic data of Fenton reactions.

  4. Application of Fenton process to remove organic matter and PCBs from waste (fuller's earth) contaminated with insulating oil.

    Science.gov (United States)

    da Silva, Milady Renata Apolinário; Rodrigues, Eduardo de Oliveira; Espanhol-Soares, Melina; Silva, Flavio Soares; Kondo, Márcia Matiko; Gimenes, Rossano

    2018-01-09

    Polychlorinated biphenyls (PCBs) are carcinogenic to humans and can be found in fuller's earth used for the treatment of used transformer oil. This work describes an optimization of the Fenton process for the removal of contaminants from fuller's earth. The effects of pH (2.5 and 4.0), [H 2 O 2 ] (1.47 and 2.07 mol L -1 ), and [Fe 2+ ] (1.7 and 40 mmol L -1 ) were studied. The Fenton process efficiency was monitored using the decreases in the chemical oxygen demand (COD) and the concentrations of oil and grease, total carbon (TC), PCBs, and H 2 O 2 . The fuller's earth contaminated with insulating oil presented 35% (w/w) of TC, 34% (w/w) of oil and grease, 297.0 g L -1 COD, and 64 mg of PCBs per kg. The material could therefore be considered a dangerous waste. After Fenton treatment, using a slurry mode, there was a removal of 55% of COD, 20% of oil and grease, and 20% of TC, achieved at pH 2.5 using 2.07 mol L -1 of H 2 O 2 and 40.0 mmol L -1 of Fe 2+ . No PCBs were detected in the samples after the Fenton treatment, even using smaller amounts of Fenton reagents (1.47 mol L -1 of H 2 O 2 , 1.7 mmol L -1 of Fe 2+ , pH 2.5). The results indicated that the treated fuller's earth was free from PCB residues and could be disposed of in a simple landfill, in accordance with Brazilian PCB regulations.

  5. Solar photo-Fenton mineralization of antipyrine in aqueous solution.

    Science.gov (United States)

    Durán, A; Monteagudo, J M; Sanmartín, I; Carrasco, A

    2013-11-30

    The mineralization of an aqueous solution of antipyrine (C11H12N2O), an emerging contaminant, using a solar photocatalytic oxidation process assisted with ferrioxalate was evaluated in a compound parabolic collector (CPC) pilot plant. Under the selected operating conditions ([H2O2] = 250 ppm, [Fe] = 14 ppm, pH = 2.7, and [(COOH)2·2H2O] = 80 ppm), 60% of TOC is removed just 5 min after treating an aqueous solution containing 50 ppm of antipyrine. The addition of oxalic acid up to a maximum concentration of 80 ppm significantly increases the mineralization rate during the first 15 min of the reaction. The synergism between the solar and dark H2O2/ferrioxalate process was quantified at 79%, calculated from the pseudo first-order mineralization rate constants. The operational costs due to the consumption of electrical energy, reagents and catalysts were calculated from the optimal conditions and compared with a novel sono-photocatalytic process using artificial UV-light. The results showed that the ferrioxalate-assisted solar photo-Fenton process was economically feasible, being able to achieve up to 60% mineralization with a total cost of 4.5 cent €/g TOC removed (1.1 €/m(3)). Copyright © 2013 Elsevier Ltd. All rights reserved.

  6. Treatment of Furfural Wastewater by (AOPs Photo-Fenton Method

    Directory of Open Access Journals (Sweden)

    Yasmen A. Mustafa

    2015-03-01

    Full Text Available The objective of this study is to investigate the application of advanced oxidation processes (AOPs in the treatment of wastewater contaminated with furfural. The AOPs investigated is the homogeneous photo-Fenton (UV/H2O2/Fe+2 process. The experiments were conducted by using cylindrical stainless steel batch photo-reactor. The influence of different variables: initial concentration of H2O2 (300-1300mg/L, Fe+2(20-70mg/L, pH(2-7 and initial concentration of furfural (50-300 mg/L and their relationship with the mineralization efficiency were studied. Complete mineralization for the system UV/H2O2/Fe+2 was achieved at: initial H2O2 = 1300mg/L, Fe+2 = 30mg/L, pH=3, temperature =30oC and irradiation time of 60 min, for 300mg/L furfural concentration. The results have shown that the oxidation reagent H2O2 plays a very important role in the furfural mineralization.

  7. Degradation of dyestuff materials by fenton oxidation, Part 4

    International Nuclear Information System (INIS)

    Shahrour, Kh.; Hachem, Ch.; Karabet, F.

    2008-01-01

    The oxidative degradation of various kinds of dyes (Azo carmine B, Tartrazine, Calcon, Methyle Orange, and Coomassie Brilliant Blue G 250, Methylene Blue, Bismark Brown Y(G) and Black 5) have been studied using Fenton's reagent (Fe 2+ and H 2 O 2 ). Many experiments were carried out on Azo carmine B as a model with initial concentration of 10 -4 to investigate the process's optimal conditions, pH, H 2 O 2 dosage, Fe 2+ dosage , temperature. The optimal conditions found were: pH=3, [H 2 O 2 ]=3 x 10 -3 M, [Fe 2+ ]=10 -4 M, t=60 Centigrade. under these contritions it was observed that Azo carmine B can be degraded at high extent (96.46%) after 50 min, however, the mineralization reached only (31.2%) in term of TOC and (41.1%) in term of COD. Results show that dyes are decomposed in two-stage reaction. In the first stage (Fe 2= /H 2 O 2 ) dyes decomposes rapidly within 0.5-5 min and the reaction obeys the pseudo-first-order. In the second stage (Fe 3+ /H 2 O 2 ) the dye decomposition is somewhat less rapidly, and the reaction follows the first order rate kinetic with respect to the dye concentration. (author)

  8. The reaction of organocerium reagents with easily enolizable ketones

    International Nuclear Information System (INIS)

    Imamoto, Tsuneo; Kusumoto, Tetsuo; Sugiura, Yasushi; Suzuki, Nobuyo; Takiyama, Nobuyuki

    1985-01-01

    Organocerium (III) reagents were conveniently generated by the reaction of organolithium compounds with anhydrous cerium (III) chloride. The reagents are less basic than organolithiums and Grignard reagents, and they react readily at -78 deg C with easily enolizable ketones such as 2-tetralone to afford addition products in high yields. Cerium (III) enolates were also generated from lithium enolates and cerium (III) chloride. The cerium (III) enolates undergo aldol addition with ketones or sterically crowded aldehyde to give the corresponding β-hydroxy ketones in good to high yields. (author)

  9. Cosmetic wastewater treatment using the Fenton, Photo-Fenton and H2O2/UV processes.

    Science.gov (United States)

    Marcinowski, Piotr P; Bogacki, Jan P; Naumczyk, Jeremi H

    2014-01-01

    Advanced Oxidation Processes (AOPs), such as the Fenton, photo-Fenton and H2O2/UV processes, have been investigated for the treatment of cosmetic wastewaters that were previously coagulated by FeCl3. The Photo-Fenton process at pH 3.0 with 1000/100 mg L(-1) H2O2/Fe(2+) was the most effective (74.0% Chemical Oxygen Demand (COD) removal). The Fenton process with 1200/500 mg L(-1) H2O2/Fe(2+) achieved a COD removal of 72.0%, and the H2O2/UV process achieved a COD removal of 47.0%. Spreading the H2O2 doses over time to obtain optimal conditions did not improve COD removal. The kinetics of the Fenton and photo-Fenton processes may be described by the following equation: d[COD]/dt = -a[COD] t(m) (t represents time and a and m are constants). The rate of COD removal by the H2O2/UV process may be described by a second-order reaction equation. Head Space, Solid-Phase MicroExtraction, Gas Chromatography and Mass Spectrometry (HS-SPME-GC-MS) were used to identify 48 substances in precoagulated wastewater. Among these substances, 26 were fragrances. Under optimal AOP conditions, over 99% of the identified substances were removed in 120 min.

  10. SIMULTANEOUS DEGRADATION OF SOME PHTHALATE ESTERS UNDER FENTON AND PHOTO-FENTON OXIDATION PROCESSES

    Directory of Open Access Journals (Sweden)

    BELDEAN-GALEA M.S.

    2015-03-01

    Full Text Available In this study the assessment of the degradation efficiency of five phthalates, DEP, BBP, DEHP, DINP and DIDP, found in a mixture in a liquid phase, using the Fenton and Photo Fenton oxidation processes, was conducted. It was observed that the main parameters that influence the Fenton oxidative processes of phthalates were the concentration of the oxidizing agent, H2O2, the concentration of the catalyst used, Fe2+, the pH value, UV irradiation and the reaction time. For the Fenton oxidative process, the highest degradation efficiencies were 19% for DEP, 50% for BBP, 84% for DEHP, 90% for DINP and 48% for DIDP, when the experiments were carried out using concentrations of 20 mg L-1 phthalate mixture, 100 mg L-1 H2O2, 10 mg L-1 Fe2+ at a pH value of 3, with a total reaction time of 30 minutes. For the Photo-Fenton oxidative process carried out in the same conditions as Fenton oxidative process, it was observed that after an irradiation time of 90 minutes under UV radiation the degradation efficiencies of phthalates were improved, being 22% for DEP, 71% for BBP, 97% for DEHP, 97% for DINP and 81% for DIDP.

  11. Constructing New Bioorthogonal Reagents and Reactions.

    Science.gov (United States)

    Row, R David; Prescher, Jennifer A

    2018-05-15

    Chemical tools are transforming our understanding of biomolecules and living systems. Included in this group are bioorthogonal reagents-functional groups that are inert to most biological species, but can be selectively ligated with complementary probes, even in live cells and whole organisms. Applications of these tools have revealed fundamental new insights into biomolecule structure and function-information often beyond the reach of genetic approaches. In many cases, the knowledge gained from bioorthogonal probes has enabled new questions to be asked and innovative research to be pursued. Thus, the continued development and application of these tools promises to both refine our view of biological systems and facilitate new discoveries. Despite decades of achievements in bioorthogonal chemistry, limitations remain. Several reagents are too large or insufficiently stable for use in cellular environments. Many bioorthogonal groups also cross-react with one another, restricting them to singular tasks. In this Account, we describe our work to address some of the voids in the bioorthogonal toolbox. Our efforts to date have focused on small reagents with a high degree of tunability: cyclopropenes, triazines, and cyclopropenones. These motifs react selectively with complementary reagents, and their unique features are enabling new pursuits in biology. The Account is organized by common themes that emerged in our development of novel bioorthogonal reagents and reactions. First, natural product structures can serve as valuable starting points for probe design. Cyclopropene, triazine, and cyclopropenone motifs are all found in natural products, suggesting that they would be metabolically stable and compatible with a variety of living systems. Second, fine-tuning bioorthogonal reagents is essential for their successful translation to biological systems. Different applications demand different types of probes; thus, generating a collection of tools that span a continuum of

  12. Photo-Fenton degradation of the insecticide esfenvalerate in aqueous medium using a recirculation flow-through UV photoreactor

    International Nuclear Information System (INIS)

    Colombo, Renata; Ferreira, Tanare C.R.; Alves, Suellen A.; Lanza, Marcos R.V.

    2011-01-01

    Highlights: ► The photo-Fenton reaction provides an efficient process by which to degrade esfenvalerate in aqueous suspensions. ► Photo-Fenton oxidation with Fe 3+ is more efficient in degrading esfenvalerate than the Fe 2+ -based reaction. ► Esfenvalerate was degraded most efficiently by photo-Fenton reaction in the presence of 5 mM Fe 3+ complex and 25 mM hydrogen peroxide at pH 2.5. ► The degradation of esfenvalerate by photo-Fenton (Fe 3+ ) generates organic by-products. ► Organic compounds present in commercial esfenvalerate-based insecticides affect the degradation process. - Abstract: The aim of the study was to evaluate the efficiencies of photo-Fenton (Fe 2+ ) and (Fe 3+ ) processes in the degradation of high-concentrations of esfenvalerate (in the form of aqueous emulsion of a commercial formulation) using a recirculation flow-through photoreactor irradiated with UV light from a 15 W lamp (254 nm emission peak). The results obtained using a basic photo-Fenton (Fe 2+ ) reaction (esfenvalerate 17 mg L −1 ; ferrous sulphate 1 mM; hydrogen peroxide 25 mM; pH 2.5) were compared with those acquired when ferrioxalate (1, 3 or 5 mM) served as the iron source. Degradation of the active component of the commercial formulation was significantly greater, and the rate of oxidation more rapid, using a photo-Fenton (Fe 3+ ) process compared with its Fe 2+ counterpart. The most efficient degradation of the insecticide (75% in 180 min) was achieved with a reaction mixture containing 5 mM ferrioxalate. However, under the same experimental conditions, degradation of pure esfenvalerate preceded much faster (99% in 60 min) and was 100% complete within 180 min reaction time.

  13. Application of Electro-Fenton Technology to Remediation of Polluted Effluents by Self-Sustaining Process

    Directory of Open Access Journals (Sweden)

    Maria Ángeles Fernández de Dios

    2014-01-01

    Full Text Available The applicability of electro-Fenton technology to remediation of wastewater contaminated by several organic pollutants such as dyes and polycyclic aromatic hydrocarbons has been evaluated using iron-enriched zeolite as heterogeneous catalyst. The electro-Fenton technology is an advanced oxidation process that is efficient for the degradation of organic pollutants, but it suffers from the high operating costs due to the need for power investment. For this reason, in this study microbial fuel cells (MFCs were designed in order to supply electricity to electro-Fenton processes and to achieve high treatment efficiency at low cost. Initially, the effect of key parameters on the MFC power generation was evaluated. Afterwards, the degradation of Reactive Black 5 dye and phenanthrene was evaluated in an electro-Fenton reactor, containing iron-enriched zeolite as catalyst, using the electricity supplied by the MFC. Near complete dye decolourization and 78% of phenanthrene degradation were reached after 90 min and 30 h, respectively. Furthermore, preliminary reusability tests of the developed catalyst showed high degradation levels for successive cycles. The results permit concluding that the integrated system is adequate to achieve high treatment efficiency with low electrical consumption.

  14. Application of Electro-Fenton Technology to Remediation of Polluted Effluents by Self-Sustaining Process

    Science.gov (United States)

    Fernández de Dios, Maria Ángeles; Iglesias, Olaia; Pazos, Marta; Sanromán, Maria Ángeles

    2014-01-01

    The applicability of electro-Fenton technology to remediation of wastewater contaminated by several organic pollutants such as dyes and polycyclic aromatic hydrocarbons has been evaluated using iron-enriched zeolite as heterogeneous catalyst. The electro-Fenton technology is an advanced oxidation process that is efficient for the degradation of organic pollutants, but it suffers from the high operating costs due to the need for power investment. For this reason, in this study microbial fuel cells (MFCs) were designed in order to supply electricity to electro-Fenton processes and to achieve high treatment efficiency at low cost. Initially, the effect of key parameters on the MFC power generation was evaluated. Afterwards, the degradation of Reactive Black 5 dye and phenanthrene was evaluated in an electro-Fenton reactor, containing iron-enriched zeolite as catalyst, using the electricity supplied by the MFC. Near complete dye decolourization and 78% of phenanthrene degradation were reached after 90 min and 30 h, respectively. Furthermore, preliminary reusability tests of the developed catalyst showed high degradation levels for successive cycles. The results permit concluding that the integrated system is adequate to achieve high treatment efficiency with low electrical consumption. PMID:24723828

  15. Fenton oxidation treatment of spent wash-off liquor for reuse in reactive dying

    International Nuclear Information System (INIS)

    Mangat, A.; Shaikh, I.A.; Ahmed, F.; Baqar, M

    2014-01-01

    The use of clean and high quality water in textile dyeing process is very expensive. In this study, the potential of reusing Fenton treated wash-off wastewater generated at the end of reactive dyeing was investigated. The treated wastewater was used in several dyeings employing three widely used reactive dyes, C. I. Reactive Yellow 145, C. I. Reactive Red 194, and C. I. Reactive Blue 221. Experimental results showed that at acidic pH (3.5) using optimized quantities of FeSO/sub 4/ and H/sub 2/O/sub 2/, Fenton process yielded a significant reduction (80-99%) of colour and COD in 30 minutes of treatment time. New dyeings were then carried out in Fenton decolourized wash-off wastewater, and dyed fabric samples were subjected to quality evaluations in terms of wash fastness, crock fastness, and colour difference properties (delta L*, delta c*, delta h*, and delta E*). This study concluded that Fenton oxidation was an efficient method for the treatment of textile wash-off wastewater, and treated liquor can be effectively recycled in next dyeing, without compromising quality parameters. This method proved to be an eco-friendly process owing to the fact that it did not use any fresh water. (author)

  16. Development of a trickle bed reactor of electro-Fenton process for wastewater treatment

    Energy Technology Data Exchange (ETDEWEB)

    Lei, Yangming [Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 401122 (China); School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Liu, Hong, E-mail: liuhong@cigit.ac.cn [Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 401122 (China); Shen, Zhemin, E-mail: zmshen@sjtu.edu.cn [School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Wang, Wenhua [School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2013-10-15

    Highlights: • An electrochemical trickle bed reactor was composed of C-PTFE-coated graphite chips. • The trickle bed reactor had a high H{sub 2}O{sub 2} production rate in a dilute electrolyte. • An azo dye was effectively decomposed by the electro-Fenton process in the reactor. -- Abstract: To avoid electrolyte leakage and gas bubbles in the electro-Fenton (E-Fenton) reactors using a gas diffusion cathode, we developed a trickle bed cathode by coating a layer composed of carbon black and polytetrafluoroethylene (C-PTFE) onto graphite chips instead of carbon cloth. The trickle bed cathode was optimized by single-factor and orthogonal experiments, in which carbon black, PTFE, and a surfactant were considered as the determinant of the performance of graphite chips. In the reactor assembled by the trickle bed cathode, H{sub 2}O{sub 2} was generated with a current of 0.3 A and a current efficiency of 60%. This performance was attributed to the fine distribution of electrolyte and air, as well as the effective oxygen transfer from the gas phase to the electrolyte–cathode interface. In terms of H{sub 2}O{sub 2} generation and current efficiency, the developed trickle bed reactor had a performance comparable to that of the conventional E-Fenton reactor using a gas diffusion cathode. Further, 123 mg L{sup −1} of reactive brilliant red X-3B in aqueous solution was decomposed in the optimized trickle bed reactor as E-Fenton reactor. The decolorization ratio reached 97% within 20 min, and the mineralization reached 87% within 3 h.

  17. Development of a trickle bed reactor of electro-Fenton process for wastewater treatment

    International Nuclear Information System (INIS)

    Lei, Yangming; Liu, Hong; Shen, Zhemin; Wang, Wenhua

    2013-01-01

    Highlights: • An electrochemical trickle bed reactor was composed of C-PTFE-coated graphite chips. • The trickle bed reactor had a high H 2 O 2 production rate in a dilute electrolyte. • An azo dye was effectively decomposed by the electro-Fenton process in the reactor. -- Abstract: To avoid electrolyte leakage and gas bubbles in the electro-Fenton (E-Fenton) reactors using a gas diffusion cathode, we developed a trickle bed cathode by coating a layer composed of carbon black and polytetrafluoroethylene (C-PTFE) onto graphite chips instead of carbon cloth. The trickle bed cathode was optimized by single-factor and orthogonal experiments, in which carbon black, PTFE, and a surfactant were considered as the determinant of the performance of graphite chips. In the reactor assembled by the trickle bed cathode, H 2 O 2 was generated with a current of 0.3 A and a current efficiency of 60%. This performance was attributed to the fine distribution of electrolyte and air, as well as the effective oxygen transfer from the gas phase to the electrolyte–cathode interface. In terms of H 2 O 2 generation and current efficiency, the developed trickle bed reactor had a performance comparable to that of the conventional E-Fenton reactor using a gas diffusion cathode. Further, 123 mg L −1 of reactive brilliant red X-3B in aqueous solution was decomposed in the optimized trickle bed reactor as E-Fenton reactor. The decolorization ratio reached 97% within 20 min, and the mineralization reached 87% within 3 h

  18. Fast biosensor with reagent layer

    NARCIS (Netherlands)

    2008-01-01

    A detection system and a sensor chip for detecting target mols., and thus corresponding analytes in a sample is described. Typically the detection system includes a sensor chip. The sensor chip (1) comprises on its detection surface a dissolvable reagent layer. When the dissolvable reagent layer is

  19. Degradation of flumequine by the Fenton and photo-Fenton processes: Evaluation of residual antimicrobial activity

    International Nuclear Information System (INIS)

    Rodrigues-Silva, Caio; Maniero, Milena Guedes; Rath, Susanne; Guimarães, José Roberto

    2013-01-01

    Flumequine is a broad-spectrum antimicrobial agent of the quinolone class, and it is widely used as a veterinary drug in food-producing animals. The presence of flumequine in the environment may contribute to the development of drug resistant bacterial strains. In this study, water samples fortified with flumequine (500 μg L −1 ) were degraded using the Fenton and photo-Fenton processes. The maximum degradation efficiency for flumequine by the Fenton process was approximately 40% (0.5 mmol L −1 Fe(II), 2.0 mmol L −1 H 2 O 2 and 15 min). By applying UV radiation (photo-Fenton process), the efficiency reached more than 94% in 60 min when 0.25 mmol L −1 Fe(II) and 10.0 mmol L −1 H 2 O 2 were used. Under these conditions, the Fenton process was able to reduce the biological activity, whereas the photo-Fenton process eliminated almost all of the antimicrobial activity because it was not detected. Four byproducts with an m/z of 244, 238, 220 and 202 were identified by mass spectrometry, and a degradation pathway for flumequine was proposed. The byproducts were derived from decarboxylation and defluorination reactions and from modifications in the alkylamino chain of the fluoroquinolone. - Highlights: ► Photo-Fenton process achieved the maximum performance, degrading 94% of flumequine. ► As the flumequine concentration decreased, antimicrobial activity also decreased. ► Four byproducts with m/z of 244, 238, 220 and 202 were identified. ► A degradation pathway for flumequine was proposed

  20. Degradation of flumequine by the Fenton and photo-Fenton processes: Evaluation of residual antimicrobial activity

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues-Silva, Caio; Maniero, Milena Guedes [School of Civil Engineering, Architecture and Urbanism, University of Campinas — UNICAMP, P.O. Box 6021, CEP 13083-852, Campinas, SP (Brazil); Rath, Susanne [Chemistry Institute, University of Campinas — UNICAMP, P.O. Box 6154, CEP 13084-971, Campinas, SP (Brazil); Guimarães, José Roberto, E-mail: jorober@fec.unicamp.br [School of Civil Engineering, Architecture and Urbanism, University of Campinas — UNICAMP, P.O. Box 6021, CEP 13083-852, Campinas, SP (Brazil)

    2013-02-15

    Flumequine is a broad-spectrum antimicrobial agent of the quinolone class, and it is widely used as a veterinary drug in food-producing animals. The presence of flumequine in the environment may contribute to the development of drug resistant bacterial strains. In this study, water samples fortified with flumequine (500 μg L{sup −1}) were degraded using the Fenton and photo-Fenton processes. The maximum degradation efficiency for flumequine by the Fenton process was approximately 40% (0.5 mmol L{sup −1} Fe(II), 2.0 mmol L{sup −1} H{sub 2}O{sub 2} and 15 min). By applying UV radiation (photo-Fenton process), the efficiency reached more than 94% in 60 min when 0.25 mmol L{sup −1} Fe(II) and 10.0 mmol L{sup −1} H{sub 2}O{sub 2} were used. Under these conditions, the Fenton process was able to reduce the biological activity, whereas the photo-Fenton process eliminated almost all of the antimicrobial activity because it was not detected. Four byproducts with an m/z of 244, 238, 220 and 202 were identified by mass spectrometry, and a degradation pathway for flumequine was proposed. The byproducts were derived from decarboxylation and defluorination reactions and from modifications in the alkylamino chain of the fluoroquinolone. - Highlights: ► Photo-Fenton process achieved the maximum performance, degrading 94% of flumequine. ► As the flumequine concentration decreased, antimicrobial activity also decreased. ► Four byproducts with m/z of 244, 238, 220 and 202 were identified. ► A degradation pathway for flumequine was proposed.

  1. Using single-chamber microbial fuel cells as renewable power sources of electro-Fenton reactors for organic pollutant treatment

    International Nuclear Information System (INIS)

    Zhu, Xiuping; Logan, Bruce E.

    2013-01-01

    Highlights: ► A new type of electro-Fenton system was developed for wastewater treatment. ► Degradation efficiency of organic pollutants was substantially improved. ► Operation cost was greatly reduced compared to other microbial fuel cell designs. -- Abstract: Electro-Fenton reactions can be very effective for organic pollutant degradation, but they typically require non-sustainable electrical power to produce hydrogen peroxide. Two-chamber microbial fuel cells (MFCs) have been proposed for pollutant treatment using Fenton-based reactions, but these types of MFCs have low power densities and require expensive membranes. Here, more efficient dual reactor systems were developed using a single-chamber MFC as a low-voltage power source to simultaneously accomplish H 2 O 2 generation and Fe 2+ release for the Fenton reaction. In tests using phenol, 75 ± 2% of the total organic carbon (TOC) was removed in the electro-Fenton reactor in one cycle (22 h), and phenol was completely degraded to simple and readily biodegradable organic acids. Compared to previously developed systems based on two-chamber MFCs, the degradation efficiency of organic pollutants was substantially improved. These results demonstrate that this system is an energy-efficient and cost-effective approach for industrial wastewater treatment of certain pollutants

  2. The reactor design and comparison of Fenton, electro-Fenton and photoelectro-Fenton processes for mineralization of benzene sulfonic acid (BSA)

    International Nuclear Information System (INIS)

    Ting, W.-P.; Lu, M.-C.; Huang, Y.-H.

    2008-01-01

    A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed. The use of UVA light and electric current as electron donors can efficiently initiate the Fenton reaction. Benzene sulfonic acid (BSA) was the target compound in this study. The parameters investigated to evaluate the reactor design include the electrode working area, electrode distance, energy consumption. Furthermore, the study also contains the intermediates and the mineralization efficiency of electrolysis, Fenton, electro-Fenton and photoelectro-Fenton process. Oxalic acid, the major intermediate of aromatic compound degradation, can complex with ferric ions. Meanwhile, a double cathode reactor could increase the current efficiency by 7%, which would translate to greater ferrous production and a higher degradation rate. Although the current efficiency of an electrode distance 5.5 cm device is 19% higher than 3.0 cm, results show that after 2 h of electrolysis the electronic expense using an electrode gap of 5.5 cm is much higher than 3.0 cm. The final TOC removal efficiency was 46, 64 and 72% using the Fenton, electro-Fenton and photoelectron-Fenton processes, respectively

  3. Optimization of the electro-Fenton and solar photoelectro-Fenton treatments of sulfanilic acid solutions using a pre-pilot flow plant by response surface methodology

    International Nuclear Information System (INIS)

    El-Ghenymy, Abdellatif; Garcia-Segura, Sergi; Rodríguez, Rosa María; Brillas, Enric; El Begrani, Mohamed Soussi; Abdelouahid, Ben Ali

    2012-01-01

    Highlights: ► Quicker degradation of sulfanilic acid by solar photoelectro-Fenton than electro-Fenton. ► The same optimized current density, Fe 2+ content and pH for both processes by CCRD. ► Description of TOC, energy cost and current efficiency by response surface methodology. ► Fe(III)–carboxylate complexes as main by-products after electro-Fenton. ► Photolysis of these complexes by UV irradiation of sunlight in solar photoelectro-Fenton. - Abstract: A central composite rotatable design and response surface methodology were used to optimize the experimental variables of the electro-Fenton (EF) and solar photoelectro-Fenton (SPEF) degradations of 2.5 L of sulfanilic acid solutions in 0.05 M Na 2 SO 4 . Electrolyses were performed with a pre-pilot flow plant containing a Pt/air diffusion reactor generating H 2 O 2 . In SPEF, it was coupled with a solar photoreactor under an UV irradiation intensity of ca. 31 W m −2 . Optimum variables of 100 mA cm −2 , 0.5 mM Fe 2+ and pH 4.0 were determined after 240 min of EF and 120 min of SPEF. Under these conditions, EF gave 47% of mineralization, whereas SPEF was much more powerful yielding 76% mineralization with 275 kWh kg −1 total organic carbon (TOC) energy consumption and 52% current efficiency. Sulfanilic acid decayed at similar rate in both treatments following a pseudo-first-order kinetics. The final solution treated by EF contained a stable mixture of tartaric, acetic, oxalic and oxamic acids, which form Fe(III) complexes that are not attacked by hydroxyl radicals formed from H 2 O 2 and added Fe 2+ . The quick photolysis of these complexes by UV light of sunlight explains the higher oxidation power of SPEF. NH 4 + was the main inorganic nitrogen ion released in both processes.

  4. How does intensification influence the operational and environmental performance of photo-Fenton processes at acidic and circumneutral pH.

    Science.gov (United States)

    Salazar, Luis Miguel; Grisales, Claudia Mildred; Garcia, Dorian Prato

    2018-05-31

    This study evaluates the technical, economical, and environmental impact of sodium persulfate (Na 2 S 2 O 8 ) as an enhancing agent in a photo-Fenton process within a solar-pond type reactor (SPR). Photo-Fenton (PF) and photo-Fenton intensified with the addition of persulfate (PFPS) processes decolorize 97% the azo dye direct blue 71 (DB71) and allow producing a highly biodegradable effluent. Intensification with persulfate allowed reducing treatment time in 33% (from 120 to 80 min) and the consumption of chemical auxiliaries needed for pH adjustment. Energy, reagents, and chemical auxiliaries are still and environmental hotspot for PF and PFPS; however, it is worth mentioning that their environmental footprint is lower than that observed for compound parabolic concentrator (CPC)-type reactors. A life-cycle assessment (LCA) confirms that H 2 O 2 , NaOH, and energy consumption are the variables with the highest impact from an environmental standpoint. The use of persulfate reduced the relative impact in 1.2 to 12% in 12 of the 18 environmental categories studied using the ReCiPe method. The PFPS process emits 1.23 kg CO 2 (CO 2 -Eqv/m 3 treated water). On the other hand, the PF process emits 1.28 kg CO 2 (CO 2 -Eqv/m 3 treated water). Process intensification, chemometric techniques, and the use of SPRs minimize the impact of some barriers (reagent and energy consumption, technical complexity of reactors, pressure drops, dirt on the reflecting surfaces, fragility of reactor materials), limiting the application of advanced oxidation systems at an industrial level, and decrease treatment cost as well as potential environmental impacts associated with energy and reagents consumption. Treatment costs for PF processes (US$0.78/m 3 ) and PFPS processes (US$0.63/m 3 ) were 20 times lower than those reported for photo-Fenton processes in CPC-type reactors.

  5. Comparison of Fenton and Fenton-like oxidation for the treatment of cosmetic wastewater.

    Science.gov (United States)

    Bautista, P; Casas, J A; Zazo, J A; Rodriguez, J J; Mohedano, A F

    2014-01-01

    The treatment of cosmetic wastewaters by Fenton (Fe²⁺/H₂O₂) and Fenton-like (Fe³⁺/H₂O₂) oxidation has been studied. From batch and continuous experiments it has been proved that both versions of the Fenton process lead to quite similar results in terms of chemical oxygen demand (COD) and total organic carbon reduction although the COD shows a slightly higher rate in the early stages of reaction. COD reductions of around 55% after 2 h reaction time and 75-80% with 4 h residence time were reached in batch and continuous experiments, respectively, conducted at pH around 3, ambient temperature (20 °C), with 200 mg/L of Fe dose and an initial H₂O₂/COD weight ratio corresponding to the theoretical stoichiometric value. Achieving the locally allowable limit of COD for industrial wastewater discharge into the municipal sewer system takes no more than 30 min reaction time under those conditions by both Fenton systems. However, the Fenton-like process, where iron is fed as Fe(3+), would be preferable for industrial applications since the ferric sludge resulting upon final neutralization of the effluent can be recycled to the process. A second-order kinetic equation with respect to COD fitted fairly well the experimental results at different temperatures, thus providing a simple practical tool for design purposes.

  6. Alternate switching between microbial fuel cell and microbial electrolysis cell operation as a new method to control H2O2 level in Bioelectro-Fenton system

    DEFF Research Database (Denmark)

    Zhang, Yifeng; Wang, Yong; Angelidaki, Irini

    2015-01-01

    cell (MEC) and microbial fuel cell (MFC) mode of operation was developed to meet the challenges. In the MEC mode, a bioelectrochemical system (BES) produces H2O2 which reacts with Fenton's reagent (Fe II) to form hydroxyradical. The unused H2O2 (residual H2O2) is removed as electron acceptor...... by switching the system to MFC mode of operation. Complete decolorization and mineralization of 50 mg L−1 methylene blue (MB) was achieved in the MEC mode with apparent first order rate constants of 0.43 and 0.22 h−1, respectively. After switching to the MFC mode, residual H2O2 of 180 mg L−1 was removed...... at a removal rate of 4.61 mg L−1 h−1 while generating a maximum current density of 0.49 A m−2. The MB degradation and residual H2O2 removal were affected by external resistance, cathode pH and initial MB concentration. Furthermore, the system performance was enhanced under stack operation. This study provides...

  7. A Bio-Electro-Fenton System Employing the Composite FePc/CNT/SS316 Cathode

    Directory of Open Access Journals (Sweden)

    Yi-Ta Wang

    2017-02-01

    Full Text Available Bio-electro-Fenton microbial fuel cells generate energy through the decomposition of organic matter by microorganisms. The generated electricity drives a Fenton reaction in a cathode chamber, which can be used for the decolorization of dye wastewater. Most of the previous works added expensive platinum catalyst to improve the electrical property of the system. In this research, aligned carbon nanotubes (CNTs were generated on the surface of SS316 stainless steel by chemical vapor deposition, and an iron phthalocyanine (FePc catalyst was added to fabricate a compound (FePc/CNT/SS316 that was applied to the cathode electrode of the fuel cell system. This was expected to improve the overall electricity generation efficiency and extent of decolorization of the system. The results showed that the maximum current density of the system with the modified electrode was 3206.30 mA/m2, and the maximum power was 726.55 mW/m2, which were increased by 937 and 2594 times, respectively, compared to the current and power densities of a system where only the SS316 stainless steel electrode was used. In addition, the decolorization of RB5 dye reached 84.6% within 12 h. Measurements of the electrical properties of bio-electro-Fenton microbial fuel cells and dye decolorization experiments with the FePc/CNT/SS316 electrode showed good results.

  8. Evaluation of Fenton's Reagent and Activated Persulfate for Treatment of a Pharmaceutical Waste Mixture in Groundwater

    DEFF Research Database (Denmark)

    Bennedsen, Lars Rønn; Søgaard, Erik Gydesen; Kakarla, Prasad

    2010-01-01

    Soil and groundwater beneath the Kærgård Plantage megasite in Denmark are contaminated with a complex mixture of pharmaceutical wastes, including sulfonamides, barbiturates, aniline, pyridine chlorinated solvents (DNAPL), benzene, toluene, mercury, and cyanide. Regulatory agencies in Denmark...... capacity of the aquifer sediments, pH dropped to within the range of 1 to 3 for all tests. Due to the presence of significant quantities of mercury and cyanide in the target treatment zone and the lowering of pH, batch and continuous-flow column reactors were used to measure mobilization of the mercury......, cyanide, chromium and other metals both within the aqueous and vapour phases. Except the alkaline activation, all the investigated techniques for activating persulfate were able to remove more than 80% of the primary contaminants. Optimization and more dosages led to 98-99% destruction of primary...

  9. IN-PLACE REGENERATION OF SVE LOADED GAC USING FENTON'S REAGENTS

    Science.gov (United States)

    Ten out of the 25 most frequently detected groundwater contaminants at hazardous waste sites are chlorinated volatile organic compounds (VOCs) 1 . Trichloroethylene (TCE) and tetrachloroethylene (PCE) are among the top three 1 . Granular activated carbon (GAC) adsorption is w...

  10. REMEDIATION OF MTBE - CONTAMINATED WATER: STUDIES ON THE DEGRADATION OF MTBE INTERMEDIATES USING THE FENTON'S REAGENT

    Science.gov (United States)

    The recent findings of unusual oncentrations of MTBE in groundwater aquifers and surface waters [1] originated most probably from the leaking of underground storage gasoline tanks [2[ has led to a series of judicial and legislative actions, especially in the state of California w...

  11. The study of a pilot-scale aerobic/Fenton/anoxic/aerobic process system for the treatment of landfill leachate.

    Science.gov (United States)

    Hu, Wenyong; Zhou, Yu; Min, Xiaobo; Liu, Jingyi; Li, Xinyu; Luo, Lin; Zhang, Jiachao; Mao, Qiming; Chai, Liyuan; Zhou, YaoYu

    2017-06-29

    In this study, a combined aerobic-Fenton-anoxic/aerobic system was designed for the remediation of raw landfill leachate in a pilot-scale experiment. This system included (i) a granular sludge biological oxidation procedure that achieves the accumulation of nitrite nitrogen ([Formula: see text]) under aerobic conditions; (ii) a Fenton process that improves the biodegradability of the biotreated leachate and (iii) an activated sludge biological oxidation component under anoxic and aerobic conditions. Additionally, a shortcut nitrification and denitrification pathway was achieved. The effects of free ammonia, temperature and pH on nitrite accumulation were discussed. The change in the biochemical oxygen demand/chemical oxygen demand ratio of the effluent after shortcut nitrification was also analysed. The microbial community in the reactor were also investigated. The problem of the lack of carbon source in the denitrification process can be solved by the Fenton reagent method. Moreover, it was beneficial to achieving nitrogen removal as well as the more extensive removal of organic matter. The treatment strategy employed in this study exhibited good results and provided the potential practical application for treating landfill leachate.

  12. Surface treatment with Fenton for separation of acrylonitrile-butadiene-styrene and polyvinylchloride waste plastics by flotation.

    Science.gov (United States)

    Wang, Jian-Chao; Wang, Hui; Huang, Luo-Luo; Wang, Chong-Qing

    2017-09-01

    Surface treatment with Fenton was applied to flotation separation of acrylonitrile-butadienestyrene (ABS) and polyvinylchloride (PVC). After treatment, the floatability of ABS has a dramatic decrease, while the floatability of PVC is not affected. Fourier transform infrared spectroscopy (FT-IR) spectra and X-ray photoelectron spectroscopy (XPS) spectra were recorded to ascertain the mechanism of Fenton treatment. FT-IR and XPS analysis confirms that the introduction of oxygen-containing group occurs on the surface of ABS. The optimum conditions are molar ration (H 2 O 2 :Fe 2+ ) 10000, H 2 O 2 concentration 0.4M/L, pH 5.8, treatment time 2min and temperature 25°C, frother concentration 15mg/L and flotation time 3min. Particle sizes and mixing ratios were also investigated. Plastic mixtures of ABS and PVC with different particle sizes and mixing ratios can be effectively separated. The purity of ABS and PVC are up to 100% and 99.78%, respectively; the recovery of ABS and PVC are up to 99.89% and 100%, respectively. A practical, environmentally friendly and effective reagent, namely Fenton, was originally applied to surface treatment of ABS and PVC waste plastics for flotation separation of their mixtures. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. Paracetamol degradation intermediates and toxicity during photo-Fenton treatment using different iron species.

    Science.gov (United States)

    Trovó, Alam G; Pupo Nogueira, Raquel F; Agüera, Ana; Fernandez-Alba, Amadeo R; Malato, Sixto

    2012-10-15

    The photo-Fenton degradation of paracetamol (PCT) was evaluated using FeSO(4) and the iron complex potassium ferrioxalate (FeOx) as iron source under simulated solar light. The efficiency of the degradation process was evaluated considering the decay of PCT and total organic carbon concentration and the generation of carboxylic acids, ammonium and nitrate, expressed as total nitrogen. The results showed that the degradation was favored in the presence of FeSO(4) in relation to FeOx. The higher concentration of hydroxylated intermediates generated in the presence of FeSO(4) in relation to FeOx probably enhanced the reduction of Fe(III) to Fe(II) improving the degradation efficiency. The degradation products were determined using liquid chromatography electrospray time-of-flight mass spectrometry. Although at different concentrations, the same intermediates were generated using either FeSO(4) or FeOx, which were mainly products of hydroxylation reactions and acetamide. The toxicity of the sample for Vibrio fischeri and Daphnia magna decreased from 100% to less than 40% during photo-Fenton treatment in the presence of both iron species, except for D. magna in the presence of FeOx due to the toxicity of oxalate to this organism. The considerable decrease of the sample toxicity during photo-Fenton treatment using FeSO(4) indicates a safe application of the process for the removal of this pharmaceutical. Copyright © 2012 Elsevier Ltd. All rights reserved.

  14. Removal of residual contaminants in petroleum-contaminated soil by Fenton-like oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Lu Mang [School of Material Science and Engineering, Jingdezhen Ceramic Institute, Jingdezhen, 333001, Jiangxi Province (China); State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249 (China); Zhang Zhongzhi, E-mail: zzzhang1955@hotmail.com [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249 (China); Qiao Wei; Guan Yueming; Xiao Meng; Peng Chong [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249 (China)

    2010-07-15

    The degradation of bioremediation residues by hydrogen peroxide in petroleum-contaminated soil was investigated at circumneutral pH using a Fenton-like reagent (ferric ion chelated with EDTA). Batch tests were done on 20 g soil suspended in 60 mL aqueous solution containing hydrogen peroxide and Fe{sup 3+}-EDTA complex under constant stirring. A slurry reactor was used to treat the soil based on the optimal reactant conditions. Contaminants were characterized by Fourier transform infrared spectroscopy and Fourier transform ion cyclotron resonance mass spectrometry. The results showed that the optimal treatment condition was: the molar ratio of hydrogen peroxide to iron = 200:1, and pH 7.0. Under the optimum condition, total dichloromethane-extractable organics were reduced from 14,800 to 2300 mg kg{sup -1} soil when the accumulative H{sub 2}O{sub 2} dosage was 2.45 mol kg{sup -1} soil during the reactor treatment. Abundance of viable cells was lower in incubated Fenton-like treated soil than in untreated soil. Oxidation of contaminants produced remarkable compositional and structural modifications. A fused ring compound, identified as C{sub 34}H{sub 38}N{sub 1}, was found to exhibit the greatest resistance to oxidation.

  15. Fenton-like initiation of a toluene transformation mechanism

    Science.gov (United States)

    In Fenton-driven oxidation treatment systems, reaction intermediates derived from parent compounds can play a significant role in the overall treatment process. Fenton-like reactions in the presence of toluene or benzene, involved a transformation mechanism that was highly effici...

  16. Stabilization of hydrogen peroxide using tartaric acids in Fenton and fenton-like oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Hyung Suk; Kim, Jeong-Jin; Kim, Young-Hun [Andong National University, Andong (Korea, Republic of)

    2016-03-15

    The stabilization of hydrogen peroxide is a key factor in the efficiency of a Fenton reaction. The stability of hydrogen peroxide was evaluated in a Fenton reaction and Fenton-like reactions in the presence of tartaric acid as a stabilizer. The interactions between ferrous or ferric iron and tartaric acid were observed through spectroscopic monitoring at variable pH around pKa{sub 1} and pKa{sub 2} of the stabilizer. Ferric iron had a strong interaction with the stabilizer, and the strong interaction was dominant above pKa{sub 2}. At a low pH, below pKa{sub 1}, the stabilizing effect was at its maximum and the prolonged life-time of hydrogen peroxide gave a higher efficiency to the oxidative degradation of nitrobenzene. In Fenton-like reactions with hematite, the acidic conditions caused dissolution of iron from an iron oxide, and an increase in iron species was the result. Tartaric acid showed a stabilizing effect on hydrogen peroxide in the Fentonlike system. The stabilization by tartaric acid might be due to an inhibition of catalytic activity of dissolved iron, and the stabilization strongly depends on the ionization state of the stabilizer.

  17. Fenton and solar photo-Fenton processes for the removal of ...

    African Journals Online (AJOL)

    Fenton (H2O2/Fe2+/solar light) processes was investigated. A laboratory-scale reactor was designed to evaluate and select the optimal oxidation condition. The degradation rate is strongly dependent on pH, temperature, H2O2 dosing rate, ...

  18. Response to Fenton and Fenton: evidence does not support the alkaline diet

    Science.gov (United States)

    In the space available in this broad review, we focused on large trials published since the 2011 Fenton meta-analysis. This included two trials published in 2013 and one in 2015. These trials found favorable effects of supplementation with alkaline salts of potassium, in amounts of 60 mmol/day and h...

  19. Stabilization of hydrogen peroxide using tartaric acids in Fenton and fenton-like oxidation

    International Nuclear Information System (INIS)

    Oh, Hyung Suk; Kim, Jeong-Jin; Kim, Young-Hun

    2016-01-01

    The stabilization of hydrogen peroxide is a key factor in the efficiency of a Fenton reaction. The stability of hydrogen peroxide was evaluated in a Fenton reaction and Fenton-like reactions in the presence of tartaric acid as a stabilizer. The interactions between ferrous or ferric iron and tartaric acid were observed through spectroscopic monitoring at variable pH around pKa 1 and pKa 2 of the stabilizer. Ferric iron had a strong interaction with the stabilizer, and the strong interaction was dominant above pKa 2 . At a low pH, below pKa 1 , the stabilizing effect was at its maximum and the prolonged life-time of hydrogen peroxide gave a higher efficiency to the oxidative degradation of nitrobenzene. In Fenton-like reactions with hematite, the acidic conditions caused dissolution of iron from an iron oxide, and an increase in iron species was the result. Tartaric acid showed a stabilizing effect on hydrogen peroxide in the Fentonlike system. The stabilization by tartaric acid might be due to an inhibition of catalytic activity of dissolved iron, and the stabilization strongly depends on the ionization state of the stabilizer.

  20. Bio-Electron-Fenton (BEF) process driven by microbial fuel cells for triphenyltin chloride (TPTC) degradation

    Energy Technology Data Exchange (ETDEWEB)

    Yong, Xiao-Yu; Gu, Dong-Yan; Wu, Yuan-Dong [College of Biotechnology and Pharmaceutical Engineering, Nanjing TECH University, Nanjing 211816 (China); Bioenergy Research Institute, Nanjing TECH University, Nanjing 211816 (China); Yan, Zhi-Ying [Key Laboratory of Environmental and Applied Microbiology, Environmental Microbiology, Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Science, Chengdu 610041 (China); Zhou, Jun; Wu, Xia-Yuan [College of Biotechnology and Pharmaceutical Engineering, Nanjing TECH University, Nanjing 211816 (China); Bioenergy Research Institute, Nanjing TECH University, Nanjing 211816 (China); Wei, Ping [College of Biotechnology and Pharmaceutical Engineering, Nanjing TECH University, Nanjing 211816 (China); Jia, Hong-Hua [College of Biotechnology and Pharmaceutical Engineering, Nanjing TECH University, Nanjing 211816 (China); Bioenergy Research Institute, Nanjing TECH University, Nanjing 211816 (China); Zheng, Tao, E-mail: zhengtao@ms.giec.ac.cn [Guangzhou Institute of Energy Conversion, Chinese Academy of Science, Nengyuan Road, Guangzhou 510640 (China); Yong, Yang-Chun, E-mail: ycyong@ujs.edu.cn [Biofuels Institute, School of the Environment, Jiangsu University, Zhenjiang 212013 (China); Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, Nanjing University of Science and Technology, Nanjing 210094 (China)

    2017-02-15

    Graphical abstract: Schematic diagram of the Bio-Electron-Fenton (BEF) process for TPTC degradation. - Highlights: • A Bio-Electro-Fenton process was performed for TPTC degradation. • TPTC removal efficiency achieved 78.32 ± 2.07% within 100 h. • The TPTC degradation rate (0.775 ± 0.021 μmol L{sup −1} h{sup −1}) was much higher than previous reports. - Abstract: The intensive use of triphenyltin chloride (TPTC) has caused serious environmental pollution. In this study, an effective method for TPTC degradation was proposed based on the Bio-Electron-Fenton process in microbial fuel cells (MFCs). The maximum voltage of the MFC with graphite felt as electrode was 278.47% higher than that of carbon cloth. The electricity generated by MFC can be used for in situ generation of H{sub 2}O{sub 2} to a maximum of 135.96 μmol L{sup −1} at the Fe@Fe{sub 2}O{sub 3(*)}/graphite felt composite cathode, which further reacted with leached Fe{sup 2+} to produce hydroxyl radicals. While 100 μmol L{sup −1} TPTC was added to the cathodic chamber, the degradation efficiency of TPTC reached 78.32 ± 2.07%, with a rate of 0.775 ± 0.021 μmol L{sup −1} h{sup −1}. This Bio-Electron-Fenton driving TPTC degradation might involve in Sn−C bonds breaking and the main process is probably a stepwise dephenylation until the formation of inorganic tin and CO{sub 2}. This study provides an energy saving and efficient approach for TPTC degradation.

  1. Bio-Electron-Fenton (BEF) process driven by microbial fuel cells for triphenyltin chloride (TPTC) degradation

    International Nuclear Information System (INIS)

    Yong, Xiao-Yu; Gu, Dong-Yan; Wu, Yuan-Dong; Yan, Zhi-Ying; Zhou, Jun; Wu, Xia-Yuan; Wei, Ping; Jia, Hong-Hua; Zheng, Tao; Yong, Yang-Chun

    2017-01-01

    Graphical abstract: Schematic diagram of the Bio-Electron-Fenton (BEF) process for TPTC degradation. - Highlights: • A Bio-Electro-Fenton process was performed for TPTC degradation. • TPTC removal efficiency achieved 78.32 ± 2.07% within 100 h. • The TPTC degradation rate (0.775 ± 0.021 μmol L"−"1 h"−"1) was much higher than previous reports. - Abstract: The intensive use of triphenyltin chloride (TPTC) has caused serious environmental pollution. In this study, an effective method for TPTC degradation was proposed based on the Bio-Electron-Fenton process in microbial fuel cells (MFCs). The maximum voltage of the MFC with graphite felt as electrode was 278.47% higher than that of carbon cloth. The electricity generated by MFC can be used for in situ generation of H_2O_2 to a maximum of 135.96 μmol L"−"1 at the Fe@Fe_2O_3_(_*_)/graphite felt composite cathode, which further reacted with leached Fe"2"+ to produce hydroxyl radicals. While 100 μmol L"−"1 TPTC was added to the cathodic chamber, the degradation efficiency of TPTC reached 78.32 ± 2.07%, with a rate of 0.775 ± 0.021 μmol L"−"1 h"−"1. This Bio-Electron-Fenton driving TPTC degradation might involve in Sn−C bonds breaking and the main process is probably a stepwise dephenylation until the formation of inorganic tin and CO_2. This study provides an energy saving and efficient approach for TPTC degradation.

  2. Estudo da degradação do metil parabeno utilizando processos Fenton, foto-Fenton e eletro-Fenton

    OpenAIRE

    Carlos Dante Gamarra Güere

    2014-01-01

    Os disruptores endócrinos são frequentemente relatados na literatura como contaminantes de ambientes aquáticos. Por isso, os processos oxidativos avançados (POAs) têm sido estudados como alternativa para o tratamento em meio aquoso. Os POAs consistem na oxidação de compostos orgânicos por radicais hidroxilas com alto poder oxidante. Diante desses aspectos, o presente trabalho tem como principal objetivo o estudo da degradação do metil parabeno (MeP) por processos Fenton, utilizando planejame...

  3. Evaluation of Efficacy of Advanced Oxidation Processes Fenton, Fenton-like and Photo-Fenton for Removal of Phenol from Aqueous Solutions

    International Nuclear Information System (INIS)

    Mofrad, M. R.; Akbari, H.; Miranzadeh, M. B.; Nezhad, M. E.; Atharizade, M.

    2015-01-01

    Contamination of water, soil and groundwater caused by aromatic compounds induces great concern in most world areas. Among organic pollutants, phenol is mostly considered dangerous due to its high toxicity for human and animal. Advanced oxidation processes (AOPs) is considered as a most efficient method also the best one for purifying organic compounds which are resistant to conventional physical and chemical processes. This experimental study was carried out in laboratory scale. First, a synthetic solution was made of phenol. Then, Fenton, Fenton-like and photo-Fenton processes were applied removing phenol from aquatic solution. The effects of Hydrogen Peroxide concentration, catalyst, pH and time were studied to phenol removal efficiency. Results showed that Photo-Fenton process with removal efficiency (97.5 percentage) is more efficient than Fenton and Fenton-like processes with removal efficiency (78.7 percentage and 82.5 percentage respectively), in pH=3, (H/sub 2/O/sub 2/)= 3mM, (Fe2+)= 0.1 mM, phenol concentration 100 mg L-1 and time reaction 60 min, the phenol removal was 97.5 percentage. (author)

  4. Simultaneous Transformation of Commingled Trichloroethylene, Tetrachloroethylene, and 1,4-Dioxane by a Microbially Driven Fenton Reaction in Batch Liquid Cultures

    Science.gov (United States)

    Sekar, Ramanan; Taillefert, Martial

    2016-01-01

    ABSTRACT Improper disposal of 1,4-dioxane and the chlorinated organic solvents trichloroethylene (TCE) and tetrachloroethylene (also known as perchloroethylene [PCE]) has resulted in widespread contamination of soil and groundwater. In the present study, a previously designed microbially driven Fenton reaction system was reconfigured to generate hydroxyl (HO˙) radicals for simultaneous transformation of source zone levels of single, binary, and ternary mixtures of TCE, PCE, and 1,4-dioxane. The reconfigured Fenton reaction system was driven by fed batch cultures of the Fe(III)-reducing facultative anaerobe Shewanella oneidensis amended with lactate, Fe(III), and contaminants and exposed to alternating anaerobic and aerobic conditions. To avoid contaminant loss due to volatility, the Fe(II)-generating, hydrogen peroxide-generating, and contaminant transformation phases of the microbially driven Fenton reaction system were separated. The reconfigured Fenton reaction system transformed TCE, PCE, and 1,4-dioxane either as single contaminants or as binary and ternary mixtures. In the presence of equimolar concentrations of PCE and TCE, the ratio of the experimentally derived rates of PCE and TCE transformation was nearly identical to the ratio of the corresponding HO˙ radical reaction rate constants. The reconfigured Fenton reaction system may be applied as an ex situ platform for simultaneous degradation of commingled TCE, PCE, and 1,4-dioxane and provides valuable information for future development of in situ remediation technologies. IMPORTANCE A microbially driven Fenton reaction system [driven by the Fe(III)-reducing facultative anaerobe S. oneidensis] was reconfigured to transform source zone levels of TCE, PCE, and 1,4-dioxane as single contaminants or as binary and ternary mixtures. The microbially driven Fenton reaction may thus be applied as an ex situ platform for simultaneous degradation of at least three (and potentially more) commingled contaminants

  5. Enhanced heterogeneous photo-Fenton process modified by magnetite and EDDS: BPA degradation.

    Science.gov (United States)

    Huang, Wenyu; Luo, Mengqi; Wei, Chaoshuai; Wang, Yinghui; Hanna, Khalil; Mailhot, Gilles

    2017-04-01

    In this research, magnetite and ethylenediamine-N,N'-disuccinic acid (EDDS) are used in a heterogeneous photo-Fenton system in order to find a new way to remove organic contaminants from water. Influence of different parameters including magnetite dosage, EDDS concentration, H 2 O 2 concentration, and pH value were evaluated. The effect of different radical species including HO · and HO 2 · /O 2 ·- was investigated by addition of different scavengers into the system. The addition of EDDS improved the heterogeneous photo-Fenton degradation of bisphenol A (BPA) through the formation of photochemically efficient Fe-EDDS complex. This effect is dependent on the H 2 O 2 and EDDS concentrations and pH value. The high performance observed at pH 6.2 could be explained by the ability of O 2 ·- to generate Fe(II) from Fe(III) species reduction. GC-MS analysis suggested that the cleavage of the two benzene rings is the first degradation step followed by oxidation leading to the formation of the benzene derivatives. Then, the benzene ring was opened due to the attack of HO · radicals producing short-chain organic compounds of low molecular weight like glycerol and ethylene glycol. These findings regarding the capability of EDDS/magnetite system to promote heterogeneous photo-Fenton oxidation have important practical implications for water treatment technologies.

  6. Methyl-orange and cadmium simultaneous removal using fly ash and photo-Fenton systems

    International Nuclear Information System (INIS)

    Visa, Maria; Duta, Anca

    2013-01-01

    Highlights: ► The mixed substrates of FA-M + TiO 2 proved to be highly efficient in adsorption. ► FA-M + photo-Fenton are a low-cost material for advanced treatment of wastewater. ► The adsorbed MO may act as a complexion agent, increasing the affinity for metals. ► Dye removal by photodegradation is the favourable mechanism compared to adsorption. -- Abstract: Wastewaters resulting from the textile and dye finishing industries need complex treatment for efficient removal of colour and other compounds existent in the dyeing and rising baths (heavy metals, surfactants, equalizers, etc.). Modified fly ash (FA) mixed with TiO 2 photocatalyst represent a viable option for simultaneous removal of dyes and heavy metals, and the optimized conditions are discussed in this paper for synthetic wastewaters containing methyl-orange (MO) and cadmium. For a cost-effective dye removal process, further tests were done, replacing the photocatalyst with a (photo)Fenton system. The optimized technological parameters (contact time, amount of fly ash and amount of Fe 2+ /H 2 O 2 ) allow to reach removal efficiencies up to 88% for the heavy metal and up to 70% for the dye. The adsorption mechanisms and the process kinetic are discussed, also considering the possibility of in situ generation of the Fenton system, due to the fly ash composition

  7. Methyl-orange and cadmium simultaneous removal using fly ash and photo-Fenton systems

    Energy Technology Data Exchange (ETDEWEB)

    Visa, Maria, E-mail: visamro2000@yahoo.com [Transilvania University of Brasov, Department of Renewable Energy Systems and Recycling, Eroilor 29, 500036 Brasov (Romania); Duta, Anca, E-mail: a.duta@unitbv.ro [Transilvania University of Brasov, Department of Renewable Energy Systems and Recycling, Eroilor 29, 500036 Brasov (Romania)

    2013-01-15

    Highlights: ► The mixed substrates of FA-M + TiO{sub 2} proved to be highly efficient in adsorption. ► FA-M + photo-Fenton are a low-cost material for advanced treatment of wastewater. ► The adsorbed MO may act as a complexion agent, increasing the affinity for metals. ► Dye removal by photodegradation is the favourable mechanism compared to adsorption. -- Abstract: Wastewaters resulting from the textile and dye finishing industries need complex treatment for efficient removal of colour and other compounds existent in the dyeing and rising baths (heavy metals, surfactants, equalizers, etc.). Modified fly ash (FA) mixed with TiO{sub 2} photocatalyst represent a viable option for simultaneous removal of dyes and heavy metals, and the optimized conditions are discussed in this paper for synthetic wastewaters containing methyl-orange (MO) and cadmium. For a cost-effective dye removal process, further tests were done, replacing the photocatalyst with a (photo)Fenton system. The optimized technological parameters (contact time, amount of fly ash and amount of Fe{sup 2+}/H{sub 2}O{sub 2}) allow to reach removal efficiencies up to 88% for the heavy metal and up to 70% for the dye. The adsorption mechanisms and the process kinetic are discussed, also considering the possibility of in situ generation of the Fenton system, due to the fly ash composition.

  8. Decontaminating reagents for radioactive systems

    International Nuclear Information System (INIS)

    Seddon, W.A.

    1982-01-01

    A decontaminating reagent composition has been developed comprising EDTA, citric acid, oxalic acid, and formic acid. Formic acid inhibits the decomposition of both EDTA and citric acid, and yields oxalic acid as a result of its own radiolysis. The invention includes the improvement of initially incorporating formic acid in the mixture and maintaining the presence of formic acid by at least one further addition

  9. On extraction reagents for hydrometallurgy

    International Nuclear Information System (INIS)

    Zolotov, Yu.A.

    1975-01-01

    Fundamental requirements to the extractants are considered. Ways of obtaining selective extractants are discussed in particular on the basis of coordination chemistry achivements. Attention is drawn to expediency of study (as extractants) of flotation reagents, additions to the oil, pesticides, accelerators of caoutchouc vulcanization

  10. Roles of free radicals in NO oxidation by Fenton system and the enhancement on NO oxidation and H2O2 utilization efficiency.

    Science.gov (United States)

    Zhao, Haiqian; Dong, Ming; Wang, Zhonghua; Wang, Huaiyuan; Qi, Hanbing

    2018-06-20

    Low H 2 O 2 utilization efficiency is the main problem when Fenton system was used to oxidize NO in flue gas. To understand the behavior of the free radicals during NO oxidation process in Fenton system is crucial to solving this problem. The oxidation capacity of ·OH and HO 2 · on NO in Fenton system was compared and the useless consumption path of ·OH and HO 2 · that caused the low utilization efficiency of H 2 O 2 were studied. A method to enhance the oxidation ability and H 2 O 2 utilization efficiency by adding reducing additives in Fenton system was proposed. The results showed that both of ·OH and HO 2 · were active substances that oxidize NO. However, the oxidation ability of ·OH radicals was stronger. The vast majority of ·OH and HO 2 · was consumed by rapid reaction ·OH+HO 2 ·→H 2 O+O 2 , which was the primary reason for the low utilization efficiency of H 2 O 2 in Fenton system. Hydroxylamine hydrochloride and ascorbic acid could accelerate the conversion of Fe 3+ to Fe 2+ , thereby increase the generation rate of ·OH and decrease the generation rate of HO 2 ·. As a result, the oxidation ability and H 2 O 2 utilization efficiency were enhanced.

  11. Combined photo-Fenton and biological treatment for Diuron and Linuron removal from water containing humic acid

    International Nuclear Information System (INIS)

    Farre, Maria Jose; Domenech, Xavier; Peral, Jose

    2007-01-01

    A combined chemical (photo-Fenton) and biological treatment has been proposed for Diuron and Linuron degradation in water containing natural dissolved organic matter (DOM). Humic acid (HA) was used to simulate the DOM. During the photo-Fenton process ([Fe(II)]=15.9mgL -1 , [H 2 O 2 ]=202mgL -1 , 60min of UVA irradiation time), the chemical oxygen demand (COD), total organic carbon (TOC), toxicity (EC 50 15 ) and biodegradability (BOD 5 /COD) of the generated intermediates were assessed. A reduction of photo-Fenton efficiency was observed when HA was present in solution. This effect has been explained as the result of a UVA light screening as well as a OH? radical quenching process by the HA. After the photo-Fenton process, the initial toxic and non-biodegradable herbicides were transformed into intermediates suitable for a subsequent aerobic biological treatment that was performed in a sequencing batch reactor (SBR). Complete elimination of the intermediates in presence of HA was reached at the end of the chemical-biological coupled system. Biosorption of HA onto the aerobic biomass was characterized. The results indicate that the Freundlich model adequately describes the adsorption of HA, a phenomena that follows a pseudo second-order adsorption kinetic model

  12. Effect of a solar Fered-Fenton system using a recirculation reactor on biologically treated landfill leachate.

    Science.gov (United States)

    Ye, Zhihong; Zhang, Hui; Yang, Lin; Wu, Luxue; Qian, Yue; Geng, Jinyao; Chen, Mengmeng

    2016-12-05

    The effects of electrochemical oxidation (EO), Fered-Fenton and solar Fered-Fenton processes using a recirculation flow system containing an electrochemical cell and a solar photo-reactor on biochemically treated landfill leachate were investigated. The most successful method was solar Fered-Fenton which achieved 66.5% COD removal after 120min treatment utilizing the optimum operating conditions of 47mM H2O2, 0.29mM Fe(2+), pH0 of 3.0 and a current density of 60mA/cm(2). The generation of hydroxyl radicals (OH) are mainly from Fered-Fenton process, which is enhanced by the introduction of renewable solar energy. Moreover, Fe(2+)/chlorine and UV/chlorine processes taking place in this system also result in additional production of OH due to the relatively high concentration of chloride ions contained in the leachate. The energy consumption was 74.5kWh/kg COD and the current efficiency was 36.4% for 2h treatment. In addition, the molecular weight (MW) distribution analysis and PARAFAC analysis of excitation emission matrix (EEM) fluorescence spectroscopy for different leachate samples indicated that the organics in the leachate were significantly degraded into either small molecular weight species or inorganics. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Using single-chamber microbial fuel cells as renewable power sources of electro-Fenton reactors for organic pollutant treatment

    KAUST Repository

    Zhu, Xiuping

    2013-05-01

    Electro-Fenton reactions can be very effective for organic pollutant degradation, but they typically require non-sustainable electrical power to produce hydrogen peroxide. Two-chamber microbial fuel cells (MFCs) have been proposed for pollutant treatment using Fenton-based reactions, but these types of MFCs have low power densities and require expensive membranes. Here, more efficient dual reactor systems were developed using a single-chamber MFC as a low-voltage power source to simultaneously accomplish H2O2 generation and Fe2+ release for the Fenton reaction. In tests using phenol, 75±2% of the total organic carbon (TOC) was removed in the electro-Fenton reactor in one cycle (22h), and phenol was completely degraded to simple and readily biodegradable organic acids. Compared to previously developed systems based on two-chamber MFCs, the degradation efficiency of organic pollutants was substantially improved. These results demonstrate that this system is an energy-efficient and cost-effective approach for industrial wastewater treatment of certain pollutants. © 2013 Elsevier B.V.

  14. Combined photo-Fenton and biological treatment for Diuron and Linuron removal from water containing humic acid

    Energy Technology Data Exchange (ETDEWEB)

    Farre, Maria Jose [Departament de Quimica, Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain); Domenech, Xavier [Departament de Quimica, Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain); Peral, Jose [Departament de Quimica, Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain)]. E-mail: jose.peral@uab.es

    2007-08-17

    A combined chemical (photo-Fenton) and biological treatment has been proposed for Diuron and Linuron degradation in water containing natural dissolved organic matter (DOM). Humic acid (HA) was used to simulate the DOM. During the photo-Fenton process ([Fe(II)]=15.9mgL{sup -1}, [H{sub 2}O{sub 2}]=202mgL{sup -1}, 60min of UVA irradiation time), the chemical oxygen demand (COD), total organic carbon (TOC), toxicity (EC{sub 50}{sup 15}) and biodegradability (BOD{sub 5}/COD) of the generated intermediates were assessed. A reduction of photo-Fenton efficiency was observed when HA was present in solution. This effect has been explained as the result of a UVA light screening as well as a OH? radical quenching process by the HA. After the photo-Fenton process, the initial toxic and non-biodegradable herbicides were transformed into intermediates suitable for a subsequent aerobic biological treatment that was performed in a sequencing batch reactor (SBR). Complete elimination of the intermediates in presence of HA was reached at the end of the chemical-biological coupled system. Biosorption of HA onto the aerobic biomass was characterized. The results indicate that the Freundlich model adequately describes the adsorption of HA, a phenomena that follows a pseudo second-order adsorption kinetic model.

  15. Leachate treatment system using constructed wetlands, Town of Fenton sanitary landfill, Broome County, New York. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1993-11-01

    Municipal sanitary landfills generate leachate that New York State regulations require to be collected and treated to avoid contaminating surface water and groundwater. One option for treating leachate is to haul it to municipal wastewater treatment facility. This option may be expensive, may require excessive energy for transportation, and may require pretreatment to protect the receiving facility`s processes. An alternative is on-site treatment and discharge. Personnel from the Town of Fenton, New York; Hawk Engineering, P.C.; Cornell University; and Ithaca College designed, built, and operated a pilot constructed wetland for treating leachate at the Town of Fenton`s municipal landfill. The system, consisting of two overland flow beds and two subsurface flow beds has been effective for 18 months in reducing levels of ammonia (averaging 85% removal by volatilization and denitrification) and total iron (averaging 95% removal by precipitation and sedimentation), two key constituents of the Fenton landfill`s leachate. The system effects these reductions with zero chemical and energy inputs and minimal maintenance. A third key constituent of the leachate, manganese, apparently passes through the beds with minimal removal. Details and wetland considerations are described.

  16. Sulfamethoxazole abatement by photo-Fenton

    International Nuclear Information System (INIS)

    Gonzalez, Oscar; Sans, Carme; Esplugas, Santiago

    2007-01-01

    The objective of this work was to study the abatement of 200 mg L -1 sulfamethoxazole (SMX) solution by means of photo-Fenton process. Biodegradability of the treated solutions was followed by the ratio biochemical oxygen demand at five days/chemical oxygen demand (BOD 5 /COD) and toxicity by Microtox[reg] and inhibition tests. Experiments with different initial concentration of H 2 O 2 were carried out. The initial amount of Fe 2+ and pH of the solution were set at 10 mg L -1 and 2.8 respectively. The temperature of the reactor was kept constant in all the experiments (25 ± 0.8 deg. C). Photo-Fenton process is thought to be a successful treatment step to improve the biodegradability of wastewater containing SMX. The complete antibiotic removal was achieved for a H 2 O 2 dose over 300 mg L -1 . Biodegradability (BOD 5 /COD) rose from zero (SMX solution) to values higher than 0.3 (treated solutions). Toxicity and inhibition tests pointed out in the same direction: oxidized intermediates for initial H 2 O 2 dose over 300 mg L -1 showed no toxicity effects on pure bacteria and no inhibition on activated sludge activity

  17. Electro-Fenton and photoelectro-Fenton degradations of the drug beta-blocker propranolol using a Pt anode: Identification and evolution of oxidation products

    Energy Technology Data Exchange (ETDEWEB)

    Isarain-Chavez, Eloy; Cabot, Pere Lluis; Centellas, Francesc; Rodriguez, Rosa Maria; Arias, Conchita; Garrido, Jose Antonio [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Brillas, Enric, E-mail: brillas@ub.edu [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2011-01-30

    The beta-blocker propranolol hydrochloride has been degraded by electrochemical advanced oxidation processes like electro-Fenton (EF) and photoelectro-Fenton (PEF) using a single cell with a Pt anode and an air diffusion cathode (ADE) for H{sub 2}O{sub 2} electrogeneration and a combined system containing the above Pt/ADE pair coupled in parallel to a Pt/carbon-felt (CF) cell. Organics are mainly oxidized with hydroxyl radical ({center_dot}OH) formed from Fenton's reaction between added Fe{sup 2+} and electrogenerated H{sub 2}O{sub 2}. The PEF treatment in Pt/ADE-Pt/CF system yields almost total mineralization because {center_dot}OH production is enhanced by Fe{sup 2+} regeneration from Fe{sup 3+} reduction at the CF cathode and Fe(III) complexes with generated carboxylic acids are rapidly photodecarboxylated under UVA irradiation. Lower mineralization degree is found for PEF in Pt/ADE cell due to the little influence of UVA light on Fe{sup 2+} regeneration. The homologous EF processes are much less potent as a result of the persistence of Fe(III)-carboxylate complexes. Aromatic intermediates such as 1-naphthol, 1,4-naphthoquinone and phthalic acid and generated carboxylic acids such as pyruvic, glycolic, malonic, maleic, oxamic, oxalic and formic are identified. While chloride ion remains stable, NH{sub 4}{sup +} and NO{sub 3}{sup -} ions are released to the medium. A reaction sequence for propranolol hydrochloride mineralization is proposed.

  18. Pyrimethanil degradation by photo-Fenton process: Influence of iron and irradiance level on treatment cost.

    Science.gov (United States)

    Cabrera Reina, A; Miralles-Cuevas, S; Casas López, J L; Sánchez Pérez, J A

    2017-12-15

    This study evaluates the combined effect of photo-catalyst concentration and irradiance level on photo-Fenton efficiency when this treatment is applied to industrial wastewater decontamination. Three levels of irradiance (18, 32 and 46W/m 2 ) and three iron concentrations (8, 20 and 32mg/L) were selected and their influence over the process studied using a raceway pond reactor placed inside a solar box. For 8mg/L, it was found that there was a lack of catalyst to make use of all the available photons. For 20mg/L, the treatment always improved with irradiance indicating that the process was photo-limited. For 32mg/L, the excess of iron caused an excess of radicals production which proved to be counter-productive for the overall process efficiency. The economic assessment showed that acquisition and maintenance costs represent the lowest relative values. The highest cost was found to be the cost of the reagents consumed. Both sulfuric acid and sodium hydroxide are negligible in terms of costs. Iron cost percentages were also very low and never higher than 10.5% while the highest cost was always that of hydrogen peroxide, representing at least 85% of the reagent costs. Thus, the total costs were between 0.76 and 1.39€/m 3 . Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Electrochemical destruction of chlorophenoxy herbicides by anodic oxidation and electro-Fenton using a boron-doped diamond electrode

    International Nuclear Information System (INIS)

    Brillas, Enric; Boye, Birame; Sires, Ignasi; Garrido, Jose Antonio; Rodriguez, Rosa Maria; Arias, Conchita; Cabot, Pere-Lluis; Comninellis, Christos

    2004-01-01

    The degradation of herbicides 4-chlorophenoxyacetic acid (4-CPA), 4-chloro-2-methylphenoxyacetic acid (MCPA), 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) in aqueous medium of pH 3.0 has been comparatively studied by anodic oxidation and electro-Fenton using a boron-doped diamond (BDD) anode. All solutions are totally mineralized by electro-Fenton, even at low current, being the process more efficient with 1 mM Fe 2+ as catalyst. This is due to the production of large amounts of oxidant hydroxyl radical (OH·) on the BDD surface by water oxidation and from Fenton's reaction between added Fe 2+ and H 2 O 2 electrogenerated at the O 2 -diffusion cathode. The herbicide solutions are also completely depolluted by anodic oxidation. Although a quicker degradation is found at the first stages of electro-Fenton, similar times are required for achieving overall mineralization in both methods. The decay kinetics of all herbicides always follows a pseudo first-order reaction. Reversed-phase chromatography allows detecting 4-chlorophenol, 4-chloro-o-cresol, 2,4-dichlorophenol and 2,4,5-trichlorophenol as primary aromatic intermediates of 4-CPA, MCPA, 2,4-D and 2,4,5-T, respectively. Dechlorination of these products gives Cl - , which is slowly oxidized on BDD. Ion-exclusion chromatography reveals the presence of persistent oxalic acid in electro-Fenton by formation of Fe 3+ -oxalato complexes, which are slowly destroyed by OH· adsorbed on BDD. In anodic oxidation, oxalic acid is mineralized practically at the same rate as generated

  20. A highly energy-efficient flow-through electro-Fenton process for organic pollutants degradation

    International Nuclear Information System (INIS)

    Ma, Liang; Zhou, Minghua; Ren, Gengbo; Yang, Weilu; Liang, Liang

    2016-01-01

    Highlights: • A highly energy-efficient flow-through electro-Fenton reactor was designed. • It had high H 2 O 2 yield and low energy consumption for organic pollutants degradation. • The effect of operational parameters was optimized and possible process mechanism was studied. • The novel system performed wide practicability and potential for organic pollutants degradation. - Abstract: A highly energy-efficient flow-through Electro-Fenton (E-Fenton) reactor for oxidation of methylene blue (MB) from aqueous solution was designed using a perforated DSA as anode and the graphite felt modified by carbon black and polytetrafluoroethylene (PTFE) as cathode for the in situ generation of H 2 O 2 . The modified cathode had a high H 2 O 2 production with low energy consumption, which was characterized by scanning electron microscopy (SEM), nitrogen adsorption-desorption study and contact angle. The flow-through E-Fenton system was compared to the flow-by and regular one, and confirmed to be best on MB removal and TOC degradation. The operational parameters such as current density, pH, Fe 2+ concentration and flow rate were optimized. The MB and TOC removal efficiency of the effluents could keep above 90% and 50%, respectively, and the energy consumption was 23.0 kWh/kgTOC at the current density of 50 mA, pH 3, 0.3 mM Fe 2+ , and the flow rate of 7 mL/min. ·OH was proved to be the main oxidizing species in this system. After 5 times operation, the system, especially cathode, still showed good stability. Five more organic pollutants including orange II (OG), tartrazine, acetylsalicylic acid (ASA), tetracycline (TC) and 2,4-dichlorophen (2,4-DCP) were investigated and the electric energy consumption (EEC) was compared with literatures. All results demonstrated that this flow-through E-Fenton system was energy-efficient and potential for degradation of organic pollutants.

  1. Pretreatment of furfural industrial wastewater by Fenton, electro-Fenton and Fe(II)-activated peroxydisulfate processes: a comparative study.

    Science.gov (United States)

    Yang, C W; Wang, D; Tang, Q

    2014-01-01

    The Fenton, electro-Fenton and Fe(II)-activated peroxydisulfate (PDS) processes have been applied for the treatment of actual furfural industrial wastewater in this paper. Through the comparative study of the three processes, a suitable pretreatment technology for actual furfural wastewater treatment was obtained, and the mechanism and dynamics process of this technology is discussed. The experimental results show that Fenton technology has a good and stable effect without adjusting pH of furfural wastewater. At optimal conditions, which were 40 mmol/L H₂O₂ initial concentration and 10 mmol/L Fe²⁺ initial concentration, the chemical oxygen demand (COD) removal rate can reach 81.2% after 90 min reaction at 80 °C temperature. The PDS process also has a good performance. The COD removal rate could attain 80.3% when Na₂S₂O₈ initial concentration was 4.2 mmol/L, Fe²⁺ initial concentration was 0.1 mol/L, the temperature remained at 70 °C, and pH value remained at 2.0. The electro-Fenton process was not competent to deal with the high-temperature furfural industrial wastewater and only 10.2% COD was degraded at 80 °C temperature in the optimal conditions (2.25 mA/cm² current density, 4 mg/L Na₂SO₄, 0.3 m³/h aeration rate). For the Fenton, electro-Fenton and PDS processes in pretreatment of furfural wastewater, their kinetic processes follow the pseudo first order kinetics law. The pretreatment pathways of furfural wastewater degradation are also investigated in this study. The results show that furfural and furan formic acid in furfural wastewater were preferentially degraded by Fenton technology. Furfural can be degraded into low-toxicity or nontoxic compounds by Fenton pretreatment technology, which could make furfural wastewater harmless and even reusable.

  2. Design of a visible light driven photo-electrochemical/electro-Fenton coupling oxidation system for wastewater treatment

    International Nuclear Information System (INIS)

    Ding, Xing; Ai, Zhihui; Zhang, Lizhi

    2012-01-01

    Highlights: ► Coupling PEC and EF oxidation significantly improves pollutant degradation efficiency. ► The degradation of the PEC/EF system was increased by 154%. ► The instantaneous current efficiency of the PEC/EF system was increased by 26%. - Abstract: In this study, we report on a photo-electrochemical/electro-Fenton oxidation (PEC/EF) system by coupling visible light driven photo-electrochemical oxidation (PEC) and electro-Fenton oxidation (EF) in an undivided cell. Bi 2 WO 6 nanoplates deposited on FTO glass (Bi 2 WO 6 /FTO) and Fe-Fe 2 O 3 core–shell nanowires supported on activated carbon fiber (Fe-Fe 2 O 3 /ACF) were used as the anode and the cathode in the PEC/EF system, respectively. This novel PEC/EF system showed much higher activity than the single PEC and EF systems on degradation of rhodamine B in aqueous solution at natural pH. Moreover, the degradation and the instantaneous current efficiencies of the PEC/EF system were increased by 154% and 26% in comparison with the sum of those of single PEC and EF systems, respectively. These significant enhancements could be attributed to the synergetic effect from better separation of photo-generated carriers in the photo-anode and the transfer of photo-electrons to the oxygen diffusion cathode to generate more electro-generated H 2 O 2 and hydroxyl radicals on the Fenton cathode. The better separation of photo-generated carriers contribute more to the overall degradation enhancement than the photo-electrons generated H 2 O 2 and the subsequent Fenton reaction on the cathode during the PEC/EF process.

  3. Mineralization of hetero bi-functional reactive dye in aqueous solution by Fenton and photo-Fenton reactions.

    Science.gov (United States)

    Torrades, Francesc; García-Hortal, José Antonio; García-Montaño, Julia

    2015-01-01

    This study focused on the advanced oxidation of the hetero bi-functional reactive dye Sumifix Supra Yellow 3RF (CI Reactive Yellow 145) using dark Fenton and photo-Fenton conditions in a lab-scale experiment. A 2(3) factorial design was used to evaluate the effects of the three key factors: temperature, Fe(II) and H2O2 concentrations, for a dye concentration of 250 mg L(-1) with chemical oxygen demand (COD) of 172 mg L(-1) O2 at pH=3. The response function was the COD reduction. This methodology lets us find the effects and interactions of the studied variables and their roles in the efficiency of the treatment process. In the optimization, the correlation coefficients for the model (R2) were 0.948 and 0.965 for Fenton and photo-Fenton treatments, respectively. Under optimized reaction conditions: pH=3, temperature=298 K, [H2O2]=11.765 mM and [Fe(II)]=1.075 mM; 60 min of treatment resulted in a 79% and 92.2% decrease in COD, for the dye taken as the model organic compound, after Fenton and photo-Fenton treatments, respectively.

  4. FENTON-DRIVEN REGENERATION OF GRANULAR ACTIVATED CARBON: A TECHNOLOGY OVERVIEW

    Science.gov (United States)

    A Fenton-driven mechanism for regenerating spent granular activated carbon (GAC) involves the combined, synergistic use of two reliable and well established treatment technologies - adsorption onto activated carbon and Fenton oxidation. During carbon adsorption treatment, enviro...

  5. Citric Acid-Modified Fenton's Reaction for the Oxidation of Chlorinated Ethylenes in Soil Solution Systems

    Energy Technology Data Exchange (ETDEWEB)

    Seol, Yongkoo; Javandel, Iraj

    2008-03-15

    Fenton's reagent, a solution of hydrogen peroxide and ferrous iron catalyst, is used for an in-situ chemical oxidation of organic contaminants. Sulfuric acid is commonly used to create an acidic condition needed for catalytic oxidation. Fenton's reaction often involves pressure buildup and precipitation of reaction products, which can cause safety hazards and diminish efficiency. We selected citric acid, a food-grade substance, as an acidifying agent to evaluate its efficiencies for organic contaminant removal in Fenton's reaction, and examined the impacts of using citric acid on the unwanted reaction products. A series of batch and column experiments were performed with varying H{sub 2}O{sub 2} concentrations to decompose selected chlorinated ethylenes. Either dissolved iron from soil or iron sulfate salt was added to provide the iron catalyst in the batch tests. Batch experiments revealed that both citric and sulfuric acid systems achieved over 90% contaminant removal rates, and the presence of iron catalyst was essential for effective decontamination. Batch tests with citric acid showed no signs of pressure accumulation and solid precipitations, however the results suggested that an excessive usage of H{sub 2}O{sub 2} relative to iron catalysts (Fe{sup 2+}/H{sub 2}O{sub 2} < 1/330) would result in lowering the efficiency of contaminant removal by iron chelations in the citric acid system. Column tests confirmed that citric acid could provide suitable acidic conditions to achieve higher than 55% contaminant removal rates.

  6. Environmental sustainability of the solar photo-Fenton process for wastewater treatment and pharmaceuticals mineralization at semi-industrial scale.

    Science.gov (United States)

    Foteinis, Spyros; Monteagudo, Jose Maria; Durán, Antonio; Chatzisymeon, Efthalia

    2018-01-15

    The environmental sustainability of a semi-industrial solar photo-Fenton reactor, treating real effluents emanating from a pharmaceutical laboratory, is assessed herein. The life cycle assessment/analysis (LCA) methodology was employed and real life cycle inventory (LCI) data was collected from a ferrioxalate-assisted homogeneous solar photo-Fenton wastewater treatment plant (WWTP), at Ciudad Real, Spain. Electricity was provided by photovoltaic (PV) panels in tandem with a battery bank, making the plant autonomous from the local grid. The effective treatment of 1m 3 of secondary-treated pharmaceutical wastewater, containing antipyrine, was used as a functional unit. The main environmental hotspot was identified to be the chemical reagents used to enhance treatment efficiency, mainly hydrogen peroxide (H 2 O 2 ) and to a smaller degree oxalic acid. On the other hand, land use, PV panels, battery units, compound parabolic collectors (CPC), tanks, pipes and pumps, as materials, had a low contribution, ranging from as little as 0.06% up to about 2% on the total CO 2eq emissions. Overall, the solar photo-Fenton process was found to be a sustainable technology for treating wastewater containing micropollutants at semi-industrial level, since the total environmental footprint was found to be 2.71kgCO 2 m -3 or 272mPtm -3 , using IPCC 2013 and ReCiPe impact assessment methods, respectively. A sensitivity analysis revealed that if the excess of solar power is fed back into the grid then the total environmental footprint is reduced. Depending on the amount of solar power fed back into the grid the process could have a near zero total environmental footprint. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Treatment of hazardous landfill leachate using Fenton process followed by a combined (UASB/DHS) system.

    Science.gov (United States)

    Ismail, Sherif; Tawfik, Ahmed

    2016-01-01

    Fenton process for pre-treatment of hazardous landfill leachate (HLL) was investigated. Total, particulate and soluble chemical oxygen demand (CODt, CODp and CODs) removal efficiency amounted to 67%, 47% and 64%, respectively, at pH value of 3.5, molar ratio (H2O2/Fe(2+)) of 5, H2O2 dosage of 25 ml/L and contact time of 15 min. Various treatment scenarios were attempted and focused on studying the effect of pre-catalytic oxidation process on the performance of up-flow anaerobic sludge blanket (UASB), UASB/down-flow hanging sponge (DHS) and DHS system. The results obtained indicated that pre-catalytic oxidation process improved the CODt removal efficiency in the UASB reactor by a value of 51.4%. Overall removal efficiencies of CODt, CODs and CODp were 80 ± 6%, 80 ± 7% and 78 ± 16% for UASB/DHS treating pre-catalytic oxidation effluent, respectively. The removal efficiencies of CODt, CODs and CODp were, respectively, decreased to 54 ± 2%, 49 ± 2% and 71 ± 16% for UASB/DHS system without pre-treatment. However, the results for the combined process (UASB/DHS) system is almost similar to those obtained for UASB reactor treating pre-catalytic oxidation effluent. The DHS system achieved average removal efficiencies of 52 ± 4% for CODt, 51 ± 4% for CODs and 52 ± 15% for CODp. A higher COD fractions removal was obtained when HLL was pre-treated by Fenton reagent. The combined processes provided a removal efficiency of 85 ± 1% for CODt, 85 ± 1% for CODs and 83 ± 8% for CODp. The DHS system is not only effective for organics degradation but also for ammonia oxidation. Almost complete ammonia (NH4-N) removal (92 ± 3.6%) was occurred and the nitrate production amounted to 37 ± 6 mg/L in the treated effluent. This study strongly recommends applying Fenton process followed by DHS system for treatment of HLL.

  8. Degradation of trans-ferulic acid in acidic aqueous medium by anodic oxidation, electro-Fenton and photoelectro-Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Flores, Nelly; Sirés, Ignasi; Garrido, José Antonio; Centellas, Francesc; Rodríguez, Rosa María; Cabot, Pere Lluís; Brillas, Enric, E-mail: brillas@ub.edu

    2016-12-05

    Highlights: • trans-Ferulic acid degradation by EAOPs using a stirred BDD/air-diffusion cell. • Slow substrate abatement and poor mineralization by AO-H{sub 2}O{sub 2}. • 98% Mineralization by PEF, but with rapid and similar substrate decay than by EF. • Quicker degradation by SPEF due to the more potent photolytic action of sunlight. • Reaction pathway with four primary aromatic products and three final carboxylic acids. - Abstract: Solutions of pH 3.0 containing trans-ferulic acid, a phenolic compound in olive oil mill wastewater, have been comparatively degraded by anodic oxidation with electrogenerated H{sub 2}O{sub 2} (AO-H{sub 2}O{sub 2}), electro-Fenton (EF) and photoelectro-Fenton (PEF). Trials were performed with a BDD/air-diffusion cell, where oxidizing ·OH was produced from water discharge at the BDD anode and/or in the solution bulk from Fenton’s reaction between cathodically generated H{sub 2}O{sub 2} and added catalytic Fe{sup 2+}. The substrate was very slowly removed by AO-H{sub 2}O{sub 2}, whereas it was very rapidly abated by EF and PEF, at similar rate in both cases, due to its fast reaction with ·OH in the bulk. The AO-H{sub 2}O{sub 2} process yielded a slightly lower mineralization than EF, which promoted the accumulation of barely oxidizable products like Fe(III) complexes. In contrast, the fast photolysis of these latter species under irradiation with UVA light in PEF led to an almost total mineralization with 98% total organic carbon decay. The effect of current density and substrate concentration on the performance of all treatments was examined. Several solar PEF (SPEF) trials showed its viability for the treatment of wastewater containing trans-ferulic acid at larger scale. Four primary aromatic products were identified by GC–MS analysis of electrolyzed solutions, and final carboxylic acids like fumaric, acetic and oxalic were detected by ion-exclusion HPLC. A reaction sequence for trans-ferulic acid mineralization

  9. Combined photo-Fenton-SBR process for antibiotic wastewater treatment

    Energy Technology Data Exchange (ETDEWEB)

    Elmolla, Emad S., E-mail: em_civil@yahoo.com [Department of Civil Engineering, Faculty of Engineering, Al-Azhar University, Cairo (Egypt); Chaudhuri, Malay [Department of Civil Engineering, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia)

    2011-09-15

    Highlights: {center_dot} The work focused on hazardous wastewater (antibiotic wastewater) treatment. {center_dot} Complete degradation of the antibiotics achieved by the treatment process. {center_dot} The SBR performance was found to be very sensitive to BOD{sub 5}/COD ratio below 0.40. {center_dot} Combined photo-Fenton-SBR process is a feasible treatment process for the antibiotic wastewater. - Abstract: The study examined combined photo-Fenton-SBR treatment of an antibiotic wastewater containing amoxicillin and cloxacillin. Optimum H{sub 2}O{sub 2}/COD and H{sub 2}O{sub 2}/Fe{sup 2+} molar ratio of the photo-Fenton pretreatment were observed to be 2.5 and 20, respectively. Complete degradation of the antibiotics occurred in one min. The sequencing batch reactor (SBR) was operated at different hydraulic retention times (HRTs) with the wastewater treated under different photo-Fenton operating conditions (H{sub 2}O{sub 2}/COD and H{sub 2}O{sub 2}/Fe{sup 2+} molar ratio). The SBR performance was found to be very sensitive to BOD{sub 5}/COD ratio of the photo-Fenton treated wastewater. Statistical analysis of the results indicated that it was possible to reduce the Fe{sup 2+} dose and increase the irradiation time of the photo-Fenton pretreatment. The best operating conditions of the combined photo-Fenton-SBR treatment were observed to be H{sub 2}O{sub 2}/COD molar ratio 2, H{sub 2}O{sub 2}/Fe{sup 2+} molar ratio 150, irradiation time 90 min and HRT of 12 h. Under the best operating conditions, 89% removal of sCOD with complete nitrification was achieved and the SBR effluent met the discharge standards.

  10. Combined photo-Fenton-SBR process for antibiotic wastewater treatment

    International Nuclear Information System (INIS)

    Elmolla, Emad S.; Chaudhuri, Malay

    2011-01-01

    Highlights: · The work focused on hazardous wastewater (antibiotic wastewater) treatment. · Complete degradation of the antibiotics achieved by the treatment process. · The SBR performance was found to be very sensitive to BOD 5 /COD ratio below 0.40. · Combined photo-Fenton-SBR process is a feasible treatment process for the antibiotic wastewater. - Abstract: The study examined combined photo-Fenton-SBR treatment of an antibiotic wastewater containing amoxicillin and cloxacillin. Optimum H 2 O 2 /COD and H 2 O 2 /Fe 2+ molar ratio of the photo-Fenton pretreatment were observed to be 2.5 and 20, respectively. Complete degradation of the antibiotics occurred in one min. The sequencing batch reactor (SBR) was operated at different hydraulic retention times (HRTs) with the wastewater treated under different photo-Fenton operating conditions (H 2 O 2 /COD and H 2 O 2 /Fe 2+ molar ratio). The SBR performance was found to be very sensitive to BOD 5 /COD ratio of the photo-Fenton treated wastewater. Statistical analysis of the results indicated that it was possible to reduce the Fe 2+ dose and increase the irradiation time of the photo-Fenton pretreatment. The best operating conditions of the combined photo-Fenton-SBR treatment were observed to be H 2 O 2 /COD molar ratio 2, H 2 O 2 /Fe 2+ molar ratio 150, irradiation time 90 min and HRT of 12 h. Under the best operating conditions, 89% removal of sCOD with complete nitrification was achieved and the SBR effluent met the discharge standards.

  11. Investigation of optimum conditions and costs estimation for degradation of phenol by solar photo-Fenton process

    Science.gov (United States)

    Gar Alalm, Mohamed; Tawfik, Ahmed; Ookawara, Shinichi

    2017-03-01

    In this study, solar photo-Fenton reaction using compound parabolic collectors reactor was assessed for removal of phenol from aqueous solution. The effect of irradiation time, initial concentration, initial pH, and dosage of Fenton reagent were investigated. H2O2 and aromatic intermediates (catechol, benzoquinone, and hydroquinone) were quantified during the reaction to study the pathways of the oxidation process. Complete degradation of phenol was achieved after 45 min of irradiation when the initial concentration was 100 mg/L. However, increasing the initial concentration up to 500 mg/L inhibited the degradation efficiency. The dosage of H2O2 and Fe+2 significantly affected the degradation efficiency of phenol. The observed optimum pH for the reaction was 3.1. Phenol degradation at different concentration was fitted to the pseudo-first order kinetic according to Langmuir-Hinshelwood model. Costs estimation for a large scale reactor based was performed. The total costs of the best economic condition with maximum degradation of phenol are 2.54 €/m3.

  12. Response surface modeling for optimization heterocatalytic Fenton oxidation of persistence organic pollution in high total dissolved solid containing wastewater.

    Science.gov (United States)

    Sekaran, G; Karthikeyan, S; Boopathy, R; Maharaja, P; Gupta, V K; Anandan, C

    2014-01-01

    The rice-husk-based mesoporous activated carbon (MAC) used in this study was precarbonized and activated using phosphoric acid. N2 adsorption/desorption isotherm, X-ray powder diffraction, electron spin resonance, X-ray photoelectron spectroscopy and scanning electron microscopy, transmission electron microscopy, (29)Si-NMR spectroscopy, and diffuse reflectance spectroscopy were used to characterize the MAC. The tannery wastewater carrying high total dissolved solids (TDS) discharged from leather industry lacks biodegradability despite the presence of dissolved protein. This paper demonstrates the application of free electron-rich MAC as heterogeneous catalyst along with Fenton reagent for the oxidation of persistence organic compounds in high TDS wastewater. The heterogeneous Fenton oxidation of the pretreated wastewater at optimum pH (3.5), H2O2 (4 mmol/L), FeSO4[Symbol: see text]7H2O (0.2 mmol/L), and time (4 h) removed chemical oxygen demand, biochemical oxygen demand, total organic carbon and dissolved protein by 86, 91, 83, and 90%, respectively.

  13. Characterization of Reagent Pencils for Deposition of Reagents onto Paper-Based Microfluidic Devices

    Directory of Open Access Journals (Sweden)

    Cheyenne H. Liu

    2017-08-01

    Full Text Available Reagent pencils allow for solvent-free deposition of reagents onto paper-based microfluidic devices. The pencils are portable, easy to use, extend the shelf-life of reagents, and offer a platform for customizing diagnostic devices at the point of care. In this work, reagent pencils were characterized by measuring the wear resistance of pencil cores made from polyethylene glycols (PEGs with different molecular weights and incorporating various concentrations of three different reagents using a standard pin abrasion test, as well as by measuring the efficiency of reagent delivery from the pencils to the test zones of paper-based microfluidic devices using absorption spectroscopy and digital image colorimetry. The molecular weight of the PEG, concentration of the reagent, and the molecular weight of the reagent were all found to have an inverse correlation with the wear of the pencil cores, but the amount of reagent delivered to the test zone of a device correlated most strongly with the concentration of the reagent in the pencil core. Up to 49% of the total reagent deposited on a device with a pencil was released into the test zone, compared to 58% for reagents deposited from a solution. The results suggest that reagent pencils can be prepared for a variety of reagents using PEGs with molecular weights in the range of 2000 to 6000 g/mol.

  14. On-surface Fenton and Fenton-like reactions appraised by paper spray ionization mass spectrometry.

    Science.gov (United States)

    Resende, S F; Oliveira, B S; Augusti, R

    2018-06-21

    On-surface degradation of sildenafil (an adequate substrate as it contains assorted functional groups in its structure) promoted by the Fenton (Fe 2+ / H 2 O 2 ) and Fenton-like (M n+ / H 2 O 2 ; M n+ = Fe 3+ , Co 2+ , Cu 2+ , Mn 2+ ) systems was investigated by using paper spray ionization mass spectrometry (PS-MS). The performance of each system was compared by measuring the ratio between the relative intensities of the ions of m/z 475 (protonated sildenafil) and m/z 235 (protonated lidocaine, used as a convenient internal standard and added to the paper just before the PS-MS analyzes). The results indicated the following order in the rates of such reactions: Fe 2+ /H 2 O 2 > H 2 O 2 > Cu 2+ /H 2 O 2 > M n+ / H 2 O 2 (M n+ = Fe 3+ , Co 2+ , Mn 2+ ) ~ M n+ (M n+ = Fe 2+ , Fe 3+ , Co 2+ , Cu 2+ , Mn 2 . The superior capability of Fe 2+ /H 2 O 2 in causing the degradation of sildenafil indicates that Fe 2+ efficiently decomposes H 2 O 2 to yield hydroxyl radicals, quite reactive species that cause the substrate oxidation. The results also indicate that H 2 O 2 can spontaneously decompose likely to yield hydroxyl radicals, although in a much smaller extension than the Fenton system. This effect, however, is strongly inhibited by the presence of the other cations, i. e. Fe 3+ , Co 2+ , Cu 2+ and Mn 2+ . A unique oxidation by-product was detected in the reaction between Fe 2+ /H 2 O 2 with sildenafil and a possible structure for it was proposed based on the MS/MS data. The on-surface reaction of other substrates (trimethoprim and tamoxifen) with the Fenton system was also investigated. In conclusion, PS-MS shown to be a convenient platform to promptly monitor on-surface oxidation reactions. This article is protected by copyright. All rights reserved.

  15. Enhancement of oxygen diffusion process on a rotating disk electrode for the electro-Fenton degradation of tetracycline

    International Nuclear Information System (INIS)

    Zhang, Yan; Gao, Ming-Ming; Wang, Xin-Hua; Wang, Shu-Guang; Liu, Rui-Ting

    2015-01-01

    An electro-Fenton process was developed for wastewater treatment in which hydrogen peroxide was generated in situ with a rotating graphite disk electrode as cathode. The maximum H 2 O 2 generation rate for the RDE reached 0.90 mg/L/h/cm 2 under the rotation speed of 400 rpm at pH 3, and −0.8 V vs SCE. The performance of this electro-Fenton reactor was assessed by tetracycline degradation in an aqueous solution. Experimental results showed the rotation of disk cathode resulted in the efficient production of H 2 O 2 without oxygen aeration, and excellent ability for degrading organic pollutants compared to the electro-Fenton system with fixed cathode. Tetracycline of 50 mg/L was degraded completely within 2 h with the addition of ferrous ion (1.0 mM). The chronoamperometry analysis was employed to investigate the oxygen diffusion on the rotating cathode. The results demonstrated that the diffusion coefficients of dissolved oxygen is 19.45 × 10 −5 cm 2 /s, which is greater than that reported in the literature. Further calculation indicated that oxygen is able to diffuse through the film on the rotating cathode within the contact time in each circle. This study proves that enhancement of oxygen diffusion on RDE is benefit for H 2 O 2 generation, thus provides a promising method for organic pollutants degradation by the combination of RDE with electro-Fenton reactor and offers a new insight on the oxygen transform process in this new system.

  16. Fenton treatment of bio-treated fermentation-based pharmaceutical wastewater: removal and conversion of organic pollutants as well as estimation of operational costs.

    Science.gov (United States)

    Cheng, Yunqin; Chen, Yunlu; Lu, Juncheng; Nie, Jianxin; Liu, Yan

    2018-04-01

    The Fenton process is used as a tertiary treatment to remove organic pollutants from the effluent of bio-treated pharmaceutical wastewater (EBPW). The optimal and most appropriate Fenton conditions were determined by an orthogonal array test and single-factor experiments. The removal of chemical oxygen demand (COD) was influenced by the following factors in a descending order: H 2 O 2 /Fe(II) molar ratio > H 2 O 2 dosage > reaction time. Under the most appropriate Fenton conditions (H 2 O 2 /Fe(II) molar ratio of 1:1, H 2 O 2 dosage of 120 mg L -1 and reaction time of 10 min), the COD and dissolved organic carbon (DOC) were removed with efficiencies of 62 and 53%, respectively, which met the national discharge standard (GB 21903-2008) for the Lake Tai Basin, China. However, the Fenton treatment was inadequate for removal of N compounds, and the removal of organic nitrogen led to an increment in N-NH 3 from 3.28 to 19.71 mg L -1 . Proteins and polysaccharides were completely removed, and humic acids (HAs) were partly removed with an efficiency of 55%. Three-dimensional excitation/emission matrix spectra (3DEEMs) indicated complete removal of fulvic acid-like substances and 90% reduction in the florescence intensity of humic acid-like substances. Organic pollutants with molecular weights (MW) > 10 kDa were completely removed, MW 5-10 kDa were degraded into smaller MW ones, and some low molecular weight acids (MW 0.1-1 kDa) were mineralized during the Fenton process. Some species, including pharmaceutical intermediates and solvents were detected by gas chromatography-mass spectrometry (GC-MS). The operational costs of the Fenton's treatment were estimated to be 0.58 yuan RMB/m 3 EBPW based on reagent usage and iron sludge treatment and disposal.

  17. A reagent for processing drilling muds

    Energy Technology Data Exchange (ETDEWEB)

    Polyakov, G.A.; Khon-Pak, A.T.; Khon, A.V.; Normatov, L.N.; Telegin, B.V.

    1983-01-01

    A reagent is proposed for processing drilling muds. It contains an acrylic polymer and potassium permanganate. The reagent is distinguished by the fact that in order to improve the quality of the drilling muds by increasing their salt resistance, the reagent contains hydrolized nitron fiber as the acrylic polymer with the following component relationship (in percent by weight): potassium permanganate, 0.015 to 0.065 and hydrolyzed nitron fiber, the remainder.

  18. Magnetic minerals from volcanic Ultisols as heterogeneous Fenton catalysts

    International Nuclear Information System (INIS)

    Aravena, S.; Pizarro, C.; Rubio, M. A.; Cavalcante, L. C. D.; Garg, V. K.; Pereira, M. C.; Fabris, J. D.

    2010-01-01

    This study was devoted to the evaluation of the effectiveness of Fenton catalysts, based on magnetically-concentrated portions of iron oxide-rich sand fractions from two magnetic Ultisols, derived from volcanic materials of southern Chile. The samples were labeled according to the municipality where the sample sites are geographically located, namely Metrenco and Collipulli, and were characterized with Moessbauer spectroscopy at 298 K and saturation magnetization (σ) measurements. Moessbauer data revealed a complex magnetic hyperfine structure for these magnetic portions from both soil-sand materials, suggesting relatively complex mineral assemblages. The monitored rate of H 2 O 2 decomposition via heterogeneous Fenton reaction revealed that materials from the Collipulli soil are more efficient Fenton catalyst than are those from the Metrenco soil. The reasons for these differences are from now on being explored on basis of a more detailed chemical investigation of these samples.

  19. Remediation of Cu metal-induced accelerated Fenton reaction by potato peels bio-sorbent.

    Science.gov (United States)

    Azmat, Rafia; Moin, Sumeira; Saleem, Ailyan

    2016-12-01

    This article has allied exposure to Ecological Particulate Matter (EPM) and its remediation using potato peel surface (PPC) bio-sorbent on two important edible crops Spinacia oleracea and Luffa acutangula. Fenton reaction acceleration was one of the major stress oxidation reactions as a consequence of iron and copper toxicity, which involve in the formation of hydroxyl radical (OH) through EPM. Results showed that the oxidative stress encouraged by Cu in both species that recruits the degradation of photosynthetic pigments, initiating decline in growth, reduced leaf area and degrade proteins. The plants were cultivated in natural environmental condition in three pots with three replicates like (a) control, (b) Cu treated and (c) treated water. Oxidative stress initiated by metal activity in Cu accumulated plant (b) were controlled, through bio-sorption of metal from contaminated water using PPC; arranged at laboratory scale. The acceleration of Fenton reaction was verified in terms of OH radical generation. These radicals were tested in aqueous extract of leaves of three types of plants via benzoic acid. The benzoic acid acts as a scavenger of OH radical due to which the decarboxylation of benzoic acid cured. Observation on (b) showed more rapid decarboxylation as compared to other plants which showed that Cu activity was much higher in (b) as compared to (a) and (c). The rapid decarboxylation of benzoic acid and lower chlorophyll contents in (b) suggest that Fenton reaction system was much enhanced by Cu-O and Fe-O chemistry that was successfully controlled by PPC which results in restoring the metabolic pathway and nullifying oxidative stress in (c).

  20. A Catalyst-Free Amination of Functional Organolithium Reagents by Flow Chemistry.

    Science.gov (United States)

    Kim, Heejin; Yonekura, Yuya; Yoshida, Jun-Ichi

    2018-04-03

    Reported is the electrophilic amination of functional organolithium intermediates with well-designed aminating reagents under mild reaction conditions using flow microreactors. The aminating reagents were optimized to achieve efficient C-N bond formation without using any catalyst. The electrophilic amination reactions of functionalized aryllithiums were successfully conducted under mild reaction conditions, within 1 minute, by using flow microreactors. The aminating reagent was also prepared by the flow method. Based on stopped-flow NMR analysis, the reaction time for the preparation of the aminating reagent was quickly optimized without the necessity of work-up. Integrated one-flow synthesis consisting of the generation of an aryllithium, the preparation of an aminating reagent, and their combined reaction was successfully achieved to give the desired amine within 5 minutes of total reaction time. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Niobium substituted magnetite as a strong heterogeneous Fenton catalyst for wastewater treatment

    Energy Technology Data Exchange (ETDEWEB)

    Rahim Pouran, Shima, E-mail: rahimpooran@yahoo.com [Chemical Engineering Department, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Abdul Aziz, A.R., E-mail: azizraman@um.edu.my [Chemical Engineering Department, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Wan Daud, Wan Mohd Ashri, E-mail: ashri@um.edu.my [Chemical Engineering Department, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Embong, Zaidi, E-mail: zembong@gmail.com [Faculty of Science, Technology and Human Development, University Tun Hussein Onn Malaysia, 86400 Johor (Malaysia)

    2015-10-01

    Highlights: • A series of Nb substituted magnetite samples were prepared and characterized. • Samples had inverse spinel structure, good magnetic property, and durability. • Increased surface area resulted in higher adsorption capacity of the samples. • Nb incorporation enhanced degradation of methylene blue through Fenton reaction. • The activity of the catalysts increased by increment in Nb content of the samples. - Abstract: In this study, a series of Nb substituted magnetites; Fe{sub 3−x}Nb{sub x}O{sub 4} (x = 0.0, 0.022, 0.049, 0.099, and 0.19) were prepared and characterized by XRD, BET surface area, TEM, VSM, XPS, and chemical experiments. The magnetite inverse spinel structure and magnetic property were maintained in all the synthetized samples. A significant decrease in crystal size (≈two times) and increase in specific surface area (≈three times) were observed with increased Nb content, resulting in higher adsorption capacity of the samples. In addition, the reactivity of the synthetized samples was examined through degradation of methylene blue solution using Fenton-like reaction. It was found that the incorporation of niobium significantly improved the degradation of methylene blue of which total MB removal was achieved within 180 min at higher molar ratios of Nb (x = 0.19). This could be attributed to the generated oxygen vacancies on the surface of catalysts, the contribution of the introduced Nb cations in Fenton oxidation cycle for regeneration of Fe{sup 2+} cations, and increase in adsorption capacity of the samples due to larger surface area. The MB degradation through Fe{sub 2.79}Nb{sub 0.19}O{sub 4}/H{sub 2}O{sub 2} system was well described by the pseudo-first-order equation in kinetics. All samples showed good stability under the studied pH conditions. The amount of niobium leached was not detectable in neutral and basic solutions and the samples could be reused in oxidation process for several times without a significant

  2. Study of the intensification of solar photo-Fenton degradation of carbamazepine with ferrioxalate complexes and ultrasound.

    Science.gov (United States)

    Expósito, A J; Monteagudo, J M; Durán, A; San Martín, I; González, L

    2018-01-15

    The intensification of the solar photo-Fenton system with ferrioxalate photoactive complexes and ultrasound applied to the mineralization of 15mg/L carbamazepine aqueous solution (CBZ) was evaluated. The experiments were carried out in a solar compound parabolic collector (CPC) pilot plant reactor coupled to an ultrasonic processor. The dynamic behavior of hydroxyl radicals generated under the different studied reaction systems was discussed. The initial concentrations of hydrogen peroxide and ferrous/oxalic acid and pH were found to be the most significant variables (32.79%, 25.98% and 26.04%, respectively). Under the selected optimal conditions ([H 2 O 2 ] 0 =150mg/L; [Fe 2+ ] 0 =2.5mg/L/[(COOH) 2 ] 0 =12.1mg/L; pH=5) CBZ was fully degraded after 5min and 80% of TOC was removed using a solar photo-Fenton system intensified with ferrioxalate (SPFF). However, no improvement in the mineralization using SPFF process combined with ultrasound was observed. More mild pH conditions could be used in the SPFF system if compared to the traditional photo-Fenton (pH 3) acidic systems. Finally, a possible reaction pathway for the mineralization of CBZ by the SPFF system was proposed and therein discussed. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Elimination of pyraclostrobin by simultaneous microbial degradation coupled with the Fenton process in microbial fuel cells and the microbial community.

    Science.gov (United States)

    Zhao, Huanhuan; Kong, Chui-Hua

    2018-06-01

    The elimination of pyraclostrobin by simultaneous microbial degradation and Fenton oxidation was achieved in a microbial fuel cell (MFC) system. After 12 h of incubation, the removal rate of pyraclostrobin was 1.4 mg/L/h at the anode and 1.7 mg/L/h at the cathode. The pyraclostrobin concentration was less than the detection limit (0.1 mg/L) after 72 h at the anode and 24 h at the cathode. The air flow rate, temperature, and pH of the catholyte had significant effects on the generation of H 2 O 2 . The maximum production of H 2 O 2 was 1.2 mg/L after reaction for 20 h during the Fenton process. Microbial community analysis indicated that functional bacteria in the genera Chryseobacterium, Stenotrophomonas, Arcobacter, and Comamonas were predominant in the anodic biofilm. In conclusion, the MFC-Fenton system provides an effective approach for treating environmental contaminants. Copyright © 2018 Elsevier Ltd. All rights reserved.

  4. Comparison of TiO2 photocatalysis, electrochemically assisted Fenton reaction and direct electrochemistry for simulation of phase I metabolism reactions of drugs.

    Science.gov (United States)

    Ruokolainen, Miina; Gul, Turan; Permentier, Hjalmar; Sikanen, Tiina; Kostiainen, Risto; Kotiaho, Tapio

    2016-02-15

    The feasibility of titanium dioxide (TiO2) photocatalysis, electrochemically assisted Fenton reaction (EC-Fenton) and direct electrochemical oxidation (EC) for simulation of phase I metabolism of drugs was studied by comparing the reaction products of buspirone, promazine, testosterone and 7-ethoxycoumarin with phase I metabolites of the same compounds produced in vitro by human liver microsomes (HLM). Reaction products were analysed by UHPLC-MS. TiO2 photocatalysis simulated the in vitro phase I metabolism in HLM more comprehensively than did EC-Fenton or EC. Even though TiO2 photocatalysis, EC-Fenton and EC do not allow comprehensive prediction of phase I metabolism, all three methods produce several important metabolites without the need for demanding purification steps to remove the biological matrix. Importantly, TiO2 photocatalysis produces aliphatic and aromatic hydroxylation products where direct EC fails. Furthermore, TiO2 photocatalysis is an extremely rapid, simple and inexpensive way to generate oxidation products in a clean matrix and the reaction can be simply initiated and quenched by switching the UV lamp on/off. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Fenton Redox Chemistry : Arsenite Oxidation by Metallic Surfaces

    NARCIS (Netherlands)

    Borges Freitas, S.C.; Van Halem, D.; Badruzzaman, A.B.M.; Van der Meer, W.G.J.

    2014-01-01

    Pre-oxidation of As(III) is necessary in arsenic removal processes in order to increase its efficiency. Therefore, the Fenton Redox Chemistry is defined by catalytic activation of H2O2 and currently common used for its redox oxidative properties. In this study the effect of H2O2 production catalysed

  6. Influence of dihydroxybenzenes on paracetamol and ciprofloxacin degradation and iron(III) reduction in Fenton processes.

    Science.gov (United States)

    Costa E Silva, Beatriz; de Lima Perini, João Angelo; Nogueira, Raquel F Pupo

    2017-03-01

    The degradation of paracetamol (PCT) and ciprofloxacin (CIP) was compared in relation to the generation of dihydroxylated products, Fe(III) reduction and reaction rate in the presence of dihydroxybenzene (DHB) compounds, or under irradiation with free iron (Fe 3+ ) or citrate complex (Fecit) in Fenton or photo-Fenton process. The formation of hydroquinone (HQ) was observed only during PCT degradation in the dark, which increased drastically the rate of PCT degradation, since HQ formed was able to reduce Fe 3+ and contributed to PCT degradation efficiency. When HQ was initially added, PCT and CIP degradation rate in the dark was much higher in comparison to the absence of HQ, due to the higher and faster formation of Fe 2+ at the beginning of reaction. In the absence of HQ, no CIP degradation was observed; however, when HQ was added after 30 min, the degradation rate increased drastically. Ten PCT hydroxylated intermediates were identified in the absence of HQ, which could contribute for Fe(III) reduction and consequently to the degradation in a similar way as HQ. During CIP degradation, only one product of hydroxyl radical attack on benzene ring and substitution of the fluorine atom was identified when HQ was added to the reaction medium.

  7. Decontamination of industrial wastewater from sugarcane crops by combining solar photo-Fenton and biological treatments

    Energy Technology Data Exchange (ETDEWEB)

    Mendoza-Marin, Claudia; Osorio, Paula [Department of Chemistry, Faculty of Science, Universidad del Valle, A.A. 25360 Cali (Colombia); Benitez, Norberto, E-mail: lubenite@univalle.edu.co [Department of Chemistry, Faculty of Science, Universidad del Valle, A.A. 25360 Cali (Colombia)

    2010-05-15

    The department of Valle del Cauca is the region with the largest sugarcane production in Colombia. This agricultural activity uses high quantities of herbicides, mainly Diuron and 2,4-Dichlorophenoxyacetic acid. Wastewater generated in the washing process of spray equipment and empty pesticide containers must be treated to keep natural water sources from being polluted with these pesticides when these effluents are disposed off. Conventional biological treatments are not able to remove recalcitrant substances like Diuron and 2,4-Dichlorophenoxyacetic acid; therefore, it is essential to have alternative treatment systems. In recent years, photocatalytic processes have been proven efficient methods in treating polluted water with recalcitrant organic substances. This study sought to evaluate the efficiency of a coupled treatment constituted for a solar photo-Fenton treatment and a biological system like an immobilized biological reactor to treat industrial wastewater containing pesticides (2,4-Dichlorophenoxyacetic acid and Diuron). The mineralization and degradation of pesticides were followed by measuring the dissolved organic carbon and pesticide concentrations. The results revealed that industrial wastewaters with high Diuron and 2,4-Dichlorophenoxyacetic acid concentrations can be successfully treated by a combined solar photo-Fenton-biological system, achieving mineralization of 79.8% in prepared wastewater and 82.5% in real industrial wastewater by using low Fe{sup 2+} and H{sub 2}O{sub 2} concentrations.

  8. Decontamination of industrial wastewater from sugarcane crops by combining solar photo-Fenton and biological treatments

    International Nuclear Information System (INIS)

    Mendoza-Marin, Claudia; Osorio, Paula; Benitez, Norberto

    2010-01-01

    The department of Valle del Cauca is the region with the largest sugarcane production in Colombia. This agricultural activity uses high quantities of herbicides, mainly Diuron and 2,4-Dichlorophenoxyacetic acid. Wastewater generated in the washing process of spray equipment and empty pesticide containers must be treated to keep natural water sources from being polluted with these pesticides when these effluents are disposed off. Conventional biological treatments are not able to remove recalcitrant substances like Diuron and 2,4-Dichlorophenoxyacetic acid; therefore, it is essential to have alternative treatment systems. In recent years, photocatalytic processes have been proven efficient methods in treating polluted water with recalcitrant organic substances. This study sought to evaluate the efficiency of a coupled treatment constituted for a solar photo-Fenton treatment and a biological system like an immobilized biological reactor to treat industrial wastewater containing pesticides (2,4-Dichlorophenoxyacetic acid and Diuron). The mineralization and degradation of pesticides were followed by measuring the dissolved organic carbon and pesticide concentrations. The results revealed that industrial wastewaters with high Diuron and 2,4-Dichlorophenoxyacetic acid concentrations can be successfully treated by a combined solar photo-Fenton-biological system, achieving mineralization of 79.8% in prepared wastewater and 82.5% in real industrial wastewater by using low Fe 2+ and H 2 O 2 concentrations.

  9. Hydrothermal synthesis of bismuth ferrite Fenton-like catalysts and their properties

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Min; Li, Wenjuan, E-mail: liwenjuan2801@163.com; Du, Yong; Kong, Defen; Wang, Ze; Meng, Yi; Sun, Xiaolan; Yan, Tingjiang; Kong, Desheng; You, Jinmao [Qufu Normal University, Shandong Province Key Laboratory of Life-Organic Analysis (China)

    2016-11-15

    Bismuth ferrite, Fenton-like catalysts have been successfully synthesized via simple hydrothermal methods without any templates. Through changing the molar ratio of Bi/Fe, the two main phases BiFeO{sub 3} and Bi{sub 25}FeO{sub 40} can be synthesized under different temperatures. Furthermore, different morphologies of the BiFeO{sub 3} phase can be adjusted by changing different concentrations of HNO{sub 3} and NaOH which were used to dissolve the reactants and adjust the pH values in the prepared process. When the concentration of HNO{sub 3}/NaOH was 8/12 M, some uniform cylindrical bodies with equal height (1 μm) and width (0.6 μm) were obtained, which have not been reported before. The uniform structures exhibited better activities in the photoassisted Fenton-like oxidation process for the degradation of rhodamine B (RhB) under visible light irradiation (420 nm < λ < 800 nm). Through the detection of the degradation mechanism, it showed that the concerted effect of the catalysts and H{sub 2}O{sub 2} can increase the generation of the charge carriers and accelerate the photogenerated charge transfer between the catalysts and dyes. The BiFeO{sub 3} samples also showed magnetic properties at room temperature, which may have potential applications in multiferroic or magnetoelectric sensors and devices.

  10. Enhanced electro-Fenton Mineralization of Acid Orange 7 Using a Carbon Nanotube Fiber Based Cathode

    Science.gov (United States)

    Huong Le, Thi Xuan; Alemán, Belén; Vilatela, Juan J.; Bechelany, Mikhael; Cretin, Marc

    2018-02-01

    A new cathodic material for electro-Fenton (EF) process was prepared based on a macroscopic fiber (CNTF) made of mm long carbon nanotubes directly spun from the gas phase by floating catalyst CVD, on a carbon fiber (CF) substrate. CNTF@CF electrode is a highly graphitic material combining a high surface area ( 260 m2/g) with high electrical conductivity and electrochemical stability . One kind of azo dye, acid orange 7 (AO7), was used as model bio-refractory pollutant to be treated at CNTF@CF cathode in acidic aqueous medium (pH 3.0). The experimental results pointed out that AO7 and its organic intermediate compounds were totally mineralized by hydroxyl radical generated from Fenton reaction. In fact, 96.7 % of the initial TOC was eliminated in 8h of electrolysis by applying a current of -25 mA and ferrous ions as catalyst at concentration of 0.2 mM. At the same electrolysis time, only 23.7 % of TOC removal found on CF support which proved the high mineralization efficiency of new material thanks to CNTs deposition. The CNTF@CF cathode maintained stable its activity during five experimental cycles of EF set-up. The results indicated that CNTF@CF material could be a potential choice for wastewater treatment containing bio-refractory by electrochemical advanced oxidation processes (EAOPs).

  11. Inactivation of rabies diagnostic reagents by gamma radiation

    International Nuclear Information System (INIS)

    Gamble, W.C.; Chappell, W.A.; George, E.H.

    1980-01-01

    Treatment of CVS-11 rabies adsorbing suspensions and street rabies infected mouse brains with gamma radiation resulted in inactivated reagents that are safer to distribute and use. These irradiated reagents were as sensitive and reactive as the nonirradiated control reagents

  12. 21 CFR 866.3780 - Toxoplasma gondii serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3780 Toxoplasma... (immunofluorescent reagents) used to identify Toxoplasma gondii from clinical specimens. The identification aids in...

  13. 21 CFR 866.3375 - Mycoplasma spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3375 Mycoplasma... fluorescent dye (immunofluorescent reagents) used to identify Mycoplasma spp. directly from clinical specimens...

  14. 21 CFR 866.3220 - Entamoeba histolytica serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3220... fluorescent dye (immunofluorescent reagents) used to identify Entamoeba histolytica directly from clinical...

  15. Degradation alternatives for a commercial fungicide in water: biological, photo-Fenton, and coupled biological photo-Fenton processes.

    Science.gov (United States)

    López-Loveira, Elsa; Ariganello, Federico; Medina, María Sara; Centrón, Daniela; Candal, Roberto; Curutchet, Gustavo

    2017-11-01

    Imazalil (IMZ) is a widely used fungicide for the post-harvest treatment of citrus, classified as "likely to be carcinogenic in humans" for EPA, that can be only partially removed by conventional biological treatment. Consequently, specific or combined processes should be applied to prevent its release to the environment. Biological treatment with adapted microorganism consortium, photo-Fenton, and coupled biological photo-Fenton processes were tested as alternatives for the purification of water containing high concentration of the fungicide and the coadjutants present in the commercial formulation. IMZ-resistant consortium with the capacity to degrade IMZ in the presence of a C-rich co-substrate was isolated from sludge coming from a fruit packaging company wastewater treatment plant. This consortium was adapted to resist and degrade the organics present in photo-Fenton-oxidized IMZ water solution. Bacteria colonies from the consortia were isolated and identified. The effect of H 2 O 2 initial concentration and dosage on IMZ degradation rate, average oxidation state (AOS), organic acid concentration, oxidation, and mineralization percentage after photo-Fenton process was determined. The application of biological treatment to the oxidized solutions notably decreased the total organic carbon (TOC) in solution. The effect of the oxidation degree, limited by H 2 O 2 concentration and dosage, on the percentage of mineralization obtained after the biological treatment was determined and explained in terms of changes in AOS. The concentration of H 2 O 2 necessary to eliminate IMZ by photo-Fenton and to reduce TOC and chemical oxygen demand (COD) by biological treatment, in order to allow the release of the effluents to rivers with different flows, was estimated.

  16. Development of national immunoassay reagent programmes

    International Nuclear Information System (INIS)

    Sufi, S.B.; Micallef, J.V.; Ahsan, R.; Goncharov, N.P.

    1992-01-01

    Despite the existence of networks of fully equipped laboratories with well-trained staff, the availability of immunodiagnostic services in developing countries is often limited by the high cost of imported kits. There are a number of ways of tackling this problem, ranging from bulk purchase of kits or reagents to local development and production of assay systems. Argentina/Chile, China, Cuba/Mexico, and Thailand are amongst the countries which have established local immunoassay reagent programmes to manufacture low cost, high quality immunoassay reagents. Kits from these projects are now beginning to become available, and it is hoped that they will promote national diagnostic services and research, as well as stimulating the development of reagent programmes for other analytes. (author). 4 refs, 1 tab

  17. Heterogeneous photo-Fenton degradation of acid red B over Fe{sub 2}O{sub 3} supported on activated carbon fiber

    Energy Technology Data Exchange (ETDEWEB)

    Lan, Huachun [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences,China (China); Wang, Aiming [Department of Municipal and Environmental Engineering, School of Civil Engineering, Beijing Jiaotong University,China (China); Liu, Ruiping, E-mail: liuruiping@rcees.ac.cn [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences,China (China); Liu, Huijuan; Qu, Jiuhui [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences,China (China)

    2015-03-21

    Highlights: • Fe{sub 2}O{sub 3} with small particle size was highly dispersed on activated carbon fiber. • Fe{sub 2}O{sub 3}/ACF exhibited higher photo-Fenton activity toward ARB degradation. • Fe{sub 2}O{sub 3}/ACF has an excellent long-term stability without obvious deactivation. - Abstract: Fe{sub 2}O{sub 3} supported on activated carbon fiber (Fe{sub 2}O{sub 3}/ACF) was prepared via an impregnation method and characterized by X-ray diffraction, scanning electron microscopy and BET analysis. The results indicated that Fe{sub 2}O{sub 3} with small particle size was highly dispersed on the surface of the ACF and the introduction of Fe{sub 2}O{sub 3} did not change the ACF pore structure. Fe{sub 2}O{sub 3}/ACF exhibited a higher Fenton efficiency for the degradation of acid red B (ARB), especially under simulated solar irradiation. Complete decoloration of the ARB solution and 43% removal of TOC could be achieved within 200 min under optimal conditions. It was verified that more ·OH radicals were generated in the photo-assisted Fenton process and involved as active species in ARB degradation. FTIR analysis indicated that the degradation of ARB was initiated through the cleavage of −N=N−, followed by hydroxylation and opening of phenyl rings to form aliphatic acids, and further oxidation of aliphatic acids would produce CO{sub 2} and H{sub 2}O. Moreover, Fe{sub 2}O{sub 3}/ACF maintained its activity after being reused 4 times and the release of iron from the catalyst was found to be insignificant during the Fenton and photo-Fenton processes, indicating that Fe{sub 2}O{sub 3}/ACF had good long-term stability.

  18. Degradação de Corantes Indigoides com Reagente de Fenton para tratamento de efluentes na Industria Têxtil

    OpenAIRE

    Meira, Luís

    2014-01-01

    A indústria têxtil gera grandes quantidades de efluentes, que não sendo tratados podem contaminar os cursos de água. É uma fonte de poluição visível e com produtos tóxicos que perturbam os ecossistemas. Torna-se por isso necessário encontrar tratamentos de efluentes têxteis simples e economicamente viáveis para não acrescentar maior custo ao produto. Pretendeu-se encontrar as condições ideais para a degradação de uma solução de corante Índigo Carmim com diferentes solventes,...

  19. MTBE DEGRADATION USING FENTON'S REAGENT: THE EFFECT OF FERROUS AND FERRIC IRON MIXTURES ON THE EFFICIENCY OF THE OVERALL REACTION

    Science.gov (United States)

    The gasoline additive MTBE has been extensively used in the U.S. since the late 70's to increase the octane rating in reformulated gasoline, replacing toxic organo-lead compounds. However, its use was boosted during the late 80's, when the study of additional physico-chemical pro...

  20. Evaluation of adsorption and Fenton-adsorption processes for landfill leachate treatment

    OpenAIRE

    San Pedro-Cedillo, L.; Méndez-Novelo, R.I.; Rojas-Valencia, M.N.; Barceló-Quintal, M.; Castillo-Borges, E.R.; Sauri-Riancho, M.R.; Marrufo-Gómez, J.M.

    2015-01-01

    The objective of this research was to compare the adsorption and Fenton-adsorption treatments for the removal of contaminants in leachate from landfills and thus determine the most efficient one. The adsorption process with granular activated carbon was tested in two types of samples: raw leachate and leachate treated by Fenton. The results showed color, chemical oxygen demand (COD), total nitrogen and total organic carbon (TOC) removal rates higher than 99% through the Fenton-adsorption proc...

  1. Treatment of amoxicillin by O3/Fenton process in a rotating packed bed.

    Science.gov (United States)

    Li, Mo; Zeng, Zequan; Li, Yingwen; Arowo, Moses; Chen, Jianfeng; Meng, Hong; Shao, Lei

    2015-03-01

    In this study, simulated amoxicillin wastewater was treated by the O3/Fenton process in a rotating packed bed (RPB) and the results were compared with the Fenton process and the O3 followed by Fenton (O3 + Fenton) process. The chemical oxygen demand (COD) removal rate and the ratio of 5-day biological oxygen demand to chemical oxygen demand (BOD5/COD) in the O3/Fenton process were approximately 17% and 26%, respectively, higher than those in the O3 + Fenton process with an initial pH of 3. The COD removal rate of the amoxicillin solution reached maximum at the Fe(II) concentration of 0.6 mM, temperature of 25 °C, rotation speed of 800 rpm and initial pH of 3. The BOD5/COD of the amoxicillin solution increased from 0 to 0.38 after the solution was treated by the O3/Fenton process. Analysis of the intermediates indicated that the pathway of amoxicillin degradation in the O3/Fenton process was similar to that in the O3 + Fenton process. Contrast experiment results showed that amoxicillin degradation was significantly intensified in the RPB. Copyright © 2014 Elsevier Ltd. All rights reserved.

  2. Preparation of a new Fenton-like catalyst from red mud using molasses wastewater as partial acidifying agent.

    Science.gov (United States)

    Wei, Guangtao; Shao, Luhua; Mo, Jihua; Li, Zhongmin; Zhang, Linye

    2017-06-01

    Using molasses wastewater as partial acidifying agent, a new Fenton-like catalyst (ACRM sm ) was prepared through a simple process of acidification and calcination using red mud as main material. With molasses wastewater, both the free alkali and the chemically bonded alkali in red mud were effectively removed under the action of H 2 SO 4 and molasses wastewater, and the prepared ACRM sm was a near-neutral catalyst. The ACRM sm preparation conditions were as follows: for 3 g of red mud, 9 mL of 0.7 mol/L H 2 SO 4 plus 2 g of molasses wastewater as the acidifying agent, calcination temperature 573 K, and calcination time 1 h. Iron phase of ACRM sm was mainly α-Fe 2 O 3 and trace amount of carbon existed in ACRM sm . The addition of molasses wastewater not only effectively reduced the consumption of H 2 SO 4 in acidification of red mud but also resulted in the generation of carbon and significantly improved the distribution of macropore in prepared ACRM sm . It was found that near-neutral pH of catalyst, generated carbon, and wide distribution of macropore were the main reasons for the high catalytic activity of ACRM sm . The generated carbon and wide distribution of macropore were entirely due to the molasses wastewater added. In degradation of orange II, ACRM sm retained most of its catalytic stability and activity after five recycling times, indicating ACRM sm had an excellent long-term stability in the Fenton-like process. Furthermore, the performance test of settling showed ACRM sm had an excellent settleability. ACRM sm was a safe and green catalytic material used in Fenton-like oxidation for wastewater treatment.

  3. Application of the response surface and desirability design to the Lambda-cyhalothrin degradation using photo-Fenton reaction.

    Science.gov (United States)

    Colombo, Renata; Ferreira, Tanare C R; Alves, Suellen A; Carneiro, Renato L; Lanza, Marcos R V

    2013-03-30

    Lambda-cyhalothrin is a potent pyrethroid insecticide used widely in pest management. Detectable levels of the pyrethroid in agricultural watersheds are potentially toxic to aquatic organisms. There is little information in the scientific literature about degradation in aqueous media of the Lambda-cyhalothrin by Advanced Oxidative Process. A mathematical approach for the degradation of this compound has not yet been fully explored… The Central composite design (CCD) and response surface method (RSM) were applied to evaluate and optimize the interactive effects of two operating variables. The initial dosages of H2O2 and Fe(2+) on photo-Fenton degradation of an aqueous solution of Lambda-cyhalothrin in a recirculation flow-through UV photoreactor were used. The remaining concentration of Lambda-cyhalothrin (y1) and the percentage removal of total organic carbon (y2) were the monitored factors since they are dependent parameters of y1 and y2. According to analysis of variances (ANOVA) results, two proposed models can be used to navigate the design space with regression coefficient R(2) - 0.834 and 0.843 for y1 and y2, respectively. A multi-response optimization procedure, based on the global desirability of the factors, was performed to establish the best concentrations of hydrogen peroxide and ferrous sulfate that would allow the most efficient degradation of Lambda-cyhalothrin concomitant with a maximal removal of total organic carbon. The global desirability surface revealed that 0.295 mmol L(-1) of ferrous sulfate and 3.85 mmol L(-1) of hydrogen peroxide were close to the optimum conditions to satisfy both factors simultaneously using minimal amounts of reagents. These photo-Fenton conditions promoted 100% of Lambda-cyhalothrin degradation and 79.83% TOC removal (mineralization) in 120 min of reaction time. Copyright © 2013 Elsevier Ltd. All rights reserved.

  4. The experimental study of a hybrid solar photo-Fenton and photovoltaic system for water purification

    International Nuclear Information System (INIS)

    Jin, Yanchao; Wang, Yiping; Huang, Qunwu; Zhu, Li; Cui, Yong; Cui, Lingyun; Lin, Chunyan

    2017-01-01

    Highlights: • A new solar photo-Fenton and photovoltaic system was performed for the first time. • Acid Red 26, Malachite Green and Reactive Blue 4 were discolored using the system. • The PV panel of the hybrid system could work under lower temperature. • The system achieved self-sufficient energy and could work autonomously. • Solar spectrum could be made full use for power generation and water purification. - Abstract: A new hybrid system that integrated a photovoltaic (PV) panel with a solar photo-Fenton (SPF) reactor was constructed to treat wastewater and generate electricity for the first time. The decolorization and photovoltaic performances of the hybrid system were tested outdoors by discoloring three dyes: Acid Red 26 (AR26), Malachite Green (MG) and Reactive Blue 4 (RB4). Lab scale experiments also had been done to confirm the impact of temperature on the SPF process. The lab scale results show that SPF process was more efficiency for decoloring the different dyes, compared with dark Fenton. The SPF followed a pseudo-first-order reaction and the reaction rate constant was improved about 3.5, 4.5 and 0.61 times for AR26, RB4 and MG respectively as the wastewater temperature increased from 20 to 50 °C. The decolorization difficulty of the three dyes followed this order: MG > AR26 > RB4. The results of the hybrid systems tested outdoors show that 200 mg/L MG had achieved 98.6% color removal after 3 h of treatment at a low catalyst dose (Fe"2"+ = 5 mg/L) under sunlight. For 100 mg/L MG, 99.3% color removal was observed after 70 min. The treatment time required for decolorization of AR26 and RB4 was more shorter. In the present of the water layer, the wastewater temperature was increased and that of the hybrid system was decreased. The average output power of the hybrid system was more than 12 W and sufficient to drive the system during all of the outdoor experiments. Our results suggest that the system could realize decolorization of different

  5. The adsorption of chelating reagents on oxide minerals

    International Nuclear Information System (INIS)

    Bryson, M.A.W.

    1984-06-01

    This work constitutes a fundamental study of the interaction between chelating reagents and oxide minerals. The adsorption mechanisms have been elucidated for most of the systems generated by the oxides of copper(II) or iron(III) and chelating reagents octyl hydroxamate, N-phenylbenzohydroxamate, salicylaldoxime, 5-nitro-salicylaldoxime or 8-hydroxyquinoline. In order to better understand the adsorption process associated with copper(II) oxide, the oxide was recrystallized to produce a coarser material with a more uniform surface. This allowed the oxide surface to be viewed under the scanning electron microscope. A detailed investigation of the effect of the system variables; pH, conditioning period, concentration, temperature, surface area and dispersing reagent on the rate of precipitation of the copper chelate species of general form, Cu(chel) 2 , was made. In addition the chemical nature of the adsorbed species and the structural form of the precipitates were determined with the aid of infra-red spectroscopy and the scanning electron microscope. On the basis of these results a model has been formulated for the adsorption processes. The precipitation process was examined in more detail by the study of the adsorption of chelate on copper metal. Contact angle measurements of air bubbles on copper metal conditioned with chelate were related to the adsorption results in an attempt to isolate the optimum conditions for flotation of oxide minerals

  6. 21 CFR 866.3200 - Echinococcus spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Echinococcus spp. serological reagents. 866.3200... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3200 Echinococcus spp. serological reagents. (a) Identification. Echinococcus spp. serological reagents are devices that...

  7. 21 CFR 866.3405 - Poliovirus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Poliovirus serological reagents. 866.3405 Section... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3405 Poliovirus serological reagents. (a) Identification. Poliovirus serological reagents are devices that consist of antigens...

  8. 21 CFR 866.3415 - Pseudomonas spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Pseudomonas spp. serological reagents. 866.3415... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3415 Pseudomonas spp. serological reagents. (a) Identification. Pseudomonas spp. serological reagents are devices that...

  9. 21 CFR 866.3350 - Leptospira spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Leptospira spp. serological reagents. 866.3350... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3350 Leptospira spp. serological reagents. (a) Identification. Leptospira spp. serological reagents are devices that...

  10. 21 CFR 866.3500 - Rickettsia serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Rickettsia serological reagents. 866.3500 Section... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3500 Rickettsia serological reagents. (a) Identification. Rickettsia serological reagents are devices that consist of antigens...

  11. Enhancement of activated sludge disintegration and dewaterability by Fenton process

    Science.gov (United States)

    Heng, G. C.; Isa, M. H.

    2016-06-01

    Municipal and industrial wastewater treatment plants produce large amounts of sludge. This excess sludge is an inevitable drawback inherent to the activated sludge process. In this study, the waste activated sludge was obtained from the campus wastewater treatment plant at Universiti Teknologi PETRONAS (UTP), Malaysia. Fenton pretreatment was optimized by using the response surface methodology (RSM) to study the effects of three operating conditions including the dosage of H2O2 (g H2O2/kg TS), the molar ratio of H2O2/Fe2+ and reaction time. The optimum operating variables to achieve MLVSS removal 65%, CST reduction 28%, sCOD 11000 mg/L and EPS 500 mg/L were: 1000 g H2O2/kg TS, H2O2/Fe2+ molar ratio 70 and reaction time 45 min. Fenton process was proved to be able to enhance the sludge disintegration and dewaterability.

  12. Application of Fenton oxidation to cosmetic wastewaters treatment.

    Science.gov (United States)

    Bautista, P; Mohedano, A F; Gilarranz, M A; Casas, J A; Rodriguez, J J

    2007-05-08

    The removal of organic matter (TOC and COD) from a cosmetic wastewater by Fenton oxidation treatment has been evaluated. The operating conditions (temperature as well as ferrous ion and hydrogen peroxide dosage) have been optimized. Working at an initial pH equal to 3.0, a Fe(2+) concentration of 200 mg/L and a H(2)O(2) concentration to COD initial weight ratio corresponding to the theoretical stoichiometric value (2.12), a TOC conversion higher than 45% at 25 degrees C and 60% at 50 degrees C was achieved. Application of the Fenton oxidation process allows to reach the COD regional limit for industrial wastewaters discharges to the municipal sewer system. A simple kinetic analysis based on TOC was carried out. A second-order equation describes well the overall kinetics of the process within a wide TOC conversion range covering up to the 80-90% of the maximum achievable conversion.

  13. Abatement of phenolic mixtures by catalytic wet oxidation enhanced by Fenton's pretreatment: Effect of H2O2 dosage and temperature

    International Nuclear Information System (INIS)

    Santos, A.; Yustos, P.; Rodriguez, S.; Simon, E.; Garcia-Ochoa, F.

    2007-01-01

    Catalytic wet oxidation (CWO) of a phenolic mixture containing phenol, o-cresol and p-cresol (500 mg/L on each pollutant) has been carried out using a commercial activated carbon (AC) as catalyst, placed in a continuous three-phase reactor. Total pressure was 16 bar and temperature was 127 deg. C. Pollutant conversion, mineralization, intermediate distribution, and toxicity were measured at the reactor outlet. Under these conditions no detoxification of the inlet effluent was found even at the highest catalyst weight (W) to liquid flow rate (Q L ) ratio used. On the other hand, some Fenton Runs (FR) have been carried out in a batch way using the same phenolic aqueous mixture previously cited. The concentration of Fe 2+ was set to 10 mg/L. The influence of the H 2 O 2 amount (between 10 and 100% of the stoichiometric dose) and temperature (30, 50, and 70 deg. C) on phenols conversion, mineralization, and detoxification have been analyzed. Phenols conversion was near unity at low hydrogen peroxide dosage but mineralization and detoxification achieved an asymptotic value at each temperature conditions. The integration of Fenton reagent as pretreatment of the CWO process remarkably improves the efficiency of the CWO reactor and allows to obtain detoxified effluents at mild temperature conditions and relatively low W/Q L values. For a given phenolic mixture a temperature range of 30-50 deg. C in the Fenton pretreatment with a H 2 O 2 dosage between 20 and 40% of the stoichiometric amount required can be proposed

  14. Potential of Wood-Rotting Fungi to Attack Polystyrene Sulfonate and Its Depolymerisation by Gloeophyllum trabeum via Hydroquinone-Driven Fenton Chemistry.

    Directory of Open Access Journals (Sweden)

    Martin C Krueger

    Full Text Available Synthetic polymers often pose environmental hazards due to low biodegradation rates and resulting accumulation. In this study, a selection of wood-rotting fungi representing different lignocellulose decay types was screened for oxidative biodegradation of the polymer polystyrene sulfonate (PSS. Brown-rot basidiomycetes showed PSS depolymerisation of up to 50 % reduction in number-average molecular mass (Mn within 20 days. In-depth investigations with the most efficient depolymeriser, a Gloeophyllum trabeum strain, pointed at extracellular hydroquinone-driven Fenton chemistry responsible for depolymerisation. Detection of hydroxyl radicals present in the culture supernatants showed good compliance with depolymerisation over the time course of PSS degradation. 2,5-Dimethoxy-1,4-hydroquinone (2,5-DMHQ, which was detected in supernatants of active cultures via liquid chromatography and mass spectrometry, was demonstrated to drive the Fenton processes in G. trabeum cultures. Up to 80% reduction in Mn of PSS where observed when fungal cultures were additionally supplemented with 2,5-dimethoxy benzoquinone, the oxidized from of 2,5-DMHQ. Furthermore, 2,5-DMHQ could initiate the Fenton's reagent-mediated PSS depolymerisation in cell-free systems. In contrast, white-rot fungi were unable to cause substantial depolymerising effects despite the expression of lignin-modifying exo-enzymes. Detailed investigations with laccase from Trametes versicolor revealed that only in presence of certain redox mediators limited PSS depolymerisation occurred. Our results indicate that brown-rot fungi might be suitable organisms for the biodegradation of recalcitrant synthetic polymeric pollutants.

  15. Degradation of the azo dye Acid Red 1 by anodic oxidation and indirect electrochemical processes based on Fenton's reaction chemistry. Relationship between decolorization, mineralization and products

    International Nuclear Information System (INIS)

    Florenza, Xavier; Solano, Aline Maria Sales; Centellas, Francesc; Martínez-Huitle, Carlos Alberto

    2014-01-01

    Highlights: • Degradation of Acid Red 1 by anodic oxidation, electro-Fenton and photoelectro-Fenton • Quicker and similar decolorization by electro-Fenton and photoelectro-Fenton due to oxidation with ● OH in the bulk • Almost total mineralization by photoelectro-Fenton with Pt or BDD due to fast photolysis of products by UVA light • Detection of 11 aromatic products, 15 hydroxylated compounds, 13 desulfonated derivatives and 7 carboxylic acids • Release of NH 4 + , NO 3 − and SO 4 2− ions, and generation of persistent N-products of low molecular mass - Abstract: Solutions of 236 mg dm −3 Acid Red 1 (AR1), an azo dye widely used in textile dying industries, at pH 3.0 have been comparatively treated by anodic oxidation with electrogenerated H 2 O 2 (AO-H 2 O 2 ), electro-Fenton (EF) and photoelectro-Fenton (PEF) at constant current density (j). Assays were performed with a stirred tank reactor equipped with a Pt or boron-doped diamond (BDD) anode and an air-diffusion cathode for H 2 O 2 generation from O 2 reduction. The main oxidizing agents were hydroxyl radicals produced at the anode from water oxidation in all methods and in the bulk from Fenton's reaction between generated H 2 O 2 and 0.5 mmol dm −3 Fe 2+ in EF and PEF. For each anode, higher oxidation power was found in the sequence AO-H 2 O 2 < EF < PEF. The oxidation ability of the BDD anode was always superior to that of Pt. Faster and similar decolorization efficiency was achieved in EF and PEF owing to the quicker destruction of aromatics with hydroxyl radicals produced in the bulk. The PEF process with BDD was the most potent method yielding almost total mineralization due to the additional rapid photolysis of recalcitrant intermediates like Fe(III)-carboxylate complexes under UVA irradiation. The increase in j always enhanced the decolorization and mineralization processes because of the greater production of hydroxyl radicals, but decreases the mineralization current efficiency

  16. Kinetic Modeling of a Heterogeneous Fenton Oxidative Treatment of Petroleum Refining Wastewater

    Science.gov (United States)

    Basheer Hasan, Diya'uddeen; Abdul Raman, Abdul Aziz; Wan Daud, Wan Mohd Ashri

    2014-01-01

    The mineralisation kinetics of petroleum refinery effluent (PRE) by Fenton oxidation were evaluated. Within the ambit of the experimental data generated, first-order kinetic model (FKM), generalised lumped kinetic model (GLKM), and generalized kinetic model (GKM) were tested. The obtained apparent kinetic rate constants for the initial oxidation step (k 2′), their final oxidation step (k 1′), and the direct conversion to endproducts step (k 3′) were 10.12, 3.78, and 0.24 min−1 for GKM; 0.98, 0.98, and nil min−1 for GLKM; and nil, nil, and >0.005 min−1 for FKM. The findings showed that GKM is superior in estimating the mineralization kinetics. PMID:24592152

  17. Heterogeneous electro-Fenton catalyst for 1-butylpyridinium chloride degradation.

    Science.gov (United States)

    Meijide, Jessica; Pazos, Marta; Sanromán, Maria Ángeles

    2017-10-15

    The application of the electro-Fenton process for organic compound mineralisation has been widely reported over the past years. However, operational problems related to the use of soluble iron salt as a homogeneous catalyst involve the development of novel catalysts that are able to operate in a wide pH range. For this purpose, polyvinyl alcohol-alginate beads, containing goethite as iron, were synthesised and evaluated as heterogeneous electro-Fenton catalyst for 1-butylpyridinium chloride mineralisation. The influence of catalyst dosage and pH solution on ionic liquid degradation was analysed, achieving almost total oxidation after 60 min under optimal conditions (2 g/L catalyst concentration and pH 3). The results showed good catalyst stability and reusability, although its effectiveness decreases slightly after three successive cycles. Furthermore, a plausible mineralisation pathway was proposed based on the oxidation byproducts determined by chromatographic techniques. Finally, the Microtox® test revealed notable detoxification after treatment which demonstrates high catalyst ability for pyridinium-based ionic liquid degradation by the electro-Fenton process.

  18. Removal of organic pollutants from produced water using Fenton oxidation

    Directory of Open Access Journals (Sweden)

    Afzal Talia

    2018-01-01

    Full Text Available Produced water (PW is the largest stream of wastewater from oil and gas exploration. It is highly polluted and requires proper treatment before disposal. The main objective of this study was to investigate the effectiveness of Fenton oxidation in degradation of organic matter in PW. The role of operating factors viz., H2O2 concentration (0.12 × 10-3 moles/L to 3 moles/L, [H2O2]/[Fe2+] molar ratio (2 to 75, and reaction time (30 to 200 minutes, on COD removal was determined through a series of batch experiments conducted in acidic environment at room temperature. The experiments were conducted with 500 mL PW samples in 1L glass beakers covered on the outside with aluminum foil to protect them from sunlight. Pre-decided amounts of ferrous sulfate heptahydrate (FeSO4.7H2O and hydrogen peroxide (H2O2 were added to initiate the Fenton reaction. An increase in COD removal was observed with increase in reaction time and [H2O2]/[Fe2+] molar ratio. COD removal also increased with H2O2 concentration up to 0.01 moles/L; further increase in H2O2 concentration decreased the COD removal efficiency. Over 90% COD removal was achieved under optimum reaction conditions. The study indicates that Fenton oxidation is effective for remediation of PW in terms of organic matter removal.

  19. Treatment of real paracetamol wastewater by fenton process

    Directory of Open Access Journals (Sweden)

    Dalgic Gamze

    2017-01-01

    Full Text Available The study investigated the pretreatment of real paracetamol (PCT wastewater of a pharmaceutical industry by Fenton process. At the best experimental conditions (COD/H2O2 = 1/1, Fe+2/H2O2 = 1/70, settling method:centrifuging, pH 6 at settling step, 92.7, 92.7, 95.5, 99.1, 99.9 and 99.4% of chemical oxygen demand (COD, total organic carbon (TOC, 5-day biological oxygen demand (BOD5, PCT, para-amino phenol (PAP and aniline were removed, respectively. Changes in the concentrations of these parameters were also investigated for both oxidation and settling steps of Fenton process. It was found that COD and TOC were removed at the settling step (precipitation whereas PCT, PAP and aniline were removed at the oxidation step. Mass balance calculations were also studied to show the mass distributions of COD in different phases (gas + foam, effluent and sludge. Fenton process was found as an effective method for the pretreatment of real PCT wastewater for discharging in a determined collective treatment plant.

  20. Removal of organic pollutants from produced water using Fenton oxidation

    Science.gov (United States)

    Afzal, Talia; Hasnain Isa, Mohamed; Mustafa, Muhammad Raza ul

    2018-03-01

    Produced water (PW) is the largest stream of wastewater from oil and gas exploration. It is highly polluted and requires proper treatment before disposal. The main objective of this study was to investigate the effectiveness of Fenton oxidation in degradation of organic matter in PW. The role of operating factors viz., H2O2 concentration (0.12 × 10-3 moles/L to 3 moles/L), [H2O2]/[Fe2+] molar ratio (2 to 75), and reaction time (30 to 200 minutes), on COD removal was determined through a series of batch experiments conducted in acidic environment at room temperature. The experiments were conducted with 500 mL PW samples in 1L glass beakers covered on the outside with aluminum foil to protect them from sunlight. Pre-decided amounts of ferrous sulfate heptahydrate (FeSO4.7H2O) and hydrogen peroxide (H2O2) were added to initiate the Fenton reaction. An increase in COD removal was observed with increase in reaction time and [H2O2]/[Fe2+] molar ratio. COD removal also increased with H2O2 concentration up to 0.01 moles/L; further increase in H2O2 concentration decreased the COD removal efficiency. Over 90% COD removal was achieved under optimum reaction conditions. The study indicates that Fenton oxidation is effective for remediation of PW in terms of organic matter removal.

  1. Production of reagents for cleaning fluids

    Energy Technology Data Exchange (ETDEWEB)

    Grunberg, I V; Korostyleva, R N; Pytel, S P; Spasskii, P I; Titarenko, N K; Trachtenberg, S I; Yushkevich, V I

    1980-10-25

    A method for producing reagents for cleaning fluids is proposed using polymerization of acrylonitril, metachrylate or a mixture of the two in water and saponification of the polymers with alakali. To reduce the consumption of monomers and increase the quality of the reagents, 0.4-1.0 parts humic substances, 0.2-1.0 parts hydrolizate from tanning waste products and 1.2-4.0 parts monomers are added to the reaction medium, followed by copolymerization in an acid medium. The proposed method ensures quality reagents which combine lower water yield with a moderate increase in viscosity when acting on clay solutions. Compared with the current method, this method lowers the consumption of an expensive and hard-to-find monomer 1.2-1.4X for one ton of reagent, which lowers the cost of raw material by 1.3-1.7X. This results in a savings of 195-385 rubles per ton of reagent, 600-1200 thousand at 3000 tons/yr.

  2. Comparison of Fenton, UV-Fenton and nano-Fe3O4 catalyzed UV-Fenton in degradation of phloroglucinol under neutral and alkaline conditions: Role of complexation of Fe3+ with hydroxyl group in phloroglucinol

    DEFF Research Database (Denmark)

    Wang, Yong; Lin, Xihuang; Shao, Zongze

    2017-01-01

    difference in TOC removal efficiency: about 90% for UV-Fenton, nearly 60% for Fenton and Hetero-Fenton. Increasing initial pH from 7.0 to 9.0, there was an obvious decline in the degradation rate. The average values of H2O2 utilization efficiency were 0.65 ± 0.01 for Fenton, 0.66 ± 0.09 for UV...

  3. Particle Size Effects on Fenton Regeneration of MTBE-spent Activated Carbon

    Science.gov (United States)

    Fenton-driven regeneration of spent granular activated carbon (GAC) is a developing technology that may reduce water treatment costs. In this study, the effect of GAC particle size on Fenton-driven oxidation of methyl tert-butyl ether (MTBE)-spent GAC was evaluated. The GAC was...

  4. Reactivity of catecholamine-driven Fenton reaction and its relationships with iron(III) speciation.

    Science.gov (United States)

    Melin, Victoria; Henríquez, Adolfo; Freer, Juanita; Contreras, David

    2015-03-01

    Fenton reaction is the main source of free radicals in biological systems. The reactivity of this reaction can be modified by several factors, among these iron ligands are important. Catecholamine (dopamine, epinephrine, and norepinephrine) are able to form Fe(III) complexes whose extension in the coordination number depends upon the pH. Fe(III)-catecholamine complexes have been related with the development of several pathologies. In this work, the ability of catecholamines to enhance the oxidative degradation of an organic substrate (veratryl alcohol, VA) through Fenton and Fenton-like reactions was studied. The initial VA degradation rate at different pH values and its relationship to the different iron species present in solution were determined. Furthermore, the oxidative degradation of VA after 24 hours of reaction and its main oxidation products were also determined. The catecholamine-driven Fenton and Fenton-like systems showed higher VA degradation compared to unmodified Fenton or Fenton-like systems, which also showed an increase in the oxidation state of the VA degradation product. All of this oxidative degradation takes place at pH values lower than 5.50, where the primarily responsible species would be the Fe(III) mono-complex. The presence of Fe(III) mono-complex is essential in the ability of catecholamines to increase the oxidative capacity of Fenton systems.

  5. Improved removal performance and mechanism investigation of papermaking wastewater treatment using manganese enhanced Fenton reaction.

    Science.gov (United States)

    Wang, Yingcai; Wang, Can; Shi, Shuai; Fang, Shuai

    2018-06-01

    The effects of Mn(II) on Fenton system to treat papermaking wastewater and the mechanism of Mn(II) enhanced Fenton reaction were investigated in this study. The chemical oxygen demand (COD) removal efficiency was enhanced in the presence of Mn(II), which increased by 19% compared with that of the Fenton system alone. The pseudo-first order reaction kinetic rate constant of Mn(II)/Fenton system was 2.11 times higher than that of Fenton system. 67%-81% COD were removed with the increasing Mn(II) concentration from 0 to 0.8 g/L. COD removal efficiency was also enhanced in a wider pH range (3-7), which indicated the operation parameters of Fenton technology could be broadened to a milder condition. The study of the mechanism showed that Mn(II) participated in the oxidation and coagulation stages in Fenton system. In the oxidation stage, Mn(II) promotes the production of HO 2 •/ O 2 • - , then HO 2 •/ O 2 • - reacts with Fe(III) to accelerate the formation of Fe(II), and finally accelerates the production of HO•. Meantime MnMnO 3 and Fe(OH) 3 forms in the coagulation stage, facilitating the removal of suspended substances and a large amount of COD, which enhances the overall COD removal of papermaking wastewater. This study provided a detailed mechanism to improve practical applications of Fenton technology.

  6. Fenton-Driven Regeneration of MTBE-spent Granular Activated Carbon

    Science.gov (United States)

    Fenton-driven regeneration of Methyl tert-butyl ether (MTBE)-spent granular activated carbon (GAC) involves the combined, synergistic use of two treatment technologies: adsorption of organic chemicals onto activated carbon and Fenton-driven oxidation regeneration of the spent-GAC...

  7. Reagent for treating clay drilling muds

    Energy Technology Data Exchange (ETDEWEB)

    Tkachenko, P V; Leshchinskiy, P A; Shnaper, B I; Zinchuk, I F; Zlobin, V P

    1982-01-01

    A reagent is proposed for treating clay drilling muds. It contains lignite, caustic soda and modifying agent. It is distinguished by the fact that in order to reduce the cost of the reagent with simultaneous decrease in the viscosity and static shear stress of the drilling mud, it additionally contains iron sulfate, and the modifying agent contained is wastes of carbonic acid production with the following ratio of components (parts by weight): lignite 10.0-15.0, caustic soda 2.0-3.0, wastes of carbonic acid production 0.5-0.75; iron sulfate 1.0-2.0.

  8. Kinetic studies on the degradation of crystal violet by the Fenton oxidation process.

    Science.gov (United States)

    Wu, H; Fan, M M; Li, C F; Peng, M; Sheng, L J; Pan, Q; Song, G W

    2010-01-01

    The degradation of dye crystal violet (CV) by Fenton oxidation process was investigated. The UV-Vis spectrogram has shown that CV can be degraded effectively by Fenton oxidation process. Different system variables namely initial H(2)O(2) concentration, initial Fe(2 + ) concentration and reaction temperature, which have effect on the degradation of CV by Fenton oxidation process, have been studied systematically. The degradation kinetics of CV was also elucidated based on the experimental data. The degradation of CV obeys the first-order reaction kinetics. The kinetic model can be described as k=1.5 exp(-(7.5)/(RT))[H(2)O(2)](0)(0.8718)[Fe(2+)](0)(0.5062). According to the IR spectrogram, it is concluded that the benzene ring of crystal violet has been destroyed by Fenton oxidation. The result will be useful in treating dyeing wastewater containing CV by Fenton oxidation process.

  9. Decolorization and mineralization of Diarylide Yellow 12 (PY12) by photo-Fenton process: the Response Surface Methodology as the optimization tool.

    Science.gov (United States)

    GilPavas, Edison; Dobrosz-Gómez, Izabela; Gómez-García, Miguel Ángel

    2012-01-01

    The Response Surface Methodology (RSM) was applied as a tool for the optimization of the operational conditions of the photo-degradation of highly concentrated PY12 wastewater, resulting from a textile industry located in the suburbs of Medellin (Colombia). The Box-Behnken experimental Design (BBD) was chosen for the purpose of response optimization. The photo-Fenton process was carried out in a laboratory-scale batch photo-reactor. A multifactorial experimental design was proposed, including the following variables: the initial dyestuff concentration, the H(2)O(2) and the Fe(+2) concentrations, as well as the UV wavelength radiation. The photo-Fenton process performed at the optimized conditions resulted in ca. 100% of dyestuff decolorization, 92% of COD and 82% of TOC degradation. A kinetic study was accomplished, including the identification of some intermediate compounds generated during the oxidation process. The water biodegradability reached a final DBO(5)/DQO = 0.86 value.

  10. Optimization of photo-Fenton process for the treatment of prednisolone.

    Science.gov (United States)

    Díez, Aida María; Ribeiro, Ana Sofia; Sanromán, Maria Angeles; Pazos, Marta

    2018-03-29

    Prednisolone is a widely prescribed synthetic glucocorticoid and stated to be toxic to a number of non-target aquatic organisms. Its extensive consumption generates environmental concern due to its detection in wastewater samples at concentrations ranged from ng/L to μg/L that requests the application of suitable degradation processes. Regarding the actual treatment options, advanced oxidation processes (AOPs) are presented as a viable alternative. In this work, the comparison in terms of pollutant removal and energetic efficiencies, between different AOPs such as Fenton (F), photo-Fenton (UV/F), photolysis (UV), and hydrogen peroxide/photolysis (UV/H 2 O 2 ), was carried out. Light diode emission (LED) was the selected source to provide the UV radiation. The UV/F process revealed the best performance, reaching high levels of both degradation and mineralization with low energy consumption. Its optimization was conducted and the operational parameters were iron and H 2 O 2 concentrations and the working volume. Using the response surface methodology with the Box-Behnken design, the effect of independent variables and their interactions on the process response were effectively evaluated. Different responses were analyzed taking into account the prednisolone removal (TOC and drug abatements) and the energy consumptions associated. The obtained model showed an improvement of the UV/F process when treating smaller volumes and when adding high concentrations of H 2 O 2 and Fe 2+ . The validation of this model was successfully carried out, having only 5% of discrepancy between the model and the experimental results. Finally, the performance of the process when having a real wastewater matrix was also tested, achieving complete mineralization and detoxification after 8 h. In addition, prednisolone degradation products were identified. Finally, the obtained low energy permitted to confirm the viability of the process.

  11. [Sensing of Cu²⁺ Based on Fenton Reaction and Unmodified Gold Nanoparticles].

    Science.gov (United States)

    Xing, Yun-peng; Liu, Chun; Zhou, Xiao-hong; Zhang, Li-pei; Shi, Han-chang

    2015-11-01

    Heavy metal pollution has received great attentions in recent years. The traditional methods for heavy metal detection rely on the expensive laboratory instruments and need time-consuming preparation steps; therefore, it is urgent to develop quick and highly sensitive new technologies for heavy metal detection. The colorimetric method based on the gold nanoparticles (AuNPs) features with simple operation, high sensitivity and low cost, therefore, enabling it widely concerned and used in the environmental monitoring, food safety and chemical and biological sensing fields. This work developed a simple, rapid and highly sensitive strategy based on the Fenton reaction and unmodified AuNPs for the detection of Cu²⁺ in water samples. The hydroxyl radical ( · OH) generated by the Fenton reaction between the Cu²⁺ and sodium ascorbate (SA) oxidized the single stranded DNA (ssDNA) attached on the AuNPs surface into variable sequence fragments. The cleavage of ssDNA induced the aggregation of AuNPs in a certain salt solution, therefore, resulting in the changes on the absorbance of solution. The assay conditions were optimized to be pH value of 7.9, 11 mg · L⁻¹ ssDNA, 8 mmol · L⁻¹ SA and 70 mmol · L⁻¹ NaCl. Results showed that the absorbance ratio values at the wavelengths of 700 and 525 nm (A₇₀₀/A₅₂₅) were linearly correlated with the Cu²⁺ concentrations. The linear detection range was 0.1-10.0 µmol · L⁻¹ with a detection limit of 24 nmol · L⁻¹ (3σ). Spiked recoveries ranged from 87%-120% in three sorts of water, including drinking water, tap water and lake water, which confirmed that the potentials of the proposed assay for Cu²⁺ detection in reality.

  12. Inactivation of microbiota from urban wastewater by single and sequential electrocoagulation and electro-Fenton treatments.

    Science.gov (United States)

    Anfruns-Estrada, Eduard; Bruguera-Casamada, Carmina; Salvadó, Humbert; Brillas, Enric; Sirés, Ignasi; Araujo, Rosa M

    2017-12-01

    This work aims at comparing the ability of two kinds of electrochemical technologies, namely electrocoagulation (EC) and electro-Fenton (EF), to disinfect primary and secondary effluents from municipal wastewater treatment plants. Heterotrophic bacteria, Escherichia coli, enterococci, Clostridium perfringens spores, somatic coliphages and eukaryotes (amoebae, flagellates, ciliates and metazoa) were tested as indicator microorganisms. EC with an Fe/Fe cell at 200 A m -2 and natural pH allowed >5 log unit removal of E. coli and final concentration below 1 bacteria mL -1 of coliphages and eukaryotes from both effluents in ca. 60 min, whereas heterotrophic bacteria, enterococci and spores were more resistant. A larger removal was obtained for the primary effluent, probably because the flocs remove higher amount of total organic carbon (TOC), entrapping more easily the microbiota. EF with a boron-doped diamond (BDD) anode and an air-diffusion cathode that produces H 2 O 2 on site was first performed at pH 3.0, with large or even total inactivation of microorganisms within 30 min. A more effective microorganism removal was attained as compared to EC thanks to • OH formed from Fenton's reaction. A quicker disinfection was observed for the secondary effluent owing to its lower TOC content, allowing the attack of greater quantities of electrogenerated oxidants on microorganisms. Wastewater disinfection by EF was also feasible at natural pH (∼7), showing similar abatement of active microorganisms as a result of the synergistic action of generated oxidants like active chlorine and coagulation with iron hydroxides. A sequential EC/EF treatment (30 min each) was more effective for a combined decontamination and disinfection of urban wastewater. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. Anodic oxidation, electro-Fenton and photoelectro-Fenton degradations of pyridinium- and imidazolium-based ionic liquids in waters using a BDD/air-diffusion cell

    International Nuclear Information System (INIS)

    Garcia-Segura, Sergi; Lima, Álvaro Silva; Cavalcanti, Eliane Bezerra; Brillas, Enric

    2016-01-01

    Highlights: • Treatment of 1-butyl-4-methylpyridinium chloride and 1-ethyl-3-methylimidazolium chloride. • Almost total mineralization of both compounds by AO-H_2O_2, EF and PEF at high current density. • Release of NH_4"+ and NO_3"− in different proportion depending on the ionic liquid. • Large decay of initial Cl"− with main formation of ClO_3"− and, in lesser extent, of ClO_4"−. • Detection of primary heteroaromatic products and carboxylic acids generated. - Abstract: The degradation of two representative ionic liquids, 1-butyl-4-methylpyridinium chloride and 1-ethyl-3-methylimidazolium chloride, has been studied in 100 cm"3 of aqueous sulfate medium of pH 3.0 by electrochemical advanced oxidation processes (EAOPs) like anodic oxidation with electrogenerated H_2O_2 (AO-H_2O_2), electro-Fenton (EF) and photoelectro-Fenton (PEF). The electrolytic cell contained a boron-doped diamond (BDD) anode and an air diffusion cathode. The main oxidants were hydroxyl radicals formed at the anode surface from water discharge and in the bulk from Fenton’s reaction between generated H_2O_2 and added Fe"2"+. The solutions of both compounds underwent an almost total mineralization with 97% and 94% of dissolved organic abatement by the most powerful PEF at high current density, being similar and slightly lower for AO-H_2O_2 and EF, respectively. At low current density, the pyridinium-based ionic liquid showed similar mineralization rate by AO-H_2O_2 and PEF, whereas the imidazolium-based ionic liquid was more rapidly degraded in the sequence: AO-H_2O_2 < EF < PEF, where the positive effect of UVA irradiation in PEF was more apparent. The current efficiency decreased gradually with increasing current density in all EAOPs and its value was always superior for the latter compound. The NO_3"− and NH_4"+ concentrations produced in each process were quantified by ion chromatography. This technique confirmed a drastic oxidation of Cl"− contained in the parent

  14. Novel RGO/α-FeOOH supported catalyst for Fenton oxidation of phenol at a wide pH range using solar-light-driven irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ying, E-mail: yingwang@bnu.edu.cn [The Key Laboratory of Water and Sediment Sciences, Ministry of Education, School of Environment, Beijing Normal University, Beijing 100875 (China); Fang, Jiasheng, E-mail: fangfangcanfly@163.com [The Key Laboratory of Water and Sediment Sciences, Ministry of Education, School of Environment, Beijing Normal University, Beijing 100875 (China); School of Chemistry and Chemical Engineering, Southeast University, Jiangsu Optoelectronic Functional Materials and Engineering Laboratory, Nanjing 211189 (China); Crittenden, John C., E-mail: John.Crittenden@ce.gatech.edu [School of Civil and Environmental Engineering and the Brook Byers Institute for Sustainable Systems, Georgia Institute of Technology, Atlanta, GA 30332-0595 (United States); Shen, Chanchan [The Key Laboratory of Water and Sediment Sciences, Ministry of Education, School of Environment, Beijing Normal University, Beijing 100875 (China)

    2017-05-05

    Graphical abstract: Schematic of the preparation of RF supported catalysts and the reaction mechanism for SLD Fenton catalytic degradation of aqueous phenol. - Highlights: • Novel SLD Fenton catalyst was synthesized via in-situ induced self-assembly process. • RGO improved light-harvesting capacity and enhanced electro-transport performance. • Visible light irradiation accelerated reaction and extended operating pHs (4.0–8.0). • H{sub 2}O{sub 2} reduction and H{sub 2}O oxidation yielded ·OH in Fe{sup Ⅱ}/Fe{sup Ⅲ} and Fe{sup Ⅲ}/Fe{sup Ⅳ} cycling process. - Abstract: A novel solar-light-driven (SLD) Fenton catalyst was developed by reducing the ferrous-ion onto graphene oxide (GO) and forming reduced graphene oxide/α-FeOOH composites (RF) via in-situ induced self-assembly process. The RF was supported on several mesoporous supports (i.e., Al-MCM-41, MCM-41 and γ-Al{sub 2}O{sub 3}). The activity, stability and energy use for phenol oxidation were systematically studied for a wide pH range. Furthermore, the catalytic mechanism at acid and alkaline aqueous conditions was also elucidated. The results showed that Fe(II) was reduced onto GO nanosheets and α-FeOOH crystals were formed during the self-assembly process. Compared with Fenton reaction without SLD irradiation, the visible light irradiation not only dramatically accelerated the rate of Fenton-based reactions, but also extended the operating pH for the Fenton reaction (from 4.0 to 8.0). The phenol oxidation on RF supported catalysts was fitting well with the pseudo-first-order kinetics, and needed low initiating energy, insensitive to the reacting temperature changes (273–318 K). The Al-MCM-41 supported RF was a more highly energy-efficient catalyst with the prominent catalytic activity at wide operating pHs. During the reaction, ·OH radicals were generated by the SLD irradiation from H{sub 2}O{sub 2} reduction and H{sub 2}O oxidation in the Fe{sup Ⅱ}/Fe{sup Ⅲ} and Fe{sup Ⅲ}/Fe{sup

  15. Oxidação em processos Fenton e Foto-Fenton em efluentes de curtumes - DOI: 10.4025/actascitechnol.v25i1.2254

    Directory of Open Access Journals (Sweden)

    Tirzhá Lins Porto Dantas

    2003-04-01

    Full Text Available Os processos Fenton e Foto-fenton são alternativas atraentes no tratamento de efluentes, especialmente aplicados àqueles contendo compostos recalcitrantes. Neste trabalho foi avaliada a remoção de DQO e amônia durante o tratamento de efluentes de curtumes pelos processos Fenton e Foto-Fenton. A cinética de degradação foi dividida em dois estágios, sendo um processo inicial rápido, no qual 70% da DQO inicial é removida; seguido por uma etapa lenta que acontece em até 4 horas de reação, alcançando cerca de 90% de remoção da DQO inicial. Diferentes proporções mássicas Fé2+/H2O2 foram testadas e os resultados mostraram que a eficiência dos processos Fenton e Foto-Fenton aumenta de 65 até 90% à medida que a produção de radicais livres hidroxil aumenta. Nenhuma diferença apreciável na degradação de nitrogênio amoniacal foi observada entre os processos Fenton e Foto-Fenton, mesmo após a coagulação. A remoção de amônia foi atribuída à oxidação de compostos orgânicos, formando N2 e íons nitrato. A toxicidade do efluente tratado diminuiu até a dosagem de 9g/L de H2O2 e aumentou para maiores dosagens, devido ao residual peróxido de hidrogênio ou a formação de produtos oxidados mais tóxicos.

  16. Enhancement of Fenton and photo-Fenton processes at initial circumneutral pH for the degradation of the β-blocker metoprolol.

    Science.gov (United States)

    Romero, V; Acevedo, S; Marco, P; Giménez, J; Esplugas, S

    2016-01-01

    The need for acidification in the Fenton and photo-Fenton process is often outlined as one of its major drawbacks, thus in this work the acidification of the Metoprolol (MET) is avoided by the addition of resorcinol (RES), which is used to simulate model organic matter. The experiments were carried out at natural pH (6.2) with different Fe(2+) (1, 2.5, 5, and 10 mg/L) and H2O2 (25, 50, 125 and 150 mg/L) concentrations. The performance of MET and RES degradation was assessed along the reaction time. Working with the highest concentrations (5 and 10 mg/L of ferrous iron and 125 and 150 mg/L of H2O2) more than 90% of MET and RES removals were reached within 50 and 20 min of treatment, respectively, by Fenton process. However a low mineralization was achieved in both cases, likely, due to by-products accumulation. Regarding to photo-Fenton process, within 3 min with the highest iron and hydrogen peroxide concentrations, a complete MET degradation was obtained and 95% of RES conversion was achieved. Parameters such Total Organic Carbon, Chemical Oxygen Demand, and AOS were measured. Intermediates were identified and MET degradation path was proposed in the presence of resorcinol. Finally, a comparison between Fenton and photo-Fenton processes at acid pH and at initial circumneutral pH was discussed. The positive effect of RES on Fenton and photo-Fenton systems has been confirmed, allowing the work at circumneutral pH. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. A Snippet of Grignard Reagent's History

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 18; Issue 8. A Snippet of Grignard Reagent's History. Sujan Singh Dua. Classroom Volume 18 Issue 8 August 2013 pp 777-780. Fulltext. Click here to view fulltext PDF. Permanent link: https://www.ias.ac.in/article/fulltext/reso/018/08/0777-0780. Keywords.

  18. Environmental application of millimetre-scale sponge iron (s-Fe"0) particles (IV): New insights into visible light photo-Fenton-like process with optimum dosage of H_2O_2 and RhB photosensitizers

    International Nuclear Information System (INIS)

    Ju, Yongming; Yu, Yunjiang; Wang, Xiaoyan; Xiang, Mingdeng; Li, Liangzhong; Deng, Dongyang; Dionysiou, Dionysios D.

    2017-01-01

    Highlights: • Synergistic action of Rhodamine B (RhB), visible light, H_2O_2 and s-Fe"0 is essential. • The complexes of RhB and Fe"3"+ eject one electron via ligand-to-metal charge-transfer. • RhB assists the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). - Abstract: In this study, we firstly develop the photo-Fenton-like system with millimetric sponge iron (s-Fe"0), H_2O_2, visible light (vis, λ ≥ 420 nm) and rhodamine B (RhB), and present a comprehensive study concerning the mechanism. Thus, we investigate (1) the adsorption of RhB onto s-Fe"0, (2) the photo-Fenton-like removal of RhB over iron oxides generated from the corrosion of s-Fe"0, (3) the homogeneous photo-Fenton removal of RhB over Fe"2"+ or Fe"3"+, (4) the Fe"3"+-RhB complexes, and (5) the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). The results show that neither the adsorption process over s-Fe"0 nor the photo-Fenton-like process over FeOOH, Fe_3O_4 and Fe_2O_3, achieved efficient removal of RhB. For comparison, in homogeneous photo-Fenton process, the presence of Fe"3"+ ions, rather than Fe"2"+ ions, effectively eliminated RhB. Furthermore, the UV–vis spectra showing new absorbance at ∼ 285 nm indicate the complexes of RhB and Fe"3"+ ions, adopting vis photons to form excited state and further eject one electron via ligand-to-metal charge-transfer to activate H_2O_2. Additionally, efficient TBBPA removal was obtained only in the presence of RhB. Accordingly, the s-Fe"0– based photo-Fenton-like process assisted with dyestuff wastewater is promising for removing a series of persistent organic pollutants.

  19. Fast decolorization of azo methyl orange via heterogeneous Fenton and Fenton-like reactions using alginate-Fe2+/Fe3+ films as catalysts.

    Science.gov (United States)

    Quadrado, Rafael F N; Fajardo, André R

    2017-12-01

    The efficiency of Fenton and Fenton-like processes can be seriously affected by the continuous loss of iron ions and by the formation of solid sludge. Here, alginate (Alg) films were synthesized to stabilize iron ions (Fe 2+ and Fe 3+ ) and to enhance their catalytic activities towards the decolorization of methyl orange via heterogeneous Fenton and Fenton-like processes. Iron ions were ionically bond to the Alg molecules resulting in a three-dimensional network with specific structural and morphological features according to the valence states of iron. Our results demonstrated that both Alg-Fe 2+ and Alg-Fe 3+ films show highlighted catalytic activity for the decolorization of MO and high decolorization rates. Reuse experiments demonstrated that both films could be employed in at least five consecutive decolorization processes without losing their catalytic efficiency or stability. Taken together, our findings reveal that the Alg-Fe 2+ and Alg-Fe 3+ films may be suitable low-cost catalysts in heterogeneous Fenton and Fenton-like processes. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Total organic carbon removal from a chemical lab’s wastewater using Fenton’s reagent

    Directory of Open Access Journals (Sweden)

    Oscar Mauricio Martínez Ávila

    2013-05-01

    Full Text Available Treating industrial wastewater represents a serious problem nowadays; it requires a strong understanding of the particular systems and (in most of cases ad hoc solutions. This work describes the use of Fenton’s reagent (reaction between H2O2 and Fe(II for removing total organic carbon (TOC from a particular chemical laboratory’s lab-scale batch reactor wastewater. Some operating variables (hydrogen peroxide and ferrous ion concentration, temperature and pH were evaluated regarding final TOC removal. An economic optimisation was made by means of a second order polynomial model representing these variables’ behaviour regarding TOC removal (0.94 R2. The highest experimentally reached TOC removal was 88.8% at 50 mg/L [Fe(II]0, 50 mM [H2O2]0 , pH=2.8 at 80oC, while 53.9% was obtained in optimised conditions, i.e. 36 mg/L [Fe(II]0 , 45.5 mM [H2O2]0 , pH=2.6 at 20°C. It was found that the Fenton process could achieve 41% removal, even in adverse conditions (pH close to 6. It was noted from the analysis that both H2O2 concentration and temperature had a powerful effect on organic matter degradation efficiency, as well as on total treatment cost.

  1. Evaluation of Fenton Process in Removal of Direct Red 81

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Baghapour

    2016-01-01

    Full Text Available Background: Dyes are visible materials and are considered as one of the hazardous components that make up the industrial waste. Dye compounds in natural water, even in very low concentrations, will lead to environmental problems. Azo dyes are compounds with one or more –N=N– groups and are used in textile industry. Because of its low price, solubility, and stability, azo dyes are widely used in the textile industry. Direct Red 81 (DR81 is one of the azo dyes, which is removed from bodies of water, using various methods. This study aimed to assess DR81 dye removal by Fenton oxidation and the effects of various parameters on this process. Methods: Decolorization tests by Fenton oxidation were performed at dye concentrations of 50, 500, 100 and 1000 mg/L; hydrogen peroxide concentrations of 0, 10, 30, 60 and 120 mg/L; iron (II sulfate heptahydrate concentrations of 0, 3, 5, 20 and 50 mg/L; and pH levels of 3, 5, 7 and 10 for durations of 5, 10, 20, 30, 60 and 180 minutes. Results: The optimal condition occurred at a dye concentration of 20 mg/L, hydrogen peroxide concentration of 120 mg/L, bivalent iron concentration of 100 mg/L, pH of 3, and duration of 30 minutes. Under such conditions, the maximum dye removal rate was 88.98%. Conclusion: The results showed that DR81 could be decomposed and removed by Fenton oxidation. In addition, the removal of Direct Red 81 (DR81 depends on several factors such as dye concentration, reaction time, concentrations of hydrogen peroxide and iron, and pH

  2. Decolorization of Diazo Dye Ponceau S by Fenton Process

    Directory of Open Access Journals (Sweden)

    Muhammad Muslim

    2013-12-01

    Full Text Available An attempt has been taken to decolorize and mineralize Ponceau S (PS, a diazo dye, in aqueous solution by Fenton process. Effects of solution pH, concentrations of H2O2, Fe(II and PS on the decolorization of PS have also been studied through batch experiments. About 90% decolorization was found under the optimal conditions [PS]: [H2O2]: [Fe(II] = 1:12:2 and [H2O2]/[Fe(II] = 6 at pH 2.85 in 40 minutes. The overall results revealed that mineralization was rather slower as compared with the decolorization.

  3. Water quality in vicinity of Fenton Hill Site, 1974

    International Nuclear Information System (INIS)

    Purtymun, W.D.; Adams, W.H.; Owens, J.W.

    1975-09-01

    The water quality at nine surface water stations, eight ground water stations, and the drilling operations at the Fenton Hill Site have been studied as a measure of the environmental impact of the Los Alamos Scientific Laboratory geothermal experimental studies in the Jemez Mountains. Surface water quality in the Jemez River drainage area is affected by the quality of the inflow from thermal and mineral springs. Ground water discharges from the Cenozoic Volcanics are similar in chemical quality. Water in the main zone of saturation penetrated by test hole GT-2 is highly mineralized, whereas water in the lower section of the hole, which is in granite, contains a higher concentration of uranium

  4. Comparative use of anodic oxidation, electro-Fenton and photoelectro-Fenton with Pt or boron-doped diamond anode to decolorize and mineralize Malachite Green oxalate dye

    International Nuclear Information System (INIS)

    El-Ghenymy, Abdellatif; Centellas, Francesc; Rodríguez, Rosa María; Cabot, Pere Lluís; Garrido, José Antonio; Sirés, Ignasi; Brillas, Enric

    2015-01-01

    Highlights: • Degradation of Malachite Green oxalate solutions at pH 3.0 by AO, AO-H 2 O 2 , EF and PEF. • A Pt anode leads to slower decolorization and mineralization than BDD. • Up to 97% mineralization by the most powerful PEF process with BDD at 100 mA cm −2 . • Study of the evolution of seven final short-chain aliphatic carboxylic acids. • Conversion of the initial N atoms of the dye mainly into NH 4 + , along with small amounts of NO 3 − . - Abstract: The degradation of 100 cm 3 of 177 mg dm −3 of the triphenylmethane dye Malachite Green oxalate at pH 3.0 was studied by anodic oxidation with stainless steel cathode (AO-SS), AO with air-diffusion cathode (AO-H 2 O 2 ), electro-Fenton (EF) and photoelectro-Fenton (PEF) with UVA light. The main oxidizing species were hydroxyl radicals formed from either water oxidation at the anode surface or in the bulk between added Fe 2+ and H 2 O 2 generated at the air-diffusion cathode. The use of a Pt anode led to slower decolorization and mineralization than BDD in all treatments because of the higher oxidation power of the latter. The decolorization was much faster for EF and PEF compared to AO-SS and AO-H 2 O 2 due to the contribution of hydroxyl radicals in the bulk. PEF allowed the quickest color removal by the rapid Fe 2+ regeneration from the photolysis of Fe(III) complexes with oxalate. The most powerful process was PEF with BDD, which yielded total decolorization in 6 min and 97% mineralization at 240 min operating at 100 mA cm −2 , thanks to hydroxyl radicals formed at the anode surface and in the bulk along with the photolytic action of UVA radiation. The evolution of final carboxylic acids like maleic, fumaric, succinic, acetic, oxalic, formic and oxamic was followed by ion-exclusion HPLC. All these acids and their Fe(III) complexes were removed more slowly with Pt anode. The initial N atoms of the dye were pre-eminently accumulated as NH 4 + ion, along with small amounts of NO 3 − ion.

  5. Degradation of Anthraquinone Dye Reactive Blue 4 in Pyrite Ash Catalyzed Fenton Reaction

    Directory of Open Access Journals (Sweden)

    Milena Becelic-Tomin

    2014-01-01

    Full Text Available Pyrite ash (PA is created by burning pyrite in the chemical production of sulphuric acid. The high concentration of iron oxide, mostly hematite, present in pyrite ash, gives the basis for its application as a source of catalytic iron in a modified Fenton process for anthraquinone dye reactive blue 4 (RB4 degradation. The effect of various operating variables such as catalyst and oxidant concentration, initial pH and RB4 concentration on the abatement of total organic carbon, and dye has been assessed in this study. Here we show that degradation of RB4 in the modified Fenton reaction was efficient under the following conditions: pH=2.5; [PA]0=0.2 g L−1; [H2O2]0=5 mM and initial RB4 concentration up to 100 mg L−1. The pyrite ash Fenton reaction can overcome limitations observed from the classic Fenton reaction, such as the early termination of the Fenton reaction. Metal (Pb, Zn, and Cu content of the solution after the process suggests that an additional treatment step is necessary to remove the remaining metals from the water. These results provide basic knowledge to better understand the modified, heterogeneous Fenton process and apply the PA Fenton reaction for the treatment of wastewaters which contains anthraquinone dyes.

  6. Degradation of azo dyes by sequential Fenton's oxidation and aerobic biological treatment

    International Nuclear Information System (INIS)

    Tantak, Nilesh P.; Chaudhari, Sanjeev

    2006-01-01

    A two stage sequential Fenton's oxidation followed by aerobic biological treatment train was used to achieve decolorization and to enhance mineralization of azo dyes, viz. Reactive Black 5 (RB5), Reactive Blue 13 (RB13), and Acid Orange 7 (AO7). In the first stage, Fenton's oxidation process was used while in the second stage aerobic sequential batch reactors (SBRs) were used as biological process. Study was done to evaluate effect of pH on Fenton's oxidation process. Results reveal that pH 3 was optimum pH for achieving decolorization and dearomatization of dyes by Fenton's process. Degradation of dye was assessed by COD reduction and reduction in aromatic amines (naphthalene chromophores) which was measured by reduction in absorbance at 200 nm. More than 95% of color was removed with Fenton's oxidation process in all dyes. In overall treatment train 81.95, 85.57, and 77.83% of COD reduction was achieved in RB5, RB13, and AO7 dyes, respectively. In the Fenton's oxidation process 56, 24.5, and 80% reduction in naphthalene group was observed in RB5, RB13, and AO7, respectively, which further increased to 81.34, 68.73, and 92% after aerobic treatment. Fenton's oxidation process followed by aerobic SBRs treatment sequence seems to be viable method for achieving significant degradation of azo dye

  7. Coupled solar photo-Fenton and biological treatment for the degradation of diuron and linuron herbicides at pilot scale.

    Science.gov (United States)

    Farré, Maria José; Maldonado, Manuel Ignacio; Gernjak, Wolfgang; Oller, Isabel; Malato, Sixto; Domènech, Xavier; Peral, José

    2008-06-01

    A coupled solar photo-Fenton (chemical) and biological treatment has been used to remove biorecalcitrant diuron (42 mg l(-1)) and linuron (75 mg l(-1)) herbicides from water at pilot plant scale. The chemical process has been carried out in a 82 l solar pilot plant made up by four compound parabolic collector units, and it was followed by a biological treatment performed in a 40 l sequencing batch reactor. Two Fe(II) doses (2 and 5 mg l(-1)) and sequential additions of H2O2 (20 mg l(-1)) have been used to chemically degrade the initially polluted effluent. Next, biodegradability at different oxidation states has been assessed by means of BOD/COD ratio. A reagent dose of Fe=5 mg l(-1) and H2O2=100 mg l(-1) has been required to obtain a biodegradable effluent after 100 min of irradiation time. Finally, the organic content of the photo-treated solution has been completely assimilated by a biomass consortium in the sequencing batch reactor using a total suspended solids concentration of 0.2 g l(-1) and a hydraulic retention time of 24h. Comparison between the data obtained at pilot plant scale (specially the one corresponding to the chemical step) and previously published data from a similar system performing at laboratory scale, has been carried out.

  8. Electrocatalytic properties of N-doped graphite felt in electro-Fenton process and degradation mechanism of levofloxacin.

    Science.gov (United States)

    Liu, Xiaocheng; Yang, Danxing; Zhou, Yaoyu; Zhang, Jiachao; Luo, Lin; Meng, Sijun; Chen, Song; Tan, Mengjiao; Li, Zhicheng; Tang, Lin

    2017-09-01

    The degradation of antibiotic levofloxacin was investigated by dimensionally stable anode as well as modified cathode using low-cost chemical reagents of hydrazine hydrate and ethanol for electro-Fenton in an undivided cell at pH 3.0 under room temperature. Comparison of unmodified and modified cathode was performed. The apparent rate constant of levofloxacin decay was found to be 0.2883 min -1 for graphite felt-10 with the best performance at 200 mA, which is lower than graphite felt at 400 mA. The optimum modified cathode showed a significant improvement of complete mineralization of levofloxacin, reaching a 92% TOC removal at 200 mA for 480 min higher than unmodified one at twice the current. Surface physicochemical properties and morphology were investigated by scanning electron microscope, contact angle and X-ray photoelectron spectroscopy. The electrochemical characterization of hydrogen evolution reaction was adopted to clarify a possible pathway for the higher mineralization of levofloxacin, indicating a potential pilot-scale study to the pollution with the similar structure. Copyright © 2017 Elsevier Ltd. All rights reserved.

  9. Treatment of real effluents from the pharmaceutical industry: A comparison between Fenton oxidation and conductive-diamond electro-oxidation.

    Science.gov (United States)

    Pérez, J F; Llanos, J; Sáez, C; López, C; Cañizares, P; Rodrigo, M A

    2017-06-15

    Wastewater produced in pharmaceutical manufacturing plants (PMPs), especially the one coming from organic-synthesis facilities, is characterized by its large variability due to the wide range of solvents and chemical reagents used in the different stages of the production of medicines. Normally, the toxicity of the organic compounds prevent the utilization of biological processes and more powerful treatments are needed becoming advanced oxidation processes (AOPs) a valid alternative. In this work, the efficiency in abatement of pollution by Fenton oxidation (FO) and conductive-diamond electro-oxidation (CDEO) are compared in the treatment of 60 real effluents coming from different processes carried out in a pharmaceutical facility, using standardized tests. In 80% of the samples, CDEO was found to be more efficient than FO and in the remaining 20%, coagulation was found to exhibit a great significance in the COD abatement mechanism during FO, pointing out the effectiveness of the oxidation promoted by the electrochemical technology. Mean oxidation state of carbon was found to be a relevant parameter to understand the behavior of the oxidation technologies. It varied inversely proportional to efficiency in FO and it showed practically no influence in the case of CDEO. Copyright © 2016 Elsevier Ltd. All rights reserved.

  10. Fast Fenton footprinting: a laboratory-based method for the time-resolved analysis of DNA, RNA and proteins

    Science.gov (United States)

    Shcherbakova, Inna; Mitra, Somdeb; Beer, Robert H.; Brenowitz, Michael

    2006-01-01

    ‘Footprinting’ describes assays in which ligand binding or structure formation protects polymers such as nucleic acids and proteins from either cleavage or modification; footprinting allows the accessibility of individual residues to be mapped in solution. Equilibrium and time-dependent footprinting links site-specific structural information with thermodynamic and kinetic transitions. The hydroxyl radical (·OH) is a particularly valuable footprinting probe by virtue of it being among the most reactive of chemical oxidants; it reports the solvent accessibility of reactive sites on macromolecules with as fine as a single residue resolution. A novel method of millisecond time-resolved ·OH footprinting has been developed based on the Fenton reaction, Fe(II) + H2O2 → Fe(III) + ·OH + OH−. This method can be implemented in laboratories using widely available three-syringe quench flow mixers and inexpensive reagents to study local changes in the solvent accessibility of DNA, RNA and proteins associated with their biological function. PMID:16582097

  11. Efficient treatment of an electroplating wastewater containing heavy metal ions, cyanide, and organics by H2O2 oxidation followed by the anodic Fenton process.

    Science.gov (United States)

    Zhao, Xu; Wang, Haidong; Chen, Fayuan; Mao, Ran; Liu, Huijuan; Qu, Jiuhui

    2013-01-01

    A real electroplating wastewater, containing heavy metals, cyanide, and organic contaminants, was treated by electrocoagulation (EC), H2O2 oxidation, H2O2 pre-oxidation followed by EC, and the anodic Fenton process and the efficacy of the processes was compared. Concentration of cyanide, Cu, Ni, Zn, and Cr was largely decreased by EC within 5 min. When the reaction time was extended, removal of residual cyanide, Cu, and Ni was limited. In H2O2 oxidation, the concentration of cyanide decreased from initial 75 to 12 mg L(-1) in 30 min. The effluents from the H2O2 oxidation were further treated by EC or anodic Fenton. In EC, the concentration of total cyanide, Ni, and Cu decreased to below 0.3, 0.5, and 1.5 mg L(-1), respectively. Removal efficiency of chemical oxygen demand by EC was less than 20.0%. By contrast, there was 73.5% reduction by the anodic Fenton process with 5 mM H2O2 at 30 min; this can be attributed to the oxidation induced by hydroxyl radicals generated by the reaction of H2O2 with the electrogenerated Fe(2+). Meanwhile, residual cyanide, Cu, and Ni can also be efficiently removed. Transformation of organic components in various processes was analyzed using UV-visible and fluorescence excitation-emission spectra.

  12. Fenton's process applied to wastewaters treatment

    OpenAIRE

    Rossi, André Fernandes

    2014-01-01

    Tese de doutoramento em Engenharia Química, apresentada à Faculdade de Ciências e Tecnologia da Universidade de Coimbra Water resources are not infinite. If even nowadays some people do not have proper access to this vital supply, humanity must do much more effort aiming its preservation in consideration with the future of the generations to come. Avoiding all types of pollutants from contaminating water cycles is currently one of the current utmost matters to be faced by government polici...

  13. 21 CFR 660.30 - Reagent Red Blood Cells.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 7 2010-04-01 2010-04-01 false Reagent Red Blood Cells. 660.30 Section 660.30...) BIOLOGICS ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS Reagent Red Blood Cells § 660.30 Reagent Red Blood Cells. (a) Proper name and definition. The proper name of the product shall be...

  14. 21 CFR 866.3255 - Escherichia coli serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Escherichia coli serological reagents. 866.3255... coli serological reagents. (a) Identification. Escherichia coli serological reagents are devices that consist of antigens and antisera used in serological tests to identify Escherichia coli from cultured...

  15. 21 CFR 864.8100 - Bothrops atrox reagent.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Bothrops atrox reagent. 864.8100 Section 864.8100 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Hematology Reagents § 864.8100 Bothrops atrox reagent. (a...

  16. 21 CFR 864.8540 - Red cell lysing reagent.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Red cell lysing reagent. 864.8540 Section 864.8540 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Hematology Reagents § 864.8540 Red cell lysing reagent...

  17. Selenium and tellurium reagents in organic synthesis

    International Nuclear Information System (INIS)

    Comasseto, J.V.

    1984-01-01

    A review of the contribution of the University of Sao Paulo (SP, Brazil) to the organic synthesis of selenium and tellurium reagents is made. Major reactions amoung selenium compounds and insaturated substrates, phosphorus, ester enolates as well as the use of phase transference catalysed reactions to produce arylselenolate are described. For tellurium, interactions of its compounds with organic substrates and reactive intermediates (e.g. benzino diazomethane) are reported. (C.L.B.) [pt

  18. Magnetic field assisted Fenton reactions for the enhanced degradation of methyl blue

    Institute of Scientific and Technical Information of China (English)

    Xiao Long Hao; Lu Yi Zou; Guang Sheng Zhang; Yi Bo Zhang

    2009-01-01

    Magnetic field was tentatively introduced into Fenton reactions system for the degradation and discoloration of methyl blue as the represent of organic chemical dye, which was a bio-refractory organic pollutant in industry wastewater. It was found that under optimal Fenton reaction conditions, with the assistant of magnetic field in Fenton reactions, the degradation rate of methyl blue, the decomposition rate of H2O2 and the conversion rate of Fe2+ were accelerated, the extent of them would be improved by the increase of magnetic field intensity. Meanwhile, the mineralization of methyl blue (CODcr) was improved by over 10% with magnetic fiold.

  19. Oxidative degradation of phenols in sono-Fenton-like systems upon high-frequency ultrasound irradiation

    Science.gov (United States)

    Aseev, D. G.; Sizykh, M. R.; Batoeva, A. A.

    2017-12-01

    The kinetics of oxidative degradation of phenol and chlorophenols upon acoustic cavitation in the megahertz range (1.7 MHz) is studied experimentally in model systems, and the involvement of in situ generated reactive oxygen species (ROSs) is demonstrated. The phenols subjected to high frequency ultrasound (HFUS) are ranked in terms of their rate of conversion: 2,4,6-trichlorophenol > 2,4-dichlorophenol 2-chlorophenol > 4-chlorophenol phenol. Oxidative degradation upon HFUS irradiation is most efficient at low concentrations of pollutants, due to the low steady-state concentrations of the in situ generated ROSs. A dramatic increase is observed in the efficiency of oxidation in several sonochemical oxidative systems (HFUS in combination with other chemical oxidative factors). The system with added Fe2+ (a sono-Fenton system) derives its efficiency from hydrogen peroxide generated in situ as a result of the recombination of OH radicals. The S2O8 2-/Fe2+/HFUS system has a synergetic effect on substrate oxidation that is attributed to a radical chain mechanism. In terms of the oxidation rates, degrees of conversion, and specific energy efficiencies of 4-chlorophenol oxidation based on the amount of oxidized substance per unit of expended energy the considered sonochemical oxidative systems form the series HFUS < S2O8 2-/HFUS < S2O8 2-/Fe2+/HFUS.

  20. Improved multiple displacement amplification (iMDA) and ultraclean reagents.

    Science.gov (United States)

    Motley, S Timothy; Picuri, John M; Crowder, Chris D; Minich, Jeremiah J; Hofstadler, Steven A; Eshoo, Mark W

    2014-06-06

    Next-generation sequencing sample preparation requires nanogram to microgram quantities of DNA; however, many relevant samples are comprised of only a few cells. Genomic analysis of these samples requires a whole genome amplification method that is unbiased and free of exogenous DNA contamination. To address these challenges we have developed protocols for the production of DNA-free consumables including reagents and have improved upon multiple displacement amplification (iMDA). A specialized ethylene oxide treatment was developed that renders free DNA and DNA present within Gram positive bacterial cells undetectable by qPCR. To reduce DNA contamination in amplification reagents, a combination of ion exchange chromatography, filtration, and lot testing protocols were developed. Our multiple displacement amplification protocol employs a second strand-displacing DNA polymerase, improved buffers, improved reaction conditions and DNA free reagents. The iMDA protocol, when used in combination with DNA-free laboratory consumables and reagents, significantly improved efficiency and accuracy of amplification and sequencing of specimens with moderate to low levels of DNA. The sensitivity and specificity of sequencing of amplified DNA prepared using iMDA was compared to that of DNA obtained with two commercial whole genome amplification kits using 10 fg (~1-2 bacterial cells worth) of bacterial genomic DNA as a template. Analysis showed >99% of the iMDA reads mapped to the template organism whereas only 0.02% of the reads from the commercial kits mapped to the template. To assess the ability of iMDA to achieve balanced genomic coverage, a non-stochastic amount of bacterial genomic DNA (1 pg) was amplified and sequenced, and data obtained were compared to sequencing data obtained directly from genomic DNA. The iMDA DNA and genomic DNA sequencing had comparable coverage 99.98% of the reference genome at ≥1X coverage and 99.9% at ≥5X coverage while maintaining both balance

  1. Enhanced Electro-Fenton Mineralization of Acid Orange 7 Using a Carbon Nanotube Fiber-Based Cathode

    Directory of Open Access Journals (Sweden)

    Thi Xuan Huong Le

    2018-02-01

    Full Text Available A new cathodic material for electro-Fenton (EF process was prepared based on a macroscopic fiber (CNTF made of mm-long carbon nanotubes directly spun from the gas phase by floating catalyst CVD, on a carbon fiber (CF substrate. CNTF@CF electrode is a highly graphitic material combining a high surface area (~260 m2/g with high electrical conductivity and electrochemical stability. One kind of azo dye, acid orange 7 (AO7, was used as model bio-refractory pollutant to be treated at CNTF@CF cathode in acidic aqueous medium (pH 3.0. The experimental results pointed out that AO7 and its organic intermediate compounds were totally mineralized by hydroxyl radical generated from Fenton reaction. In fact, 96.7% of the initial total organic carbon (TOC was eliminated in 8 h of electrolysis by applying a current of −25 mA and ferrous ions as catalyst at concentration of 0.2 mM. At the same electrolysis time, only 23.7% of TOC removal found on CF support which proved the high mineralization efficiency of new material thanks to CNTF deposition. The CNTF@CF cathode maintained stable its activity during five experimental cycles of EF setup. The results indicated that CNTF@CF material could be a potential choice for wastewater treatment containing bio-refractory by electrochemical advanced oxidation processes.

  2. Efficient mineralization of the antibiotic trimethoprim by solar assisted photoelectro-Fenton process driven by a photovoltaic cell.

    Science.gov (United States)

    Zhang, Yanyu; Wang, Aimin; Tian, Xiujun; Wen, Zhenjun; Lv, Hanjiao; Li, Desheng; Li, Jiuyi

    2016-11-15

    In this study, a novel self-sustainable solar assisted photoelectro-Fenton (SPEF) system driven by a solar photovoltaic cell was developed for the efficient mineralization of antibiotic trimethoprim (TMP) in water. A comparative degradation of 200mgL(-1) TMP by RuO2/Ti anodic oxidation (AO), anodic oxidation with H2O2 electrogeneration (AO-H2O2), electro-Fenton (EF) and SPEF was investigated. SPEF was proved to exhibit the highest oxidation power, i.e., more than 80% TOC was removed after 360min SPEF treatment of 200mgL(-1) of TMP under optimal conditions at pH 3.0, 1.0mM Fe(2+) and 18mAcm(-2). Influences of current density, pH, initial Fe(2+) and initial TMP concentration on SPEF process were also studied. Ten aromatic intermediates generated from hydroxylation, carbonylation and demethylation reactions were identified using UPLC-QTOF-MS/MS system during the SPEF treatment, together with three carboxylic acids (oxamic, oxalic and formic acids) and two inorganic ions (NH4(+) and NO3(-)) measured. Therefore, a reasonable pathway of TMP degradation in SPEF process was proposed. Copyright © 2016 Elsevier B.V. All rights reserved.

  3. Carbon isotope effects associated with Fenton-like degradation of toluene: Potential for differentiation of abiotic and biotic degradation

    International Nuclear Information System (INIS)

    Ahad, Jason M.E.; Slater, Greg F.

    2008-01-01

    Hydrogen peroxide (H 2 O 2 )-mediated oxygenation to enhance subsurface aerobic biodegradation is a frequently employed remediation technique. However, it may be unclear whether observed organic contaminant mass loss is caused by biodegradation or chemical oxidation via hydroxyl radicals generated during catalyzed Fenton-like reactions. Compound-specific carbon isotope analysis has the potential to discriminate between these processes. Here we report laboratory experiments demonstrating no significant carbon isotope fractionation during Fenton-like hydroxyl radical oxidation of toluene. This implies that observation of significant isotopic fractionation of toluene at a site undergoing H 2 O 2 -mediated remediation would provide direct evidence of biodegradation. We applied this approach at a field site that had undergone 27 months of H 2 O 2 -mediated subsurface oxygenation. Despite substantial decreases (> 68%) in groundwater toluene concentrations carbon isotope signatures of toluene (δ 13 C tol ) showed no significant variation (mean = - 27.5 ±0.3 per mille, n = 13) over a range of concentrations from 11.1 to 669.0 mg L -1 . Given that aerobic degradation by ring attack has also been shown to result in no significant isotopic fractionation during degradation, at this site we were unable to discern the mechanism of degradation. However, such differentiation is possible at sites where aerobic degradation by methyl group attack results in significant isotopic fractionation

  4. The application of a monolithic triphenylphosphine reagent for conducting Appel reactions in flow microreactors

    Directory of Open Access Journals (Sweden)

    Kimberley A. Roper

    2011-12-01

    Full Text Available Herein we describe the application of a monolithic triphenylphosphine reagent to the Appel reaction in flow-chemistry processing, to generate various brominated products with high purity and in excellent yields, and with no requirement for further off-line purification.

  5. The application of a monolithic triphenylphosphine reagent for conducting Appel reactions in flow microreactors.

    Science.gov (United States)

    Roper, Kimberley A; Lange, Heiko; Polyzos, Anastasios; Berry, Malcolm B; Baxendale, Ian R; Ley, Steven V

    2011-01-01

    Herein we describe the application of a monolithic triphenylphosphine reagent to the Appel reaction in flow-chemistry processing, to generate various brominated products with high purity and in excellent yields, and with no requirement for further off-line purification.

  6. Microwave-Assisted Organic Synthesis Using Benign Reaction Medium and Reagents

    Science.gov (United States)

    Account of chemical reactions expedited by microwave (MW) exposure of neat reactants for the rapid one-pot assembly of heterocyclic compounds from in situ generated reactive intermediates via enamines or using hypervalent iodine reagents will be described that can be adapted for ...

  7. Catalytic enantioselective addition of organometallic reagents to N-formylimines using monodentate phosphoramidite ligands

    NARCIS (Netherlands)

    Pizzuti, Maria Gabriella; Minnaard, Adriaan J.; Feringa, Ben L.

    2008-01-01

    [GRAPHICS] The asymmetric synthesis of protected amines via the copper/phosphoramidite-catalyzed addition of organozine and organoaluminum reagents to N-acylimines, generated in situ from aromatic and aliphatic alpha-amidosulfones, is reported. High yields of optically active N-formyl-protected

  8. Catalytic Enantioselective Addition of Organometallic Reagents to N-Formylimines Using Monodentate Phosphoramidite Ligands

    NARCIS (Netherlands)

    Pizzuti, Maria Gabriella; Minnaard, Adriaan J.; Feringa, Bernard

    2008-01-01

    The asymmetric synthesis of protected amines via the copper/phosphoramidite-catalyzed addition of organozinc and organoaluminum reagents to N-acylimines, generated in situ from aromatic and aliphatic α-amidosulfones, is reported. High yields of optically active N-formyl-protected amines and

  9. A Dramatic Classroom Demonstration of Limiting Reagent Using the Vinegar and Sodium Hydrogen Carbonate Reaction

    Science.gov (United States)

    Artdej, Romklao; Thongpanchang, Tienthong

    2008-01-01

    This demonstration is designed to illustrate the concept of limiting reagent in a spectacular way. Via a series of experiments where the amount of vinegar is fixed and the amount of NaHCO[subscript 3] is gradually increased, the volume of CO[subscript 2] generated from the reaction varies corresponding to the amount of NaHCO[subscript 3] until it…

  10. Reagent' sets for the concentration of sup(99m)Tc and sup(113m)In

    International Nuclear Information System (INIS)

    Bianco de Salas, G.N.; Arciprete, J.; Mitta, A.E.A.

    1976-10-01

    A simple technique for the concentration of the eluates from 99 Mo/sup(99m)Tc and 113 Sn/sup(113m)In generators is described. The reagents' sets provided by the C.N.E.A. for the labelling of different radiopharmaceuticals can be used by only reducing their volumes proportionally. Both concentration techniques for Tc-99m and In-113m will be supplied to users as reagents' sets. (author) [es

  11. Decolorization of C.I. Acid Blue 9 solution by UV/Nano-TiO{sub 2}, Fenton, Fenton-like, electro-Fenton and electrocoagulation processes: A comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Khataee, A.R. [Water and Wastewater Treatment Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of)], E-mail: a_khataee@tabrizu.ac.ir; Vatanpour, V. [Water and Wastewater Treatment Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of)], E-mail: vahidvatanpoor@yahoo.com; Amani Ghadim, A.R. [Water and Wastewater Treatment Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of)], E-mail: a.r_amani@yahoo.com

    2009-01-30

    This study makes a comparison between UV/Nano-TiO{sub 2}, Fenton, Fenton-like, electro-Fenton (EF) and electrocoagulation (EC) treatment methods to investigate the removal of C.I. Acid Blue 9 (AB9), which was chosen as the model organic contaminant. Results indicated that the decolorization efficiency was in order of Fenton > EC > UV/Nano-TiO{sub 2} > Fenton-like > EF. Desired concentrations of Fe{sup 2+} and H{sub 2}O{sub 2} for the abatement of AB9 in the Fenton-based processes were found to be 10{sup -4} M and 2 x 10{sup -3} M, respectively. In the case of UV/Nano-TiO{sub 2} process, we have studied the influence of the basic photocatalytic parameters such as the irradiation time, pH of the solution and amount of TiO{sub 2} nanoparticles on the photocatalytic decolorization efficiency of AB9. Accordingly, it could be stated that the complete removal of color, after selecting desired operational parameters could be achieved in a relatively short time, about 25 min. Our results also revealed that the most effective decomposition of AB9 was observed with 150 mg/l of TiO{sub 2} nanoparticles in acidic condition. The effect of operational parameters including current density, initial pH and time of electrolysis were studied in electrocoagulation process. The results indicated that for a solution of 20 mg/l AB9, almost 98% color were removed, when the pH was about 6, the time of electrolysis was 8 min and the current density was approximately 25 A/m{sup 2} in electrocoagulation process.

  12. Decolorization of C.I. Acid Blue 9 solution by UV/Nano-TiO2, Fenton, Fenton-like, electro-Fenton and electrocoagulation processes: A comparative study

    International Nuclear Information System (INIS)

    Khataee, A.R.; Vatanpour, V.; Amani Ghadim, A.R.

    2009-01-01

    This study makes a comparison between UV/Nano-TiO 2 , Fenton, Fenton-like, electro-Fenton (EF) and electrocoagulation (EC) treatment methods to investigate the removal of C.I. Acid Blue 9 (AB9), which was chosen as the model organic contaminant. Results indicated that the decolorization efficiency was in order of Fenton > EC > UV/Nano-TiO 2 > Fenton-like > EF. Desired concentrations of Fe 2+ and H 2 O 2 for the abatement of AB9 in the Fenton-based processes were found to be 10 -4 M and 2 x 10 -3 M, respectively. In the case of UV/Nano-TiO 2 process, we have studied the influence of the basic photocatalytic parameters such as the irradiation time, pH of the solution and amount of TiO 2 nanoparticles on the photocatalytic decolorization efficiency of AB9. Accordingly, it could be stated that the complete removal of color, after selecting desired operational parameters could be achieved in a relatively short time, about 25 min. Our results also revealed that the most effective decomposition of AB9 was observed with 150 mg/l of TiO 2 nanoparticles in acidic condition. The effect of operational parameters including current density, initial pH and time of electrolysis were studied in electrocoagulation process. The results indicated that for a solution of 20 mg/l AB9, almost 98% color were removed, when the pH was about 6, the time of electrolysis was 8 min and the current density was approximately 25 A/m 2 in electrocoagulation process

  13. Copper-Catalyzed Oxy-Alkynylation of Diazo Compounds with Hypervalent Iodine Reagents.

    Science.gov (United States)

    Hari, Durga Prasad; Waser, Jerome

    2016-02-24

    Alkynes have found widespread applications in synthetic chemistry, biology, and materials sciences. In recent years, methods based on electrophilic alkynylation with hypervalent iodine reagents have made acetylene synthesis more flexible and efficient, but they lead to the formation of one equivalent of an iodoarene as side-product. Herein, a more efficient strategy involving a copper-catalyzed oxy-alkynylation of diazo compounds with ethynylbenziodoxol(on)e (EBX) reagents is described, which proceeds with generation of nitrogen gas as the only waste. This reaction is remarkable for its broad scope in both EBX reagents and diazo compounds. In addition, vinyl diazo compounds gave enynes selectively as single geometric isomers. The functional groups introduced during the transformation served as easy handles to access useful building blocks for synthetic and medicinal chemistry.

  14. Sperm cell purification from mock forensic swabs using SOMAmer™ affinity reagents.

    Science.gov (United States)

    Katilius, Evaldas; Carmel, Andrew B; Koss, Heidi; O'Connell, Dan; Smith, Breanna C; Sanders, Glenn M; LaBerge, Greggory S

    2018-03-27

    We have demonstrated a proof of concept with affinity-based purification of sperm cells from mock forensic samples using SOMAmer™ reagents, DNA-based affinity reagents developed by SomaLogic, Inc. SOMAmer reagents were selected in vitro using whole-cell SELEX to bind specifically with intact, detergent-treated sperm cells. Successful separation of sperm from epithelial cells and their debris was demonstrated using buccal swabs with added semen. Primarily male DNA profiles were generated from sperm cells eluted from the types of cotton swabs typically used for rape kit evidence collection. The quality of sperm DNA isolated from samples purified using SOMAmers is comparable to existing commercially available differential extraction-based methods at higher sperm concentrations. This purification method is simple, offers relatively rapid (forensic casework. Copyright © 2018. Published by Elsevier B.V.

  15. Effects of reaction conditions on nuclear laundry water treatment in Fenton process

    International Nuclear Information System (INIS)

    Vilve, Miia; Hirvonen, Arja; Sillanpaeae, Mika

    2009-01-01

    This study presents the efficiency of Fenton process in the degradation of organic compounds of nuclear laundry water. The influence of Fe 2+ and hydrogen peroxide ratio, hydrogen peroxide dose, pH and treatment time were investigated. The degradation of non-ionic surfactant and other organic compounds was analysed as COD, TOC and molecular weight distribution (MWD). The most cost-effective degradation conditions were at H 2 O 2 /Fe 2+ stoichiometric molar ratio of 2 with 5 min mixing and H 2 O 2 dose of 1000 mg l -1 . With the initial pH of 6, the reductions of COD and TOC were 85% and 69%, respectively. However, the removal of the organic compounds was mainly carried out by Fenton-based Fe 3+ coagulation rather than Fenton oxidation. Fenton process proved to be much more efficient than previously performed ozone-based oxidation processes.

  16. Fenton- and Persulfate-driven Regeneration of Contaminant-spent Granular Activated Carbon

    Science.gov (United States)

    Fenton- or persulfate-driven chemical oxidation regeneration of spent granular activated carbon (GAC) involves the combined, synergistic use of two treatment technologies: adsorption of organic chemicals onto GAC and chemical oxidation regeneration of the spent-GAC. Environmental...

  17. Degradation of p-nitrophenol using acoustic cavitation and Fenton chemistry

    International Nuclear Information System (INIS)

    Pradhan, Amey A.; Gogate, Parag R.

    2010-01-01

    Due to increasing human requirements, newer chemical species are being observed in the effluent streams with higher loadings such that efficacy of conventional treatment techniques is decreased and a combination of advanced oxidation processes is implemented for enhanced treatment ability and better energy efficiency. In the present work, the efficacy of combination of sonochemistry and Fenton chemistry has been investigated for wastewater treatment considering p-nitrophenol as model pollutant at pilot scale operation. Degradation of p-nitrophenol has been investigated under various operating conditions based on the use of ultrasound, Fenton process, ultrasound and H 2 O 2 , ultrasound and Fe, ultrasound and FeSO 4 , ultrasound and conventional Fenton process and ultrasound and advanced Fenton process. Two different initial concentrations of 0.5 and 1% of p-nitrophenol have been used for the experiments. In conventional Fenton and advanced Fenton process, two loadings of FeSO 4 and Fe powder 0.5 and 1 g/l and three ratios of FeSO 4 :H 2 O 2 and Fe:H 2 O 2 (1:5, 1:7.5 and 1:10) were investigated respectively. In all the systems investigated, maximum extent of degradation (66.4%) was observed for 0.5% p-nitrophenol concentration (w/v) using a combination of ultrasound and advanced Fenton process. The novelty of the work is in terms of investigating the efficacies of combined advanced oxidation processes based on the use of cavitation and Fenton chemistry at pilot scale operation and tries to establish the missing design related information for large scale operation of wastewater treatment.

  18. Heterogeneous activation of H{sub 2}O{sub 2} by defect-engineered TiO{sub 2−x} single crystals for refractory pollutants degradation: A Fenton-like mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Ai-Yong, E-mail: ayzhang@hfut.edu.cn; Lin, Tan; He, Yuan-Yi; Mou, Yu-Xuan

    2016-07-05

    Highlights: • Facet- and defect-engineered TiO{sub 2} is proposed for water treatment as Fenton-like catalyst. • The =Ti(III) center serves as lattice shuttle for electron transfer in H{sub 2}O{sub 2} activation. • TiO{sub 2} is promising due to low cost, high abundance, no toxicity and stable performance. - Abstract: The heterogeneous catalyst plays a key role in Fenton-like reaction for advanced oxidation of refractory pollutants in water treatment. Titanium dioxide (TiO{sub 2}) is a typical semiconductor with high industrial importance due to its earth abundance, low cost and no toxicity. In this work, it is found that TiO{sub 2} can heterogeneously activate hydrogen peroxide (H{sub 2}O{sub 2}, E° = 1.78 eV), a common chemical oxidant, to efficiently generate highly-powerful hydroxyl radical, ·OH (E{sup 0} = 2.80 eV), for advanced water treatment, when its crystal shape, exposed facet and oxygen-stoichiometry are finely tuned. The defect-engineered TiO{sub 2} single crystals exposed by high-energy {0 0 1} facets exhibited an excellent Fenton-like activity and stability for degrading typical refractory organic pollutants such as methyl orange and p-nitrophenol. Its defect-centered Fenton-like superiority is mainly attributed to the crystal oxygen-vacancy, single-crystalline structure and exposed polar {0 0 1} facet. Our findings could provide new chance to utilize TiO{sub 2} for Fenton-like technology, and develop novel heterogeneous catalyst for advanced water treatment.

  19. Heterogeneous activation of H_2O_2 by defect-engineered TiO_2_−_x single crystals for refractory pollutants degradation: A Fenton-like mechanism

    International Nuclear Information System (INIS)

    Zhang, Ai-Yong; Lin, Tan; He, Yuan-Yi; Mou, Yu-Xuan

    2016-01-01

    Highlights: • Facet- and defect-engineered TiO_2 is proposed for water treatment as Fenton-like catalyst. • The =Ti(III) center serves as lattice shuttle for electron transfer in H_2O_2 activation. • TiO_2 is promising due to low cost, high abundance, no toxicity and stable performance. - Abstract: The heterogeneous catalyst plays a key role in Fenton-like reaction for advanced oxidation of refractory pollutants in water treatment. Titanium dioxide (TiO_2) is a typical semiconductor with high industrial importance due to its earth abundance, low cost and no toxicity. In this work, it is found that TiO_2 can heterogeneously activate hydrogen peroxide (H_2O_2, E° = 1.78 eV), a common chemical oxidant, to efficiently generate highly-powerful hydroxyl radical, ·OH (E"0 = 2.80 eV), for advanced water treatment, when its crystal shape, exposed facet and oxygen-stoichiometry are finely tuned. The defect-engineered TiO_2 single crystals exposed by high-energy {0 0 1} facets exhibited an excellent Fenton-like activity and stability for degrading typical refractory organic pollutants such as methyl orange and p-nitrophenol. Its defect-centered Fenton-like superiority is mainly attributed to the crystal oxygen-vacancy, single-crystalline structure and exposed polar {0 0 1} facet. Our findings could provide new chance to utilize TiO_2 for Fenton-like technology, and develop novel heterogeneous catalyst for advanced water treatment.

  20. Feasibility of bioleaching combined with Fenton oxidation to improve sewage sludge dewaterability.

    Science.gov (United States)

    Liu, Changgeng; Zhang, Panyue; Zeng, Chenghua; Zeng, Guangming; Xu, Guoyin; Huang, Yi

    2015-02-01

    A novel joint method of bioleaching with Fenton oxidation was applied to condition sewage sludge. The specific resistance to filtration (SRF) and moisture of sludge cake (MSC) were adopted to evaluate the improvement of sludge dewaterability. After 2-day bioleaching, the sludge pH dropped to about 2.5 which satisfied the acidic condition for Fenton oxidation. Meanwhile, the SRF declined from 6.45×10(10) to 2.07×10(10) s2/g, and MSC decreased from 91.42% to 87.66%. The bioleached sludge was further conditioned with Fenton oxidation. From an economical point of view, the optimal dosages of H2O2 and Fe2+ were 0.12 and 0.036 mol/L, respectively, and the optimal reaction time was 60 min. Under optimal conditions, SRF, volatile solids reduction, and MSC were 3.43×10(8) s2/g, 36.93%, and 79.58%, respectively. The stability and settleability of sewage sludge were both improved significantly. Besides, the results indicated that bioleaching-Fenton oxidation was more efficient in dewatering the sewage sludge than traditional Fenton oxidation. The sludge conditioning mechanisms by bioleaching-Fenton oxidation might mainly include the flocculation effects and the releases of extracellular polymeric substances-bound water and intercellular water. Copyright © 2014. Published by Elsevier B.V.

  1. Photonic efficiency of the photodegradation of paracetamol in water by the photo-Fenton process.

    Science.gov (United States)

    Yamal-Turbay, E; Ortega, E; Conte, L O; Graells, M; Mansilla, H D; Alfano, O M; Pérez-Moya, M

    2015-01-01

    An experimental study of the homogeneous Fenton and photo-Fenton degradation of 4-amidophenol (paracetamol, PCT) is presented. For all the operation conditions evaluated, PCT degradation is efficiently attained by both Fenton and photo-Fenton processes. Also, photonic efficiencies of PCT degradation and mineralization are determined under different experimental conditions, characterizing the influence of hydrogen peroxide (H2O2) and Fe(II) on both contaminant degradation and sample mineralization. The maximum photonic degradation efficiencies for 5 and 10 mg L(-1) Fe(II) were 3.9 (H2O2 = 189 mg L(-1)) and 5 (H2O2 = 378 mg L(-1)), respectively. For higher concentrations of oxidant, H2O2 acts as a "scavenger" radical, competing in pollutant degradation and reducing the reaction rate. Moreover, in order to quantify the consumption of the oxidizing agent, the specific consumption of the hydrogen peroxide was also evaluated. For all operating conditions of both hydrogen peroxide and Fe(II) concentration, the consumption values obtained for Fenton process were always higher than the corresponding values observed for photo-Fenton. This implies a less efficient use of the oxidizing agent for dark conditions.

  2. Combined heterogeneous Electro-Fenton and biological process for the treatment of stabilized landfill leachate.

    Science.gov (United States)

    Baiju, Archa; Gandhimathi, R; Ramesh, S T; Nidheesh, P V

    2018-03-15

    Treatment of stabilized landfill leachate is a great challenge due to its poor biodegradability. Present study made an attempt to treat this wastewater by combining electro-Fenton (E-Fenton) and biological process. E-Fenton treatment was applied prior to biological process to enhance the biodegradability of leachate, which will be beneficial for the subsequent biological process. This study also investigates the efficiency of iron molybdophosphate (FeMoPO) nanoparticles as a heterogeneous catalyst in E-Fenton process. The effects of initial pH, catalyst dosage, applied voltage and electrode spacing on Chemical Oxygen Demand (COD) removal efficiency were analyzed to determine the optimum conditions. Heterogeneous E-Fenton process gave 82% COD removal at pH 2, catalyst dosage of 50 mg/L, voltage 5 V, electrode spacing 3 cm and electrode area 25 cm 2 . Combined E-Fenton and biological treatment resulted an overall COD removal of 97%, bringing down the final COD to 192 mg/L. Copyright © 2018 Elsevier Ltd. All rights reserved.

  3. A Brief History With Lessons Learned From The Hot Dry Rock Geothermal Energy Program At Fenton Hill, New Mexico, USA

    Science.gov (United States)

    Kelkar, S.; Woldegabriel, G. W.; Rehfeldt, K. R.

    2009-12-01

    and tracer data led to the conclusion that having multiple production wells could lead to improved energy extraction. Geochemical techniques were refined and tests were designed to use reactive tracers that could provide estimates of the reservoir temperature profiles. Water-rock interactions were found to be modest and did not significantly impact the surface plant operations. Numerous small seismic events were generated during hydraulic stimulations but they were of a very small magnitude and none caused noticeable movement at the land surface. The effects of reservoir stimulation were found to persist over a period of nearly 2 years after shut in. Cyclic flow tests demonstrated the ability of the HDR reservoir at Fenton Hill to regulate peak load demands, and the ability to act as an energy storage system. These tests demonstrated actual increase in the thermal output of the reservoir during cyclic production tests.HDR Reservoir Characteristics at Fenton Hill

  4. Decolorization of Diazo Dye Ponceau S by Fenton Process

    International Nuclear Information System (INIS)

    Muslim, M.; Habib, M.A.; Islam, T.S.A.; Mahmood, A.J.; Ismail, I.M.I.

    2013-01-01

    An attempt has been taken to decolorize and mineralize Ponceau S (PS), a diazo dye, in aqueous solution by Fenton process. Effects of solution pH, concentrations of H/sub 2/O/sub 2/, Fe(II) and PS on the decolorization of PS have also been studied through batch experiments. About 90percentage decolorization was found under the optimal conditions (PS): (H/sub 2/O/sub 2/): (Fe(II)) = 1:12:2 and (H/sub 2/O/sub 2/)/(Fe(II)) = 6 at pH 2.85 in 40 minutes. The overall results revealed that mineralization was rather slower as compared with the decolorization. (author)

  5. Fenton-enhanced {gamma}-radiolysis of cyanuric acid

    Energy Technology Data Exchange (ETDEWEB)

    Varghese, Rani [School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686560, Kerala (India); Aravind, Usha K. [School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686560, Kerala (India); Aravindakumar, Charuvila T. [School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686560, Kerala (India)]. E-mail: CT-Aravindakumar@rocketmail.com

    2007-04-02

    Degradation of cyanuric acid (OOOT), a stable end product of oxidative decomposition of atrazine, is investigated in a combined field of gamma radiolysis and fenton reaction. The reaction of hydroxyl radical ({center_dot}OH) at pH 6 was carried out by irradiating N{sub 2}O saturated aqueous solutions containing OOOT (1 x 10{sup -3} mol dm{sup -3}), and this resulted only a marginal degradation (20%). However, when the same reaction was carried out in the presence of varying concentrations of ferrous sulfate ((5-10) x 10{sup -5} mol dm{sup -3}), the decay of OOOT has been enhanced to more than 80%. This decay followed a first order kinetics. Nearly similar effects were observed with another triazine derivative, 2,4-dioxohexahydro-1,3,5-triazine (DHT). Two major reaction mechanisms are proposed for the enhanced decay of OOOT. The formation of unstable hydroxyl radical adducts from the reaction of {center_dot}OH which is the result of gamma radiolysis and the Fenton reaction (resulting from the reaction of the added Fe(II) and of the H{sub 2}O{sub 2} from the radiolysis of water), is proposed as the first mechanism. The second mechanism, which is likely the major contributor to degradation, is proposed as the reaction of a nucleophilic adduct, Fe(II)OOH, which could directly react with the electron deficient triazine ring. It is highlighted that such degradation reactions must be explored for the complete degradation of the byproducts of the oxidative decomposition of atrazine.

  6. Winery wastewater treatment by heterogeneous Photo-Fenton process and activated sludges; Depuracion de efluentes vinicolas ediante tratamientos Foto-Fenton en fase heterogenea y lodos activos

    Energy Technology Data Exchange (ETDEWEB)

    Mosteo, R.; Lalinde, N.; Ormad, Maria O. M.; Ovelleiro, J. L.

    2007-07-01

    The system composed by heterogeneous Photon-Fenton assisted by solar light and biological treatment based on activated sludge process treats adequately real winery wastewaters. the previous stage based on heterogeneous Photo-Fenton process produces a partial degradation of winery wastewaters and achieves a yield of degradation of organic matter (measured as TOC) close to 50%. The activated sludge process in simple stage doesn't present any operation problems (bulking phenomenon) and achieves a yield of degradation of organic matter of 90%. (Author) 16 refs.

  7. Solar photoelectro-Fenton degradation of the herbicide 4-chloro-2-methylphenoxyacetic acid optimized by response surface methodology

    International Nuclear Information System (INIS)

    Garcia-Segura, Sergi; Almeida, Lucio Cesar; Bocchi, Nerilso; Brillas, Enric

    2011-01-01

    Highlights: → The herbicide MCPA is quickly mineralized by solar photoelectro-Fenton. → A CCRD allowed the optimization of current, Fe 2+ content and solution pH. → TOC, MCE and energy consumption are described by response surface methodology. → Generated hydroxyl radical destroys MCPA and its aromatic oxidation by-products. → UV light of solar irradiation photolyzes the Fe(III)-carboxylate complexes produced. - Abstract: A central composite rotatable design and response surface methodology (RSM) were used to optimize the experimental variables of the solar photoelectro-Fenton (SPEF) treatment of the herbicide 4-chloro-2-methylphenoxyacetic acid (MCPA). The experiments were made with a flow plant containing a Pt/air-diffusion reactor coupled to a solar compound parabolic collector (CPC) under recirculation of 10 L of 186 mg L -1 MCPA solutions in 0.05 M Na 2 SO 4 at a liquid flow rate of 180 L h -1 with an average UV irradiation intensity of about 32 W m -2 . The optimum variables found for the SPEF process were 5.0 A, 1.0 mM Fe 2+ and pH 3.0 after 120 min of electrolysis. Under these conditions, 75% of mineralization with 71% of current efficiency and 87.7 kWh kg -1 TOC of energy consumption were obtained. MCPA decayed under the attack of generated hydroxyl radicals following a pseudo-first-order kinetics. Hydroxyl radicals also destroyed 4-chloro-2-methylphenol, methylhydroquinone and methyl-p-benzoquinone detected as aromatic by-products. Glycolic, maleic, fumaric, malic, succinic, tartronic, oxalic and formic acids were identified as generated carboxylic acids, which form Fe(III) complexes that are quickly photodecarboxylated by the UV irradiation of sunlight at the CPC photoreactor. A reaction sequence for the SPEF degradation of MCPA was proposed.

  8. A Snippet of Grignard Reagent's Histroy There are very few reagents ...

    Indian Academy of Sciences (India)

    IAS Admin

    with bromine, (eq.1). But he failed to notice the formation of phenylmagnesium bromide, because he was using excess bromine which destroyed it. Hence, he could isolate only bromobenzene,. (eq.2). Had he used only one molar equivalent of bromine, perhaps the organomagnesium reagent would bear his name today.

  9. Dissolved Organic Carbon Determination Using FIA and Photo-Fenton Reaction

    Directory of Open Access Journals (Sweden)

    Márcia M. Kondo

    2002-03-01

    Full Text Available The FIA-photo-Fenton system is based on the flow oxidation of the organic matter. A small amount of the sample containing H2O2 is injected into the acidic flow solution of Fe2+, which passes through a tubular PTFE reactor irradiated with UV light. The generated CO2 is quantified by a conductometric detector and is directly proportional to the dissolved organic carbon concentration in the sample. The optimization studies were performed using EDTA solutions. The average recovery of organic carbon was 83% with a relative standard deviation of 3.7% using a 1:5 molar ratio of Fe2+:H2O2, pH 2.0, 100 muL of sample injection and a liquid flow of 1 mL min-1. After optimization, the DOC concentration was quantified using 13 different organic compounds, where the average recovery was 90%. The rate of the analysis was in average 50 samples hour-1.O sistema FIA-foto-Fenton é baseado na oxidação em fluxo da matéria orgânica. Uma pequena quantidade de amostra contendo H2O2 é introduzida no fluxo de uma solução ácida de Fe2+, que passa por um reator tubular de PTFE irradiado com luz UV. O CO2 gerado é quantificado condutometricamente e é diretamente proporcional à concentração de carbono orgânico dissolvido na amostra. Os estudos de otimização foram realizados empregando soluções de EDTA. A recuperação média de carbono orgânico foi de 83% com desvio padrão relativo de 3,7% empregando 100 miL de amostra, pH 2,0, razão molar entre Fe2+ e H2O2 de 1:5 e uma vazão de 1 mL.min-1. Após otimização as concentrações de DOC foram quantificadas em 13 diferentes compostos orgânicos, com uma recuperação média de 90%. A velocidade de análise foi em média 50 amostras/h.

  10. Treatment of azo dye-containing wastewater by a Fenton-like process in a continuous packed-bed reactor filled with activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Mesquita, Isabel; Matos, Luis C. [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); Duarte, Filipa [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal); Maldonado-Hodar, F.J. [Department of Inorganic Chemistry, Faculty of Sciences, University of Granada, Av. Fuentenueva, 18071 Granada (Spain); Mendes, Adelio [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal); Madeira, Luis M., E-mail: mmadeira@fe.up.pt [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal)

    2012-10-30

    Highlights: Black-Right-Pointing-Pointer Oxidation with the Fenton's reagent was carried out in a packed-bed reactor. Black-Right-Pointing-Pointer The packed-bed was filled with iron-impregnated activated carbon. Black-Right-Pointing-Pointer The increment of temperature increases the Chicago Sky Blue removal and mineralization. Black-Right-Pointing-Pointer The values of iron leaching were below 0.4 ppm in the outlet effluent. Black-Right-Pointing-Pointer It was possible to reach a dye conversion of 88% in steady-state. - Abstract: In this work, oxidation with a Fenton-like process of a dye solution was carried out in a packed-bed reactor. Activated carbon Norit RX 3 Extra was impregnated with ferrous sulfate and used as catalyst (7 wt.% of iron). The effect of the main operating conditions in the Chicago Sky Blue (CSB) degradation was analyzed. It was found that the increase in temperature leads to a higher removal of the dye and an increased mineralization. However, it also increases the iron leaching, but the values observed were below 0.4 ppm (thus, far below European Union limits). It was possible to reach, at steady-state, a dye conversion of 88%, with a total organic carbon (TOC) removal of ca. 47%, being the reactor operated at 50 Degree-Sign C, pH 3, W{sub cat}/Q = 4.1 g min mL{sup -1} (W{sub cat} is the mass of catalyst and Q the total feed flow rate) and a H{sub 2}O{sub 2} feed concentration of 2.25 mM (for a CSB feed concentration of 0.012 mM). The same performance was reached in three consecutive cycles.

  11. Mineralization of phthalic acid by solar photoelectro-Fenton with a stirred boron-doped diamond/air-diffusion tank reactor: Influence of Fe3+ and Cu2+ catalysts and identification of oxidation products

    International Nuclear Information System (INIS)

    Garcia-Segura, Sergi; Salazar, Ricardo; Brillas, Enric

    2013-01-01

    Highlights: • Almost total mineralization of phthalic acid by solar photoelectro-Fenton with Fe 3+ , Cu 2+ and Fe 3+ –Cu 2+ mixtures. • Hydroxyl radical generation from photo-Fenton reaction under solar radiation. • Enhancement of the mineralization rate using Fe 3+ and small amounts of Cu 2+ . • Detection of eleven aromatic intermediates and six short-linear carboxylic acids. • Oxidation of Cu(II)-carboxylate complexes with ·OH and photolysis of Fe(III)-carboxylate species. -- Abstract: Here, the substrate decay and mineralization rate for 100 cm 3 of a 2.0 mM phthalic acid solution in 0.10 M Na 2 SO 4 of pH 3.0 have been studied by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF). The electrochemical cell was a stirred tank reactor containing a 3 cm 2 boron-doped diamond (BDD) anode and a 3 cm 2 air-diffusion cathode that generates H 2 O 2 . Cu 2+ and/or Fe 3+ were added as catalysts with total concentration of 0.50 mM and a constant current density of 33.3 mA cm −2 was applied. In EF with Cu 2+ or Fe 3+ alone and SPEF with only Cu 2+ , phthalic acid decayed slowly and poor mineralization was reached because the main oxidant was ·OH produced at the BDD surface from water oxidation. In contrast, the substrate destruction was largely enhanced using SPEF with 0.50 mM Fe 3+ since a high quantity of oxidant ·OH was produced in the bulk induced by photo-Fenton reaction. This treatment led to an almost total mineralization by the photolysis of generated Fe(III)-carboxylate complexes. In all cases, the decay of phthalic acid obeyed a pseudo-first-order reaction. The combination of Cu 2+ and Fe 3+ as catalysts accelerated the mineralization process in SPEF because Cu(II)-carboxylate complexes were also removed with ·OH formed from photo-Fenton reaction. The best SPEF process was found for 0.125 mM Cu 2+ + 0.375 mM Fe 3+ , giving rise to 99% mineralization with 40% current efficiency and 0.294 kWh g −1 TOC energy consumption. Eleven aromatics

  12. Activated sludge treatment by electro-Fenton process: Parameter optimization and degradation mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Rahmani, Ali Reza; Azarian, Ghasem; Berizi, Zohreh [Hamadan University of Medical Sciences, Hamadan (Iran, Islamic Republic of); Nematollahi, Davood [Bu-Ali-Sina University, Hamadan (Iran, Islamic Republic of); Godini, Kazem [Ilam University of Medical Sciences, Ilam (Iran, Islamic Republic of)

    2015-08-15

    This study was conducted to evaluate the mineralization of activated sludge (MAS) by a facile and environmentally friendly electro-Fenton process (EFP). The effects of initial H{sub 2}O{sub 2} concentration, pH value, applied current density and operating time on MAS through determining the removal rate of chemical oxygen demand (COD) and total coliform (TC) were studied. 72% of COD was removed by indirect oxidation double-mediated based on the electro- generation of hydroxyl radical and active chlorine, under the following optimum conditions: 127mmol L{sup -}1 of hydrogen peroxide, pH=3.0, 10 mA cm{sup -}2 of DC current, 120min of operating time, and 0.22mol L{sup -}1 of NaCl as the supporting electrolyte. Only in 10 min and pH 3.0 approximately 100% of TC was removed. The findings indicated that EFP can be applied efficiently for MAS by selecting appropriate operating conditions. The bottom line is that the process is entirely effective owing to the application of green oxidants (hydroxyl radical and active chlorine) and lack of being influenced by environmental situations, which can be introduced as an alternative to current conventional methods.

  13. Landfill leachate treatment by coagulation/flocculation combined with microelectrolysis-Fenton processes.

    Science.gov (United States)

    Luo, Kun; Pang, Ya; Li, Xue; Chen, Fei; Liao, Xingsheng; Lei, Min; Song, Yong

    2018-02-07

    Landfill leachate was pretreated by chemical flocculation with polyaluminum chloride (PAC) as a flocculant, and subsequently purified by the microelectrolysis-Fenton (MEF) process. Response surface methodology was employed to optimize the MEF process, and the optimal conditions were initial pH 3.20, H 2 O 2 concentration 3.57 g/L, and Fe-C dosage 104.52 g/L. The PAC coagulation combined with MEF processes obtained a superior decontamination performance, and the predicted chemical oxygen demand (COD) and humic acids (HA) removal were respectively 90.27% and 93.79%. The strong fluorescence peak at 425 nm and the trapping experiment showed that [Formula: see text] was generated during MEF, which had a strong oxidation ability to degrade organic recalcitrant pollutants. The ultraviolet-visible spectra and three-dimensional excitation-emission matrices spectra (3D-EEMs) indicated that PAC coagulation could preferentially remove protein-like substances, while the MEF process was effective in destructing organic recalcitrant pollutants, especially humic-like and fulvic-like substances.

  14. Activated sludge treatment by electro-Fenton process: Parameter optimization and degradation mechanism

    International Nuclear Information System (INIS)

    Rahmani, Ali Reza; Azarian, Ghasem; Berizi, Zohreh; Nematollahi, Davood; Godini, Kazem

    2015-01-01

    This study was conducted to evaluate the mineralization of activated sludge (MAS) by a facile and environmentally friendly electro-Fenton process (EFP). The effects of initial H 2 O 2 concentration, pH value, applied current density and operating time on MAS through determining the removal rate of chemical oxygen demand (COD) and total coliform (TC) were studied. 72% of COD was removed by indirect oxidation double-mediated based on the electro- generation of hydroxyl radical and active chlorine, under the following optimum conditions: 127mmol L - 1 of hydrogen peroxide, pH=3.0, 10 mA cm - 2 of DC current, 120min of operating time, and 0.22mol L - 1 of NaCl as the supporting electrolyte. Only in 10 min and pH 3.0 approximately 100% of TC was removed. The findings indicated that EFP can be applied efficiently for MAS by selecting appropriate operating conditions. The bottom line is that the process is entirely effective owing to the application of green oxidants (hydroxyl radical and active chlorine) and lack of being influenced by environmental situations, which can be introduced as an alternative to current conventional methods.

  15. 21 CFR 866.3120 - Chlamydia serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3120 Chlamydia... and antisera used in serological tests to identify antibodies to chlamydia in serum. Additionally...

  16. 21 CFR 866.3490 - Rhinovirus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3490 Rhinovirus... and antisera used in serological tests to identify antibodies to rhinovirus in serum. The...

  17. 21 CFR 866.3240 - Equine encephalomyelitis virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... HUMAN SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents... these viruses. Equine encephalomyelitis viruses are transmitted to humans by the bite of insects, such...

  18. 21 CFR 866.3165 - Cryptococcus neoformans serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3165... clinical specimens or from cultured isolates derived from clinical specimens. The identification aids in...

  19. 21 CFR 866.3020 - Adenovirus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3020 Adenovirus... identify adenoviruses directly from clinical specimens. The identification aids in the diagnosis of disease...

  20. 21 CFR 866.3480 - Respiratory syncytial virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3480... respiratory syncytial viruses from clinical specimens or from tissue culture isolates derived from clinical...

  1. 21 CFR 866.3140 - Corynebacterium spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3140.... from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria...

  2. 21 CFR 866.3250 - Erysipelothrix rhusiopathiae serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3250... Erysipelothrix rhusiopathiae from cultured isolates derived from clinical specimens. The identification aids in...

  3. 21 CFR 866.3270 - Flavobacterium spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3270.... from cultured isolates derived from clinical specimens. The identification aids in the diagnosis of...

  4. 21 CFR 866.3205 - Echovirus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3205 Echovirus... echoviruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The...

  5. 21 CFR 866.3110 - Campylobacter fetus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3110 Campylobacter... clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the...

  6. 21 CFR 866.3320 - Histoplasma capsulatum serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3320... capsulatum from clinical specimens or cultured isolates derived from clinical specimens. The identification...

  7. 21 CFR 866.3340 - Klebsiella spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3340 Klebsiella... from clinical specimens. The identification aids in the diagnosis of diseases caused by bacteria...

  8. 21 CFR 866.3930 - Vibrio cholerae serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3930 Vibrio... from cultured isolates derived from clinical specimens. The identification aids in the diagnosis of...

  9. 21 CFR 866.3010 - Acinetobacter calcoaceticus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3010... this bacterium from cultured isolates derived from clinical specimens. The identification aids in the...

  10. 21 CFR 866.3370 - Mycobacterium tuberculosis immunofluorescent reagents.

    Science.gov (United States)

    2010-04-01

    ... HUMAN SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents... used to identify Mycobacterium tuberculosis directly from clinical specimens. The identification aids...

  11. New data on masking reagents in complexometry

    International Nuclear Information System (INIS)

    Yurist, I.M.; Talmud, M.M.; Zajtsev, P.M.

    1985-01-01

    Recent literature data on employing inorganic and organic oxygen-, nitrogen- and sulfur-containing substances as masking reagents (MR) in complexonometry of alkali earths, rare earths and transition elements are reviewed for the period of 1971-1983. Effectiveness of any type of MR is shown to be dependent on the electron configuration of a cation being masked. Sr, La, Th, V(6), Zr, Hf, V(5), Nb(5), Ta(5), Mo(6), W(6) a.o. are masked by oxygen-containing ligands. Zn, Cd, Fe(2, 3), Co(2, 3), Ni, etc. are masked by nitrogen- and sulfur-bearing ligands. Thiocompounds mask mainly In, Tl(3), Sn(2), Pb, Bi

  12. ESTUDO MECANÍSTICO DAS REAÇÕES FENTON E CUPRO-FENTON POR ANÁLISE VOLTAMÉTRICA IN SITU

    Directory of Open Access Journals (Sweden)

    Leidi C. Friedrich

    Full Text Available Although the classical Fenton process exhibits a high initial rate of the organic compounds degradation, this process is not complete due to the formation of refractory compounds which resist the attack of the hydroxyl radicals. In the presence of Cu(II, the degradation is slower, but results in a greater reduction of TOC (total organic carbon measurements of net mineralization at the end of the reaction (t=120min. The addition of Cu(II ions to classical Fenton reaction conditions (Fe(II plus H2O2 at pH 3 is shown to accelerate the degradation of organic compounds. This synergic effect causes an approximately 15% additional reduction of the TOC. Voltammetric studies confirm the catalytic role of catechol in the presence of Fe(III/Fe(II and Cu(II/Cu(I. Addition of aliphatic acids to the reaction medium, did not interfere with the cupro-Fenton reaction, but had an inhibitory effect on the classical Fenton reaction, consistent with the following order of interaction with the ion Fe(III: Oxalic Acid (OA >> Formic Acid (FA ~ Acetic acid (AA.

  13. Degradation of the beta-blocker propranolol by electrochemical advanced oxidation processes based on Fenton's reaction chemistry using a boron-doped diamond anode

    Energy Technology Data Exchange (ETDEWEB)

    Isarain-Chavez, Eloy; Rodriguez, Rosa Maria; Garrido, Jose Antonio; Arias, Conchita; Centellas, Francesc; Cabot, Pere Lluis [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Brillas, Enric, E-mail: brillas@ub.ed [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-12-15

    The electro-Fenton (EF) and photoelectro-Fenton (PEF) degradation of solutions of the beta-blocker propranolol hydrochloride with 0.5 mmol dm{sup -3} Fe{sup 2+} at pH 3.0 has been studied using a single cell with a boron-doped diamond (BDD) anode and an air diffusion cathode (ADE) for H{sub 2}O{sub 2} electrogeneration and a combined cell containing the above BDD/ADE pair coupled in parallel to a Pt/carbon felt (CF) cell. This naphthalene derivative can be mineralized by both methods with a BDD anode. Almost overall mineralization is attained for the PEF treatments, more rapidly with the combined system due to the generation of higher amounts of hydroxyl radical from Fenton's reaction by the continuous Fe{sup 2+} regeneration at the CF cathode, accelerating the oxidation of organics to Fe(III)-carboxylate complexes that are more quickly photolyzed by UVA light. The homologous EF processes are less potent giving partial mineralization. The effect of current density, pH and Fe{sup 2+} and drug concentrations on the oxidation power of PEF process in combined cell is examined. Propranolol decay follows a pseudo first-order reaction in most cases. Aromatic intermediates such as 1-naphthol and phthalic acid and generated carboxylic acids such as maleic, formic, oxalic and oxamic are detected and quantified by high-performance liquid chromatography. The chloride ions present in the starting solution are slowly oxidized at the BDD anode. In PEF treatments, all initial N of propranolol is completely transformed into inorganic ions, with predominance of NH{sub 4}{sup +} over NO{sub 3}{sup -} ion.

  14. Development of versatile isotopic labeling reagents for profiling the amine submetabolome by liquid chromatography–mass spectrometry

    International Nuclear Information System (INIS)

    Zhou, Ruokun; Huan, Tao; Li, Liang

    2015-01-01

    Highlights: • Two new reagents were developed for chemical isotope labeling mass spectrometry (MS). • They could be used to label amine-containing metabolites in a metabolomic sample. • The labeled metabolites could be detected with much improved sensitivity in MS. • One of the reagents could also help generate useful MS/MS spectra for structural analysis. • These reagents should be useful for quantitative metabolomics. - Abstract: Metabolomic profiling involves relative quantification of metabolites in comparative samples and identification of the significant metabolites that differentiate different groups (e.g., diseased vs. controls). Chemical isotope labeling (CIL) liquid chromatography–mass spectrometry (LC–MS) is an enabling technique that can provide improved metabolome coverage and metabolite quantification. However, chemical identification of labeled metabolites can still be a challenge. In this work, a new set of isotopic labeling reagents offering versatile properties to enhance both detection and identification are described. They were prepared by a glycine molecule (or its isotopic counterpart) and an aromatic acid with varying structures through a simple three-step synthesis route. In addition to relatively low costs of synthesizing the reagents, this reaction route allows adjusting reagent property in accordance with the desired application objective. To date, two isotopic reagents, 4-dimethylaminobenzoylamido acetic acid N-hydroxylsuccinimide ester (DBAA-NHS) and 4-methoxybenzoylamido acetic acid N-hydroxylsuccinimide ester (MBAA-NHS), for labeling the amine-containing metabolites (i.e., amine submetabolome) have been synthesized. The labeling conditions and the related LC–MS method have been optimized. We demonstrate that DBAA labeling can increase the metabolite detectability because of the presence of an electrospray ionization (ESI)-active dimethylaminobenzoyl group. On the other hand, MBAA labeled metabolites can be fragmented

  15. Development of versatile isotopic labeling reagents for profiling the amine submetabolome by liquid chromatography–mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Ruokun; Huan, Tao; Li, Liang, E-mail: Liang.Li@ualberta.ca

    2015-06-30

    Highlights: • Two new reagents were developed for chemical isotope labeling mass spectrometry (MS). • They could be used to label amine-containing metabolites in a metabolomic sample. • The labeled metabolites could be detected with much improved sensitivity in MS. • One of the reagents could also help generate useful MS/MS spectra for structural analysis. • These reagents should be useful for quantitative metabolomics. - Abstract: Metabolomic profiling involves relative quantification of metabolites in comparative samples and identification of the significant metabolites that differentiate different groups (e.g., diseased vs. controls). Chemical isotope labeling (CIL) liquid chromatography–mass spectrometry (LC–MS) is an enabling technique that can provide improved metabolome coverage and metabolite quantification. However, chemical identification of labeled metabolites can still be a challenge. In this work, a new set of isotopic labeling reagents offering versatile properties to enhance both detection and identification are described. They were prepared by a glycine molecule (or its isotopic counterpart) and an aromatic acid with varying structures through a simple three-step synthesis route. In addition to relatively low costs of synthesizing the reagents, this reaction route allows adjusting reagent property in accordance with the desired application objective. To date, two isotopic reagents, 4-dimethylaminobenzoylamido acetic acid N-hydroxylsuccinimide ester (DBAA-NHS) and 4-methoxybenzoylamido acetic acid N-hydroxylsuccinimide ester (MBAA-NHS), for labeling the amine-containing metabolites (i.e., amine submetabolome) have been synthesized. The labeling conditions and the related LC–MS method have been optimized. We demonstrate that DBAA labeling can increase the metabolite detectability because of the presence of an electrospray ionization (ESI)-active dimethylaminobenzoyl group. On the other hand, MBAA labeled metabolites can be fragmented

  16. Alkylation of pyridines at their 4-positions with styrenes plus yttrium reagent or benzyl Grignard reagents.

    Science.gov (United States)

    Mizumori, Tomoya; Hata, Takeshi; Urabe, Hirokazu

    2015-01-02

    A new regioselective alkylation of pyridines at their 4-position was achieved with styrenes in the presence of yttrium trichloride, BuLi, and diisobutylaluminium hydride (DIBAL-H) in THF. Alternatively, similar products were more simply prepared from pyridines and benzyl Grignard reagents. These reactions are not only a useful preparation of 4-substituted pyridines but are also complementary to other relevant reactions usually giving 2-substituted pyridines. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Effect of reagent charge on the labeling of erythrocyte membrane proteins by photoactivated reagents

    International Nuclear Information System (INIS)

    Schaeffer, J.C.; Hakimian, R.; Shimer, M.L.

    1986-01-01

    Leaky erythrocyte ghosts were labeled with 3 H-[2-(4-azido-2-nitroanilino)ethyl]trimethylammonium iodide (cationic label) or 3 H-N-(4-azido-2-nitrophenyl)-β-alanine (anionic label). After the membranes were thoroughly washed, seven times as much cationic label was associated with the membranes as anionic label at 5 μM, whereas at 50 μM the cationic label was favored 15-fold. The distribution of label in the membrane proteins was ascertain by SDS-gel electrophoresis followed by autoradiography. At 50 μM cationic label, erythrocyte membrane protein bands 1,2,3,4.2, and 5 were intensely labeled, while band 6 was labeled weakly. At 5 μM cationic label, bands 1 and 4.2 were heavily labeled, while 2,3 and 5 were labeled less well. At both 50 μM and 5 μM anionic label, bands 1 and 6 were most prominently labeled. Bands 2,3,4.2 and 5 were labeled also at 50 μM, but they were labeled only very weakly at 5 μM. Band 4.1 was labeled very poorly if at all by either reagent. A mixture of the reagents gave an additive pattern. Thus, the charge and concentration of these reagents appear to play a major role in their ability to label membrane proteins indiscriminately. Because these reagents contain the same chromophore, 4-azido-2-nitroaniline, and differ mainly only in their charge, they may prove useful in assessing the location of charged sites on proteins in supramolecular complexes

  18. Fenton chemistry-based detemplation of an industrially relevant microcrystalline beta zeolite. Optimization and scaling-up studies

    NARCIS (Netherlands)

    Ortiz-Iniesta, Maria Jesus; Melian-Cabrera, Ignacio

    A mild template removal of microcrystalline beta zeolite, based on Fenton chemistry, was optimized. Fenton detemplation was studied in terms of applicability conditions window, reaction rate and scale up. TGA and CHN elemental analysis were used to evaluate the detemplation effectiveness, while 'CP,

  19. Removal of Refractory Organics from Biologically Treated Landfill Leachate by Microwave Discharge Electrodeless Lamp Assisted Fenton Process

    Directory of Open Access Journals (Sweden)

    Jiuyi Li

    2015-01-01

    Full Text Available Biologically treated leachate usually contains considerable amount of refractory organics and trace concentrations of xenobiotic pollutants. Removal of refractory organics from biologically treated landfill leachate by a novel microwave discharge electrodeless lamp (MDEL assisted Fenton process was investigated in the present study in comparison to conventional Fenton and ultraviolet Fenton processes. Conventional Fenton and ultraviolet Fenton processes could substantially remove up to 70% of the refractory organics in a membrane bioreactor treated leachate. MDEL assisted Fenton process achieved excellent removal performance of the refractory components, and the effluent chemical oxygen demand concentration was lower than 100 mg L−1. Most organic matters were transformed into smaller compounds with molecular weights less than 1000 Da. Ten different polycyclic aromatic hydrocarbons were detected in the biologically treated leachate, most of which were effectively removed by MDEL-Fenton treatment. MDEL-Fenton process provides powerful capability in degradation of refractory and xenobiotic organic pollutants in landfill leachate and could be adopted as a single-stage polishing process for biologically treated landfill leachate to meet the stringent discharge limit.

  20. Fenton-driven regeneration of MTBE-spent granular activated carbon - Effects of particle size and Iron Amendment Procedures

    Science.gov (United States)

    Fenton-driven regeneration of spent granular activated carbon (GAC) is a technology being developed to regenerate organic contaminant-spent GAC. Here, the effect of GAC particle size (>2 mm to <0.35 mm) on Fenton-driven oxidation of methyl tert-butyl ether (MTBE)-spent GAC was ev...

  1. Fenton-driven regeneration of MTBE-spent granular activated carbon - Effects of particle size and Iron Amendment Procedures

    Science.gov (United States)

    Fenton-driven regeneration of spent granular activated carbon (GAC) is a technology being developed to regenerate organic contaminant-spent GAC. Here, the effect of GAC particle size (>2 mm to Fenton-driven oxidation of methyl tert-butyl ether (MTBE)-spent GAC was ev...

  2. Photo-assisted Fenton type processes for the degradation of phenol: A kinetic study

    International Nuclear Information System (INIS)

    Kusic, Hrvoje; Koprivanac, Natalija; Bozic, Ana Loncaric; Selanec, Iva

    2006-01-01

    In this study the application of advanced oxidation processes (AOPs), dark Fenton and photo-assisted Fenton type processes; Fe 2+ /H 2 O 2 , Fe 3+ /H 2 O 2 , Fe 0 /H 2 O 2 , UV/Fe 2+ /H 2 O 2 , UV/Fe 3+ /H 2 O 2 and UV/Fe 0 /H 2 O 2 , for degradation of phenol as a model organic pollutant in the wastewater was investigated. A detail kinetic modeling which describes the degradation of phenol was performed. Mathematical models which predict phenol decomposition and formation of primary oxidation by-products: catechol, hydroquinone and benzoquinone, by applied processes were developed. The study also consist the modeling of mineralization kinetic of the phenol solution by applied AOPs. This part, besides well known reactions of Fenton and photo-Fenton chemistry, involves additional reactions which describe removal of iron from catalytic cycle through formation of ferric complexes and its regeneration induced by UV radiation. Phenol decomposition kinetic was monitored by HPLC analysis and total organic carbon content measurements (TOC). Complete phenol removal was obtained by all applied processes. Residual TOC by applied Fenton type processes ranged between 60.2 and 44.7%, while the efficiency of those processes was significantly enhanced in the presence of UV light, where residual TOC ranged between 15.2 and 2.4%

  3. The catalytic oxidation of malachite green by the microwave-Fenton processes.

    Science.gov (United States)

    Zheng, Huaili; Zhang, Huiqin; Sun, Xiaonan; Zhang, Peng; Tshukudu, Tiroyaone; Zhu, Guocheng

    2010-01-01

    Catalytic oxidation of malachite green using the microwave-Fenton process was investigated. 0% of malachite green de-colorization using the microwave process and 23.5% of malachite green de-colorization using the Fenton process were observed within 5 minutes. In contrast 95.4% of malachite green de-colorization using the microwave-Fenton was observed in 5 minutes. During the microwave-Fenton process, the optimum operating conditions for malachite green de-colorization were found to be 3.40 of initial pH, 0.08 mmol/L of Fe2+ concentration and 12.5 mmol/L of H2O2 concentration. Confirmatory tests were carried out under the optimum conditions and the COD removal rate of 82.0% and the de-colorization rate of 99.0% were observed in 5 minutes. The apparent kinetics equation of -dC/dt=0.0337 [malachite green]0.9860[Fe2+)]0.8234[H2O2]0.1663 for malachite green de-colorization was calculated, which implied that malachite green was the dominant factor in determining the removal efficiency of malachite green based on microwave-Fenton process.

  4. Iron-chelating agents never suppress Fenton reaction but participate in quenching spin-trapped radicals

    International Nuclear Information System (INIS)

    Li Linxiang; Abe, Yoshihiro; Kanagawa, Kiyotada; Shoji, Tomoko; Mashino, Tadahiko; Mochizuki, Masataka; Tanaka, Miho; Miyata, Naoki

    2007-01-01

    Hydroxyl radical formation by Fenton reaction in the presence of an iron-chelating agent such as EDTA was traced by two different assay methods; an electron spin resonance (ESR) spin-trapping method with 5,5-dimethyl-1-pyrroline N-oxide (DMPO), and high Performance liquid chromatography (HPLC)-fluorescence detection with terephthalic acid (TPA), a fluorescent probe for hydroxyl radicals. From the ESR spin-trapping measurement, it was observed that EDTA seemed to suppress hydroxyl radical formation with the increase of its concentration. On the other hand, hydroxyl radical formation by Fenton reaction was not affected by EDTA monitored by HPLC assay. Similar inconsistent effects of other iron-chelating agents such as nitrylotriacetic acid (NTA), diethylenetriamine penta acetic acid (DTPA), oxalate and citrate were also observed. On the addition of EDTA solution to the reaction mixture 10 min after the Fenton reaction started, when hydroxyl radical formation should have almost ceased but the ESR signal of DMPO-OH radicals could be detected, it was observed that the DMPO-OH· signal disappeared rapidly. With the simultaneous addition of Fe(II) solution and EDTA after the Fenton reaction ceased, the DMPO-OH· signal disappeared more rapidly. The results indicated that these chelating agents should enhance the quenching of [DMPO-OH]· radicals by Fe(II), but they did not suppress Fenton reaction by forming chelates with iron ions

  5. Synergetic pretreatment of waste activated sludge by hydrodynamic cavitation combined with Fenton reaction for enhanced dewatering.

    Science.gov (United States)

    Cai, Meiqiang; Hu, Jianqiang; Lian, Guanghu; Xiao, Ruiyang; Song, Zhijun; Jin, Micong; Dong, Chunying; Wang, Quanyuan; Luo, Dewen; Wei, Zongsu

    2018-04-01

    The dewatering of waste activated sludge by integrated hydrodynamic cavitation (HC) and Fenton reaction was explored in this study. We first investigated the effects of initial pH, sludge concentration, flow rate, and H 2 O 2 concentration on the sludge dewaterability represented by water content, capillary suction time and specific resistance to filtration. The results of dewatering tests showed that acidic pH and low sludge concentration were favorable to improve dewatering performance in the HC/Fenton system, whereas optimal flow rate and H 2 O 2 concentration applied depended on the system operation. To reveal the synergism of HC/Fenton treatment, a suite of analysis were implemented: three-dimensional excitation emission matrix (3-DEEM) spectra of extracellular polymeric substances (EPS) such as proteins and polysaccharides, zeta potential and particle size of sludge flocs, and SEM/TEM imaging of sludge morphology. The characterization results indicate a three-step mechanism, namely HC fracture of different EPS in sludge flocs, Fenton oxidation of the released EPS, and Fe(III) re-flocculation, that is responsible for the synergistically enhanced sludge dewatering. Results of current study provide a basis to improve our understanding on the sludge dewatering performance by HC/Fenton treatment and possible scale-up of the technology for use in wastewater treatment plants. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Electrokinetic-Fenton remediation of organochlorine pesticides from historically polluted soil.

    Science.gov (United States)

    Ni, Maofei; Tian, Shulei; Huang, Qifei; Yang, Yanmei

    2018-04-01

    Soil contamination by persistent organic pollutants (POPs) poses a great threat to historically polluted soil worldwide. In this study, soils were characterized, and organochlorine pesticides contained in the soils were identified and quantified. Individual electrokinetic (IE), EK-Fenton-coupled technologies (EF), and enhanced EK-Fenton treatment (E-1, E-2, and E-3) were applied to remediate soils contaminated with hexachloro-cyclohexane soprocide (HCH) and dichloro-diphenyl-trichloroethane (DDT). Variation of pH, electrical conductivity, and electroosmotic flow was evaluated during the EK-Fenton process. The IE treatment showed low removal efficiency for HCHs (30.5%) and DDTs (25.9%). In the EF treatment, the highest removal level (60.9%) was obtained for α-HCH, whereas P,P-DDT was the lowest (40.0%). Low solubility of pollutants impeded the HCH and DDT removal. After enhanced EK-Fenton treatment, final removal of pollutants decreased as follows: β-HCH (82.6%) > γ-HCH (81.6%) > α-HCH (81.2%) > δ-HCH (80.0%) > P,P-DDD (73.8%) > P,P-DDE (73.1%) > P,P-DDT (72.6%) > O,P-DDT (71.5%). The results demonstrate that EK-Fenton is a promising technology for POP removal in historically polluted soil.

  7. Evaluation of the mercaptobenzothiazole degradation by combined adsorption process and Fenton reaction using iron mining residue.

    Science.gov (United States)

    Martins, Adriana Lau da Silva; Teixeira, Luís Alberto César; da Fonseca, Fabiana Valéria; Yokoyama, Lídia

    2017-08-01

    The present study investigated the degradation of mercaptobenzothiazole (MBT), evaluating homogeneous and heterogeneous systems. An iron mineral residue from the desliming step of iron mining was used as a source in the Fenton-like reaction (advanced oxidation process). A granulometric analysis of the residue was performed and yielded fractions with high hematite (Fe 2 O 3 ) and low quartz content in sieves from 74 to below 44 mm. In this particle size range, the hematite content from 58.9% to 67.4% and the Brunauer-Emmett-Teller area from 0.1345 to 1.3137 m 2  g -1 were obtained. The zeta potential curves as a function of pH were obtained for the residue, the MBT solution and mixtures thereof. The adsorption of MBT in the residue and its degradation through the Fenton-like reaction were investigated. Adsorption tests and the Fenton-like reaction were carried out, where the MBT species and the residue are oppositely charged, yielding, respectively, 10% MBT adsorption on the surface of the residue and 100% MBT degradation by the Fenton-like reaction at pH 3, hydrogen peroxide concentration of 25 mg L -1 , residue concentration of 3 g L -1 , 200 rpm and 25°C, from a 100 mg L -1 MBT solution. MBT degradation was found to occur mainly by the heterogeneous Fenton-like process.

  8. Review Article: Toxic Effects of Some Reagents Used in Electron ...

    African Journals Online (AJOL)

    Ultrathin sections prepared for electron microscopy and histochemistry are indispensable in cytological, histological and histochemical studies. The paper discusses the various reagents used in these fields of study. Unfortunately, these reagents and chemicals are hazardous to health. There is wisdom in informing the ...

  9. Physically absorbable reagents-collectors in elementary flotation

    Energy Technology Data Exchange (ETDEWEB)

    S.A. Kondrat' ev; I.G. Bochkarev [Russian Academy of Sciences, Novosibirsk (Russian Federation). Institute of Mining

    2007-09-15

    Based on the reviewed researches held at the Institute of Mining, Siberian Branch, Russian Academy of Sciences, the effect of physically absorbable reagents-collectors on formation of a flotation complex and its stability in turbulent pulp flows in flotation machines of basic types is considered. The basic requirements for physically absorbable reagents-collectors at different flotation stages are established.

  10. 21 CFR 866.3520 - Rubeola (measles) virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Rubeola (measles) virus serological reagents. 866... Rubeola (measles) virus serological reagents. (a) Identification. Rubeola (measles) virus serological... to rubeola virus in serum. The identification aids in the diagnosis of measles and provides...

  11. 21 CFR 866.3355 - Listeria spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3355 Listeria spp... from clinical specimens. Additionally, some of these reagents consist of Listeria spp. antisera... clinical specimens. The identification aids in the diagnosis of listeriosis, a disease caused by bacteria...

  12. 21 CFR 866.3550 - Salmonella spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3550 Salmonella... isolates derived from clinical specimens. Additionally, some of these reagents consist of antisera... clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the...

  13. Reagents for the assay of cardenolide glycosides and aglycones

    International Nuclear Information System (INIS)

    Wilkinson, S.

    1976-01-01

    Some novel reagents are described for use in the radioimmunoassay of the 3-glycone derivatives of cardenolides (cardiac glycosides) and more especially digoxin, digitoxin, gitoxin, periplocin and lanatosides. Using these reagents these cardenolides and their derivatives may be assayed both in aqueous solution and in urine. A method is also described for performing such assays, including a suitable kit. (U.K.)

  14. 21 CFR 864.4020 - Analyte specific reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Analyte specific reagents. 864.4020 Section 864.4020 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Specimen Preparation Reagents § 864.4020 Analyte specific...

  15. 21 CFR 864.8950 - Russell viper venom reagent.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Russell viper venom reagent. 864.8950 Section 864.8950 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Hematology Reagents § 864.8950 Russell viper venom...

  16. 21 CFR 864.4010 - General purpose reagent.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false General purpose reagent. 864.4010 Section 864.4010 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Specimen Preparation Reagents § 864.4010 General purpose...

  17. Use of Competition Kinetics with Fast Reactions of Grignard Reagents

    DEFF Research Database (Denmark)

    Holm, Torkil

    2000-01-01

    small.This is concluded from experiments in which results obtained by competition kinetics are compared with results obtained directly by flow stream procedures. A clearer picture of the reactivity ratios is obtained when the highly reactive reagent is highly diluted with its competitor. A fast reagent...

  18. Spectrophotometric determination of tannins by phosphotungstic-phosphomolybdic reagent

    Energy Technology Data Exchange (ETDEWEB)

    Reicher, F; Sierakowski, M R; Correa, J B.C. [Parana Univ., Curitiba (Brazil). Dept. de Bioquimica

    1981-01-01

    There are several colorimetric techniques to determine tannins in plant extracts. One frequently used is the Folin method (phosphotungstic acid reagent) that procedures a blue color with phenolic compounds. However, this coloured complex is unstable. With the Folin-Ciocalteau reagent, used in protein determination (Lowry et al. J.B.C. 193: 265, 1951) good results were obtained, even in the absence of cooper solution. Using phosphotungstic-phosphomolybdic reagent (Folin-Denis), it was obtained maximum color with 1,0 ml of the reagent in 20 minutes, after the additon of 10 ml 20% sodium carbonate solution. Tannins samples containing 10 to 200 ..mu..g/ml were analysed. Absorbances are determined at 720 or 600 nm. Tannins of commercial preparations from Acacia negra were analysed by the phosphotungstic-phosphomolybdic reagent before (A) and after (B) treatment with chromate hyde powder. By this procedure hydrolysible tannins were determined (A-B).

  19. Spectrophotometric determination of tannins by phosphotungstic-phosphomolibdic reagent

    International Nuclear Information System (INIS)

    Reicher, F.; Sierakowski, M.R.; Correa, J.B.C.

    1981-01-01

    There are several colorimetric techniques to determine tannins in plant extracts. One frequently used is the Folin method (phosphotungstic acid reagent) that procedures a blue color with phenolic compounds. However, this coloured complex is unstable. With the Folin-Ciocalteau reagent, used in protein determination (Lowry et al. J.B.C. 193: 265, 1951) good results were obtained, even in the absence of cooper solution. Using phosphotungstic-phosphomolibdic reagent (Folin-Denis), it was obtained maximum color with 1,0 ml of the reagent in 20 minutes, after the adition of 10 ml 20% sodium carbonate solution. Tannins samples containing 10 to 200 μg/ml were analysed. Absorbances are determined at 720 or 600 nm. Tannins of commercial preparations from Acacia negra were analysed by the phosphotungstic-phosphomolibdic reagent before (A) and after (B) treatment with chromate hyde powder. By this procedure hydrolysible tannins were determined (A-B). (Author) [pt

  20. Reagent-loaded plastic microfluidic chips for detecting homocysteine

    International Nuclear Information System (INIS)

    Suk, Ji Won; Jang, Jae-Young; Cho, Jun-Hyeong

    2008-01-01

    This report describes the preliminary study on plastic microfluidic chips with pre-loaded reagents for detecting homocysteine (Hcy). All reagents needed in an Hcy immunoassay were included in a microfluidic chip to remove tedious assay steps. A simple and cost-effective bonding method was developed to realize reagent-loaded microfluidic chips. This technique uses an intermediate layer between two plastic substrates by selectively patterning polydimethylsiloxane (PDMS) on the embossed surface of microchannels and fixing the substrates under pressure. Using this bonding method, the competitive immunoassay for SAH, a converted form of Hcy, was performed without any damage to reagents in chips, and the results showed that the fluorescent signal from antibody antigen binding decreased as the SAH concentration increased. Based on the SAH immunoassay, whole immunoassay steps for Hcy detection were carried out in plastic microfluidic chips with all necessary reagents. These experiments demonstrated the feasibility of the Hcy immunoassay in microfluidic devices

  1. Advances in solar photoelectro-Fenton: Decolorization and mineralization of the Direct Yellow 4 diazo dye using an autonomous solar pre-pilot plant

    International Nuclear Information System (INIS)

    Garcia-Segura, Sergi; Brillas, Enric

    2014-01-01

    Highlights: • Assessment of an autonomous solar pre-pilot plant for solar photoelectro-Fenton. • Total decolorization and 96-97% mineralization for solutions of Direct Yellow 4 diazo dye at pH 3.0. • More rapid dye decay and mineralization at 0.50 mmol dm −3 Fe 2+ and maximum current of 5.0 A. • 11 aromatics, 22 hydroxylated derivatives and 9 carboxylic acids detected as intermediates. • Release of NH 4 + and SO 4 2− as main inorganic ions. - Abstract: Here, an overview on the advances in solar photoelectro-Fenton (SPEF) is initially presented to show that it is the more potent electrochemical advanced oxidation process based on Fenton's reaction chemistry to remove organic pollutants from waters, due to the synergistic action of generated hydroxyl radicals and solar irradiation. As a novel advance for SPEF, an autonomous solar pre-pilot plant is proposed to make an energetically inexpensive process that can be viable at industrial level. The plant of 10 dm 3 capacity contained a Pt/air-diffusion cell with 90.2 cm 2 electrode area, coupled to a solar compound parabolic collectors (CPCs) photoreactor of 1.57 dm 3 irradiation volume and to a solar photovoltaic panel that provides a maximum average current of 5.0 A. The oxidation ability of this plant was assessed by studying the degradation of Direct Yellow 4 (DY4) diazo dye, which involved the predominant destruction of organics by ·OH formed from Fenton's reaction between H 2 O 2 generated at the cathode and added Fe 2+ , along with the photolysis of Fe(III)-carboxylate complexes with sunlight in the CPCs photoreactor. The effect of Fe 2+ and dye contents as well as current on decolorization rate, substrate decay and mineralization rate was examined. About 96-97% mineralization was rapidly attained using 0.50 mmol dm −3 Fe 2+ and up to 0.32 mmol dm −3 DY4 at 5.0 A. The DY4 decay always obeyed a pseudo-first-order kinetics. Eleven aromatic products, twenty two hydroxylated derivatives

  2. Role of sulfate, chloride, and nitrate anions on the degradation of fluoroquinolone antibiotics by photoelectro-Fenton.

    Science.gov (United States)

    Villegas-Guzman, Paola; Hofer, Florian; Silva-Agredo, Javier; Torres-Palma, Ricardo A

    2017-12-01

    Taking ciprofloxacin (CIP) as a fluoroquinolone antibiotic model, this work explores the role of common anions (sulfate, nitrate, and chloride) during the application of photoelectro-Fenton (PEF) at natural pH to degrade this type of compound in water. The system was composed of an IrO 2 anode, Ti, or gas diffusion electrode (GDE) as cathode, Fe 2+ , and UV (254 nm). To determine the implications of these anions, the degradation pathway and efficiency of the PEF sub-processes (UV photolysis, anodic oxidation, and electro-Fenton at natural pH) were studied in the individual presence of the anions. The results highlight that degradation routes and kinetics are strongly dependent on electrolytes. When chloride and nitrate ions were present, indirect electro-chemical oxidation was identified by electro-generated HOCl and nitrogenated oxidative species, respectively. Additionally, direct photolysis and direct oxidation at the anode surface were identified as degradation routes. As a consequence of the different pathways, six primary CIP by-products were identified. Therefore, a scheme was proposed representing the pathways involved in the degradation of CIP when submitted to PEF in water with chloride, nitrate, and sulfate ions, showing the complexity of this process. Promoted by individual and synergistic actions of this process, the PEF system leads to a complete elimination of CIP with total removal of antibiotic activity against Staphylococcus aureus and Escherichia coli, and significant mineralization. Finally, the role of the anions was tested in seawater containing CIP, in which the positive contributions of the anions were partially suppressed by its OH radical scavenger action. The findings are of interest for the understanding of the degradation of antibiotics via the PEF process in different matrices containing sulfate, nitrate, and chloride ions.

  3. Coupling Fenton and biological oxidation for the removal of nitrochlorinated herbicides from water.

    Science.gov (United States)

    Sanchis, S; Polo, A M; Tobajas, M; Rodriguez, J J; Mohedano, A F

    2014-02-01

    The combination of Fenton and biological oxidation for the removal of the nitrochlorinated herbicides alachlor, atrazine and diuron in aqueous solution has been studied. The H2O2 dose was varied from 20 to 100% of the stoichiometric amount related to the initial chemical oxygen demand (COD). The effluents from Fenton oxidation were analyzed for ecotoxicity, biodegradability, total organic carbon (TOC), COD and intermediate byproducts. The chemical step resulted in a significant improvement of the biodegradability in spite of its negligible or even slightly negative effect on the ecotoxicity. Working at 60% of the stoichiometric H2O2 dose allowed obtaining highly biodegradable effluents in the cases of alachlor and atrazine. That dose was even lower (40% of the stoichiometric) for diuron. The subsequent biological treatment was carried out in a sequencing batch reactor (SBR) and the combined Fenton-biological treatment allowed up to around 80% of COD reduction. Copyright © 2013 Elsevier Ltd. All rights reserved.

  4. For the Fenton process in a sequential downflow and upflow system to treat textile dyeing wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Bae, W.K.; Ko, G.B.; Cho, S.J. [Dept. of Civil and Environmental Engineering, Hanyang Univ., Kyounggi (Korea); Lee, S.H. [Dept. of Environmental Engineering, Sangmyung Univ., Cheonan (Korea)

    2003-07-01

    Wastewater from textile dyeing industry is characterized by high temperature, pH, pollution loading such as color and COD which are containing refractory, toxic and high molecular weight compounds. It is therefore, presumed to be very resistant to microbial degradation. Textile dyeing wastewater is therefore, presumed to be very resistant to microbial degradation. Combined processes are usually applied, which are chemical oxidation and biological process for textile dyeing wastewater in order to satisfy water quality standards. Fenton process as advanced oxidation process is well known as effective process for the removal of color and recalcitrant organics. However, the exactly predominant reaction mechanisms during Fenton process are not well explained among coagulation, oxidation and sedimentation so far. This research attempts to evaluate the predominant reaction with comparable results of ferric coagulation and oxidation for the Fenton process. (orig.)

  5. Fenton-like reaction: a possible way to efficiently remove illicit drugs and pharmaceuticals from wastewater.

    Science.gov (United States)

    Mackuľak, Tomáš; Mosný, Michal; Grabic, Roman; Golovko, Oksana; Koba, Olga; Birošová, Lucia

    2015-03-01

    We analyzed 13 psychoactive pharmaceuticals, illicit drugs and their metabolites in wastewater treatment plant influent and effluent and the possibility of their degradation by biological and chemical processes. Tramadol (413-853 ng/L) and methamphetamine (460-682 ng/L) were the most concentrated compounds in the wastewater in winter and summer, respectively. A significant decrease in the concentration of tramadol in wastewater was measured during the summer. The lowest efficiency was observed for tramadol, venlafaxine, citalopram and oxazepam (∼ 10%) and the highest efficiency was observed for amphetamine and THC-COOH (∼ 80%). The efficiency of compound degradation via the Fenton reaction, a modified Fenton reaction and different degradation (by algae, wood-rotting fungi and enzymes at influent versus effluent) was determined. The Fenton reaction and its modification were efficient at eliminating these substances in comparison with the tested biological processes. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Sequential solar photo-fenton-biological system for the treatment of winery wastewaters.

    Science.gov (United States)

    Mosteo, R; Sarasa, J; Ormad, Maria P; Ovelleiro, J L

    2008-08-27

    In this study, winery wastewaters are considered for degradation using heterogeneous photo-Fenton as a preliminary step before biotreatment. The heterogeneous photo-Fenton process assisted by solar light is able to partially degrade the organic matter present in winery wastewaters. When an initial hydrogen peroxide concentration of 0.1 M is used over 24 h of treatment, a degradation yield of organic matter (measured as TOC) of around 50% is reached. The later treatment (activated sludge process) allows the elimination of 90% of the initial TOC present in pretreated winery wastewaters without producing nondesired side-effects, such as the bulking phenomenon, which is usually detected when this treatment is used alone. The final effluent contains a concentration of organic matter (measured as COD) of 128 mg O2/L. The coupled system comprising the heterogeneous photo-Fenton process and biological treatment based on activated sludge in simple stage is a real alternative for the treatment of winery wastewater.

  7. Fenton degradation of Cartap hydrochloride: identification of the main intermediates and the degradation pathway.

    Science.gov (United States)

    Tian, Kaixun; Ming, Cuixiang; Dai, Youzhi; Honore Ake, Kouassi Marius

    2015-01-01

    The advanced oxidation of Cartap hydrochloride (Cartap) promoted by the Fenton system in an aqueous medium was investigated. Based on total organic carbon, chemical oxygen demand and high-performance liquid chromatography, the oxidation of Cartap is quite efficient by the Fenton system. Its long chain is easily destroyed, but the reaction does not proceed to complete mineralization. Ion chromatography detection indicated the formation of acetic acid, propionic acid, formic acid, nitrous acid and sulfuric acid in the reaction mixtures. Further evidence of nitrogen monoxide and sulfur dioxide formation was obtained by using a flue gas analyzer. Monitoring by gas chromatograph-mass spectrometer demonstrated the formation of oxalic acid, ethanol, carbon dioxide, and L-alanine ethylamide. Based on these experimental results, plausible degradation pathways for Cartap mineralization in an aqueous medium by the Fenton system are proposed.

  8. Applying fenton process in acrylic fiber wastewater treatment and practice teaching

    Science.gov (United States)

    Zhang, Chunhui; Jiang, Shan

    2018-02-01

    Acrylic fiber manufacturing wastewater, containing a wider range of pollutants, high concentration of refractory organics, poisonous and harmful matters, was significant to treat from the effluents of wastewater treatment plants (WWTPs). In this work, a Fenton reactor was employed for advanced treatment of the WWTP effluents. An orthogonal test and a parametric study were carried out to determine the effect of the main operating conditions and the Fenton process attain excellent performance on the degradation of pollutants under an optimal condition of ferrous dosage was 6.25 mM, hydrogen peroxide was 75 mM and initial pH value was 3.0 in 90 min reaction time. The removal efficiency of COD, TOC, NH4 +-N and TN reached from 45% to 69%. Lastly, as a teaching advice, the Fenton reactor was used in practicing teaching nicely.

  9. Research on the Treatment of Aluminum Alloy Chemical Milling Wastewater with Fenton Process

    Science.gov (United States)

    Zong-liang, Huang; Ru, Li; Peng, Luo; Jun-li, Gu

    2018-03-01

    The aluminum alloy chemical milling wastewater was treated by Fenton method. The effect of pH value, reaction time, rotational speed, H2O2 dosage, Fe2+ dosage and the molar ratio between H2O2 and Fe2+ on the COD removal rate of aluminum alloy chemical milling wastewater were investigated by single factor experiment and orthogonal experiment. The results showed that the optimum operating conditions for Fenton oxidation were as follows: the initial pH value was 3, the rotational speed was 250r/min, the molar ratio of H2O2 and Fe2+ was 8, the reaction time was 90 min. Under the optimum conditions, the removal rate of the wastewater’s COD is about 72.36%. In the reaction kinetics that aluminum alloy chemical milling wastewater was oxidized and degraded by Fenton method under the optimum conditions, the reaction sequence of the initial COD was 0.8204.

  10. Degradation of 1-butyl-3-methylimidazolium chloride ionic liquid in a Fenton-like system

    International Nuclear Information System (INIS)

    Siedlecka, E.M.; Mrozik, W.; Kaczynski, Z.; Stepnowski, P.

    2008-01-01

    The study examined the usefulness of a Fenton-like system for the degradation of ionic liquid residues in water. The ionic liquid was oxidized in a dilute aqueous solution of 1-butyl-3-methylimidazolium chloride (bmimCl). The ionic liquid decomposes readily and rapidly in aqueous solution by chemical degradation in a Fenton-like system. Under chosen conditions the initial bmimCl solution was reduced by a factor of 0.973 within 90 min. Additional results showed that bmimCl degradations in a Fenton-like system in excess H 2 O 2 could be interpreted as a combined oxidation-reduction mechanism. Preliminary investigations of the mechanism of such degradations have indicated that initial OH· radicals can attack any one of the three carbon atoms on the imidazolium ring. The intermediates of this reaction may be mono- di- or amino- carboxylic acids

  11. Simple preparation of Fenton catalyst@bacterial cellulose for waste water treatment

    Science.gov (United States)

    Wibowo, Arie; Febi Indrawan, Radian; Triadhi, Untung; Hasdi Aimon, Akfiny; Iskandar, Ferry; Ardy, Husaini

    2018-02-01

    Heterogeneous fenton catalyst is one of the attractive technologies for destruction of persistent and non-biodegradable pollutant in wastewater, because it can be used in wide range of pH and recyclable. Herein, commercial bacterial celluloses (BCs) were used as an alternative support of fenton catalyst to improve their catalytic activity. Scanning Electron Microscope (SEM) observations indicated that the presence of BCs and decreasing precursor concentration might promote formation of smaller particle sizes of catalyst from 3.5 μm of bare catalyst to 0.7 μm of catalyst@BC. UV-vis measurement showed that fast degradation of dyes with half-time degradation at around 25 min was observed in sample using catalyst@BCs with precursor concentration of 0.01 M. Successful preparation of heterogeneous fenton catalyst with smaller particle size and better catalytic activity is important for their application in wastewater treatment.

  12. Environmental application of millimetre-scale sponge iron (s-Fe{sup 0}) particles (IV): New insights into visible light photo-Fenton-like process with optimum dosage of H{sub 2}O{sub 2} and RhB photosensitizers

    Energy Technology Data Exchange (ETDEWEB)

    Ju, Yongming, E-mail: juyongming@scies.org [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Innovative Laboratory for Environmental Functional Materials and Environmental Applications of Microwave Irradiation, South China Subcenter of State Environmental Dioxin Monitoring Center, Guangzhou 510655 (China); Guangdong Key Laboratory of Agro-Environment Integrated Control, South China Institute of Environmental Sciences, Guangzhou 510655 (China); Yu, Yunjiang, E-mail: yuyunjiang@scies.org [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Wang, Xiaoyan; Xiang, Mingdeng; Li, Liangzhong [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Deng, Dongyang [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Innovative Laboratory for Environmental Functional Materials and Environmental Applications of Microwave Irradiation, South China Subcenter of State Environmental Dioxin Monitoring Center, Guangzhou 510655 (China); Guangdong Key Laboratory of Agro-Environment Integrated Control, South China Institute of Environmental Sciences, Guangzhou 510655 (China); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, Department of Biomedical, Chemical and Environmental Engineering (DBCEE), University of Cincinnati, Cincinnati, Ohio, 45221-0012 (United States)

    2017-02-05

    Highlights: • Synergistic action of Rhodamine B (RhB), visible light, H{sub 2}O{sub 2} and s-Fe{sup 0} is essential. • The complexes of RhB and Fe{sup 3+} eject one electron via ligand-to-metal charge-transfer. • RhB assists the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). - Abstract: In this study, we firstly develop the photo-Fenton-like system with millimetric sponge iron (s-Fe{sup 0}), H{sub 2}O{sub 2}, visible light (vis, λ ≥ 420 nm) and rhodamine B (RhB), and present a comprehensive study concerning the mechanism. Thus, we investigate (1) the adsorption of RhB onto s-Fe{sup 0}, (2) the photo-Fenton-like removal of RhB over iron oxides generated from the corrosion of s-Fe{sup 0}, (3) the homogeneous photo-Fenton removal of RhB over Fe{sup 2+} or Fe{sup 3+}, (4) the Fe{sup 3+}-RhB complexes, and (5) the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). The results show that neither the adsorption process over s-Fe{sup 0} nor the photo-Fenton-like process over FeOOH, Fe{sub 3}O{sub 4} and Fe{sub 2}O{sub 3}, achieved efficient removal of RhB. For comparison, in homogeneous photo-Fenton process, the presence of Fe{sup 3+} ions, rather than Fe{sup 2+} ions, effectively eliminated RhB. Furthermore, the UV–vis spectra showing new absorbance at ∼ 285 nm indicate the complexes of RhB and Fe{sup 3+} ions, adopting vis photons to form excited state and further eject one electron via ligand-to-metal charge-transfer to activate H{sub 2}O{sub 2}. Additionally, efficient TBBPA removal was obtained only in the presence of RhB. Accordingly, the s-Fe{sup 0}– based photo-Fenton-like process assisted with dyestuff wastewater is promising for removing a series of persistent organic pollutants.

  13. Heterogeneous photo-Fenton decolorization of Orange II over Al-pillared Fe-smectite: Response surface approach, degradation pathway, and toxicity evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Li, Huiyuan; Li, Yanli [Department of Environmental Engineering, Wuhan University, Wuhan 430079 (China); Xiang, Luojing [Department of Environmental Engineering, Wuhan University, Wuhan 430079 (China); Université de Poitiers, UMR CNRS 7285, IC2MP, ENSIP, B1, 1 rue Marcel Doré, TSA 41105, Poitiers 86073 Cedex 9 (France); Huang, Qianqian; Qiu, Juanjuan [Department of Environmental Engineering, Wuhan University, Wuhan 430079 (China); Zhang, Hui, E-mail: eeng@whu.edu.cn [Department of Environmental Engineering, Wuhan University, Wuhan 430079 (China); Sivaiah, Matte Venkata; Baron, Fabien; Barrault, Joel; Petit, Sabine [Université de Poitiers, UMR CNRS 7285, IC2MP, ENSIP, B1, 1 rue Marcel Doré, TSA 41105, Poitiers 86073 Cedex 9 (France); Valange, Sabine, E-mail: sabine.valange@univ-poitiers.fr [Université de Poitiers, UMR CNRS 7285, IC2MP, ENSIP, B1, 1 rue Marcel Doré, TSA 41105, Poitiers 86073 Cedex 9 (France)

    2015-04-28

    Highlights: • Al-pillared Fe-smectite was synthesized and used as the photo-Fenton catalyst. • Response surface methodology was used to study the effects of reaction parameters. • The main intermediate products were identified by GC–MS technique. • A possible degradation pathway of Orange II was proposed. • All the generated products of Orange II were less toxic than the original dye. - Abstract: A ferric smectite clay material was synthesized and further intercalated with Al{sub 2}O{sub 3} pillars for the first time with the aim of evaluating its ability to be used as heterogeneous catalyst for the photo-Fenton decolorization of azo dye Orange II. UV irradiation was found to enhance the activity of the catalyst in the heterogeneous photo-Fenton process. Catalyst loading of 0.5 g/L and hydrogen peroxide concentration of 13.5 mM yielded a remarkable color removal, accompanied by excellent catalyst stability. The decolorization of Orange II followed the pseudo-first-order kinetics for initial dye concentrations from 20 to 160 mg/L. The central composite design (CCD) based on the response surface methodology (RSM) was applied to evaluate the effects of several operating parameters, namely initial pH, catalyst loading and hydrogen peroxide concentration, on the decolorization efficiency. The RSM model was derived and the response surface plots were developed based on the results. Moreover, the main intermediate products were separated and identified using gas chromatography–mass spectrometry (GC–MS) and a possible degradation pathway was proposed accordingly. The acute toxicity experiments illustrated that the Daphniamagna immobilization rate continuously decreased during 150 min reaction, indicating that the effluent was suitable for sequential biological treatment.

  14. Hepatitis A Virus Disinfection in Water by Solar Photo-Fenton Systems.

    Science.gov (United States)

    Polo, David; García-Fernández, Irene; Fernández-Ibañez, Pilar; Romalde, Jesús L

    2018-06-01

    This study evaluates and compares the effectiveness of solar photo-Fenton systems for the inactivation of hepatitis A virus (HAV) in water. The effect of solar irradiance, dark- Fenton reaction and three different reactant concentrations (2.5/5, 5/10 and 10/20 mg/L of Fe 2+ /H 2 O 2 ) on the photo-Fenton process were tested in glass bottle reactors (200 mL) during 6 h under natural sunlight. Disinfection kinetics were determined both by RT-qPCR and infectivity assays. Mean water temperatures ranged from 25 to 27.3 °C, with a maximum local noon UV irradiances of 22.36 W/m 2 . Photo-Fenton systems yielded increased viral reduction rates in comparison with the isolated effect under the Fenton reaction in darkness (negligible viral reduction) or the solar radiation (0.25 Log of RNA reduction). With the highest concentration employed (10-20 mg/L Fe 2+ -H 2 O 2 ), an average RNA reduction rate of ~ 1.8 Log (initial concentration of 10 5 pfu/mL) and a reduction of 80% in the infectivity capacity were reached. Results showed a strong synergistic effect between Fe 2+ /H 2 O 2 and sunlight, demonstrating that significant disinfection rates of HAV under photo-Fenton systems may occur with relatively higher efficiency at middle environmental temperatures and without the need for an energy-intensive light source.

  15. A bionic system with Fenton reaction and bacteria as a model for bioprocessing lignocellulosic biomass.

    Science.gov (United States)

    Zhang, Kejing; Si, Mengying; Liu, Dan; Zhuo, Shengnan; Liu, Mingren; Liu, Hui; Yan, Xu; Shi, Yan

    2018-01-01

    The recalcitrance of lignocellulosic biomass offers a series of challenges for biochemical processing into biofuels and bio-products. For the first time, we address these challenges with a biomimetic system via a mild yet rapid Fenton reaction and lignocellulose-degrading bacterial strain Cupriavidus basilensis B-8 (here after B-8) to pretreat the rice straw (RS) by mimicking the natural fungal invasion process. Here, we also elaborated the mechanism through conducting a systematic study of physicochemical changes before and after pretreatment. After synergistic Fenton and B-8 pretreatment, the reducing sugar yield was increased by 15.6-56.6% over Fenton pretreatment alone and 2.7-5.2 times over untreated RS (98 mg g -1 ). Morphological analysis revealed that pretreatment changed the surface morphology of the RS, and the increase in roughness and hydrophilic sites enhanced lignocellulose bioavailability. Chemical components analyses showed that B-8 removed part of the lignin and hemicellulose which caused the cellulose content to increase. In addition, the important chemical modifications also occurred in lignin, 2D NMR analysis of the lignin in residues indicated that the Fenton pretreatment caused partial depolymerization of lignin mainly by cleaving the β- O -4 linkages and by demethoxylation to remove the syringyl (S) and guaiacyl (G) units. B-8 could depolymerize amount of the G units by cleaving the β-5 linkages that interconnect the lignin subunits. A biomimetic system with a biochemical Fenton reaction and lignocellulose-degrading bacteria was confirmed to be able for the pretreatment of RS to enhance enzymatic hydrolysis under mild conditions. The high digestibility was attributed to the destruction of the lignin structure, partial hydrolysis of the hemicellulose and partial surface oxidation of the cellulose. The mechanism of synergistic Fenton and B-8 pretreatment was also explored to understand the change in the RS and the bacterial effects on

  16. The contributions of the music of George Fenton to the fi lms of Ken Loach

    OpenAIRE

    Sofía López Hernández

    2018-01-01

    Ken Loach is a high profile British film director. Since the mid 1960’s, he has made numerous films for cinema and television. There is already a lot written about his way of filming and yet very little is written about the music for his films. To be able to get inside the music of Ken Loach’s films, we must first talk about George Fenton as he has been Loach’s usual composer since 1994. The object of this article is to fill this gap: to discover what musical characteristics Fenton contri...

  17. The contributions of the music of George Fenton to the fi lms of Ken Loach

    Directory of Open Access Journals (Sweden)

    Sofía López Hernández

    2018-01-01

    Full Text Available Ken Loach is a high profile British film director. Since the mid 1960’s, he has made numerous films for cinema and television. There is already a lot written about his way of filming and yet very little is written about the music for his films. To be able to get inside the music of Ken Loach’s films, we must first talk about George Fenton as he has been Loach’s usual composer since 1994. The object of this article is to fill this gap: to discover what musical characteristics Fenton contributes to Loach’s cinema.

  18. Personal Review: Progress and prospect in electro-Fenton process for wastewater treatment

    Institute of Scientific and Technical Information of China (English)

    JIANG Cheng-chun; ZHANG Jia-fa

    2007-01-01

    As a novel advanced oxidation process (AOP), electro-Fenton process is powerful for degrading most organic compounds including toxic and non-biodegradable ones, and so has attracted great attention. This paper reviews this process in detail including the mechanism, electrolytic bath, electrode materials, aerations and operation parameters. The application of electro-Fenton method in wastewater treatment is evaluated and summarized. Future work in this field is suggested, and three main directions of new electrode exploitation, development of assisted technologies and mechanistic study should be strengthened.

  19. STUDY ON OIL WASTEWATER TREATMENT WITH POLYMERIC REAGENTS

    Directory of Open Access Journals (Sweden)

    RODICA BUCUROIU

    2016-04-01

    Full Text Available Used the polymeric reagents in oil wastewater treatment is an effective method of eliminate hydrocarbons. The present study aims to finding reagents that lead to lowering of extractible (EXT, suspended solids (SS and chemical oxygen demand (COD of industrial wastewater from washing cars in loading ramps petroleum products. For this purpose five reagents were tested, namely: polyamines, cationic polyacrylamides, polydiallydimethyl ammonium chloride (PolyDADMAC, melamine formaldehyde polymer resin and polydicyandiamide polymer resin. Obtaining removal degrees over 80 % justifies using this method in the industrial practice.

  20. N-tritioacetoxyphthalimide: A new high specific activity tritioacetylating reagent

    International Nuclear Information System (INIS)

    Saljoughian, M.; Morimoto, Hiromi; Than, Chit

    1996-01-01

    The authors' aim was to develop a nonvolatile, stable, and facile tritioacetylating reagent and to demonstrate its use on simple peptides. Accordingly, the authors made the synthesis of high specific activity N-(tritioacetoxy) derivatives of succinimide, phthalimide, and naphthalimide a major focus. As the preferred approach, N-(tritioacetoxy)phthalimide was prepared by radical dehalogenation of N-(iodoacetoxy)phthalimide using high specific activity tributyltin tritide. This tritiated acetylation reagent was characterized by 3 H and 1 H NMR spectroscopy and by radio-HPLC. Efficacy of the reagent was investigated by tritioacetylation of several peptides at their N-terminal amino group. 26 refs., 1 fig

  1. Sequential Combination of Electro-Fenton and Electrochemical Chlorination Processes for the Treatment of Anaerobically-Digested Food Wastewater.

    Science.gov (United States)

    Shin, Yong-Uk; Yoo, Ha-Young; Kim, Seonghun; Chung, Kyung-Mi; Park, Yong-Gyun; Hwang, Kwang-Hyun; Hong, Seok Won; Park, Hyunwoong; Cho, Kangwoo; Lee, Jaesang

    2017-09-19

    A two-stage sequential electro-Fenton (E-Fenton) oxidation followed by electrochemical chlorination (EC) was demonstrated to concomitantly treat high concentrations of organic carbon and ammonium nitrogen (NH 4 + -N) in real anaerobically digested food wastewater (ADFW). The anodic Fenton process caused the rapid mineralization of phenol as a model substrate through the production of hydroxyl radical as the main oxidant. The electrochemical oxidation of NH 4 + by a dimensionally stable anode (DSA) resulted in temporal concentration profiles of combined and free chlorine species that were analogous to those during the conventional breakpoint chlorination of NH 4 + . Together with the minimal production of nitrate, this confirmed that the conversion of NH 4 + to nitrogen gas was electrochemically achievable. The monitoring of treatment performance with varying key parameters (e.g., current density, H 2 O 2 feeding rate, pH, NaCl loading, and DSA type) led to the optimization of two component systems. The comparative evaluation of two sequentially combined systems (i.e., the E-Fenton-EC system versus the EC-E-Fenton system) using the mixture of phenol and NH 4 + under the predetermined optimal conditions suggested the superiority of the E-Fenton-EC system in terms of treatment efficiency and energy consumption. Finally, the sequential E-Fenton-EC process effectively mineralized organic carbon and decomposed NH 4 + -N in the real ADFW without external supply of NaCl.

  2. Sono-photo-Fenton oxidation of bisphenol-A over a LaFeO3 perovskite catalyst.

    Science.gov (United States)

    Dükkancı, Meral

    2018-01-01

    In this study, oxidation of bisphenol-A (IUPAC name - 2,2-(4,4-dihydroxyphenyl, BPA), which is an endocrine disrupting phenolic compound used in the polycarbonate plastic and epoxy resin industry, was investigated using sono-photo-Fenton process under visible light irradiation in the presence of an iron containing perovskite catalyst, LaFeO 3 . The catalyst prepared by sol-gel method, calcined at 500°C showed a catalytic activity in BPA oxidation using sono-photo-Fenton process with a degradation degree and a chemical oxygen demand (COD) reduction of 21.8% and 11.2%, respectively. Degradation of BPA was studied by using individual and combined advanced oxidation techniques including sonication, heterogeneous Fenton reaction and photo oxidation over this catalyst to understand the effect of each process on degradation of BPA. It was seen, the role of sonication was very important in hybrid sono-photo-Fenton process due to the pyrolysis and sonoluminescence effects caused by ultrasonic irradiation. The prepared LaFeO 3 perovskite catalyst was a good sonocatalyst rather than a photocatalyst. Sonication was not only the effective process to degrade BPA but also it was the cost effective process in terms of energy consumption. The studies show that the energy consumption is lower in the sono-Fenton process than those in the photo-Fenton and sono-photo- Fenton processes. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Quick photo-Fenton degradation of phenolic compounds by Cu/Al2O3-MCM-41 under visible light irradiation: small particle size, stabilization of copper, easy reducibility of Cu and visible light active material.

    Science.gov (United States)

    Pradhan, Amaresh C; Nanda, Binita; Parida, K M; Das, Mira

    2013-01-14

    The present study reports the photo-Fenton degradation of phenolic compounds (phenol, 2-chloro-4-nitrophenol and 4-chloro-2-nitrophenol) in aqueous solution using mesoporous Cu/Al(2)O(3)-MCM-41 nanocomposite as a heterogeneous photo-Fenton-like catalyst. The in situ incorporation of mesoporous Al(2)O(3) (MA) into the framework of MCM-41 (sol-gel method) forms Al(2)O(3)-MCM-41 and wetness impregnation of Cu(II) on Al(2)O(3)-MCM-41 generates mesoporous Cu/Al(2)O(3)-MCM-41 composite. The effects of pH and H(2)O(2) concentration on degradation of phenol, 2-chloro-4-nitrophenol and 4-chloro-2-nitrophenol are studied. Kinetics analysis shows that the photocatalytic degradation reaction follows a first-order rate equation. Mesoporous 5 Cu/Al(2)O(3)-MCM-41 is found to be an efficient photo-Fenton-like catalyst for the degradation of phenolic compounds. It shows nearly 100% degradation in 45 min at pH 4. The combined effect of small particle size, stabilization of Cu(2+) on the support Al(2)O(3)-MCM-41, ease reducibility of Cu(2+) and visible light activeness are the key factors for quick degradation of phenolic compounds by Cu/Al(2)O(3)-MCM-41.

  4. Application of the Fenton's process in a bubble column reactor for hydroquinone degradation.

    Science.gov (United States)

    Lima, Vanessa N; Rodrigues, Carmen S D; Madeira, Luis M

    2017-11-27

    The aim of this study was to assess the degradation and mineralization of hydroquinone (HQ) by the Fenton's process in a bubble column reactor (BCR). The effect of the main operating variables, namely, air flow rate, effluent volume, hydrogen peroxide (H 2 O 2 ) concentration, catalyst (Fe 2+ ) dose, initial pH, and temperature, were assessed. For all air flow rates tested, no concentration gradients along the column were noticed, evidencing that a good mixing was reached in the BCR. For the best conditions tested ([H 2 O 2 ] = 500 mg/L, [Fe 2+ ] = 45 mg/L, T = 24 °C, Q air  = 2.5 mL/min, pH = 3.0, and V = 5 L), complete HQ degradation was reached, with ~ 39% of total organic carbon (TOC) removal, and an efficiency of the oxidant use-η H2O2 -of 0.39 (ratio between TOC removed per H 2 O 2 consumed normalized by the theoretical stoichiometric value); moreover, a non-toxic effluent was generated. Under these conditions, the intermediates and final oxidation compounds identified and quantified were a few carboxylic acids, namely, maleic, pyruvic, and oxalic. As a strategy to improve the TOC removal, a gradual dosage of the optimal H 2 O 2 concentration was implemented, being obtained ~ 55% of mineralization (with complete HQ degradation). Finally, the matrix effect was evaluated, for which a real wastewater was spiked with 100 mg/L of HQ; no reduction in terms of HQ degradation and mineralization was observed compared to the solution in distilled water.

  5. A convenient method to synthesize N-[3H]methyl-N-nitrosocarbamate transfer reagents

    International Nuclear Information System (INIS)

    Mehta, P.; Gold, B.; Konakahara, T.

    1992-01-01

    Activated N-alkyl-N-nitrosocarbamates are useful acyl transfer reagents that are employed in the synthesis of N-alkyl-N-nitrosoureas and related N-nitroso compounds. The nitrosourea products are of chemical and biological interest because they provide access to the in situ generation of highly reactive carbonium type intermediates, which, depending on their structure, can be powerful carcinogens or antineoplastic agents. The availability of radiolabeled nitrosoureas greatly facilitates studies on their chemical and biological activities. Generally, the synthesis of activated nitrosocarbamates requires condensation of radiolabeled alkylisocyanates with the appropriate alcohol. Because radiolabeled alkylisocyanates are not commercially available and/or troublesome to synthesize, we have developed an easy and economical method for preparing N-[ 3 H]methyl-N-nitrosocarbamates suitable for use as transfer reagents utilizing 1,2,2,2-tetrachloroethyl chloroformate and [ 3 H]methylamine hydrochloride as starting materials. (author)

  6. A convenient method to synthesize N-[[sup 3]H]methyl-N-nitrosocarbamate transfer reagents

    Energy Technology Data Exchange (ETDEWEB)

    Mehta, P.; Gold, B. (Nebraska Univ., Omaha, NE (United States). Eppley Inst. for Research in Cancer); Konakahara, T. (Science Univiversity of Tokyo, Noda, Chiba (Japan). Faculty of Science and Technology)

    1992-11-01

    Activated N-alkyl-N-nitrosocarbamates are useful acyl transfer reagents that are employed in the synthesis of N-alkyl-N-nitrosoureas and related N-nitroso compounds. The nitrosourea products are of chemical and biological interest because they provide access to the in situ generation of highly reactive carbonium type intermediates, which, depending on their structure, can be powerful carcinogens or antineoplastic agents. The availability of radiolabeled nitrosoureas greatly facilitates studies on their chemical and biological activities. Generally, the synthesis of activated nitrosocarbamates requires condensation of radiolabeled alkylisocyanates with the appropriate alcohol. Because radiolabeled alkylisocyanates are not commercially available and/or troublesome to synthesize, we have developed an easy and economical method for preparing N-[[sup 3]H]methyl-N-nitrosocarbamates suitable for use as transfer reagents utilizing 1,2,2,2-tetrachloroethyl chloroformate and [[sup 3]H]methylamine hydrochloride as starting materials. (author).

  7. Tetrameric DABCO™-Bromine: an Efficient and Versatile Reagent ...

    African Journals Online (AJOL)

    NJD

    Reagent for Bromination of Various Organic Compounds. Majid M. Heravi,a* ... aDepartment of Chemistry, School of Sciences, Azzahra University, Vanak, Tehran, Iran. bChemistry ... Synthesis of "-bromo ketones and nitriles has also been ...

  8. 21 CFR 866.3470 - Reovirus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3470 Reovirus... and antisera used in serological tests to identify antibodies to reovirus in serum. The identification...

  9. 21 CFR 866.3870 - Trypanosoma spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3870 Trypanosoma... consist of antigens and antisera used in serological tests to identify antibodies to Trypanosoma spp. in...

  10. 21 CFR 866.3630 - Serratia spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3630 Serratia spp... antigens and antisera used in serological tests to identify Serratia spp. from cultured isolates. The...

  11. 21 CFR 866.3850 - Trichinella spiralis serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3850... devices that consist of antigens and antisera used in serological tests to identify antibodies to...

  12. 21 CFR 866.3680 - Sporothrix schenckii serological reagents.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3680... devices that consist of antigens and antisera used in serological tests to identify antibodies to...

  13. 21 CFR 866.3660 - Shigella spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3660 Shigella spp...), used in serological tests to identify Shigella spp. from cultured isolates. The identification aids in...

  14. 21 CFR 866.3400 - Parainfluenza virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3400 Parainfluenza... that consist of antigens and antisera used in serological tests to identify antibodies to parainfluenza...

  15. 21 CFR 866.3040 - Aspergillus spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3040 Aspergillus... consist of antigens and antisera used in various serological tests to identify antibodies to Aspergillus...

  16. 21 CFR 866.3330 - Influenza virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3330 Influenza... consist of antigens and antisera used in serological tests to identify antibodies to influenza in serum...

  17. 21 CFR 866.3125 - Citrobacter spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3125 Citrobacter... isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by...

  18. 21 CFR 866.3940 - West Nile virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3940 West Nile... detection aids in the clinical laboratory diagnosis of viral meningitis/encephalitis caused by West Nile...

  19. 21 CFR 866.3740 - Streptococcus spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3740 Streptococcus... derived from clinical specimens. The identification aids in the diagnosis of diseases caused by bacteria...

  20. 21 CFR 866.3065 - Bordetella spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3065 Bordetella... serological tests to identify Bordetella spp. from cultured isolates or directly from clinical specimens. The...

  1. 21 CFR 866.3035 - Arizona spp. serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3035 Arizona spp... antisera and antigens used to identify Arizona spp. in cultured isolates derived from clinical specimens...

  2. 21 CFR 866.3380 - Mumps virus serological reagents.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3380 Mumps virus... serological tests to identify mumps viruses from tissue culture isolates derived from clinical specimens. The...

  3. Reagent and process for detaching furfural in petroleum products

    Energy Technology Data Exchange (ETDEWEB)

    Orelup, R.B.

    1987-07-14

    A two-component liquid reagent and process is provided for detecting the presence of furfural in petroleum products. The reagent comprises two components which are stored separately from each other and are combined prior to admixture with the petroleum product. The process comprises combining the two separate components of the liquid reagent with each other prior to use, admixing the combined components with a petroleum product containing furfural, shaking the resultant mixture, allowing the mixture to separate and observing a red color characteristic of furfural in the lower layer. Alternately, the process may be carried out by combining the second component of the two-component liquid reagent with the petroleum product, followed by admixture with the first component to obtain two separate layers in which the red color characteristic of furfural is observed in the lower layer.

  4. Photo-Fenton and Fenton-like processes for the treatment of the antineoplastic drug 5-fluorouracil under simulated solar radiation.

    Science.gov (United States)

    Koltsakidou, Α; Antonopoulou, M; Sykiotou, M; Εvgenidou, Ε; Konstantinou, I; Lambropoulou, D A

    2017-02-01

    In the present study, photo-Fenton and Fenton-like processes were investigated for the degradation and mineralization of the antineoplastic drug 5-fluorouracil (5-FU). For the optimization of photo-Fenton treatment under simulated solar light (SSL) radiation, the effects of several operating parameters (i.e., 5-FU concentration, Fe 3+ , and oxidant concentration) on the treatment efficiency were studied. According to the results, SSL/[Fe(C 2 Ο 4 ) 3 ] 3- /Η 2 Ο 2 process was the most efficient, since faster degradation of 5-FU and higher mineralization percentages were achieved. All the applied processes followed quite similar transformation routes which include defluorination-hydroxylation as well as pyrimidine ring opening, as demonstrated by the transformation products identified by high resolution mass spectrometry analysis. The toxicity of the treated solutions was evaluated using the Microtox assay. In general, low toxicity was recorded for the initial solution and the solution at the end of the photocatalytic treatment, while an increase in the overall toxicity was observed only at the first stages of SSL/Fe 3+ /Η 2 Ο 2 and SSL/Fe 3+ /S 2 O 8 2- processes.

  5. Method for controlled introduction of reagent into a liquid

    Energy Technology Data Exchange (ETDEWEB)

    Newlove, J.C.; McDougall, L.A.

    1988-11-29

    It is an object of this invention to provide a method for using an article to enhance the production of hydrocarbons from geological reservoirs, more particularly from fractured formations. It is an additional object to devise a method for providing controlled release of a reagent downhole, in a pipeline, or in other oil-containing environments or fluids. Thus, there is provided a method for releasing a treating reagent, such as a wax crystal modifier, scale inhibitor, demulsifier, corrosion inhibitor, antioxidant, and biocide, into a liquid hydrocarbon stream. A plurality of porous, substantially wax-free, plastic particles having a softening point above 60/sup 0/C and being chemically resistant to the hydrocarbon stream are placed in the stream. The said particles contain the treating reagent in their pores, said reagent being insoluble in water and in the particles and being leachable on contact with the stream. The hydrocarbon stream is then flowed past said particles and the reagent is leached from the particle pores. In a specific aspect of this invention, a method is provided for recovering crude oil from an underground formation by means of: depositing the aforementioned particles, containing a suitable reagent, downhole in the oil-producing region of the formation; flowing the oil through the deposited particles, thereby leaching the reagent into the oil; and recovering the oil modified by the presence of an active amount of said reagent. Experiments are described to illustrate ways of producing the polymeric particles of the invention and to illustrate the processes of the invention.

  6. Electro-Fenton decolourisation of dyes in an airlift continuous reactor using iron alginate beads.

    Science.gov (United States)

    Iglesias, O; Rosales, E; Pazos, M; Sanromán, M A

    2013-04-01

    In this study, electro-Fenton dye degradation was performed in an airlift continuous reactor configuration by harnessing the catalytic activity of Fe alginate gel beads. Electro-Fenton experiments were carried out in an airlift reactor with a working volume of 1.5 L, air flow of 1.5 L/min and 115 g of Fe alginate gel beads. An electric field was applied by two graphite bars connected to a direct current power supply with a constant potential drop. In this study, Lissamine Green B and Reactive Black 5 were selected as model dyes. Fe alginate gel beads can be used as an effective heterogeneous catalyst for the degradation of organic dyes in the electro-Fenton process, as they are more efficient than the conventional electrochemical techniques. At optimal working conditions (3 V and pH 2), the continuous process was performed. For both dyes, the degree of decolourisation increases when the residence time augments. Taking into account hydrodynamic and kinetic behaviour, a model to describe the reactor profile was obtained, and the standard deviation between experimental and theoretical data was lower than 6%. The results indicate the suitability of the electro-Fenton technique to oxidise polluted effluents in the presence of Fe alginate gel beads. Moreover, the operation is possible in a continuous airlift reactor, due to the entrapment of iron in the alginate matrix.

  7. Feasibility of bioleaching combined with Fenton-like reaction to remove heavy metals from sewage sludge.

    Science.gov (United States)

    Zhu, Yi; Zeng, Guangming; Zhang, Panyue; Zhang, Chang; Ren, Miaomiao; Zhang, Jiachao; Chen, Ming

    2013-08-01

    Feasibility of bioleaching combining with Fenton-like reaction to remove heavy metals from sewage sludge was investigated. After 5-day bioleaching, the sludge pH decreased from 6.95 to 2.50, which satisfied the acidic conditions for Fenton-like reaction. Meanwhile, more than 50% of sludge-borne heavy metals were dissolved except for Pb. The bioleached sludge was further oxidized with Fenton-like reaction, with an optimal H2O2 dosage of 5 g/L, the Cu, Zn, Pb and Cd removal reached up to 75.3%, 72.6%, 34.5% and 65.4%, respectively, and the residual content of heavy metals in treated sludge meets the requirement of Disposal of Sludge from Municipal Wastewater Treatment Plant - Control Standards for Agricultural Use (CJ/T 309-2009) of China for A grade sludge. Bioleaching combined with Fenton-like reaction was the most effective method for heavy metal removal, compared with 15-day bioleaching and inorganic acid leaching with 10% H2SO4, 10% HCl and 10% HNO3. Copyright © 2013 Elsevier Ltd. All rights reserved.

  8. Effect of Fenton treatment on the aquatic toxicity of bisphenol A in different water matrices

    DEFF Research Database (Denmark)

    Arslan-Alaton, Idil; Aytac, Ece; Kusk, Kresten Ole

    2014-01-01

    products. For this purpose, BPA was subjected to Fenton treatment in the growth medium of the test organisms employed as well as in real lake water. Treatment results indicated that BPA removals were fast and complete within less than a minute, whereas total organic carbon (TOC) removals were rather...

  9. Electro-Fenton oxidation of reverse osmosis concentrate from sanitary landfill leachate: Evaluation of operational parameters.

    Science.gov (United States)

    Fernandes, Annabel; Labiadh, Lazhar; Ciríaco, Lurdes; Pacheco, Maria José; Gadri, Abdellatif; Ammar, Salah; Lopes, Ana

    2017-10-01

    The electro-Fenton oxidation of a concentrate from reverse osmosis of a sanitary landfill leachate, with an initial chemical oxygen demand (COD) of 42 g L -1 , was carried out using a carbon-felt cathode and a boron doped diamond anode. The influence of the applied current intensity, initial pH and dissolved iron initial concentration on the electro-Fenton process was assessed. For the experimental conditions used, results showed that the initial pH is the parameter that more strongly influences the current efficiency of the electro-Fenton process, being this influence more pronounced on the oxidation rate than on the mineralization rate of the organic matter. The increase in iron initial concentration was found to be detrimental, since the natural amount of iron present in the effluent, 73 mg L -1 of total iron and 61 mg L -1 of dissolved iron, was sufficient to ensure the electro-Fenton process at the applied intensities - 0.2-1.4 A. For the more favourable conditions studied, initial pH of 3 and natural iron concentration, it was found an increase in the organic load and nitrogen removals with the applied current intensity. For the highest current intensity applied, a COD removal of 16.7 g L -1 was achieved after 8-h experiments. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Integrating Fenton's process and ion exchange for olive mill wastewater treatment and iron recovery.

    Science.gov (United States)

    Reis, Patrícia M; Martins, Pedro J M; Martins, Rui C; Gando-Ferreira, Licínio M; Quinta-Ferreira, Rosa M

    2018-02-01

    A novel integrated methodology involving Fenton's process followed by ion exchange (IE) was proposed for the treatment of olive mill wastewater. Fenton's process was optimized and it was able to remove up to 81% of chemical oxygen demand when pH 3.5, reaction time 1 h, [Fe 2+ ] = 50 mg L -1 and [Fe 2+ ]/[H 2 O 2 ] = 0.002 were applied. In spite of the potential of this treatment approach, final iron removal from the liquid typically entails pH increase and iron sludge production. The integration of an IE procedure using Lewatit TP 207 resin was found to be able to overcome this important environmental shortcoming. The resin showed higher affinity toward Fe 3+ than to Fe 2+ . However, the iron removal efficiency of an effluent coming from Fenton's was independent of the type of the initial iron used in the process. The presence of organic matter had no significant effect over the resin iron removal efficiency. Even if some efficiency decrease was observed when a high initial iron load was applied, the adsorbent mass quantity can be easily adapted to reach the desired iron removal. The use of IE is an interesting industrial approach able to surpass Fenton's peroxidation drawback and will surely boost its full-scale application in the treatment of bio-refractory effluents.

  11. Fenton-Like Oxidation of Malachite Green Solutions: Kinetic and Thermodynamic Study

    Directory of Open Access Journals (Sweden)

    Saeedeh Hashemian

    2013-01-01

    Full Text Available Oxidation by Fenton-like (Fe3+/H2O2 reactions is proven to be an economically feasible process for destruction of a variety of hazardous pollutants in wastewater. In this study, the degradation and mineralization of malachite green dye are reported using Fenton-like reaction. The effects of different parameters like pH of the solution, the initial concentrations of Fe3+, H2O2, and dye, temperature, and added electrolytes (Cl− and on the oxidation of the dye were investigated. Optimized condition was determined. The efficiency of 95.5% degradation of MAG after 15 minutes of reaction at pH 3 was obtained. TOC removal indicates partial and insignificant mineralization of malachite green dye. The results of experiments showed that degradation of malachite green dye in Fenton-like oxidation process can be described with a pseudo-second-order kinetic model. The thermodynamic constants of the Fenton oxidation process were evaluated. The results implied that the oxidation process was feasible, spontaneous, and endothermic. The results will be useful for designing the treatment systems of various dye-containing wastewaters.

  12. ADVANTAGES/DISADVANTAGES FOR ISCO METHODS IN-SITU FENTON OXIDATION IN-SITU PERMANGANATE OXIDATION

    Science.gov (United States)

    The advantages and disadvantages of in-situ Fenton oxidation and in-situ permanganate oxidation will be presented. This presentation will provide a brief overview of each technology and a detailed analysis of the advantages and disadvantages of each technology. Included in the ...

  13. Integrating the Fenton's Process with Biofiltration by to Reduce Chemical Oxygen Demand of Winery Effluents.

    Science.gov (United States)

    Pipolo, Marco; Martins, Rui C; Quinta-Ferreira, Rosa M; Costa, Raquel

    2017-03-01

    The discharge of poorly decontaminated winery wastewater remains a serious environmental problem in many regions, and the industry is welcoming improved treatment methods. Here, an innovative decontamination approach integrating Fenton's process with biofiltration by Asian clams is proposed. The potential of this approach was assessed at the pilot scale using real effluent and by taking an actual industrial treatment system as a benchmark. Fenton peroxidation was observed to remove 84% of the effluent's chemical oxygen demand (COD), reducing it to 205 mg L. Subsequent biofiltration decreased the effluent's COD to approximately zero, well below the legal discharge limit of 150 mg L, in just 3 d. The reduction of the effluent's organic load through Fenton's process did not decrease its toxicity toward , but the effluent was much less harmful after biofiltration. The performance of the treatment proposed exceeded that of the integrated Fenton's process-sequencing batch reactor design implemented in the winery practice, where a residence time of around 10 d in the biological step typically results in 80 to 90% of COD removal. The method proposed is effective and compatible with typical winery budgets and potentially contributes to the management of a nuisance species. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  14. Use of Fenton oxidation to improve the biodegradability of a pharmaceutical wastewater

    International Nuclear Information System (INIS)

    Tekin, Huseyin; Bilkay, Okan; Ataberk, Selale S.; Balta, Tolga H.; Ceribasi, I. Haluk; Sanin, F. Dilek; Dilek, Filiz B.; Yetis, Ulku

    2006-01-01

    The applicability of Fenton's oxidation to improve the biodegradability of a pharmaceutical wastewater to be treated biologically was investigated. The wastewater was originated from a factory producing a variety of pharmaceutical chemicals. Treatability studies were conducted under laboratory conditions with all chemicals (having COD varying from 900 to 7000 mg/L) produced in the factory in order to determine the operational conditions to utilize in the full-scale treatment plant. Optimum pH was determined as 3.5 and 7.0 for the first (oxidation) and second stage (coagulation) of the Fenton process, respectively. For all chemicals, COD removal efficiency was highest when the molar ratio of H 2 O 2 /Fe 2+ was 150-250. At H 2 O 2 /Fe 2+ ratio of 155, 0.3 M H 2 O 2 and 0.002 M Fe 2+ , provided 45-65% COD removal. The wastewater treatment plant that employs Fenton oxidation followed by aerobic degradation in sequencing batch reactors (SBR), built after these treatability studies provided an overall COD removal efficiency of 98%, and compliance with the discharge limits. The efficiency of the Fenton's oxidation was around 45-50% and the efficiency in the SBR system which has two reactors each having a volume of 8 m 3 and operated with a total cycle time of 1 day, was around 98%, regarding the COD removal

  15. IRON OPTIMIZATION FOR FENTON-DRIVEN OXIDATION OF MTBE-SPENT GRANULAR ACTIVATED CARBON

    Science.gov (United States)

    Fenton-driven chemical regeneration of granular activated carbon (GAC) is accomplished through the addition of H2O2 and iron (Fe) to spent GAC. The overall objective of this treatment process is to transform target contaminants into less toxic byproducts, re-establish the sorpti...

  16. Iron Amendment and Fenton Oxidation of MTBE-Spent Granular Activated Carbon

    Science.gov (United States)

    Fenton-driven regeneration of Methyl tert-butyl ether (MTBE)-spent granular activated carbon (GAC) involves Fe amendment to the GAC to catalyze H2O2 reactions and to enhance the rate of MTBE oxidation and GAC regeneration. Four forms of iron (ferric sulfate, ferric chloride, fer...

  17. Sequential pretreatment for cell disintegration of municipal sludge in a neutral Bio-electro-Fenton system.

    Science.gov (United States)

    Yu, Qilin; Jin, Xiaochen; Zhang, Yaobin

    2018-05-15

    Sludge cell disruption was generally considered as the rate-limiting step for the anaerobic digestion of waste activated sludge (WAS). Advanced oxidation processes and bio-electro-chemical systems were recently reported to enhance the hydrolysis of WAS and sludge cell disruption, while the cell-breaking processes of these systems remain unclear yet. In this study, an innovative Bio-electro-Fenton system was developed to pretreat the WAS sequentially with cathode Fenton process and anode anaerobic digestion. Significant cell disruption and dissolution intracellular organics were founded after the treatment. X-ray photoelectron spectroscopy (XPS) analysis and fourier transform infrared spectroscopy (FT-IR) spectra indicated that Gram-negative bacteria were more sensitive to free radicals yielded in cathode to induce a chain reaction that destroyed the lipid-contained outer membrane, while Gram-positive bacteria with thick peptidoglycan layer were liable to be biologically decomposed in the anode. Compared with the oxidation of organic matters in the cathode Fenton, the secretion of enzyme increased in the anode which was beneficial to break down the complex matters (peptidoglycans) into simples that were available for anode oxidation by exoelectrogens. The results also showed a possible prospect for the application of this sequential pretreatment in bio-electro-Fenton systems to disrupt sludge cells and enhance the anaerobic digestion. Copyright © 2018 Elsevier Ltd. All rights reserved.

  18. Fenton-like Degradation of MTBE: Effects of Iron Counter Anion and Radical Scavengers

    Science.gov (United States)

    Fenton-driven oxidation of Methyl tert-butyl ether (MTBE) (0.11-0.16 mM) in batch reactors containing ferric iron (5 mM), hydrogen peroxide (H2O2) (6 mM) (pH=3) was performed to investigate MTBE transformation mechanisms. Independent variables included the form of iron (Fe) (Fe2(...

  19. Efficient mineralization of antibiotic ciprofloxacin in acid aqueous medium by a novel photoelectro-Fenton process using a microwave discharge electrodeless lamp irradiation.

    Science.gov (United States)

    Wang, Aimin; Zhang, Yanyu; Zhong, Huihui; Chen, Yu; Tian, Xiujun; Li, Desheng; Li, Jiuyi

    2018-01-15

    In this study, a novel photoelectro-Fenton (PEF) process using microwave discharge electrodeless lamp (MDEL) as a UV irradiation source was developed for the removal of antibiotic ciprofloxacin (CIP) in water. Comparative degradation of 200mgL -1 CIP was studied by direct MDEL photolysis, anodic oxidation (AO), AO in presence of electrogenerated H 2 O 2 (AO-H 2 O 2 ), AO-H 2 O 2 under MDEL irradiation (MDEL-AO-H 2 O 2 ), electro-Fenton (EF) and MDEL-PEF processes. Higher oxidation power was found in the sequence: MDEL photolysis < AO < AO-H 2 O 2 < MDEL-AO-H 2 O 2 < EF < MDEL-PEF. Effects of current density, pH, initial Fe 2+ concentration and initial CIP concentration on TOC removal in MDEL-PEF process were examined, and the optimal conditions were ascertained. The releases of three inorganic ions (F - , NH 4 + and NO 3 - ) and two carboxylic acids (oxalic and formic acids) were qualified. Seven aromatic intermediates mainly generated from hydroxylation, dealkylation and defluorination of CIP were detected by UPLC-QTOF-MS/MS technology. Therefore, plausible degradation sequences for CIP degradation in MDEL-PEF process including all detected products were proposed. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. A histone-like protein of mycobacteria possesses ferritin superfamily protein-like activity and protects against DNA damage by Fenton reaction.

    Directory of Open Access Journals (Sweden)

    Masaki Takatsuka

    Full Text Available Iron is an essential metal for living organisms but its level must be strictly controlled in cells, because ferrous ion induces toxicity by generating highly active reactive oxygen, hydroxyl radicals, through the Fenton reaction. In addition, ferric ion shows low solubility under physiological conditions. To overcome these obstacles living organisms possess Ferritin superfamily proteins that are distributed in all three domains of life: bacteria, archaea, and eukaryotes. These proteins minimize hydroxyl radical formation by ferroxidase activity that converts Fe(2+ into Fe(3+ and sequesters iron by storing it as a mineral inside a protein cage. In this study, we discovered that mycobacterial DNA-binding protein 1 (MDP1, a histone-like protein, has similar activity to ferritin superfamily proteins. MDP1 prevented the Fenton reaction and protects DNA by the ferroxidase activity. The K(m values of the ferroxidase activity by MDP1 of Mycobacterium bovis bacillus Calmette-Guérin (BCG-3007c, Mycobacterium tuberculosis (Rv2986c, and Mycobacterium leprae (ML1683; ML-LBP were 0.292, 0.252, and 0.129 mM, respectively. Furthermore, one MDP1 molecule directly captured 81.4±19.1 iron atoms, suggesting the role of this protein in iron storage. This study describes for the first time a ferroxidase-iron storage protein outside of the ferritin superfamily proteins and the protective role of this bacterial protein from DNA damage.

  1. The photodeposition of surface plasmon Ag metal on SiO2@α-Fe2O3 nanocomposites sphere for enhancement of the photo-Fenton behavior

    Science.gov (United States)

    Uma, Kasimayan; Arjun, Nadarajan; Pan, Guan-Ting; Yang, Thomas C.-K.

    2017-12-01

    In this study, a simple sol-gel method was used for the synthesis of a core-shell structure of SiO2@α-Fe2O3 nanocomposites for employment as a visible light photocatalyst. It was observed that Ag nanoparticles about 20 nm in size were successfully deposited on the surface of the SiO2@α-Fe2O3 nanocomposites. The photocatalytic activity of the Ag-SiO2@α-Fe2O3 nanocomposites catalyst was investigated by observing the degradation of methylene blue (MB) dye in a photo-Fenton process. The results showed that the Ag nanoparticles acted as centers for photo induced electron transfer. The catalytic activity in the SiO2@α-Fe2O3 nanocomposites were enhanced due to the plasmoni c effect of Ag metal under visible light irradiation. The addition of H2O2 played an important role, generating more OH radicals which improved the photo-Fenton catalytic activity, resulting in quicker degradation of the MB dye using the Ag-SiO2@α-Fe2O3 nanocomposite catalyst.

  2. Evaluation of novel derivatisation reagents for the analysis of oxysterols

    Energy Technology Data Exchange (ETDEWEB)

    Crick, Peter J., E-mail: p.j.crick@swansea.ac.uk [Institute of Mass Spectrometry, College of Medicine, Swansea University, Singleton Park, Swansea SA2 8PP (United Kingdom); Aponte, Jennifer; Bentley, T. William [Institute of Mass Spectrometry, College of Medicine, Swansea University, Singleton Park, Swansea SA2 8PP (United Kingdom); Matthews, Ian [College of Engineering, Swansea University, Singleton Park, Swansea SA2 8PP (United Kingdom); Wang, Yuqin [Institute of Mass Spectrometry, College of Medicine, Swansea University, Singleton Park, Swansea SA2 8PP (United Kingdom); Griffiths, William J., E-mail: w.j.griffiths@swansea.ac.uk [Institute of Mass Spectrometry, College of Medicine, Swansea University, Singleton Park, Swansea SA2 8PP (United Kingdom)

    2014-04-11

    Graphical abstract: - Highlights: • New derivatisation reagents for LC–MS analysis of oxysterols. • New reagents based on Girard P give high ion-currents and informative LC–MS{sup n} spectra. • Permanent charge is vital for efficient MS{sup n} fragmentation. • New reagents offer greater scope for incorporation of isotope labels. - Abstract: Oxysterols are oxidised forms of cholesterol that are intermediates in the synthesis of bile acids and steroid hormones. They are also ligands to nuclear and G protein-coupled receptors. Analysis of oxysterols in biological systems is challenging due to their low abundance coupled with their lack of a strong chromophore and poor ionisation characteristics in mass spectrometry (MS). We have previously used enzyme-assisted derivatisation for sterol analysis (EADSA) to identify and quantitate oxysterols in biological samples. This technique relies on tagging sterols with the Girard P reagent to introduce a charged quaternary ammonium group. Here, we have compared several modified Girard-like reagents and show that the permanent charge is vital for efficient MS{sup n} fragmentation. However, we find that the reagent can be extended to include sites for potential stable isotope labels without a loss of performance.

  3. Decolourisation of dyes under electro-Fenton process using Fe alginate gel beads

    Energy Technology Data Exchange (ETDEWEB)

    Rosales, E.; Iglesias, O.; Pazos, M. [Department of Chemical Engineering, University of Vigo, Isaac Newton Building, Campus As Lagoas, Marcosende 36310, Vigo (Spain); Sanroman, M.A., E-mail: sanroman@uvigo.es [Department of Chemical Engineering, University of Vigo, Isaac Newton Building, Campus As Lagoas, Marcosende 36310, Vigo (Spain)

    2012-04-30

    Highlights: Black-Right-Pointing-Pointer Catalytic activity of Fe alginate gel beads for the remediation of wastewater was tested. Black-Right-Pointing-Pointer New electro-Fenton process for the remediation of polluted wastewater. Black-Right-Pointing-Pointer Continuous dye treatment without operational problem with high removal. - Abstract: This study focuses on the application of electro-Fenton technique by use of catalytic activity of Fe alginate gel beads for the remediation of wastewater contaminated with synthetic dyes. The Fe alginate gel beads were evaluated for decolourisation of two typical dyes, Lissamine Green B and Azure B under electro-Fenton process. After characterization of Fe alginate gel beads, the pH effect on the process with Fe alginate beads and a comparative study of the electro-Fenton process with free Fe and Fe alginate bead was done. The results showed that the use of Fe alginate beads increases the efficiency of the process; moreover the developed particles show a physical integrity in a wide range of pH (2-8). Around 98-100% of dye decolourisation was obtained for both dyes by electro-Fenton process in successive batches. Therefore, the process was performed with Fe alginate beads in a bubble continuous reactor. High color removal (87-98%) was attained for both dyes operating at a residence time of 30 min, without operational problems and maintaining particle shapes throughout the oxidation process. Consequently, the stable performance of Fe alginate beads opens promising perspectives for fast and economical treatment of wastewater polluted by dyes or similar organic contaminants.

  4. Decolourisation of dyes under electro-Fenton process using Fe alginate gel beads

    International Nuclear Information System (INIS)

    Rosales, E.; Iglesias, O.; Pazos, M.; Sanromán, M.A.

    2012-01-01

    Highlights: ► Catalytic activity of Fe alginate gel beads for the remediation of wastewater was tested. ► New electro-Fenton process for the remediation of polluted wastewater. ► Continuous dye treatment without operational problem with high removal. - Abstract: This study focuses on the application of electro-Fenton technique by use of catalytic activity of Fe alginate gel beads for the remediation of wastewater contaminated with synthetic dyes. The Fe alginate gel beads were evaluated for decolourisation of two typical dyes, Lissamine Green B and Azure B under electro-Fenton process. After characterization of Fe alginate gel beads, the pH effect on the process with Fe alginate beads and a comparative study of the electro-Fenton process with free Fe and Fe alginate bead was done. The results showed that the use of Fe alginate beads increases the efficiency of the process; moreover the developed particles show a physical integrity in a wide range of pH (2–8). Around 98–100% of dye decolourisation was obtained for both dyes by electro-Fenton process in successive batches. Therefore, the process was performed with Fe alginate beads in a bubble continuous reactor. High color removal (87–98%) was attained for both dyes operating at a residence time of 30 min, without operational problems and maintaining particle shapes throughout the oxidation process. Consequently, the stable performance of Fe alginate beads opens promising perspectives for fast and economical treatment of wastewater polluted by dyes or similar organic contaminants.

  5. Sodium hypochlorite as an alternative to hydrogen peroxide in Fenton process for industrial scale.

    Science.gov (United States)

    Behin, Jamshid; Akbari, Abbas; Mahmoudi, Mohsen; Khajeh, Mehdi

    2017-09-15

    In present work, the treatment of aromatic compounds of simulated wastewater was performed by Fenton and NaOCl/Fe 2+ processes. The model solution was prepared based on the wastewater composition of Diisocyanate unit of Karoon Petrochemical Company/Iran containing Diamino-toluenes, Nitro-phenol, Mononitro-toluene, Nitro-cresol, and Dinitro-toluene. Experiments were conducted in a batch mode to examine the effects of operating variables such as pH, oxidant dosages, ferrous ion concentration and numbers of feeding on COD removal. Taguchi experimental design was used to determine the optimum conditions. The COD removal efficiency under optimum conditions (suggested by Taguchi design) in Fenton and NaOCl/Fe 2+ processes was 88.7% and 83.4%, respectively. The highest contribution factor in Fenton process belongs to pH (47.47%) and in NaOCl/Fe 2+ process belongs to NaOCl/pollutants (50.26%). High regression coefficient (R 2 : 0.98) obtained for Taguchi method, indicates that models are statistically significant and are in well agreement with each other. The NaOCl/Fe 2+ process utilizing a conventional oxidant, in comparison to hydrogen peroxide, is an efficient cost effective process for COD removal from real wastewater, although the removal efficiency is not as high as in Fenton process; however it is a suitable process to replace Fenton process in industrial scale for wastewater involved aromatic compounds with high COD. This process was successfully applied in Karoon Petrochemical Company/Iran. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Microwave enhanced Fenton-like process for the treatment of high concentration pharmaceutical wastewater

    International Nuclear Information System (INIS)

    Yang Yu; Wang Peng; Shi Shujie; Liu Yuan

    2009-01-01

    This paper explored a novel process for wastewater treatment, i.e. microwave enhanced Fenton-like process. This novel process was introduced to treat high concentration pharmaceutical wastewater with initial COD loading of 49,912.5 mg L -1 . Operating parameters were investigated and the optimal condition included as follows: microwave power was 300 W, radiation time was 6 min, initial pH was 4.42, H 2 O 2 dosage was 1300 mg L -1 and Fe 2 (SO 4 ) 3 dosage was 4900 mg L -1 , respectively. Within the present experimental condition used, the COD removal and UV 254 removal reached to 57.53% and 55.06%, respectively, and BOD 5 /COD was enhanced from 0.165 to 0.470. The variation of molecular weight distribution indicated that both macromolecular substances and micromolecular substances were eliminated quite well. The structure of flocs revealed that one ferric hydrated ion seemed to connect with another ferric hydrated ion and/or organic compound molecule to form large-scale particles by means of van der waals force and/or hydrogen bond. Subsequently, these particles aggregated to form flocs and settled down. Comparing with traditional Fenton-like reaction and conventional heating assisted Fenton-like reaction, microwave enhanced Fenton-like process displayed superior treatment efficiency. Microwave was in favor of improving the degradation efficiency, the settling quality of sludge, as well as reducing the yield of sludge and enhancing the biodegradability of effluent. Microwave enhanced Fenton-like process is believed to be a promising treatment technology for high concentration and biorefractory wastewater.

  7. Immobilizing LaFeO3 nanoparticles on carbon spheres for enhanced heterogeneous photo-Fenton like performance

    Science.gov (United States)

    Wang, Kaixuan; Niu, Helin; Chen, Jingshuai; Song, Jiming; Mao, Changjie; Zhang, Shengyi; Gao, Yuanhao

    2017-05-01

    LaFeO3 nanoparticles immobilized on the surface of monodisperse carbon spheres have been obtained through a facile and environmentally friendly ultrasonic assisted surface ions adsorption method. The LaFeO3/C nanocomposite was evaluated as photo-Fenton like catalyst for the degradation of Rhodamine B (RhB) under visible light irradiation (λ > 420 nm). The LaFeO3/C nanocomposite possesses high specific surface area compared with pure LaFeO3 and significantly enhanced photo-Fenton like catalytic performance. The possible formation process of the LaFeO3/C nanocomposite and the mechanism for photo-Fenton like reaction were discussed. The superior property was attributed to the synergistic effects from the photo-Fenton like process and the presence of carbon spheres. In addition, the heterogeneous process led to better recyclability of this type of catalyst.

  8. Study of the removal of metronidazole from aqueous solutions using Electro/ Fenton process and graphite and iron electrodes

    Directory of Open Access Journals (Sweden)

    Bahram Kamarehie

    2018-04-01

    Conclusion: The Electro-Fenton process can effectively remove metronidazole from aquatic solutions in environmentally convenient conditions. This process can be used as an efficient method for removing other persistent pollutants from the environment.

  9. Novel bio-electro-Fenton technology for azo dye wastewater treatment using microbial reverse-electrodialysis electrolysis cell

    DEFF Research Database (Denmark)

    Li, Xiaohu; Jin, Xiangdan; Zhao, Nannan

    2017-01-01

    Development of sustanaible technologies for treatment of azo dyes containing wastewaters has long been of great interest. In this study, we proposed an innovative concept of using microbial reverse-electrodialysis electrolysis cell (MREC) based Fenton process to treat azo dye wastewater. In such ......Development of sustanaible technologies for treatment of azo dyes containing wastewaters has long been of great interest. In this study, we proposed an innovative concept of using microbial reverse-electrodialysis electrolysis cell (MREC) based Fenton process to treat azo dye wastewater....... In such MREC-Fenton integrated process, the production of H2O2 which is the key reactant of fenton-reaction was driven by the electrons harvested from the exoelectrogens and salinity-gradient between sea water and fresh water in MREC. Complete decolorization and mineralization of 400 mg L-1 Orange G...

  10. The behavior of thiourea and flotation reagents in zinc electrowinning circuits

    Science.gov (United States)

    MacKinnon, D. J.; Dutrizac, J. E.; Brannen, J. M.; Hardy, D. J.

    1988-04-01

    The effect of thiourea and flotation reagents on the electrowinning of zinc from industrial electrolytes was studied, and all the compounds were found to reduce the zinc deposition current efficiency and to change the properties of the zinc deposits. The effectiveness of activated carbon, two-stage cementation, and hot acid leaching on the destruction/removal of the organic compounds also was addressed. Activated carbon pretreatment of thiourea-containing electrolytes restored the current efficiency for 1-hour zinc deposits to values comparable to those obtained for thiourea-free electrolytes. The activated carbon pretreatment, however, altered the deposit morphology and orientation, but produced a cyclic voltammogram similar to that of the thiourea-free solution. Two-stage cementation did not counteract the harmful effects of thiourea. Hot acid leaching destroyed the thiourea but generated large concentrations of ferrous ion that reduced the current efficiency. The ferrous concentrations, however, were readily controlled by KMnO4 or MnO2 oxidation. None of the treatment options (activated carbon, two-stage cementation, or hot acid leaching) was effective in controlling the flotation reagents, and their moderately harmful effect on zinc electrowinning persisted. Even low concentrations of these reagents polarized zinc deposition, and this resulted in a “glue-type” zinc deposit.

  11. Treatment of reverse osmosis (RO) concentrate by the combined Fe/Cu/air and Fenton process (1stFe/Cu/air-Fenton-2ndFe/Cu/air).

    Science.gov (United States)

    Ren, Yi; Yuan, Yue; Lai, Bo; Zhou, Yuexi; Wang, Juling

    2016-01-25

    To decompose or transform the toxic and refractory reverse osmosis (RO) concentrate and improve the biodegradability, 1stFe/Cu/air-Fenton-2ndFe/Cu/air were developed to treat RO concentrate obtained from an amino acid production plant in northern China. First, their operating conditions were optimized thoroughly. Furthermore, 5 control experiments were setup to confirm the superiority of 1stFe/Cu/air-Fenton-2ndFe/Cu/air and synergistic reaction between Fe/Cu/air and Fenton. The results suggest that the developed method could obtain high COD removal (65.1%) and BOD5/COD ratio (0.26) due to the synergistic reaction between Fe/Cu/air and Fenton. Under the optimal conditions, the influent and effluent of 1stFe/Cu/air-Fenton-2ndFe/Cu/air and 5 control experiments were analyzed by using UV, FTIR, EEM and LC, which confirm the superiority of 1stFe/Cu/air-Fenton-2ndFe/Cu/air. Therefore, the developed method in this study is a promising process for treatment of RO concentrate. Copyright © 2015 Elsevier B.V. All rights reserved.

  12. Reagent conditions of the flotation of copper, copper - molybdenum and copper -zinc ores in foreing countries

    International Nuclear Information System (INIS)

    Nevaeva, L.M.

    1983-01-01

    Reagents-collectors and frothers, used abroad in reagent regimes of flotation of copper, copper-molybdenum and copper zinc ores, have been considered. Xanthogenates, aerofloats, xanthogenformiates, thionocarbamates are mainly used as reagents-collectors. Methylizobutylcarbinol and Daufros are used as reagents-frothers

  13. 21 CFR 866.3720 - Streptococcus spp. exo-enzyme reagents.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Streptococcus spp. exo-enzyme reagents. 866.3720... (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Serological Reagents § 866.3720 Streptococcus spp. exo-enzyme reagents. (a) Identification. Streptococcus spp. exoenzyme reagents are devices used...

  14. Alkaline phosphatase-fused repebody as a new format of immuno-reagent for an immunoassay

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Hyo-Deok; Lee, Joong-jae [Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of); Kim, Yu Jung [Industrial Biotechnology and Bioenergy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon (Korea, Republic of); Hantschel, Oliver [School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne (Switzerland); Lee, Seung-Goo [Industrial Biotechnology and Bioenergy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon (Korea, Republic of); Kim, Hak-Sung, E-mail: hskim76@kaist.ac.kr [Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of)

    2017-01-15

    Enzyme-linked immunoassays based on an antibody-antigen interaction are widely used in biological and medical sciences. However, the conjugation of an enzyme to antibodies needs an additional chemical process, usually resulting in randomly cross-linked molecules and a loss of the binding affinity and enzyme activity. Herein, we present the development of an alkaline phosphatase-fused repebody as a new format of immuno-reagent for immunoassays. A repebody specifically binding to human TNF-α (hTNF-α) was selected through a phage display, and its binding affinity was increased up to 49 nM using a modular engineering approach. A monomeric alkaline phosphatase (mAP), which was previously isolated from a metagenome library, was genetically fused to the repebody as a signal generator, and the resulting repebody-mAP fusion protein was used for direct and sandwich immunoassays of hTNF-α. We demonstrate the utility and potential of the repebody-mAP fusion protein as an immuno-reagent by showing the sensitivity of 216 pg mL{sup −1} for hTNF-α in a sandwich immunoassay. Furthermore, this repebody-mAP fusion protein enabled the detection of hTNF-α spiked in a serum-supplemented medium with high accuracy and reproducibility. It is thus expected that a mAP-fused repebody can be broadly used as an immuno-reagent in immunoassays. - Highlights: • A human TNF-α (hTNF-α)-specific repebody was selected using a phage display. • A monomeric alkaline phosphatase (mAP) was genetically fused to the repebody. • mAP-fused repebody enabled detection of hTNF-α with high sensitivity and accuracy. • mAP-fused repebody can be widely used as a new immuno-reagent in immunoassays.

  15. Solar photoelectro-Fenton degradation of the herbicide 4-chloro-2-methylphenoxyacetic acid optimized by response surface methodology.

    Science.gov (United States)

    Garcia-Segura, Sergi; Almeida, Lucio Cesar; Bocchi, Nerilso; Brillas, Enric

    2011-10-30

    A central composite rotatable design and response surface methodology (RSM) were used to optimize the experimental variables of the solar photoelectro-Fenton (SPEF) treatment of the herbicide 4-chloro-2-methylphenoxyacetic acid (MCPA). The experiments were made with a flow plant containing a Pt/air-diffusion reactor coupled to a solar compound parabolic collector (CPC) under recirculation of 10 L of 186 mg L(-1) MCPA solutions in 0.05 M Na(2)SO(4) at a liquid flow rate of 180 L h(-1) with an average UV irradiation intensity of about 32 Wm(-2). The optimum variables found for the SPEF process were 5.0 A, 1.0mM Fe(2+) and pH 3.0 after 120 min of electrolysis. Under these conditions, 75% of mineralization with 71% of current efficiency and 87.7 k Wh kg(-1) TOC of energy consumption were obtained. MCPA decayed under the attack of generated hydroxyl radicals following a pseudo-first-order kinetics. Hydroxyl radicals also destroyed 4-chloro-2-methylphenol, methylhydroquinone and methyl-p-benzoquinone detected as aromatic by-products. Glycolic, maleic, fumaric, malic, succinic, tartronic, oxalic and formic acids were identified as generated carboxylic acids, which form Fe(III) complexes that are quickly photodecarboxylated by the UV irradiation of sunlight at the CPC photoreactor. A reaction sequence for the SPEF degradation of MCPA was proposed. Copyright © 2011 Elsevier B.V. All rights reserved.

  16. Detoxification and biodegradability enhancement of aqueous solutions of four commercial pesticides along a Photo-Fenton treatment

    Energy Technology Data Exchange (ETDEWEB)

    Amat, A. M.; Arques, A.; Domenech, A.; Garcia-Ripoll, A.; Vicente, R.

    2009-07-01

    Photo-Fenton treatment has proven to be efficient to remove recalcitrant pollutants as commercial pesticides commonly employed in citric cultivars in the Mediterranean coast of Spain as Laition, Sevnol, Ultracid and Metasystox. However, the photon-Fenton treatment resulted to be less efficient to remove organic matter; nevertheless it could be employed as a pre-treatment to couple with biological processes, widely used in wastewater treatment. (Author)

  17. Detoxification and biodegradability enhancement of aqueous solutions of four commercial pesticides along a Photo-Fenton treatment

    International Nuclear Information System (INIS)

    Amat, A. M.; Arques, A.; Domenech, A.; Garcia-Ripoll, A.; Vicente, R.

    2009-01-01

    Photo-Fenton treatment has proven to be efficient to remove recalcitrant pollutants as commercial pesticides commonly employed in citric cultivars in the Mediterranean coast of Spain as Laition, Sevnol, Ultracid and Metasystox. However, the photon-Fenton treatment resulted to be less efficient to remove organic matter; nevertheless it could be employed as a pre-treatment to couple with biological processes, widely used in wastewater treatment. (Author)

  18. Ferrous ions reused as catalysts in Fenton-like reactions for remediation of agro-food industrial wastewater.

    Science.gov (United States)

    Leifeld, Vanessa; Dos Santos, Tâmisa Pires Machado; Zelinski, Danielle Wisniewski; Igarashi-Mafra, Luciana

    2018-09-15

    Cassava is the most important tuberous root in tropical and subtropical regions of the world, being the third largest source of carbohydrates. The root processing is related to the production of starch, an important industrial input, which releases a highly toxic liquid wastewater due to its complex composition, which inhibits high performances of conventional effluent treatments. This study aims to evaluate Fenton-like and photo-Fenton-like reactions for treatment of cassava wastewater, reusing ferrous ions from the preliminary coagulation stage. Pre-treated cassava wastewater was submitted to oxidation in three variations of hydrogen peroxide concentrations, with more relevant analytical responses verified in color, turbidity, COD (Chemical Oxygen Demand), and acute toxicity in Artemia salina, besides the action of radicals during Fenton-like reactions. At higher peroxide concentrations, a decrease of 68% in turbidity and 70% in COD on the photo-Fenton-like system was observed, even at slow reaction rates (fastest rate constant k = 2 × 10 -4 min -1 ). Inclusion of UV increases the viability of the Fenton-like reactions by supplementing the reaction medium with hydroxyl radicals, verified by the tert-butanol tests. The oxidation process leads to high EC 50 values in 24 h of incubation in Fenton-like reactions and 48 h in photo-Fenton-like reactions. Final COD and turbidity suggests that the reuse of iron, which remains in the preliminary treatment step shows a great potential as a catalyst for Fenton-like advanced oxidation processes. Tertiary treatment can be less expensive and harmful to the environment, reducing production of residual sludge and metal content in the final effluent, which reduces polluting potential of the effluent regarding solid waste. Copyright © 2018 Elsevier Ltd. All rights reserved.

  19. Immobilizing LaFeO{sub 3} nanoparticles on carbon spheres for enhanced heterogeneous photo-Fenton like performance

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Kaixuan [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230601 (China); Niu, Helin, E-mail: niuhelin@ahu.edu.cn [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230601 (China); Chen, Jingshuai; Song, Jiming; Mao, Changjie; Zhang, Shengyi [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230601 (China); Gao, Yuanhao [Institute of Surface Micro and Nano Materials, Xuchang University, Henan 461000 (China)

    2017-05-15

    Highlights: • LaFeO{sub 3} nanoparticles sub–10 nm were successfully immobilized on monodisperse carbon spheres for the first time through a facile and environmental friendly ultrasonic assisted surface ions adsorption method. • LaFeO{sub 3}/C nanocomposite exhibits much higher photo-Fenton like catalytic activity than LaFeO{sub 3}. • The superior property was attributed to the synergistic effects from the photo-Fenton like process and the presence of monodisperse carbon spheres. - Abstract: LaFeO{sub 3} nanoparticles immobilized on the surface of monodisperse carbon spheres have been obtained through a facile and environmentally friendly ultrasonic assisted surface ions adsorption method. The LaFeO{sub 3}/C nanocomposite was evaluated as photo-Fenton like catalyst for the degradation of Rhodamine B (RhB) under visible light irradiation (λ > 420 nm). The LaFeO{sub 3}/C nanocomposite possesses high specific surface area compared with pure LaFeO{sub 3} and significantly enhanced photo-Fenton like catalytic performance. The possible formation process of the LaFeO{sub 3}/C nanocomposite and the mechanism for photo-Fenton like reaction were discussed. The superior property was attributed to the synergistic effects from the photo-Fenton like process and the presence of carbon spheres. In addition, the heterogeneous process led to better recyclability of this type of catalyst.

  20. Reuse of recalcitrant-rich anaerobic effluent as dilution water after enhancement of biodegradability by Fenton processes.

    Science.gov (United States)

    Arimi, Milton M; Zhang, Yongjun; Namango, Saul S; Geißen, Sven-Uwe

    2016-03-01

    Anaerobic digestion is used to treat effluents with a lot of organics, such as molasses distillery wastewater (MDW) which is the effluent of bioethanol production from molasses. The raw MDW requires a lot of dilution water before biodigestion, while the digested MDW has high level of recalcitrants which are problematic for its discharge. This study investigated ferric coagulation, Fenton, Fenton-like (with ferric ions as catalyst) processes and their combinations on the biodegradability of digested MDW. The Fenton and Fenton-like processes after coagulation increased the MDW biodegradability defined by (BOD5/COD) from 0.07 to (0.4-0.6) and saved 50% of H2O2 consumed in the classic Fenton process. The effluent from coagulation coupled to a Fenton-like process was used as dilution water for the raw MDW before the anaerobic digestion. The process was stable with volumetric loading of approx. 2.7 g COD/L/d. It resulted in increased overall biogas recovery and significantly decreased the demand for the dilution water. Copyright © 2015 Elsevier Ltd. All rights reserved.