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Sample records for chelate-modified fenton reaction

  1. Chelate-Modified Fenton Reaction for the Degradation of Trichloroethylene in Aqueous and Two-Phase Systems

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    Lewis, Scott [Univ of KY, dept of chemical and materials engineering; lynch, Andrew [Univ of KY, dept of chemical and materials engineering; Bachas, Leonidas [Univ of KY, Dept of Chemistry; hampson, Steve [Univ of KY Center for Applied Energy Research - KY Research Consortium of Energy and Environment; Ormsbee, Lindelle [Univ of KY Center for Applied Energy Research - KY Research Consortium of Energy and Environment; Bhattacharyya, Dibakar [Univ of KY, dept of chemical and materials engineering

    2008-06-01

    The Standard Fenton reaction has been used for In-Situ Chemical Oxidation (ISCO) of toxic organics in groundwater. However, it requires low pH operating conditions, and thus has limitations for in situ applications. In addition, hydroxyl radicals are rapidly consumed by hydroxyl scavengers found in the subsurface. These problems are alleviated through the chelate-modified Fenton (hydroxyl radical) reaction, which includes the addition of nontoxic chelate (L) such as citrate or gluconic acid. This chelate allows the reaction to take place at bear neutral pH and control hydrogen peroxide consumption by binding to Fe(II), forming an FeL complex. The chelate also binds to Fe(III), preventing its precipitation as ferric hydroxide and thus prevents problems associated with injection well plugging. The rate of TCE dechlorination in chelate-modified Fenton systems is a function of pH, H2O2 concentration, and FE:L ratio. The primary objective of this research is to model and apply this process to the destruction of trichloroethylene (TCE) present in both the aqueous and organic (in the form of droplets) phases. Experimentation proved the chelate-modified Fenton reaction effectively dechlorinates TCE in both the aqueous and organic phases at near-neutral pH. Other focuses of this work include determining the effect of [L]:[Fe] ratios on H2O2 and TCE degradation as well as reusability of the FE citrate solution under repeated H2O2 injections. Generalized models were developed to predict the concentration of TCE in the aqueous phase and TCE droplet radius as a function of time using established hydroxyl radial kinetics and mass transfer relationships.

  2. 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.

  3. 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.

  4. 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.

  5. Effects of Fenton Reaction on Human Serum Albumin: An In Vitro Study

    Science.gov (United States)

    Khosravifarsani, Meysam; Monfared, Ali Shabestani; Pouramir, Mahdi; Zabihi, Ebrahim

    2016-01-01

    Introduction Human serum albumin (HSA) is a critical protein in human blood plasma, which can be highly damaged by oxidative stress. The aim of this study was to analyze modifications of this protein after oxidation using a Fenton system. Methods In this 2015 experiment, different ratios of Fenton reagent (Fe2+/H2O2) was incubated with one concentration of human serum albumin (1mg/ml). Hence, HSA was incubated 30 min with various combinations of a Fenton system and quantified oxidation products such as carbonyl groups, fragmentations, degradations, and oxidized free thiol group using reliable techniques. Image and data analysis were carried out using ImageJ software and Excel (version 2007), respectively. Results An SDS-PAGE profile showed no cross link and aggregation. However, protein band intensity has decreased to 50% in the highest ratio of H2O2/Fe. Carbonylation assay indicated carbonyl/protein (molc/molp) ratio increased linearly in lower ratios and the values plateau at higher levels of H2O2/Fe 2+. The only free sulfhydryl group on HSA was oxidized in all ratios of the Fenton system. Conclusion To sum, the structure of HSA has been changed following treatment with Hydroxyl Radical as the main product of Fenton reaction. These data confirm the antioxidant activity of HSA.

  6. Kinetics and reaction pathways of formaldehyde degradation using the UV-fenton method.

    Science.gov (United States)

    Liu, Xiangxuan; Liang, Jiantao; Wang, Xuanjun

    2011-05-01

    This study was based on the purpose of investigating the reaction rules of formaldehyde (HCHO) as an intermediate product in the degradation of many other organic wastewaters. The process conditions of UV-Fenton method for the degradation of the low concentrations of HCHO were studied in a batch photochemical reactor. The results showed that, when the original HCHO concentration was 30 mg/L, at an operating temperature of 23 degrees C, pH = 3, an H202 dosage of 68 mg/L, and an H2O2-to-Fe2+ mole ratio (H2O2:Fe2+) of 5, 91.89% of the HCHO was removed after 30 minutes. The degradation of HCHO in the UV-Fenton system was basically in accordance with the exponential decay. The kinetic study results showed that the reaction orders of HCHO, Fe2+, and H2O2 in the system were 1.054, 0.510, and 0.728, respectively, and the activation energy (Ea) was 9.85 kJ/mol. The comparison of UV/H2O2, Fenton, and UV-Fenton systems for the degradation of HCHO, and the results of iron catalyst tests showed that the mechanism of UV-Fenton on the degradation of HCHO was through a synergistic effect of Fe2+ and UV light to catalyze the decomposition of H2O2. The introduction of UV irradiation to the Fenton system largely increased the degradation rate of HCHO, mainly as a result of the accelerating effect on the formation of the Fe2+/Fe3+ cycle. The reaction products were analyzed by gas chromatography-mass spectrometry and a chemical oxygen demand (COD) analyzer. The effluent gases also were analyzed by gas chromatography. Based on those results, the reaction pathways of HCHO in the UV-Fenton system were proposed. The qualitative and quantitative analysis of the reaction products and the COD showed that the main intermediate product of the reaction was formic acid, and the further oxidation of it was the rate-limiting step for the degradation of HCHO.

  7. Discoloration of Rhodamine B dyeing wastewater by schorl-catalyzed Fenton-like reaction

    Institute of Scientific and Technical Information of China (English)

    Murari; PRASAD

    2009-01-01

    As other natural iron-bearing minerals, schorl could be taken as an effective iron source for degradation of organic pollutants by mineral-catalyzed Fenton-like system. In our present study, the schorl-catalyzed Fenton-like system has been successfully developed for discoloration of an active commercial dye, Rhodamine B (RhB), in an aqueous solution. Through a number of batch discoloration experiments under various conditions, it was found that the reactivity of the system increased by, respectively, increasing schorl dosage, temperature, hydrogen peroxide starting concentration and by decreasing the pH. Over 90% of discoloration ratio could be gained in less than 30 min, and nearly 70% of total organic carbon (TOC) could be removed in less than 200 min. And, the schorl catalyst could be repeatedly used at least ten times, still with high catalytic activity. Comparative studies indicated that the RhB discoloration ratios were much higher in presence of schorl and H2O2 than those in presence of schorl or H2O2 only, which suggested that the schorl-catalyzed Fenton-like reaction governed the RhB discoloration process. The content of Fe ion leaching in the solution was also measured using inductively coupling plasma-atomic emission spectra (ICP-AES). A mechanism proposed herein suggested that adsorption and Fenton-like reaction (heterogeneous and homogeneous) were responsible for the discoloration of RhB.

  8. Application of Fenton's reaction to steam explosion prehydrolysates from poplar biomass.

    Science.gov (United States)

    Oliva, J M; Manzanares, P; Ballesteros, I; Negro, M J; González, A; Ballesteros, M

    2005-01-01

    The application of Fenton's reaction to enhance the fermentability of prehydrolysates obtained from steam explosion pretreatment of poplar biomass was studied. Reaction conditions of temperature and H2O2 and Fe(II) concentrations were studied. The fermentability of prehydrolysate treated by Fenton's reaction was tested by using different inoculum sizes of thermotolerant strain Kluyveromyces marxianus CECT 10875. The highest percentages of toxic compound degradation (ranging from 71 to 93% removal) were obtained at the highest H2O2 concentration tested (50 mM). However, a negative effect on fermentability was observed at this H2O2 concentration at the lower inoculum loading. An increase in inoculum size to 0.6 g/L resulted in an enhanced ethanol fermentation yield of 95% relative to control.

  9. Fenton reaction induced cancer in wild type rats recapitulates genomic alterations observed in human cancer.

    Directory of Open Access Journals (Sweden)

    Shinya Akatsuka

    Full Text Available Iron overload has been associated with carcinogenesis in humans. Intraperitoneal administration of ferric nitrilotriacetate initiates a Fenton reaction in renal proximal tubules of rodents that ultimately leads to a high incidence of renal cell carcinoma (RCC after repeated treatments. We performed high-resolution microarray comparative genomic hybridization to identify characteristics in the genomic profiles of this oxidative stress-induced rat RCCs. The results revealed extensive large-scale genomic alterations with a preference for deletions. Deletions and amplifications were numerous and sometimes fragmented, demonstrating that a Fenton reaction is a cause of such genomic alterations in vivo. Frequency plotting indicated that two of the most commonly altered loci corresponded to a Cdkn2a/2b deletion and a Met amplification. Tumor sizes were proportionally associated with Met expression and/or amplification, and clustering analysis confirmed our results. Furthermore, we developed a procedure to compare whole genomic patterns of the copy number alterations among different species based on chromosomal syntenic relationship. Patterns of the rat RCCs showed the strongest similarity to the human RCCs among five types of human cancers, followed by human malignant mesothelioma, an iron overload-associated cancer. Therefore, an iron-dependent Fenton chemical reaction causes large-scale genomic alterations during carcinogenesis, which may result in distinct genomic profiles. Based on the characteristics of extensive genome alterations in human cancer, our results suggest that this chemical reaction may play a major role during human carcinogenesis.

  10. Fenton reaction-based colorimetric immunoassay for sensitive detection of brevetoxin B.

    Science.gov (United States)

    Lai, Wenqiang; Wei, Qiaohua; Zhuang, Junyang; Lu, Minghua; Tang, Dianping

    2016-06-15

    We designed a new colorimetric immunoassay for sensitive monitoring of brevetoxin B (BTB) using enzyme-controlled Fenton reaction with a high-resolution 3,3',5,5'-tetramethylbenzidine (TMB)-based visual colored system. Upon addition of hydrogen peroxide (H2O2), the equivalent iron(II) could be first converted into iron(III) and free hydroxyl radical (•OH) via the classical Fenton reaction. Then the as-produced iron(III) and •OH could cause a perceptible change from colorless to blue with the increasing H2O2 concentration in the presence of TMB. Based on Fenton reaction-triggered visual colored system, a novel competitive-type colorimetric enzyme immunoassay was developed for the quantitative screening of target BTB on the bovine serum albumin-BTB-modified magnetic bead using glucose oxidase/anti-BTB antibody-labeled gold nanoparticle as the signal-transduction tag. Upon target BTB introduction, the analyte competed with the conjugated BTB on the magnetic bead for anti-BTB antibody on gold nanoparticle. The carried glucose oxidase with the gold nanoparticle could implement the oxidation of glucose to produce H2O2, and the generated H2O2 promoted the above-mentioned Fenton reaction for color development. Under the optimal conditions, the absorbance decreased with the increasing target BTB in the range from 0.1 to 150 ng kg(-1) with a low detection limit (LOD) of 0.076 ng kg(-1). The LOD was 500-fold lower than that of commercialized Abraxis BTB ELISA kit. Non-specific adsorption was not observed. The precision, reproducibility and specificity were acceptable. Finally, the method accuracy was also validated for monitoring spiked seafood samples, giving results well matched with the referenced brevetoxin ELISA kit. PMID:26851583

  11. 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.

  12. Accelerated Catalytic Fenton Reaction with Traces of Iron: An Fe-Pd-Multicatalysis Approach.

    Science.gov (United States)

    Georgi, Anett; Velasco Polo, Miriam; Crincoli, Klara; Mackenzie, Katrin; Kopinke, Frank-Dieter

    2016-06-01

    An accelerated catalytic Fenton (ACF) reaction was developed based upon a multicatalysis approach, facilitating efficient contaminant oxidation at trace levels of dissolved iron. Beside the Fe(II)/H2O2 catalyst/oxidant pair for production of OH-radicals, the ACF system contains Pd/H2 as catalyst/reductant pair for fast reduction of Fe(III) back to Fe(II) which accelerates the Fenton cycle and leads to faster contaminant degradation. By this means, the concentration of the dissolved iron catalyst can be reduced to trace levels (1 mg L(-1)) below common discharge limits, thus eliminating the need for iron sludge removal, which is one of the major drawbacks of conventional Fenton processes. ACF provides fast degradation of the model contaminant methyl tert-butyl ether (MTBE, C0 = 0.17 mM) with a half-life of 11 min with 1 mg L(-1) dissolved iron, 500 mg L(-1) H2O2, 5 mg L(-1) Pd (as suspended Pd/Al2O3 catalyst) and 0.1 MPa H2, pH 3. The effects of pH, H2 partial pressure and H2O2 concentration on MTBE degradation rates were studied. Results on kinetic deuterium isotope effect and quenching studies are in conformity with OH-radicals as main oxidant. The heterogeneous Pd/Al2O3 catalyst was reused within six cycles without significant loss in activity. PMID:27167833

  13. A Peptide-mediated Fenton Reaction in Wood-degrading Fungi

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Gt factor is a low-molecular-weight peptide isolated from the extracellular culture of wood-degrading fungus Gloeophyllum trabeum. It is capable of enhancing degradation of cellulose. Its action mechanism was investigated and it was found that Gt factor could reduce Fe3+ to Fe2+. Electron paramagnetic resonance (EPR) spectroscopy revealed in the presence of O2, Gt factor could drive the formation of H2O2 via a superoxide anion O2.- intermediate and mediate the generation of hydroxyl radical HO˙ in a Fenton-type reaction. All these provided evidence for the formation of HO˙ in some wood-degrading fungi.

  14. Catalytic degradation of methylene blue by Fenton like system:model to the environmental reaction

    Institute of Scientific and Technical Information of China (English)

    Sanjay R. Thakare

    2004-01-01

    To develop more efficient chemical methods for the demineralization of organic pollutants from waterbodies, which one was also mimic to the nature, a degradation of methylene blue by Fe( Ⅲ ) and H2O2 in theabsence of light instead of Fe( Ⅱ ) and H2O2 was studied. Results showed that use of Fe ( Ⅲ ) is more promisingthan Fe( Ⅱ ). The present study reflects that Fenton reaction is more efficient, in the presence of a small amount ofsalicylic acid is added which is a one of the priority pollutant.

  15. Sulfurized limonite as material for fast decomposition of organic compounds by heterogeneous Fenton reaction

    Energy Technology Data Exchange (ETDEWEB)

    Toda, Kei, E-mail: todakei@sci.kumamoto-u.ac.jp [Department of Chemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Tanaka, Toshinori; Tsuda, Yutaka; Ban, Masahiro; Koveke, Edwin P. [Department of Chemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Koinuma, Michio [Department of Chemistry and Biochemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Ohira, Shin-Ichi [Department of Chemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan)

    2014-08-15

    Graphical abstract: - Highlights: • Used limonite degrades organic compounds by heterogeneous Fenton reaction. • Sulfurized limonite removes methylene blue color in seconds. • Recycled limonite can be used for biogas purification and wastewater treatment. - Abstract: Rapid decomposition of wastewater contaminants using sulfurized limonite (S-limonite) was investigated. Limonite is used for desulfurization of biogases, and S-limonite is obtained from desulfurization plants as solid waste. In this work, the profitable use of S-limonite in water treatment was examined. The divalent Fe in S-limonite was expected to produce OH radicals, as Fe{sup 2+} ions and limonite thermally treated with H{sub 2} do. Methylene blue was used for batch-wise monitoring of the decomposition performance. The decomposition rate was fast and the methylene blue solution color disappeared in only 10 s when a small amount of H{sub 2}O{sub 2} was added (1 mM in the sample solution) in the presence of S-limonite. The OH radicals were formed by a heterogeneous reaction on the S-limonite surface and Fenton reaction with dissolved Fe{sup 2+}. The decomposition of pentachlorophenol was also examined; it was successfully decomposed in batch-wise tests. The surfaces of limonite before sulfurization, S-limonite, and S-limonite after use for water treatment were performed using scanning electron microscopy and X-ray photoelectron spectroscopy. The results show that S-limonite reverted to limonite after being used for water treatment.

  16. Application of non-thermal plasma reactor and Fenton reaction for degradation of ibuprofen

    Energy Technology Data Exchange (ETDEWEB)

    Marković, Marijana [Center of Chemistry, Institute of Chemistry, Technology and Metallurgy, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia); Jović, Milica; Stanković, Dalibor [Innovation Center, Faculty of Chemistry, University of Belgrade, P.O. Box 51, 11058 Belgrade 118 (Serbia); Kovačević, Vesna [Faculty of Physics, University of Belgrade, P.O. Box 44, 11000 Belgrade (Serbia); Roglić, Goran [Faculty of Chemistry, University of Belgrade, P.O. Box 51, 11058 Belgrade 118 (Serbia); Gojgić-Cvijović, Gordana [Center of Chemistry, Institute of Chemistry, Technology and Metallurgy, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia); Manojlović, Dragan, E-mail: manojlo@chem.bg.ac.rs [Faculty of Chemistry, University of Belgrade, P.O. Box 51, 11058 Belgrade 118 (Serbia)

    2015-02-01

    Pharmaceutical compounds have been detected frequently in surface and ground water. Advanced Oxidation Processes (AOPs) were reported as very efficient for removal of various organic compounds. Nevertheless, due to incomplete degradation, toxic intermediates can induce more severe effects than the parent compound. Therefore, toxicity studies are necessary for the evaluation of possible uses of AOPs. In this study the effectiveness and capacity for environmental application of three different AOPs were estimated. They were applied and evaluated for removal of ibuprofen from water solutions. Therefore, two treatments were performed in a non-thermal plasma reactor with dielectric barrier discharge with and without a homogenous catalyst (Fe{sup 2+}). The third treatment was the Fenton reaction. The degradation rate of ibuprofen was measured by HPLC-DAD and the main degradation products were identified using LC–MS TOF. Twelve degradation products were identified, and there were differences according to the various treatments applied. Toxicity effects were determined with two bioassays: Vibrio fischeri and Artemia salina. The efficiency of AOPs was demonstrated for all treatments, where after 15 min degradation percentage was over 80% accompanied by opening of the aromatic ring. In the treatment with homogenous catalyst degradation reached 99%. V. fischeri toxicity test has shown greater sensitivity to ibuprofen solution after the Fenton treatment in comparison to A. salina. - Highlights: • Twelve ibuprofen degradation products were identified in total. • The degradation percentage differed between treatments (DBD/Fe{sup 2+} was 99%). • In DBD/Fe{sup 2+} only aliphatic degradation products were identified. • V. fischeri was sensitive to ibuprofen solution after the Fenton treatment. • A. salina showed no toxic effect when exposed to all post treatment solutions.

  17. Chemical oxidation of anthracite with hydrogen peroxide via the Fenton reaction

    Science.gov (United States)

    Heard, I.; Senftle, F.E.

    1984-01-01

    Solutions of 30% H2O2 ranging from pH = 0 to pH = 11.5 have been used to oxidize anthracite at room temperature. The inorganic impurities, primarily pyrite, catalysed the oxidation and reduction of H2O2 (the Fenton reaction) to form the hydroxyl radical; the oxidation of the organic matter was minimal and was observed only in strong acidic solutions (pH reactions were completed in a much shorter time, the oxidation mechanism must have been of a different nature than that for the untreated anthracite. A qualitative model based on the catalytic decomposition of H2O2 by activated carbon sites in the coal surface is used to explain the oxidation of the demineralized anthracite. ?? 1984.

  18. Degradation of polyvinyl alcohol (PVA) by homogeneous and heterogeneous photocatalysis applied to the photochemically enhanced Fenton reaction.

    Science.gov (United States)

    Bossmann, S H; Oliveros, E; Göb, S; Kantor, M; Göppert, A; Lei, L; Yue, P L; Braun, A M

    2001-01-01

    The reaction mechanism of the oxidative degradation of polyvinyl alcohol (PVA) by the photochemically enhanced Fenton reaction was studied using a homogeneous (Fe2+(aq) + H2O2) and a heterogeneous reaction system (iron(III)-exchanged zeolite Y+ H2O2). In the homogeneous Fenton system, efficient degradation was observed in a batch reactor, equipped with a medium pressure mercury arc in a Pyrex envelope and employing 80% of the stoichiometric amount of H2O2 required for the total oxidation of PVA and a concentration ratio as low as I mole of iron(II) sulfate per 20 moles of PVA sub-units (C2H40). Model PVA polymers of three different molecular weights (15,000, 49,000 and 100,000 g mol(-1)) were found to follow identical degradation patterns. Strong experimental evidence supports the formation of supermacromolecules (MW: 1-5 x 10(6) g/mol) consisting of oxidized PVA and trapped iron(III) at an early reaction stage. Low molecular weight intermediates, such as oxalic acid, formic acid or formaldehyde were not found during PVA degradation in the homogeneous Fenton system, and we may deduce that the manifold of degradation reactions is mainly taking place within the super-macromolecules from which CO2 is directly released. However, in the heterogeneous Fenton system, the reaction behavior was found to be distinctly different: a decrease of the molecular weights of all three tested monodisperse PVA samples was observed by the broadening of the GPC-traces during irradiation, and oxalic acid was formed. The results lead to the mechanistic hypothesis that during the heterogeneous Fenton process, the cleavage of the PVA-chains may occur at random positions, the reactive centres being located inside the iron(III)-doped zeolite Y photocatalysts.

  19. Synthesis of iron/GAC catalyst for wastewater treatment using heterogeneous Fenton reaction

    Indian Academy of Sciences (India)

    S T T Le; T T Ngo; W Khanitchaidecha; A Nakaruk

    2015-08-01

    Iron catalyst dispersed on granular activated carbon (GAC) was prepared by impregnating Fe(NO3)3 solution on GAC. The mixed solution was annealed at 600°C in muffle furnace under ambient condition for 1 h. The structural property of the catalyst was investigated using X-ray diffraction (XRD). The catalyst’s activity and lifetime were tested using the degradation of 50 ppm methyl orange (MO) solution. In addition, the optimum conditions of the Fenton reaction such as initial pH, initial MO concentration hydrogen peroxide concentration and the amount of catalyst were also investigated. The XRD results showed that magnetite and haematite were two main compositions of the synthesized catalyst. The investigation of optimum conditions suggested that initial pH at 3 provided the highest efficiency of MO removal. In addition, the concentration of hydrogen peroxide at 8 ppm was the most suitable. The optimum condition of amount of catalyst was 5 g l−1. The efficiencies of MO removal reached 95% at 60 min of reaction time at low initial MO concentration (25–500 mg l−1). In the meantime, the removal efficiency was found to decrease with the increase in the initial MO concentration. The efficiency decreased to 70 and 30% at 1000 and 3000 mg l−1 of initial MO concentration, respectively. Additionally, after reuse the synthesized catalyst 3 times the MO removal efficiency still remained over 90%. In conclusion, the iron/GAC catalyst was successfully synthesized and applied to dye treatment using heterogeneous Fenton reaction. The catalyst showed high efficiency of MO removal and could be reused many times.

  20. 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.

  1. Enhancing enzymolysis and fermentation efficiency of sugarcane bagasse by synergistic pretreatment of Fenton reaction and sodium hydroxide extraction.

    Science.gov (United States)

    Zhang, Teng; Zhu, Ming-Jun

    2016-08-01

    A study on the synergistic pretreatment of sugarcane bagasse (SCB) using Fenton reaction and NaOH extraction was conducted. The optimized process conditions for Fenton pretreatment were 10% (w/w) of H2O2, 20mM of Fe(2+), pH 2.5, pretreatment time 6h, and pretreatment temperature 55°C. Sequential pretreatments were performed in combination with NaOH extraction (NaOH 1% (w/w), 80°C, 5% of solid loading, 1h). Among all the pretreatments, Fenton pretreatment followed by NaOH extraction had the highest efficiency of 64.7% and 108.3% for enzymolysis and simultaneous saccharification fermentation (SSF) with an ethanol concentration of 17.44g/L. The analyses by the scanning electron microscopy, X-ray diffraction and confocal laser scanning microscopy revealed that Fenton pretreatment disrupts the structure of SCB to facilitate the degradation of lignin by NaOH. The overall data suggest that this combinatorial strategy is a promising process for SCB pretreatment. PMID:27213578

  2. Degradation of Corn Oil Wastes by Fenton Reaction and Under Mildly Basic Media in the Presence of Oxidants Assisted with Sun Light

    OpenAIRE

    Josefina V.  Sanchez; Susana S.  Martinez; Maria D.F.T.  Hernandez

    2008-01-01

    The degradation of water soluble corn oil wastes was carried out by Fenton reaction and also under mildly basic media in the presence of oxidants, such as hydrogen peroxide and persulfate, assisted with solar light. The degradation efficiency was obtained by analysis of chemical oxygen demand, carbon dioxide and gas chromatography. Over 90% of both chemical oxygen demand abatement and carbon dioxide recovery was accomplished by Fenton reaction. The presence of oxidants during the photodegrada...

  3. Simultaneous photoinduced generation of Fe(2+) and H2O2 in rivers: An indicator for photo-Fenton reaction.

    Science.gov (United States)

    Mostofa, Khan M G; Sakugawa, Hiroshi

    2016-09-01

    The photo-Fenton reaction is a key source of the highly reactive hydroxyl radical (HO) that is produced by the reaction of simultaneous photo-induced generation of Fe(2)(+)-dissolved organic matter (DOM) with H2O2 in sunlit surface waters as well as in the treatment of organic pollutants in the advanced oxidation processes (AOPs). Concentrations of both H2O2 and Fe(2)(+)-DOM were dependent on time and total solar intensity flux, and their levels were highest in the diurnal samples collected at noon compared with the samples collected during the period before sunrise and after sunset. H2O2 and Fe(2)(+)-DOM concentrations during monthly readings were also found higher in comparison with the diurnal samples, shortly before sunrise or after sunset. A π-electron bonding system is formed between Fe and the functional groups in DOM (Fe-DOM), through electron donation from the functional groups of DOM to an empty d-orbital of Fe. The π-electron is loosely bound and is highly susceptible to a rapid excitation upon light exposure that will provide better understanding of the formation of aqueous electrons, superoxide radical anions, H2O2 and finally, photo-Fenton reactions, too. Our results imply that simultaneous generation of H2O2 and Fe(2)(+)-DOM upon sunlight exposure during the daytime is most likely to be the key photo-Fenton reaction pathway, taking place in surface waters. PMID:27593270

  4. Simultaneous photoinduced generation of Fe(2+) and H2O2 in rivers: An indicator for photo-Fenton reaction.

    Science.gov (United States)

    Mostofa, Khan M G; Sakugawa, Hiroshi

    2016-09-01

    The photo-Fenton reaction is a key source of the highly reactive hydroxyl radical (HO) that is produced by the reaction of simultaneous photo-induced generation of Fe(2)(+)-dissolved organic matter (DOM) with H2O2 in sunlit surface waters as well as in the treatment of organic pollutants in the advanced oxidation processes (AOPs). Concentrations of both H2O2 and Fe(2)(+)-DOM were dependent on time and total solar intensity flux, and their levels were highest in the diurnal samples collected at noon compared with the samples collected during the period before sunrise and after sunset. H2O2 and Fe(2)(+)-DOM concentrations during monthly readings were also found higher in comparison with the diurnal samples, shortly before sunrise or after sunset. A π-electron bonding system is formed between Fe and the functional groups in DOM (Fe-DOM), through electron donation from the functional groups of DOM to an empty d-orbital of Fe. The π-electron is loosely bound and is highly susceptible to a rapid excitation upon light exposure that will provide better understanding of the formation of aqueous electrons, superoxide radical anions, H2O2 and finally, photo-Fenton reactions, too. Our results imply that simultaneous generation of H2O2 and Fe(2)(+)-DOM upon sunlight exposure during the daytime is most likely to be the key photo-Fenton reaction pathway, taking place in surface waters.

  5. A fluorescence turn on assay for alkaline phosphatase based on the Cu(2+) catalyzed Fenton-like reaction.

    Science.gov (United States)

    Zhang, Qingfeng; Zhang, Cuiyun; Shahzad, Sohail Anjum; Yu, Cong

    2016-09-01

    A fluorescence turn-on assay was established for ALP (alkaline phosphatase) based on Cu(2+) catalyzed Fenton-like reaction and Graphene Oxide (GO). GO was utilized to quench the fluorescence of fluorescein (FAM) labeled single strand DNA (F-DNA). ALP can remove the phosphate group in sodium ascorbyl phosphate (SAP), and convert it into reducing ascorbate. Highly reactive hydroxyl radicals (·OH) were generated in the presence of ascorbate and Cu(2+) through the Fenton-like reaction. The reactive radicals generated in situ caused the cleavage of F-DNA into small fragments. When GO was added, the fluorescence emission of the sample without ALP was quenched and fluorescence emission recovered in the presence of ALP. The intensity of the recovered fluorescence was directly related to the concentration of ALP in the assay solution, and a sensitive and selective facile ALP assay is therefore established. PMID:27343614

  6. Degradation of aniline by heterogeneous Fenton's reaction using a Ni-Fe oxalate complex catalyst.

    Science.gov (United States)

    Liu, Yucan; Zhang, Guangming; Fang, Shunyan; Chong, Shan; Zhu, Jia

    2016-11-01

    A Ni-Fe oxalate complex catalyst was synthesized and characterized by means of Brunauer-Emmet-Teller (BET) method, scanning electron microscope (SEM) and X-ray photo-electron spectroscopy (XPS). The catalyst showed good catalytic activity for aniline degradation by heterogeneous Fenton's reaction, in which the synergetic index was 9.3. The effects of reaction temperature, catalyst dosage, hydrogen peroxide concentration and initial pH were investigated. Under the optimum conditions (T = 293 K, catalyst dosage = 0.2 g/L, H2O2 concentration = 4 mmol/L and initial pH = 5.4), 100% aniline could be removed within 35 min, and approximately 88% deamination efficiency was achieved in 60 min. The aniline degradation process followed the pseudo-first-order kinetic (k = 0.177 min(-1)) with activation energy (Ea) of 49.4 kJ mol(-1). Aniline could be removed in a broad initial pH (3-8) due to the excellent pH-tolerance property of the catalyst. The detected ammonium ion indicated that deamination occurred during aniline degradation. It was proposed that deamination synchronized with aniline removal, and aniline was attacked by free radicals to generate benzoquinonimine and phenol. This system is promising for the removal of aniline from water.

  7. Integrated treatment of olive mill wastewater (OMW) by the combination of Fenton's reaction and anaerobic treatment

    International Nuclear Information System (INIS)

    The use of an integrated treatment scheme consisting of wet hydrogen peroxide catalytic oxidation (WHPCO) followed by two-stage upflow anaerobic sludge blanket (UASB) reactor (10 l each) for the treatment of olive mill wastewater was the subject of this study. The diluted wastewater (1:1) was pre-treated using Fenton's reaction. Optimum operating conditions namely, pH, H2O2 dose, Fe+2, COD:H2O2 ratio and Fe+2:H2O2 ratio were determined. The UASB reactor was fed continuously with the pre-treated wastewater. The hydraulic retention time was kept constant at 48 h (24 h for each stage). The conventional parameters such as COD, BOD, TOC, TKN, TP, TSS, oil and grease, and total phenols were determined. The concentrations of polyphenolic compounds in raw wastewater and effluents of each treatment step were measured using HPLC. The results indicated a good quality final effluent. Residual concentrations of individual organic compounds ranged from 0.432 mg l-1 for ρ-hydroxy-benzaldhyde to 3.273 mg l-1 for cinnamic acid

  8. Removal of trace metals and improvement of dredged sediment dewaterability by bioleaching combined with Fenton-like reaction.

    Science.gov (United States)

    Zeng, Xiangfeng; Twardowska, Irena; Wei, Shuhe; Sun, Lina; Wang, Jun; Zhu, Jianyu; Cai, Jianchao

    2015-05-15

    Bioleaching by Aspergillus niger strain SY1 combined with Fenton-like reaction was optimized to improve trace metal removal and dewaterability of dredged sediments. The major optimized parameters were the duration of bioleaching and H₂O₂ dose in Fenton-like process (5 days and 2g H₂O₂/L, respectively). Bioleaching resulted in the removal of ≈90% of Cd, ≈60% of Zn and Cu, ≈20% of Pb, and in decrease of sediment pH from 6.6 to 2.5 due to organic acids produced by A. niger. After addition of H₂O₂, Fenton-like reaction was initiated and further metal removal occurred. Overall efficiency of the combined process comprised: (i) reduction of Cd content in sediment by 99.5%, Cu and Zn by >70% and Pb by 39% as a result of metal release bound in all mobilizable fractions; (ii) decrease of sediment capillary suction time (CST) from 98.2s to 10.1s (by 89.8%) and specific resistance to filtration (SRF) from 37.4×10(12)m/kg to 6.2×10(12)m/kg (by 83.8%), due to reducing amount of extracellular polymeric substances (EPS) by 68.7% and bound water content by 79.1%. The combined process was found to be an efficient method to remove trace metals and improve dewaterability of contaminated dredged sediments. PMID:25682517

  9. Ultradispersed Cobalt Ferrite Nanoparticles Assembled in Graphene Aerogel for Continuous Photo-Fenton Reaction and Enhanced Lithium Storage Performance.

    Science.gov (United States)

    Qiu, Bocheng; Deng, Yuanxin; Du, Mengmeng; Xing, Mingyang; Zhang, Jinlong

    2016-07-04

    The Photo-Fenton reaction is an advanced technology to eliminate organic pollutants in environmental chemistry. Moreover, the conversion rate of Fe(3+)/Fe(2+) and utilization rate of H2O2 are significant factors in Photo-Fenton reaction. In this work, we reported three dimensional (3D) hierarchical cobalt ferrite/graphene aerogels (CoFe2O4/GAs) composites by the in situ growing CoFe2O4 crystal seeds on the graphene oxide (GO) followed by the hydrothermal process. The resulting CoFe2O4/GAs composites demonstrated 3D hierarchical pore structure with mesopores (14~18 nm), macropores (50~125 nm), and a remarkable surface area (177.8 m(2 )g(-1)). These properties endowed this hybrid with the high and recyclable Photo-Fenton activity for methyl orange pollutant degradation. More importantly, the CoFe2O4/GAs composites can keep high Photo-Fenton activity in a wide pH. Besides, the CoFe2O4/GAs composites also exhibited excellent cyclic performance and good rate capability. The 3D framework can not only effectively prevent the volume expansion and aggregation of CoFe2O4 nanoparticles during the charge/discharge processes for Lithium-ion batteries (LIBs), but also shorten lithium ions and electron diffusion length in 3D pathways. These results indicated a broaden application prospect of 3D-graphene based hybrids in wastewater treatment and energy storage.

  10. Ultradispersed Cobalt Ferrite Nanoparticles Assembled in Graphene Aerogel for Continuous Photo-Fenton Reaction and Enhanced Lithium Storage Performance.

    Science.gov (United States)

    Qiu, Bocheng; Deng, Yuanxin; Du, Mengmeng; Xing, Mingyang; Zhang, Jinlong

    2016-01-01

    The Photo-Fenton reaction is an advanced technology to eliminate organic pollutants in environmental chemistry. Moreover, the conversion rate of Fe(3+)/Fe(2+) and utilization rate of H2O2 are significant factors in Photo-Fenton reaction. In this work, we reported three dimensional (3D) hierarchical cobalt ferrite/graphene aerogels (CoFe2O4/GAs) composites by the in situ growing CoFe2O4 crystal seeds on the graphene oxide (GO) followed by the hydrothermal process. The resulting CoFe2O4/GAs composites demonstrated 3D hierarchical pore structure with mesopores (14~18 nm), macropores (50~125 nm), and a remarkable surface area (177.8 m(2 )g(-1)). These properties endowed this hybrid with the high and recyclable Photo-Fenton activity for methyl orange pollutant degradation. More importantly, the CoFe2O4/GAs composites can keep high Photo-Fenton activity in a wide pH. Besides, the CoFe2O4/GAs composites also exhibited excellent cyclic performance and good rate capability. The 3D framework can not only effectively prevent the volume expansion and aggregation of CoFe2O4 nanoparticles during the charge/discharge processes for Lithium-ion batteries (LIBs), but also shorten lithium ions and electron diffusion length in 3D pathways. These results indicated a broaden application prospect of 3D-graphene based hybrids in wastewater treatment and energy storage. PMID:27373343

  11. Ultradispersed Cobalt Ferrite Nanoparticles Assembled in Graphene Aerogel for Continuous Photo-Fenton Reaction and Enhanced Lithium Storage Performance

    Science.gov (United States)

    Qiu, Bocheng; Deng, Yuanxin; Du, Mengmeng; Xing, Mingyang; Zhang, Jinlong

    2016-01-01

    The Photo-Fenton reaction is an advanced technology to eliminate organic pollutants in environmental chemistry. Moreover, the conversion rate of Fe3+/Fe2+ and utilization rate of H2O2 are significant factors in Photo-Fenton reaction. In this work, we reported three dimensional (3D) hierarchical cobalt ferrite/graphene aerogels (CoFe2O4/GAs) composites by the in situ growing CoFe2O4 crystal seeds on the graphene oxide (GO) followed by the hydrothermal process. The resulting CoFe2O4/GAs composites demonstrated 3D hierarchical pore structure with mesopores (14~18 nm), macropores (50~125 nm), and a remarkable surface area (177.8 m2 g−1). These properties endowed this hybrid with the high and recyclable Photo-Fenton activity for methyl orange pollutant degradation. More importantly, the CoFe2O4/GAs composites can keep high Photo-Fenton activity in a wide pH. Besides, the CoFe2O4/GAs composites also exhibited excellent cyclic performance and good rate capability. The 3D framework can not only effectively prevent the volume expansion and aggregation of CoFe2O4 nanoparticles during the charge/discharge processes for Lithium-ion batteries (LIBs), but also shorten lithium ions and electron diffusion length in 3D pathways. These results indicated a broaden application prospect of 3D-graphene based hybrids in wastewater treatment and energy storage. PMID:27373343

  12. Ultradispersed Cobalt Ferrite Nanoparticles Assembled in Graphene Aerogel for Continuous Photo-Fenton Reaction and Enhanced Lithium Storage Performance

    Science.gov (United States)

    Qiu, Bocheng; Deng, Yuanxin; Du, Mengmeng; Xing, Mingyang; Zhang, Jinlong

    2016-07-01

    The Photo-Fenton reaction is an advanced technology to eliminate organic pollutants in environmental chemistry. Moreover, the conversion rate of Fe3+/Fe2+ and utilization rate of H2O2 are significant factors in Photo-Fenton reaction. In this work, we reported three dimensional (3D) hierarchical cobalt ferrite/graphene aerogels (CoFe2O4/GAs) composites by the in situ growing CoFe2O4 crystal seeds on the graphene oxide (GO) followed by the hydrothermal process. The resulting CoFe2O4/GAs composites demonstrated 3D hierarchical pore structure with mesopores (14~18 nm), macropores (50~125 nm), and a remarkable surface area (177.8 m2 g-1). These properties endowed this hybrid with the high and recyclable Photo-Fenton activity for methyl orange pollutant degradation. More importantly, the CoFe2O4/GAs composites can keep high Photo-Fenton activity in a wide pH. Besides, the CoFe2O4/GAs composites also exhibited excellent cyclic performance and good rate capability. The 3D framework can not only effectively prevent the volume expansion and aggregation of CoFe2O4 nanoparticles during the charge/discharge processes for Lithium-ion batteries (LIBs), but also shorten lithium ions and electron diffusion length in 3D pathways. These results indicated a broaden application prospect of 3D-graphene based hybrids in wastewater treatment and energy storage.

  13. Ultradispersed Cobalt Ferrite Nanoparticles Assembled in Graphene Aerogel for Continuous Photo-Fenton Reaction and Enhanced Lithium Storage Performance

    Science.gov (United States)

    Qiu, Bocheng; Deng, Yuanxin; Du, Mengmeng; Xing, Mingyang; Zhang, Jinlong

    2016-07-01

    The Photo-Fenton reaction is an advanced technology to eliminate organic pollutants in environmental chemistry. Moreover, the conversion rate of Fe3+/Fe2+ and utilization rate of H2O2 are significant factors in Photo-Fenton reaction. In this work, we reported three dimensional (3D) hierarchical cobalt ferrite/graphene aerogels (CoFe2O4/GAs) composites by the in situ growing CoFe2O4 crystal seeds on the graphene oxide (GO) followed by the hydrothermal process. The resulting CoFe2O4/GAs composites demonstrated 3D hierarchical pore structure with mesopores (14~18 nm), macropores (50~125 nm), and a remarkable surface area (177.8 m2 g‑1). These properties endowed this hybrid with the high and recyclable Photo-Fenton activity for methyl orange pollutant degradation. More importantly, the CoFe2O4/GAs composites can keep high Photo-Fenton activity in a wide pH. Besides, the CoFe2O4/GAs composites also exhibited excellent cyclic performance and good rate capability. The 3D framework can not only effectively prevent the volume expansion and aggregation of CoFe2O4 nanoparticles during the charge/discharge processes for Lithium-ion batteries (LIBs), but also shorten lithium ions and electron diffusion length in 3D pathways. These results indicated a broaden application prospect of 3D-graphene based hybrids in wastewater treatment and energy storage.

  14. Plausible mechanisms of the fenton-like reactions, M = Fe(II) and Co(II), in the presence of RCO2(-) substrates: are OH(•) radicals formed in the process?

    Science.gov (United States)

    Kornweitz, Haya; Burg, Ariela; Meyerstein, Dan

    2015-05-01

    DFT calculations concerning the plausible mechanism of Fenton-like reactions catalyzed by Fe(II) and Co(II) cations in the presence of carboxylate ligands suggest that hydroxyl radicals are not formed in these reactions. This conclusion suggests that the commonly accepted mechanisms of Fenton-like reactions induced oxidative stress and advanced oxidation processes have to be reconsidered.

  15. Supported Nanosized α-FeOOH Improves Efficiency of Photoelectro-Fenton Process with Reaction-Controlled pH Adjustment for Sustainable Water Treatment

    Directory of Open Access Journals (Sweden)

    Chuan Wang

    2012-01-01

    Full Text Available The overall photoelectro-Fenton (PE-Fenton process for water treatment with neutral initial pH includes three steps of pH reduction, PE-Fenton reaction, and pH elevation. Reaction-controlled pH adjustment (RCpA, which utilizes the intrinsic electrochemical reactions instead of chemical addition, has been employed to lower the pH, maintain the lowered pH for the Fenton reaction, and recover the pH for final effluent discharge. This study demonstrated that the overall efficiency of this sustainable PE-Fenton process was improved by rapidly recycling the iron substance. Nanosized iron oxide was prepared and employed to ensure such rapid recycling. SEM and XRD results showed that the as-prepared iron oxide was α-FeOOH with 20 nm in size. The experimental results of dimethyl phthalate (DMP degradation showed that diatomite-supported α-FeOOH (N-α-FeOOH/diatomite could efficiently reduce the DMP concentration and total organic carbon. Furthermore, compared with Fe3+, the N-α-FeOOH/diatomite saved 160 min for iron settlement at 20 mg L−1 DMP concentration. Also, with the increment in the initial DMP concentration, extra energy consumed by the individual step of PE-Fenton reaction using the N-α-FeOOH/diatomite became negligible compared with that using free iron ions with the increment in the initial DMP concentration. This development is expected to be a major step of the PE-Fenton process with RCpA towards actual water treatment.

  16. 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.

  17. Degradation of Corn Oil Wastes by Fenton Reaction and Under Mildly Basic Media in the Presence of Oxidants Assisted with Sun Light

    Directory of Open Access Journals (Sweden)

    Josefina V.  Sanchez

    2008-01-01

    Full Text Available The degradation of water soluble corn oil wastes was carried out by Fenton reaction and also under mildly basic media in the presence of oxidants, such as hydrogen peroxide and persulfate, assisted with solar light. The degradation efficiency was obtained by analysis of chemical oxygen demand, carbon dioxide and gas chromatography. Over 90% of both chemical oxygen demand abatement and carbon dioxide recovery was accomplished by Fenton reaction. The presence of oxidants during the photodegradation resulted in high chemical oxygen demand abatement of the oil waste with the disappearance of the majority of the initial fatty acids present in the oil waste before treatment.

  18. Potential of modified iron-rich foundry waste for environmental applications: Fenton reaction and Cr(VI) reduction.

    Science.gov (United States)

    Oliveira, Patrícia E F; Oliveira, Leandro D; Ardisson, José D; Lago, Rochel M

    2011-10-30

    A magnetic fraction (15%) from a waste of foundry sand (WFS), composed of sand, carbon, bentonite clay and iron (10%) was modified by thermal treatment at 400, 600 and 800°C under inert atmosphere. Mössbauer analyses showed that the thermal treatment increased the amount of Fe(3)O(4) from 25 to 55% by reduction of Fe(2)O(3) and highly dispersed Fe(3+) by the carbon present in the waste. The Fe(3)O(4) caused a significant increase on the activity of two important reactions with application in environmental remediation: the Fenton oxidation of indigo carmine dye with H(2)O(2) and the reduction of Cr(VI) to Cr(III). The magnetic fraction of WFS was also mixed with hematite (Fe(2)O(3)) and thermally treated at 400, 600 and 800°C. This treatment produced large amounts of surface Fe(3)O(4) and increased substantially the rate of Fenton reaction as well as Cr(VI) reduction. This reactivity combined with the presence of carbon (an adsorbent for organic contaminants), bentonite clay (an adsorbent for metallic contaminants) and the granulometry/packing/hydrodynamic features make WFS a promising material for use in reactive permeable barriers. PMID:21890267

  19. Ex Vivo Antioxidant Activity of Selected Medicinal Plants against Fenton Reaction-Mediated Oxidation of Biological Lipid Substrates

    Directory of Open Access Journals (Sweden)

    Namratha Pai Kotebagilu

    2015-01-01

    Full Text Available Free radical-mediated oxidation is often linked to various degenerative diseases. Biological substrates with lipids as major components are susceptible to oxygen-derived lipid peroxidation due to their composition. Lipid peroxide products act as biomarkers in evaluating the antioxidant potential of various plants and functional foods. The study focused on evaluation of the antioxidant potential of two extracts (methanol and 80% methanol of four medicinal plants, Andrographis paniculata, Costus speciosus, Canthium parviflorum, and Abrus precatorius, against Fenton reaction-mediated oxidation of three biological lipid substrates; cholesterol, low-density lipoprotein, and brain homogenate. The antioxidant activity of the extracts was measured by thiobarbituric acid reactive substances method. Also, the correlation between the polyphenol, flavonoid content, and the antioxidant activity in biological substrates was analyzed. Results indicated highest antioxidant potential by 80% methanol extract of Canthium parviflorum (97.55%, methanol extract of Andrographis paniculata (72.15%, and methanol extract of Canthium parviflorum (49.55% in cholesterol, low-density lipoprotein, and brain, respectively. The polyphenol and flavonoid contents of methanol extract of Andrographis paniculata in cholesterol (r=0.816 and low-density lipoprotein (r=0.948 and Costus speciosus in brain (r=0.977, polyphenols, and r=0.949, flavonoids correlated well with the antioxidant activity. The findings prove the antioxidant potential of the selected medicinal plants against Fenton reaction in biological lipid substrates.

  20. Ex Vivo Antioxidant Activity of Selected Medicinal Plants against Fenton Reaction-Mediated Oxidation of Biological Lipid Substrates.

    Science.gov (United States)

    Pai Kotebagilu, Namratha; Reddy Palvai, Vanitha; Urooj, Asna

    2015-01-01

    Free radical-mediated oxidation is often linked to various degenerative diseases. Biological substrates with lipids as major components are susceptible to oxygen-derived lipid peroxidation due to their composition. Lipid peroxide products act as biomarkers in evaluating the antioxidant potential of various plants and functional foods. The study focused on evaluation of the antioxidant potential of two extracts (methanol and 80% methanol) of four medicinal plants, Andrographis paniculata, Costus speciosus, Canthium parviflorum, and Abrus precatorius, against Fenton reaction-mediated oxidation of three biological lipid substrates; cholesterol, low-density lipoprotein, and brain homogenate. The antioxidant activity of the extracts was measured by thiobarbituric acid reactive substances method. Also, the correlation between the polyphenol, flavonoid content, and the antioxidant activity in biological substrates was analyzed. Results indicated highest antioxidant potential by 80% methanol extract of Canthium parviflorum (97.55%), methanol extract of Andrographis paniculata (72.15%), and methanol extract of Canthium parviflorum (49.55%) in cholesterol, low-density lipoprotein, and brain, respectively. The polyphenol and flavonoid contents of methanol extract of Andrographis paniculata in cholesterol (r = 0.816) and low-density lipoprotein (r = 0.948) and Costus speciosus in brain (r = 0.977, polyphenols, and r = 0.949, flavonoids) correlated well with the antioxidant activity. The findings prove the antioxidant potential of the selected medicinal plants against Fenton reaction in biological lipid substrates. PMID:26933511

  1. The decolorization of Acid Orange II in non-homogeneous Fenton reaction catalyzed by natural vanadium-titanium magnetite

    Energy Technology Data Exchange (ETDEWEB)

    Liang Xiaoliang; Zhong Yuanhong [Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 (China); Graduate University of the Chinese Academy of Sciences, Beijing 100049 (China); Zhu Sanyuan; Zhu Jianxi; Yuan Peng [Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 (China); He Hongping, E-mail: hehp@gig.ac.cn [Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 (China); Zhang Jing [Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)

    2010-09-15

    The catalytic activity of natural vanadium-titanium magnetite was investigated in the decolorization of Acid Orange II by non-homogeneous Fenton process. The natural catalysts purified by magnetic separation were characterized using X-ray diffraction (XRD), polarizing microscope, X-ray absorption fine structure (XAFS) analysis and Moessbauer spectroscopy. The obtained results show that the natural samples after magnetic separation mainly contain titanomagnetite, with a small amount of ilmenite and chlorite. Titanomagnetite is doped with vanadium, whose the valency is mainly +3 and occupies the octahedral site. Batch decolorization studies were performed to evaluate the influences of various experimental parameters like initial pH, the amount of catalyst and initial concentration of hydrogen peroxide on the decolorization efficiency of Acid Orange II. The decolorization of the dye mainly relied on degradation. The degradation efficiency was strongly dependent on pH of the medium where it increased as the pH decreased in acid range. The increase of catalyst and hydrogen peroxide could accelerate the degradation. The catalytic property of natural vanadium-titanium magnetite in the degradation of Acid Orange II was stronger than that of synthetic magnetite (Fe{sub 3}O{sub 4}). The catalytic activity of the natural samples was greatly related to the titanomagnetite content. The degradation process was dominated by heterogeneous Fenton reaction, complying with pseudo-first-order rate law. The natural catalyst has a good catalytic stability.

  2. Combination of heterogeneous Fenton-like reaction and photocatalysis using Co-TiO2 nanocatalyst for activation of KHSO5 with visible light irradiation at ambient conditions

    Institute of Scientific and Technical Information of China (English)

    Qingkong Chen; Fangying Ji; Qian Guo; Jianping Fan; Xuan Xu

    2014-01-01

    A novel coupled system using Co-TiO2 was successfully designed which combined two different heterogeneous advanced oxidation processes,sulfate radical based Fenton-like reaction (SR-Fenton) and visible light photocatalysis (Vis-Photo),for degradation of organic contaminants.The synergistic effect of SR-Fenton and Vis-Photo was observed through comparative tests of 50 mg/L Rhodamine B (RhB) degradation and TOC removal.The Rhodamine B degradation rate and TOC removal were 100% and 68.1% using the SR-Fenton/Vis-Photo combined process under ambient conditions,respectively.Moreover,based on XRD,XPS and UV-DRS characterization,it can be deduced that tricobalt tetroxide located on the surface of the catalyst is the SR-Fenton active site,and cobalt ion implanted in the TiO2 lattice is the reason for the visible light photocatalytic activity of Co-TiO2.Finally,the effects of the calcination temperature and cobalt concentration on the synergistic performance were also investigated and a possible mechanism for the synergistic system was proposed.This coupled system exhibited excellent catalytic stability and reusability,and almost no dissolution of Co2+ was found.

  3. Hydrogenated Graphene as Metal-free Catalyst for Fenton-like Reaction

    Institute of Scientific and Technical Information of China (English)

    Yi Zhao; Wu-feng Chen; Cheng-fei Yuan; Zi-ye Zhu; Li-feng Yan

    2012-01-01

    Carbonaceous catalysts are potential alternatives to metal catalysts.Graphene has been paid much attention for its high surface area and light weight.Here,hydrogenated graphene has been prepared by a simple gamma ray irradiation of graphene oxide aqueous suspension at room temperature.Transmission electron microscopic,element analysis,X-ray photoelectron spectroscopy,and UV-Vis spectrophotometer studies verified the hydrogenation of graphene.The as-prepared hydrogenated graphene can be used as a metal-free carbonaceous catalyst for the Fenton-like degradation of organic dye in water.

  4. Dissolved Organic Carbon Determination Using FIA and Photo-Fenton Reaction

    Directory of Open Access Journals (Sweden)

    Kondo Márcia M.

    2002-01-01

    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.

  5. Synergetic Effect of Ultrasound, the Heterogeneous Fenton Reaction and Photocatalysis by TiO2 Loaded on Nickel Foam on the Degradation of Pollutants

    Directory of Open Access Journals (Sweden)

    Shan Qiu

    2016-06-01

    Full Text Available The synergistic effect of ultrasound, the heterogeneous Fenton reaction and photocatalysis was studied using a nickel foam (NF-supporting TiO2 system and rhodamine B (RhB as a target. The NF-supporting TiO2 system was prepared by depositing TiO2 on the skeleton of NF repeatedly and then calcining it. To optimize the conditions and parameters, the catalytic activity was tested in four systems (ultrasound alone (US, nickel foam (NF, US/NF and NF/US/H2O2. The optimal conditions were fixed at 0.1 g/mL NF, initial 5.00 mg/L RhB, 300 W ultrasonic power, pH = 3 and 5.00 mg/L H2O2. The effects of the dissolution of nickel from NF and quenching of the Fenton reaction were studied on degradation efficiency. When the heterogeneous Fenton reaction is combined with TiO2-photocatalysis, the pollutant removal efficiency is enhanced significantly. Through this synergistic effect, 22% and 80% acetochlor was degraded within 10 min and 80 min, respectively.

  6. Integrated treatment of olive mill wastewater (OMW) by the combination of Fenton's reaction and anaerobic treatment

    Energy Technology Data Exchange (ETDEWEB)

    El-Gohary, F.A.; Badawy, M.I. [Water Pollution Department, National Research Center (NRC), Dokki, Cairo (Egypt); El-Khateeb, M.A. [Water Pollution Department, National Research Center (NRC), Dokki, Cairo (Egypt)], E-mail: elkhateebcairo@yahoo.com; El-Kalliny, A.S. [Water Pollution Department, National Research Center (NRC), Dokki, Cairo (Egypt)

    2009-03-15

    The use of an integrated treatment scheme consisting of wet hydrogen peroxide catalytic oxidation (WHPCO) followed by two-stage upflow anaerobic sludge blanket (UASB) reactor (10 l each) for the treatment of olive mill wastewater was the subject of this study. The diluted wastewater (1:1) was pre-treated using Fenton's reaction. Optimum operating conditions namely, pH, H{sub 2}O{sub 2} dose, Fe{sup +2}, COD:H{sub 2}O{sub 2} ratio and Fe{sup +2}:H{sub 2}O{sub 2} ratio were determined. The UASB reactor was fed continuously with the pre-treated wastewater. The hydraulic retention time was kept constant at 48 h (24 h for each stage). The conventional parameters such as COD, BOD, TOC, TKN, TP, TSS, oil and grease, and total phenols were determined. The concentrations of polyphenolic compounds in raw wastewater and effluents of each treatment step were measured using HPLC. The results indicated a good quality final effluent. Residual concentrations of individual organic compounds ranged from 0.432 mg l{sup -1} for {rho}-hydroxy-benzaldhyde to 3.273 mg l{sup -1} for cinnamic acid.

  7. Electrochemical detection of in situ DNA damage induced by enzyme-catalyzed Fenton reaction. Part I: In phosphate buffer solution

    International Nuclear Information System (INIS)

    We report on a biosensor for the electrochemical detection of the damage of DNA and of antioxidant protecting DNA. The biosensor was constructed by co-immobilization of DNA and glucose oxidase (GOx) on a glassy carbon electrode. Under aerobic conditions, GOx catalyzes the oxidation of glucose, and the hydrogen peroxide produced reacts with ferrous ions in a Fenton-type reaction to generate hydroxy radical. This was validated by UV-vis spectroscopy. The hydroxy radical can cause serious oxidative damage to DNA, and this can be detected by square wave voltammetry of the electroactive indicator Co(bpy)33+. The effects of pH value, incubation time, and the concentration of glucose and ferrous ion were optimized. The effects of the antioxidants ascorbic acid and aloe emodin on DNA damage were also investigated within the concentration range from 0.05 to 200 μM. This work provides an in-vitro model system to mimic the processes in oxidative DNA damage by a simple electrochemical approach. (author)

  8. Using Central Composite Experimental Design to Optimize the Degradation of Tylosin from Aqueous Solution by Photo-Fenton Reaction

    Directory of Open Access Journals (Sweden)

    Abd Elaziz Sarrai

    2016-05-01

    Full Text Available The feasibility of the application of the Photo-Fenton process in the treatment of aqueous solution contaminated by Tylosin antibiotic was evaluated. The Response Surface Methodology (RSM based on Central Composite Design (CCD was used to evaluate and optimize the effect of hydrogen peroxide, ferrous ion concentration and initial pH as independent variables on the total organic carbon (TOC removal as the response function. The interaction effects and optimal parameters were obtained by using MODDE software. The significance of the independent variables and their interactions was tested by means of analysis of variance (ANOVA with a 95% confidence level. Results show that the concentration of the ferrous ion and pH were the main parameters affecting TOC removal, while peroxide concentration had a slight effect on the reaction. The optimum operating conditions to achieve maximum TOC removal were determined. The model prediction for maximum TOC removal was compared to the experimental result at optimal operating conditions. A good agreement between the model prediction and experimental results confirms the soundness of the developed model.

  9. Effect and Cost Research for Leachate Treatment in PAC/Fenton and Fenton/PAC Technology

    Institute of Scientific and Technical Information of China (English)

    JIANG Bao-jun; YIN Jun; WU Xiao-yan; Zhao Yu-xin

    2010-01-01

    To compare the treatment effects and the costs of coagulation/Fenton process and Fenton/coagulation process in leachate treatment,fresh and old leachates were respestively treated with these two techniques.The experimental results indicate that the highest chemical oxygen demand(COD)removal rate of Fenton reaction on leachate can be acquired under the conditions of pH = 3.5,nH2O2/nFe2+= 6,mH2O2/mCOD = 3,and reaction time = 4 h.Polyaluminium chloride(PAC)coagulation has the highest COD removal rate on leachate under the condition of mPAC/mCOD = 0.6.Under the optimum reaction conditions,coagulation/Fenton and Fenton/coagulation processes were respestively adopted to treat raw leachate.The data also show that COD removal rate of coagulation/Fenton process on fresh and old leachates are90.56% and 86.52% respectively and that of Fenton/coagulation process 89.99% and 85.99%,so there is no obvious difference.But the cost of coagulation/Fenton process for leachate treatment is RMB 62.6,lower than that of Fenton/coagulation process.Therefore,coagulation/Fenton process is more optimized than Fenton/coagulation process for leachate treatment.

  10. Comparative study of radical oxidation of DNA and its nucleosides by hydroxyl radicals and ferryl ions generated by the Fenton reaction. Etude comparative de l'oxydation radicalaire de l'ADN et de ses nucleosides par les radicaux hydroxyles et les ions ferryles issus de la reaction de Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Mouret, J.F.; Berger, M.; Anselmino, C.; Polverelli, M.; Cadet, J. (CEA Centre d' Etudes Nucleaires de Grenoble, 38 (FR). Dept. de Recherche Fondamentale)

    1991-06-01

    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.

  11. 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.

  12. 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.

  13. Oxygen Reduction Reaction on Graphene in an Electro-Fenton System: In Situ Generation of H2 O2 for the Oxidation of Organic Compounds.

    Science.gov (United States)

    Chen, Chen-Yu; Tang, Cheng; Wang, Hao-Fan; Chen, Cheng-Meng; Zhang, Xiaoyuan; Huang, Xia; Zhang, Qiang

    2016-05-23

    Fenton oxidation using an aqueous mixture of Fe(2+) and H2 O2 is a promising environmental remediation strategy. However, the difficulty of storage and shipment of concentrated H2 O2 and the generation of iron sludge limit its broad application. Therefore, highly efficient and cost-effective electrocatalysts are in great need. Herein, a graphene catalyst is proposed for the electro-Fenton process, in which H2 O2 is generated in situ by the two-electron reduction of the dissolved O2 on the cathode and then decomposes to generate (.) OH in acidic solution with Fe(2+) . The π bond of the oxygen is broken whereas the σ bond is generally preserved on the metal-free reduced graphene oxide owing to the high free energy change. Consequently, the oxygen is reduced to H2 O2 through a two-electron pathway. The thermally reduced graphene with a high specific surface area (308.8 m(2)  g(-1) ) and a large oxygen content (10.3 at %) exhibits excellent reactivity for the two-electron oxygen reduction reaction to H2 O2 . A highly efficient peroxide yield (64.2 %) and a remarkable decolorization of methylene blue (12 mg L(-1) ) of over 97 % in 160 min are obtained. The degradation of methylene blue with hydroxyl radicals generated in situ is described by a pseudo first-order kinetics model. This provides a proof-of-concept of an environmentally friendly electro-Fenton process using graphene for the oxygen reduction reaction in an acidic solution to generate H2 O2 . PMID:27098063

  14. Fenton reaction-mediated fluorescence quenching of N-acetyl-L-cysteine-protected gold nanoclusters: analytical applications of hydrogen peroxide, glucose, and catalase detection.

    Science.gov (United States)

    Deng, Hao-Hua; Wu, Gang-Wei; He, Dong; Peng, Hua-Ping; Liu, Ai-Lin; Xia, Xing-Hua; Chen, Wei

    2015-11-21

    Given the importance of hydrogen peroxide (H2O2) in many biological processes and its wide application in various industries, the demand for sensitive, accurate, and economical H2O2 sensors is high. In this study, we used Fenton reaction-stimulated fluorescence quenching of N-acetyl-L-cysteine-protected gold nanoclusters (NAC-AuNCs) as a reporter system for the determination of H2O2. After the experimental conditions were optimized, the sensing platform enabled the analysis of H2O2 with a limit of detection (LOD) as low as 0.027 μM. As the glucose oxidase cascade leads to the generation of H2O2 and catalase catalyzes the decomposition of H2O2, these two biocatalytic procedures can be probed by the Fenton reaction-mediated quenching of NAC-AuNCs. The LOD for glucose was found to be 0.18 μM, and the linear range was 0.39-27.22 μM. The LOD for catalase was 0.002 U mL(-1), and the linear range was 0.01-0.3 U mL(-1). Moreover, the proposed sensing methods were successfully applied for human serum glucose detection and the non-invasive determination of catalase activity in human saliva, demonstrating their great potential for practical applications.

  15. Biodegradability enhancement of a leachate after biological lagooning using a solar driven photo-Fenton reaction, and further combination with an activated sludge biological process, at pre-industrial scale.

    Science.gov (United States)

    Silva, Tânia F C V; Fonseca, Amélia; Saraiva, Isabel; Vilar, Vítor J P; Boaventura, Rui A R

    2013-06-15

    This work proposes an integrated leachate treatment strategy, combining a solar photo-Fenton reaction, to enhance the biodegradability of the leachate from an aerated lagoon, with an activated sludge process, under aerobic and anoxic conditions, to achieve COD target values and nitrogen content according to the legislation. The efficiency and performance of the photo-Fenton reaction, concerning a sludge removal step after acidification, defining the optimum phototreatment time to reach a biodegradable wastewater that can be further oxidized in a biological reactor and, activation sludge biological process, defining the nitrification and denitrification reaction rates, alkalinity balance and methanol dose necessary as external carbon source, was evaluated in the integrated system at a scale close to industrial. The pre-industrial plant presents a photocatalytic system with 39.52 m(2) of compound parabolic collectors (CPCs) and 2 m(3) recirculation tank and, an activated sludge biological reactor with 3 m(3) capacity. Leachate biodegradability enhancement by means of a solar driven photo-Fenton process was evaluated using direct biodegradability tests, as Zahn-Wellens method, and indirect measure according to average oxidation state (AOS), low molecular carboxylic acids content (fast biodegradable character) and humic substances (recalcitrant character) concentration. Due to high variability of leachate composition, UV absorbance on-line measurement was established as a useful parameter for photo-Fenton reaction control.

  16. Biodegradability enhancement of a leachate after biological lagooning using a solar driven photo-Fenton reaction, and further combination with an activated sludge biological process, at pre-industrial scale.

    Science.gov (United States)

    Silva, Tânia F C V; Fonseca, Amélia; Saraiva, Isabel; Vilar, Vítor J P; Boaventura, Rui A R

    2013-06-15

    This work proposes an integrated leachate treatment strategy, combining a solar photo-Fenton reaction, to enhance the biodegradability of the leachate from an aerated lagoon, with an activated sludge process, under aerobic and anoxic conditions, to achieve COD target values and nitrogen content according to the legislation. The efficiency and performance of the photo-Fenton reaction, concerning a sludge removal step after acidification, defining the optimum phototreatment time to reach a biodegradable wastewater that can be further oxidized in a biological reactor and, activation sludge biological process, defining the nitrification and denitrification reaction rates, alkalinity balance and methanol dose necessary as external carbon source, was evaluated in the integrated system at a scale close to industrial. The pre-industrial plant presents a photocatalytic system with 39.52 m(2) of compound parabolic collectors (CPCs) and 2 m(3) recirculation tank and, an activated sludge biological reactor with 3 m(3) capacity. Leachate biodegradability enhancement by means of a solar driven photo-Fenton process was evaluated using direct biodegradability tests, as Zahn-Wellens method, and indirect measure according to average oxidation state (AOS), low molecular carboxylic acids content (fast biodegradable character) and humic substances (recalcitrant character) concentration. Due to high variability of leachate composition, UV absorbance on-line measurement was established as a useful parameter for photo-Fenton reaction control. PMID:23642652

  17. Treating leachate by Fenton oxidation

    Directory of Open Access Journals (Sweden)

    Roger Iván Méndez Novelo

    2010-05-01

    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.

  18. Electrochemical detection of in situ DNA damage induced by enzyme-catalyzed Fenton reaction. Part II in hydrophobic room temperature ionic liquid

    International Nuclear Information System (INIS)

    A hydrophobic room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]), was applied as nonaqueous solvent for the generation of hydroxy radical (.OH) through glucose oxidase-catalyzed Fenton reaction. The enzyme catalyzes the oxidation of glucose, and the produced H2O2 further reacts with transition metal ions, generating hydroxyl radicals. They attacked DNA and led its damage. This was detected by square wave voltammetry (SWV) of the electroactive indicator Co(bpy)33+. It bound more strongly to intact DNA, and the SWV peak currents decreased at the potential of 0.064 V when DNA was damaged. The experimental results testified that the antioxidants, ascorbic acid, aloe-emodin and rutin, inhibited oxidative DNA damage by hydroxyl radicals. The method is promising for rapid, sensitive, and inexpensive detection of DNA damage. (author)

  19. Mechanism of Photo-Fenton Degradation of Ethanol and PVA

    Institute of Scientific and Technical Information of China (English)

    雷乐成; 沈学优; 何锋

    2003-01-01

    Contrast degradation experiments between ethanol and polyvinyl alcohol (PVA) were conducted during H2O2, UV/H2O2, Fenton, and Photo-Fenton processes in this study. UV/VIS spectra showed: that complexes between Fe(Ⅲ) and organics were easily formed and degraded within reaction time. Compared with.the degradation of complex, hydroxyl radicals acted weakly in Fenton or Photo-Fenton process. Hydroxyl radicals involved in Photo-Fenton process were deemed to be generated from the split decomposition of H202, photolysis of Feaq3+, and degradation of hydrated Fe(IV)-complex but not traditional Fenton reaction. Experimental evidence to support this point was presented in this paper.

  20. Rapid and facile preparation of zinc ferrite (ZnFe2O4) oxide by microwave-solvothermal technique and its catalytic activity in heterogeneous photo-Fenton reaction

    International Nuclear Information System (INIS)

    In this work zinc ferrite (ZnFe2O4) oxide was rapidly and easily prepared by microwave-solvothermal route and its catalytic property in photo-Fenton reaction was evaluated. The effects of microwave heating time and power on the properties of produced particles were investigated. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), atomic force microscopy (AFM) and nitrogen adsorption–desorption isotherms were the techniques used for characterizing the solid products. The synthesized material was tested as a catalyst in the degradation of the textile dye molecule by the heterogeneous photo-Fenton process. Characterization results showed that the microwave heating time and power have significant influences on the formation of the phase spinel as well as on its physical properties. The reaction results showed that the ZnFe2O4 oxide has good photocatalytic activity, which can be attributed to high surface area and pore volume, and large pore size. The ZnFe2O4 oxide produced by the microwave irradiation exhibited promising photocatalytic activity for the removal of textile dye, reaching nearly 100% of decolorization at 40 min and 60% of mineralization at 240 min. Therefore, ZnFe2O4 particles rapidly prepared by the microwave route have the potential for use in treatment of textile wastewater by the heterogeneous photo-Fenton process. - Highlights: • ZnFe2O4 was synthesized by microwave-solvothermal method. • ZnFe2O4 was prepared by different microwave heating times and powers. • ZnFe2O4 was used as heterogeneous photo-Fenton catalyst. • Degradation of Procion red dye using heterogeneous photo-Fenton process. • ZnFe2O4 was highly efficient to degrade textile dye under visible light

  1. Rapid and facile preparation of zinc ferrite (ZnFe{sub 2}O{sub 4}) oxide by microwave-solvothermal technique and its catalytic activity in heterogeneous photo-Fenton reaction

    Energy Technology Data Exchange (ETDEWEB)

    Anchieta, Chayene G.; Severo, Eric C.; Rigo, Caroline; Mazutti, Marcio A. [Department of Chemical Engineering, Federal University of Santa Maria, 97105-900, Santa Maria (Brazil); Kuhn, Raquel C., E-mail: raquelckuhn@yahoo.com.br [Department of Chemical Engineering, Federal University of Santa Maria, 97105-900, Santa Maria (Brazil); Muller, Edson I.; Flores, Erico M.M. [Department of Chemistry, Federal University of Santa Maria, 97105-900, Santa Maria (Brazil); Moreira, Regina F.P.M. [Department of Chemical Engineering and Food Engineering, Federal University of Santa Catarina, 88040-970, Florianópolis (Brazil); Foletto, Edson L. [Department of Chemical Engineering, Federal University of Santa Maria, 97105-900, Santa Maria (Brazil)

    2015-06-15

    In this work zinc ferrite (ZnFe{sub 2}O{sub 4}) oxide was rapidly and easily prepared by microwave-solvothermal route and its catalytic property in photo-Fenton reaction was evaluated. The effects of microwave heating time and power on the properties of produced particles were investigated. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), atomic force microscopy (AFM) and nitrogen adsorption–desorption isotherms were the techniques used for characterizing the solid products. The synthesized material was tested as a catalyst in the degradation of the textile dye molecule by the heterogeneous photo-Fenton process. Characterization results showed that the microwave heating time and power have significant influences on the formation of the phase spinel as well as on its physical properties. The reaction results showed that the ZnFe{sub 2}O{sub 4} oxide has good photocatalytic activity, which can be attributed to high surface area and pore volume, and large pore size. The ZnFe{sub 2}O{sub 4} oxide produced by the microwave irradiation exhibited promising photocatalytic activity for the removal of textile dye, reaching nearly 100% of decolorization at 40 min and 60% of mineralization at 240 min. Therefore, ZnFe{sub 2}O{sub 4} particles rapidly prepared by the microwave route have the potential for use in treatment of textile wastewater by the heterogeneous photo-Fenton process. - Highlights: • ZnFe{sub 2}O{sub 4} was synthesized by microwave-solvothermal method. • ZnFe{sub 2}O{sub 4} was prepared by different microwave heating times and powers. • ZnFe{sub 2}O{sub 4} was used as heterogeneous photo-Fenton catalyst. • Degradation of Procion red dye using heterogeneous photo-Fenton process. • ZnFe{sub 2}O{sub 4} was highly efficient to degrade textile dye under visible light.

  2. 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)

  3. Experimental Design of Photo-Fenton Reactions for the Treatment of Car Wash Wastewater Effluents by Response Surface Methodological Analysis

    Directory of Open Access Journals (Sweden)

    Maha A. Tony

    2014-01-01

    Full Text Available Establishing a treatment process for practical and economic disposal of car wash wastewater has become an urgent environmental concern. Photo-Fenton’s process as one of the advanced oxidation processes is a potentially useful oxidation process in treating such wastewater. Lab-scale experiments with UV source, coupled with Fenton’s reagent, showed that hydrocarbon oil is degradable through such a process. The feasibility of photo-Fenton’s process to treat wastewater from a car wash is investigated in the present study. A factorial design based on the response surface methodology was applied to optimize the photo-Fenton oxidation process conditions using chemical oxygen demand (COD reduction as the target parameter to optimize. The reagent (Fe2+ and H2O2 concentration and pH are used as the controlling factors to be optimized. Maximal COD reduction (91.7% was achieved when wastewater samples were treated at pH 3.5 in the presence of hydrogen peroxide and iron in amounts of 403.9 and 48.4 mg/L, respectively.

  4. Evidence against hydroxyl radical mechanism in photo-Fenton degradation of p-chlorophenol

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    This paper provides evidence for the degradation of organic pollutant by the photo-Fenton complex mechanism. Both the tum yield. The hydroxyl radical involved in the photo-Fenton process can also be generated from the decomposition of H2O2,photolysis of Fe3+ and degradation of hydrated Fe(Ⅵ)-complex, excepting the traditional Fenton reaction.

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

    OpenAIRE

    Gong Cheng; Jing Lin; Jian Lu; Xi Zhao; Zhengqing Cai; Jie Fu

    2015-01-01

    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 desc...

  6. RhB Adsorption Performance of Magnetic Adsorbent Fe3O4/RGO Composite and Its Regeneration through A Fenton-like Reaction

    Institute of Scientific and Technical Information of China (English)

    Yalin Qin; Mingce Long∗; Beihui Tan; Baoxue Zhou

    2014-01-01

    Adsorption is one of the most effective technologies in the treatment of colored matter containing wastewater. Graphene related composites display potential to be an effective adsorbent. However, the adsorp-tion mechanism and their regeneration approach are still demanding more efforts. An effective magnetically separable absorbent, Fe3O4 and reduced graphene oxide (RGO) composite has been prepared by an in situ coprecipitation and reduction method. According to the characterizations of TEM, XRD, XPS, Raman spectra and BET analyses, Fe3O4 nanoparticles in sizes of 10-20 nm are well dispersed over the RGO nanosheets, re-sulting in a highest specific area of 296.2 m2/g. The rhodamine B adsorption mechanism on the composites was investigated by the adsorption kinetics and isotherms. The isotherms are fitting better by Langmuir model, and the adsorption kinetic rates depend much on the chemical components of RGO. Compared to active carbon, the composite shows 3.7 times higher adsorption capacity and thirty times faster adsorption rates. Furthermore, with Fe3O4 nanoparticles as the in situ catalysts, the adsorption performance of composites can be restored by carrying out a Fenton-like reaction, which could be a promising regeneration way for the adsorbents in the organic pollutant removal of wastewater.

  7. Pyrite cinder as a cost-effective heterogeneous catalyst in heterogeneous Fenton reaction: decomposition of H(2)O(2) and degradation of Acid Red B.

    Science.gov (United States)

    Wu, Deli; Liu, Yanxia; Duan, Dong; Ma, Luming

    2014-01-01

    Pyrite cinder (PyC) was employed as a heterogeneous Fenton-like catalyst, and its catalytic activity was evaluated in view of the effects of catalyst dosage, pH and leaching metal ions. PyC showed significant reactivity, and the pseudo-first-order kinetic rate constant for decomposition of H(2)O(2) and degradation of Acid Red B (ARB) were 3.4 and 14.89 (10⁻³ min⁻¹) respectively when pH = 5. When 20 g/L PyC was added into 10 mM H(2)O(2) solution in neutral pH, H(2)O(2) could be completely degraded within 4 h, and more than 90% ARB was removed. Leaching metal ions from PyC were found to have little effect on decomposition of H(2)O(2) or on degradation of ARB. PyC still had high catalytic activity after five successive runs. The decomposition mechanism of H(2)O(2) was analyzed and the Haber-Weiss mechanism was employed in this paper. The electron spin resonance image showed •OH was produced and increased between 3 and 5 min in the PyC catalyzing H(2)O(2) reaction, which demonstrated that PyC had a durable ability to produce •OH.

  8. 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. PMID:26780702

  9. Degradação de corantes têxteis e remediação de resíduos de tingimento por processos Fenton, foto-Fenton e eletro-Fenton

    Directory of Open Access Journals (Sweden)

    Terezinha Salvador

    2012-01-01

    Full Text Available In this work the degradation of textile dyes were evaluated, using Fenton, photo-Fenton and electro-Fenton processes. Under optimized conditions Fenton and photo-Fenton processes showed high decolorization capacity of the model dyes. The electro-Fenton process was carried out in an undivided electrochemical reactor (1000 mL equipped with a carbon-felt cathode (253 cm² and a platinum gauze anode (6 cm². Under optimal conditions (J: 1.6 mA cm-2, Na2SO4: 0.075 mol L-1, pH: 3 H2O2 concentration of about 60 mg L-1 was observed. The addition of Fe2+ (15 mg L-1 induces Fenton reactions that permit almost total decolorization of textile dyes.

  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. Photo degradation of methyl orange an azo dye by advanced Fenton process using zero valent metallic iron: influence of various reaction parameters and its degradation mechanism.

    Science.gov (United States)

    Gomathi Devi, L; Girish Kumar, S; Mohan Reddy, K; Munikrishnappa, C

    2009-05-30

    Advanced Fenton process (AFP) using zero valent metallic iron (ZVMI) is studied as a potential technique to degrade the azo dye in the aqueous medium. The influence of various reaction parameters like effect of iron dosage, concentration of H(2)O(2)/ammonium per sulfate (APS), initial dye concentration, effect of pH and the influence of radical scavenger are studied and optimum conditions are reported. The degradation rate decreased at higher iron dosages and also at higher oxidant concentrations due to the surface precipitation which deactivates the iron surface. The rate constant for the processes Fe(0)/UV and Fe(0)/APS/UV is twice compared to their respective Fe(0)/dark and Fe(0)/APS/dark processes. The rate constant for Fe(0)/H(2)O(2)/UV process is four times higher than Fe(0)/H(2)O(2)/dark process. The increase in the efficiency of Fe(0)/UV process is attributed to the cleavage of stable iron complexes which produces Fe(2+) ions that participates in cyclic Fenton mechanism for the generation of hydroxyl radicals. The increase in the efficiency of Fe(0)/APS/UV or H(2)O(2) compared to dark process is due to continuous generation of hydroxyl radicals and also due to the frequent photo reduction of Fe(3+) ions to Fe(2+) ions. Though H(2)O(2) is a better oxidant than APS in all respects, but it is more susceptible to deactivation by hydroxyl radical scavengers. The decrease in the rate constant in the presence of hydroxyl radical scavenger is more for H(2)O(2) than APS. Iron powder retains its recycling efficiency better in the presence of H(2)O(2) than APS. The decrease in the degradation rate in the presence of APS as an oxidant is due to the fact that generation of free radicals on iron surface is slower compared to H(2)O(2). Also, the excess acidity provided by APS retards the degradation rate as excess H(+) ions acts as hydroxyl radical scavenger. The degradation of Methyl Orange (MO) using Fe(0) is an acid driven process shows higher efficiency at pH 3. The

  12. 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.

  13. INFLUENCE OF PEAT ON FENTON OXIDATION

    Science.gov (United States)

    A diagnostic probe was used to estimate the activity of Fenton-derived hydroxyl radicals (@OH), reaction kinetics, and oxidation efficiency in batch suspensions comprised of silica sand, crushed goethite ("-FeOOH) ore, peat, and H2O2 (0.13 mM). A simple method of kinetic analysi...

  14. Study on condition of CaO2-based Fenton reaction by methylene blue spectrophotometric method%亚甲基蓝光度法研究基于CaO2的Fenton反应条件

    Institute of Scientific and Technical Information of China (English)

    刘娇; 孟范平; 王震宇; 刘启元

    2011-01-01

    The potential of calcium peroxide (CaO2) as a source of hydrogen peroxide (H2O2) in Fenton oxidation has been gradually taken note. In order to understand the characteristics of CaO2-based Fenton reactions, experiments were conducted using methylene blue spectrophotometric method to investigate effect of catalyst type, initial pH, CaO2 dose, molar ratio of catalyst to CaO2 (?Fe/?cao2 )? And phosphate buffer concentration on production of hydroxyl radicals (HO ? ). The results showed that under the experimental conditions Fez+ had better catalytic ability than Fe3+ and Cu2+. The optimal Fenton reaction conditions were; Fe2+ as catalyst, initial buffer pH = 4, CaO2 dose 1 mmol ? L"1 , wF,/?cao2 = 1/5, phosphate buffer concentration 40 mmol ? L"1. It was also indicated that the release of H2O2 and Fenton reaction were regulated by the dissolution process of CaO2 that could be a potential substitute for H2O2 in in-situ Fenton oxidations, because of decrease of H2O2 loss as well as negative impact of Fenton processes on the environment.%CaO2作为原位Fenton氧化修复中H2O2持续供源的作用逐渐受到关注.利用亚甲基蓝分光光度法评价了基于CaO2的Fenton反应中催化剂种类、初始pH值、CaO2用最、催化剂和CaO2比例、磷酸缓冲溶液浓度对羟基自由基(HO·)产率的影响.结果表明,采用Fe2作为催化剂,在pH值为4、CaO2用量为1 mmo1·L-1,催化剂CaO2摩尔比(nFe/nCaO2.)为1/5、磷酸缓冲溶液浓度为40 mmol·L-1时HO·产率较高,Fe2+催化作用最显著.CaO2溶解过程对H2O2的释放和Fenton反应起到一定调节作用,以CaO2取代H2O2可减少氧化剂的流失及其对环境产生的不利影响.

  15. Graphene quantum dots from a facile sono-Fenton reaction and its hybrid with a polythiophene graft copolymer toward photovoltaic application.

    Science.gov (United States)

    Routh, Parimal; Das, Sandip; Shit, Arnab; Bairi, Partha; Das, Pradip; Nandi, Arun K

    2013-12-11

    A new and facile approach for synthesizing graphene quantum dots (GQDs) using sono-Fenton reaction in an aqueous dispersion of graphene oxide (GO) is reported. The transmission electron microscopy (TEM) micrographs of GQDs indicate its average diameter as ∼5.6 ± 1.4 nm having a lattice parameter of 0.24 nm. GQDs are used to fabricate composites (PG) with a water-soluble polymer, polythiophene-g-poly[(diethylene glycol methyl ether methacrylate)-co-poly(N,N-dimethylaminoethyl methacrylate)] [PT-g-P(MeO2MA-co-DMAEMA), P]. TEM micrographs indicate that both P and PG possess distinct core-shell morphology and the average particle size of P (0.16 ± 0.08 μm) increases in PG (0.95 ± 0.45 μm). Fourier transform infrared and X-ray photoelectron spectrometry spectra suggest an interaction between -OH and -COOH groups of GQDs and -NMe2 groups of P. A decrease of the intensity ratio of Raman D and G bands (ID/IG) is noticed during GQD and PG formation. In contrast to GO, GQDs do not exhibit any absorption peak for its smaller-sized sp(2) domain, and in PG, the π-π* absorption of polythiophene (430 nm) of P disappears. The photoluminescence (PL) peak of GQD shifts from 450 to 580 nm upon a change in excitation from 270 to 540 nm. PL emission of PG at 537 nm is quenched, and it shifts toward lower wavelength (∼430 nm) with increasing aging time for energy transfer from P to GQDs followed by up-converted emission of GQDs. Both P and PG exhibit semiconducting behavior, and PG produces an almost reproducible photocurrent. Dye-sensitized solar cells (DSSCs) fabricated with an indium-titanium oxide/PG/graphite device using the N719 dye exhibit a short-circuit current (Jsc) of 4.36 mA/cm(2), an open-circuit voltage (Voc) of 0.78 V, a fill factor of 0.52, and a power conversion efficiency (PCE, η) of 1.76%. Extending the use of GQDs to fabricate DSSCs with polypyrrole, both Voc and Jsc increase with increasing GQD concentration, showing a maximum PCE of 2.09%. The PG

  16. Removal of Textile Dyes from Aqueous Solution by Heterogeneous Photo-Fenton Reaction Using Modified PAN Nanofiber Fe Complex as Catalyst

    OpenAIRE

    Xueting Zhao; Yongchun Dong; Bowen Cheng; Weimin Kang

    2013-01-01

    The modified PAN nanofiber Fe complex was prepared by the amidoximation and Fe coordination of PAN nanofiber was obtained using electrospinning technique and then used for the heterogeneous Fenton degradation of textile dyes as a novel catalyst. Some main factors affecting dye degradation such as Fe content of catalyst, irradiation intensity, H2O2 initial concentration, the solution pH as well as dye structure, and initial concentration were investigated. UV-Vis spectrum analysis and TOC meas...

  17. 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.

  18. 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.

  19. Comparative analysis of trace contaminants in leachates before and after a pre-oxidation using a solar photo-Fenton reaction.

    Science.gov (United States)

    Rocha, Elisangela M R; Mota, Francisco S; Vilar, Vítor J P; Boaventura, Rui A R

    2013-09-01

    Sanitary landfill leachates are a complex mixture of high-strength organic and inorganic persistent contaminants, which constitute a serious environmental problem. In this study, trace contaminants present in leachates were investigated by gas chromatography-mass spectrometry and gas chromatography-flame ionization detector before and after a pre-oxidation step using a solar photo-Fenton process. More than 40 organic compounds were detected and identified as benzene (0.09 ± 0.07 mg L(-1)), trichlorophenol (TCP) (0.18 ± 0.12 mg L(-1)), phthalate esters (Di-n-butyl phthalate (DBP), Butyl benzyl phthalate (BBP), Di(2-ethylhexyl) phthalate (DEHP)) (DBP: 0.47 ± 0.01 mg L(-1); BBP: 0.36 ± 0.02 mg L(-1); DEHP: 0.18 ± 0.01 mg L(-1)), among others. Toluene, pentachlorophenol, dimethyl phthalate, diethyl phthalate, and Di-n-octyl phthalate were never detected in any of the samples. After the photo-Fenton treatment process, TCP decreased to levels below its detection limit, benzene concentration increased approximately three times, and DBP concentration decreased about 77 % comparatively to the raw leachate sample. The solar photo-Fenton process was considered to be very efficient for the treatment of sanitary landfill leachates, leading to the complete elimination of 24 of the detected micropollutants to levels below their respective detection limits and low to significant abatement of seven other organic compounds, thus resulting in an increase of the leachate biodegradability. PMID:23519479

  20. Comparative analysis of trace contaminants in leachates before and after a pre-oxidation using a solar photo-Fenton reaction.

    Science.gov (United States)

    Rocha, Elisangela M R; Mota, Francisco S; Vilar, Vítor J P; Boaventura, Rui A R

    2013-09-01

    Sanitary landfill leachates are a complex mixture of high-strength organic and inorganic persistent contaminants, which constitute a serious environmental problem. In this study, trace contaminants present in leachates were investigated by gas chromatography-mass spectrometry and gas chromatography-flame ionization detector before and after a pre-oxidation step using a solar photo-Fenton process. More than 40 organic compounds were detected and identified as benzene (0.09 ± 0.07 mg L(-1)), trichlorophenol (TCP) (0.18 ± 0.12 mg L(-1)), phthalate esters (Di-n-butyl phthalate (DBP), Butyl benzyl phthalate (BBP), Di(2-ethylhexyl) phthalate (DEHP)) (DBP: 0.47 ± 0.01 mg L(-1); BBP: 0.36 ± 0.02 mg L(-1); DEHP: 0.18 ± 0.01 mg L(-1)), among others. Toluene, pentachlorophenol, dimethyl phthalate, diethyl phthalate, and Di-n-octyl phthalate were never detected in any of the samples. After the photo-Fenton treatment process, TCP decreased to levels below its detection limit, benzene concentration increased approximately three times, and DBP concentration decreased about 77 % comparatively to the raw leachate sample. The solar photo-Fenton process was considered to be very efficient for the treatment of sanitary landfill leachates, leading to the complete elimination of 24 of the detected micropollutants to levels below their respective detection limits and low to significant abatement of seven other organic compounds, thus resulting in an increase of the leachate biodegradability.

  1. 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)

    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)

  2. Effect of Particles on Fenton Oxidation of Organic Contaminated Groundwater

    Science.gov (United States)

    Lee, J.; Kim, Y.; Gwak, J.; Lee, C.; Ha, J.

    2009-12-01

    Fenton oxidation has been widely applied for a variety of water treatment due to non-selectively oxidative capability at a high reaction rate and cost effectiveness. Even though wide and deep range of studies were conducted for understanding the Fenton reaction with various contaminants, effect of particles on Fenton reaction has been little studied. This study explored the performance of Fenton oxidation for organic contaminated groundwater treatment in the presence of particles. The contaminated groundwater was a free oil separated groundwater obtained from a pilot scale bioslurping process for LNAPL treatment. The groundwater was characterized by a high suspended solid (SS) concentration relative to total organic carbon (TOC) concentration varying from 4 to 7.3. It was found that the optimum ratio of Fenton’s reagent (Fe2+:H2O2) was 1:10 in terms of TOC removal efficiency. Presence of solid particles significantly affected the TOC removal efficiency by Fenton’s reaction accounting for 37% for raw groundwater and 61% for soluble groundwater. Particles larger than 5 µm could be effectively settled out by a quiescent settling for 3 hr based on particle size distribution analysis. The TOC removal efficiency for the supernatant after settling was a similar to that of soluble sample. Total petroleum hydrocarbon (TPH) was mostly present in the adsorbed form to the particles in the groundwater and was potentially persistent to Fenton oxidation. TPH removal efficiency by Fenton oxidation was 24% which was less than that of the total groundwater indicating that hydroxyl radicals generated from Fenton oxidation did not directly attack the adsorbed organic carbon and removal of the adsorbed organic carbon was dependent on its mass transfer to bulk region. The concept for particle effect on Fenton oxidation was confirmed in another experiment spiking washed soil to the soluble groundwater. TOC removal efficiency was lowered by addition of the soil probably because the

  3. 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.

  4. Mineralization of sulfamethizole in photo-Fenton and photo-Fenton-like systems.

    Science.gov (United States)

    Wu, C H; Wu, J T; Lin, Y H

    2016-01-01

    In this investigation, UV/H2O2, UV/H2O2/Fe(2+) (photo-Fenton) and UV/H2O2/Fe(3+) (photo-Fenton-like) systems were used to mineralize sulfamethizole (SFZ). The optimal doses of H2O2 (1-20 mM) in UV/H2O2 and iron (0.1-1 mM) in photo-Fenton and photo-Fenton-like systems were determined. Direct photolysis by UV irradiation and direct oxidation by added H2O2, Fe(2+) and Fe(3+) did not mineralize SFZ. The optimal dose of H2O2 was 10 mM in UV/H2O2 and that of iron (Fe(2+) or Fe(3+)) was 0.2 mM in both UV/H2O2/Fe(2+) and UV/H2O2/Fe(3+) systems. Under the best experimental conditions and after 60 min of reaction, the SFZ mineralization percentages in UV/H2O2, UV/H2O2/Fe(2+) and UV/H2O2/Fe(3+) systems were 16, 90 and 88%, respectively. The UV/H2O2/Fe(2+) and UV/H2O2/Fe(3+) systems effectively mineralized SFZ.

  5. Avaliação da reação foto-fenton na decomposição de resíduos de carrapaticida Evaluation of the photo-fenton reaction in the decomposition of tick residues

    Directory of Open Access Journals (Sweden)

    Caio Fernando Gromboni

    2007-04-01

    Full Text Available Experimental procedures based on factorial design and surface response methodology were applied to establishe experimental conditions for the decomposition of a 1:400 (v/v Supocade® (chlorfenvinphos 13.8% and cypermethrin 2.6% solution, used to control cattle ticks. Experiments exploring photo-oxidative reactions were performed with and without UV radiation, fixing exposition time and pesticide volume, and varying the oxidant mixture. The use of 3.6 mmol L-1 Fe2+ plus 1.9 mol L-1 H2O2 plus UV radiation provided destruction of 94% of the original carbon content and reduction of aromatic, aliphatic and carbinolic compounds, evaluated by determination of residual carbon content by ICP OES and NMR analysis.

  6. Chemical oxidation of sulfadiazine by the Fenton process: kinetics, pathways, toxicity evaluation.

    Science.gov (United States)

    Yang, Ji-Feng; Zhou, Shi-Biao; Xiao, An-Guo; Li, Wen-Jun; Ying, Guang-Guo

    2014-01-01

    This paper investigated sulfadiazine oxidation by the Fenton process under various reaction conditions. The reaction conditions tested in the experiments included the initial pH value of reaction solutions, and the dosages of ferrous ions and hydrogen peroxide. Under the reaction conditions with pH 3, 0.25 mM of ferrous ion and 2 mM of hydrogen peroxide, a removal efficiency of nearly 100% was achieved for sulfadiazine. A series of intermediate products including 4-OH-sulfadiazine/or 5-OH-sulfadiazine, 2-aminopyrimidine, sulfanilamide, formic acid, and oxalic acid were identified. Based on these products, the possible oxidation pathway of sulfadiazine by Fenton's reagent was proposed. The toxicity evaluation of reaction solutions showed increased antimicrobial effects following the Fenton oxidation process. The results from this study suggest that the Fenton oxidation process could remove sulfadiazine, but also increase solution toxicity due to the presence of more toxic products. PMID:25310806

  7. Sulfate radicals induced from peroxymonosulfate by cobalt manganese oxides (Co{sub x}Mn{sub 3−x}O{sub 4}) for Fenton-Like reaction in water

    Energy Technology Data Exchange (ETDEWEB)

    Yao, Yunjin, E-mail: yaoyunjin@gmail.com [Anhui Key Lab of Controllable Chemical Reaction & Material Chemical Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Tunxi Road 193, Hefei 230009 (China); State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China); School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui 230026 (China); Cai, Yunmu; Wu, Guodong; Wei, Fengyu [Anhui Key Lab of Controllable Chemical Reaction & Material Chemical Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Tunxi Road 193, Hefei 230009 (China); Li, Xingya [School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui 230026 (China); Chen, Hao [Anhui Key Lab of Controllable Chemical Reaction & Material Chemical Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Tunxi Road 193, Hefei 230009 (China); Wang, Shaobin, E-mail: shaobin.wang@curtin.edu.au [Department of Chemical Engineering, Curtin University, G.P.O. Box U1987, Perth, Western Australia 6845 (Australia)

    2015-10-15

    Highlights: • A series of Co{sub x}Mn{sub 3−x}O{sub 4} particles as Fenton-like solid catalysts were synthesized. • CoMn{sub 2}O{sub 4}/PMS exhibits high activity due to synergistic effects of Co and Mn species. • Reaction conditions and degradation mechanism have been analyzed. • Contributions from SO{sub 4}·{sup −} and HO· radicals to the reaction were measured using scavengers. • The catalyst had good stability and reusability during the five successive runs. - Abstract: A series of Co{sub x}Mn{sub 3−x}O{sub 4} particles as Fenton-like solid catalysts were synthesized, and their catalytic performance in oxidative degradation of organic dye compounds in water was investigated. The surface morphology and structure of the Co{sub x}Mn{sub 3−x}O{sub 4} catalysts were characterized by field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), powder X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The results showed that, as an oxide composite of Co and Mn elements, CoMn{sub 2}O{sub 4} showed much stronger catalytic activity in peroxymonosulfate (PMS) oxidation than Co{sub 3}O{sub 4}, Mn{sub 2}O{sub 3,} and their physical mixture. Typically, the uses of 0.02 g/dm{sup 3} CoMn{sub 2}O{sub 4} and 0.2 g/dm{sup 3} PMS yielded a nearly complete removal of Rhodamine B (0.03 g/dm{sup 3}) in 80 min at 25 °C. The efficiency of Rhodamine B decomposition increased with increasing temperature (15–55 °C), but decreased with the increase of fulvic acid concentration (0–0.08 g/dm{sup 3}). Furthermore, CoMn{sub 2}O{sub 4} could maintain its catalytic activity in the repeated batch experiments. Moreover, HO· and SO{sub 4}·{sup −} radicals participating in the process were evidenced using quenching experiments, and a rational mechanism was proposed. PMS oxidation with CoMn{sub 2}O{sub 4} is an efficient technique for remediation of organic contaminants in

  8. 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)

    The mineralization of acidic aqueous solutions with 230 and 115 ppm of herbicide 3,6-dichloro-2-methoxybenzoic acid (dicamba) in 0.05 M Na2SO4 of pH 3.0 has been studied by electro-Fenton and photoelectro-Fenton using a Pt anode and an O2-diffusion cathode, where oxidizing hydroxyl radicals are produced from Fenton's reaction between added Fe2+ and H2O2 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 H2O2 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 CO2, and maleic acid is completely converted into oxalic acid, remaining stable Fe3+-oxalato complexes in the solution. The fast mineralization of such complexes by UV light explains the highest oxidative ability of photoelectro-Fenton

  9. Sulfate radicals induced from peroxymonosulfate by cobalt manganese oxides (Co(x)Mn(3-x)O4) for Fenton-Like reaction in water.

    Science.gov (United States)

    Yao, Yunjin; Cai, Yunmu; Wu, Guodong; Wei, Fengyu; Li, Xingya; Chen, Hao; Wang, Shaobin

    2015-10-15

    A series of CoxMn3-xO4 particles as Fenton-like solid catalysts were synthesized, and their catalytic performance in oxidative degradation of organic dye compounds in water was investigated. The surface morphology and structure of the CoxMn3-xO4 catalysts were characterized by field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), powder X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The results showed that, as an oxide composite of Co and Mn elements, CoMn2O4 showed much stronger catalytic activity in peroxymonosulfate (PMS) oxidation than Co3O4, Mn2O3, and their physical mixture. Typically, the uses of 0.02 g/dm(3) CoMn2O4 and 0.2 g/dm(3) PMS yielded a nearly complete removal of Rhodamine B (0.03 g/dm(3)) in 80 min at 25 °C. The efficiency of Rhodamine B decomposition increased with increasing temperature (15-55 °C), but decreased with the increase of fulvic acid concentration (0-0.08 g/dm(3)). Furthermore, CoMn2O4 could maintain its catalytic activity in the repeated batch experiments. Moreover, HO· and SO4(·-) radicals participating in the process were evidenced using quenching experiments, and a rational mechanism was proposed. PMS oxidation with CoMn2O4 is an efficient technique for remediation of organic contaminants in wastewater. PMID:25913679

  10. Magnetic minerals from volcanic Ultisols as heterogeneous Fenton catalysts

    International Nuclear Information System (INIS)

    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 H2O2 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.

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

    Directory of Open Access Journals (Sweden)

    Zazouli Mohammad

    2012-08-01

    Full Text Available 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 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Bandala, Erick R. [Instituto Mexicano de Tecnologia del Agua, Paseo Cuauhnahuac 8532, Progreso Jiutepec, Morelos 62550 (Mexico)], E-mail: ebandala@tlaloc.imta.mx; Pelaez, Miguel A.; Salgado, Maria J. [Instituto Mexicano de Tecnologia del Agua, Paseo Cuauhnahuac 8532, Progreso Jiutepec, Morelos 62550 (Mexico); Torres, Luis [Instituto de Ingenieria, Universidad Nacional Autonoma de Mexico (UNAM) (Mexico)

    2008-03-01

    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{sub 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{sub 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{sub 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. 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.

  14. Fenton Oxidation of Methyl Violet in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Saeedeh Hashemian

    2013-01-01

    Full Text Available In this study, oxidative discoloration of methyl violet (MV dye in aqueous solution has been studied using Fenton (Fe2+/H2O2 process. The parameters such as concentration of Fe2+, H2O2, MV, temperature, and Cl− and ions that affected of discoloration in Fenton process were investigated. The rate of degradation is dependent on initial concentration of Fe2+ ion, initial concentration of H2O2, and pH of media. Discoloration of MV was increased by increasing the temperature of reaction. Optimized condition was determined and it was found that the obtained efficiency was about 95.5% after 15 minutes of reaction at pH 3. TOC of dye sample, before and after the oxidation process, was determined. TOC removal indicates partial and significant mineralization of MV dye. The results of experiments showed that degradation of MV dye in Fenton oxidation can be described with a pseudo-irst-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.

  15. 乙醇和PVA的光助Fenton降解机理%Mechanism of Photo-Fenton Degradation of Ethanol and PVA

    Institute of Scientific and Technical Information of China (English)

    雷乐成; 沈学优; 何锋

    2003-01-01

    Contrast degradation experiments between ethanol and polyvinyl alcohol (PVA) were conducted during H2O2, UV/H2O2, Fenton, and Photo-Fenton processes in this study. UV/VIS spectra showed. that complexes between Fe(Ⅲ) and organics were easily formed and degraded within reaction time. Compared with the degradation of complex, hydroxyl radicals acted weakly in Fenton or Photo-Fenton process. Hydroxyl radicals involved in Photo-Fenton process were deemed to be generated from the split decomposition of H2O2, photolysis of Fe3+/aq, and degradation of hydrated Fe(Ⅳ)-complex but not traditional Fenton reaction. Experimental evidence to support this point was presented in this paper.

  16. Electrochemical dissolution of steel as a typical catalyst for electro-Fenton oxidation

    OpenAIRE

    Kočanová, Veronika; Dušek, Libor

    2016-01-01

    Abstract Although traditional Fenton reaction is known for a long time, it is still a perspective method for removal of pollution from wastewater. Applications of electro-Fenton oxidation are commonly used in wastewater treatment. These methods are classified into groups—electrochemical advanced oxidation processes. Typical catalysts for these technologies are Fe2+ ions. Comparison between two material types of steel was investigated in this paper. Alloy steel Cr–Ni and non-alloy steel were u...

  17. Combined UV/ Fenton and SBR Treatment of a Semi-aerobic Landfill Leachate

    International Nuclear Information System (INIS)

    This study examined the combined UV/ Fenton and sequencing batch biological reactor (SBR) treatment of a semi-aerobic landfill leachate. Fenton pretreatment of the leachate was optimized by the response surface methodology (RSM). UV/ Fenton pretreatment of the leachate was performed under the optimum operating conditions of the Fenton pretreatment (H2O2/ COD molar ratio 2.25, H2O2/ Fe2+ molar ratio 10.0 and reaction/ irradiation time 1.5 h). The characteristics of the UV/ Fenton pretreated leachate were: COD 390 mg/ L, sCOD 330 mg/L, BOD5 136 mg/L, BOD5/ COD ratio 0.35, NH3-N 112 mg/ L, TKN 157 mg/ L, NO3--N 6.8 mg/ L and colour 99 Pt-Co Unit. SBR treatment of the UV/ Fenton pretreated leachate resulted in sCOD, BOD5 and NH3-N removal of 78 %, 81 % and 88 %, respectively. The final effluent characteristics were: COD 92 mg/ L, sCOD 71 mg/L, BOD5 26 mg/ L, NH3-N 7 mg/ L, NO3--N 27 mg/ L, TKN 13 mg/ L and TSS 38 mg/ L. The effluent met the Malaysian discharge standard (B) - COD 100 mg/ L, BOD5 50 mg/ L and TSS 100 mg/ L. Combined UV/ Fenton and SBR is an effective treatment for mature leachate from semi-aerobic landfill. (author)

  18. 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.

  19. Effect of Hydrogen Peroxide Induced Fenton Reaction on Biomass of Rice in Soil Contaminated by Cd and As%H2O2介导的Fenton反应对砷镉污染下水稻生物量的影响

    Institute of Scientific and Technical Information of China (English)

    黎俏文; 秦俊豪; 陈桂葵; 黎华寿

    2015-01-01

    A pot experiment using a rhizo-bag system filled with soil and sand was conducted to investigate if rice growth was influenced by Fenton Reaction induced by hydrogen peroxide at micro molar level from simulated rain water in arsenic and/or cadmium contaminated pad-dy soil under all-time flooding and partial flooding. Results show that the Fenton Reaction significantly improved the dry weight and fresh weight of rice at tillering stage in the treatment with 30 mg As·kg-1 soil, and at maturing stage in the treatment with both 30 mg As·kg-1 soil and 0.3 mg Cd·kg-1 soil. Fenton Reaction also improved the weight of rice grain in treatments with 0.3 mg Cd·kg-1 soil and 3 mg Cd·kg-1 soil. These findings prove that Fenton Reaction could reduce the negative impacts of arsenic and cadmium contamination on rice growth and increase rice biomass and yield.%采用土壤-石英砂根袋法,研究了淹水和干湿交替两种水分条件下,模拟天然降雨中微摩尔级浓度H2O2介导Fenton反应对砷镉污染土壤上水稻生长的影响。结果表明,添加砷浓度30 mg·kg-1处理组在有Fenton反应的情况下显著提高了水稻在分蘖期的干重和鲜重,在添加砷浓度30 mg·kg-1和镉浓度0.3 mg·kg-1的复合污染处理组Fenton反应也提高了水稻在成熟期的干重和鲜重,同时Fenton反应增加了添加镉浓度为0.3、3 mg·kg-1处理组的稻谷产量。模拟研究证明,H2O2介导的Fenton反应可以缓解砷、镉污染对水稻的胁迫作用,提高水稻的生物量和产量。

  20. 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.

  1. Improvement in carbofuran degradation by different Fenton's reagent dosing processes.

    Science.gov (United States)

    Ma, Ying-Shih

    2011-11-01

    Attempts were made in this study to examine the efficiency of Fenton's reagent with different dosing processes and H(2)O(2) and Fe(2+) concentrations for the treatment of carbofuran wastewater. Carbofuran degradation, total organic carbon (TOC) removal and H(2)O(2) consumption were determined during the experiments. Increases in H(2)O(2) and Fe(2+) concentrations led to an increase in the degradation of carbofuran. Almost 100% of carbofuran could be degraded at pH 3, 120 mg L(-1) H(2)O(2), 24 mg L(-1) Fe(2+) and 30 minutes reaction time; removals of TOC were among 48.8%-53.3% under different dosing processes. A continuous dosing process was beneficial to improve the removal of TOC by Fenton's reagent. Rate constants of carbofuran degradation could be calculated by the first-order kinetics; increase in the Fenton's reagent generally increased the rate constants. Gas chromatography-mass spectrometry analysis found five degradation products by hydroxyl radicals attack. Thus, this study might offer an effective dosing way for carbofuran wastewater treatment by Fenton's reagent.

  2. Avaliação da potencialidade de processos pseudo-fenton para remediação de solos contaminados por diesel Evaluation of potencial fenton-like process to the remediation of contaminated soils by diesel

    Directory of Open Access Journals (Sweden)

    Carolina Acioli Pereira

    2009-01-01

    Full Text Available The use of the Fenton's reagent process has been investigated for the remediation of a Brazilian soil contaminated by diesel. Laboratory experiments were conducted in batch experiments. Slurries, consisting of 10 g of diesel-contaminated soil and 30 mL of Fenton's Reagent (0.41 mol L-1 H(20(2 and 0.18 mol L-1 FeSO4. The experiments were monitored during 24, 48 and 72 h. The efficiency of the Fenton treatment was dependent on the time of contact between soil and Fenton's reagents and matrix characteristics, probably iron content. Data suggested that no iron addition is needed for the application of Fenton-like treatment for the remediation of diesel-contaminated iron rich soils after 72 h reaction.

  3. 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.

  4. 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. 

  5. Experimental study on the pre-treatment of flotation wastewater by UV/Fenton oxidation-coagulation process%UV/Fenton -混凝法对浮选废水预处理研究

    Institute of Scientific and Technical Information of China (English)

    吕春玲; 王莹; 刘强

    2015-01-01

    试验考察了UV/Fenton法和CCG788/UV/Fenton法对浮选废水进行预氧化后,废水中COD去除效果的影响因素。其结果表明:UV/Fenton 法处理效果明显优于普通 Fenton 法,而CCG788的加入提高了 UV/Fenton 体系对紫外光的利用率,不仅氧化效果更好,还可以促进UV/Fenton氧化反应的进行,缩短反应时间。在前述试验结果基础上,对CCG788/UV/Fenton法处理后的浮选废水投加CCG158进行了二次氧化,COD去除率可提高到87%,并缩短了总反应时长。%Pre-oxidation of flotation wastewater by UV/Fenton and CCG 788/UV/Fenton process was exploredin terms of the influence factors on COD removal.The experiment results show that UV/Fenton oxidation process is much more effective for the pre-treatment of flotation wastewater than Fenton oxidation process.In addition,the introduction of CCG788 into UV/Fenton system improves the utilization of ultraviolet ray( UV) and removal rates of COD,as well as promotes oxidation reaction and shortens the reaction time.Furthermore,the total removal rate of COD can reach 87 %by secondary oxidation of CCG788/UV/Fenton flotation wastewater with CCG158,and the reaction time is shortened.

  6. 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.

  7. Design of an electro-Fenton system with a novel sandwich film cathode for wastewater treatment.

    Science.gov (United States)

    Fan, Yan; Ai, Zhihui; Zhang, Lizhi

    2010-04-15

    In this study, we demonstrate an electro-Fenton (E-Fenton) system constructed with a novel sandwich film cathode (SFC). For the fabrication of SFC, Fe(2+)-chitosan (Fe-CHI) was first deposited on foam nickel (Fe-CHI/Ni). Then two pieces of Fe-CHI/Ni was used to fasten one piece of activated carbon fiber (ACF) to obtain a Fe-CHI/Ni|ACF|Fe-CHI/Ni sandwich film cathode. We interestingly found that this SFC based E-Fenton system could effectively degrade rodamine B with in situ generating both hydrogen peroxide and iron ions. Its degradation efficiency was significantly higher than those of the E-Fenton systems constructed with composite cathodes of carbon nanotubes with Fe@Fe(2)O(3) core-shell nanowires or Cu(2)O nanocubes reported in our previous studies. Hydrogen peroxide electrogenerated through the reduction of O(2) adsorbed on the sandwich film cathode and the iron ions produced by the leakage from Fe(2+)-chitosan film during the E-Fenton reaction were, respectively, monitored, providing clues to understand the high efficiency of this novel SFC based E-Fenton system. More importantly, this low-cost sandwich film cathode was very stable and could be reused without catalytic activity decrease, suggesting its potential application in the wastewater treatment.

  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. Degradation of carbofuran in aqueous solution by ultrasound and Fenton processes: Effect of system parameters and kinetic study.

    Science.gov (United States)

    Ma, Ying-Shih; Sung, Chi-Fanga; Lin, Jih-Gaw

    2010-06-15

    To establish an efficient oxidation process for carbofuran degradation, the effects of some operating parameters such as dosages of H(2)O(2), Fe(2+) and initial carbofuran concentrations were observed during carbofuran degradation by the ultrasound process, Fenton process and a combined ultrasound/Fenton process. The degradation kinetics of carbofuran was also examined based on the experimental data. The results show that more than 99% of the carbofuran was degraded by the ultrasound/Fenton process within short reaction time periods. Increased dosages of H(2)O(2) and Fe(2+) enhanced the degradation of carbofuran in the ultrasound and Fenton oxidation processes, but initial carbofuran concentrations decreased carbofuran degradation in both the Fenton and ultrasound/Fenton processes. The degradation kinetics of carbofuran by the three oxidation processes was found to be in accordance with first-order reaction kinetics. The results provide fundamental information about the treatment of carbofuran wastewater and/or other pesticides by the ultrasound/Fenton oxidation process.

  10. Efficiency and toxicity: comparison between the Fenton and electrochemical processes.

    Science.gov (United States)

    Tavares, Marcela Gomes; Santos, Danilo Henrique da Silva; Torres, Sheyla Jaqueline Albuquerque; Pimentel, Wagner Roberto Oliveira; Tonholo, Josealdo; Zanta, Carmem Lucia de Paiva E Silva

    2016-01-01

    This study aimed to determine the best method to treat a textile effluent containing the dye basic blue 99 (BB). Treatments by the electrochemical and the Fenton processes were compared by means of a 2(3) experimental design, and the interaction of experimental conditions for BB oxidation were determined. The electrochemical treatment gave better results in the presence of NaCl as electrolyte and high current density (30 mA cm(-2)); the Fenton reaction provided better results at H2O2 and Fe(2+) concentrations of 10 mg L(-1) and 0.5 mmol L(-1), respectively. Electrochemical treatment was 23 times faster than the Fenton reaction because formation of chlorinated species during electrooxidation significantly contributed to dye oxidation. Although the electrochemical process was more efficient, the resulting treated effluent was more toxic to Lactuca sativa germination and growth, which indicated some biotoxicity. Results demonstrated that both processes efficiently remediated effluents containing the dye BB, but they need to be combined with other processes to ensure complete adequacy of the effluent for disposal. PMID:27642834

  11. Electro-Fenton degradation of antimicrobials triclosan and triclocarban

    International Nuclear Information System (INIS)

    The antimicrobials triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether) and triclocarban (N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl)urea) have been degraded by four electro-Fenton systems using undivided electrolytic cells with a Pt or boron-doped diamond (BDD) anode and a carbon felt or O2 diffusion cathode. The main oxidant is hydroxyl radical (·OH) produced both on the anode surface from water oxidation and in the medium by Fenton's reaction, which takes place between electrogenerated H2O2 and Fe2+ coming from cathodic reduction of O2 and Fe3+, respectively. Triclosan from saturated aqueous solutions of pH 3.0 is completely removed in all cells, decreasing its decay rate in the order: Pt/carbon felt > BDD/carbon felt > Pt/O2 diffusion > BDD/O2 diffusion, in agreement with their ·OH generation ability from Fenton's reaction. Glyoxylic, maleic and oxalic acids are identified as aliphatic intermediates. Complexes between oxalic acid and iron ions persist largely in solution, although Fe2+-oxalato complexes are mineralized by ·OH in the medium and Fe3+-oxalato complexes are destroyed by ·OH on BDD. Analogous treatments of more concentrated triclosan solutions using a 20:80 (v/v) acetonitrile/water mixture as solvent evidence the role of hydroxyl radicals along the degradation. In this hydroorganic medium hydroxylated derivatives such as 2,4-dichlorophenol, 4-chlorocatechol, chlorohydroquinone and chloro-p-benzoquinone, and carboxylic acids such as maleic, oxalic, formic and acetic acids are detected as products. Complete destruction of iron-oxalato complexes and released Cl- ion involves some oxidizing species coming from parallel acetonitrile oxidation. The same electro-Fenton systems also yield the overall removal of triclocarban in acetonitrile/water mixtures, giving rise to urea, hydroquinone, chlorohydroquinone, 1-chloro-4-nitrobenzene and 1,2-dichloro-4-nitrobenzene as primary intermediates

  12. Fenton-Like Oxidation of Malachite Green Solutions: Kinetic and Thermodynamic Study

    OpenAIRE

    Saeedeh Hashemian

    2013-01-01

    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 con...

  13. Biosynthetic Schwertmannite as Catalyst in Fenton-liKe Reactions for Degradation of Methyl Orange%生物合成施氏矿物作为类芬顿反应催化剂降解甲基橙的研究

    Institute of Scientific and Technical Information of China (English)

    汪快兵; 方迪; 徐峙晖; 施瑛; 郑冠宇; 周立祥

    2015-01-01

    应用生物合成施氏矿物作为光助类芬顿反应催化剂促进甲基橙的降解.施氏矿物通过A. f-LX5细胞悬浮液在初始pH值2.5和28℃时氧化FeSO43d生成,并进行X射线衍射和扫描电子显微镜表征.本研究分析了不同初始pH、H2 O2浓度及催化剂装载量对在光助类芬顿反应中甲基橙氧化降解效率的影响.结果表明,生物合成施氏矿物具有较高的催化活性,并且通过羟基自由基机制使甲基橙降解.在近中性、较高Cl-、SO2-4及NO3-浓度条件下,施氏矿物仍然能保持较高催化甲基橙降解的效率.本研究验证了以生物合成施氏矿物作为催化剂的异相光助类芬顿反应是一种处理含甲基橙废水有应用前景的高级氧化技术.%Biosynthesized schwertmannite was used as catalyst in photo-Fenton-like reaction to facilitate the degradation of methyl orange ( MO) . Schwertmannite was synthesized through the oxidation of FeSO4 by Acidithiobacillus ferrooxidans LX5 cell suspension at an initial pH 2. 5 and 28℃ for 3 days and characterized using X-ray diffraction spectroscopy and scanning electron microscope. The oxidative degradation of MO in the photo-Fenton-like reaction was studied at different initial pH values of suspension, concentrations of H2 O2 and dosages of catalyst. The results suggested that the biosynthetic schwertmannite showed a good catalytic activity in the MO degradation via ·OH radical mechanism. Considerable degradation efficiency of MO was still obtained in approximately neutral condition or in the presence of high concentrations of chloride, sulfate and nitrate. This work demonstrated that the heterogeneous photo-Fenton-like reaction catalyzed by the biosynthetic schwertmannite is a promising advanced oxidation technology for the treatment of wastewater containing MO.

  14. Fe2O3/H2O2类芬顿法处理阴离子表面活性剂废水的试验%Experiment of Fenton-Like Fe2O3/H2O2 Reaction Process for Treatment of Wastewater with Anionic Surfactant

    Institute of Scientific and Technical Information of China (English)

    张婷; 冯辉霞; 张娟; 苑晓微

    2013-01-01

    Fe2O/H2O2, a kind of Fenton-like agent, was used to degrade sodium dodecyl benzene sulfonate (SDBS). Effect of H2O2 concentration, Fe2O3 dosage, pH value and reaction temperature on SDBS degradation was studied. Remits show the degradation of SDBS increases with temperature increasing. The SDBS degradation ratio is high when H2O2/Fe2O3 is 1.568. pH value has unmarked effect on degradation of system. When pH is 2~10, the system maintains high degradation rate. Fenton-like Fe2O3/H2O2 reaction almost has the same efficiency as homogeneous Fenton reaction, while the former has a widely pH range and Fe2O3 can be separated easily and has no secondary pollution.%该文采用Fe2O3/H2O2类芬顿试剂处理阴离子表面活性剂——十二烷基苯磺酸钠(SDBS),研究了H2O2浓度、Fe2O3投加量、pH值及反应温度对处理效果的影响,结果表明SDBS的降解率随温度的升高而升高;当H2O2/Fe2O3=1.568(物质的量比)时体系具有较高的降解率;pH对体系降解率影响不大,在2-10的范围内降解率均较高;Fe2O3/H2O2非均相体系类F.nt.n试剂和Fe2+/H2O2均相体系Fenton试剂的降解效果相差不大,但前者具有pH范围宽,易分离,不产生二次污染的特点.

  15. 2-chlorophenol oxidation kinetic by photo-assisted Fenton process

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Experimental data are presented to test and validate a kinetic model for the oxidation of 2-chlorophenol wastewater by photo-assistedFenton process. The data showed that this process had produced good effects under acidic conductions. Up to 90% 2-chlorophenol was removedafter 90-minute reaction time with H2 O2 of 25 % CODcr in while in UV/H2 O2 system only 16.8% 2-chlorophenol was removed after one hourtreatment. The optimal pH in this reaction occurred between pH 3.0 and pH 4.0. The reaction kinetics for photo-assisted Fenton processexperimented in this research was investigated. Kinetic models were proposed for the treatment of 2-chlorophenol wastewater. The reaction wasfound to follow the 2nd order. The equations of reaction kinetics are as follows: - dt/d[RH]= KRH [ RH] [ H2O2 ]0exp(-KH2O2t); -dt/d[CODcr]= KCODCr[CODCr][ H2O2 ]0exp( - K't). The prediction of the models was found to be in a good agreement with experimentalresults, thus confirming the proposed reaction mechanism.

  16. Glutamic acid modified fenton system for degradation of BTEX contamination

    Energy Technology Data Exchange (ETDEWEB)

    Yehia, Fatma Z.; Badawi, Abdelfatah M.; Mady, Amr H. [Department of Petrochemicals, Egyptian Petroleum Research Institute, Nasr City, Cairo (Egypt); Kandile, Nadia G. [Faculty of Women, Department of Chemistry, Ain Shams University, Heliopolis, Cairo (Egypt)

    2012-07-15

    The present study employed a modified Fenton system that aims to extend the optimum pH range towards neutral conditions for studying the oxidation of benzene, toluene, ethyl benzene, xylenes (BTEX) using glutamic acid (Glu) as an iron chelator. Addition of 20 mM Glu greatly enhanced the oxidation rate of BTEX in modified Fenton system at pH 5-7. A rapid mass destruction (>97% after 1 h) of BTEX as a water contaminant carried out in the presence of 500 mM H{sub 2}O{sub 2}, 10 mM Fe{sup 2+}, and 20 mM Glu at pH 5 could be shown. The efficiency of this modified Fenton's system for mass destruction of BTEX in contaminated water was measured to estimate the impact of the major process variables that include initial concentrations of soluble Fe, H{sub 2}O{sub 2}, Glu (as metal chelating agent), and reaction time. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Photo-Fenton and Fenton Oxidation of Recalcitrant Industrial Wastewater Using Nanoscale Zero-Valent Iron

    OpenAIRE

    Henrik Hansson; Fabio Kaczala; Marcia Marques; William Hogland

    2012-01-01

    There is a need for the development of on-site wastewater treatment technologies suitable for “dry-process industries,” such as the wood-floor sector. Due to the nature of their activities, these industries generate lower volumes of highly polluted wastewaters after cleaning activities. Advanced oxidation processes such as Fenton and photo-Fenton, are potentially feasible options for treatment of these wastewaters. One of the disadvantages of the Fenton process is the formation of large amoun...

  18. Fundamentos e aplicações ambientais dos processos fenton e foto-fenton Fundaments and environmental applications of fenton and photo-fenton processes

    Directory of Open Access Journals (Sweden)

    Raquel F. Pupo Nogueira

    2007-04-01

    Full Text Available Wastewater and soil treatment processes based on Fenton's reagent have gained great attention in recent years due to its high oxidation power. This review describes the fundaments of the Fenton and photo-Fenton processes and discusses the main aspects related to the degradation of organic contaminants in water such as the complexation of iron, the use of solar light as the source of irradiation and the most important reactor types used. An overview of the main applications of the process to a variety of industrial wastewater and soil remediations is presented.

  19. Application of Fenton-like oxidation as pre-treatment for carbamazepine biodegradation

    OpenAIRE

    Monsalvo, VM.; Pedro, ZM. de; M. Muñoz; Casas, JA; Mohedano, AF.; Rodríguez, JJ

    2015-01-01

    Degradation of carbamazepine (CBZ) upon Fenton-like oxidation has been investigated analyzing the effect of H2O2 dose and temperature at a very low catalyst concentration (2mgL-1 of Fe3+). Fenton-like oxidation allowed complete conversion of CBZ, the oxidation rate depending on the amount of H2O2 used. The addition of the theoretical stoichiometric amount of H2O2 led to the complete conversion of CBZ in 1h reaction time. The reduction of the H2O2 initial concentration down to 10% of the stoic...

  20. 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.

  1. 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.

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

    Science.gov (United States)

    Flores, Nelly; Sirés, Ignasi; Garrido, José Antonio; Centellas, Francesc; Rodríguez, Rosa María; Cabot, Pere Lluís; Brillas, Enric

    2016-12-01

    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 H2O2 (AO-H2O2), 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 H2O2 and added catalytic Fe(2+). The substrate was very slowly removed by AO-H2O2, 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-H2O2 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 involving all the detected products is finally proposed.

  3. Treatment of oilfield wastewater by Fenton's process.

    Science.gov (United States)

    Gao, Y X; Yang, M; Zhang, Y; Hu, J Y

    2004-01-01

    A combination of coagulation and Fenton's process was used for the removal of total oxygen carbon (TOC) from oilfield wastewater. Compared with aluminium sulfate, ferric coagulant had better TOC removal efficiency at the same mass dosage. In Fenton's process, the effect of H2O2 and Fe2+ dose on the removal of TOC was studied. The optimum conditions required for TOC removal were an Fe3+ concentration of 40-50 mg/L, an H2O2 dose of 50 mmol/L and an Fe2+ concentration of 1.0 mmol/L. GC-MS chromatographic analysis indicated that most of the alkyl hydrocarbons of carbon numbers < 21 were removed in the first minute of Fenton's process mainly through adsorption. Alkyl hydrocarbons and phenols were oxidized almost completely following 120 min of treatment. The pathway of newly formed intermediates in Fenton's process was proposed on the basis of the GC/MS chromatogram. PMID:15077956

  4. AN ADVANCED OXIDATION PROCESS : FENTON PROCESS

    OpenAIRE

    Engin GÜRTEKİN; Nusret ŞEKERDAĞ

    2008-01-01

    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 ...

  5. UV/Fenton及Fenton体系降解愈创木酚的机理探讨%Discussion on the Mechanism of Guaiacol Degradation by UV/Fenton and Fenton Processes

    Institute of Scientific and Technical Information of China (English)

    刘芳; 杨艳明; 王昶

    2011-01-01

    This paper selected guaiacol, one model compound of lignin, as the target compound to study the degradation of guaiacol by UV/ Fenton and Fenton processes. With the help of guaiacol UV-visible spectrum changes, comparison of guaiacol removal rate and mineralization rate, the degradation mechanism of guaiacol by UV/Fenton and Fenton processes treatment was discussed. The experimental results showed that UV/Fenton and Fenton processes are not simply free radical reactions. Fe2+ and H202 can generate high iron complexes. The guaiacol is degraded with the electron transfer of complexes.%选择木素类模型物愈创木酚作为目标化合物,对UV/Fenton和Fenton体系降解愈创木酚的过程进行研究,结合愈创木酚紫外-可见光谱的变化、愈创木酚去除率和矿化率的比较,对UV/Fenton和Fenton体系降解愈创木酚的机理加以探讨.实验发现,UV/Fenton和Fenton体系不只是单纯的自由基反应,Fe2+还可以和H2 02生成高价铁配合物,通过配合物的电子转移使愈刨木酚得到氧化.

  6. Using Fenton Oxidation to Simultaneously Remove Different Estrogens from Cow Manure.

    Science.gov (United States)

    Sun, Minxia; Xu, Defu; Ji, Yuefei; Liu, Juan; Ling, Wanting; Li, Shunyao; Chen, Mindong

    2016-01-01

    The presence of estrogens in livestock excrement has raised concerns about their potential negative influence on animals and the overall food cycle. This is the first investigation to simultaneously remove estrogens, including estriol (E3), bisphenol A (BPA), diethylstilbestrol (DES), estradiol (E2), and ethinyl estradiol (EE2), from cow manure using a Fenton oxidation technique. Based on the residual concentrations and removal efficiency of estrogens, the Fenton oxidation reaction conditions were optimized as follows: a H₂O₂ dosage of 2.56 mmol/g, a Fe(II) to H₂O₂ molar ratio of 0.125 M/M, a solid to water mass ratio of 2 g/mL, an initial pH of 3, and a reaction time of 24 h. Under these conditions, the simultaneous removal efficiencies of E3, BPA, DES, E2, and EE2, with initial concentrations in cow manure of 97.40, 96.54, 100.22, 95.01, and 72.49 mg/kg, were 84.9%, 99.5%, 99.1%, 97.8%, and 84.5%, respectively. We clarified the possible Fenton oxidation reaction mechanisms that governed the degradation of estrogens. We concluded that Fenton oxidation technique could be effective for efficient removal of estrogens in livestock excrement. Results are of great importance for cow manure reuse in agricultural management, and can be used to reduce the threat of environmental estrogens to human health and ecological safety. PMID:27649223

  7. 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.

  8. Using Fenton Oxidation to Simultaneously Remove Different Estrogens from Cow Manure

    Science.gov (United States)

    Sun, Minxia; Xu, Defu; Ji, Yuefei; Liu, Juan; Ling, Wanting; Li, Shunyao; Chen, Mindong

    2016-01-01

    The presence of estrogens in livestock excrement has raised concerns about their potential negative influence on animals and the overall food cycle. This is the first investigation to simultaneously remove estrogens, including estriol (E3), bisphenol A (BPA), diethylstilbestrol (DES), estradiol (E2), and ethinyl estradiol (EE2), from cow manure using a Fenton oxidation technique. Based on the residual concentrations and removal efficiency of estrogens, the Fenton oxidation reaction conditions were optimized as follows: a H2O2 dosage of 2.56 mmol/g, a Fe(II) to H2O2 molar ratio of 0.125 M/M, a solid to water mass ratio of 2 g/mL, an initial pH of 3, and a reaction time of 24 h. Under these conditions, the simultaneous removal efficiencies of E3, BPA, DES, E2, and EE2, with initial concentrations in cow manure of 97.40, 96.54, 100.22, 95.01, and 72.49 mg/kg, were 84.9%, 99.5%, 99.1%, 97.8%, and 84.5%, respectively. We clarified the possible Fenton oxidation reaction mechanisms that governed the degradation of estrogens. We concluded that Fenton oxidation technique could be effective for efficient removal of estrogens in livestock excrement. Results are of great importance for cow manure reuse in agricultural management, and can be used to reduce the threat of environmental estrogens to human health and ecological safety. PMID:27649223

  9. Exploitation of Fenton and Fenton-like reagents as alternative conditioners for alum sludge conditioning

    Institute of Scientific and Technical Information of China (English)

    Maha A. Tony; Y. Q. Zhao; Aghareed M. Tayeb

    2009-01-01

    The use of Fenton's reagent (Fe2+/H2O2) and Fenton-like reagents containing transition metals of Cu(II), Zn(II), Co(II), and Mn(II) for an alum sludge conditioning to improve its dewaterability was investigated in this study. The results obtained were compared with those obtained from conditioning the same alum sludge using cationic and anionic polymers. Experimental results show that Fenton's reagent was the best among the Fenton and Fenton-like reagents for the alum sludge conditioning. A considerable effectiveness of capillary suction time (CST) reduction efficiency of 47% can be achieved under test conditions of Fe2+/H2O2 = 20/125 mg/gDS (dry solid) and pH = 6.0. The observation of floc-like particles after Fenton's reagent conditioning of alum sludge suggests that the mechanism of Fenton's reagent conditioning was different with that of polymer conditioning. In spite of the less efficiency in the CST reduction of Fenton's reagent in alum sludge conditioning compared with that of polymer conditioning, is less than that of polymer conditioning.[b1] This study provided an example of proactive treatment engineering, which is aimed at seeking a safe alternative to the use of polymers in sludge conditioning towards achieving a more sustainable sludge management strategy.

  10. Photo-Fenton and Fenton Oxidation of Recalcitrant Wastewater from the Wooden Floor Industry.

    Science.gov (United States)

    Hansson, Henrik; Kaczala, Fabio; Marques, Marcia; Hogland, William

    2015-06-01

    There is a need for development of on-site wastewater treatment technologies suitable to "dry-process" industries, such as the wooden floor sector. Due to the nature of their activities, these industries generate low volumes of highly polluted and recalcitrant wastewaters due to washing and cleaning surfaces and machinery. Advanced oxidation processes such as Fenton and photo-Fenton are potentially feasible options for the treatment of wastewaters with not easily biodegradable pollutants. The wastewater from a wooden floor industry with initial COD value of 4956 mg/L and TOC value of 2730 mg/L was treated with Fenton (Fe/H2O2) and photo-Fenton (Fe/H2O2/UV) applying a 2-level full-factorial experimental design. The highest removals of COD and TOC (79% and 62% respectively) were achieved when photo-Fenton was applied. In conclusion, Fenton and photo-Fenton are promising treatment options for these highly recalcitrant wastewaters, photo-Fenton being a more promising option according to the results.

  11. Electro-Fenton degradation of antimicrobials triclosan and triclocarban

    Energy Technology Data Exchange (ETDEWEB)

    Sires, Ignasi [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); Oturan, Nihal [Universite de Marne la Vallee, Laboratoire des Geomateriaux et Geologie de l' Ingenieur, 5 Boulevard Descartes, Champs-sur-Marne, 77454 Marne-la-Vallee Cedex 2 (France); Oturan, Mehmet A. [Universite de Marne la Vallee, Laboratoire des Geomateriaux et Geologie de l' Ingenieur, 5 Boulevard Descartes, Champs-sur-Marne, 77454 Marne-la-Vallee Cedex 2 (France); Rodriguez, Rosa Maria [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); 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 [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

    2007-05-05

    The antimicrobials triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether) and triclocarban (N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl)urea) have been degraded by four electro-Fenton systems using undivided electrolytic cells with a Pt or boron-doped diamond (BDD) anode and a carbon felt or O{sub 2} diffusion cathode. The main oxidant is hydroxyl radical ({center_dot}OH) produced both on the anode surface from water oxidation and in the medium by Fenton's reaction, which takes place between electrogenerated H{sub 2}O{sub 2} and Fe{sup 2+} coming from cathodic reduction of O{sub 2} and Fe{sup 3+}, respectively. Triclosan from saturated aqueous solutions of pH 3.0 is completely removed in all cells, decreasing its decay rate in the order: Pt/carbon felt > BDD/carbon felt > Pt/O{sub 2} diffusion > BDD/O{sub 2} diffusion, in agreement with their {center_dot}OH generation ability from Fenton's reaction. Glyoxylic, maleic and oxalic acids are identified as aliphatic intermediates. Complexes between oxalic acid and iron ions persist largely in solution, although Fe{sup 2+}-oxalato complexes are mineralized by {center_dot}OH in the medium and Fe{sup 3+}-oxalato complexes are destroyed by {center_dot}OH on BDD. Analogous treatments of more concentrated triclosan solutions using a 20:80 (v/v) acetonitrile/water mixture as solvent evidence the role of hydroxyl radicals along the degradation. In this hydroorganic medium hydroxylated derivatives such as 2,4-dichlorophenol, 4-chlorocatechol, chlorohydroquinone and chloro-p-benzoquinone, and carboxylic acids such as maleic, oxalic, formic and acetic acids are detected as products. Complete destruction of iron-oxalato complexes and released Cl{sup -} ion involves some oxidizing species coming from parallel acetonitrile oxidation. The same electro-Fenton systems also yield the overall removal of triclocarban in acetonitrile/water mixtures, giving rise to urea, hydroquinone, chlorohydroquinone, 1-chloro-4

  12. Study of solar photo-Fenton system applied to removal of phenol from water.

    Science.gov (United States)

    Freire, Layla F A; da Fonseca, Fabiana Valéria; Yokoyama, Lidia; Teixeira, Luiz Alberto Cesar

    2014-01-01

    This study evaluated the use of a Fenton's reaction in a falling film solar reactor (FFR), as a possible advanced oxidation process for the mineralization of the organic compound phenol in water. Preliminary tests were carried out to evaluate phenol degradation by photolysis and to select the optimal residence time in which to carry out the process using a solar photo-Fenton system. The variables studied were the initial phenol concentration (100 to 300 mg L(-1)), the [Phenol]:[H2O2] mass ratio (1.0 to 2.0) and the [H2O2]/[Fe2+] molar ratio (5 to 10). Phenol degradation of 99% and chemical oxygen demand (COD) reduction of 97% were obtained under the following reaction conditions: phenol concentration=200 mg L(-1), mass ratio [Phenol]:[H2O2]=1.5 and molar ratio [H2O2]/[Fe2+]=7.5. Overall mineralization was achieved using the solar photo-Fenton process to destroy phenol and COD. The solar photo-Fenton process using a FFR appears to be a viable method for removing phenols in wastewaters on an industrial scale.

  13. Treatment of mature landfill leachate by chemical precipitation and Fenton advanced oxidation process

    Directory of Open Access Journals (Sweden)

    Nemat Alah Jaafarzadeh Haghighi Fard

    2016-03-01

    Full Text Available Background: Mature landfill leachate is a complicated mixture which is resistant to biological treatment processes. The treatment of mature landfill leachate by struvite precipitation and Fenton oxidation was the main objective of the current research. Methods: Struvite with the phosphate/ammonia/magnesium molar ratio of 1/1/1.05 was considered during all experiments. Five initial pHs of 3, 4, 5, 6, and 7, four different H2O2/Fe mass ratios of 50, 100, 200, and 400, and reaction times of 20, 40, 80, 120, and 160 minutes were examined for the Fenton oxidation process. Results: A leachate sample with average chemical oxygen demand (COD, BOD5, and NH4 concentrations of 7350, 2220, and 2280 mg L-1, respectively, and a BOD5/COD ratio of 0.3 was introduced to the chemical precipitation unit. An NH4 removal efficiency of 87% was obtained at pH 8.5 for struvite precipitation. Under optimum conditions of Fenton oxidation, including pH 3, an H2O2/Fe2+ mass ratio of 200, and a reaction time of 160 min, more than 95% COD and BOD5 removal was observed. Conclusion: Struvite precipitation and Fenton oxidation are reliable and efficient alternatives for mature landfill treatment.

  14. Landfill Leachates Treatment by /UV, /, Modified Fenton, and Modified Photo-Fenton Methods

    Directory of Open Access Journals (Sweden)

    Jeremi Naumczyk

    2012-01-01

    Full Text Available Advanced oxidation processes (AOPs such as H2O2/UV, O3/H2O2, modified Fenton, and modified photo-Fenton processes have been investigated in terms of the treatment of landfill leachate with ratio of BOD5/COD in the range of 0.22 to 0.24. The modification of Fenton and photo-Fenton processes consisted in the inclusion of precipitation and separation of humic substances at pH 3. Due to the precipitation, the value of COD decreased by 39% and BOD5 by 7.1%. The modification of the processes allowed us to improve the efficiency and to decrease the doses of reagents necessary to continue the process. Modified photo-Fenton process proved to be the most effective (92.7% COD removal of all processes investigated. Additionally, modified-Fenton process was much more effective than the other two processes when compared up to 120 min, while after longer times it gave the least satisfactory results. After 30 min of modified-Fenton process BOD5/COD ratio increased to 0.43. The parameter referred to as “efficiency of oxidants” was used to estimate the efficiency of all the processes—its value varied from 178 to 239%. Various substances including phthalates, hydrocarbons, silanes, and siloxanes were identified in raw and treated leachate.

  15. A Novel Mechanism for Halogenated Quinone- Mediated and Metal-Independent Organic Fenton-Like Reaction%不依赖于过渡金属离子的卤代醌介导的新型有机类Fenton反应机理

    Institute of Scientific and Technical Information of China (English)

    朱本占; 任福荣; 夏海英; 邵杰

    2012-01-01

    卤代醌是许多卤芳香持久有机污染物的致癌代谢产物和饮用水消毒副产物.羟基自由基(OH)被公认为生物系统中最具活性的活性氧物种,能导致生物体内DNA等生物大分子的氧化损伤.目前,最被广泛接受的OH产生机理是过渡金属离子催化的Fenton反应.综合采用电子自旋共振二级自旋捕获和其他分析方法,发现四氯苯醌和其它卤代醌皆可通过不依赖于过渡金属离子的途径,显著促进氢过氧化物(H2O2或有机氢过氧化物)的分解而产生OH或烷氧自由基,并首次检测到一种新型的、以碳为中心的醌自由基.基于以上研究,提出一类不依赖于过渡金属离子的卤代醌介导的新型有机类Fenton反应机理.%Halogenated quinones are a class of carcinogenic metabolites of many halogenated persistent organic pollutants and new chlorination disinfection byproducts in drinking water. The hydroxyl radical ("OH) has been considered to be one of the most reactive oxygen species produced in biological systems. It has been shown that 'OH can cause oxidative damage to DNA and other macromolecuies. One of the most widely accepted mechanisms for OH production is through the transition metal-catalyzed Fenton reaction. Through the complementary application of electron spin resonance (ESR) secondary spin-trapping and other analytical methods, we found that tetrachloro-1,4-benzoquinone (TCBQ) and other halogenated quinones could markedly enhance the decomposition of hydroperoxides (H2O2 and organic hydroperoxides) and formation of "OH and alkoxyl radicals independent of transition metal ions. A novel carbon-centered quinone ketoxy radical was also detected and identified for the first time. Based on these data, we proposed a novel mechanism for metal-independent and halogenated quinone-mediated organic Fenton-like reaction.

  16. 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.

  17. 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.

  18. Electro-fenton and photoelectro-fenton degradation of sulfanilic acid using a boron-doped diamond anode and an air diffusion cathode.

    Science.gov (United States)

    El-Ghenymy, Abdellatif; Garrido, José Antonio; Centellas, Francesc; Arias, Conchita; Cabot, Pere Lluís; Rodríguez, Rosa María; Brillas, Enric

    2012-04-01

    The mineralization of sulfanilic acid has been studied by electro-Fenton (EF) and photoelectro-Fenton (PEF) reaction with UVA light using an undivided electrochemical cell with a boron-doped diamond (BDD) anode and an air diffusion cathode able to generate H(2)O(2). Organics were then oxidized by hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between generated H(2)O(2) and added Fe(2+). The UVA irradiation in PEF enhanced the production of hydroxyl radicals in the bulk, accelerating the removal of organics and photodecomposed intermediates like Fe(III)-carboxylate complexes. Partial decontamination of 1.39 mM sulfanilic acid solutions was achieved by EF until 100 mA cm(-2) at optimum conditions of 0.4 mM Fe(2+) and pH 3.0. The increase in current density and substrate content led to an almost total mineralization. In contrast, the PEF process was more powerful, yielding almost complete mineralization in less electrolysis time under comparable conditions. The kinetics for sulfanilic acid decay always followed a pseudo-first-order reaction. Hydroquinone and p-benzoquinone were detected as aromatic intermediates, whereas acetic, maleic, formic, oxalic, and oxamic acids were identified as generated carboxylic acids. NH(4)(+) ion was preferentially released in both treatments, along with NO(3)(-) ion in smaller proportion.

  19. Use of Enzymatic Bio-Fenton as a New Approach in Decolorization of Malachite Green

    Directory of Open Access Journals (Sweden)

    Afzal Karimi

    2012-01-01

    Full Text Available An enzymatic reaction using glucose oxidase was applied for in situ production of hydrogen peroxide for use in simultaneously Fenton's reaction in decolorization of malachite green. It was found that decolorization rate increased by increasing of glucose concentration from 0.2 g/L to 1.5 g/L. Decolorization rate showed different behaviors versus temperature changes. Initial rate of decolorization process was increased by increasing of temperature; after 30 minutes, especially at temperatures above 30°C, the decolorization rate was gradually reduced. The pH value in the reaction media was decreased from natural to about pH=3 which had synergic effect on the Fenton process by stabilizing of Fe2+ ions.

  20. A combined process of adsorption and Fenton-like oxidation for furfural removal using zero-valent iron residue.

    Science.gov (United States)

    Li, Furong; Bao, Jianguo; Zhang, Tian C; Lei, Yutian

    2015-01-01

    In this study, the feasibility of using a combined adsorption and Fenton-like oxidation process (with zero-valent iron (ZVI) residue from heat wraps as an absorbent and catalyst) to remove furfural in the solution was evaluated. The influencing parameters (e.g. pH, H2O2 concentration, initial furfural concentration) and the reusability of ZVI residue (to replace the iron powder) were estimated. The ZVI residue was found to have much better adsorption effect on furfural at pH 2.0 compared with pH 6.7. For Fenton-like reaction alone with ZVI residue, the highest furfural removal of 97.5% was observed at the concentration of 0.176 mol/L H2O2, and all of the samples had >80% removal efficiency at different initial furfural concentrations of 2, 10, 20, 30 and 40 mmol/L. However, with a combined adsorption and Fenton-like oxidation, the removal efficiency of furfural was nearly 100% for all treatments. The ZVI residue used for furfural removal was much better than that of iron powder in the Fenton-like reaction at a seven-cycle experiment. This study suggests the combined process of adsorption and Fenton-like oxidation using ZVI residue is effective for the treatment of furfural in the liquid.

  1. Degradation of carbofuran-contaminated water by the Fenton process.

    Science.gov (United States)

    Ma, Ying-Shih; Kumar, Mathava; Lin, Jih-Gaw

    2009-07-15

    In this study, the Fenton process was applied for the degradation of carbofuran from aqueous system. Batch experiments were conducted at two different carbofuran concentrations i.e., 10 and 50 mg/L, and at pH 3. Batch experiments at each carbofuran concentration were designed by central composite design (CCD) with two independent variables i.e. Fe2+ and H2O2. Experimental results indicate that more than 90% of carbofuran removal was observed within 5 mins of Fenton reaction at 5 mg/L of Fe2+ concentration and 100 mg/L of H202 concentration. Increases in Fe2+ and/or H2O2 concentrations beyond 5 and 100 mg/L, respectively produced 100% carbofuran removal. Based on the experimental observations, the optimal Fe2+ and H2O2 dosages required for 10 mg/L of aqueous carbofuran removal were estimated as 7.4 and 143 mg/L, respectively. During this study, three carbofuran intermediates such as 7-benzofuranol,2,3,-dihydro-2,2-dimethyl, 7-hydroxy-2,2-dimethyl-benzofuran-3-one and 1,4-Benzene-di-carboxaldehyde were identified using GC/MS analyses.

  2. Photo-Fenton-like treatment of K-acid: assessment of treatability, toxicity and oxidation products.

    Science.gov (United States)

    Olmez-Hanci, Tugba; Arslan-Alaton, Idil; Gelegen, Ozlem

    2014-01-01

    Photo-Fenton-like treatment of the commercially important naphthalene sulphonate K-acid (2-naphthylamine-3,6,8-trisulphonic acid) was investigated using UV-C, UV-A and visible light irradiation. Changes in toxicity patterns were followed by the Vibrio fischeri bioassay. Rapid and complete degradation of K-acid accompanied with nearly complete oxidation and mineralization rates (>90%) were achieved for all studied irradiation types. On the other hand, detoxification was rather limited and did not change significantly during photo-Fenton-like treatment. Several oxidation products could be identified via liquid chromatograph-mass spectrometer analyses, such as desulphonated and hydroxylated naphthalene derivatives, quinones, and ring-opening as well as dimerization products. Photo-Fenton-like treatment of K-acid with UV-C, UV-A and visible light irradiation occurred through a series of hydroxylation and desulphonation reactions, followed by ring cleavage. A common degradation pathway for photo-Fenton-like treatment of K-acid using different irradiation types was proposed. PMID:25259495

  3. Treatability assessment of polycyclic aromatic hydrocarbons contaminated marine sediments using permanganate, persulfate and Fenton oxidation processes.

    Science.gov (United States)

    Shih, Yu-Jen; Binh, Nguyen Thanh; Chen, Chiu-Wen; Chen, Chih-Feng; Dong, Cheng-Di

    2016-05-01

    Various chemical oxidation techniques, such as potassium permanganate (KMnO4), sodium persulfate (Na2S2O8), Fenton (H2O2/Fe(2+)), and the modified persulfate and Fenton reagents (activated by ferrous complexes), were carried out to treat marine sediments that were contaminated with polycyclic aromatic hydrocarbons (PAHs) and dredged from Kaohsiung Harbor in Taiwan. Experimental results revealed that KMnO4 was the most effective of the tested oxidants in PAH degradation. Owing to the high organic matter content in the sediment that reduced the efficiencies of Na2S2O8 and regular Fenton reactions, a large excess of oxidant was required. Nevertheless, KH2PO4, Na4P2O7 and four chelating agents (EDTA, sodium citrate, oxalic acid, and sodium oxalate) were utilized to stabilize Fe(II) in activating the Na2S2O8 and Fenton oxidations, while Fe(II)-citrate remarkably promoted the PAH degradation. Increasing the molecular weight and number of rings of PAH did not affect the overall removal efficiencies. The correlation between the effectiveness of the oxidation processes and the physicochemical properties of individual PAH was statistically analyzed. The data implied that the reactivity of PAH (electron affinity and ionization potential) affected its treatability more than did its hydrophobicity (Kow, Koc and Sw), particularly using experimental conditions under which PAHs could be effectively oxidized. PMID:26915591

  4. Effects of inorganic anions on carbon isotope fractionation during Fenton-like degradation of trichloroethene.

    Science.gov (United States)

    Liu, Yunde; Zhou, Aiguo; Gan, Yiqun; Li, Xiaoqian

    2016-05-01

    Understanding the magnitude and variability in isotope fractionation with respect to specific processes is crucial to the application of stable isotopic analysis as a tool to infer and quantify transformation processes. The variability of carbon isotope fractionation during Fenton-like degradation of trichloroethene (TCE) in the presence of different inorganic ions (nitrate, sulfate, and chloride), was investigated to evaluate the potential effects of inorganic anions on carbon isotope enrichment factor (ε value). A comparison of ε values obtained in deionized water, nitrate solution, and sulfate solution demonstrated that the ε values were identical and not affected by the presence of nitrate and sulfate. In the presence of chloride, however, the ε values (ranging from -6.3±0.8 to 10±1.3‰) were variable and depended on the chloride concentration, indicating that chloride could significantly affect carbon isotope fractionation during Fenton-like degradation of TCE. Thus, caution should be exercised in selecting appropriate ε values for the field application of stable isotope analysis, as various chloride concentrations may be present due to naturally present or introduced with pH adjustment and iron salts during Fenton-like remediation. Furthermore, the effects of chloride on carbon isotope fractionation may be able to provide new insights about reaction mechanisms of Fenton-like processes. PMID:26835895

  5. Review of iron-free Fenton-like systems for activating H2O2 in advanced oxidation processes

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Elements with multiple redox states efficiently decompose H2O2 at neutral pH. • Activation of H2O2 is entirely governed by solution pH and catalyst composition. • Metal leaching and toxicity is an important factor for practical applications. • Iron-free Fenton systems work only in specialized reaction conditions. - Abstract: Iron-catalyzed hydrogen peroxide decomposition for in situ generation of hydroxyl radicals (HO• ) has been extensively developed as advanced oxidation processes (AOPs) for environmental applications. A variety of catalytic iron species constituting metal salts (in Fe2+ or Fe3+ form), metal oxides (e.g., Fe2O3, Fe3O4), and zero-valent metal (Fe0) have been exploited for chemical (classical Fenton), photochemical (photo-Fenton) and electrochemical (electro-Fenton) degradation pathways. However, the requirement of strict acidic conditions to prevent iron precipitation still remains the bottleneck for iron-based AOPs. In this article, we present a thorough review of alternative non-iron Fenton catalysts and their reactivity towards hydrogen peroxide activation. Elements with multiple redox states (like chromium, cerium, copper, cobalt, manganese and ruthenium) all directly decompose H2O2 into HO• through conventional Fenton-like pathways. The in situ formation of H2O2 and decomposition into HO• can be also achieved using electron transfer mechanism in zero-valent aluminum/O2 system. Although these Fenton systems (except aluminum) work efficiently even at neutral pH, the H2O2 activation mechanism is very specific to the nature of the catalyst and critically depends on its composition. This review describes in detail the complex mechanisms and emphasizes on practical limitations influencing their environmental applications

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

    OpenAIRE

    Marco A. Benedetti Durigan; Sergio Renato Vaz; Patricio Peralta-Zamora

    2012-01-01

    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...

  7. Oxidation of Levafix CA reactive azo-dyes in industrial wastewater of textile dyeing by electro-generated Fenton's reagent.

    Science.gov (United States)

    El-Desoky, Hanaa S; Ghoneim, Mohamed M; El-Sheikh, Ragaa; Zidan, Naglaa M

    2010-03-15

    The indirect electrochemical removal of pollutants from effluents has become an attractive method in recent years. Removal (decolorization and mineralization) of Levafix Blue CA and Levafix Red CA reactive azo-dyes from aqueous media by electro-generated Fenton's reagent (Fe(2+)/H(2)O(2)) using a reticulated vitreous carbon cathode and a platinum gauze anode was optimized. Progress of oxidation (decolorization and mineralization) of the investigated azo-dyes with time of electro-Fenton's reaction was monitored by UV-visible absorbance measurements, Chemical oxygen demand (COD) removal and HPLC analysis. The results indicated that the electro-Fenton's oxidation system is efficient for treatment of such types of reactive dyes. Oxidation of each of the investigated azo-dyes by electro-generated Fenton's reagent up to complete decolorization and approximately 90-95% mineralization was achieved. Moreover, the optimized electro-Fenton's oxidation was successfully applied for complete decolorization and approximately 85-90% mineralization of both azo-dyes in real industrial wastewater samples collected from textile dyeing house at El-Mahalla El-Kobra, Egypt.

  8. Impact of Fenton and ozone on oxidation of wastewater containing nitroaromatic compounds

    Institute of Scientific and Technical Information of China (English)

    Fares Al Momani; Mo'ayyad Shawaqfah; Ahmad Shawaqfeh; Mohammad Al-Shannag

    2008-01-01

    Fenton and ozone treatment was investigated at laboratory scale for the degradation of aqueous solutions of nitrobenzene (NB).Effects of reactants concentration (O3,H2O2,and Fe(II)),temperature,and pH on NB degradation were monitored.Reaction kinetic of these processes was also assessed.A rapid reaction took place for Fenton process at higher initial concentration of H2O2,higher temperatures,and more acidic conditions(pH 3).Similarly, ozonation reaction exhibited rapid rates for higher ozone dose,higher temperatures,and more basic conditions(pH 11).Complete NB degradation in 65 min Was achieved using Fenton process.The conditions of complete elimination of 100 mg/L of initial NB concentration,were 250 mg/L of H2O2 concentration,pH 3,and 10 mg/L of Fe(Ⅱ) concentration.Under these conditions,55% organic carbon elimination Was achieved.Total organic carbon mineralization Was attained in 240 min reaction time by Fenton process with 900 mg/L of H2O2 concentration,and 30 mg/L of Fe(II) concentration.Fenton reaction showed a pseudo-first order kinetic;the reaction rate constant Was ranged from 0.0226 to 0.0658 min-1.Complete NB degradation wag also achieyed for an ozone dose of the order of 2.5 g/L.The ozonation Was studied at different ozone doses.different initial pH(7-11)and at difierent temperatures(15-35℃).NB ozonation kinetic Was represented by a bi-molecular kinetic model which was reduced to pseudo-first order kinetic.The pseudo-first order reaction rate constant was determined to increase at 20℃ from 0.004 to 0.020 min-1 as the used ozone increased from 0.4 to 1.9g/L.

  9. 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.

  10. Heterogeneous photo-assisted Fenton catalytic removal of tetracycline using Fe-Ce pillared bentonite

    Institute of Scientific and Technical Information of China (English)

    张亚平; 贾成光; 彭然; 马丰; 欧光南

    2014-01-01

    In the present work, a novel heterogeneous photo-Fenton catalyst was prepared by iron and cerium pillared bentonite. The catalyst Fe-Ce/bentonite was characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), Brunauer-Emmett-Teller (BET) and scanning electron microscopy (SEM) methods. It is found that Fe and Ce intercalate into the silicate layers of bentonite successfully. Tetracycline was removed by heterogeneous photo-Fenton reaction using the catalyst in this work. The effects of different reaction systems, hydrogen peroxide concentration, initial pH, catalyst dosage, UV power and introduction of different anions on degradation were investigated in details. The stability of catalyst was investigated through recycling experiment. The results show that removal rate of tetracycline is 98.13%under the conditions of 15 mmol/L H2O2, 0.50 g/L catalyst dosage, initial pH 3.0, 11 W UV lamp power and 60 min reaction time. However, the removal rate decreases after adding some anions. The hydroxyl radical plays an important role in heterogeneous photo-assisted Fenton degradation of tetracycline. The catalyst is very stable and can be recycled many times.

  11. Advanced treatment of pharmaceutical wastewater by Fenton reagent oxidation process

    Directory of Open Access Journals (Sweden)

    Yanan YANG

    2015-12-01

    Full Text Available Avermectin-salinomycin waster is hard to be further biodegraded after treated by anaerobic-aerobiotic process, so Fenton oxidation process is studied for its advanced treatment. Influencing factors of pH, reaction time, H2O2 dosage and H2O2/Fe2+ on COD removal are investigated, respectively. When pH value is 3.0, the dosage of H2O2 is 1.5 mL/L, and the mole ratio of H2O2/Fe2+ is 5∶1, the effluent COD mass concentrations decreases from 224 to 64.3 mg/L, namely the COD removal efficiency reaches 71.3%.

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

    Energy Technology Data Exchange (ETDEWEB)

    Colombo, Renata, E-mail: colombo@iqsc.usp.br [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, Caixa Postal 780, 13560-970 Sao Carlos, SP (Brazil); Ferreira, Tanare C.R.; Alves, Suellen A.; Lanza, Marcos R.V. [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, Caixa Postal 780, 13560-970 Sao Carlos, SP (Brazil)

    2011-12-30

    Highlights: Black-Right-Pointing-Pointer The photo-Fenton reaction provides an efficient process by which to degrade esfenvalerate in aqueous suspensions. Black-Right-Pointing-Pointer Photo-Fenton oxidation with Fe{sup 3+} is more efficient in degrading esfenvalerate than the Fe{sup 2+}-based reaction. Black-Right-Pointing-Pointer Esfenvalerate was degraded most efficiently by photo-Fenton reaction in the presence of 5 mM Fe{sup 3+} complex and 25 mM hydrogen peroxide at pH 2.5. Black-Right-Pointing-Pointer The degradation of esfenvalerate by photo-Fenton (Fe{sup 3+}) generates organic by-products. Black-Right-Pointing-Pointer 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{sup 2+}) and (Fe{sup 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{sup 2+}) reaction (esfenvalerate 17 mg L{sup -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{sup 3+}) process compared with its Fe{sup 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. 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. 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.

  15. 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.

  16. Fenton oxidation of 2, 4-and 2, 6-dinitrotoluene and acetone inhibition

    Institute of Scientific and Technical Information of China (English)

    Yiliang HE; Bin ZHAO; Joseph B.HUGHES; Sunh Soo HAN

    2008-01-01

    The performances and kinetic parameters of Fenton oxidation of 2, 4- and 2, 6-dinitrotoluene (DNT) in water-acetone mixtures and explosive contaminated soil washing-out solutions were investigated at a labor-atory scale. The experimental results show that acetone can be a significant hydroxyl radical scavenger and result in serious inhibition of Fenton oxidation of 2, 4- and 2, 6-DNT. Although no serious inhibition was found in con-taminated soil washing-out solutions, longer reaction time was needed to remove 2, 4- and 2, 6-DNT completely, mainly due to the competition of hydroxyl radicals. Fenton oxidation of 2, 4- and 2, 6-DNT fit well with the first-order kinetics and the presence of acetone also reduced DNT's degradation kinetics. Based on the com-parison and matching of retention time and ultraviolet (UV) spectra between high performance liquid chromato-graphy (HPLC) and standards, the following reaction pathway for 2, 4-DNT primary degradation was pro-posed: 2, 4-DNT→2, 4-dinitro-benzaldehyde→2, 4-dini-trobenzoic acid→1, 3-dinitrobenzene→3-nitrophenol.

  17. Treatment of Effluent from a Factory of Paints Using Solar Photo-Fenton Process

    Directory of Open Access Journals (Sweden)

    Alam Gustavo Trovó

    2013-01-01

    Full Text Available We evaluated the use of Fenton reactions induced by solar radiation in the treatment of effluent from a factory of paints for buildings, after prior removal of the suspended solids. The increase of H2O2 concentration from 100 to 2500 mg L−1 for a [Fe2+] = 105 mg L−1 contributed to the reduction of DOC, COD, and toxicity. Our best results were achieved using 1600 mg L−1 H2O2, with 90% of DOC and COD removal and a complete removal of the toxicity with respect to Artemia salina. Additionally, through increasing Fe2+ concentration from 15 to 45 mg L−1, the DOC removal rate increased 11 times, remaining almost constant in the range above 45 until 105 mg L−1. Under our best experimental conditions, 80% of DOC removal was achieved after an accumulated dose of 130 kJ m−2 of UVA radiation (82±17 min of solar irradiation under an average UVA irradiance of 34.1±7.3 W m−2, while 40% of DOC removal was reached after 150 min under only thermal Fenton reactions. The results suggest the effectiveness of implementation of solar photo-Fenton process in the decontamination and detoxification of effluents from factories of paints for buildings.

  18. Roles of TaON and Ta(3)N(5) in the visible-Fenton-like degradation of atrazine.

    Science.gov (United States)

    Du, Yingxun; Zhao, Lu; Zhang, Yuanyuan

    2014-02-28

    In this study, the roles of TaON and Ta3N5 in the degradation of atrazine by the visible-Fenton-like system were examined in detail. The TaON and Ta3N5 samples prepared by the nitridation of Ta2O5 and characterized by XRD, DRS, BET and PL analyses. The results showed that the TaON sample had weaker absorption in the visible region but higher specific surface area than the Ta3N5 sample. The degradation rate of atrazine in visible-TaON-Fenton-like system was 2.64 times than that in visible-Ta3N5-Fenton-like system. Both Fe(2+) and H2O2 could be reduced by eCB (electrons in the conduction band) in TaON or Ta3N5, while atrazine could not be oxidized by hVB (holes in the valance band). OH is the active species for the degradation of atrazine in visible-TaON/Ta3N5-Fenton-like systems. Majority of OH originated from Fenton reaction. After Fe(3+) was reduced by eCB to Fe(2+), Fe(2+) reacted quickly with H2O2 to generate OH. In addition, by capturing eCB, a little of H2O2 was reduced to yield OH, which contributed a small fraction of atrazine degradation. Based on the experimental results, the roles of TaON and Ta3N5 in the visible-Fenton-like system were proposed. And the higher photocatalytic activity of TaON than Ta3N5 was suggested to be due to the higher separation efficiency of electrons and holes, which may be related to the larger specific surface area. PMID:24413052

  19. ROLE OF THE PHOTO-FENTON REACTION IN THE PRODUCTION OF HYDROXYL RADICALS AND PHOTOBLEACHING OF COLORED DISSOLVED ORGANIC MATTER IN A COASTAL RIVER OF THE SOUTHEASTERN UNITED STATES

    Science.gov (United States)

    Photochemical reactions involving colored dissolved organic matter (CDOM) in natural waters are important determinants of nutrient cycling, trace gas production and control of light penetration into the water column. In this study the role of the hydroxyl radical ((OH)-O-.) in CD...

  20. Fenton's Reagent. Innovative Technology Summary Report

    International Nuclear Information System (INIS)

    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

  1. Heterogeneous fenton process using the mineral hematite for the discolouration of a reactive dye solution

    Directory of Open Access Journals (Sweden)

    F. V. F. Araujo

    2011-12-01

    Full Text Available This work reports a study on the heterogeneous Fenton reaction using hematite powder (Fe2O3 in suspension for the discolouration of the reactive dye Drimarene Red X-6BN in aqueous solutions. The efficiency of the process was studied as a function of the experimental conditions: initial pH; H2O2 dose; and hematite powder concentration; all of which showed a strong effect on the reaction kinetics. Under the best experimental conditions: pH = 2.5; H2O2 dose = 800 mg/L; and [Hematite] = 20 g/L, it was possible to remove about 99% of the initial colour in 120 minutes in a batch reaction at 25ºC. The analysis of the kinetic results suggests that the reaction is initiated by heterogeneous generation of free radicals on the hematite surface, but as soluble iron (III and iron (II species are released into the solution during the course of the reaction, a simultaneous homogeneous Fenton reaction step propagates and contributes to the overall reaction.

  2. Treatment of Color Filter Wastewater by Fresnel Lens Enhanced Solar Photo-Fenton Process

    OpenAIRE

    Wen-shiuh Kuo; Chia-ling Wu

    2012-01-01

    Treatment of color filter wastewater using solar photo-Fenton process enhanced by high-concentrating Fresnel lens was investigated in this paper. Optimal reaction conditions based on response surface methodology (RSM) were established as under an initial pH of 5, a [H2O2]0/COD0 ratio of 1~1.35 and a [H2O2]0/[Fe2+]0 ratio of 15 for a reaction time of 60 min, which could reach a readily biodegradable level, that is, the biodegradability (BOD5/COD) of wastewater was more than 0.3. With the assis...

  3. Study of the Development of Fenton and Fenton Like Oxidation in High Concentration and Non-degradation Organic Wastewater Treatment%Fenton及类Fenton氧化在高浓度难降解有机废水处理中的研究进展

    Institute of Scientific and Technical Information of China (English)

    赖亦桂

    2012-01-01

    随着工业的迅速发展,越来越多的有机物被广泛运用于工业生产,高浓度难降解的有机废水成为工业水处理的一个难点。阐述了Fenton试剂及光助Fenton、电Fenton以及超声Fenton氧化法处理有机废水的特性,概述了羟基自由基(·OH)的产生机理,对Fenton试剂及类Fenton试剂在有机废水处理上的应用状况进行了总结。%With the rapid development of industry,more and more organics were widely utilized in industry,high concentration and non-degradation organic wastewater became to be a difficult point in industrial water conditioning.Expounded the features of organic wastewater treated with Fenton reagent,Photo-Fenton,Electro-Fenton,US-Fenton reagent;summarized the produced mechanism of ·OH and applied status of organic wastewater treated with Fenton and Fenton Like Reaction.

  4. Self-catalytic degradation of ortho-chlorophenol with Fenton's reagent studied by chemiluminescence

    Institute of Scientific and Technical Information of China (English)

    Zhen Lin; HuiChen; Yun Zhou; Nobuaki Ogawa; Jin-Ming Lin

    2012-01-01

    The degradation of ortho-chlorophenol using Fenton's reagent was studied by chemiluminescence(CL).Without a special CL reagent,a weak CL emission from the mixture of ferrous ion and hydrogen peroxide was observed at room temperature.The CL intensity was increased by the addition of ortho-chlorophenol into the mixed solution.When the temperature was raised to 65℃,the CL intensity was enhanced strongly.The CL mechanisms for the system H2O2-Fe2+ with and without ortho-chlorophenol were studied by examining the CL spectrum,gas chromatography-mass spectrometry and electron spin resonance spectrum.The effects of various free radical scavengers,surfactants and fluorescence compounds on the CL intensity were also investigated.A self-catalytic oxidation mechanism was proposed.The results showed that singlet oxygen was the main emitter for the system H2O2-Fe2+.The strong CL from the system H2O2-Fe2+-ortho-chlorophenol was due to singlet oxygen and electronically excited quinone.The benzenediol-like intermediate product formed during the phenol oxidation process greatly promoted the Fenton's reaction and led to higher CL intensity.Chemiluninescence is a novel approach for the investigation of the oxidation of some organic pollutants by Fenton's reagent.

  5. Photochemically enhanced degradation of phenol using heterogeneous Fenton-type catalysts

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The degradation of phenol was carried out using heterogeneous Fenton-type catalysts in the presence of H2O2 and UV. Catalysts were prepared by exchanging and immobilizing Fe2+ in zeolite 13X, silica gel or Al2O3. The concentration of phenol solution was 100 mg/L. The amount of H2O2 added was the stoichiometric amount of H2O2 required for the total oxidation of phenol. Under the irradiation of medium pressure light (300W) phenol was mineralized within 1h in the presence of Fe2+/zeolite 13X. The COD removal rate was enhanced in the presence of Fe2+/zeolite13X compared to that of Fe2+/silica gel or Fe2+/Al2O3. Analogous homogenous photo-Fenton reaction with equivalent Fe2+ was also carried out to evaluate the catalysis efficiency of Fe2+/zeolite 13X. Results showed that the COD removal rate was near to that of homogeneous Fenton, while heterogeneous Fe2+/zeolite 13X catalyst could be recycled.

  6. Fenton process for degradation of selected chlorinated aliphatic hydrocarbons exemplified by trichloroethylene, 1,1-dichloroethylene and chloroform

    Institute of Scientific and Technical Information of China (English)

    Zhimin QIANG; Weiwei BEN; ChinPao HUANG

    2008-01-01

    The degradation of selected chlorinated ali-phatic hydrocarbons (CAHs) exemplified by trichloroethy-lene (TCE), 1,1-dichloroethylene (DCE), and chloroform (CF) was investigated with Fenton oxidation process. The results indicate that the degradation rate was primarily affected by the chemical structures of organic contami-nants. Hydroxyl radicals (·OH) preferred to attack the organic contaminants with an electron-rich structure such as chlorinated alkenes (i.e., TCE and DCE). The dosing mode of Fenton's reagent, particularly of Fe2+, significantly affected the degradation efficiency of studied organic compound. A new "time-squared" kinetic model, C = Coexp(-kobst2), was developed to express the degrada-tion kinetics of selected CAHs. This model was applicable to TCE and DCE, but inapplicable to CF due to their varied reaction rate constants towards ·OH. Chloride release was monitored to examine the degree of dechlorina- tion during the oxidation of selected CAHs. TCE was more easily dechlorinated than DCE and CF. Dichloroacetic acid (DCAA) was identified as the major reaction intermediate in the oxidation of TCE, which could be completely removed as the reaction proceeded. No reaction intermedi- ates or byproducts were identified in the oxidation of DCE and CF. Based on the identified intermediate, the reaction mechanism of TCE with Fenton's reagent was proposed.

  7. 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.

  8. Fenton-like oxidation of 2,4-DCP in aqueous solution using iron-based nanoparticles as the heterogeneous catalyst.

    Science.gov (United States)

    Li, Renchao; Gao, Ying; Jin, Xiaoying; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravendra

    2015-01-15

    In this report, various iron-based nanoparticles (nZVI, n-Ni/Fe, n-Pd/Fe) were used for both heterogeneous Fenton oxidation of 2,4-dichlorophenol (2,4-DCP) and reductive dechlorination of 2,4-DCP in order to understand their roles in the Fenton oxidation and the reductive degradation of 2,4-DCP. The dechlorination efficiency of 2,4-DCP using nZVI, n-Ni/Fe, n-Fe/Pd and Fe(2)(+) was 6.48%, 6.80%, 15.95%, 5.02%, while Fenton oxidation efficiency of 2,4-DCP was 57.87%, 34.23%, 27.94%, 19.61% after 180 min, respectively. The new findings included a higher dechlorination using n-Fe/Pd due to Pd effective catalysis and the effective heterogeneous Fenton oxidation using nZVI depending on reductive dechlorination and heterogeneous Fenton oxidation occurs simultaneously. However, nZVI as the potential catalyst for heterogeneous Fenton was observed, and SEM, EDS and XRD demonstrate that change on the nZVI surface occurred due to the Fe(2+) leaching, and Total Organic Carbon (TOC) (30.71%) shows that 2,4-DCP was degraded. Furthermore, the experiment indicates that the pH values and concentration of 2,4-DCP significantly impacted on the heterogeneous Fenton oxidation of 2,4-DCP and the data fits well with the pseudo first-order kinetic model, which was a diffusion-controlled reaction. Finally, a possible mechanism for degradation of 2,4-DCP was proposed. PMID:25454429

  9. Fenton-like oxidation of 2,4-DCP in aqueous solution using iron-based nanoparticles as the heterogeneous catalyst.

    Science.gov (United States)

    Li, Renchao; Gao, Ying; Jin, Xiaoying; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravendra

    2015-01-15

    In this report, various iron-based nanoparticles (nZVI, n-Ni/Fe, n-Pd/Fe) were used for both heterogeneous Fenton oxidation of 2,4-dichlorophenol (2,4-DCP) and reductive dechlorination of 2,4-DCP in order to understand their roles in the Fenton oxidation and the reductive degradation of 2,4-DCP. The dechlorination efficiency of 2,4-DCP using nZVI, n-Ni/Fe, n-Fe/Pd and Fe(2)(+) was 6.48%, 6.80%, 15.95%, 5.02%, while Fenton oxidation efficiency of 2,4-DCP was 57.87%, 34.23%, 27.94%, 19.61% after 180 min, respectively. The new findings included a higher dechlorination using n-Fe/Pd due to Pd effective catalysis and the effective heterogeneous Fenton oxidation using nZVI depending on reductive dechlorination and heterogeneous Fenton oxidation occurs simultaneously. However, nZVI as the potential catalyst for heterogeneous Fenton was observed, and SEM, EDS and XRD demonstrate that change on the nZVI surface occurred due to the Fe(2+) leaching, and Total Organic Carbon (TOC) (30.71%) shows that 2,4-DCP was degraded. Furthermore, the experiment indicates that the pH values and concentration of 2,4-DCP significantly impacted on the heterogeneous Fenton oxidation of 2,4-DCP and the data fits well with the pseudo first-order kinetic model, which was a diffusion-controlled reaction. Finally, a possible mechanism for degradation of 2,4-DCP was proposed.

  10. The decontamination of bleaching effluent by pilot-scale solar Fenton process.

    Science.gov (United States)

    Wang, Zhaojiang; Chen, Kefu; Li, Jun; Mo, Lihuan

    2011-01-01

    A solar Fenton process was applied as post-treatment to selectively eliminate organic pollutants and toxicants in bleaching effluents of kraft pulp mills. Experiments were conducted to study the effect of system parameters (pH, initial concentration of H2O2, molar ratio of Fe2+/H2O2 and solar-UV irradiance) on the removals of chemical oxygen demand and colour. The results showed 92.8% of COD and 99.6% of colour were removed at pH 3.5, H2O2 30 mM/ L, Fe2+/H2O2 1:100, solar-UV irradiance 11070 mW/m2, reaction time 120 min. The first-order kinetic model was used to study the dependence of the reaction rate on solar-UV irradiance: a linear relationship was shown to exist between reaction rate constants and solar-UV irradiance. The results of gas chromatography mass spectrometry analysis showed that the toxicity of the bleaching effluents was mainly derived from the presence of mononuclear aromatics, polycyclic aromatic hydrocarbons and organochlorides, which were all degraded into harmless organic acids under the attack of hydroxyl radicals generated from the solar Fenton reaction. PMID:21879547

  11. Study on Treatability of Real Textile Wastewater by Electrochemically Generated  Fenton Reagent using Graphite Felt Cathode

    Directory of Open Access Journals (Sweden)

    Akbar Eslami

    2012-10-01

    Full Text Available Background and Objectives: Electro-Fenton process has been widely applied for dye removal from aqueous solution lately. Fenton's reagent is formed in the electrolysis medium through the simultaneous electrochemical reduction of O2 and Fe3+ to H2O2 and Fe2+ respectively on the cathode surface. In this paper, COD reduction potential and decolorization of real textile wastewater were evaluated by electrochemically generated Fenton reagent process. This wastewater mainly contains non-biodegradable acidic dyes, which are highly resistant against conventional oxidizing agents.Materials and Methods: Electro-Fenton process was carried out in an open and undivided cell in order to evaluate the removal of color and COD from real textile wastewater using graphite felt (cathode and Pt plate (anode at room temperature. The effects of current density, flow rate of air, electrolysis time, initial pH, and ferrous ion concentration were investigated for real textile wastewater.Results: The results showed that the optimal experimental conditions obtained in electrochemical studies were as follows: current density=4.8 mA cm-2, pH=3, flow rate of air=1.5L/min, Fe2+=3mM and reaction time=160 min. Under these conditions, COD removal and decolorization achieved were 63% and 77.2% respectively. Conclusion: According to the results achieved, electro-Fenton process can be used as a pretreatment for degradation of colored wastewater and refractory pollutants. Moreover, this feasible technology improves biodegradability of the textile wastewater.

  12. Evaluation of Electro-Fenton Process Performance for COD and Reactive Blue 19 Removal from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Mohammad Malakootian

    2013-02-01

    Full Text Available Background and Objectives: Synthetic dyes represent one of the largest groups of pollutants in wastewater of dying industries. Discharging these wastewaters into receiving streams not only affects the aesthetic but also reduces photosynthetic activity. Electrochemical advanced oxidation processes such as Electro-Fenton process are low operational and have high mineralization degree of pollutants. In this study, we investigated affective factors in this process to determine the optimum conditions for dye and COD removal from aqueous solutions containing Reactive Blue 19 dye.Materials and Methods: Synthetic samples containing Reactive Blue 19 dye were prepared by dissolving dye powder in double distilled water. and the the solution prepared was transferred into pilot electrochemical cell having two anode and cathode electrode made of iron and carbon. Electro-Fenton process was began by adding of Fe2+ ions and establishing electrical potential difference. After testing and at specified time intervals, each sample was collected from the pilot cell, and process performance was evaluated through measuring dye concentration and COD. Results: Based on the results obtained, optimum conditions of Electro-Fenton process for dye and COD removal was determined. Accordingly, potential difference of 20 volt for dye concentration up to 100 mg/L and potential difference of 30 volt for dye concentration of more than 200 mg/L, reaction time 60 minutes, 0.5 mg/L of Fe2+ concentration and suitable pH for the maximum dye removal efficiency equaled 4 respectively. Under such conditions, the dye and COD removal was 100 and 95% respectively.Conclusion: Based on the results obtained, it was revealed that Electro-Fenton process has significant ability in not only dye removal but also in COD removal. Accordingly, it was found that the effective parameters in Electro-Fenton process for removal Reactive Blue19 dye are electric potential difference, concentration of iron ions

  13. Heterogeneous photo-Fenton oxidation with natural clays for phenol and tyrosol remediation

    Directory of Open Access Journals (Sweden)

    Djeffal L.

    2013-09-01

    Full Text Available Due to their excellent properties, clays have been widely used in several applications, particularly in catalysis. In this paper, three clays were used as heterogeneous photo-Fenton catalysts for phenol and tyrosol oxidations. Particular attention was given to the effect of the main operating conditions on the process performance. A total conversion was obtained for both organic pollutants with studied catalysts in 20 minutes reaction. For phenol, a total organic carbon (TOC conversion of 93% was obtained using sieved and calcined smectite clay. The TOC conversion was 60% for tyrosol with the same catalyst. Clays were characterized by chemical analysis, BET, XRD, TPR and SEM.

  14. Treatment of mature landfill leachate by chemical precipitation and Fenton advanced oxidation process

    OpenAIRE

    Nemat Alah Jaafarzadeh Haghighi Fard; Sahand Jorfi; Mehdi Ahmadi; Samaneh Mirali; Raheleh Kujlu

    2016-01-01

    Background: Mature landfill leachate is a complicated mixture which is resistant to biological treatment processes. The treatment of mature landfill leachate by struvite precipitation and Fenton oxidation was the main objective of the current research. Methods: Struvite with the phosphate/ammonia/magnesium molar ratio of 1/1/1.05 was considered during all experiments. Five initial pHs of 3, 4, 5, 6, and 7, four different H2O2/Fe mass ratios of 50, 100, 200, and 400, and reaction times of ...

  15. Treatment of Effluent from a Factory of Paints Using Solar Photo-Fenton Process

    OpenAIRE

    Alam Gustavo Trovó; Oswaldo Gomes; Antonio Eduardo da Hora Machado

    2013-01-01

    We evaluated the use of Fenton reactions induced by solar radiation in the treatment of effluent from a factory of paints for buildings, after prior removal of the suspended solids. The increase of H2O2 concentration from 100 to 2500 mg L−1 for a [Fe2+] = 105 mg L−1 contributed to the reduction of DOC, COD, and toxicity. Our best results were achieved using 1600 mg L−1 H2O2, with 90% of DOC and COD removal and a complete removal of the toxicity with respect to Artemia salina. Additionally, th...

  16. FePt nanoparticles as heterogeneous Fenton-like catalysts for hydrogen peroxide decomposition and the decolorization of methylene blue

    International Nuclear Information System (INIS)

    In this report, we show that superparamagnetic FePt nanoparticles are highly efficient heterogeneous Fenton-like oxidation catalysts and compare their performance to Fe3O4 nanoparticles using methylene blue dye as the target organic. X-ray diffraction and transmission electron microscopy were used to characterize the structure of the nanoparticles, a superconducting quantum interference device confirmed the magnetic properties, X-ray photoelectron spectroscopy characterized the chemical state of Fe in the nanoparticles, and ultraviolet–visible spectroscopy was used to monitor the heterogeneous Fenton-like reaction. The pseudo-first-order reaction rate constant for 5 ppm FePt nanoparticles was approximately 100 times faster than for 5 ppm Fe3O4 nanoparticles under otherwise identical conditions. Furthermore, a concentration of 2,500 ppm Fe3O4 was required to achieve the same reaction extent as 5 ppm FePt. Thus, FePt nanoparticles are more efficient heterogeneous Fenton-like catalyst for H2O2 decomposition and methylene blue decolorization than Fe3O4. Further, as both types of nanoparticles are superparamagnetic, they can easily be reclaimed and reused.

  17. Degradation kinetics and mechanisms of phenolin photo-Fenton process

    Institute of Scientific and Technical Information of China (English)

    何锋; 雷乐成

    2004-01-01

    Phenol degradation in photochemically enhanced Fenton process was investigated in this work. UV-VIS spectra of phenol degradation showed the difference between photo-Fenton process and UV/H2O2, which is a typical hydroxyl radical process. A possible pathway diagram for phenol degradation in photo-Fenton process was proposed, and a mathematical model for chemical oxygen demand (COD) removal was developed. Operating parameters such as dosage of H2O2 and ferrous ions, pH, suitable carrier gas were found to impact the removal of COD significantly. The results and analysis of kinetic parameters calculated from the kinetic model showed that complex degradation of phenol was the main pathway for removal of COD: while hydroxyl radicals acted weakly in the photo-Fenton degradation of phenol.

  18. Fenton coupled with nanofiltration for elimination of Bisphenol A

    OpenAIRE

    I. Escalona; Fortuny Sanromá, Agustín; Stueber, Frank; Bengoa, Christophe José; Fabregat Llangotera, Azael; Font Capafons, Josep

    2014-01-01

    Bisphenol A (BPA) is a typical Endocrine Disrupting Chemical (EDC), which is potentially harmful during wastewater reclamation. In this study, its degradation during Fenton's process under different operational conditions was investigated in combination with subsequent nanofiltration of low concentration remnant BPA and compounds derived from oxidation. The results indicate that BPA could be degraded efficiently in aqueous phase by Fenton, even at very low hydrogen peroxide doses. The treatme...

  19. Treatment of pharmaceutical wastewater containing recalcitrant compounds in a Fenton-coagulation process

    Institute of Scientific and Technical Information of China (English)

    XING Mei-yan; DENG Can; Bukuru Godefroid; YANG Jian

    2006-01-01

    The advanced treatment using integrated Fenton's reaction and coagulation process was investigated in this study. Before the advancement, the pharmaceutical wastewater containing lincomycin hydrochloride was pretreated by UASB (upflow anaerobic sludge bed) and a SBR (sequencing batch reactor) process. The residual recalcitrant compounds, measured by gas chromatographymass spectrometry (GC-MS), mainly consisted of alcohols, phenols, and nitrogenous and sulfur compounds. The experimental results indicated that when the Fenton' s reaction was conducted at pH=3.0, H2O2/CODCr = 0.27, H2O2/Fe2+ = 3:1 and 30 min of reaction time,and the coagulation process operated at a sulfate aluminum concentration of 800 mg/L and pH value of 5.0, the color and COD in the wastewater decreased by 94% and 73%, respectively; with a finale COD concentration of 267 mg/L and color level of 40 units,meeting the secondary standard of GB8978-1996 for industrial wastewater.

  20. Kinetics of acetaminophen degradation by Fenton oxidation in a fluidized-bed reactor.

    Science.gov (United States)

    de Luna, Mark Daniel G; Briones, Rowena M; Su, Chia-Chi; Lu, Ming-Chun

    2013-01-01

    Acetaminophen (ACT), an analgesic and antipyretic substance, is one of the most commonly detected pharmaceutical compound in surface waters and wastewaters. In this study, fluidized-bed Fenton (FB-Fenton) was used to decompose ACT into its final degradation products. The 1.45-L cylindrical glass reactor had inlet, outlet and recirculating sections. SiO(2) carrier particles were supported by glass beads with 2-4 mm in diameter. ACT concentration was determined by high performance liquid chromatography (HPLC). During the first 40 min of reaction, a fast initial ACT removal was observed and the "two-stage" ACT degradation conformed to a pseudo reaction kinetics. The effects of ferrous ion dosage and [Fe(2+)]/[H(2)O(2)] (FH ratio) were integrated into the derived pseudo second-order kinetic model. A reaction pathway was proposed based on the intermediates detected through SPME/GC-MS. The aromatic intermediates identified were hydroquinone, benzaldehydes and benzoic acids while the non-aromatic substances include alcohols, ketones, aldehydes and carboxylic acids. Rapid initial ACT degradation rate can be accomplished by high initial ferrous ion concentration and/or low FH ratio.

  1. A study of catalytic behaviour of aromatic additives on the photo-Fenton degradation of phenol red

    Indian Academy of Sciences (India)

    Abhilasha Jain; Savitri Lodha; P B Punjabi; V K Sharma; Suresh C Ameta

    2009-11-01

    The present study describes the photochemical degradation of phenol-red using photo-Fenton reaction. The progress of the reaction has been monitored spectrophotometrically. The effect of various organic additives e.g. hydroquinone, resorcinol and catechol on the rate of photodegradation has been observed. The effect of variation of various parameters such as pH, concentration of dye, Fe3+ ion and additives, amount of H2O2, and light intensity on the rate of photodegradation was also observed. A tentative mechanism of the reaction has been proposed.

  2. The Study of Fenton Performance in Removal of  Cyanide from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Somayeh Golbaz

    2013-02-01

    Full Text Available Background and Objectives: Cyanide is a toxic pollutant existing in the various industrial effluents such as iron and steel, coal mining, non-ferrous metals manufacturing and metal plating. Its presence in water resources and wastewater, as serious hazardous substances leads to undesirable effects on both the environment and human. Thus, its concentration control is essential for human health. The main goal of this study was to evaluate Fenton process efficiency in cyanide removal from aqueous solution.Materials and Methods: This is an experimental study Conducted at Lab scale in a batch system. We investigated effect of different variables including; pH, mole ratio of Fe2+/ H2O2, contact time, and initial concentration of cyanide. Data were analyzed using Excel software.Results: We found that cyanide with initial concentrations of 0.4 mM/L was reduced by 92 %. This removal result was related to oxidizing agent of hydroxyl radicals under optimum conditions including; pH = 4, molar ratio Fe2+/ H2O2= 0.046 (Fe2+=0.27 mM/L after 6o min reaction time. An increase in reaction time was not improved cyanide removal efficiency. Moreover, the Fenton process efficiency in cyanide removal decreased from 92 to 60 %, by increasing the initial cyanide concentration from 0.4 to 0.6 mM/L.Conclusion: It can be concluded that Fenton oxidation Process can be considered as a suitable alternative for cyanide removal to achieve environmental standards.

  3. 二甲基亚砜捕获Fenton体系生成的·OH的研究%Investigation on Scavenging of Fenton Produced Hydroxyl Radical by Dimethyl Sulfoxide

    Institute of Scientific and Technical Information of China (English)

    陆彬

    2012-01-01

    Fenton体系是H2O2与Fe(II)反应产生.OH的过程。本文主要研究了二甲基亚砜对Fenton体系产生的.OH的捕获,通过分析产物HCHO的浓度,确定.OH的生成量。同时,建立了DMSO捕获Fenton体系产.OH过程的化学反应模型,考察了DMSO初始浓度、pH值对Fenton体系的影响。结果表明DMSO浓度达到246 mmol/L时能够基本完全捕获Fenton体系所产生的.OH;pH值小于5时,Fenton体系受到H+激发释放较多的.OH,pH值不大于5时,H+对Fenton体系的激发能力不足。%Fenton was a reaction between H2O2 with Fe(II) in solution,which could produce ·OH radical.The scavenging of hydroxyl radical produced from Fenton reaction using dimethyl sulfoxide(DMSO) was mainly investigated.Through analysis of the generation of the intermediate by-product of HCHO,the amount of produced hydroxyl radical could be estimated.Besides,the chemical reaction modeling of the reaction between DMSO with Fenton reagents was also performed to investigate the effects of DMSO initial concentration and solution pH on production of hydroxyl radical.The results were that ·OH was completely scavenged by 246 mmol/L of DMSO,when pH5,the oxidation potential of Fenton system was enhanced through increasing H+,and when pH5,the oxidation potential of Fenton system was weakened.

  4. Degradation of Phenol with Fenton-like Treatment by Using Heterogeneous Catalyst (Modified Iron Oxide) and Hydrogen Peroxide

    International Nuclear Information System (INIS)

    Goethite, hematite, magnetite and synthesized iron oxide are used as catalysts for Fenton-type oxidation of phenol. The synthesized iron oxides were characterized by X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The catalytic activity of these materials is classified according to the observed rate of phenol oxidation. The effectiveness of the catalysts followed the sequence: ferrous ion > synthesized iron oxide >> magnetite hematite > goethite. According to these results, the most effective iron oxide catalyst had the structure similar to natural hematite. The surface oxidation state of the catalyst was between magnetite and hematite (+2.5 ∼ +3.0). Phenol degraded completely in 40 min at neutral pH (pH = 7). Soluble ferric and ferrous ions were not detected in the filtrate from Fenton reaction solution by AAS. The formation of hydroxyl radicals was confirmed by EPR

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

    International Nuclear Information System (INIS)

    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; Fe3−xNbxO4 (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 Fe2+ cations, and increase in adsorption capacity of the samples due to larger surface area. The MB degradation through Fe2.79Nb0.19O4/H2O2 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 decrease in their catalytic efficiency. The results proved

  6. 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

  7. Development of MCM-41 based catalysts for the photo-Fenton's degradation of dye pollutants

    Science.gov (United States)

    Lam, Leung Yuk Frank

    The continuous advancement in most industries has resulted in serious water pollution problems. The industrial effluents contain a variety of highly toxic organics such as dye pollutants. Numerous processes have been demonstrated for treating such pollutants. Among them, photo-Fenton's reaction is effective for organic mineralization by hydroxyl radicals generated from the Fenton's reagents (Fe2+ and H2O2). However, there is a drawback in that it requires a separation system to recover the homogeneous ferrous ion in the treated wastewater. In this research, new heterogeneous Fenton's catalysts are developed to solve such a problem and to achieve an efficient mineralization of dye pollutants. Two methods for catalyst preparation, including sol-gel hydrothermal (SG) and metal-organic chemical vapor deposition (MOCVD) techniques, were studied in this work. For SG-prepared catalysts, the iron element was successfully doped into the MCM-41 structure. These catalysts demonstrated a good catalytic efficiency but leaching of metal ions from the developed catalyst was found. In the MOCVD technique, a rotated tubular reactor system was developed to synthesize Fe/MCM-41 catalyst with uniform metal dispersion. It was found that using oxygen as a carrier gas during metal deposition was able to increase the stability of the deposited metal. In degradation of a model dye pollutant, Orange II, a total of 85% TOC mineralization was achieved at pH 3. A disadvantage of using Fe/MCM-41 was the reduced efficiency at higher pH. Cu/MCM-41 was thus developed and showed better catalytic activities than Fe/MCM-41 at neutral pH. Having the specific catalytic properties of Fe/MCM-41 and Cu/MCM-41, bimetallic (Fe+Cu) catalysts supported on MCM-41 were developed which show better activities in the Orange II mineralization than those monometallic (Fe or Cu) catalysts. The preparation conditions of the catalysts were experimentally optimized. The effects of catalyst dosage, metal loading

  8. Efficient degradation of Acid Orange 7 in aqueous solution by iron ore tailing Fenton-like process.

    Science.gov (United States)

    Zheng, Jianming; Gao, Zhanqi; He, Huan; Yang, Shaogui; Sun, Cheng

    2016-05-01

    An effective method based on iron ore tailing Fenton-like process was studied for removing an azo dye, Acid Orange 7 (AO7) in aqueous solution. Five tailings were characterized by X-ray fluorescence spectroscope (XFS), Brunner-Emmet-Teller (BET) measurement, and Scanning Electron Microscope (SEM). The result of XFS showed that Fe, Si and Ca were the most abundant elements and some toxic heavy metals were also present in the studied tailings. The result of BET analysis indicated that the studied tailings had very low surface areas (0.64-5.68 m(2) g(-1)). The degradation efficiencies of AO7 were positively correlated with the content of iron oxide and cupric oxide, and not related with the BET surface area of the tailings. The co-existing metal elements, particularly Cu, might accelerate the heterogeneous Fenton-like reaction. The effects of other parameters on heterogeneous Fenton-like degradation of AO7 by a converter slag iron tailing (tailing E) which contains highest iron oxide were also investigated. The tailing could be reused 10 times without significant decrease of the catalytic capacity. Very low amount of iron species and almost undetectable toxic elements were leached in the catalytic degradation of AO7 by the tailing E. The reaction products were identified by gas chromatography-mass spectrometry and a possible pathway of AO7 degradation was proposed. This study not only provides an effective method for removing azo dyes in polluted water by employing waste tailings as Fenton-like catalysts, but also uses waste tailings as the secondary resource. PMID:26891355

  9. Municipal Leachate Treatment by Fenton Process: Effect of Some Variable and Kinetics

    Directory of Open Access Journals (Sweden)

    Mohammad Ahmadian

    2013-01-01

    Full Text Available Due to complex composition of leachate, the comprehensive leachate treatment methods have been not demonstrated. Moreover, the improper management of leachate can lead to many environmental problems. The aim of this study was application of Fenton process for decreasing the major pollutants of landfill leachate on Kermanshah city. The leachate was collected from Kermanshah landfill site and treated by Fenton process. The effect of various parameters including solution pH, Fe2+ and H2O2 dosage, Fe2+/H2O2 molar ratio, and reaction time was investigated. The result showed that with increasing Fe2+ and H2O2 dosage, Fe2+/H2O2 molar ratio, and reaction time, the COD, TOC, TSS, and color removal increased. The maximum COD, TOC, TSS, and color removal were obtained at low pH (pH: 3. The kinetic data were analyzed in term of zero-order, first-order, and second-order expressions. First-order kinetic model described the removal of COD, TOC, TSS, and color from leachate better than two other kinetic models. In spite of extremely difficulty of leachate treatment, the previous results seem rather encouraging on the application of Fenton’s oxidation.

  10. Combined treatment of retting flax wastewater using Fenton oxidation and granular activated carbon

    Directory of Open Access Journals (Sweden)

    Sohair I. Abou-Elela

    2016-07-01

    Full Text Available The process of retting flax produces a huge amount of wastewater which is characterized with bad unpleasant smell and high concentration of organic materials. Treatment of such waste had always been difficult because of the presence of refractory organic pollutants such as lignin. In this study, treatment of retting wastewater was carried out using combined system of Fenton oxidation process followed by adsorption on granular activated carbon (GAC. The effects of operating condition on Fenton oxidation process such as hydrogen peroxide and iron concentration were investigated. In addition, kinetic study of the adsorption process was elaborated. The obtained results indicated that degradation of organic matters follows a pseudo-first order reaction with regression coefficient of 0.98. The kinetic model suggested that the rate of reaction was highly affected by the concentration of hydrogen peroxide. Moreover, the results indicated that the treatment module was very efficient in removing the organic and inorganic pollutants. The average percentage removal of chemical oxygen demand (COD, total suspended solid (TSS, oil, and grease was 98.60%, 86.60%, and 94.22% with residual values of 44, 20, and 5 mg/L, respectively. The treated effluent was complying with the National Regulatory Standards for wastewater discharge into surface water or reuse in the retting process.

  11. Selective and sensitive colorimetric detection of stringent alarmone ppGpp with Fenton-like reagent.

    Science.gov (United States)

    Zheng, Lin Ling; Huang, Cheng Zhi

    2014-12-01

    Stringent alarmone, namely, guanosine 3'-diphosphate-5'-diphosphate (ppGpp), is a global regulator that plays a critical role in the survival, growth, metabolism, and many other vital processes of microorganisms. Because of its structural similarity to normal nucleotides, it is also a challenge for the selective and sensitive detection of ppGpp nowadays. Herein, we developed a colorimetric method for the selective detection of ppGpp by inhibiting the redox reaction between Fenton-like reagent (composed of Fe(3+) and H2O2) with 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS). Owing to the strong coordination affinity between ppGpp and Fe(3+), the chromogenic reaction between ABTS and Fenton-like reagent, occurred in aqueous medium at 37 °C and resulted in a bluish-green solution, which was inhibited with the addition of ppGpp. This phenomenon forms the basis for the colorimetric detection of ppGpp, with a detection limit of 0.19 μM and good selectivity for ppGpp over other nucleotides and anions. Furthermore, the results could be visualized by the naked eye, and the sensitivity of the naked-eye observation could even be further improved with the aid of the introduction of a background color.

  12. 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.

  13. Degradation of Amaranth azo dye in water by heterogeneous photo-Fenton process using FeWO4 catalyst prepared by microwave irradiation.

    Science.gov (United States)

    da Cruz Severo, Eric; Anchieta, Chayene Gonçalves; Foletto, Vitória Segabinazzi; Kuhn, Raquel Cristine; Collazzo, Gabriela Carvalho; Mazutti, Marcio Antonio; Foletto, Edson Luiz

    2016-01-01

    FeWO4 particles were synthesized by a simple, rapid and facile microwave technique and their catalytic properties in heterogeneous photo-Fenton reaction were evaluated. This material was employed in the degradation of Amaranth azo dye. Individual and interactive effects of operational parameters such as pH, dye concentration and H2O2 dosage on the decolorization efficiency of Amaranth dye were evaluated by 2(3) central composite design. According to characterization techniques, a porous material and a well-crystallized phase of FeWO4 oxide were obtained. Regarding the photo-Fenton reaction assays, up to 97% color and 58% organic carbon removal were achieved in the best experimental conditions. In addition, the photo-Fenton process maintained treatment efficiency over five catalyst reuse cycles to indicate the durability of the FeWO4 catalyst. In summary, the results reveal that the synthesized FeWO4 material is a promising catalyst for wastewater treatment by heterogeneous photo-Fenton process.

  14. Degradation of Amaranth azo dye in water by heterogeneous photo-Fenton process using FeWO4 catalyst prepared by microwave irradiation.

    Science.gov (United States)

    da Cruz Severo, Eric; Anchieta, Chayene Gonçalves; Foletto, Vitória Segabinazzi; Kuhn, Raquel Cristine; Collazzo, Gabriela Carvalho; Mazutti, Marcio Antonio; Foletto, Edson Luiz

    2016-01-01

    FeWO4 particles were synthesized by a simple, rapid and facile microwave technique and their catalytic properties in heterogeneous photo-Fenton reaction were evaluated. This material was employed in the degradation of Amaranth azo dye. Individual and interactive effects of operational parameters such as pH, dye concentration and H2O2 dosage on the decolorization efficiency of Amaranth dye were evaluated by 2(3) central composite design. According to characterization techniques, a porous material and a well-crystallized phase of FeWO4 oxide were obtained. Regarding the photo-Fenton reaction assays, up to 97% color and 58% organic carbon removal were achieved in the best experimental conditions. In addition, the photo-Fenton process maintained treatment efficiency over five catalyst reuse cycles to indicate the durability of the FeWO4 catalyst. In summary, the results reveal that the synthesized FeWO4 material is a promising catalyst for wastewater treatment by heterogeneous photo-Fenton process. PMID:26744938

  15. 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. PMID:27336472

  16. Optimization of Fenton pretreatment for 2-chlorophenol solution

    Institute of Scientific and Technical Information of China (English)

    贺仲兵; 刘云国; 肖玉

    2013-01-01

    Fenton oxidation was used as the pretreatment of 2-chlorophenol wastewater with the objective of dechlorination, as it was considered that after breakage of aryl—Cl bond, the generated intermediates may be easily biodegraded. Hence, the optimization of pH and the low Fenton reagent doses for dechlorination was investigated. More than 99% dechlorination is obtained at the optimal pH 4 and the Fenton reagent doses of 86 mmol/L H2 O2 and 2.87 mmol/L Fe2+. The corresponding 2-chlorophenol is degraded completely, 80.02% COD is also removed, and the biodegradability, evaluated in terms of the BOD5 /COD ratio, is increased up to 0.41. To test the effect of this pretreatment, the pretreated 2-chlorophenol wastewater was fed to a sequencing batch reactor(SBR). The results show that complete mineralization is achieved. It is demonstrated that, for the treatment of recalcitrant compounds like 2-chlorophenol, the Fenton pretreatment could be quite effective and economical for enhancing the biodegradability in a Fenton-biological coupled system.

  17. Fenton oxidation and combined Fenton-microbial treatment for remediation of crude oil contaminated soil in Assam - India.

    Science.gov (United States)

    Buragohain, Surabhi; Deka, Dibakar Chandra; Devi, Arundhuti

    2013-10-01

    The study is aimed at the remediation of soil spiked with crude oil (5%) by employing Fenton oxidation, biological treatment and combined Fenton-biological treatment. A spiked concentration of 5% crude oil was selected on the basis of contamination levels of 0-5% as found in the soil of upper Assam oil fields (India). The degradation of the aliphatic fraction (C14-C28) of the crude oil was investigated by gas chromatography. Fenton oxidation was carried out at different pH (3 to 8) in a laboratory batch reactor and maximum oxidative degradation was observed at pH 3-5. At pH 3, single Fenton oxidation resulted in 36 and 57% degradation in 5 and 10 days respectively. Biological treatment (with Fusarium solani) and combined Fenton-biological treatment were carried out with a one month incubation period. Biological treatment alone brought about 61% degradation of the crude oil while the combined process could achieve as much as 75% degradation of the aliphatic fractions of the crude oil. PMID:24056615

  18. Fenton oxidation and combined Fenton-microbial treatment for remediation of crude oil contaminated soil in Assam - India.

    Science.gov (United States)

    Buragohain, Surabhi; Deka, Dibakar Chandra; Devi, Arundhuti

    2013-10-01

    The study is aimed at the remediation of soil spiked with crude oil (5%) by employing Fenton oxidation, biological treatment and combined Fenton-biological treatment. A spiked concentration of 5% crude oil was selected on the basis of contamination levels of 0-5% as found in the soil of upper Assam oil fields (India). The degradation of the aliphatic fraction (C14-C28) of the crude oil was investigated by gas chromatography. Fenton oxidation was carried out at different pH (3 to 8) in a laboratory batch reactor and maximum oxidative degradation was observed at pH 3-5. At pH 3, single Fenton oxidation resulted in 36 and 57% degradation in 5 and 10 days respectively. Biological treatment (with Fusarium solani) and combined Fenton-biological treatment were carried out with a one month incubation period. Biological treatment alone brought about 61% degradation of the crude oil while the combined process could achieve as much as 75% degradation of the aliphatic fractions of the crude oil.

  19. Degradation of disperse azo dyes from waters by solar photoelectro-Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Salazar, Ricardo [Departamento de Ciencias del Ambiente, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACh, Casilla 40, Correo 33, Santiago (Chile); Garcia-Segura, Sergi [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); Ureta-Zanartu, M.S. [Departamento de Ciencias del Ambiente, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACh, Casilla 40, Correo 33, Santiago (Chile); 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)

    2011-07-15

    Highlights: > Reactive azo dyes are almost totally mineralized by solar photoelectro-Fenton. > The process yields high current efficiencies and low energy consumptions. > It is more efficient and inexpensive by decreasing current and increasing dye content. > Nitrate ions are the main inorganic ions released during the mineralization process. > The process is also effective for the remediation of textile dyeing solutions. - Abstract: Solutions of the azo dyes Disperse Red 1 (DR1) and Disperse Yellow 3 (DY3), commonly used in the Chilean textile industry, in 0.1 mol dm{sup -3} Na{sub 2}SO{sub 4} and 0.5 mmol dm{sup -3} Fe{sup 2+} of pH 3.0 were comparatively degraded by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF) using a 2.5 dm{sup 3} recirculation flow plant containing a BDD/air-diffusion cell coupled with a solar photoreactor. Organics were oxidized in EF with hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between electrogenerated H{sub 2}O{sub 2} and added Fe{sup 2+}. The oxidizing power of SPEF was enhanced by the additional production of hydroxyl radicals from the photolysis of Fe(III) hydrated species and the photodecomposition of Fe(III) complexes with intermediates by UV light of solar irradiation. Total decolorization, complete dye removal and almost overall mineralization for both dye solutions were only achieved using the most potent SPEF process, yielding higher current efficiencies and lower energy consumptions than EF. Final carboxylic acids like pyruvic, acetic, oxalic and oxamic were detected during the SPEF treatments. NO{sub 3}{sup -} ion was released as inorganic ion. The use of a solution pH of 2.0-3.0 at 50 mA cm{sup -2} was found preferable for SPEF. Synthetic textile dyeing solutions containing the dyes were treated under these conditions yielding lower decolorization rate, slower dye removal and smaller mineralization degree than only using 0.1 mol dm{sup -3} Na

  20. Investigation of acid red 88 oxidation in water by means of electro-Fenton method for water purification.

    Science.gov (United States)

    Özcan, Ali; Gençten, Metin

    2016-03-01

    In this study, electro-Fenton method was applied to acid red 88 (AR88) containing aqueous solutions for the removal of it from water. The mineralization of AR88 has been achieved by oxidation with hydroxyl radicals. These radicals were produced simultaneously by the electro-Fenton method using an electrochemical cell including a carbon felt cathode and a platinum anode. Applied current and concentrations of catalyst and supporting electrolyte were optimized to obtain the best effective parameters of 500 mA, 0.1 mM and 75 mM, respectively. The absolute rate constant for the oxidation reaction of AR88 with hydroxyl radical was determined as (1.57 ± 0.06) x 10(10) M(-1) s(-1). Total organic carbon (TOC) analysis was performed to determine whether the organics were converted to carbon dioxide or not. A two-hour electrolysis at 500 mA is enough to remove 87% of initial TOC values of 0.25 mM AR88 solution. Electro-Fenton treatment of AR88 led to the formation of five aromatic intermediates, five short-chain carboxylic acids and three inorganic ions. Identified intermediates and complete mineralization of AR88 allowed us to propose a mineralization pathway for first time in the literature.

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

    International Nuclear Information System (INIS)

    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. Bi2WO6 nanoplates deposited on FTO glass (Bi2WO6/FTO) and Fe-Fe2O3 core–shell nanowires supported on activated carbon fiber (Fe-Fe2O3/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 H2O2 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 H2O2 and the subsequent Fenton reaction on the cathode during the PEC/EF process.

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

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Xing [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Ai, Zhihui, E-mail: jennifer.ai@mail.ccnu.edu.cn [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Zhang, Lizhi, E-mail: zhanglz@mail.ccnu.edu.cn [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Coupling PEC and EF oxidation significantly improves pollutant degradation efficiency. Black-Right-Pointing-Pointer The degradation of the PEC/EF system was increased by 154%. Black-Right-Pointing-Pointer 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{sub 2}WO{sub 6} nanoplates deposited on FTO glass (Bi{sub 2}WO{sub 6}/FTO) and Fe-Fe{sub 2}O{sub 3} core-shell nanowires supported on activated carbon fiber (Fe-Fe{sub 2}O{sub 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{sub 2}O{sub 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{sub 2}O{sub 2} and the subsequent Fenton reaction on the cathode during the PEC/EF process.

  3. Monitoring ecotoxicity of disperse red 1 dye during photo-Fenton degradation.

    Science.gov (United States)

    da Silva Leite, Laís; de Souza Maselli, Bianca; de Aragão Umbuzeiro, Gisela; Pupo Nogueira, Raquel F

    2016-04-01

    The present work assessed the ecotoxicity of the commercially available form of the azo dye Disperse Red 1 (DR1) and the main degradation products generated during photo-Fenton degradation. The acute toxicity tests with the microcrustacean Daphnia similis showed that toxicity increased after 10 min of treatment, when 35% of the original concentration of the dye has been degraded but without decrease in total organic carbon concentration (TOC). The increase of toxicity was a consequence of generation of degradation products of higher toxicity than DR1, which achieved maximum concentration after 10 min reaction. The structures identified using LC/MS indicated that most of the intermediates were formed after addition of hydroxyl radical to benzenic ring but the cleavage of azo bond was also observed. The intermediates were further degraded and toxicity was then reduced to non toxic levels after 45 min experiment, when 98% of the initial concentration of DR1 was degraded and mineralization achieved 55%. The results of this study showed that the textile dye DR1 can be degraded by photo-Fenton process with removal of acute toxicity to D. similis even with incomplete mineralization.

  4. A mechanistic kinetic model for phenol degradation by the Fenton process

    International Nuclear Information System (INIS)

    The objective of this paper is to develop and validate a mechanistic model for the degradation of phenol by the Fenton process. Experiments were performed in semi-batch operation, in which phenol, catechol and hydroquinone concentrations were measured. Using the methodology described in Pontes and Pinto [R.F.F. Pontes, J.M. Pinto, Analysis of integrated kinetic and flow models for anaerobic digesters, Chemical Engineering Journal 122 (1-2) (2006) 65-80], a stoichiometric model was first developed, with 53 reactions and 26 compounds, followed by the corresponding kinetic model. Sensitivity analysis was performed to determine the most influential kinetic parameters of the model that were estimated with the obtained experimental results. The adjusted model was used to analyze the impact of the initial concentration and flow rate of reactants on the efficiency of the Fenton process to degrade phenol. Moreover, the model was applied to evaluate the treatment cost of wastewater contaminated with phenol in order to meet environmental standards.

  5. Fenton+MnO2+A/O组合工艺处理过氧化甲乙酮生产废水%Treatment of methyIethyI ketone peroxide processing wastewater by combined process,Fenton+MnO2+A/O

    Institute of Scientific and Technical Information of China (English)

    宋勇; 段钧元

    2016-01-01

    利用Fenton+MnO2+A/O组合工艺处理过氧化甲乙酮生产废水。在Fenton+MnO2预处理阶段对影响废水COD去除率的主要因素进行了考察,得到反应的最佳条件:pH=2.7,30%H2O2投加量为0.1 L/L,FeSO4·7H2O投加量为5 g/L,MnO2投加量为8 g/L,MnO2氧化反应时间为45 min。废水经Fenton+MnO2氧化预处理后可生化性由0.14提高到了0.25左右。废水经Fenton+MnO2+A/O组合工艺处理后,出水COD稳定低于500 mg/L。%The combined process,Fenton+MnO2+A/O has been used for treating methylethyl ketone peroxide proces-sing wastewater. The key factors affecting the wastewater COD removing rate in the stage of Fenton+MnO2 pretreat-ment are investigated. The results show that the optimum conditions are as follows:the pH is 2.7,dosage of 30%of H2O2 0.1 L/L,dosage of FeSO4·7H2O 5 g/L,dosage of MnO2 8 g/L,and MnO2 oxidation reaction time 45 min. After the wastewater has been pretreated by Fenton+MnO2 oxidation process,its biodegradability can be improved from 0.14 to about 0.25. After the wastewater has been treated by Fenton+MnO2+A/O process,the effluent COD is stably lower than 500 mg/L.

  6. Water quality in the vicinity of Fenton Hill, 1987 and 1988. [Fenton Hill site

    Energy Technology Data Exchange (ETDEWEB)

    Purtymun, W.D.; Ferenbaugh, R.W.; Maes, M.N.; Williams, M.C.

    1991-03-01

    Water-quality data have been collected since 1974 from established surface- and ground-water stations at, and in the vicinity of, Fenton Hill (site of the Laboratory's Hot Dry Rock Geothermal Project). The site is located on the southwest edge of the Valles Caldera in the Jemez Mountains. To determine the chemical quality of water, data were collected in 1987 and 1988 from 13 surface-water stations and 19 ground-water stations. The classification of the water quality is made on the basis of predominated ions and total dissolved solids. There are four classifications of surface water (sodium and chloride, calcium and bicarbonate, calcium and sulfate, and sodium and bicarbonate) and three classifications of ground water (sodium and chloride, calcium and bicarbonate, and sodium and bicarbonate). Variations in the chemical quality of the surface and ground water in 1987 and 1988 are apparent when data are compared with each other and with previous analyses. These variations are not considered significant, as they are in the range of normal seasonal changes. Cumulative production since 1976 from the supply well at Fenton Hill has been about 63 {times} 10{sup 6} gal, with a decline in the water level of the well of about 14 ft, or about 1.4 ft/yr. The aquifer penetrated by the well is still capable of reliable supply to the site for a number of years, based on past production. The quality of water from the well has deteriorated slightly; however, the water quality is in compliance with drinking water standards. The effects of discharge from the storage ponds into an adjacent canyon have been monitored by trace metal analyses of vegetation and soil. The study indicates minimal effects, which will be undetectable in a few years if there are no further releases of effluents into the canyon. 19 refs., 6 figs., 3 tabs.

  7. A parametric study on the decolorization and mineralization of C.I. Reactive Red 141 in water by heterogeneous Fenton-like oxidation over FeZSM-5 zeolite

    OpenAIRE

    Yaman, Ceyda; GÜNDÜZ*, Gönül

    2015-01-01

    In this study, the heterogeneous Fenton-like degradation of Reactive Red 141 (RR141) in water was investigated over iron containing ZSM-5 zeolite (Si/Al = 42) prepared by ion-exchange (FeZSM-5 (42)). The catalyst was characterized by XRD, SEM, FTIR, TPR, and ICP-AES measurements. The effects of the initial concentrations of the dye and H2O2, the initial pH of the solution, catalyst loading, and the reaction temperature were investigated on heterogeneous Fenton-like degradation of RR141. The r...

  8. 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

  9. Fenton Processes as an Alternative to the Removal of Endocrine Disruptors and other Environmental Pollutants [Processos Fenton como Alternativa na Remoção de Interferentes Endócrinos e outros Micropoluentes Ambientais

    Directory of Open Access Journals (Sweden)

    Mariana Roberto Gama

    2012-11-01

    Full Text Available Technological advances, combined to high levels of consumption by the population, led to an increase in the generation of waste, which compromise the availability of natural resources, especially water resources. Furthermore, sensitive analytical detections have increased the detection of environmental micropollutants, many highly toxic. Therefore, the search for alternatives to the removal of micropollutants from water is necessary to overcome the methods currently available. Advanced oxidative processes are efficient for the removal of micropollutants. This review summarizes the main aspects of environmental contamination by endocrine disruptors and the use of Fenton reactions as advanced oxidation processes in the removal of these micropollutants.

  10. 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

  11. Review of iron-free Fenton-like systems for activating H{sub 2}O{sub 2} in advanced oxidation processes

    Energy Technology Data Exchange (ETDEWEB)

    Bokare, Alok D.; Choi, Wonyong, E-mail: wchoi@postech.edu

    2014-06-30

    Graphical abstract: - Highlights: • Elements with multiple redox states efficiently decompose H{sub 2}O{sub 2} at neutral pH. • Activation of H{sub 2}O{sub 2} is entirely governed by solution pH and catalyst composition. • Metal leaching and toxicity is an important factor for practical applications. • Iron-free Fenton systems work only in specialized reaction conditions. - Abstract: Iron-catalyzed hydrogen peroxide decomposition for in situ generation of hydroxyl radicals (HO{sup •} ) has been extensively developed as advanced oxidation processes (AOPs) for environmental applications. A variety of catalytic iron species constituting metal salts (in Fe{sup 2+} or Fe{sup 3+} form), metal oxides (e.g., Fe{sub 2}O{sub 3}, Fe{sub 3}O{sub 4}), and zero-valent metal (Fe{sup 0}) have been exploited for chemical (classical Fenton), photochemical (photo-Fenton) and electrochemical (electro-Fenton) degradation pathways. However, the requirement of strict acidic conditions to prevent iron precipitation still remains the bottleneck for iron-based AOPs. In this article, we present a thorough review of alternative non-iron Fenton catalysts and their reactivity towards hydrogen peroxide activation. Elements with multiple redox states (like chromium, cerium, copper, cobalt, manganese and ruthenium) all directly decompose H{sub 2}O{sub 2} into HO{sup •} through conventional Fenton-like pathways. The in situ formation of H{sub 2}O{sub 2} and decomposition into HO{sup •} can be also achieved using electron transfer mechanism in zero-valent aluminum/O{sub 2} system. Although these Fenton systems (except aluminum) work efficiently even at neutral pH, the H{sub 2}O{sub 2} activation mechanism is very specific to the nature of the catalyst and critically depends on its composition. This review describes in detail the complex mechanisms and emphasizes on practical limitations influencing their environmental applications.

  12. The removal of COD and color by Fenton oxidation from leachate of Erzurum municipal solid waste landfill

    Science.gov (United States)

    Kocakaplan, Nihal; Ertugay, Neşe; Malkoç, Emine

    2016-04-01

    The optimal conditions for treatment of leachate were determined as pH = 2.5, Fe2+= 2 mg/L and H2O2= 100 mg/L. Under the optimal conditions, approximately 90% color (at 620 nm), 84% color (at 525 nm), 74% color (at 436 nm) and 47.8% COD removal efficiency from leachate were achieved after 20 min of reaction. Depending on the results obtained experiments, Fenton process has been used successfully in removal of COD and color in landfill leachate.

  13. Comparison of ultraviolet radiation/hydrogen peroxide, Fenton and photo-Fenton processes for the decolorization of reactive dyes

    Directory of Open Access Journals (Sweden)

    Radović Miljana D.

    2015-01-01

    Full Text Available The effectivness of UV/H2O2 process, Fenton and photo-Fenton process at decolorization of commercially important textile dyes Reactive Orange 4 (RO4 and Reactive Blue 19 (RB19 was evaluated. The effect of operational condition such as initial pH, initial H2O2 concentration, initial Fe2+ concentration and initial dye concentration on decolorization of RO4 and RB19 was studied. The photo-Fenton process is found to be more efficient than UV/H2O2 and Fenton process for decolorization of simulated dye bath effluent and solutions of the dyes in water alone under optimum conditions. In simulated dye bath the removal efficiency was slightly lower than for the solutions of the dyes in water alone for both dyes types. The results revealed that the tested advanced oxidation processes were very effective for decolorization of RO4 and RB19 in aqueous solution. [Projekat Ministarstva nauke Republike Srbije, br. TR34008

  14. A study on removal of elemental mercury in flue gas using fenton solution

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Yongchun [Jiangsu Province Special Equipment Safety Supervision Inspection Institute (Branch of Wuxi), Wuxi 214000 (China); Zhou, Jianfei [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Jun [Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, Southeast University, Nanjing 210096 (China)

    2015-07-15

    Highlights: • A novel technique on oxidation of Hg{sup 0} using Fenton was proposed. • The effects of several process parameters on Hg{sup 0} removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg{sup 0} removal was studied. • Simultaneous removal of Hg{sup 0}, NO and SO{sub 2} was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg{sup 0}) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H{sub 2}O{sub 2} concentration, Hg{sup 0} inlet concentration, Fe{sup 2+} concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO{sub 2}, O{sub 2}, CO{sub 2}, inorganic ions and particulate matters on Hg{sup 0} removal were studied. The results indicate that H{sub 2}O{sub 2} concentration, Fe{sup 2+} concentration, solution pH and gas flow have great effects on Hg{sup 0} removal. Solution temperature, Hg{sup 0}, NO, SO{sub 2}, CO{sub 3}{sup 2−} and HCO{sub 3}{sup −} concentrations also have significant effects on Hg{sup 0} removal. However, Cl{sup −}, SO{sub 4}{sup 2−}, NO{sub 3}{sup −}, O{sub 2} and CO{sub 2} concentrations only have slight effects on Hg{sup 0} removal. Furthermore, reaction mechanism of Hg{sup 0} removal and simultaneous removal process of Hg{sup 0}, NO and SO{sub 2} were also studied. Hg{sup 0} is removed by oxidation of ·OH and oxidation of H{sub 2}O{sub 2}. The simultaneous removal efficiencies of 100% for SO{sub 2}, 100% for Hg{sup 0} and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg{sup 0} removal and simultaneous removal of Hg{sup 0}, SO{sub 2} and NO using Fenton solution in a bubbling reactor.

  15. Study on the removal of urea in wastewater using Fenton reagent

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The great amount of NH3-N produced in biological hydrolysis process of high concentration urea can inhibit the growth of microorganisms. In allusion to this problem, the Fenton reagent was used to treat high concentration urea wastewater. And the optimum conditions of this experiment were employed as follows: Fe (Ⅱ) -H2O2mole ratio was 1/3.53, H2O2 was 4 mL (corresponding to 35.30 mmol) , pH was 3.0 -3.5. Then the experiment shows that the urea concentration decreases from 500 mg/L to less than 2 mg/L, or is even not detected; under the same dose of H2O2 , repetitious addition does better than one-off addition; the reaction time within one minute or to be prolonged has little influence on removal effect. The results verify feasibility of this method.

  16. Fenton oxidative decolorization of the azo dye Direct Blue 15 in aqueous solution

    DEFF Research Database (Denmark)

    Sun, Jian-Hui; Shi, Shao-Hui; Lee, Yi-Fan;

    2009-01-01

    and kinetic of the DB15 were studied, the operating parameters were preferred by changing one factor at one time while the other parameters were kept constant. The optimal conditions for the decolorization of DB15 were determined as pH=4.0, [H2O2] = 2.8x10(-3) mol/L, H2O2/Fe2+ ratio = 100: 1, H2O2/dye ratio...... the reaction temperature from 20 to 40 degrees C showed a positive effect on the decolorization efficiency of DB15. The present study can provide guidance to relational industry operators and planners to effectively treat the DB15 contaminated wastewater by Fenton oxidation process. (C) 2009 Elsevier B. V. All...

  17. Fenton 氧化法预处理高浓度制药废水的实验研究%The Experimental Study on the Fenton Oxidation Pretreatment of High Concentration Pharmaceutical Wastewater

    Institute of Scientific and Technical Information of China (English)

    王会芳; 杨瑞洪

    2014-01-01

    The high concentration pharmaceutical wastewater was pretreated by Fenton method , the influence of Fenton reagent oxidation pretreatment of high concentration pharmaceutical wastewater was studied.The effect on COD Cr treatment of pharmaceutical wastewater was discussed , the influence factor included the value of pH , the dosage of FeSO 4 · 7H2 O, and reaction time on Fenton oxidation.The experimental results showed that the pH value was 4, the reaction time was 100 min, the dosage of FeSO4 · 7H2O was 0.024 mol/L, the dosage ratio of H2O2/Fe2+was 11:1, the CODCr removal was 52.1%, and the biodegradability of the BOD/COD was 0.57.Under this condition , the effect was the most ideal.%采用Fenton法对高浓度制药废水进行预处理实验。主要考察了Fenton试剂氧化法预处理高浓度制药废水的影响因素,主要讨论pH值、 FeSO4·7H2 O投加量、反应时间对Fenton氧化工艺对制药废水中CODCr处理效果的影响。实验结果显示, pH值为4、反应时间100 min、 FeSO4·7H2 O投加量为0.024 mol/L、 H2 O2/Fe2+投加比为11:1, CODCr处理去除率为52.1%,可生化性BOD/COD为0.57,效果最为理想。

  18. Effect of iron ion on doxycycline photocatalytic and Fenton-based autocatatalytic decomposition.

    Science.gov (United States)

    Bolobajev, Juri; Trapido, Marina; Goi, Anna

    2016-06-01

    Doxycycline plays a key role in Fe(III)-to-Fe(II) redox cycling and therefore in controlling the overall reaction rate of the Fenton-based process (H2O2/Fe(III)). This highlights the autocatalytic profile of doxycycline degradation. Ferric iron reduction in the presence of doxycycline relied on doxycycline-to-Fe(III) complex formation with an ensuing reductive release of Fe(II). The lower ratio of OH-to-contaminant in an initial H2O2/Fe(III) oxidation step than in that of classical Fenton (H2O2/Fe(II)) decreased the doxycycline degradation rate. The quantum yield of doxycycline in direct UV-C photolysis was 3.1 × 10(-3) M E(-1). In spite of doxycycline-Fe(III) complexes could produce the adverse effect on the doxycycline degradation in the UV/Fe(III) system some acceleration of the rate was observed upon irradiation of the Fe(III)-hydroxy complex. Acidic reaction media (pH 3.0) and the molar ratio of DC/Fe(III) = 2/1 favored the complex formation. Doxycycline close degradation rates and complete mineralization achieved for 120 min (Table 1) with both UV/H2O2 and UV/H2O2/Fe(III) indicated the unsubstantial role of the reduction of Fe(III) to Fe(II) in UV/H2O2/Fe(III) system efficacy. Thus, factors such as doxycycline's ability to form complexes with ferric iron and the ability of complexes to participate in a reductive pathway should be considered at a technological level in process optimization, with chemistry based on iron ion catalysis to enhance the doxycycline oxidative pathway. PMID:27016818

  19. Stimulation of production of reactive oxygen and nitrogen species in endothelial cells by unmodified and Fenton-modified ultradisperse detonation diamond.

    Science.gov (United States)

    Solarska-Ściuk, K; Gajewska, A; Skolimowski, J; Mitura, K; Bartosz, G

    2013-01-01

    In recent years, the development of nanotechnology opens up new prospects for biomedical applications of unmodified and chemically modified diamond nanoparticles (DNPs). The problem of biocompatibility of DNPs is thus of primary importance. The first step in the modification of DNPs is usually the introduction of -OH groups, which can bind other functional groups. One of the basic methods to introduce -OH groups onto DNPs is the Fenton reaction. The aim of this study was to compare the effect of unmodified DNPs and nanoparticles modified by the Fenton reaction on human endothelial cells. Ultradisperse diamond (UDD) was modified by the Fenton reaction introducing surface -OH groups. Immortalized human umbilical cord endothelial cells (HUVEC-ST) were incubated with 2-100 µg/mL nanopowders in the opti-MEM medium. For comparison, graphite powder (GRAF and GRAF+OH) was also employed. UDD and GRAF augmented generation of reactive oxygen species in the cells after 24 H incubation, estimated by oxidation of 2',7'-dichlorofluorescin diacetate (H2DCF-DA). Cellular production of nitric oxide, estimated with DAF-FM-DA (3-amino-4-aminomethyl 2',7'-dichlorofluorescein diacetate), was also affected by UDD and GRAF after 24 H. Fenton-modified OH, in contrast to unmodified diamond, decreased NO production. Detonation nanoparticles also affected the cellular content of glutathione and activities of main antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, and glutathione S-transferase). This article was published online on 5 February 2013. Errors in the byline and affiliation line were subsequently identified. This notice is included in the online and print versions to indicate that both have been corrected 18 April 2013. PMID:23586587

  20. Assessment of PCDD/Fs formation in the Fenton oxidation of 2-chlorophenol: Influence of the iron dose applied.

    Science.gov (United States)

    Vallejo, Marta; Fernández-Castro, Pablo; San Román, M Fresnedo; Ortiz, Inmaculada

    2015-10-01

    Toxic polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) may be formed during remediation of chlorinated phenols via Fenton oxidation. To highlight the need for monitoring the production of toxic byproducts in these reactions, this work assessed the influence of iron dose (0.09-0.36 mM) on the Fenton oxidation of 2-chlorophenol (2-CP, 15.56 mM), a potential precursor of PCDD/Fs, by quantifying 2-CP removal and mineralization rates as well as byproducts yields, including PCDD/Fs. Although the increase in the iron dose showed positive contribution to 2-CP oxidation, under the operating conditions of the current study (H2O2 at 20% of the stoichiometric dose and 20 °C), there was no effect on the mineralization rate, and TOC and chlorine balances were far to be closed, depicting the presence of chlorinated organic byproducts in the reaction medium. After 4 h of treatment, the total PCDD/Fs concentrations increased by 14.5-39 times related to the untreated sample when the iron doses tested decreased from 0.36 to 0.09 mM, with preferential formation of PCDFs over PCDDs and dominance of lower chlorinated congeners such as tetra and penta-PCDD/Fs. The treatment with the highest iron dose (0.36 mM) exhibited the lowest PCDD/Fs yields and was thus most successful at mitigating toxic byproducts of the Fenton oxidation, leading to lower sample toxic equivalence (TEQ) value. PMID:26134538

  1. Use of Both Anode and Cathode Reactions in Wastewater Treatment

    Science.gov (United States)

    Brillas, Enric; Sirés, Ignasi; Cabot, Pere LluíS.

    Here, we describe the fundamentals, laboratory experiments, and environmental applications of indirect electrooxidation methods based on H2O2 electrogeneration such as electro-Fenton, photoelectro-Fenton and peroxicoagulation for the treatment of acidic wastewaters containing toxic and recalcitrant organics. These methods are electrochemical advanced oxidation processes that can be used in divided and undivided electrolytic cells in which pollutants are oxidized by hydroxyl radical (•OH) produced from anode and/or cathode reactions. H2O2 is generated from the two-electron reduction of O2 at reticulated vitreous carbon, graphite, carbon-felt, and O2-diffusion cathodes. The most usual method is electro-Fenton where Fe2 + added to the wastewater reacts with electrogenerated H2O2 to yield •OH and Fe3 + from Fenton's reaction. An advantage of this technique is that Fe2 + is continuously regenerated from cathodic reduction of Fe3 +. The characteristics of different electro-Fenton systems where pollutants are simultaneously destroyed by •OH formed in the medium from Fenton's reaction and at the anode surface from water oxidation are explained. The effect of the anode [Pt or boron-doped diamond (BDD)] and cathode (carbon-felt or O2-diffusion) on the degradation rate of persistent industrial by-products, herbicides, pharmaceuticals, dyes, etc. is examined. Initial pollutants react much more rapidly with •OH formed in the medium and their degradation sequences are discussed from aromatic intermediates and finally short aliphatic acids are detected. The synergetic positive catalytic effect of Cu2 + on the electro-Fenton process is evidenced. The photoelectro-Fenton method involves the irradiation of the wastewater with UVA light that rapidly photodecomposes complexes of Fe3 + with final carboxylic acids enhancing total decontamination. The peroxicoagulation method uses a sacrificial Fe anode that is continuously oxidized to Fe2 + and organics are either mineralized

  2. 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)

  3. 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

    Sustainable H2O2 supply and cost-effective elimination of residual H2O2 are two key challenges associated with the successful application of Fenton reaction for contaminant removal. In this study, an innovative Bioelectro-Fenton system capable of alternate switching between microbial electrolysis...... 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...... a proof-in-concept new system for efficient and cost-effective H2O2 control and recalcitrant pollutants removal....

  4. AbstractApplication of Fenton-like process using iron nano oxides for pyrene removal from contaminated soils

    Directory of Open Access Journals (Sweden)

    S. Jorfi

    2014-05-01

    Conclusion: Fenton oxidation using iron nano oxides under defined optimum conditions and neutral pH, can be a suitable alternative to conventional Fenton for remediation of soils contaminated with pyrene.

  5. Fenton-treated functionalized diamond nanoparticles as gene delivery system.

    Science.gov (United States)

    Martín, Roberto; Alvaro, Mercedes; Herance, José Raúl; García, Hermenegildo

    2010-01-26

    When raw diamond nanoparticles (Dnp, 7 nm average particle size) obtained from detonation are submitted to harsh Fenton-treatment, the resulting material becomes free of amorphous soot matter and the process maintains the crystallinity, reduces the particle size (4 nm average particle size), increases the surface OH population, and increases water solubility. All these changes are beneficial for subsequent Dnp covalent functionalization and for the ability of Dnp to cross cell membranes. Fenton-treated Dnps have been functionalized with thionine and the resulting sample has been observed in HeLa cell nuclei. A triethylammonium-functionalized Dnp pairs electrostatically with a plasmid having the green fluorescent protein gene and acts as gene delivery system permitting the plasmid to cross HeLa cell membrane, something that does not occur for the plasmid alone without assistance of polycationic Dnp. PMID:20047335

  6. Stability and performance enhancements of Electrokinetic-Fenton soil remediation

    OpenAIRE

    Ng, Y. S.; Sen Gupta, B; Hashim, M A

    2014-01-01

    Electrokinetic process is a potential in situ soil remediation process which transports the contaminants via electromigration and electroosmosis. For organic compounds contaminated soil, Fenton’s reagent is utilized as a flushing agent in electrokinetic process (Electrokinetic-Fenton) so that removal of organic contaminants could be achieved by in situ oxidation/destruction. However, this process is not applied widely in industries as the stability issue for Fenton’s reagent is the main drawb...

  7. COD Removal of Different Industrial Wastewater by Fenton Oxidation Process

    OpenAIRE

    Yogita Sindhi*1

    2014-01-01

    Advanced oxidation processes are possibly one of the most effective methods for the treatment of wastewater containing organic products (effluents from chemical and agrochemical industries, the textile industry, paints, dyes, etc.).Fenton process is a one of advanced oxidation process. Fenton’s process have been extensively used for the removal of COD, TOC, dyes, phenolic compounds other organic chemicals from industrial and municipal wastewater. In this study, the laboratory s...

  8. Rapid decolorization and mineralization of simulated textile wastewater in a heterogeneous Fenton like system with/without external energy.

    Science.gov (United States)

    Zhou, Tao; Lu, Xiaohua; Wang, Jia; Wong, Fook-Sin; Li, Yaozhong

    2009-06-15

    A novel Fenton like system, employing Zero Valent Iron (ZVI) and air bubbling, was developed to treat a simulated textile wastewater containing azo dye Reactive Black 5 (RB5) and Ethylenediaminetetraacetic acid (EDTA). By dioxygen activation, H(2)O(2) was self-produced continuously in the system through a series of iron-EDTA ligands reactions. After 3h reaction, the removal rates of RB5, EDTA, Total Organic Carbon (TOC), and Chemical Oxygen Demand (COD) were 100%, 96.5%, 68.6% and 92.2%, respectively. The effects of pH, atmosphere as well as the initial concentration of RB5, EDTA and ZVI were also investigated. Two types of external energy-Ultrasound (US) and Ultraviolet (UV) were introduced into the Fenton like system, respectively. The effect of these external energies on the degradation of the wastewater was assessed. It was demonstrated that US presented significant synergistic effect on the degradation and mineralization of both RB5 and EDTA, while UV could not achieve any improvement.

  9. Optimization of the Parameters Affecting the Fenton Process for Decolorization of Reactive Red 198 (RR-198 from the Aqueous Phase

    Directory of Open Access Journals (Sweden)

    Mansooreh Dehghani

    2015-10-01

    Full Text Available Background: Recently, there has been a great concern about the consumption of dyes because of their toxicity, mutagenicity, carcinogenicity, and persistence in the aquatic environment. Reactive dyes are widely used in textile industry. Advanced oxidation processes are one of the cost-effective methods for the removal of these dyes. The main aims of this study were determining the feasibility of using Fenton process in removing Reactive Red 198 (RR-198 dye from aqueous solution and determining the optimal conditions. Methods: This is a cross-sectional study conducted at a laboratory scale. A total of 69 samples were considered and the effect of pH, Fe (II concentration, H2O2 concentration, initial dye concentration and reaction time were investigated. Results: According to the results, a maximum removal efficiency of 92% was obtained at pH of 3 and the reaction time of 90 min; also, the concentration of Fe (II, H2O2, initial dye concentration were 100 mg/L, 50 mg/L, and 100 mg/L, respectively. The results revealed that by increasing the concentration of Fe (II, H2O2 and initial dye, the removal efficiency was increased. Conclusions: The results showed that Fenton process could be used as a cost-effective method for removing RR-198 dye from textile wastewater efficiently.

  10. Optimization of the Parameters Influencing the Photo-Fenton Process for the Decolorization of Reactive Red 198 (RR198

    Directory of Open Access Journals (Sweden)

    Dehghani

    2015-04-01

    Full Text Available Background Reactive dyes, anionic compounds with high water solubility, are widely used in textile industries. Objectives The present study aimed to assess the feasibility of the photo-Fenton process in removing Reactive Red 198 dye from aqueous solutions and determine the optimal conditions for maximum removal. Materials and Methods This study was performed on a laboratory scale using a 4-liter photochemical reactor. The spectrophotometer DR5000 (wavelength 520 nm was used to determine the dye concentration. The effect of the influencing parameters, including pH (3–9, Fe (II concentration (10–200 mg/L, H2O2 concentration (25 - 150 mg/L, initial dye concentration (50–200 mg/L, and reaction time (15 - 120 minutes were studied. Results According to the results, the photo-Fenton (UV/ H2O2/Fe (II process significantly removed dye from the aqueous solution. The Reactive Red 198 dye removal efficiency from aqueous solutions was more than 99% at optimal conditions (pH = 3, Fe (II = 10 mg/L, H2O2 = 75 mg/L, initial dye concentration = 50 mg/L, and reaction time = 120 minutes. Conclusions The present study demonstrated that the UV/ H2O2/Fe (II process could be used as an efficient, reliable method for removing Reactive Red 198 dye from textile wastewater.

  11. Microwave-assisted Fenton-like decolorization of methyl orange solution using chromium compounds

    Institute of Scientific and Technical Information of China (English)

    LIU Zuo-hua; TAO Chang-yuan; DU Jun; SUN Da-gui; LI Bai-zhan

    2008-01-01

    Azo dyes discharged in the environment are persistent organic pollutants (POPs), which are very difficult to remove. We developed a microwave-assisted Fenton-like process to degrade methyl orange (MO), an azo dye, with hydrogen peroxide (H2O2) catalyzed by chromium compounds coexisting with MO in the solution. Comparison between the Cr(III)-H2O2 and Cr(VI)-H2O2 systems shows that Cr(VI) has a stronger and more stable catalytical activity than Cr(III), and Cr(III) is more susceptible to a change in the acidity or alkalinity of the reaction system. With a Cr(VI) concentration of 10 mmol L-1 or a Cr(III) concentration of 12 mmol L-1 in the solution under the microwave irradiation of a power larger than 300 W for 3 min, 10 mmol L-1 H2O2 can degrade more than 95% of 1 000 mg L-1 methyl orange; when the microwave power is increased to 700 W, the same amount of H2O2 can degrade all methyl orange in the solution with the same amount of Cr(VI) catalyst. Ultraviolet-visible spectrography indicates the cleavage of the azo bond in methyl orange after treatment, suggesting the potential of this Fenton-like process to degrade azo dye POPs. Reusing waste chromium compounds coexisting with dyestuff in wastewater to catalyze the degradation of azo dyes could be a cost-effective technique for azo dyes and chromate manufacturers and/or users to treat their wastewater and prevent POPs from endangering the environment. This is of particular importance to controlling the water quality of the Three Gorges Reservoir.

  12. Treatment of pharmaceutical wastewater using interior micro-electrolysis/Fenton oxidation-coagulation and biological degradation.

    Science.gov (United States)

    Xu, Xiaoyi; Cheng, Yao; Zhang, Tingting; Ji, Fangying; Xu, Xuan

    2016-06-01

    The synthesis of steroid hormones produces wastewater that is difficult to manage and characterize due to its complex components and high levels of toxicity and bio-refractory compounds. In this work, interior micro-electrolysis (IME) and Fenton oxidation-coagulation (FOC) were investigated as wastewater pretreatment processes in combination with biological treatments using a hydrolysis acidification unit (HA) and two-stage biological contact oxidation (BCO) in laboratory and field experiments. In laboratory experiments with an average initial COD load of about 15,000 mg/L, pH of 4, Fe-C/water (V/V) ratio of 1:1, air/water ratio of 10, and reaction time of 180 min, IME achieved a COD removal efficiency of 31.8% and a 1.7-fold increase in the BOD5/COD (B/C) ratio of wastewater. The Fe(2+) concentration of 458.5 mg/L in the IME effluent meets the requirements of the Fenton oxidation (FO) process. FOC further reduced the COD with an efficiency of 30.1%, and the B/C ratio of the wastewater reached 0.59. Excitation-emission matrix (EEM) analysis showed that complex higher molecular weight organic compounds in the wastewater were degraded after the pretreatment process. In addition, a field experiment with a continuous flow of 96 m(3)/d was conducted for over 90 d. The combined process system operated steadily, though the Fe-C fillings should be soaked in a sulfuric acid solution (5‰) for 12 h to recover activity every two weeks. The COD and BOD5 concentrations in the final effluent were less than 90 mg/L and 15 mg/L, respectively. PMID:26953729

  13. Electrokinetic-Fenton technology for the remediation of hydrocarbons historically polluted sites.

    Science.gov (United States)

    Sandu, Ciprian; Popescu, Marius; Rosales, Emilio; Bocos, Elvira; Pazos, Marta; Lazar, Gabriel; Sanromán, M Angeles

    2016-08-01

    The feasibility of the electrokinetic-Fenton technology coupled with surfactants in the treatment of real historically hydrocarbons polluted soils has been studied. The characterisation of these soils from Spain and Romania was performed and identified as diesel and diesel-motor oil spillages, respectively. Moreover, the ageing of the spillages produced by the soil contamination was estimated showing the historical pollution of the sites (around 11 and 20 years for Romanian and Spanish soils, respectively). An ex-situ electrochemical treatment was performed to evaluate the adequacy of surfactants for the degradation of the hydrocarbons present in the soils. It was found an enhancement in the solubilisation and removal of TPHs with percentages increasing from 25.7 to 81.8% by the presence of Tween 80 for Spanish soil and from 15.1% to 71.6% for Triton X100 in Romanian soil. Therefore, the viability of coupling enhanced electrokinetic and Fenton remediation was evaluated through a simulated in-situ treatment at laboratory scale. The results demonstrated that the addition of the selected surfactants improved the solubilisation of the hydrocarbons and influenced the electroosmotic flow with a slight decrease. The efficiency of the treatment increased for both considered soil samples and a significant degradation level of the hydrocarbons compounds was observed. Buffering of pH coupled with the addition of a complexing agent showed to be important in the treatment process, facilitating the conditions for the degradation reactions that take place into the soil matrix. The results demonstrated the effectiveness of the selected techniques for remediation of the investigated soils. PMID:27183337

  14. Chelate-modified polymers for atmospheric gas chromatography

    Science.gov (United States)

    Christensen, W. W.; Mayer, L. A.; Woeller, F. H. (Inventor)

    1980-01-01

    Chromatographic materials were developed to serve as the stationary phase of columns used in the separation of atmospheric gases. These materials consist of a crosslinked porous polymer matrix, e.g., a divinylbenzene polymer, into which has been embedded an inorganic complexed ion such as N,N'-ethylene-bis-(acetylacetoniminato)-cobalt (2). Organic nitrogenous bases, such as pyridine, may be incorporated into the chelate polymer complexes to increase their chromatographic utility. With such materials, the process of gas chromatography is greatly simplified, especially in terms of time and quantity of material needed for a gas separation.

  15. Preparation of natural pyrite nanoparticles by high energy planetary ball milling as a nanocatalyst for heterogeneous Fenton process

    Energy Technology Data Exchange (ETDEWEB)

    Fathinia, Siavash [Department of Mining Engineering, Faculty of Engineering and Technology, Imam Khomeini International University, Qazvin (Iran, Islamic Republic of); Research Laboratory of Advanced Water and Wastewater Treatment Processes, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Fathinia, Mehrangiz [Research Laboratory of Advanced Water and Wastewater Treatment Processes, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Rahmani, Ali Akbar [Department of Mining Engineering, Faculty of Engineering and Technology, Imam Khomeini International University, Qazvin (Iran, Islamic Republic of); Khataee, Alireza, E-mail: a_khataee@tabrizu.ac.ir [Research Laboratory of Advanced Water and Wastewater Treatment Processes, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of)

    2015-02-01

    Graphical abstract: - Highlights: • Pyrite nanoparticles were successfully produced by planetary ball milling process. • The physical and chemical properties of pyrite nanoparticles were fully examined. • The degradation of AO7 was notably enhanced by pyrite nanoparticles Fenton system. • The influences of basic operational parameters were investigated using CCD. - Abstract: In the present study pyrite nanoparticles were prepared by high energy mechanical ball milling utilizing a planetary ball mill. Various pyrite samples were produced by changing the milling time from 2 h to 6 h, in the constant milling speed of 320 rpm. X-ray diffraction (XRD), scanning electron microscopy (SEM) linked with energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FT-IR) analysis and Brunauer–Emmett–Teller (BET) were performed to explain the characteristics of primary (unmilled) and milled pyrite samples. The average particle size distribution of the produced pyrite during 6 h milling was found to be between 20 nm and 100 nm. The catalytic performance of the different pyrite samples was examined in the heterogeneous Fenton process for degradation of C.I. Acid Orange 7 (AO7) solution. Results showed that the decolorization efficiency of AO7 in the presence of 6 h-milled pyrite sample was the highest. The impact of key parameters on the degradation efficiency of AO7 by pyrite nanoparticles catalyzed Fenton process was modeled using central composite design (CCD). Accordingly, the maximum removal efficiency of 96.30% was achieved at initial AO7 concentration of 16 mg/L, H{sub 2}O{sub 2} concentration of 5 mmol/L, catalyst amount of 0.5 g/L and reaction time of 25 min.

  16. Superiority of solar Fenton oxidation over TiO2 photocatalysis for the degradation of trimethoprim in secondary treated effluents.

    Science.gov (United States)

    Michael, I; Hapeshi, E; Michael, C; Fatta-Kassinos, D

    2013-01-01

    The overall aim of this work was to examine the degradation of trimethoprim (TMP), which is an antibacterial agent, during the application of two advanced oxidation process (AOP) systems in secondary treated domestic effluents. The homogeneous solar Fenton process (hv/Fe(2+)/H2O2) and heterogeneous photocatalysis with titanium dioxide (TiO2) suspensions were tested. It was found that the degradation of TMP depends on several parameters such as the amount of iron salt and H2O2, concentration of TiO2, pH of solution, solar irradiation, temperature and initial substrate concentration. The optimum dosages of Fe(2+) and H2O2 for homogeneous ([Fe(2+)] = 5 mg L(-1), [H2O2] = 3.062 mmol L(-1)) and TiO2 ([TiO2] = 3 g L(-1)) for heterogeneous photocatalysis were established. The study indicated that the degradation of TMP during the solar Fenton process is described by a pseudo-first-order reaction and the substrate degradation during the heterogeneous photocatalysis by the Langmuir-Hinshelwood kinetics. The toxicity of the treated samples was evaluated using a Daphnia magna bioassay and was finally decreased by both processes. The results indicated that solar Fenton is more effective than the solar TiO2 process, yielding complete degradation of the examined substrate within 30 min of illumination and dissolved organic carbon (DOC) reduction of about 44% whereas the respective values for the TiO2 process were ∼70% degradation of TMP within 120 min of treatment and 13% DOC removal. PMID:23508150

  17. Mineralization of the textile dye acid yellow 42 by solar photoelectro-Fenton in a lab-pilot plant.

    Science.gov (United States)

    Espinoza, Carolina; Romero, Julio; Villegas, Loreto; Cornejo-Ponce, Lorena; Salazar, Ricardo

    2016-12-01

    A complete mineralization of a textile dye widely used in the Chilean textile industry, acid yellow 42 (AY42), was studied. Degradation was carried out in an aqueous solution containing 100mgL(-1) of total organic carbon (TOC) of dye using the advanced solar photoelectro-Fenton (SPEF) process in a lab-scale pilot plant consisting of a filter press cell, which contains a boron doped diamond electrode and an air diffusion cathode (BDD/air-diffusion cell), coupled with a solar photoreactor for treat 8L of wastewater during 270min of electrolysis. The main results obtained during the degradation of the textile dye were that a complete transformation to CO2 depends directly on the applied current density, the concentration of Fe(2+) used as catalyst, and the solar radiation intensity. The elimination of AY42 and its organic intermediates was due to hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between electrogenerated H2O2 and added Fe(2+). The application of solar radiation in the process (SPEF) yield higher current efficiencies and lower energy consumptions than electro-Fenton (EF) and electro-oxidation with electrogenerated H2O2 (E OH2O2) by the additional production of hydroxyl radicals from the photolysis of Fe(III) hydrated species and the photodecomposition of Fe(III) complexes with organic intermediates. Moreover, some products and intermediates formed during mineralization of dye, such as inorganic ions, carboxylic acids and aromatic compounds were determined by photometric and chromatographic methods. An oxidation pathway is proposed for the complete conversion to CO2. PMID:26971051

  18. Superiority of solar Fenton oxidation over TiO2 photocatalysis for the degradation of trimethoprim in secondary treated effluents.

    Science.gov (United States)

    Michael, I; Hapeshi, E; Michael, C; Fatta-Kassinos, D

    2013-01-01

    The overall aim of this work was to examine the degradation of trimethoprim (TMP), which is an antibacterial agent, during the application of two advanced oxidation process (AOP) systems in secondary treated domestic effluents. The homogeneous solar Fenton process (hv/Fe(2+)/H2O2) and heterogeneous photocatalysis with titanium dioxide (TiO2) suspensions were tested. It was found that the degradation of TMP depends on several parameters such as the amount of iron salt and H2O2, concentration of TiO2, pH of solution, solar irradiation, temperature and initial substrate concentration. The optimum dosages of Fe(2+) and H2O2 for homogeneous ([Fe(2+)] = 5 mg L(-1), [H2O2] = 3.062 mmol L(-1)) and TiO2 ([TiO2] = 3 g L(-1)) for heterogeneous photocatalysis were established. The study indicated that the degradation of TMP during the solar Fenton process is described by a pseudo-first-order reaction and the substrate degradation during the heterogeneous photocatalysis by the Langmuir-Hinshelwood kinetics. The toxicity of the treated samples was evaluated using a Daphnia magna bioassay and was finally decreased by both processes. The results indicated that solar Fenton is more effective than the solar TiO2 process, yielding complete degradation of the examined substrate within 30 min of illumination and dissolved organic carbon (DOC) reduction of about 44% whereas the respective values for the TiO2 process were ∼70% degradation of TMP within 120 min of treatment and 13% DOC removal.

  19. Mineralization of the textile dye acid yellow 42 by solar photoelectro-Fenton in a lab-pilot plant.

    Science.gov (United States)

    Espinoza, Carolina; Romero, Julio; Villegas, Loreto; Cornejo-Ponce, Lorena; Salazar, Ricardo

    2016-12-01

    A complete mineralization of a textile dye widely used in the Chilean textile industry, acid yellow 42 (AY42), was studied. Degradation was carried out in an aqueous solution containing 100mgL(-1) of total organic carbon (TOC) of dye using the advanced solar photoelectro-Fenton (SPEF) process in a lab-scale pilot plant consisting of a filter press cell, which contains a boron doped diamond electrode and an air diffusion cathode (BDD/air-diffusion cell), coupled with a solar photoreactor for treat 8L of wastewater during 270min of electrolysis. The main results obtained during the degradation of the textile dye were that a complete transformation to CO2 depends directly on the applied current density, the concentration of Fe(2+) used as catalyst, and the solar radiation intensity. The elimination of AY42 and its organic intermediates was due to hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between electrogenerated H2O2 and added Fe(2+). The application of solar radiation in the process (SPEF) yield higher current efficiencies and lower energy consumptions than electro-Fenton (EF) and electro-oxidation with electrogenerated H2O2 (E OH2O2) by the additional production of hydroxyl radicals from the photolysis of Fe(III) hydrated species and the photodecomposition of Fe(III) complexes with organic intermediates. Moreover, some products and intermediates formed during mineralization of dye, such as inorganic ions, carboxylic acids and aromatic compounds were determined by photometric and chromatographic methods. An oxidation pathway is proposed for the complete conversion to CO2.

  20. Salicylic acid degradation by advanced oxidation processes. Coupling of solar photoelectro-Fenton and solar heterogeneous photocatalysis.

    Science.gov (United States)

    Garza-Campos, Benjamin; Brillas, Enric; Hernández-Ramírez, Aracely; El-Ghenymy, Abdellatif; Guzmán-Mar, Jorge Luis; Ruiz-Ruiz, Edgar J

    2016-12-01

    A 3.0 L solar flow plant with a Pt/air-diffusion (anode/cathode) cell, a solar photoreactor and a photocatalytic photoreactor filled with TiO2-coated glass spheres has been utilized to couple solar photoelectro-Fenton (SPEF) and solar heterogeneous photocatalysis (SPC) for treating a 165mgL(-1) salicylic acid solution of pH 3.0. Organics were destroyed by OH radicals formed on the TiO2 photocatalyst and at the Pt anode during water oxidation and in the bulk from Fenton's reaction between added Fe(2+) and cathodically generated H2O2, along with the photolytic action of sunlight. Poor salicylic acid removal and mineralization were attained using SPC, anodic oxidation with electrogenerated H2O2 (AO-H2O2) and coupled AO-H2O2-SPC. The electro-Fenton process accelerated the substrate decay, but with low mineralization by the formation of byproducts that are hardly destroyed by OH. The mineralization was strongly increased by SPEF due to the photolysis of products by sunlight, being enhanced by coupled SPEF-SPC due to the additional oxidation by OH at the TiO2 surface. The effect of current density on the performance of both processes was examined. The most potent SPEF-SPC process at 150mAcm(-2) yielded 87% mineralization and 13% current efficiency after consuming 6.0AhL(-1). Maleic, fumaric and oxalic acids detected as final carboxylic acids were completely removed by SPEF and SPEF-SPC.

  1. Heterogeneous UV/Fenton catalytic degradation of wastewater containing phenol with Fe-Cu-Mn-Y catalyst

    Institute of Scientific and Technical Information of China (English)

    郑展望; 雷乐成; 徐生娟; 岑沛霖

    2004-01-01

    The heterogeneous UV/Fenton process with the appropriate amount of Fe-Mn-Cu-Y as catalyst was developed and various operation conditions for the degradation of phenol were evaluated. The results indicated that by using the heterogeneous UV/Fenton process, the CODer removal rate reached almost 100% for wastewater containing phenol. Compared with the homogeneous process, the developed catalyst could be used at wider pH range in the UV/Fenton process. Comparison of various heterogeneous process showed that heterogeneous UV/Fenton process was best. The heterogeneous UV/Fenton process with Fe-Mn-Cu-Y catalyst is highly efficient in degrading various organic pollutants.

  2. Heterogeneous UV/Fenton catalytic degradation of wastewater containing phenol with Fe-Cu-Mn-Y catalyst

    Institute of Scientific and Technical Information of China (English)

    郑展望; 雷乐成; 徐生娟; 岑沛霖

    2004-01-01

    The heterogeneous UV/Fenton process with the appropriate amount of Fe-Mn-Cu-Y as catalyst was developed and various operation conditions for the degradation of phenol were evaluated. The results indicated that by using the heterogeneous UV/Fenton process, the CODcr removal rate reached almost 100% for wastewater containing phenol. Compared with the homogeneous process, the developed catalyst could be used at wider pH range in the UV/Fenton process. Comparison of various heterogeneous process showed that heterogeneous UV/Fenton process was best. The heterogeneous UV/Fenton process with Fe-Mn-Cu-Y catalyst is highly efficient in degrading various organic pollutants.

  3. 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.

  4. Heterogeneous Fenton-like discoloration of methyl orange using Fe3O4/MWCNTs as catalyst: process optimization by response surface methodology

    Science.gov (United States)

    Xu, Huan-Yan; Shi, Tian-Nuo; Zhao, Hang; Jin, Li-Guo; Wang, Feng-Chun; Wang, Chun-Yan; Qi, Shu-Yan

    2016-03-01

    Fe3O4/MWCNTs nanocomposites were prepared by chemical oxidation coprecipitation method and developed as highly efficient heterogeneous Fenton-like catalyst. XRD results revealed that Fe3O4 nanoparticles deposited onto MWCNTs surface remained the inverse spinel crystal structure of cubic Fe3O4 phase. The FTIR characteristic peaks of MWCNTs weakened or disappeared due to the anchor of Fe3O4 nanoparticles and Fe-O peak at 570 cm-1 was indicative of the formation of Fe3O4. TEM observation revealed that Fe3O4 nanoparticles were tightly anchored by MWCNTs. The Fenton-like catalytic activity of Fe3O4/MWCNTs nanocomposites for the discoloration of methyl orange (MO) was much higher than that of Fe3O4 nanoparticles. The process optimization of this heterogeneous Fenton-like system was implemented by response surface methodology (RSM). The optimum conditions for MO discoloration were determined to be of 12.3 mmol/L H2O2 concentration, 2.9 g/L catalyst dosage, solution pH 2.7 and 39.3 min reaction time, with the maximum predicted value for MO discoloration ratio of 101.85%. The corresponding experimental value under the identical conditions was obtained as 99.86%, which was very close to the predicted one with the absolute deviation of 1.99%.

  5. Treatment of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran production effluent by combination of biological treatments and Fenton's oxidation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    High strength refractory organic stream is produced during the production of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran(One Dye Black 2, abbr. ODB 2), a novel heat-sensitive material with a promising market. In this study, a combination of acidificationprecipitation, primary biological treatment, Fenton's oxidation and another biological treatment was successfully used for the removal of COD from 18000-25000 mg/L to below 200 mg/L from the ODB 2 production wastewater in a pilot experiment. A COD removal of 70%-80% was achieved by acidification-precipitation under a pH of 2.5-3.0. The first step biodegradation permitted an average COD removal of 70% under an hydraulic residence time (HRT) of 30 h. By batch tests, the optimum conditions of Fenton's oxidation were acquired as: Fe2+ dose 6.0 mmol/L; H2O2 dose 3000 mg/L; and reaction time 6 h. The second step biological treatment could ensure an effluent COD below 200 mg/L under an HRT of 10 h following the Fenton's treatment.

  6. 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)

  7. Sistema de injeção em fluxo espectrofotométrico para monitorar peróxido de hidrogênio em processo de fotodegradação por reação foto-Fenton Flow injection spectrophotometric system for hydrogen peroxide monitoring in photo-Fenton degradation processes

    Directory of Open Access Journals (Sweden)

    Mirela C. Oliveira

    2001-04-01

    Full Text Available A flow injection spectrophotometric system was projected for monitoring hydrogen peroxide during photodegradation of organic contaminants in photo-Fenton processes (Fe2+/H2O2/UV. Sample is injected manually in a carrier stream and then receives by confluence a 0.1 mol L-1 NH4VO3 solution in 0.5 mol L-1 H2SO4 medium. The product formed shows absorption at 446 nm which is recorded as a peak with height proportional to H2O2 concentration. The performance of the proposed system was evaluated by monitoring the consumption of H2O2 during the photodegradation of dichloroacetic acid solution by foto-Fenton reaction.

  8. Involutin is an Fe3+ reductant secreted by the ectomycorrhizal fungus Paxillus involutus during Fenton-based decomposition of organic matter.

    Science.gov (United States)

    Shah, Firoz; Schwenk, Daniel; Nicolás, César; Persson, Per; Hoffmeister, Dirk; Tunlid, Anders

    2015-12-01

    Ectomycorrhizal fungi play a key role in mobilizing nutrients embedded in recalcitrant organic matter complexes, thereby increasing nutrient accessibility to the host plant. Recent studies have shown that during the assimilation of nutrients, the ectomycorrhizal fungus Paxillus involutus decomposes organic matter using an oxidative mechanism involving Fenton chemistry (Fe(2+) + H2O2 + H(+) → Fe(3+) + ˙OH + H2O), similar to that of brown rot wood-decaying fungi. In such fungi, secreted metabolites are one of the components that drive one-electron reductions of Fe(3+) and O2, generating Fenton chemistry reagents. Here we investigated whether such a mechanism is also implemented by P. involutus during organic matter decomposition. Activity-guided purification was performed to isolate the Fe(3+)-reducing principle secreted by P. involutus during growth on a maize compost extract. The Fe(3+)-reducing activity correlated with the presence of one compound. Mass spectrometry and nuclear magnetic resonance (NMR) identified this compound as the diarylcyclopentenone involutin. A major part of the involutin produced by P. involutus during organic matter decomposition was secreted into the medium, and the metabolite was not detected when the fungus was grown on a mineral nutrient medium. We also demonstrated that in the presence of H2O2, involutin has the capacity to drive an in vitro Fenton reaction via Fe(3+) reduction. Our results show that the mechanism for the reduction of Fe(3+) and the generation of hydroxyl radicals via Fenton chemistry by ectomycorrhizal fungi during organic matter decomposition is similar to that employed by the evolutionarily related brown rot saprotrophs during wood decay. PMID:26431968

  9. Electro-Fenton法的影响因素及研究进展%The Influential Factors of Electro-Fenton Method and Research Progress

    Institute of Scientific and Technical Information of China (English)

    杨新涛; 马如意; 王倩; 吴玉凯

    2014-01-01

    Electro-Fenton法是一种新型的电催化氧化技术,具有“环境友好”的特点,是一种高级氧化技术(AOPs)。结合国内外Electro-Fenton法的研究近况,阐述Fenton法的作用机理及主要影响因素,主要受pH值、O2流量、温度、电流密度、Fe2+离子浓度、电极间距离、电解质及电极材料等因素影响,结合具体的废水对主要反应参数进行总结,分析作用机理。对Electro-Fenton法的研究发展趋势提出了一些观点。%Electro-Fenton method is a new type of electric catalytic ox idation technology, has the characteristics of"environmentally friendly", is a kind of Advanced Oxidation Processes (AOPs). It was combined with the research status of Electro-Fenton method in recent years, expounds the mechanism of Electro-Fenton method and main influence factors. pH, O2 flow rate, temperature, current density, ferrous ion concentration, the distance between the electrodes, electrolyte and electrode materials are the main influence factors. Combined with specific wastewater to summarize main reaction parameters, the mechanism was analyzed. Some views of the trend of research and development of the Electro-Fenton method were put forward.

  10. 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.

  11. 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. PMID:26741550

  12. 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.

  13. Photo-Fenton-like treatment of BPA: effect of UV light source and water matrix on toxicity and transformation products.

    Science.gov (United States)

    Molkenthin, Merle; Olmez-Hanci, Tugba; Jekel, Martin R; Arslan-Alaton, Idil

    2013-09-15

    UV-A (near-UV), UV-C (short-UV) and visible-light assisted Fenton-like treatment of Bisphenol A (BPA) was investigated in pure water and raw freshwater samples spiked with BPA. Treatment performances were evaluated in terms of BPA degradation, dissolved organic carbon (DOC) removal and H2O2 consumption rates. Complete BPA degradation accompanied with significant DOC removal was achieved for all studied processes. Increasing the initial solution pH only exhibited a negative effect on treatment efficiencies when bicarbonate alkalinity was used for pH adjustment, whereas the raw freshwater matrix and irradiation type also influenced oxidation rates appreciably. Acute toxicity analysis employing Vibrio fischeri revealed that the inhibitory effect of BPA decreased significantly during the course of Photo-Fenton-like treatment. Several transformation products could be identified via HPLC and GC-MS analyses including hydroxylated phenolic compounds (hydroquinone; 2-methoxy, 1-4-benzenediol; 4-isopropenylphenol; 4'-hydroxy-acetophenone; 1-(4-cyclohexylphenyl) ethanone; 4-isopropylenecatechol; 4-4'-dihydroxybenzophenone; 4-ethyl,1,3-benzenediol), as well as the ring opening products hexanoic acid methyl ester, fumaric, succinic and oxalic acids. A reaction pathway featuring hydroxylation, dimerization and ring opening steps is proposed. PMID:23866146

  14. In situ anchor of magnetic Fe3O4 nanoparticles onto natural maifanite as efficient heterogeneous Fenton-like catalyst

    Science.gov (United States)

    Zhao, Hang; Weng, Ling; Cui, Wei-Wei; Zhang, Xiao-Rui; Xu, Huan-Yan; Liu, Li-Zhu

    2016-09-01

    In situ anchor of magnetic Fe3O4 nanoparticles (NPs) onto the surface of natural maifanite was realized by chemical oxidation coprecipitation in hot alkaline solution. The Fe3O4/maifanite composites were characterized by XRD, FTIR, SEM, and TEM. These results indicated that polycrystalline Fe3O4 NPs with inverse spinel structure were formed and tightly dispersed on maifanite surface. Based on the measurement of surface Zeta potential of maifanite at different medium pHs, the possible combination mechanism between natural maifanite and Fe3O4 NPs was proposed. Then, the asobtained composites were developed as highly efficient heterogeneous Fenton-like catalyst for the discoloration of an azo dye, Methyl Orange (MO). The comparative tests on MO discoloration in different systems revealed that Fe3O4/maifanite composite exhibited much higher Fenton-like catalytic activity than Fe3O4 NPs and the heterogeneous Fentonlike reaction governed the discoloration of MO. Kinetic results clearly showed that MO discoloration process followed the second-order kinetic model. Fe3O4/maifanite composites exhibited the typical ferromagnetic property detected by VSM and could be easily separated from solution by an external magnetic field.

  15. Optimization of Fenton-based treatment of petroleum refinery wastewater with scrap iron using response surface methodology

    Science.gov (United States)

    Saber, Ali; Hasheminejad, Hasti; Taebi, Amir; Ghaffari, Ghasem

    2014-09-01

    The ever-increasing number and production capacity of petroleum refineries in recent years have intensified the need for developing an effective and practical method for treating their wastewaters. In this study, the application of Fenton process with scrap iron powder was investigated for the treatment of a bio-refractory petroleum refinery effluent. Response surface methodology was employed with a cubic IV optimal design to optimize the process using chemical oxygen demand (COD) removal as the target response. H2O2/COD, and H2O2/Fe mass ratios as well as pH were considered as the relevant parameters. A COD removal of more than 83 % was achieved under optimal conditions (H2O2/COD 10.03, H2O2/Fe 2.66 and pH 3.0) within 90 min. Kinetics studies were conducted to investigate the effect of reaction time on COD removal. In addition, the role of post-coagulation on COD removal under optimal conditions was investigated and it was found that 37 % of COD removal occurred due to coagulation, indicating its high potential in the Fenton process.

  16. Effects of operating parameters on advanced oxidation of diuron by the Fenton's reagent: a statistical design approach.

    Science.gov (United States)

    Catalkaya, Ebru Cokay; Kargi, Fikret

    2007-09-01

    Advanced oxidation of diuron in aqueous solution by Fenton's reagent using FeSO(4) as source of Fe(II) was investigated in the absence of light. Effects of operating parameters namely the concentrations of pesticide (diuron), H(2)O(2) and Fe(II) on oxidation of diuron was investigated by using Box-Behnken statistical experiment design and the surface response analysis. Diuron oxidation by the Fenton reagent was evaluated by determining the total organic carbon (TOC), diuron, and adsorbable organic halogen (AOX) removals. Concentration ranges of the reagents resulting in the highest level of diuron oxidation were determined. Diuron removal increased with increasing H(2)O(2) and Fe(II) concentrations up to a certain level. Diuron concentration had a more profound effect than H(2)O(2) and Fe(II) in removal of diuron, TOC and AOX from the aqueous solution. Nearly complete (98.5%) disappearance of diuron was achieved after 15min reaction period. However, only 58% of diuron was mineralized after 240min under optimal operating conditions indicating formation of some intermediate products. Optimal H(2)O(2)/Fe(II)/diuron ratio resulting in the maximum diuron removal (98.5%) was found to be 302/38/20 (mgl(-1)).

  17. 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. PMID:27434735

  18. 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)

    Highlights: • Almost total mineralization of phthalic acid by solar photoelectro-Fenton with Fe3+, Cu2+ and Fe3+–Cu2+ mixtures. • Hydroxyl radical generation from photo-Fenton reaction under solar radiation. • Enhancement of the mineralization rate using Fe3+ and small amounts of Cu2+. • 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 cm3 of a 2.0 mM phthalic acid solution in 0.10 M Na2SO4 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 cm2 boron-doped diamond (BDD) anode and a 3 cm2 air-diffusion cathode that generates H2O2. Cu2+ and/or Fe3+ 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 Cu2+ or Fe3+ alone and SPEF with only Cu2+, 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 Fe3+ 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 Cu2+ and Fe3+ 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 Cu2+ + 0.375 mM Fe3+, giving rise to 99% mineralization with 40% current efficiency and 0.294 kWh g−1 TOC energy consumption. Eleven aromatics and six short-linear carboxylic

  19. Importance of iron complexation for Fenton-mediated hydroxyl radical production at circumneutral pH

    Directory of Open Access Journals (Sweden)

    Christopher J. Miller

    2016-08-01

    Full Text Available The reaction between Fe(II and H2O2 to yield hydroxyl radicals (HO•, the Fenton reaction, is of interest due to its role in trace metal and natural organic matter biogeochemistry, its utility in water treatment and its role in oxidative cell degradation and associated human disease. There is significant dispute over whether HO•, the most reactive of the so-called reactive oxygen species, is formed in this reaction, particularly under circumneutral conditions relevant to natural systems. In this work we have studied the oxidation kinetics of Fe(II complexed by L = citrate, ethylenediaminetetraacetic acid (EDTA and diethylenetriaminepentaacetic acid (DTPA and also measured HO• production using phthalhydrazide as a probe compound at pH 8.2. It is shown that HO• is the sole product of the Fe(IIL-H2O2 reaction for L = EDTA and DTPA, with kinetic modelling of the full reaction pathway utilized to confirm this finding. Quantitative HO• production also appears likely for L = citrate, although uncertainties with the speciation of Fe(II-citrate complexes as well as difficulties in modelling the oxidation kinetics of these complexes has prevented a definitive conclusion. In the absence of ligands at circumneutral pH, inorganic Fe(II reacts with H2O2 to yield a species other than HO•, contrary to the well-established production of HO• from inorganic Fe(II at low pH. Our results suggest that at high pH Fe(II must be complexed for HO• production to occur.

  20. DI-(2-ETHYLHEXYL PHTHALATE OXIDATIVE DEGRADATION BY FENTON PROCESS IN SYNTHETIC AND REAL PETROCHEMICAL WASTEWATER

    Directory of Open Access Journals (Sweden)

    R. Esmaeli

    2011-09-01

    Full Text Available Di-(2-Ethylhexyl phthalate (DEHP belongs to the class of phthalate esters and is used as an additive in many products including plastics, paints and inks or as a solvent in industrial formulations. The degradation of DEHP in aqueous solution using oxidative Fenton reaction (H2O2/Fe2+ was carried out in this study. It was found that H2O2 concentration, Fe2+ concentration, and pH were the three main factors that could significantly influence the degradation rates of DEHP. The highest degradation percentage (85.6 % of DEHP was observed within 60 min at pH 3 in H2O2/Fe2+ system. The results of our study suggested that the concentration with 90 mg/L H2O2, 5 mg/L Fe2+, and 20 mg/L DEHP in the solution at pH 3 were the optimal conditions. The optimized reaction parameters were preceded for treatment of real wastewater obtained from a petrochemical plant.

  1. Decoloration and mineralization of yeast wastewater by using Ce-Fe/Al2O3 as heterogeneous photo-Fenton catalyst

    Institute of Scientific and Technical Information of China (English)

    WEI Chao-hai; ZHANG Ya-ping; WU Chao-fei; HU Cheng-sheng

    2006-01-01

    Decoloration and mineralization of yeast wastewater were investigated by using Ce-Fe/Al2O3 as a heterogeneous photo-Fenton catalyst in fluidized bed reactor in order to solve the problem of yeast wastewater discharge.The experimental results were assessed in terms of total organic carbon(TOC) reduction. The operational and reaction conditions affecting the efficiencies of TOC removal such as initial pH value, H2O2 concentration, catalyst loading and UV power were studied. The results show that TOC is reduced from 347.6 mg/L to 10.8 mg/L, color is changed from 500 units to 0 under the conditions as follows: initial pH value 6. 0, H2O2 concentration of 1.000 g/L,catalyst loading of 5 g/L, reaction duration of 120 min and reaction temperature of 30 ℃. The irradiated Ce-Fe/Al2O3 catalyst was complexed with 1,10-phenanthroline and then it was subjected to Fourier transform infrared spectroscopy and diffuse reflectance spectroscopy to confirm the formation of Fe( Ⅱ ) in the solid state. Heterogeneous photo-Fenton reaction proves to be effective for the treatment of yeast wastewater.

  2. UV/Fenton/杂多酸体系对染料曙红Y的光解作用研究%Study on UV/Fenton/Heteropoly Acid System Photolysis of Dye Eosin Y

    Institute of Scientific and Technical Information of China (English)

    高航; 马威; 李海霞; 高梅; 李松田

    2012-01-01

    In order to improve oxidation efficiency of Fenton reaction,heteropoly acid was chosen as activator.A new photocatalysis system was established.In photochemical reactor,uv lamp was used as light sources,phosphotungstic acid as photocatalysis additives,UV/Fenton/heteropoly acid system effect to photocatalysis degradation on eosin Y simulative dyeing was studied.Heteropoly acid photocatalysis degradation mechanism to dye,factors that could affect photocatalysis degradation rate of dye,ways to improve photocatalysis degradation efficiency to dye were preliminary studied.Experiments results showed that: H2O2 addition amount to the solution,Fe^2+ concentration,pH value of the solution could affect photocatalysis degradation result.From the experiments,optimum reaction conditions were: pH value was 5-6,30% H2O2 addition amount was 2 mL,FeSO4 dose was 0.02 g/L.%为改善Fenton反应的氧化效率,选择杂多酸为活化剂,建立了一种新的光催化体系。在光化学反应器中,以紫外灯为光源,以磷钨酸为光催化助剂,研究了UV/Fenton/杂多酸体系对曙红Y模拟染料废水的光催化降解的影响,并就杂多酸辅助光催化降解染料的机理,影响染料光催化降解速率的因素,提高染料光催化降解效率的途径进行了初步探讨。结果表明,溶液中H2O2投加量、Fe^2+浓度、溶液pH值是影响催化光解效果的重要因素。实验得出反应的适宜条件是:pH为5~6,30%H2O2的投加量为2 mL,FeSO4的剂量约为0.02 g/L。

  3. 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.

  4. Soil washing in combination with homogeneous Fenton-like oxidation for the removal of 2,4,4'-trichlorodiphenyl from soil contaminated with capacitor oil.

    Science.gov (United States)

    Ma, Xiao-Hong; Zhao, Ling; Lin, Zhi-Rong; Dong, Yuan-Hua

    2016-04-01

    Detoxification by chemical oxidation of polychlorinated biphenyls (PCBs) in contaminated soils is very difficult and inefficient because PCBs typically associate with the solid phase or exist as non-aqueous-phase liquids due to their low solubility and slow desorption rates, and thus, they are difficult to remove from soils by using traditional, water-based elution techniques. Surfactant can enhance washing efficiency of PCBs from contaminated soils. This study used Brij 58, Brij 30, Tween 80, and 2-hydroxypropyl-β-cyclodextrin (HPCD) to solubilize 2,4,4'-trichlorodiphenyl (PCB28) from soil contaminated with capacitor oil into solution. The feasibility of PCB28 oxidation in soil washing wastewater through a Fe(3+)-catalyzed Fenton-like reaction was subsequently examined. Washing with 10 g L(-1) Brij 58 solution showed the highest extraction efficiency (up to 61.5 %) compared with that of the three other surfactants. The total concentration of PCB28 in contaminated soil at 25 °C after 48-h extraction was 286 mg L(-1). In contrast to conditions in which no washing agent was added, addition of the four washing agents decreased the efficiency of PCB28 degradation by the Fenton-like reaction, with the decrease due to addition of 10 g L(-1) Brij 58 solution being the smallest. The optimal concentration of H2O2 for preventing its useless decomposition was found to be 50 mM. The efficiency of PCB28 removal was lower when the initial concentration of PCB28 treated in the Fenton-like reaction was higher. The degradation efficiencies of PCB28 at initial concentrations of 0.1, 10, and 176 mg L(-1) in 10 g L(-1) Brij 58 solution at 25 °C and pH 3.0 and 9 h of reaction using 50 mM H2O2 were 64.1, 42.0, and 34.6 %, respectively. This result indicates that soil washing combined with Fenton-like oxidation may be a practical approach for the remediation of PCB-contaminated soil.

  5. Soil washing in combination with homogeneous Fenton-like oxidation for the removal of 2,4,4'-trichlorodiphenyl from soil contaminated with capacitor oil.

    Science.gov (United States)

    Ma, Xiao-Hong; Zhao, Ling; Lin, Zhi-Rong; Dong, Yuan-Hua

    2016-04-01

    Detoxification by chemical oxidation of polychlorinated biphenyls (PCBs) in contaminated soils is very difficult and inefficient because PCBs typically associate with the solid phase or exist as non-aqueous-phase liquids due to their low solubility and slow desorption rates, and thus, they are difficult to remove from soils by using traditional, water-based elution techniques. Surfactant can enhance washing efficiency of PCBs from contaminated soils. This study used Brij 58, Brij 30, Tween 80, and 2-hydroxypropyl-β-cyclodextrin (HPCD) to solubilize 2,4,4'-trichlorodiphenyl (PCB28) from soil contaminated with capacitor oil into solution. The feasibility of PCB28 oxidation in soil washing wastewater through a Fe(3+)-catalyzed Fenton-like reaction was subsequently examined. Washing with 10 g L(-1) Brij 58 solution showed the highest extraction efficiency (up to 61.5 %) compared with that of the three other surfactants. The total concentration of PCB28 in contaminated soil at 25 °C after 48-h extraction was 286 mg L(-1). In contrast to conditions in which no washing agent was added, addition of the four washing agents decreased the efficiency of PCB28 degradation by the Fenton-like reaction, with the decrease due to addition of 10 g L(-1) Brij 58 solution being the smallest. The optimal concentration of H2O2 for preventing its useless decomposition was found to be 50 mM. The efficiency of PCB28 removal was lower when the initial concentration of PCB28 treated in the Fenton-like reaction was higher. The degradation efficiencies of PCB28 at initial concentrations of 0.1, 10, and 176 mg L(-1) in 10 g L(-1) Brij 58 solution at 25 °C and pH 3.0 and 9 h of reaction using 50 mM H2O2 were 64.1, 42.0, and 34.6 %, respectively. This result indicates that soil washing combined with Fenton-like oxidation may be a practical approach for the remediation of PCB-contaminated soil. PMID:26762933

  6. Degradation kinetics and mechanisms of phenol in photo-Fenton process

    Institute of Scientific and Technical Information of China (English)

    何锋; 雷乐成

    2004-01-01

    Phenol degradation in photochemically enhanced Fenton process was investigated in this work. UV-VIS spectra of phenol degradation showed the difference between photo-Fenton process and UV/H2O2, which is a typical hydroxyl radical process. A possible pathway diagram for phenol degradation in photo-Fenton process was proposed, and a mathematical model for chemical oxygen demand (COD) removal was developed. Operating parameters such as dosage of H2O2 and ferrous ions, pH, suitable carrier gas were found to impact the removal of COD significantly. The results and analysis of kinetic parameters calculated from the kinetic model showed that complex degradation of phenol was the main pathway for removal of COD; while hydroxyl radicals acted weakly in the photo-Fenton degradation of phenol.

  7. 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...

  8. Élimination des polluants organiques de l'eau par les procédés électrochimiques : procédés électro-Fenton et électro-Fenton modifiés

    OpenAIRE

    Lin, Heng

    2015-01-01

    In this paper, electro-Fenton and sulfate radical-based electro-Fenton-like processes were used to degrade artificial sweeteners and azo dye. The results obtained during the research concern the removal efficiency, the oxidation mechanism, degradation pathway and toxicity evolution of target pollutants.(1) Electro-Fenton process was a effective method for the degradation of ASP in water. The removal and mineralization rate was affected by the Fe2+ concentration and applied current. The absolu...

  9. BİR İLERİ OKSİDASYON PROSESİ : FENTON PROSES

    OpenAIRE

    Engin GÜRTEKİN; Nusret ŞEKERDAĞ

    2008-01-01

    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 ...

  10. Biological hazard evaluation of a pharmaceutical effluent before and after a photo-Fenton treatment.

    Science.gov (United States)

    Novoa-Luna, Karen Adriana; Mendoza-Zepeda, Arisbeht; Natividad, Reyna; Romero, Rubi; Galar-Martínez, Marcela; Gómez-Oliván, Leobardo Manuel

    2016-11-01

    The aim of this study was to evaluate the biological hazard of a pharmaceutical effluent before and after treatment. For the former, the determined 96h-LC50 value was 1.2%. The photo-Fenton treatment catalyzed with an iron-pillared clay reduced this parameter by 341.7%. Statistically significant increases with respect to the control group (Pphoto-Fenton process decreases the presence of PCT, oxidative stress, genotoxic damage and LC50 in Hyalella azteca.

  11. Degradation of n-butyl xanthate using fly ash as heterogeneous Fenton-like catalyst

    Institute of Scientific and Technical Information of China (English)

    陈绍华; 杜冬云

    2014-01-01

    Heterogeneous Fenton-like process using fly ash as a catalyst was studied to degrade n-butyl xanthate form aqueous solution. The different reaction parameters on the degradation efficiency of the process were investigated. The fly ash/H2O2 catalyst possesses a high oxidation activity for n-butyl xanthate degradation in aqueous solution. It is found that both the dosage of catalyst and initial solution pH significantly affect the n-butyl xanthate conversion efficient. The results indicate that by using 1.176 mmol/L H2O2 and 1.0 g/L fly ash catalyst with mass fraction of 4.14%Fe(III) oxide at pH 3.0, almost 96.90%n-butyl xanthate conversion and over 96.66%COD removal can be achieved within 120 min with heterogeneous catalysis by fly ash. CS2 as an intermediate of n-butyl xanthate oxidation. Finally, it is demonstrated that the fly ash/H2O2 catalytic oxidation process can be an efficient method for the treatment of n-butyl xanthate containing wastewater.

  12. Degradation of hydroxycinnamic acid mixtures in aqueous sucrose solutions by the Fenton process.

    Science.gov (United States)

    Nguyen, Danny M T; Zhang, Zhanying; Doherty, William O S

    2015-02-11

    The degradation efficiencies and behaviors of caffeic acid (CaA), p-coumaric acid (pCoA), and ferulic acid (FeA) in aqueous sucrose solutions containing the mixture of these hydroxycinnamic acids (HCAs) were studied by the Fenton oxidation process. Central composite design and multiresponse surface methodology were used to evaluate and optimize the interactive effects of process parameters. Four quadratic polynomial models were developed for the degradation of each individual acid in the mixture and the total HCAs degraded. Sucrose was the most influential parameter that significantly affected the total amount of HCA degraded. Under the conditions studied there was a sucrose in all reactions. The optimal values of the process parameters for a 200 mg/L HCA mixture in water (pH 4.73, 25.15 °C) and sucrose solution (13 mass %, pH 5.39, 35.98 °C) were 77% and 57%, respectively. Regression analysis showed goodness of fit between the experimental results and the predicted values. The degradation behavior of CaA differed from those of pCoA and FeA, where further CaA degradation is observed at increasing sucrose and decreasing solution pH. The differences (established using UV/vis and ATR-FTIR spectroscopy) were because, unlike the other acids, CaA formed a complex with Fe(III) or with Fe(III) hydrogen-bonded to sucrose and coprecipitated with lepidocrocite, an iron oxyhydroxide.

  13. Combined Chemical Activation and Fenton Degradation to Convert Waste Polyethylene into High-Value Fine Chemicals.

    Science.gov (United States)

    Chow, Cheuk-Fai; Wong, Wing-Leung; Ho, Keith Yat-Fung; Chan, Chung-Sum; Gong, Cheng-Bin

    2016-07-01

    Plastic waste is a valuable organic resource. However, proper technologies to recover usable materials from plastic are still very rare. Although the conversion/cracking/degradation of certain plastics into chemicals has drawn much attention, effective and selective cracking of the major waste plastic polyethylene is extremely difficult, with degradation of C-C/C-H bonds identified as the bottleneck. Pyrolysis, for example, is a nonselective degradation method used to crack plastics, but it requires a very high energy input. To solve the current plastic pollution crisis, more effective technologies are needed for converting plastic waste into useful substances that can be fed into the energy cycle or used to produce fine chemicals for industry. In this study, we demonstrate a new and effective chemical approach by using the Fenton reaction to convert polyethylene plastic waste into carboxylic acids under ambient conditions. Understanding the fundamentals of this new chemical process provides a possible protocol to solve global plastic-waste problems. PMID:27168079

  14. Modified Fe3O4- hydroxyapatite nanocomposites as heterogeneous catalysts in three UV, Vis and Fenton like degradation systems

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Photocatalytic degradation of dye by Ag modified HAP under visible light. • Study of Fenton like degradation of dye by transition metal ions modified HAP. • Comparison of catalytic systems according to Langmuir-Hinshelwood kinetic expression. - Abstract: The magnetite-hydroxyapatite (M-HAP) nanocomposites were prepared by a chemical co- precipitation procedure and characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and diffuse reflectance spectra (DRS). The ability of the synthesized catalyst for photocatalytic degradation of Acid Blue 25 (AB25), as an organic dye, under UV irradiation was studied. The catalyst was modified employing transition metals (Mn, Fe, Co, Ni, Cu and Zn) trying to improve the catalytic performance of HAP in absence of UV irradiation and in the presence of hydrogen peroxide i.e. a Fenton like reaction. The best results obtained for Cu and Co modified M-HAPs and the effect of operational parameters such pH, amount of catalyst and hydrogen peroxide concentration was studied. In order to investigate the performance of HAP based photocatalyst in visible light region, M-HAP was modified with silver ions. At the end, Langmuir-Hinshelwood kinetic expression used to evaluate and compare the catalytic systems. The strongest degradation activity was observed for Ag-M-HAP/Vis system because of Ag3PO4 formation. Apparent reaction rate constant (Kapp) by Ag-M-HAP/Vis was 63, 36 and 19 times faster than Cu-M-HAP(II)/H2O2, Co-M-HAP(II)/H2O2 and M-HAP (I)/UV systems, respectively

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

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Leandro G.; Goes, Marcos M.; Marumo, Julio T., E-mail: jtmarumo@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    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{sub 3} as a white precipitate resulting from the reaction between the Ca(OH){sub 2} and the CO{sub 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)

  16. Efficient photo-assisted Fenton oxidation treatment of multi-walled carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    FAN CaiLing; LI Wei; LI Xin; ZHAO ShiJu; ZHANG Ling; MO YuJun; CHENG RongMing

    2007-01-01

    In this paper, a new and efficient way to oxidize and functionalize the multi-walled carbon nanotubes (MWNTs) has been developed by using a combination of ultraviolet (UV) irradiation and Fenton oxidation process, namely UV/Fenton oxidation treatment. Comparing with conventionally individual Fenton oxidation treatment of MWNTs, UV/Fenton combined treatment improved the etching rates and efficiencies and hence reduced the time for surface modification of MWNTs, which was proved to be an effective method in etching and functionalizing CNTs. The formation of new functional groups, structural changes and thermal stability during oxidation period were characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and could be clarified by thermogravimetric analysis (TGA), which showed that it was under UV irradiation conditions that MWNTs could be rapidly functionalized with hydroxyl, carbonyl and carboxyl groups in the presence of Fenton reagents, originating from the increase in the gross HO·concentration and the existent synergetic effect when using UV irradiation combing with Fenton oxidation process. Introduction of such new oxygen-containing functional groups was attributed to attacks of HO·on defect sites and unsaturated bonds of C=C in the MWNTs sample, which should play an important role in accounting for the FTIR and Raman spectral changes.

  17. Toxicity assessment of tannery effluent treated by an optimized photo-Fenton process.

    Science.gov (United States)

    Borba, Fernando Henrique; Módenes, Aparecido Nivaldo; Espinoza-Quiñones, Fernando Rodolfo; Manenti, Diego Ricieri; Bergamasco, Rosangela; Mora, Nora Diaz

    2013-01-01

    In this work, an optimized photo-Fenton process was applied to remove pollutants from tannery industrial effluent (TIE) with its final toxicity level being assessed by a lettuce-seed-based bioassay test. A full 33 factorial design was applied for the optimization of long-term photo-Fenton experiments. The oPtimum conditions of the photo-Fenton process were attained at concentration values of 0.3 g Fe(2+) L(-1) and 20 g H2O2 L(-1) and pH3, for 120 min UV irradiation time. Reactor operating parameter (ROP) effects on the removal of chemical oxygen demand, colour, turbidity, total suspended solids and total volatile solids were evaluated, suggesting that a broad range of ROP values are also suitable to give results very near to those of the photo-Fenton experiments under optimal conditions. Based on the low calculated median lethal dose (LD50) values from a lettuce-seed-based bioassay test, we suggest that recalcitrant substances are present in treated TIE samples. A possible cause of the high toxicity level could partly be attributed to the nitrate concentration, which was not completely abated by the photo-Fenton process. Apart from this, the photo-Fenton process can be used as a part of an industrial effluent treatment system in order to abate high organic pollutant loads. PMID:23837315

  18. Study on Treatability of Real Textile Wastewater by Electrochemically Generated  Fenton Reagent using Graphite Felt Cathode

    OpenAIRE

    Akbar Eslami; Mohammad Reza Massoudinejad; Farshid Ghanbari; Mahsa Moradi

    2012-01-01

    Background and Objectives: Electro-Fenton process has been widely applied for dye removal from aqueous solution lately. Fenton's reagent is formed in the electrolysis medium through the simultaneous electrochemical reduction of O2 and Fe3+ to H2O2 and Fe2+ respectively on the cathode surface. In this paper, COD reduction potential and decolorization of real textile wastewater were evaluated by electrochemically generated Fenton reagent process. This wastewater mainly contains non-biodegradabl...

  19. Photo-Fenton oxidation of phenol and organochlorides (2,4-DCP and 2,4-D) in aqueous alkaline medium with high chloride concentration.

    Science.gov (United States)

    Luna, Airton J; Chiavone-Filho, Osvaldo; Machulek, Amilcar; de Moraes, José Ermírio F; Nascimento, Cláudio A O

    2012-11-30

    A highly concentrated aqueous saline-containing solution of phenol, 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4-dichlorophenol (2,4-DCP) was treated by the photo-Fenton process in a system composed of an annular reactor with a quartz immersion well and a medium-pressure mercury lamp (450 W). The study was conducted under special conditions to minimize the costs of acidification and neutralization, which are usual steps in this type of process. Photochemical reactions were carried out to investigate the influence of some process variables such as the initial concentration of Fe(2+) ([Fe(2+)](0)) from 1.0 up to 2.5 mM, the rate in mmol of H(2)O(2) fed into the system (FH(2)O(2);in) from 3.67 up to 7.33 mmol of H(2)O(2)/min during 120 min of reaction time, and the initial pH (pH(0)) from 3.0 up to 9.0 in the presence and absence of NaCl (60.0 g/L). Although the optimum pH for the photo-Fenton process is about 3.0, this particular system performed well in experimental conditions starting at alkaline and neutral pH. The results obtained here are promising for industrial applications, particularly in view of the high concentration of chloride, a known hydroxyl radical scavenger and the main oxidant present in photo-Fenton processes. PMID:22809483

  20. Heterogeneous photo-Fenton decolorization of Orange II over Al-pillared Fe-smectite: Response surface approach, degradation pathway, and toxicity evaluation

    International Nuclear Information System (INIS)

    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 Al2O3 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

  1. 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.

  2. Photo-Fenton oxidation of phenol and organochlorides (2,4-DCP and 2,4-D) in aqueous alkaline medium with high chloride concentration.

    Science.gov (United States)

    Luna, Airton J; Chiavone-Filho, Osvaldo; Machulek, Amilcar; de Moraes, José Ermírio F; Nascimento, Cláudio A O

    2012-11-30

    A highly concentrated aqueous saline-containing solution of phenol, 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4-dichlorophenol (2,4-DCP) was treated by the photo-Fenton process in a system composed of an annular reactor with a quartz immersion well and a medium-pressure mercury lamp (450 W). The study was conducted under special conditions to minimize the costs of acidification and neutralization, which are usual steps in this type of process. Photochemical reactions were carried out to investigate the influence of some process variables such as the initial concentration of Fe(2+) ([Fe(2+)](0)) from 1.0 up to 2.5 mM, the rate in mmol of H(2)O(2) fed into the system (FH(2)O(2);in) from 3.67 up to 7.33 mmol of H(2)O(2)/min during 120 min of reaction time, and the initial pH (pH(0)) from 3.0 up to 9.0 in the presence and absence of NaCl (60.0 g/L). Although the optimum pH for the photo-Fenton process is about 3.0, this particular system performed well in experimental conditions starting at alkaline and neutral pH. The results obtained here are promising for industrial applications, particularly in view of the high concentration of chloride, a known hydroxyl radical scavenger and the main oxidant present in photo-Fenton processes.

  3. 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)

    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 Fe2+ and maximum current of 5.0 A. • 11 aromatics, 22 hydroxylated derivatives and 9 carboxylic acids detected as intermediates. • Release of NH4+ and SO42−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 dm3 capacity contained a Pt/air-diffusion cell with 90.2 cm2 electrode area, coupled to a solar compound parabolic collectors (CPCs) photoreactor of 1.57 dm3 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 H2O2 generated at the cathode and added Fe2+, along with the photolysis of Fe(III)-carboxylate complexes with sunlight in the CPCs photoreactor. The effect of Fe2+ 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 Fe2+ 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 and nine short

  4. Fenton peroxidation improves the drying performance of waste activated sludge.

    Science.gov (United States)

    Dewil, Raf; Baeyens, Jan; Neyens, Elisabeth

    2005-01-31

    Advanced sludge treatment processes (AST) reduce the amount of sludge produced and improve the dewaterability, thus probably also affecting the heat transfer properties and the drying characteristics of the sludge. This paper studies the influence of the Fenton peroxidation on the thermal conductivity of the sludge. Results demonstrate that the Fenton's peroxidation positively influences the sludge cake consistency and hence enhances the mechanical dewaterability and the drying characteristics of the dewatered sludge. For the two sludges used in this study, i.e. obtained from the wastewater treatment plants (WWTP) of Tienen and Sint-Niklaas--the dry solids content of the mechanically dewatered sludge increased from 22.5% to 40.3% and from 18.7% to 35.2%, respectively. The effective thermal conductivity k(e) of the untreated and the peroxidized sludges is measured and used to determine the heat transfer coefficient h(s). An average improvement for k(e) of 16.7% (Tienen) and 5.8% (Sint-Niklaas) was observed. Consequently the value of h(s) increased with 15.6% (Tienen) and 5.0% (Sint-Niklaas). This increased heat transfer coefficient in combination with the increased dewaterability has direct implications on the design of sludge dryers. A plate-to-plate calculation of a multiple hearth dryer illustrates that the number of plates required to dry the peroxidized sludge to 90% DS is less than half the number of plates needed to dry untreated sludge. This results in reduced dryer dimensions or a higher capacity for an existing dryer of given dimensions. PMID:15629575

  5. Fuzzy-logic modeling of Fenton's strong chemical oxidation process treating three types of landfill leachates.

    Science.gov (United States)

    Sari, Hanife; Yetilmezsoy, Kaan; Ilhan, Fatih; Yazici, Senem; Kurt, Ugur; Apaydin, Omer

    2013-06-01

    Three multiple input and multiple output-type fuzzy-logic-based models were developed as an artificial intelligence-based approach to model a novel integrated process (UF-IER-EDBM-FO) consisted of ultrafiltration (UF), ion exchange resins (IER), electrodialysis with bipolar membrane (EDBM), and Fenton's oxidation (FO) units treating young, middle-aged, and stabilized landfill leachates. The FO unit was considered as the key process for implementation of the proposed modeling scheme. Four input components such as H(2)O(2)/chemical oxygen demand ratio, H(2)O(2)/Fe(2+) ratio, reaction pH, and reaction time were fuzzified in a Mamdani-type fuzzy inference system to predict the removal efficiencies of chemical oxygen demand, total organic carbon, color, and ammonia nitrogen. A total of 200 rules in the IF-THEN format were established within the framework of a graphical user interface for each fuzzy-logic model. The product (prod) and the center of gravity (centroid) methods were performed as the inference operator and defuzzification methods, respectively, for the proposed prognostic models. Fuzzy-logic predicted results were compared to the outputs of multiple regression models by means of various descriptive statistical indicators, and the proposed methodology was tested against the experimental data. The testing results clearly revealed that the proposed prognostic models showed a superior predictive performance with very high determination coefficients (R (2)) between 0.930 and 0.991. This study indicated a simple means of modeling and potential of a knowledge-based approach for capturing complicated inter-relationships in a highly non-linear problem. Clearly, it was shown that the proposed prognostic models provided a well-suited and cost-effective method to predict removal efficiencies of wastewater parameters prior to discharge to receiving streams.

  6. Preservation of glutamic acid-iron chelate into montmorillonite to efficiently degrade Reactive Blue 19 in a Fenton system under sunlight irradiation at neutral pH

    Science.gov (United States)

    Huang, Zhujian; Wu, Pingxiao; Gong, Beini; Yang, Shanshan; Li, Hailing; Zhu, Ziao; Cui, Lihua

    2016-05-01

    To further enhance the visible light responsive property and the chemical stability of Fe/clay mineral catalysts, glutamic acid-iron chelate intercalated montmorillonite (G-Fe-Mt) was developed. The physiochemical properties of G-Fe-Mt were investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), etc. The results showed that glutamic acid-iron chelates were successfully intercalated into the gallery of montmorillonite and the intercalated glutamic acid-iron chelate molecules were well preserved. The product G-Fe-Mt displayed excellent catalytic performance in heterogeneous photo-Fenton reaction under sunlight irradiation at acidic and neutral pH values. The chelation and the visible light responsiveness of glutamic acid produce a synergistic effect leading to greatly enhanced sunlight-Fenton reaction catalyzed by the heterogeneous G-Fe-Mt under neutral pH. G-Fe-Mt is a promising catalyst for advanced oxidation processes.

  7. Chlorinated and brominated phosphatidylcholines are generated under the influence of the Fenton reagent at low pH-a MALDI-TOF MS study.

    Science.gov (United States)

    Wu, Jianqing; Teuber, Kristin; Eibisch, Mandy; Fuchs, Beate; Schiller, Jürgen

    2011-01-01

    Lipid (phospholipid) oxidation is an increasingly important research topic due to the significant physiological relevance. The Fenton reaction, i.e. the transition metal catalyzed decomposition of H(2)O(2) is frequently used to generate hydroxyl radicals (HO*). Lipids with unsaturated fatty acyl residues are primarily converted by HO* radicals into peroxides. In contrast, chloro- and bromohydrins as well as dihalogenides are formed by the addition of HOCl or HOBr to the olefinic groups of the fatty acyl residues of lipids or under the influence of the enzyme myeloperoxidase (MPO) from Cl(-) and H(2)O(2). We will show here by using MALDI-TOF MS for product analysis that halogenated products may also be generated in the presence of the Fenton reagent, if either FeCl(2) or FeBr(2) is used. In the presence of FeSO(4), however, peroxides are exclusively generated. It will also be shown that the generation of halogen-containing products is a competing reaction with the cleavage of the double bond under generation of the corresponding aldehyde or carboxylic acid that is favored at prolonged incubation times and at elevated pH. PMID:20932962

  8. A novel Electro-Fenton-Like system using PW11O39Fe(III)(H2O)4- as an electrocatalyst for wastewater treatment

    International Nuclear Information System (INIS)

    A novel Electro-Fenton-Like (EFL) system was developed using the Keggin-type iron-substituted heteropolytungstate anion PW11O39Fe(III)(H2O)4- to substitute for Fe3+ in the conventional Electro-Fenton (EF) system for treatment of water polluted with organic compounds. The EFL system overcomes the drawback of low pH in conventional EF approaches and can be directly applied to neutral water treatment without any pH adjustment. Experimental results for dimethylphthalate (DMP) revealed complete degradation in 2 flow rate of 60 mL min-1. Total organic carbon removal of ∼56% was achieved at 120 min. Comparison with conventional EF oxidation revealed better efficiency of the present system for DMP degradation, suggesting its potential in treatment of water and wastewater with a relaxed pH requirement. The cumulative H2O2 concentration generated in situ at the electrode was monitored and the observed degradation rate constants kobs were determined for different initial DMP concentrations. The ligand exchange reaction of PW11O39Fe(III)(H2O)4- with H2O2 and the electron transfer resulting in hydroxyl radicals were examined using HPLC and electrochemical impedance spectroscopy. An electrocatalytic model involving inner-sphere electron transfer and a reaction mechanism for PW11O39Fe(III)(H2O)4- electrocatalytic reduction of H2O2 are proposed.

  9. UV light photo-Fenton degradation of polyphenols in oolong tea manufacturing wastewater.

    Science.gov (United States)

    Sabaikai, Waraluk; Sekine, Makoto; Tokumura, Masahiro; Kawase, Yoshinori

    2014-01-01

    The UV light photo-Fenton degradation of oolong tea polyphenols in tea manufacturing effluent that color the wastewater to a dark brown has been examined. In order to elucidate the photo-Fenton degradation mechanism of oolong tea polyphenols and find the optimal dosages of the Fenton reagents, systematic study has been conducted. For the UV light photo-Fenton degradation of oolong tea effluent being 70 mg-(polyphenol) L(-1), the optimum dosages of Fenton reagents were found to be 20 mgL(-1) of total Fe and 500 mgL(-1) of H2O2. The polyphenol degradation could be divided into two stages. The polyphenols concentration rapidly decreased to around 30% of the initial concentration within 2 min and the degradation rate significantly slowed down in the subsequent stage. After 60 min of UV light irradiation, 97% polyphenol removal was obtained. The initial quick degradation of oolong tea polyphenols suggests that hydroxyl radical generated by the photo-Fenton process might preferentially attack polyphenols having high antioxidant activity by scavenging hydroxyl radicals. Almost complete decolorization of the oolong tea effluent was achieved after 80 min. About 96% mineralization of 63 mgL(-1) TOC loading was achieved within 60 min and then further mineralization was rather slow. The complete COD removal of 239 mgL(-1) COD loading was obtained after 100 min. The present results indicate that the UV light photo-Fenton degradation process can treat tea manufacturing wastewaters very effectively.

  10. Solar photoelectro-Fenton degradation of the herbicide 4-chloro-2-methylphenoxyacetic acid optimized by response surface methodology

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Segura, Sergi [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); Almeida, Lucio Cesar; Bocchi, Nerilso [Laboratorio de Pesquisas em Eletroquimica, Departamento de Quimica, Universidade Federal de Sao Carlos, C.P. 676, 13560-970 Sao Carlos - SP (Brazil); 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)

    2011-10-30

    Highlights: {yields} The herbicide MCPA is quickly mineralized by solar photoelectro-Fenton. {yields} A CCRD allowed the optimization of current, Fe{sup 2+} content and solution pH. {yields} TOC, MCE and energy consumption are described by response surface methodology. {yields} Generated hydroxyl radical destroys MCPA and its aromatic oxidation by-products. {yields} 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{sup -1} MCPA solutions in 0.05 M Na{sub 2}SO{sub 4} at a liquid flow rate of 180 L h{sup -1} with an average UV irradiation intensity of about 32 W m{sup -2}. The optimum variables found for the SPEF process were 5.0 A, 1.0 mM Fe{sup 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{sup -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.

  11. Investigation on pretreatment of centrifugal mother liquid produced in the production of polyvinyl chloride by air-Fenton technique.

    Science.gov (United States)

    Sun, Yingying; Hua, Xiuyi; Ge, Rui; Guo, Aitong; Guo, Zhiyong; Dong, Deming; Sun, Wentian

    2013-08-01

    Centrifugal mother liquid (CML) is one of the main sources of wastewater produced during the production of polyvinyl chloride in chlor-alkali industry. CML is a typical poorly biodegradable organic wastewater, containing many kinds of refractory pollutants. Specifically, it contains dissolved refractory polymers, especially polyvinyl alcohol (PVA), which can pass though the biotreatment processes and clog the membranes used for further treatment. In this study, to ensure the CML applicable to biotreatment and membrane treatment, a novel efficient and mild technique, air-Fenton treatment, was employed as a pretreatment technique to improve biodegradability of the CML and to break down the polymers in the CML. Firstly, the technique was optimized for the CML treatment by optimizing the main parameters, including the dosage of ferrous sulfate, initial pH of the wastewater, [H2O2]/[Fe(2+)], aeration rate, reaction time, and temperature, based on removal efficiency of COD and PVA from the CML. Then, the optimized technique was tested and evaluated. The results indicated that under the optimized conditions, the air-Fenton treatment could remove 66, 98, and 55 % of the COD, PVA, and TOC, respectively, from the CML. After the treatment, biodegradability of the wastewater increased significantly (BOD/COD increased from 0.31 to 0.68), and almost all of the PVA polymers were removed or broken down. Meanwhile, concentration of the remaining iron ions, which were added during the treatment, was also quite low (only 2.9 mg/L). Furthermore, most of the suspended materials and ammonia nitrogen, and some of the phosphorus in the wastewater were removed simultaneously.

  12. Fabrication of magnetic carbon composites from peanut shells and its application as a heterogeneous Fenton catalyst in removal of methylene blue

    International Nuclear Information System (INIS)

    Graphical abstract: Peanut shell magnetic carbon (PMC) were fabricated by carbonized the mixture of peanut shells and (NH4)3Fe(C2O4)3. The obtained PMC exhibit high efficiency in catalysis oxidation methylene blue with the help of K2S2O8 and it can be easily separated from aqueous by external magnetic field. Meanwhile, the catalyst can be reused for seven times almost without decreased of activity. - Highlights: • Novel peanut shell magnetic carbon (PMC) catalysts were successfully synthesized. • PMC exhibited superior activity as a heterogeneous Fenton-like catalyst. • A high efficient Fenton-like system was set up for removal MB. • PMC posed excellent catalysis oxidation quality, stability and good reusability. - Abstract: Magnetic carbons were prepared from agricultural waste peanut shells and Ferric ammonium oxalate via a simple impregnation and carbonization process. The obtained composites were characterized by element analysis, MÖssbauer spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, X-ray diffraction, vibrating sample magnetometry and the Brunauer-Emmett-Teller surface area method, respectively. The magnetic carbon material was used as catalyst of heterogeneous Fenton reaction to remove methylene blue with the help of persulfate in waste water. The results indicated that both the removal rate and removal efficiency of this catalytic system are very excellent. The degradation efficiency was best (90% within 30 min) using initial concentrations of 0.5 g L−1 persulfate and 40 mg L−1 methylene blue. The removal mechanism was investigated by LC-MS. The catalyst retained its activity after seven reuses, indicating its good stability and reusability. It is inexpensive because it consists mainly of agricultural waste. Its porosity contributed to its high activity, which was achieved without any additional activation process. These indicating that the catalyst is potentially useful in the treatment of wastewater

  13. Fenton/BAF组合工艺处理全棉机织布印染废水研究%Fenton Oxidation/BAF Process for Advanced Treatment of Wastewater from Dyeing and Finishing of Cotton Woven Fabrics

    Institute of Scientific and Technical Information of China (English)

    文淦斌; 黄瑞敏; 黄春梅; 王君

    2011-01-01

    The dyeing and finishing processes of cotton woven fabrics need a lot of sizing agents toimprove the smoothness and wear resistance of the fabrics, thus the discharged wastewater often contains a lot of desizing wastewater, which has high concentration of COD, strong alkalinity and poor biodegradability. The biodegradability is difficult to be improved using conventional coagulation sedimentation/anaerobic/aerobic process, and the effluent COD and color are difficult to meet the standards. According to the characteristics above, the combined process of Fenton oxidation and biological aerated filter (BAF) was used for the advanced treatment. The results of the pilot study show that under the conditions of initial pH of 4, H2O2 dosage of 150 mg/L, Fe2+/H2O2 ratio of 1 and reaction time of 60 min in Fenton oxidation process, COD and color of the wastewater are reduced from 400 mg/L to 125 mg/L with the removal rate of 68.75% and from 200 times to less than 25 times respectively. After the Fenton oxidation,the B/C ratio is increased from 0.08 to 0.34, and the biodegradability is significantly improved. Under the condition of HRT of 2.5 h, COD in the effluent from BAF is 74.5 mg/L, with the removal rate of 40.4%. After treatment by the combined process, the removal rate of COD is more than 80% , and the color is less than 25 times, with good treatment efficiency.%全棉机织布染色加工需使用大量浆料助剂进行上浆处理以提高织物的光滑度及耐磨性,因而排放的废水中往往含有大量的退浆废水,其COD浓度高、碱度强、可生化性差,经常规的混凝沉淀/厌氧/好氧组合工艺处理后,可生化性难以改善,出水COD、色度值难以达标.采用Fen-ton/曝气生物滤池(BAF)组合工艺对其进行深度处理,中试结果表明,在Fenton工艺的初始pH值=4、H2O2投加量=150 mg/L、Fe2+/H2O2值=1、反应时间为60 min的条件下,COD由原来的400mg/L降低至125 mg/L,去除率达68.75%,色度由200

  14. Elimination of radiocontrast agent diatrizoic acid by photo-Fenton process and enhanced treatment by coupling with electro-Fenton process.

    Science.gov (United States)

    Bocos, Elvira; Oturan, Nihal; Pazos, Marta; Sanromán, M Ángeles; Oturan, Mehmet A

    2016-10-01

    The removal of radiocontrast agent diatrizoic acid (DIA) from water was performed using photo-Fenton (PF) process. First, the effect of H2O2 dosage on mineralization efficiency was determined using ultraviolet (UV) irradiation. The system reached a maximum mineralization degree of 60 % total organic carbon (TOC) removal at 4 h with 20 mM initial H2O2 concentration while further concentration values led to a decrease in TOC abatement efficiency. Then, the effect of different concentrations of Fenton's reagents was studied for homogeneous Fenton process. Obtained results revealed that 0.25 mM Fe(3+) and 20 mM H2O2 were the best conditions, achieving 80 % TOC removal efficiency at 4 h treatment. Furthermore, heterogeneous PF treatment was developed using iron-activated carbon as catalyst. It was demonstrated that this catalyst is a promising option, reaching 67 % of TOC removal within 4 h treatment without formation of iron leachate in the medium. In addition, two strategies of enhancement for process efficiency are proposed: coupling of PF with electro-Fenton (EF) process in two ways: photoelectro-Fenton (PEF) or PF followed by EF (PF-EF) treatments, achieving in both cases the complete mineralization of DIA solution within only 2 h. Finally, the Microtox tests revealed the formation of more toxic compounds than the initial DIA during PF process, while, it was possible to reach total mineralization by both proposed alternatives (PEF or PF-EF) and thus to remove the toxicity of DIA solution.

  15. 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.

  16. Learning about Regiochemistry from a Hydrogen-Atom Abstraction Reaction in Water

    Science.gov (United States)

    Sears-Dundes, Christopher; Huon, Yoeup; Hotz, Richard P.; Pinhas, Allan R.

    2011-01-01

    An experiment has been developed in which the hydrogen-atom abstraction and the coupling of propionitrile, using Fenton's reagent, are investigated. Students learn about the regiochemistry of radical formation, the stereochemistry of product formation, and the interpretation of GC-MS data, in a safe reaction that can be easily completed in one…

  17. Roles of TaON and Ta{sub 3}N{sub 5} in the visible-Fenton-like degradation of atrazine

    Energy Technology Data Exchange (ETDEWEB)

    Du, Yingxun, E-mail: yxdu@niglas.ac.cn; Zhao, Lu; Zhang, Yuanyuan

    2014-02-01

    Graphical abstract: - Highlights: • TaON exhibited higher photocatalytic activity than Ta{sub 3}N{sub 5}. • e{sub CB} is captured by either Fe{sup 3+} or H{sub 2}O{sub 2} and h{sub VB} could not oxidize atrazine. • ·OH, from the reduction of H{sub 2}O{sub 2} by Fe{sup 2+} or by e{sub CB}, is the active species. • By capturing e{sub CB}, H{sub 2}O{sub 2} was preferred to be reduced to H{sub 2}O than to ·OH. • TaON showed the higher separation efficiency of electrons and holes than Ta{sub 3}N{sub 5}. - Abstract: In this study, the roles of TaON and Ta{sub 3}N{sub 5} in the degradation of atrazine by the visible-Fenton-like system were examined in detail. The TaON and Ta{sub 3}N{sub 5} samples prepared by the nitridation of Ta{sub 2}O{sub 5} and characterized by XRD, DRS, BET and PL analyses. The results showed that the TaON sample had weaker absorption in the visible region but higher specific surface area than the Ta{sub 3}N{sub 5} sample. The degradation rate of atrazine in visible-TaON-Fenton-like system was 2.64 times than that in visible-Ta{sub 3}N{sub 5}-Fenton-like system. Both Fe{sup 2+} and H{sub 2}O{sub 2} could be reduced by e{sub CB} (electrons in the conduction band) in TaON or Ta{sub 3}N{sub 5}, while atrazine could not be oxidized by h{sub VB} (holes in the valance band). ·OH is the active species for the degradation of atrazine in visible-TaON/Ta{sub 3}N{sub 5}-Fenton-like systems. Majority of ·OH originated from Fenton reaction. After Fe{sup 3+} was reduced by e{sub CB} to Fe{sup 2+}, Fe{sup 2+} reacted quickly with H{sub 2}O{sub 2} to generate ·OH. In addition, by capturing e{sub CB}, a little of H{sub 2}O{sub 2} was reduced to yield ·OH, which contributed a small fraction of atrazine degradation. Based on the experimental results, the roles of TaON and Ta{sub 3}N{sub 5} in the visible-Fenton-like system were proposed. And the higher photocatalytic activity of TaON than Ta{sub 3}N{sub 5} was suggested to be due to the higher

  18. Aquifer evaluation at Fenton Hill, October and November 1980

    Energy Technology Data Exchange (ETDEWEB)

    Becker, N.M.; Purtymun, W.D.; Ballance, W.C.

    1981-10-01

    An aquifer test at the Fenton Hill Geothermal Site was performed on a volcanic aquifer used for water supply. The test was made to determine the yield from the aquifer and to predict the amount of depletion that would occur with increased production during the period 1981 to 1985. A step-discharge test indicated the aquifer would comfortably yield 100 gal per min (gpm) without excessive water level drawdown in the pumping well. Drawdown test results indicated that the average aquifer transmissivity and storage coefficient are 5000 gal per day per foot (gpd/ft) and 0.07, respectively. Using these parameters, a drawdown was estimated to be at least 42 ft at the pumping well due to a withdrawal of 500 acre-ft of water over 5 yr. However, the presence of ground water boundaries indicates the aquifer is of limited extent, and because of this, the water level decline would probably be much greater. Past water level data indicate that there is little recharge to the aquifer.

  19. Effect of pH and H2O2 dosage on catechol oxidation in nano-Fe3O4 catalyzing UV-Fenton and identification of reactive oxygen species

    DEFF Research Database (Denmark)

    Li, Weiguang; Wang, Yong; Angelidaki, Irini

    2014-01-01

    scavenging of HO would completely inhibit degradation. This result implied only HO was the direct product, while O21 and O2- were secondary oxidants coming from HO involved reactions. This finding increases insight into the mechanism for nano-Fe3O4 catalyzing UV-Fenton. Maintenance of catalytic ability...... dosage of 11.80mM for complete oxidation of 100mgL-1 catechol) to 1.00×δH2O2. Radical identification experiments based on inhibition of methylene blue degradation rate under respective scavenger for HO, O21 and HO2 showed HO, O21 and O2- were involved in nano-Fe3O4 catalyzing UV-Fenton, and total......This laboratory scale batch study examined catechol oxidation by UV-Fenton with commercial nanosized Fe3O4 as catalyst, focusing on influence of initial pH and H2O2 dosage on oxidation efficiency (represented by COD removal) and H2O2 utilization efficiency. In a wide initial pH range (2...

  20. Sequential treatment of olive oil mill wastewater with adsorption and biological and photo-Fenton oxidation.

    Science.gov (United States)

    Aytar, Pınar; Gedikli, Serap; Sam, Mesut; Farizoğlu, Burhanettin; Çabuk, Ahmet

    2013-05-01

    Olive oil mill wastewater (OMWW), a recalcitrant pollutant, has features including high phenolic content and dark color; thereby, several chemical or physical treatments or biological processes were not able to remediate it. In this study, the treatment efficiencies of three treatments, including adsorption, biological application, and photo-Fenton oxidation were sequentially evaluated for OMWW. Adsorption, biological treatment, and photo-Fenton caused decreasing phenolic contents of 48.69 %, 59.40 %, and 95 %, respectively. However, after three sequential treatments were performed, higher reduction percentages in phenolic (total 99 %) and organic contents (90 %) were observed. Although the studied fungus has not induced significant color reduction, photo-Fenton oxidation was considered to be an attractive solution, especially for color reduction. Besides, toxicity of OMWW treatment was significantly reduced.

  1. Investigation of a shallow aquifer near the Fenton Hill hot dry rock site using DC resistivity

    Energy Technology Data Exchange (ETDEWEB)

    Pearson, C.F.

    1981-10-01

    A shallow aquifer in the base of the Tertiary volcanic sequence was investigated using a series of 9 DC Schlumberger soundings taken within 10 km of the Fenton Hill hot dry rock geothermal site. The aquifer dips to the southwest following the top of the Abo formation, which acts as an aquiclude. Depth increases from 130 m in the eastern part of the study area to 260 m at 1.5 km west of the Fenton Hill site. Aquifer resistivities varied from 13..cap omega..-m to 126..cap omega..-m, which could be caused by variable permeability in the aquifer. Using results from empirical studies permeabilities ranging from 40 darcies to less than 0.3 darcies were estimated with the highest values occurring nearest to the Fenton Hill site.

  2. Treatment of TFT-LCD wastewater containing ethanolamine by fluidized-bed Fenton technology.

    Science.gov (United States)

    Anotai, Jin; Chen, Chia-Min; Bellotindos, Luzvisminda M; Lu, Ming-Chun

    2012-06-01

    The objectives of this study are: (1) to determine the effect of pH, initial concentration of Fe(2+) and H(2)O(2) dosage on the removal efficiency of MEA by fluidized-bed Fenton process and Fenton process, (2) to determine the optimal conditions for the degradation of ethanolamine from TFT-LCD wastewater by fluidized-bed Fenton process. In the design of experiment, the Box-Behnken design was used to optimize the operating conditions. A removal efficiency of 98.9% for 5mM MEA was achieved after 2h under optimal conditions of pH3, [Fe(2+)]=5mM and [H(2)O(2)]=60mM.

  3. Degradation of 4-Chlorophenol Solution by Synergetic Effect of Dual-frequency Ultrasound with Fenton Reagent

    Institute of Scientific and Technical Information of China (English)

    赵德明; 徐新华; 雷乐成; 汪大翚

    2005-01-01

    4-Chlorophenol (4-CP) solution was treated by dual-frequency ultrasound in conjunction with Fenton reagent, and obvious improvement in the 4-CP degradation rate was observed in this advanced oxidation process.Experimental results showed that ultrasonic intensity, saturating gas and pH value affected greatly the 4-CP removal rate. Among four different saturating gases (Ar, 02, air and N2), 4-CP degradation with Ar-saturated solution was the best. However, in the view of practical wastewater treatment, using oxygen as the saturating gas would be more economical. The addition of Fenton reagent followed the first-order kinetics and increased the 4-CP degradation rate.The 4-CP removal rate increased by around 126% within 15 rain treatment. The synergetic effect of dual-frequency ultrasound with Fenton reagent on 4-CP degradation was obviously observed.

  4. Biomimetic Fenton-catalyzed lignin depolymerization to high-value aromatics and dicarboxylic acids.

    Science.gov (United States)

    Zeng, Jijiao; Yoo, Chang Geun; Wang, Fei; Pan, Xuejun; Vermerris, Wilfred; Tong, Zhaohui

    2015-03-01

    By mimicking natural lignin degradation systems, the Fenton catalyst (Fe(3+), H2O2) can effectively facilitate lignin depolymerization in supercritical ethanol (7 MPa, 250 °C) to give organic oils that consist of mono- and oligomeric aromatics, phenols, dicarboxylic acids, and their derivatives in yields up to (66.0±8.5) %. The thermal properties, functional groups, and surface chemistry of lignin before and after Fenton treatment were examined by thermogravimetric analysis, pyrolysis-gas chromatography-mass spectrometry, (31)P NMR spectroscopy, and X-ray photoelectron spectroscopy. The results suggest that the Fenton catalyst facilitates lignin depolymerization through cleavage of β-ether bonds between lignin residues. The formation of a lignin-iron chelating complex effectively depresses lignin recondensation; thus minimizing charcoal formation and enhancing the yield of liquid products.

  5. Oxidative desulfurization of fuels catalyzed by Fenton-like ionic liquids at room temperature.

    Science.gov (United States)

    Jiang, Yunqing; Zhu, Wenshuai; Li, Huaming; Yin, Sheng; Liu, Hua; Xie, Qingjie

    2011-03-21

    Oxidation of the sulfur-containing compounds benzothiophene (BT), dibenzothiophene (DBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT) has been studied in a desulfurization system composed of model oil, hydrogen peroxide, and different types of ionic liquids [(C(8)H(17))(3)CH(3)N]Cl/FeCl(3), [(C(8)H(17))(3)CH(3)N]Cl/CuCl(2), [(C(8)H(17))(3)CH(3)N]Cl/ZnCl(2), [(C(8)H(17))(3)CH(3)N]Cl/SnCl(2), [(C(4)H(9))(3)CH(3)N]Cl/FeCl(3), [C(10)H(21)(CH(3))(3)N]Cl/FeCl(3), [(C(10)H(21))(2)(CH(3))(2)N]Cl/FeCl(3). Deep desulfurization is achieved in the Fenton-like ionic liquid [(C(8)H(17))(3)CH(3)N]Cl/FeCl(3) at 25 °C for 1 h. The desulfurization of DBT reaches 97.9%, in consuming very low amount of [(C(8)H(17))(3)CH(3)N]Cl/FeCl(3) (only 0.702 mmol). The reaction conditions, for example, the amount of [(C(8)H(17))(3)CH(3)N]Cl/FeCl(3) or H(2)O(2), the temperature, and the molar ratio of FeCl(3) to [(C(8)H(17))(3)CH(3)N]Cl, are investigated for this system. The oxidation reactivity of the different sulfur-containing compounds is found to decrease in the order of DBT>BT>4,6-DMDBT. The desulfurization system can be recycled six times without significant decrease in activity. The sulfur level of FCC gasoline could be reduced from 360 ppm to 110 ppm. PMID:21394927

  6. Iron Compound-Based Heterogeneous Fenton Catalytic Oxidation Technology%基于铁化合物的异相Fenton催化氧化技术

    Institute of Scientific and Technical Information of China (English)

    王彦斌; 赵红颖; 赵国华; 王宇晶; 杨修春

    2013-01-01

    Heterogeneous Fenton catalytic oxidation technology is a powerful method for degradation of various kinds of non-biodegradable pollutants at moderate condition.Heterogeneous Fenton as the evolution of homogeneous Fenton reaction,offer the advantage of allowing easier separation from treated water and reuse,and wider field of application.This article mainly reviews the development of various iron-based materials,such as zero-valent iron,iron oxides,iron (hydr)oxides,ferrihydrite and other iron compounds,as heterogeneous catalysts for degrading organic pollutants.The mechanisms of Fenton reaction are comprehensively illustrated,including the free radical mechanism and the high-valent iron mechanism.Particularly,the emphasis is to summarize the catalytic activity of different heterogeneous Fenton catalysts,and point out that the catalytic efficiency of heterogeneous Fenton catalyst is strongly affected by the surface oxidation state,specific surface area,kinds of doped transition metal and the crystalline phase of catalysts.The different ways to improve the catalytic efficiency of heterogeneous Fenton catalysts are also concluded as:reducing the size of catalysts to nano-scales,loading the catalysts onto carriers with high specific surface area,introducing transition metal (such as Ti,Co,Mn,Cr and V) into the structure of iron oxide.In addition,some novel catalysts such as ferrites are especially paid attention due to their high catalytic activity and stability.Finally,the prospects of the development of the heterogeneous Fenton catalytic oxidation technology is given.We believe that an ideal heterogeneous Fenton catalyst should possess high catalytic efficiency and H2O2 utilization,good chemical stability,effectiveness at extend pH range and the ability of easy to be recycled.%异相Fenton催化氧化技术是一种非常有效的处理难生物降解有机污染物的方法,它可以在温和的条件下实现反应.作为均相Fenton的发展,异相Fenton具有容

  7. Heterogeneous fenton-like degradation of an azo dye reactive brilliant orange by the combination of activated carbon-FeOOH catalyst and H 2O2

    DEFF Research Database (Denmark)

    Wu, Jinhua; Lin, Guanghui; Li, Ping;

    2013-01-01

    The decoloration of an azo dye reactive brilliant orange (X-GN) by a heterogeneous Fenton system using activated carbon-FeOOH catalyst (AC-FeOOH) and H2O2 was studied. Under typical conditions (pH 7.0, H2O2 10 mmol/L, AC-FeOOH 1.0g/L and 30°C), 98% decoloration rate of X-GN was achieved in 240 mm...... that the decoloration of X-GN followed a pseudo-first order reaction and the activation energy was 17.2 kJ/mol. Iron leaching from AC-FeOOH occurred during the reaction, but the decoloration efficiency of X-GN was still higher than 80% after four runs. The AC-FeOOH has a good stability and can be reused. Besides...

  8. Experimental Study on Treatment of Pharmaceutical Wastewater with UV-Fenton Oxidation%UV-Fenton法预处理某制药厂废水的实验研究

    Institute of Scientific and Technical Information of China (English)

    陈琳; 张争民

    2015-01-01

    The pharmaceutical wastewater, a class of industrial wastewater, is characterized by high concentra⁃tion and low bio-degradability. The treatment efficiency had been compared between Fenton and UV-Fenton of dosage, initial pH, reaction time, and so on. The results showed that the treatment efficiency of UV-Fen⁃ton oxidation process was better than Fenton. The optimal reaction conditions of Fenton were as follows: the dosage of FeSO4·7H2O and H2O2 were 0.036 mol/L and 0.128 mol/L respectively, the initial pH was 4.3, the reaction time was 2h, and the removal efficiency of CODCr was 43.9%. However, the optimal conditions of UV-Fenton were as follows: the dosage of FeSO4·7H2O and H2O2 were 0.029 mol/L and 0.102 mol/L respec⁃tively, the initial pH was 4.3, the reaction time of UV and Fenton were 7 min and 75 min respectively and the removal efficiency of CODCr was 63.5%. What’s more, the B/C was increased to 0.39, which showed that UV-Fenton oxidation could improve biodegradability of the pharmaceutical wastewater.%制药废水是一种难生物降解的高浓度有机工业废水,处理困难.研究以某制药股份有限公司综合排放废水为对象,分别采用Fenton和UV-Fenton法对制药废水进行处理,分析试剂投加量、反应初始pH和反应时间等对反应的影响.结果表明,Fenton法处理制药废水的最佳条件为:FeSO4·7H2O投加0.036 mol/L,H2O2投加0.128 mol/L,初始pH为4.3,反应时间为2 h,CODCr去除率为43.9%. UV-Fenton法处理制药废水缩短反应时间,减少试剂投加量,最佳处理条件为:UV处理时间为7 min,FeSO4·7H2O投加0.029 mol/L,H2O2投加0.102 mol/L,初始pH为4.3,反应时间为75 min,最佳条件下CODCr去除率优于Fenton法,可达63.5%,且污水B/C增至0.39,提高可生化性.

  9. Fenton氧化法修复石油污染土壤的研究进展%Remediation of petroleum contaminated soil by Fenton oxidation method: A review

    Institute of Scientific and Technical Information of China (English)

    李方敏; 柳红霞

    2012-01-01

    The traditional Fenton oxidation (Fe2+/H2 02 ) reaction has some drawbacks when used for sml remediation, including rapid reaction rate, regular additions of Fe2+ and the requirement of low pH 〈3, which limited its remediation efficiency for petroleum hydrocarbons contaminated soil. In this paper, recent progress on modified oxidants and catalysts of the Fenton reaction, and effects of the modification on removal efficiencies in petroleum-contaminated soils were reviewed. Soil properties, reaction conditions, pollutant structure and the heterogeneous catalyst specific surface areas were major factors influencing the removal efficiencies. The method of ultrasonic pre-treatment was introduced, which increases the contact probability of Fenton reagent with the petroleum contaminants petroleum hydrocarbon pollutants by the subsequent also prospected. desorbed from soils, and it improves biodegradability of microbial processes. The research trends in this field were%传统的Fenton氧化法(Fe2+/H2O2)因反应速度过快、需要定期补充Fe2+、控制pH值≤3等方面的限制而影响到石油烃类污染土壤的修复效果.本文综述了近年来Fenton反应中氧化剂、催化剂的改进及其对土壤中石油污染物的去除效率,揭示了土壤性质、反应条件、污染物结构及非均相催化剂比表面积等因素对去除效率的影响,介绍了超声波前置处理后,Fenton试剂与土壤上解吸的石油污染物接触几率的增加及石油烃类可生物降解性的提高,促进了微生物的后续处理效果,并对该领域的研究趋势进行了展望.

  10. Amorphous Fe²⁺-rich FeOx loaded in mesoporous silica as a highly efficient heterogeneous Fenton catalyst.

    Science.gov (United States)

    Wang, Min; Shu, Zhu; Zhang, Lingxia; Fan, Xiangqian; Tao, Guiju; Wang, Yongxia; Chen, Lisong; Wu, Meiying; Shi, Jianlin

    2014-06-28

    A simple physical-vapor-infiltration (PVI) method using ferrocene as the iron source, has been developed to load FeOx into the pore channels of mesoporous silica SBA-15. The obtained FeOx/SBA-15 composite has a high loading amount of FeOx (e.g. 26.64 wt% Fe content obtained at PVI duration 17 h and calcination temperature 450 °C) but unblocked pore channels thanks to the unique preparation strategy. The FeOx species are amorphous, rich of Fe(2+) and have been highly dispersed as a nanocoating onto the pore channel surface. The FeOx/SBA-15 composite was used as a heterogeneous Fenton catalyst to degrade Acid orange 7 (AO7). It showed a high catalytic activity and degradation efficiency, which was attributed to the high proportion of Fe(2+) in the amorphous FeOx and their favorable adsorption capability for the dye. The influences of the PVI duration, the calcination temperature and the Fenton reaction conditions (FeOx/SBA-15 dosages, H2O2 dosages and initial pH value) on the catalytic activity were investigated in detail. PMID:24816279

  11. Heterogeneous photo-Fenton-like catalysts Cu2V2O7 and Cr2V4O13 for an efficient removal of azo dye in water

    Directory of Open Access Journals (Sweden)

    Sangeeta Kalal

    2016-12-01

    Full Text Available This work deals with the degradation of non-biodegradable azo-dye (Evans blue by the heterogeneous photo-Fenton-like process using copper pyrovanadate (Cu2V2O7 and chromium tetravanadate (Cr2V4O13 as catalysts, which have been prepared by wet chemical method. These catalysts were characterized by different techniques such as scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and Brunauer–Emmett–Teller surface area analysis. The effect of various parameters such as initial pH, concentration of dye, amount of catalyst, amount of H2O2, and light intensity on the reaction rate has also been studied. Photodegradation efficiency was found 77.78 and 79% for copper pyrovanadate (Cu2V2O7 and chromium tetravanadate (Cr2V4O13, respectively. A tentative mechanism involving ·OH radicals as an oxidant for the degradation of dye has also been proposed. The observations revealed that the rate of photo-Fenton-like degradation of dye follows pseudo-first-order kinetics.

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

    Energy Technology Data Exchange (ETDEWEB)

    El-Ghenymy, Abdellatif [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); Departement de Chimie, Faculte des Sciences, Universite Abdelmalek Essaadi, M' Hannech II B.P.2121, C.P. 93002 Tetouan (Morocco); Garcia-Segura, Sergi; Rodriguez, Rosa Maria [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); El Begrani, Mohamed Soussi; Abdelouahid, Ben Ali [Departement de Chimie, Faculte des Sciences, Universite Abdelmalek Essaadi, M' Hannech II B.P.2121, C.P. 93002 Tetouan (Morocco)

    2012-06-30

    Highlights: Black-Right-Pointing-Pointer Quicker degradation of sulfanilic acid by solar photoelectro-Fenton than electro-Fenton. Black-Right-Pointing-Pointer The same optimized current density, Fe{sup 2+} content and pH for both processes by CCRD. Black-Right-Pointing-Pointer Description of TOC, energy cost and current efficiency by response surface methodology. Black-Right-Pointing-Pointer Fe(III)-carboxylate complexes as main by-products after electro-Fenton. Black-Right-Pointing-Pointer 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{sub 2}SO{sub 4}. Electrolyses were performed with a pre-pilot flow plant containing a Pt/air diffusion reactor generating H{sub 2}O{sub 2}. In SPEF, it was coupled with a solar photoreactor under an UV irradiation intensity of ca. 31 W m{sup -2}. Optimum variables of 100 mA cm{sup -2}, 0.5 mM Fe{sup 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{sup -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{sub 2}O{sub 2} and added Fe{sup 2+}. The quick photolysis of these complexes by UV light of sunlight explains the higher oxidation power of SPEF. NH{sub 4}{sup +} was the main inorganic nitrogen ion released in both processes.

  13. 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.

  14. Fenton法降解水中布洛芬%Degradation of ibuprofen by Fenton oxidation

    Institute of Scientific and Technical Information of China (English)

    杨丽娟; 胡翔; 吴晓楠

    2012-01-01

    采用benton法降解水中布洛芬,考察了H2O2投加量、FeSO4·7H2O与H2O2的比值、初始pH、反应时间等因素对布洛芬去除率的影响,通过正交实验确定影响作用大小依次为:[Fe2+]:[H2O2]的物质的量之比〉H2O2的投加量〉pH值,最佳的反应工艺条件为:H2O2的投加量为3mL-L1,[Fe2+]:[H2O2]的物质的量之比为1:10,反应初始pH值为3,反应时间为40min.在最佳条件下布洛芬的去除率达到86%以上.同时对布洛芬降解反应动力学进行了研究,发现Fenton降解布洛芬符合二级反应动力学规律.%The degradation of ibuprofen was investigated by using Fenton method. The effects of different tactors on the removal efficiency of ibuprofen were evaluated. The order of main factors were O O rthogo ptimal nal experiments as follow: the mole ratio of Fe2+ to H2O2 〉 H2O2 dosage 〉 reaction conditions were as follow : dosage of H2O2 was 3 mL. L- 1, the mole ratio 1 : 10, the initial pH was 3 and the reaction time was 40 min. Under such conditions, the ibuprofen was over 86%. The reaction kinetics was also investigated. The degradation of oxidation was accord with the second order kinetics.

  15. Fenton degradation of sulfanilamide in the presence of Al,Fe-pillared clay: Catalytic behavior and identification of the intermediates.

    Science.gov (United States)

    Khankhasaeva, Sesegma Ts; Dambueva, Darima V; Dashinamzhilova, Elvira Ts; Gil, Antonio; Vicente, Miguel A; Timofeeva, Maria N

    2015-08-15

    Liquid phase catalytic degradation of sulfanilamide with H2O2 was carried out in the presence of Fe,Al/M-pillared clay (Fe,Al/M-MM, M=Na(+), Ca(2+) and Ba(2+)) as heterogeneous Fenton type catalyst. Fe,Al/M-MMs were prepared by swelling of layered aluminosilicate (90-95 wt.% montmorillonite) from a bed located in Mukhortala (Buryatia, Russia) in Na(+), Ca(2+) and Ba(2+) forms by means of the exchange of these cations with bulky Fe,Al-polyoxocations prepared at Al/Fe=10/1 and OH/(Al+Fe)=2.0, and then calcinated at 500°C. XRD method and chemical analysis demonstrated that the rate of crystalline swelling was dependent on the interlayer cations and decreased in the order: Fe,Al-/Na-MM>Fe,Al/Ca-MM>Fe,Al/Ba-MM. It was found that the catalytic properties of Fe,Al/M-MMs depended on the type of exchangeable cations. The effect of the H2O2/sulfanilamide molar ratio, the catalyst content, the reaction temperature and the reaction pH on the removal rate of sulfanilamide has been studied in the presence of Fe,Al/Na-MM. The catalyst can be applied for degradation of sulfanilamide with H2O2 for at least three successive cycles without loss of activity. HPLC analyses pointed out that the main degradation intermediate products were sulfanilic acid, benzenesulfonic acid, p-benzoquinone and aliphatic carboxylic acids.

  16. Fe, Co, Ni nanocrystals encapsulated in nitrogen-doped carbon nanotubes as Fenton-like catalysts for organic pollutant removal.

    Science.gov (United States)

    Yao, Yunjin; Chen, Hao; Lian, Chao; Wei, Fengyu; Zhang, Dawei; Wu, Guodong; Chen, Benjin; Wang, Shaobin

    2016-08-15

    Magnetic metal M (M=Fe, Co, Ni) nanocrystals encapsulated in nitrogen-doped carbon nanotubes (M@N-C) were fabricated conveniently using dicyandiamide as a C/N precursor, and exhibited varying activities toward Fenton-like reaction. The surface morphology and structure of the M@N-C catalysts were characterized and an efficient catalytic degradation performance, high stability, and excellent reusability were observed. In addition, several operational factors, such as initial dye concentration, oxidant type (peroxymonosulfate, peroxydisulfate and H2O2) and dosage, reaction temperature, and dye type as well as stability of the composite were extensively evaluated in view of the practical applications. The results showed that various transition metals M significantly affected the structures and performances of the catalysts, and specially, their activity followed the order of Co>Fe>Ni in the presence of peroxymonosulfate. Moreover, HO⁡ and SO4(-) radicals participating in the process were evidenced using quenching experiments, and a rational mechanism was proposed based on a non-radical process and the free radical process. Control experiments revealed that the enhanced active sites were mainly ascribed to the synergistic effects between the metal nanocrystals and nitrogen-doped carbon. The findings of this study elucidated that encapsulation of nanocrystals in nitrogen-doped carbon nanotubes was an effective strategy to enhance the overall catalytic activity. PMID:27111426

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

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Ai, Zhihui, E-mail: jennifer.ai@mail.ccnu.edu.cn [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China); Zhang, Lizhi [Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079 (China)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer Remove RhB by a novel 3D-E-Fenton system using foam nickel as particle electrodes. Black-Right-Pointing-Pointer The 3D-E-Fenton system exhibit much higher RhB removal efficiency than the counterpart 3D-E and E-Fenton system. Black-Right-Pointing-Pointer Foam nickel as a particle electrode displays good oxygen reduction activity. Black-Right-Pointing-Pointer 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{sub 2}-IrO{sub 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 {center_dot}O{sub 2}{sup -} via a single-electron transfer pathway to subsequently generate more H{sub 2}O{sub 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.

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

    International Nuclear Information System (INIS)

    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/RuO2–IrO2 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 ·O2− via a single-electron transfer pathway to subsequently generate more H2O2 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.

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

    International Nuclear Information System (INIS)

    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, BOD5 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.

  20. 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(...

  1. Iron-loaded mangosteen as a heterogeneous Fenton catalyst for the treatment of landfill leachate.

    Science.gov (United States)

    Laiju, A R; Sivasankar, T; Nidheesh, P V

    2014-09-01

    Iron-loaded mangosteen shell powder (Fe-MSP) was found as an effective heterogeneous Fenton catalyst for the treatment of stabilized landfill leachate. Sonolytically produced catalyst has higher efficiency than other catalysts. At the optimal conditions (pH 3, catalyst concentration of 1,750 mg/L and hydrogen peroxide concentration of 0.26 M), 81 % of the chemical oxygen demand (COD) was removed effectively from the landfill leachate. But, the efficiency of Fe-MSP was reduced in the first recycling due to the poisoning of active sites. A metal leaching study indicated that the degradation of the pollutant is mainly due to solid Fe ions present in Fe-MSP rather than the leached ferrous and ferric ions. Hydroxyl radical production in the system was confirmed by the Fenton oxidation of benzoic acid. Compared to the homogeneous Fenton process, the heterogeneous Fenton process using Fe-MSP had higher COD removal efficiency, indicating the practical applicability of the prepared catalyst. PMID:24798918

  2. 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.

  3. Effect of non-modified and modified nanodiamond particles by Fenton reaction on human endothelial cells

    Directory of Open Access Journals (Sweden)

    K. Solarska

    2010-12-01

    Full Text Available Purpose: The use of carbon nanoparticles in medicine is increasing due to their high biocompatibility. Nanopowders are one of the best materials which can be used in medicine on medical implants and surgical tools. DPP (Diamond Powder Particles obtained by different methods which can be expected to affect their properties, including biocompatibility, were compared. The aim of the present study was to compare the biocompatibility of Diamond Powder Particles (DPP obtained by detonation method and graphite on the basis of their interactions with human endothelial cells.Design/methodology/approach: The effect of nanodiamonds on cell proliferation HUVEC-ST and production of reactive oxygen species (ROS and reactive nitrogen species (RNS was studied. We used FT-IR Spectroscopy attributive chemical function groups.Findings: In this subject the material characterization of nanodiamond powders and influence on endothelial cells.Practical implications: Biological research with endothelial cells and nanodiamond powder are the introduction to application in human’s treatment.Originality/value: Nanodiamond powders with chemical modified surface.

  4. Free hydroxyl radical is not involved in an important reaction of lignin degradation by Phanerochaete chrysosporium Burds.

    Science.gov (United States)

    Kirk, T K; Mozuch, M D; Tien, M

    1985-01-01

    Hydroxyl radical (HO.) has been implicated in the degradation of lignin by Phanerochaete chrysosporium. This study assessed the possible involvement of HO. in degradation of lignin substructural models by intact cultures and by an extracellular ligninase isolated from the cultures. Two non-phenolic lignin model compounds [aryl-C(alpha)HOH-C(beta)HR-C(gamma)H2OH, in which R = aryl (beta-1) or R = O-aryl (beta-O-4)] were degraded by cultures, by the purified ligninase, and by Fenton's reagent (H2O2 + Fe2+), which generates HO.. The ligninase and the cultures formed similar products, derived via an initial cleavage between C(alpha) and C(beta) (known to be an important biodegradative reaction), indicating that the ligninase is responsible for model degradation in cultures. Products from the Fenton degradation were mainly polar phenolics that exhibited little similarity to those from the biological systems. Mass-spectral analysis, however, revealed traces of the same products in the Fenton reaction as seen in the biological reactions; even so, an 18O2-incorporation study showed that the mechanism of formation differed. E.s.r. spectroscopy with a spin-trapping agent readily detected HO. in the Fenton system, but indicated that no HO. is formed during ligninase catalysis. We conclude, therefore that HO. is not involved in fungal C(alpha)-C(beta) cleavage in the beta-1 and beta-O-4 models and, by extension, in the same reaction in lignin. PMID:2986597

  5. Combined humic acid adsorption and enhanced Fenton processes for the treatment of naphthalene dye intermediate wastewater.

    Science.gov (United States)

    Gu, Lin; Zhu, Nanwen; Wang, Liang; Bing, Xiaoxiao; Chen, Xiaoliang

    2011-12-30

    In this work, an humic acid adsorption with an enhanced Fenton oxidation was employed to treat the real effluent originating from the 1-diazo-2-naphthol-4-sulfonic acid (1,2,4-Acid) production plant. In a first step, humic acid with MgSO(4) was selected as adsorbent and precipitant for physicochemical pretreatment, the synergetic effect had led to 39% of COD removal and 89% of colour removal. A multi-staged Fenton oxidation process with inner circulation was introduced subsequently. The TOC, COD, 1,2,4-Acid, NH(4)(+)-N, SS and colour were reduced from 3024 mg/L, 12,780 mg/L, 9103 mg/L, 110 mg/L, 240 mg/L and 25,600 (multiple) to 46 mg/L, 210 mg/L, 21 mg/L, 16 mg/L, 3 mg/L and 25 through the combined process, respectively. Hydrogen peroxide consumed per kg COD had saved up to 36% when two-staged Fenton process with inner circulation (flow-back to influent ratio: 3) was applied. Influence of H(2)O(2) concentration, flow-back to influent ratio and staged Fenton mode were investigated in detail in order to find out the optimal operating parameters. The kinetics of 1,2,4-Acid degradation by two-staged Fenton process was investigated. The evolution of the main intermediates during the degradation process was conducted using the LC-(ESI)-TOF-MS technique, and the results showed a staged degradation pathway from the ring opening of naphthalene compounds to the formation of benzene compounds and carboxyl acids. The combined process had been proved effective in both technical and economic aspects.

  6. Decolourisation of dyes under electro-Fenton process using Fe alginate gel beads

    International Nuclear Information System (INIS)

    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.

  7. 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.

  8. Solar photoelectro-Fenton degradation of the antibiotic metronidazole using a flow plant with a Pt/air-diffusion cell and a CPC photoreactor

    International Nuclear Information System (INIS)

    Highlights: • Degradation of metronidazole solutions at pH 3.0 by EF and SPEF in a flow plant. • High recalcitrance of the antibiotic and its products to be destroyed by ·OH radicals. • Only 53% mineralization by the most potent SPEF process at 55.4 mA cm−2. • 5 heterocyclic products, 12 hydroxylated derivatives and 2 carboxylic acids were found. • Release of NO3− ion and generation of persistent N-products and N-volatile species. - Abstract: The degradation of 10 dm3 of solutions of the heterocyclic antibiotic metronidazole in 0.10 mol dm−3 Na2SO4 of pH 3.0 has been comparatively studied by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF). Experiments were performed in a solar flow plant equipped with a Pt/air-diffusion cell and coupled to a compound parabolic collector (CPC) photoreactor. A very weak mineralization was found for the EF process in the dark, indicating a large recalcitrance of heterocyclic compounds to be destroyed by hydroxyl radicals formed at the Pt anode from water oxidation and mainly in the bulk from Fenton's reaction between added Fe2+ and cathodically generated H2O2. The quick photolysis of intermediates by UV radiation from sunlight enhanced largely the mineralization process by SPEF. The effect of applied current density and Fe2+ and drug contents on the SPEF treatment was examined. The best process was found for 1.39 mmol dm−3 metronidazole with 0.50 mmol dm−3 Fe2+ at 55.4 mA cm−2 giving 53% mineralization, 36% mineralization current efficiency and 0.339 kWh (g DOC)−1 in 300 min. Metrodinazole was completely removed and its decay obeyed a pseudo-first-order kinetics. LC-MS analysis allowed identifying five heterocyclic products and twelve hydroxylated derivatives. Ion-exclusion HPLC analysis revealed that final oxalic and oxamic acids were practically removed at the end of electrolysis due to the efficient photolysis of their Fe(III) complexes by sunlight. The initial N of metronidazole gave NO3

  9. Treatment of phenol-containing wastewater by UV-Fenton process%UV/Fenton处理苯酚废水的研究

    Institute of Scientific and Technical Information of China (English)

    王来斐

    2012-01-01

    UV—Fenton process was used to treat simulant phenol—containing wastewater, the initial mass concentrations of phenol and CODcx were 300 and 760 mg/L respectively. The effects of pH value, dosage of H2O2(30%) and FeSO4·7H2O, reaction time and some other factors on the removal rates of phenol and CODcr were discussed. The results showed that, the optimal condition for UV-Fenton process treating phenol-containing wastewater was as follows: the solution pH value was 3, the dosage of H2O2 and FeSO4·7H2O were 2.5 mL/L and 0.020 g/L respectively, the reaction time was 90 min. Under the above condition, the removal rates of phenol and CODcr reached 95% and 90% respectively. It could be seen that, UV -Fenton process was effective for the treatment of phenol-containing wastewater.%采用UV/Fenton联合体系降解苯酚模拟废水,苯酚的初始质量浓度为300 mg/L,CODCr的初始质量浓度为760 mg/L.探讨了pH值、H2O2 (30%)和FeSO4· 7H2O投加量、反应时间等因素对苯酚和CODCr去除率的影响.结果表明,UV/Fenton联合体系降解苯酚废水的最佳工艺条件是:溶液pH值为3、H2O2投加量为2.5 mL/L、FeSO4·7H2O投加量为0.020 g/L、反应时间为90 min.此时,苯酚的去除率为95%,CODCr的去除率为90%.UV/Fenton联合体系能较好地处理苯酚废水.

  10. Novel Method for Breakthrough Removal of Azo Dye from Aqueous Environment Using Integrated Coagulation and Fenton Process

    OpenAIRE

    Sherine Awad; Usama Eldemerdash

    2014-01-01

    Fenton process has proven to be efficient in the removal of color and chemical oxygen demand (COD) from the aqueous environment. However, the environment, health, and economic constraints on the dosage of hydrogen peroxide represent a limitation towards a wide practical use of this approach. In this study, a novel approach is proposed; this includes the treatment with ferrous oxide through coagulation followed by integrated Fenton process. However, the excess ferrous and ferric ions from the ...

  11. AbstractApplication of Fenton-like process using iron nano oxides for pyrene removal from contaminated soils

    OpenAIRE

    S. Jorfi; Rezaee, A.; N Jaafarzadeh Haghighifard; G.A Moheb-ali

    2014-01-01

    Background and objectives: Because of problems dealing with bioremediation including being time consuming, low efficiency and toxicity to biota, application of advanced oxidation processes with higher efficiency and shorter remediation time have been considered for removal of hydrophobic hydrocarbons from contaminated soils. A great interest has been directed to Fenton oxidation because of its simplicity and high oxidation potential. The objective of this study was to determine the Fenton-lik...

  12. Degradation of tyrosol by a novel electro-Fenton process using pyrite as heterogeneous source of iron catalyst.

    Science.gov (United States)

    Ammar, Salah; Oturan, Mehmet A; Labiadh, Lazhar; Guersalli, Amor; Abdelhedi, Ridha; Oturan, Nihal; Brillas, Enric

    2015-05-01

    Tyrosol (TY) is one of the most abundant phenolic components of olive oil mill wastewaters. Here, the degradation of synthetic aqueous solutions of 0.30 mM TY was studied by a novel heterogeneous electro-Fenton (EF) process, so-called EF-pyrite, in which pyrite powder was the source of Fe(2+) catalyst instead of a soluble iron salt used in classical EF. Experiments were performed with a cell equipped with a boron-doped diamond anode and a carbon-felt cathode, where TY and its products were destroyed by hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between Fe(2+) and H2O2 generated at the cathode. Addition of 1.0 g L(-1) pyrite provided an easily adjustable pH to 3.0 and an appropriate 0.20 mM Fe(2+) to optimize the EF-pyrite treatment. The effect of current on mineralization rate, mineralization current efficiency and specific energy consumption was examined under comparable EF and EF-pyrite conditions. The performance of EF-pyrite was 8.6% superior at 50 mA due to self-regulation of soluble Fe(2+) by pyrite. The TY decay in this process followed a pseudo-first-order kinetics. The absolute rate constant for TY hydroxylation was 3.57 × 10(9) M(-1) s(-1), as determined by the competition kinetics method. Aromatic products like 3,4-dihydroxyphenylethanol, 4-hydroxyphenylacetic acid, 4-hydroxybenzoic acid, 3,4-dihydroxybenzoic acid and catechol, as well as o-benzoquinone, were identified by GC-MS and reversed-phase HPLC. Short-chain aliphatic carboxylic acids like maleic, glycolic, acetic, oxalic and formic were quantified by ion-exclusion HPLC. Oxalic acid was the major and most persistent product found. Based on detected intermediates, a plausible mineralization pathway for TY by EF-pyrite was proposed. PMID:25720669

  13. Photo-Fenton degradation of the herbicide 2,4-D in aqueous medium at pH conditions close to neutrality.

    Science.gov (United States)

    Conte, Leandro O; Schenone, Agustina V; Alfano, Orlando M

    2016-04-01

    A theoretical and experimental study of the photo-Fenton degradation of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) in water is presented. A kinetic model derived from a reaction sequence is proposed using the ferrioxalate complex as iron source for conditions of pH = 5. The kinetic model was employed to predict the concentrations of 2,4-D, 2,4-dichlorophenol (2,4-DCP), hydrogen peroxide (HP) and oxalate (Ox) in a flat plate laboratory reactor irradiated with a solar simulator. Two types of incident irradiation levels were tested by different combinations of attenuation filters. The effects of the oxalate/Fe(+3) molar ratio (Ox/Fe), the reaction temperature (T) and the 2,4-D/HP molar ratio (R) on the photo-Fenton process were also investigated. For low radiation level and operating conditions of R = 50 and T = 50 °C, a 2,4-D conversion of 95.6% was obtained after 180 min. Moreover, the 2,4-D conversion was almost 100% in only 120 min when the system was operated under the same operating conditions and high radiation level. From the proposed model and the experimental data, the corresponding kinetic parameters were estimated applying a nonlinear regression method. A good agreement between the kinetic model and experimental data, for a wide range of simulated solar operating conditions, was observed. For 2,4-D, 2,4-DCP, HP and Ox concentrations, the calculated RMSE were 1.21 × 10(-2), 5.45 × 10(-3), 2.86 × 10(-1) and 2.65 × 10(-2) mM, respectively. PMID:26800432

  14. Optimization of the mineralization of a mixture of phenolic pollutants under a ferrioxalate-induced solar photo-Fenton process

    Energy Technology Data Exchange (ETDEWEB)

    Monteagudo, J.M., E-mail: josemaria.monteagudo@uclm.es [University of Castilla-La Mancha, Grupo IMAES, Department of Chemical Engineering, Escuela Tecnica Superior de Ingenieros Industriales, Avda. Camilo Jose Cela, 1, 13071 Ciudad Real (Spain); Duran, A.; Aguirre, M.; San Martin, I. [University of Castilla-La Mancha, Grupo IMAES, Department of Chemical Engineering, Escuela Tecnica Superior de Ingenieros Industriales, Avda. Camilo Jose Cela, 1, 13071 Ciudad Real (Spain)

    2011-01-15

    The mineralization of solutions containing a mixture of three phenolic compounds, gallic, p-coumaric and protocatechuic acids, in a ferrioxalate-induced solar photo-Fenton process was investigated. The reactions were carried out in a pilot plant consisting of a compound parabolic collector (CPC) solar reactor. An optimization study was performed combining a multivariate experimental design and neuronal networks that included the following variables: pH, temperature, solar power, air flow and initial concentrations of H{sub 2}O{sub 2}, Fe(II) and oxalic acid. Under optimal conditions, total elimination of the original compounds and 94% TOC removal of the mixture were achieved in 5 and 194 min, respectively. pH and initial concentrations of H{sub 2}O{sub 2} and Fe(II) were the most significant factors affecting the mixture mineralization. The molar correlation between consumed hydrogen peroxide and removed TOC was always between 1 and 3. A detailed analysis of the reaction was presented. The values of the pseudo-first-order mineralization kinetic rate constant, k{sub TOC}, increased as initial Fe(II) and H{sub 2}O{sub 2} concentrations and temperature increased. The optimum pH value also slightly increased with greater Fe(II) and hydrogen peroxide concentrations but decreased when temperature increased. {center_dot}OH and O{sub 2}{center_dot}{sup -} radicals were the main oxidative intermediate species in the process, although singlet oxygen ({sup 1}O{sub 2}) also played a role in the mineralization reaction.

  15. 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. PMID:26692412

  16. 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.

  17. Selection of electrode material and treatment of printing wastewater by EF-Fenton%阴极电芬顿法电极材料的选择及处理印染废水的研究

    Institute of Scientific and Technical Information of China (English)

    石申; 刘正伟; 奚吉; 金少波; 周宇松

    2014-01-01

    The selection criteria of electrode material in EF-Fenton system was discussed,and by comparing the performance, titanium coated ruthenium iridium electrode was selected as the anode material,ACF electrode as the cathode material. A self-made Electro-Fenton reactor was used to treat printing wastewater,the effects of various factors on the treatment of printing wastewater were experimentally analyzed. The results show that the EF-Fenton system is effective in the treatment of printing wastewater,and the optimal reaction conditions are as follows:reaction pH value of 3,FeSO4 dosage of 150 mg/L,aeration capacity of 0.1 m3/h,voltage of 9 V,time of 40 min. The maximum removal rate of COD reaches 73.5%.%讨论了阴极电芬顿体系中电极材料的选择标准,并通过比较选择以钛涂钌铱电极、活性碳纤维电极作为阳极、阴极材料。利用自制的电芬顿反应器,对影响体系处理印染废水效果的各相关因素进行研究。结果表明:阴极电芬顿法处理印染废水效果良好,最佳反应条件:pH值为3,FeSO4投加量为150 mg/L,曝气量为0.1 m3/h,电压为9 V,反应时间为40 min,此时COD的去除率最高,可达到73.5%。

  18. Tratamento de águas contaminadas por diesel/biodiesel utilizando processo Fenton Treatment of water contaminated by diesel/biodiesel using Fenton process

    Directory of Open Access Journals (Sweden)

    Teofani Koslides Mitre

    2012-06-01

    Full Text Available A contaminação de águas por misturas diesel/biodiesel pode causar grandes impactos ambientais, relacionados à presença de compostos orgânicos recalcitrantes e tóxicos, inviabilizando o uso de processos biológicos de tratamento. A avaliação da biodegradabilidade, nas proporções B0, B25, B50, B75 e B100 (os números especificam o percentual em massa de biodiesel na mistura, indicou que a adição de biodiesel em teores acima de 50% aumenta a biodegradabilidade, alcançando 60 e 80% para B50 e B75, respectivamente. Na aplicação do processo Fenton, a remoção da matéria orgânica foi superior a 80% em todas as misturas, exceto para B0, que apresentou remoção máxima de 50%. A oxidação por Fenton se ajustou a um modelo cinético de pseudo-segunda ordem em relação à concentração de matéria orgânica, e resultou em aumento da biodegradabilidade de até 150%.Waters contaminated with diesel/biodiesel and their blends can cause major environmental impacts, due to the presence of toxic and recalcitrant organic compounds, which invalidate the use of biological treatment processes. Evaluation of biodegradability of the blends B0, B25, B50, B75 and B100 (the numbers specify the mass percentage of biodiesel in the blend indicated that the addition of biodiesel at concentrations above 50% increased biodegradation, reaching 60 and 80% for B50 and B75, respectively. When the Fenton process was used, removal of organic matter was greater than 80 % in all blends, except for B0, which showed maximum removal of 60%. Oxidation by Fenton was fitted with a pseudo-second order kinetic model in relation to the concentration of organic matter and resulted in increased biodegradation of up to 150%.

  19. Fenton Process Coupled to Ultrasound and UV Light Irradiation for the Oxidation of a Model Pollutant

    Directory of Open Access Journals (Sweden)

    Karen E. Barrera-Salgado

    2016-01-01

    Full Text Available The Fenton process coupled to photosonolysis (UV light and Us, using Fe2O3 catalyst supported on Al2O3, was used to oxidize a model pollutant like acid green 50 textile dye (AG50. Dye degradation was followed by AG50 concentration decay analyses. It was observed that parameters like iron content on a fixed amount of catalyst supporting material, catalyst annealing temperature, initial dye concentration, and the solution pH influence the overall treatment efficiency. High removal efficiencies of the model pollutant are achieved. The stability and reusability tests of the Fe2O3 catalyst show that the catalyst can be used up to three cycles achieving high discoloration. Thus, this catalyst is highly efficient for the degradation of AG50 in the Fenton process.

  20. Applicability of nano zero valent iron (nZVI) in sono - Fenton process

    Science.gov (United States)

    Taha, M. R.; Ibrahim, A. H.; Amat, R. C.; Azhari, A. W.

    2014-04-01

    Fenton process is one of the advanced oxidation processes (AOPs) used to remove complex organic pollutants in wastewater. In this study, instead of iron sulfate (FeSO4), nano zero valent iron (nZVI) was used as a major source of ferrous iron (Fe2+). In order to enhance the process, ultrasound was utilized in this study. Results show that, with the aid of ultrasound, nZVI produced more Fe2+ compared to FeSO4 at pH 2. Furthermore, combination of higher intensity and longer sonication time in Fenton process acceleratde the chemical oxygen demand (COD) removal from palm oil mill effluent (POME). Through the process, 80% of COD content was removed within 2 hours instead of 24 hours of silent degradation.

  1. Fenton's reagent minimum dosage for remediation of water contaminated with dyes

    Directory of Open Access Journals (Sweden)

    Gina Terán

    2015-09-01

    Full Text Available Effluents from the textile industry not only represent a latent threat to biodiversity on our planet but also to humans due to the pollution generated by industrial dyes. In this study a Fenton process was evaluated for the decoloration of water contaminated with yellow 160, blue 81 and red 190 with an initial concentration of 3300 mg.L-1 and a chemical oxygen demand of 1719 mg.L-1. Changes in pH and molar doses of ferrous sulfate and hydrogen peroxide were evaluated. The Fenton process allowed 99,9% removal of organic matter and 100% removal of turbidity when it worked at pH 3,5 and molar dose Fe+2/ H2O2 between 1:3 and 1:5. By spectrophotometric scanning and measurement of redox potential, it was shown that the quality of decontaminated water resembled the ultrapure water type I.

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

    Directory of Open Access Journals (Sweden)

    Didik Setiawan

    2013-11-01

    Full Text Available Tujuan dari penelitian ini adalah untuk menentukan konsentrasi optimum dan efektifitas hidrogen peroksida dan pereaksi Fenton sebagai disinfektan dibandingkan dengan kaporit. Efektivitas disinfeksi ditentukan berdasarkan beberapa parameter yaitu: koefisien fenol disinfektan dan kualitas air yang dihasilkan yang diukur melalui pH, oksigen terlarut (DO, dissolved oxygen, dan suhunya serta harga disinfektan itu sendiri. Analisis statistik ANOVA dua arah tanpa interaksi  pada tingkat kesalahan 0.01 dilakukan guna menentukan disinfektan paling efektif dan konsentrasi optimumnya. Uji koefisien fenol dilakukan dengan mencampurkan disinfektan dengan konsentrasi tertentu dengan bakteri Salmonella typhosa dan Staphyllococcus aureuskemudian membandingkan hasilnya dengan fenol.Hasil pengamatan menunjukkan bahwa koefisien fenol dari kaporit, hidrogen peroksida, dan reagen Fenton berturut-turut adalah 4, 6, dan 6. Air yang dihasilkan oleh kaporit mempunyai pH, DO dan suhu berturut-turut adalah 10.07 - 9.2, 6.63-8.07 mgL-1, dan 28.5-28.13oC. Air yang didisinfeksi dengan hidrogen peroksida mempunyai pH,DO, dan suhu berturut-turut adalah 9.03-7.33, 6.93-9.40 mgL-1  , dan 28.5-28.03oC. Sedangkan air hasil didisinfeksi dengan reagen Fenton mempunyai pH, DO, dan suhu berturut-turut adalah 5.97-4.57, 7.40-8.57 mgL-1 , dan 28.47-28.07oC.Meskipun kaporit paling murah, namun dari segi kesehatan hidrogen peroksida merupakan reagen yang paling aman dan paling efektif karena dengan daya disinfeksi enam kali dibandingkan fenol, tidak meninggalkan residu yang membahayakan. Fenton, dilain pihak, meskipun mempunyai daya disinfeksi setara dengan hidrogen peroksida, namun menghasilkan ion Besi (III dalam air sehingga memerlukan pengolahan lebih jauh.Dengan demikian, secara keseluruhan hidrogen peroksida merupakan disinfektan paling efektif dari ketiganya. The purpose of this study is to determine the optimum concentration and the effectiveness of hydrogen peroxide and Fenton

  3. REMOVAL OF REMAZOL ROSSO RB DYE FROM AQUEOUS EFFLUENTS BY HOMOGENOUS FENTON OXIDATION PROCESSES

    OpenAIRE

    Carmen Zaharia; Victoria Fedorcea; Adrian Beda; Victor Amarandei; Augustin Muresan

    2014-01-01

    The paper presents some data from our laboratory-setup experiments of homogenous oxidative processes with hydrogen peroxide (i.e. advanced Fenton oxidation processes) applied for Remazol Rosso RB dye-containing aqueous systems, especially textile effluents. Therefore, some different operating parameters (including pH, concentration of dye, H2O2 and ferrous ions, oxidation time, temperature, stirring regime, among its) were tested for determination of the best performance in effluent decolorat...

  4. Combined treatment of retting flax wastewater using Fenton oxidation and granular activated carbon

    OpenAIRE

    Sohair I. Abou-Elela; Mohammed Eid M. Ali; Ibrahim, Hanan S.

    2016-01-01

    The process of retting flax produces a huge amount of wastewater which is characterized with bad unpleasant smell and high concentration of organic materials. Treatment of such waste had always been difficult because of the presence of refractory organic pollutants such as lignin. In this study, treatment of retting wastewater was carried out using combined system of Fenton oxidation process followed by adsorption on granular activated carbon (GAC). The effects of operating condition on Fento...

  5. Biological hazard evaluation of a pharmaceutical effluent before and after a photo-Fenton treatment.

    Science.gov (United States)

    Novoa-Luna, Karen Adriana; Mendoza-Zepeda, Arisbeht; Natividad, Reyna; Romero, Rubi; Galar-Martínez, Marcela; Gómez-Oliván, Leobardo Manuel

    2016-11-01

    The aim of this study was to evaluate the biological hazard of a pharmaceutical effluent before and after treatment. For the former, the determined 96h-LC50 value was 1.2%. The photo-Fenton treatment catalyzed with an iron-pillared clay reduced this parameter by 341.7%. Statistically significant increases with respect to the control group (PPCT, oxidative stress, genotoxic damage and LC50 in Hyalella azteca. PMID:27392336

  6. New approach to solar photo-Fenton operation. Raceway ponds as tertiary treatment technology

    Energy Technology Data Exchange (ETDEWEB)

    Carra, Irene; Santos-Juanes, Lucas [Department of Chemical Engineering, University of Almería, 04120, Almería (Spain); CIESOL, Joint Centre of the University of Almería-CIEMAT, 04120, Almería (Spain); Acién Fernández, Francisco Gabriel [Department of Chemical Engineering, University of Almería, 04120, Almería (Spain); Malato, Sixto [CIESOL, Joint Centre of the University of Almería-CIEMAT, 04120, Almería (Spain); Plataforma Solar de Almería (CIEMAT), 04200, Tabernas, Almería (Spain); Sánchez Pérez, José Antonio, E-mail: jsanchez@ual.es [Department of Chemical Engineering, University of Almería, 04120, Almería (Spain); CIESOL, Joint Centre of the University of Almería-CIEMAT, 04120, Almería (Spain)

    2014-08-30

    Graphical abstract: - Highlights: • Raceway ponds are used for the first time as photo-Fenton reactors. • Raceway ponds are effective and have high treatment capacity (48 mg/h m{sup 2} for 360 L). • The highest treatment capacity occurs with 5.5 mg Fe/L and 15 cm liquid depth. • Low iron concentrations are enough to oxidise the pesticide mixture. • Raceway ponds are a simple and low-cost alternative for micropollutant removal. - Abstract: The photo-Fenton process has proven its efficiency in the removal of micropollutants. However, the high costs usually associated with it prevent a spread of this technology. An important factor affecting costs is the kind of photoreactor used, usually tubular with a reflecting surface. Tubular reactors like compound parabolic collectors, CPCs, involve high capital costs. In comparison, the application of less costly reactors such as the extensive raceway ponds (RPRs) would help to spread the use of the photo-Fenton process as tertiary treatment at commercial scale. As far as the authors know, RPRs have never been used in advanced oxidation processes (AOPs) applications. This work is aimed at studying the applicability of RPRs to remove micropollutants with solar photo-Fenton. For this purpose, a pesticide mixture of commercial acetamiprid (ACTM) and thiabendazole (TBZ) (100 μg/L each) was used in simulated secondary effluent. Iron concentration (1, 5.5 and 10 mg/L) and liquid depth (5, 10 and 15 cm) were studied as process variables. TBZ was removed at the beginning of the treatment (less than 5 min), although ACTM removal times were longer (20–40 min for the highest iron concentrations). High treatment capacity per surface area was obtained (48 mg/h m{sup 2} with 5.5 mg Fe/L and 15 cm liquid depth), proving the feasibility of using RPRs for micropollutant removal.

  7. Photo-Fenton and Slow Sand Filtration coupling for hydroponics water reuse

    OpenAIRE

    Micó Reche, Mª del Mar

    2013-01-01

    The collaboration between the University of Barcelona and Acciona Agua was focused on optimizing greenhouses hydric resources. The functionality of a combined treatment had to be assessed, when applied to the discard stream of a recycling system of the Advanced Greenhouse leachates. The coupling consisted on an Advanced Oxidation Processes (AOP), photo-Fenton, based on hydroxyl radical oxidative potential, produced by the interaction between Fe2+ and H2O2, and a slow sand filtration column ac...

  8. Solar photo-Fenton like using persulphate for carbamazepine removal from domestic wastewater

    OpenAIRE

    Ahmed, M M; Chiron, Serge

    2014-01-01

    This work aimed at decontaminating biologically treated domestic wastewater effluent from pharmaceutical residues by using sulphate radical based homogeneous photo-Fenton involving persulphate (PS) as an oxidant, ferrous iron (Fe(II)) as a catalyst and simulated solar irradiation as a light source. This is the first time that the beneficiary use of solar energy in PS/Fe(II)/UV-Vis system was evaluated by using carbamazepine (CBZ) as a probe compound. In wastewater, CBZ was fully degraded in 3...

  9. Use of Fenton oxidation to improve the biodegradability of a pharmaceutical wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Tekin, Huseyin [ENCON Environmental Consultancy Co., Mahatma Gandhi Caddesi 75/3, Gaziosmanpasa, 06700 Ankara (Turkey); Bilkay, Okan [ENCON Environmental Consultancy Co., Mahatma Gandhi Caddesi 75/3, Gaziosmanpasa, 06700 Ankara (Turkey); Ataberk, Selale S. [ENCON Environmental Consultancy Co., Mahatma Gandhi Caddesi 75/3, Gaziosmanpasa, 06700 Ankara (Turkey); Balta, Tolga H. [ENCON Environmental Consultancy Co., Mahatma Gandhi Caddesi 75/3, Gaziosmanpasa, 06700 Ankara (Turkey); Ceribasi, I. Haluk [ENCON Environmental Consultancy Co., Mahatma Gandhi Caddesi 75/3, Gaziosmanpasa, 06700 Ankara (Turkey); Sanin, F. Dilek [Department of Environmental Engineering, Middle East Technical University, 06531 Ankara (Turkey); Dilek, Filiz B. [Department of Environmental Engineering, Middle East Technical University, 06531 Ankara (Turkey); Yetis, Ulku [Department of Environmental Engineering, Middle East Technical University, 06531 Ankara (Turkey)]. E-mail: uyetis@metu.edu.tr

    2006-08-21

    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{sub 2}O{sub 2}/Fe{sup 2+} was 150-250. At H{sub 2}O{sub 2}/Fe{sup 2+} ratio of 155, 0.3 M H{sub 2}O{sub 2} and 0.002 M Fe{sup 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{sup 3} and operated with a total cycle time of 1 day, was around 98%, regarding the COD removal.

  10. Photo-fenton process: Optimization and decolourization and mineralization of reactive blue 222 dye

    Directory of Open Access Journals (Sweden)

    Shumaila Kiran

    2012-12-01

    Full Text Available Dye house effluents of textile industries leads to severe environmental problems when disposed to aquatic bodies without proper treatment. This work was carried out to optimize the Photo-Fenton process for decolorization and mineralization of a commercial textile dye, Reactive Blue 222. The effect of different process parameters on decolorization efficiency of Photo-Fenton process was investigated. The optimal conditions for process were observed as; pH level 3.5, H2O2 concentration 1× 10-2M, FeSO4 concentration 3.5 × 10-5 mol L-1, temperature 50˚C and process time 50 min. The maximum 95% dye decolorization was achieved along with a significant (P< 0.05 reduction of chemical oxygen demand and total organic. The degradation products were characterized by UV–visible and FTIR spectral techniques. The results provide evidence that Photo-Fenton process was able to oxidize and mineralize the selected azo dye into non-toxic metabolites.

  11. Soil remediation using a coupled process: soil washing with surfactant followed by photo-Fenton oxidation

    International Nuclear Information System (INIS)

    In the present work the use of a coupled process, soil washing and photo-Fenton oxidation, was investigated for remediation of a soil contaminated with p,p'-DDT (DDT) and p,p'-DDE (DDE), and a soil artificially contaminated with diesel. In the soil washing experiments, Triton X-100 (TX-100) aqueous solutions were used at different concentrations to obtain wastewaters with different compositions. Removal efficiencies of 66% (DDT), 80% (DDE) and 100% (diesel) were achieved for three sequential washings using a TX-100 solution strength equivalent to 12 times the effective critical micelle concentration of the surfactant (12 CMCeff). The wastewater obtained was then treated using a solar photo-Fenton process. After 6 h irradiation, 99, 95 and 100% degradation efficiencies were achieved for DDT, DDE and diesel, respectively. In all experiments, the concentration of dissolved organic carbon decreased by at least 95%, indicating that residual concentration of contaminants and/or TX-100 in the wastewater was very low. The co-extraction of metals was also evaluated. Among the metals analyzed (Pb, Cr, Ni, Cu, Cd, Mn and Co), only Cr and Mn were detected in the wastewater at concentrations above the maximum value permitted by current Brazilian legislation. The effective removal of contaminants from soil by the TX-100 washing process, together with the high degradation efficiency of the solar photo-Fenton process, suggests that this procedure could be a useful option for soil remediation.

  12. Repeated oxidative degradation of methyl orange through bio-electro-Fenton in bioelectrochemical system (BES).

    Science.gov (United States)

    Ling, Ting; Huang, Bin; Zhao, Mingxing; Yan, Qun; Shen, Wei

    2016-03-01

    Composite Fe2O3/ACF electrode facilitated methyl orange (MO) oxidative degradation using bio-electro-Fenton in bioelectrochemical system (BES) was investigated. Characterized by both XPS and FT-IR techniques, it was found that the composite Fe2O3/ACF electrode with highest Fe loading capacity of 11.02% could be prepared after the carbon felt was oxidized with nitric acid. Moreover, hydrogen peroxide production reached steadily at 88.63 μmol/L with the external resistance as 100 Ω, cathodic aeration rate at 750 mL/min, and the pH of the bio-electro-Fenton system adjusted to 2. Significantly, not only the electrochemical profiles of the BES reactor as electrochemical impedance spectroscopy (EIS) was bettered, but the MO oxidative degradation could be accomplished for eight repeated batches, with the MO removal efficiency varied slightly from 73.9% to 86.7%. It indicated that the bio-electro-Fenton might be a promising eco-friendly AOP method for Azo-dye wastewater treatment. PMID:26722807

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

    International Nuclear Information System (INIS)

    Highlights: ► The mixed substrates of FA-M + TiO2 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 TiO2 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 Fe2+/H2O2) 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

  14. New approach to solar photo-Fenton operation. Raceway ponds as tertiary treatment technology.

    Science.gov (United States)

    Carra, Irene; Santos-Juanes, Lucas; Acién Fernández, Francisco Gabriel; Malato, Sixto; Sánchez Pérez, José Antonio

    2014-08-30

    The photo-Fenton process has proven its efficiency in the removal of micropollutants. However, the high costs usually associated with it prevent a spread of this technology. An important factor affecting costs is the kind of photoreactor used, usually tubular with a reflecting surface. Tubular reactors like compound parabolic collectors, CPCs, involve high capital costs. In comparison, the application of less costly reactors such as the extensive raceway ponds (RPRs) would help to spread the use of the photo-Fenton process as tertiary treatment at commercial scale. As far as the authors know, RPRs have never been used in advanced oxidation processes (AOPs) applications. This work is aimed at studying the applicability of RPRs to remove micropollutants with solar photo-Fenton. For this purpose, a pesticide mixture of commercial acetamiprid (ACTM) and thiabendazole (TBZ) (100μg/L each) was used in simulated secondary effluent. Iron concentration (1, 5.5 and 10mg/L) and liquid depth (5, 10 and 15cm) were studied as process variables. TBZ was removed at the beginning of the treatment (less than 5min), although ACTM removal times were longer (20-40min for the highest iron concentrations). High treatment capacity per surface area was obtained (48mg/hm(2) with 5.5mg Fe/L and 15cm liquid depth), proving the feasibility of using RPRs for micropollutant removal. PMID:25072137

  15. Disintegration and dissolution of spent radioactive cationic exchange resins using Fenton-like oxidation process

    International Nuclear Information System (INIS)

    Highlights: • The spent radioactive resins could be oxidized by Fenton-like process. • The influencing factors on resin oxidation were evaluated. • Chemical oxygen demand (COD) reduction rate was more than 99%. • SEM and Raman spectrum were used to analyze the resins morphological change. - Abstract: The treatment and disposal of the spent radioactive resins is essential for the sustainable development of the nuclear industry. In this paper, the disintegration and dissolution of spent cationic resins were studied by Fenton-like process. The influencing factors on resin dissolution, such as pH, temperature, type and concentration of catalysts were evaluated. The results showed that the spent resins could be effectively dissolved at pH < 1, [Fe2+] = 0.2 M and T = 97 ± 2 °C. Chemical oxygen demand (COD) reduction rate was more than 99%. The scanning electron microscopy and the Raman spectrum were used to observe the morphological changes of the spent resins during the dissolution process. Fenton-like oxidation is an efficient method for the volume reduction and stabilization of the spent resins before further immobilization

  16. 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.

  17. Photoassisted fenton oxidation of refractory organics in UASB-pretreated leachate

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Nearly 91% of organic pollutants in Hong Kong leachate could be effectively removed by the UASB (upflow anaerobic sludge blanket) process followed by the fenton coagulation.The COD (chemical oxygen demand) of leachate was lowered from an average of 5620 mg/L to 1910 mg/L after the UASB treatment at 37C,and was further lowered to 513 mg/L after fenton coagulation.The remaining refractory residues could be further removed by photochemical oxidation with the addition of H202 .The BOD/COD ratio was greatly increased from 0.062 to 0.142,indicating the biodegradability of organic residues was improved.The photochemical oxidation for the fenton-ceagulation supernatant was most effective at pH 3-4,with the addition of 800 mg/L of H202,and UV radiation time of 30 minutes.The final effluent contained only 148 mg/L of COD,21 mg/L of BOD(biochemieal oxygen demand) and 56 mg/L of TOC (total organic carbon).

  18. Disintegration and dissolution of spent radioactive cationic exchange resins using Fenton-like oxidation process

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Zhong; Xu, Lejin [Collaborative Innovation Center for Advanced Nuclear Energy Technology, INET, Tsinghua University, Beijing 100084 (China); Wang, Jianlong, E-mail: wangjl@tsinghua.edu.cn [Collaborative Innovation Center for Advanced Nuclear Energy Technology, INET, Tsinghua University, Beijing 100084 (China); Beijing Key Laboratory of Radioactive Wastes Treatment, Tsinghua University, Beijing 100084 (China)

    2015-09-15

    Highlights: • The spent radioactive resins could be oxidized by Fenton-like process. • The influencing factors on resin oxidation were evaluated. • Chemical oxygen demand (COD) reduction rate was more than 99%. • SEM and Raman spectrum were used to analyze the resins morphological change. - Abstract: The treatment and disposal of the spent radioactive resins is essential for the sustainable development of the nuclear industry. In this paper, the disintegration and dissolution of spent cationic resins were studied by Fenton-like process. The influencing factors on resin dissolution, such as pH, temperature, type and concentration of catalysts were evaluated. The results showed that the spent resins could be effectively dissolved at pH < 1, [Fe{sup 2+}] = 0.2 M and T = 97 ± 2 °C. Chemical oxygen demand (COD) reduction rate was more than 99%. The scanning electron microscopy and the Raman spectrum were used to observe the morphological changes of the spent resins during the dissolution process. Fenton-like oxidation is an efficient method for the volume reduction and stabilization of the spent resins before further immobilization.

  19. An insight in magnetic field enhanced zero-valent iron/H2O2 Fenton-like systems: Critical role and evolution of the pristine iron oxides layer

    Science.gov (United States)

    Xiang, Wei; Zhang, Beiping; Zhou, Tao; Wu, Xiaohui; Mao, Juan

    2016-04-01

    This study demonstrated the synergistic degradation of 4-chlorophenol (4-CP) achieved in a magnetic field (MF) enhanced zero-valent iron (ZVI)/H2O2 Fenton-like (FL) system and revealed an interesting correlative dependence relationship between MF and the pristine iron oxides layer (FexOy) on ZVI particles. First, a comparative investigation between the FL and MF-FL systems was conducted under different experimental conditions. The MF-FL system could suppress the duration of initial lag degradation phase one order of magnitude in addition of the significant enhancement in overall 4-CP degradation. Monitoring of intermediates/products indicated that MF would just accelerate the Fenton reactions to produce hydroxyl radical more rapidly. Evolutions of simultaneously released dissolved iron species suggested that MF would not only improve mass-transfer of the initial heterogeneous reactions, but also modify the pristine ZVI surface. Characterizations of the specific prepared ZVI samples evidenced that MF would induce a special evolution mechanism of the ZVI particles surface depending on the existence of FexOy layer. It comprised of an initial rapid point dissolution of FexOy and a following pitting corrosion of the exposed Fe0 reactive sites, finally leading to appearance of a particular rugged surface topography with numerous adjacent Fe0 pits and FexOy tubercles.

  20. Effect of iron salt counter ion in dose-response curves for inactivation of Fusarium solani in water through solar driven Fenton-like processes

    Science.gov (United States)

    Aurioles-López, Verónica; Polo-López, M. Inmaculada; Fernández-Ibáñez, Pilar; López-Malo, Aurelio; Bandala, Erick R.

    2016-02-01

    The inactivation of Fusarium solani in water was assessed by solar driven Fenton-like processes using three different iron salts: ferric acetylacetonate (Fe(acac)3), ferric chloride (FeCl3) and ferrous sulfate (FeSO4). The experimental conditions tested were [Fe] ≈ 5 mg L-1, [H2O2] ≈ 10 mg L-1 and [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1 mild and high, respectively, and pH 3.0 and 5.0, under solar radiation. The highest inactivation rates were observed at high reaction conditions for the three iron salts tested at pH 5.0 with less than 3.0 kJ L-1 of accumulate energy (QUV) to achieve over 99.9% of F. solani inactivation. Fe(acac)3 was the best iron salt to accomplishing F. solani inactivation. The modified Fermi equation was used to fix the experimental inactivation, data showed it was helpful for modeling the process, adequately describing dose-response curves. Inactivation process using FeSO4 at pH 3.0 was modeled fairly with r2 = 0.98 and 0.99 (mild and high concentration, respectively). Fe(acac)3, FeCl3 and FeSO4 at high concentration (i.e. [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1) and pH 5.0 showed the highest fitting values (r2 = 0.99). Iron salt type showed a remarkable influence on the Fenton-like inactivation process.

  1. Effect of iron salt counter ion in dose-response curves for inactivation of Fusarium solani in water through solar driven Fenton-like processes

    Science.gov (United States)

    Aurioles-López, Verónica; Polo-López, M. Inmaculada; Fernández-Ibáñez, Pilar; López-Malo, Aurelio; Bandala, Erick R.

    2016-02-01

    The inactivation of Fusarium solani in water was assessed by solar driven Fenton-like processes using three different iron salts: ferric acetylacetonate (Fe(acac)3), ferric chloride (FeCl3) and ferrous sulfate (FeSO4). The experimental conditions tested were [Fe] ≈ 5 mg L-1, [H2O2] ≈ 10 mg L-1 and [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1 mild and high, respectively, and pH 3.0 and 5.0, under solar radiation. The highest inactivation rates were observed at high reaction conditions for the three iron salts tested at pH 5.0 with less than 3.0 kJ L-1 of accumulate energy (QUV) to achieve over 99.9% of F. solani inactivation. Fe(acac)3 was the best iron salt to accomplishing F. solani inactivation. The modified Fermi equation was used to fix the experimental inactivation, data showed it was helpful for modeling the process, adequately describing dose-response curves. Inactivation process using FeSO4 at pH 3.0 was modeled fairly with r2 = 0.98 and 0.99 (mild and high concentration, respectively). Fe(acac)3, FeCl3 and FeSO4 at high concentration (i.e. [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1) and pH 5.0 showed the highest fitting values (r2 = 0.99). Iron salt type showed a remarkable influence on the Fenton-like inactivation process.

  2. Ultrasonic Fenton-like catalytic degradation of bisphenol A by ferroferric oxide (Fe₃O₄) nanoparticles prepared from steel pickling waste liquor.

    Science.gov (United States)

    Huang, Ruixiong; Fang, Zhanqiang; Fang, Xiaobo; Tsang, Eric Pokeung

    2014-12-15

    In this study, Fe3O4 NPs (named as Fe3O4 NPs-PO) were prepared by steel pickling waste liquor to reduce the cost of preparation, and were compared with those obtained by the common co-precipitation method (named as Fe3O4 NPs-CP) which prepared from chemical reagent using BET, XRD, XPS, TEM and SEM techniques. The results indicated that Fe3O4 NPs-PO nanoparticles mainly existed in the form of Fe3O4 and appeared to be roughly spherical in shape with a size range of 20-50 nm. The heterogeneous Fenton-like catalytic capacity of Fe3O4 NPs-PO in US+Fe3O4+H2O2 system was comprehensively investigated. BPA could be degraded within a wide pH range of 7-10. The removal efficiencies of BPA were close to 100% and about 45% total organic carbon (TOC) in solution was eliminated at the optimized conditions. It was found that ·OH radicals which mainly caused the degradation of BPA were promptly generated due to the catalysis of the Fe3O4 NPs-PO. Furthermore, the comparative study of catalytic activity, stability and reusability between Fe3O4 NPs-PO and Fe3O4 NPs-CP showed that the two catalysts both remained good activity after several reaction cycles and no significant change in composition and structure was observed, the loss of catalyst was negligible, which demonstrated that Fe3O4 NPs-PO were promising in ultrasonic Fenton-like process to treat refractory organics. PMID:25280370

  3. Efficient conversion of dimethylarsinate into arsenic and its simultaneous adsorption removal over FeCx/N-doped carbon fiber composite in an electro-Fenton process.

    Science.gov (United States)

    Lan, Huachun; Li, Jianfei; Sun, Meng; An, Xiaoqiang; Hu, Chengzhi; Liu, Ruiping; Liu, Huijuan; Qu, Jiuhui

    2016-09-01

    In this study, a FeCx/N-doped carbon fiber composite (FeCx/NCNFs) was developed via an electrospinning method. According to the characterization results of XRD, TEM and XPS, FeCx (a mixture of Fe7C3 and Fe3C) was either embedded in or attached to the NCNFs. It was used for the first time as a catalyst for dimethylarsinate (DMA) degradation and as an absorbent for inorganic arsenic (As (V)), with degradation and adsorption occurring simultaneously, in an electro-Fenton process. The effects of catalyst dosage, initial DMA concentration, solution pH, and applied current on the treatment efficiency and the corresponding H2O2 generation were systematically investigated. The results showed that DMA could be efficiently oxidized into As(V). 96% of DMA was degraded after reaction time of 360 min and the residual As(V) concentration in solution was below the allowable limit of 0.01 mg/L under the optimum treatment conditions. Based on an ESR and radical scavenger experiment, OH was proven to be the sole reactive oxygen species involved in the degradation process of DMA. DMA was oxidized to MMA as the primary oxidation product, which was subsequently oxidized to inorganic arsenic, As (V). TOC was also efficiently removed at the same time. The DMA removal mechanism for simultaneous degradation of dimethylarsinate and adsorption of arsenic over FeCx/NCNFs in the electro-Fenton process was also proposed based on the experimental results. PMID:27179339

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

    International Nuclear Information System (INIS)

    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 H2O2/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% nitrogen

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

    Science.gov (United States)

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

    2012-06-30

    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 2.5L of sulfanilic acid solutions in 0.05M 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. 31Wm(-2). Optimum variables of 100mAcm(-2), 0.5mM Fe(2+) and pH 4.0 were determined after 240min of EF and 120min of SPEF. Under these conditions, EF gave 47% of mineralization, whereas SPEF was much more powerful yielding 76% mineralization with 275kWh 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.

  6. Study on the sewage residue from dyeing indigo-jeans by ferric-carbon micro-electrolysis and Fenton reagent%Fenton强化微电解工艺处理靛蓝牛仔布印染废水研究

    Institute of Scientific and Technical Information of China (English)

    杨林; 王玉军

    2012-01-01

    研究了铁炭微电解- Fenton试剂作用下靛蓝牛仔布印染废水的脱色和COD去除行为,通过正交试验和单因素试验确定了微电解-Fenton反应的最佳操作条件,分析了各影响因子的作用机理.结果表明:在铁炭质量比为2∶1,pH值为3的条件下反应90 min,铁炭微电解出水COD的去除率在49.20%,色度去除率达到80%,BODs/COD值由0.248上升至0.436,可生化性提高;微电解出水在pH值为5,H2O2投加量为0.3%条件下反应60 min后,COD去除率可达84.1%,色度去除率达90%,BOD5/COD值上升至0.525;铁炭微电解- Fenton组合工艺COD的总去除率为87.26%.%The present paper is engaged in a study on the sewage residue from dyeing indigo-jeans by ferric-carbon micro-electrolysis and Fenton reagent. As is known, ferric-carbon micro-electrolysis and Fenton reagent are commonly used in pre- treating printing and dyeing sewage. For our research purpose, we have done a series of combined orthogonal experiments and the single factor experiment through the micro-electrolysis and Fenton and worked out the optimal operating conditions of COD and color removing effects. And, then, we have analyzed the mechanism of the affecting factors. The optimal conditions we have established through experiments can be stated as follows: the volume ratio of iron to carbon is equal to 2: 1, the influent pH value is 3, the ferric-carbon micro-electrolysis aeration time is 90 min. We have also enhanced the removal of COD and color, which can reach about 49% and 80% . When the treatment is over, we have found that the B0D5/C0D could be heightened from 0.248 to 0.436, with the biodegradability being improved. In addition, we have also found that Fe2 + and · OH could be generated at low cost by effective combination of micro-eSectrolysis and Fenton, which helps to overcome high cost and waste in Fenton reaction. Moreover, our study has also found the best operating conditions for Fenton reaction system: p

  7. Remoción de colorantes sintéticos mediante el proceso Fenton heterogéneo usando Fe2O3 soportado en carbón activado obtenido a partir de residuos de rosas

    Directory of Open Access Journals (Sweden)

    María Paula Castellanos

    2012-12-01

    Full Text Available To study the removal of dyes:reactive black 5 and crystal violet by the Fenton reaction using Fe2O3-catalysts (0-10% m/m of Fe supported on activated carbon obtained from rose remnants. The activated carbon was obtained from pyrolysis at 500 °C (1h followed by activation with NaOH (1:2 wt.. The support was classified using several chemical and physical techniques. Fe-catalysts were synthesized by incipient impregnation. Fenton and adsorption treatments were performed in a batch reactor, concentration of dye of 10 mgL-1, 0.25 mgmL-1 catalyst, pH = 3.7, 20 ± 2 ° C, 750 rpm and atmospheric pressure. The activated carbon used as support showed high basicity, presence of polar groups on the surface, high ash content (22.85% and oxygen (43.93% and was mostly of the microporous type with a BET surface area of 520 m2g-1. The maximum discoloration achieved for black reactive 5 was obtained with the catalyst of 3% Fe (98.33% after 180 min. while for the crystal violet it was obtained with the catalyst of 1% Fe (63.95% after 180 min. Discoloration by Fenton treatment is dependent on the Fe content, the particle size of the active site and the type of dye. The removal of reactive black 5 reached a maximum at 3% Fe while the crystal violet decreased by increasing Fe content. The treatment proposed in this paper is promising for the removal of synthetic dyes present in contaminated water.

  8. Fenton oxidation to remediate PAHs in contaminated soils: A critical review of major limitations and counter-strategies.

    Science.gov (United States)

    Usman, M; Hanna, K; Haderlein, S

    2016-11-01

    Fenton oxidation constitutes a viable remediation strategy to remove polycyclic aromatic hydrocarbons (PAHs) in contaminated soils. This review is intended to illustrate major limitations associated with this process like acidification, PAH unavailability, and deterioration of soil quality along with associated factors, followed by a critical description of various developments to overcome these constraints. Considering the limitation that its optimal pH is around 3, traditional Fenton treatment could be costly, impractical in soil due to the high buffering capacity of soils and associated hazardous effects. Use of various chelating agents (organic or inorganic) allowed oxidation at circumneutral pH but factors like higher oxidant demand, cost and toxicity should be considered. Another alternative is the use of iron minerals that can catalyze Fenton-like oxidation over a wide range of pH, but mobility of these particles in soils (i.e. saturated and unsaturated zones) should be investigated prior to in-situ applications. The PAH-unavailability is the crucial limitation hindering their effective degradation. Research data is compiled describing various strategies to address this issue like the use of availability enhancement agents, extraction or thermal pretreatment. Last section of this review is devoted to describe the effects of various developments in Fenton treatment onto soil quality and native microbiota. Finally, research gaps are discussed to suggest future directions in context of applying Fenton oxidation to remediate contaminated soils. PMID:27341118

  9. Comparative temporal analysis of multiwalled carbon nanotube oxidation reactions: Evaluating chemical modifications on true nanotube surface

    Science.gov (United States)

    Pacheco, Flávia G.; Cotta, Alexandre A. C.; Gorgulho, Honória F.; Santos, Adelina P.; Macedo, Waldemar A. A.; Furtado, Clascídia A.

    2015-12-01

    The influence of extensive purification on oxidized multiwalled carbon nanotube surface composition was studied through the characterization and differentiation of the actual surface submitted to three oxidation methods: microwave-assisted acid oxidation, hydrogen peroxide reflux, and Fenton reaction. The oxidized samples were purified by a multi-step procedure including the sequential use of basic reflux and dispersion in dimethylformamide (DMF). The results showed a significant increase in the amount of oxidation debris with hydrogen peroxide and Fenton reaction times longer than 8 h and strong surface characteristic modification. With regard to sample purification, basic reflux led to a reduction in oxygenated group concentration of only 10% in the samples treated by acid oxidation. On the other hand, the subsequent use of DMF led to a further decrease in concentration of 39%, proving to be a more efficient method for the removal of oxidation debris.

  10. 树脂吸附-Fenton 试剂氧化法预处理炼油碱渣废水%Pretreatment of Refining Alkaline Residue Wastewater by Resin Adsorption -Fenton Reagent Oxidation Process

    Institute of Scientific and Technical Information of China (English)

    张大涌; 高小青; 朱颖; 宿新泰; 甄新平; 牛春革

    2011-01-01

    采用树脂吸附-Fenton 试剂氧化组合工艺对某炼油企业炼油碱渣废水进行预处理.实验确定的最佳工艺条件为:3 种树脂串联吸附,废水流量0.33 mL/ min,H2O2加入量0.20 mol / L,n(H2O2)1 n(Fe2 +)= 12,Fenton 试剂氧化进水pH 3,Fenton 试剂氧化反应时间120 min.在此条件下,废水的COD 去除率为98.0%,BOD5 / COD 由0.09提高到0.70,可生化性有了较大的提高,为后续生化处理创造了条件.%The wastewater containing refining alkaline residue from an oil refining factory was pretreated by the resin adsorption - Fenton reagent oxidation process. The optimum process conditions are determined by experiments as follows: adsorption in series using 3 kinds of resin, wastewater flow 0. 33 mL/min, H2O2 dosage 0. 20 mol/L, n( H2O2 ): n( Fe2+ ) = 12, Fenton reagent oxidation influent pH 3, Fenton reagent oxidation time 120 min. Under these conditions, the COD removal rate is 98. 0% and BOD5/COD is increased from 0. 09 to 0. 70. The great improvement of the wastewater biodegradability creates a favorable condition for further bio-treatment.

  11. Study on the advanced treatment of synthesis pharmaceutical wastewater by fluidized bed fenton%流体化床Fenton深度处理合成制药废水研究

    Institute of Scientific and Technical Information of China (English)

    王付超; 梅荣武; 刘俊

    2012-01-01

    The fluidized-bed Fenton reactor was employed for advanced treatment of synthesis pharmaceutical wastewater.Through orthogonal tests,the best reaction conditions for synthesis pharmaceutical wastewater treatment were determined as 20 min of HRT,4.0 of initial pH value,4.0 of H2O2/CODcr mass ratio and 15 of H2O2/Fe2+ Moore ratio.Under those optimum conditions,CODcr concentration of the effluent was detected stably below 80 mg/L,which complies with the Class A of Integrated Wastewater Discharge Standard(GB8978-1996).Comparing to the standard Fenton oxidation,the application of fluidized-bed Fenton reactor resulted in an improvement of over 13% on CODcr removal efficiency,as well as a reduction of 70% on sludge yield.Accordingly,the operating costs can be reduced by 28%,which could be controlled within 3.0 yuan/tons wastewater in stable conditions.%采用流体化床Fenton装置深度处理合成制药废水,通过正交试验确定了处理合成制药废水的最佳条件是HRT为20min,初始pH值为4.0,H2O2/CODcr(质量比)为4.0,H2O2/Fe2+(摩尔比)为15,且在最佳条件下出水CODcr稳定在80mg/L以下,可以达到《污水综合排放标准》(GB8979-1996)一级标准。同时将其与标准Fenton氧化法进行对比试验,结果显示流体化床FentonCODcr去除率可提高13%以上,污泥产生量可降低70%,运行成本可减低28%,稳定运行成本可以控制在3.0元/吨废水以内。

  12. 非均相光Fenton降解4-氯酚的研究%Degradation efficiency of 4-chlorophenol via heterogeneous photo-Fenton

    Institute of Scientific and Technical Information of China (English)

    王维明; 张冉; 王树涛; 刘婷; 尤宏

    2013-01-01

    制备了以Al2O3/TiO2为载体的负载型铁氧化物催化剂,对催化剂进行SEM、XRD、UV-vis-DRS和XPS分析,考察H2O2投加量、催化剂投加量、4-氯酚初始质量浓度对4-氯酚处理效果的影响,分析了非均相光Fenton体系的氧化机理.结果表明,所制备的负载型铁氧化物催化剂为α-FeOOH与γ-Fe2O3的混合物,其表面存在较多的颗粒和孔穴,吸附性强,具有很高的催化活性.H2O2、铁氧化物催化剂、紫外灯之间存在协同作用,所构成的非均相光Fenton体系对4-氯酚具有良好的去除效果.其反应机理为表面催化,催化剂表面的Fe(Ⅲ)在光照的作用下被还原为Fe(Ⅱ).在催化剂投加量为1 g/L,H2O2浓度为7.84mmol/L时,对4-氯酚的降解效果达到最佳,反应进行30 min后4-氯酚的去除率大于99%,反应1h矿化度可达91.4%.%This paper aims to introduce our preparation of catalysts loaded on Al2O3/TiO2 and the heterogeneous photo-Fenton reaction system we have established for the study of the degradation efficiency of the 4-chlorophenol. The catalysts we have prepared are characterized by SEM, XRD, by means of which we have investigated the effect of H2O2 dosage, along with the catalyst dosage and initial concentration of the 4-chlorophenol on 4-chlorophenol degradation needed. In addition, we have also done experiments to explore the oxidation mechanism of heterogeneous photo-Fenton system. The results of our research show that the ingredients of iron oxidate catalysts loaded on Al2O3/TiO2 were the mixture of α- FeOOH and γ - Fe2O3; and, as compared with Al2O3/TiO2 carrier, it has been found that there exist more surface particles and cavity on the catalyst surface, whose specific surface area proves to be wider for its adsorption, and, therefore, helps to enhance their catalytic activity. The heterogeneous photo-Fenton system we have established proves to be highly effective for degrading 4-chlorophenol. Furthermore, we have worked out the

  13. Aerobic SMBR/reverse osmosis system enhanced by Fenton oxidation for advanced treatment of old municipal landfill leachate.

    Science.gov (United States)

    Zhang, Guoliang; Qin, Lei; Meng, Qin; Fan, Zheng; Wu, Dexin

    2013-08-01

    A novel combined process of Fenton oxidation, submerged membrane bioreactor (SMBR) and reverse osmosis (RO) was applied as an appropriate option for old municipal landfill leachate treatment. Fenton process was designed to intensively solve the problem of non-biodegradable organic pollutant removal and low biodegradability of leachate, although the removal of ammonia-nitrogen was similar to 10%. After SMBR treatment, it not only presented a higher removal efficiency of organics, but also exhibited high ammonia-nitrogen removal of 80% on average. The variation of extracellular polymeric substance (EPS) content, zeta potential, and particle size of flocs after Fenton effluent continually fed in SMBR was found to be benefit for alleviating membrane fouling. Finally, three kinds of RO membranes (RE, CPA, and BW) were applied to treat SMBR effluents and successfully met wastewater re-utilization requirement. Compared with simple RO process, the troublesome membrane fouling can be effectively reduced in the combined process. PMID:23743431

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

    International Nuclear Information System (INIS)

    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 H2O2 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

  15. 微电解-Fenton氧化法去除垃圾渗滤液中有机物%Removal of organic pollutants in landfill leachate by microelectrolysis-Fenton process

    Institute of Scientific and Technical Information of China (English)

    朱兆连; 孙敏; 杨峰; 王海玲; 徐炎华; 李爱民

    2011-01-01

    Iron-carbon microelectrolysis and its Fenton process were used to treat landfill leachate. The factors, such as pH, reagent dosage, reagent ratio, and reaction time were investigated. The landfill leachate COD decreased to 5 960 mg/L and COD removal reached 51.8% after iron-carbon microelectrolysis under the optimal conditions of initial pH value of 3, iron to carbon mass ratio of 4, iron-carbon dosage of 0. 6 g/L, and reaction time of 60 min. The optimal operating conditions of iron-carbon microelec-trolysis-Fenton process were H2O2 dosage of 11 mL/L and the reaction time of 100 min after iron-carbon microelectrolysis. The landfill leachate COD after iron-carbon microelectrolysis-Fenton process decreased to 4 480 mg/L and COD removal reached 63. 8%. Humic matters of large molecule were removed and decomposed into small molecular compounds after iron-carbon microelectrolysis and its Fenton process. Fenton process had stronger destruction performance for humic matters than iron-carbon microelectrolysis.%采用Fe/C微电解和Fe/C微电解-Fenton氧化联合工艺对垃圾渗滤液进行处理,研究了废水初始pH、药剂投加量、药剂投加比例和反应时间等对处理效果的影响,获得Fe/C微电解处理垃圾渗滤液的最佳工艺条件:初始pH =3、m(Fe)/m(C)为4、ρ(Fe/C)为0.6 g/L、反应时间为60 min,处理后COD降至5 960 mg/L,COD去除率达51.8%.Fe/C微电解-Fenton氧化处理垃圾渗滤液的最佳工艺条件:在Fe/C微电解最佳条件下,H2O2投加量为11 mL/L,反应时间为100 min,出水COD为4480 mg/L,COD总去除率为63.8%.垃圾渗滤液中的腐殖酸类有机质经过Fe/C微电解或微电解-Fenton氧化处理后变成小分子产物,与Fe/C微电解相比,Fenton氧化对腐殖酸等大分子有机质有更强的氧化降解效果.

  16. DETERMINACIÓN DE LA DOSIS ÓPTIMA DE REACTIVO FENTON EN UN TRATAMIENTO DE LIXIVIADOS POR FENTON-ADSORCIÓN

    OpenAIRE

    Roger Iván MÉNDEZ NOVELO; José Alfredo PIETROGIOVANNA BRONCA; Beatriz SANTOS OCAMPO; María Rosa SAURI RIANCHO; Germán GIÁCOMAN VALLEJOS; Elba René CASTILLO BORGES

    2010-01-01

    Los lixiviados son el resultado de la percolación de líquidos a través de los desechos sólidos en proceso de estabilización. La complejidad de su tratamiento se debe a que su composición es altamente tóxica y variable. Lo anterior y el suelo altamente permeable de la península de Yucatán, representan un alto peligro a la salud. Se ensayó un tratamiento de oxidación tipo Fenton-adsorción con el que se obtuvieron mejores resultados que con otros tratamientos fisicoquímicos o biológicos reportad...

  17. Advanced Treatment of Pulping Medium Wastewater by Fenton-UV Combined Technology%Fenton-UV偶联深度处理制浆中段废水

    Institute of Scientific and Technical Information of China (English)

    蓝惠霞; 刘晓凤; 王乐乐

    2010-01-01

    采用Fenton-UV偶联时制浆中段废水进行深度处理.实验结果表明,Fenton氧化在UV照射下的处理效果明显好于无UV照射时的废水处理效果,尤其是大功率的UV(2000W)照射时,CODCr去除率和过氧化氢利用率可达80%以上.在紫外波长为365nm处,Fenton氧化处理效果优于波长为253.7nm时的效果.随着反应时间的增加,CODCr的去除率增大,在12min以后几乎保持稳定.CODCr去除率在pH为4时最好,高达88.4%.

  18. Fate of citalopram during water treatment with O3, ClO2, UV and fenton oxidation

    DEFF Research Database (Denmark)

    Hörsing, Maritha; Kosjek, Tina; Andersen, Henrik Rasmus;

    2012-01-01

    In the present study we investigate the fate of citalopram (CIT) at neutral pH using advanced water treatment technologies that include O3, ClO2 oxidation, UV irradiation and Fenton oxidation. The ozonation resulted in 80% reduction after 30 min treatment. Oxidation with ClO2 removed >90% CIT...... at a dosage of 0.1 mg L−1. During UV irradiation 85% reduction was achieved after 5 min, while Fenton with addition of 14 mg L−1 (Fe2+) resulted in 90% reduction of CIT. During these treatment experiments transformation products (TPs) were formed from CIT, where five compounds were identified by using high...

  19. Stabilization and dewatering of wastewater treatment plants sludge using the Fenton process

    Directory of Open Access Journals (Sweden)

    Abolfazl Azhdarpoor

    2015-11-01

    Full Text Available Wastewater sludge typically contains large amounts of water and organic materials; therefore, its stabilization and dewatering is of particular importance. In this study, Fenton oxidation process is used for stabilization and dewatering of sludge in the output of a wastewater treatment plant. To evaluate the sludge stabilization and dewatering, specific resistance to filtration (SRF, volatile organic compounds (VSS, total suspended solids (TSS, soluble chemical oxygen demand (SCOD and heterotrophic bacteria were measured. During the experiment, the optimal values of various parameters such as pH (2-9, hydrogen peroxide (0.015- 0.18mol/L, Fe2+ (0.008- 0.1mol/L and time (5 - 60 minutes for optimum sludge dewatering and stabilization were investigated. The results showed that the highest percentages of SRF reduction and removal rates of SCOD, VSS and TSS were 99.48, 61, 42, and 41 percent respectively. These results were obtained in optimum pH 5, 0.05 mol/l Fe2+, 0.12 mol/l hydrogen peroxide, and the retention time of 15 minutes. The removal rate of heterotrophic bacteria increased with increasing dose of hydrogen peroxide, so that a removal rate of 84 percent was observed at a dose of 0.18 mol/l. In general, Fenton process can reduce volatile organic materials and chemical oxygen demand of the sludge resulting in its significant stabilization and dewatering. In general, Fenton process can reduce volatile organic materials and chemical oxygen demand of the sludge resulting in its significant stabilization and dewatering.

  20. REMOVAL OF REMAZOL ROSSO RB DYE FROM AQUEOUS EFFLUENTS BY HOMOGENOUS FENTON OXIDATION PROCESSES

    Directory of Open Access Journals (Sweden)

    Carmen Zaharia

    2014-06-01

    Full Text Available The paper presents some data from our laboratory-setup experiments of homogenous oxidative processes with hydrogen peroxide (i.e. advanced Fenton oxidation processes applied for Remazol Rosso RB dye-containing aqueous systems, especially textile effluents. Therefore, some different operating parameters (including pH, concentration of dye, H2O2 and ferrous ions, oxidation time, temperature, stirring regime, among its were tested for determination of the best performance in effluent decoloration and dye removal, meaning the optimal values of each studied parameters for highest decoloration or dye removal.

  1. Treatment of Actual Chemical Wastewater by a Heterogeneous Fenton Process Using Natural Pyrite

    OpenAIRE

    Liang Sun; Yan Li; Aimin Li

    2015-01-01

    Wastewater from chemical plants has remarkable antibiotic effects on the microorganisms in traditional biological treatment processes. An enhanced Fenton system catalyzed by natural pyrite was developed to degrade this kind of wastewater. Approximately 30% chemical oxygen demand (COD) was removed within 120 min when 50 mmol/L H2O2 and 10 g/L natural pyrite were used at initial pH from 1.8 to 7. A BOD5/COD enhancement efficiency of 210% and an acute biotoxicity removal efficiency of 84% were a...

  2. Application of electro-Fenton oxidation for the detoxification of olive mill wastewater phenolic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Khoufi, S.; Aouissaoui, H.; Sayadi, S. [Lab. des Bioprocedes, Centre de Biotechnologie de Sfax, Sfax (Tunisia); Penninckx, M. [UPEM, Univ. Libre de Bruxelles, Bruxelles (Belgium)

    2003-07-01

    Olive mill effluent (OMW) is an example of a wastewaters containing high concentrations of recalcitrant and toxic compounds which are polyphenolics of different molecular weight. It causes disposal problems because they contain powerful pollutants. Treatment and detoxification of phenolic fraction extracted from olive mill wastewaters as well as a synthetic phenolic mixture was investigated by electro-Fenton method. Results shows that this method is highly efficient in polymerising low molecular mass phenolics and removing a large amount of recalcitrant polyphenolic compounds. This treatment decreased 78% of the toxicity which sustained a good anaerobic post-treatment. (orig.)

  3. Treatment of pesticide rinsate towards reuse by photosensitized Fenton-like process.

    Science.gov (United States)

    Kuo, W S; Ho, Y Y

    2010-01-01

    A Fenton-like process with combination of dye has been used to enhance the treatment of carbofuran (2,3-dihydro-2,2-dimethylbenzofuran -7-yl methylcarbamate) pesticide rinsate. Results showed that as compared to Fenton-like process, this photosensitization Fenton-like process improved the degradation efficiency of carbofuran rinsate significantly. Among the conditions studied, the optimum dosage for the complete destruction of carbofuran molecular structure was found under a [H2O2]0/[Fe3+]0 ratio of 30-35 and a [Dye]0/[Fe3+]0 ratio of 2%, respectively, after an irradiance of 500 W/m2 for 20 min. As a result, the COD degradation efficiency of rinsate could be promoted from 37.1 to 61.2% and 66.0% by an addition of methylene blue (MB) and alizarin red S (ARS), respectively. Nevertheless, ARS showed a much more effective acceleration effect on the mineralization and microtoxicity reduction of carbofuran than MB. A mineralization efficiency of 57.2% and a microtoxicity reduction of 90% could be achieved with the addition of ARS. Because of its quinone structure unit, the dye ARS could play a role like hydroquinone to recycle Fe2+ from Fe3+, resulting in one more catalytic effect on the reduction of Fe3+ and thus the mineralization and microtoxicity reduction of carbofuran was greatly promoted in the presence of ARS. In addition, it was found that carbofuran molecules could be decomposed quickly to lower-molecular-weight intermediates and even mineralized by attacking of hydroxyl radicals. Carbofuran was found to be decomposed to carbofuran phenol, 3-oxo carbofuran phenol, and 3-hydroxyl carbofuran phenol initially, and then further be degraded to smaller molecules, such as NO3-, CH3COOH, (COOH)2 and CO2. Accordingly, it was believed that the Fenton-like process along with the aid of a photosensitizer, such as ARS, under an appropriate ratio could be a feasible and potential technology for the treatment of pesticide rinsate.

  4. 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;

    Groundwater beneath the Kærgård Plantage megasite in Denmark are contaminated with a complex mixtu of pharmaceutical wastes, including sulfonamides, barbiturates, aniline, pyridine chlorinated solvents, mercury, and cyanide.  Regulatory agencies in Denmark are now in the process of evaluating...... is to identify the fate of mercury and cyanide consequent to the application of Fenton's reagent and activated persulfate.  Batch and continuous-flow column reactors will be used to measure mobilization of the mercury, cyanide and other metals both within the aqueous and vapor phases.   The collective chemical...

  5. A Fenton-like degradation mechanism for 1,4-dioxane using zero-valent iron (Fe0) and UV light.

    Science.gov (United States)

    Son, Hyun-Seok; Im, Jong-Kwon; Zoh, Kyung-Duk

    2009-03-01

    In this study, the degradation mechanism of 1,4-dioxane using zero-valent iron (Fe0) in the presence of UV light was investigated kinetically. The degradation of 1,4-dioxane in Fe0-only, photolysis, and combined Fe0 and UV reactions followed the kinetics of a pseudo-first-order model. The degradation rate constant (19 x 10(-4)min(-1)) in the combined reaction with UV-C (4.2 mW cm(-2)) and Fe0 (5 mg L(-1)) was significantly enhanced compared to Fe0-only (4.8 x 10(-4) min(-1)) and photolytic reactions (2.25 x 10(-4)min(-1)), respectively. The removal efficiency of 1,4-dioxane in combined reaction with Fe0 and UV within 4 h was enhanced by increasing UV intensity at UV-C region (34% at 4.2 mW cm(-2) and 89% at 16.9 mW cm(-2)) comparing with the removal in the combined reaction with Fe0 and UV-A (29% at 2.1 mW cm(-2), and 33% at 12.6 mW cm(-2)). It indicates that 1,4-dioxane was degraded mostly by OH radicals in the combined reaction. The degradation patterns in both Fe(0)-only and combined reactions were well fitted to the Langmuir-Hinshelwood model, implying that adsorption as well as the chemical reaction occurred. The transformation of Fe0 to Fe2+ and Fe3+ was observed in the Fe0-only and combined reactions, and the transformation rate of Fe0 was improved by UV irradiation. Furthermore, the reduction of Fe3+ was identified in the combined reaction, and the reduction rate was enhanced by an increase of UV energy. Our study demonstrated that the enhancement of 1,4-dioxane removal rate occurred via an increased supply of OH radicals from the Fenton-like reaction induced by the photolysis of Fe0 and H2O, and with producing less sludge.

  6. Cold Incineration of Chlorophenols in Aqueous Solution by Advanced Electrochemical Process Electro-Fenton. Effect of Number and Position of Chlorine Atoms on the Degradation Kinetics

    Science.gov (United States)

    Oturan, Nihal; Panizza, Marco; Oturan, Mehmet A.

    2009-09-01

    This study reports the kinetics of the degradation of several chlorophenols (CPs), such as monochlorophenols (2-chlorophenol and 4-chlorophenol), dichlorophenols (2,4-dichlorophenol and 2,6- dichlorophenol), trichlorophenols (2,3,5- trichlorophenol and 2,4,5-trichlorophenol), 2,3,5,6-tetrachlorophenol, and pentachlorophenol, by the electro-Fenton process using a carbon felt cathode and a Pt anode. The effect of number and the position of the chlorine atoms in the aromatic ring on the oxidative degradation rate was evaluated and discussed. The oxidation reaction of all the CPs with hydroxyl radicals evidenced a pseudo-first-order kinetics and the rate constant decreased with increasing the number of chlorine atoms. The absolute rate constant of second-order reaction kinetics between CPs and •OH was determined by the competition kinetics method in the range of (3.56-7.75) × 109 M-1 s-1 and follows the same sequence of the apparent rate constants. The mineralization of several CPs and of a mixture of all CPs under study was monitored by the total organic carbon (TOC) removal and the chlorine release during mineralization was followed by ion chromatography. Our results demonstrated that more chlorinated phenols are more difficult to mineralize; however for all the tested CPs, almost quantitative release of chloride ions was obtained after 6 h of treatment.

  7. Degradation of polycyclic aromatic hydrocarbons (PAHs) in contaminated soils by Fenton's reagent: a multivariate evaluation of the importance of soil characteristics and PAH properties.

    Science.gov (United States)

    Jonsson, Sofia; Persson, Ylva; Frankki, Sofia; van Bavel, Bert; Lundstedt, Staffan; Haglund, Peter; Tysklind, Mats

    2007-10-01

    In this study, we investigated how the chemical degradability of polycyclic aromatic hydrocarbons (PAHs) in aged soil samples from various contaminated sites is influenced by soil characteristics and by PAH physico-chemical properties. The results were evaluated using the multivariate statistical tool, partial least squares projections to latent structures (PLS). The PAH-contaminated soil samples were characterised (by pH, conductivity, organic matter content, oxide content, particle size, specific surface area, and the time elapsed since the contamination events, i.e. age), and subjected to relatively mild, slurry-phase Fenton's reaction conditions. In general, low molecular weight PAHs were degraded to a greater extent than large, highly hydrophobic variants. Anthracene, benzo(a)pyrene, and pyrene were more susceptible to degradation than other, structurally similar, PAHs; an effect attributed to the known susceptibility of these compounds to reactions with hydroxyl radicals. The presence of organic matter and the specific surface area of the soil were clearly negatively correlated with the degradation of bi- and tri-cyclic PAHs, whereas the amount of degraded organic matter correlated positively with the degradation of PAHs with five or six fused rings. This was explained by enhanced availability of the larger PAHs, which were released from the organic matter as it degraded. Our study shows that sorption of PAHs is influenced by a combination of soil characteristics and physico-chemical properties of individual PAHs. Multivariate statistical tools have great potential for assessing the relative importance of these parameters.

  8. 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.

  9. Fenton-BAF-RO工艺处理电镀前处理废水并回用%Treatment and Reuse of Electroplating Pre-treatment Wastewater by Fenton/BAF/RO Membrane Technology

    Institute of Scientific and Technical Information of China (English)

    2013-01-01

    Pre-treatment wastewater is an important part of the plating wastewater. It has higher COD but with relatively larger reuse potential. The technology of Fenton-BAF-RO membrane separation process was used to treat electroplating Pre-treatment wastewater from a plant in Guangdong province, the results show that the pre-treatment wastewater can be advanced treated and reused effectively by this technology, and by concentrated water recirculation, zero emission was achieved. Fenton-BAF process ensure the stable operation of the RO system.%  前处理废水是电镀废水的重要组成部分,COD较高但回用潜力相对较大。采用Fenton-BAF-RO膜分离工艺处理广东省某厂电镀前处理废水,运行结果表明,该工艺可有效实现电镀前处理废水的深度处理及回用,并且通过浓水回流达到零排放,Fenton-BAF 工艺保证了 RO 系统的稳定运行。

  10. Study on the treatment of trichlorfon pesticides wastewater with UV-TiO2-Fenton-Activated carbon%UV-TiO2-Fenton-活性炭处理敌百虫农药废水的研究

    Institute of Scientific and Technical Information of China (English)

    朱丹; 王瑛瑛; 廖绍华; 赵磊

    2013-01-01

    Taking the trichlorfon wastewater as test material, the treatment effects of UV-TiO2-Fenton -Activated Carbon were studied. The result shows that treatment with UV has a great COD removal effect compa-ring to other treatments. The COD of trichlorfon wastewater would decrease from 16 675. 7 mg/L to 6 987. 1 mg/L by UV-TiO2-Fenton-Activated Carbon. The COD removal was up to 58. 1 % .%以敌百虫农药废水为研究对象,研究了UV-TiO2-Fenton-活性炭对敌百虫农药废水单独使用及复合联用的处理效果,结果表明:各方法单独使用时,UV光照对敌百虫农药废水COD的去除效果最好.将UV-TiO2-Fenton-活性炭复合联用处理敌百虫农药废水时,COD由16 675.7 mg/L变为6987.1 mg/L,COD去除率达58.1%.

  11. Pretreatment of 2,4-dinitroanisole (DNAN) producing wastewater using a combined zero-valent iron (ZVI) reduction and Fenton oxidation process

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Jinyou, E-mail: shenjinyou-1981@163.com [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu Province (China); Ou, Changjin; Zhou, Zongyuan [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu Province (China); Chen, Jun; Fang, Kexiong [Hubei Dongfang Chemical Co. Ltd., Hubei 441404 (China); Sun, Xiuyun; Li, Jiansheng [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu Province (China); Zhou, Lin [School of Mechatronical Engineering, Beijing Institute of Technology, Beijing 100081 (China); Wang, Lianjun, E-mail: wanglj@mail.njust.edu.cn [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu Province (China)

    2013-09-15

    Highlights: • ZVI-Fenton process was conducted for DNAN producing wastewater pretreatment. • Transformation of nitro to amino group by ZVI overcomes the oxidative hindrance. • Subsequent Fenton process is efficient for the removal of aromatic compounds. • ABR-MBBR process is efficient for the polishing of ZVI-Fenton effluent. -- Abstract: A combined zero-valent iron (ZVI) reduction and Fenton oxidation process was tested for the pretreatment of 2,4-dinitroanisole (DNAN) producing wastewater. Operating conditions were optimized and overall performance of the combined process was evaluated. For ZVI process, almost complete reduction of nitroaromatic compounds was observed at empty bed contact time (EBCT) of 8 h. For Fenton process, the optimal pH, H{sub 2}O{sub 2} to Fe(II) molar ratio, H{sub 2}O{sub 2} dosage and hydraulic retention time (HRT) were found to be 3.0, 15, 0.216 mol/L and 5 h, respectively. After pretreatment by the combined ZVI-Fenton process under the optimal conditions, aromatic organic compound removal was as high as 77.2%, while the majority of COD remained to be further treated by sequent biological process. The combined anaerobic-aerobic process consisted of an anaerobic baffled reactor (ABR) and a moving-bed biofilm reactor (MBBR) was operated for 3 months, fed with ZVI-Fenton effluent. The results revealed that the coupled ZVI-Fenton-ABR-MBBR system was significantly efficient in terms of correcting the effluent's main parameters of relevance, mainly aromatic compounds concentration, COD concentration, color and acute toxicity. These results indicate that the combined ZVI-Fenton process offers bright prospects for the pretreatment of wastewater containing nitroaromatic compounds.

  12. Research on Treating Dye Wastewater by Fenton Reagent%Fenton试剂对染料废水的降解脱色作用研究

    Institute of Scientific and Technical Information of China (English)

    杨威; 孔德骞; 车春波; 刘丹

    2009-01-01

    In order to research the degradation efficiency of Fenton method on some non-biodegradable organic pollutant and the factors that af-fect the degradation process, the effects d pH,dosages of H2O2 and FeSO4, reaction time,temperature on decolouration efficiency and COD removal efficiency of the dyes wastewater simulated by methyl orange solution were studied. The results showed that Fenton reagent could remove the color and COD of this dye wastewater effectively with color and COD removals of 99.66 % and 88% respectively when the concentration of dye was 200 mg/L, pH=4,temperature was 20℃,the dosages of H2O2 and FeSO4·7H2O were 0.6 mL/L and 200mg/L,and reaction time was 60min.%为了进一步探讨Fenton法对某些难降解有机物的降解效果,研究影响降解的诸多因素,以甲基橙模拟染料废水为研究对象,以色度和COD去除率为检测指标,研究了Fenton反应中pH值、H2O2浓度、Fe2+离子浓度、反应时间、温度对甲基橙模拟染料废水脱色率及COD去除率的影响规律.结果表明:Fenten试剂可有效地去除甲基橙模拟染料废水中的色度和COD.染料浓度为200mg/L时,在pH=4、20℃、H2O2=(浓度为30%)投量为0.6mL/L、硫酸亚铁投量为200mg/L时,反应60min,甲基橙模拟染料废水的色度去除率可以达到99.66%,COD的去除率可达88%.

  13. Photo-Fenton-like degradation of azo dye methyl orange using synthetic ammonium and hydronium jarosite

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zhihui [Department of Chemistry, College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Liang, Jianru [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Zhou, Lixiang, E-mail: lxzhou@njau.edu.cn [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China)

    2013-01-05

    Highlights: Black-Right-Pointing-Pointer Hydronium and ammonium jarosite could catalyze the oxidation of methyl orange in photo-Fenton-like process. Black-Right-Pointing-Pointer The oxidation process is essentially heterogeneous, not homogeneous. Black-Right-Pointing-Pointer Hydronium jarosite has stronger reactivity than ammonium jarosite. - Abstract: Ammonium and hydronium jarosite were prepared by hydrothermal method with urea as the homogeneous precipitant. X-ray diffraction, field-emission scanning electron microscope, X-ray photoelectron spectrum, UV-vis spectra and fourier transform infrared spectrum were used to characterize the resulting products. The photodegradation efficiency of the prepared ammonium and hydronium jarosite was studied in a photo-Fenton-like process using methyl orange (MO) as target pollutant. The photocatalytic degradation of MO over synthetic ammonium and hydronium jarosite under various conditions, such as catalysts loading, H{sub 2}O{sub 2} concentration and initial pH, has been investigated. Results show that ammonium and hydronium jarosite have satisfactory photocatalysis effect in degradation of MO azo dye, and that the reactivity of hydronium jarosite toward the mineralization of MO was higher than that of ammonium jarosite. The novel ammonium and hydronium jarosite catalysts would be important for industrial applications due to their high photoactivity, little iron leaching and low cost.

  14. Water quality in the vicinity of Fenton Hill. Progress report 1981 and 1982

    Energy Technology Data Exchange (ETDEWEB)

    Purtymun, W.D.; Ferenbaugh, R.W.; Becker, N.M.; Adams, W.H.; Maes, M.N.

    1983-09-01

    As part of a continuing program of environmental studies, water quality data have been collected from established surface and ground water stations and from ponds and pond discharges at Fenton Hill Site located in the Jemez Mountains. Most of these stations were established in 1973, and water quality data have been collected since that time. There have been slight variations in the chemical quality of water from the surface and ground water locations; however, these variations are within normal seasonal fluctuations. The discharge from ponds at Fenton Hill infiltrates into canyon alluvium within 400 m of the site. Monitoring surface and spring discharge downgradient from the ponds failed to detect any effects resulting from water released from the ponds. Total dissolved solids and calcium have increased in water from well FH-1, which furnishes the water supply for the site. This increase is caused by the decreasing water level in the well resulting in yield from beds with a slightly different quality than has been found in previous years.

  15. Solar photo-Fenton optimisation in treating carbofuran-contaminated water

    Directory of Open Access Journals (Sweden)

    Manuel Alejandro Hernández-Shek

    2012-04-01

    Full Text Available Box-Benkhen design response-surface methodology was developed to optimise photo-Fenton degradation of carbofuran (C12H15NO3 by using a compound parabolic collector pilot plant. The four variables considered in Box-Benkhen design model included carbofuran degradation percentage, initial carbofuran concentration, hydrogen peroxide [H2O2] concentration and iron [Fe2+] concentration. Degradation was monitored by using total organic carbon concentration and high-performance liquid chromatography. A 93.2 mg l-1 carbofuran concentration was completely degraded in t30W = 15 min with 17.1 mg l-1 Fe2+ and 121.6 mg l-1 H2O2. Photo-Fenton degradation led to 76.7% mineralisation. Biodegradability during optimisation was evaluated by using the BOD5/COD ratio; this value increased from 0.04 at the beginning of the process to 0.52 in t30W = 20 min, thereby showing the effectiveness of using biological treatments.

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

    International Nuclear Information System (INIS)

    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 Fe3+-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-1 soil when the accumulative H2O2 dosage was 2.45 mol kg-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 C34H38N1, was found to exhibit the greatest resistance to oxidation.

  17. Olive mill effluent depuration by ozonation and Fenton processes enhanced by iron wastes.

    Science.gov (United States)

    Martins, Rui C; Ramos, Carina M; Henriques, Lucy R; Quinta-Ferreira, Rosa M

    2016-01-01

    The aim of the present work was to compare the potential of iron industry wastes to enhance ozone and hydrogen peroxide action on the degradation of olive mill wastewaters (OMWs). The results attained show a higher efficiency for ozonation using a lower catalyst load. Nevertheless, Fenton's process led to a larger amount of chemical oxidation demand (COD) removed per mole of oxidant applied. It was concluded that hydroxyl radicals are responsible for the pollutant abatement. High eco-toxicity decay was observed after the treatments. Furthermore, a preliminary analysis of the iron shavings' stability was made by reusing it in two feed-batch trials. It was concluded that while activity was maintained for Fenton's, a decrease of about 20% was verified for catalytic ozonation. Comparing these results with the ones obtained for the same processes applied to an actual OMW, a lower percentage of COD abatement was achieved. However, when reporting the amount of COD removed per mole of oxidant used, the difference between effluents are not so high. This should be taken into account when deciding which process should be implemented at an industrial scale. With the outcomes of this research it was possible to conclude that integrating waste management with wastewater treatment was feasible. PMID:26942537

  18. Environmental studies conducted at the Fenton Hill Hot Dry Rock geothermal development site

    Energy Technology Data Exchange (ETDEWEB)

    Miera, F.R. Jr.; Langhorst, G.; McEllin, S.; Montoya, C.

    1984-05-01

    An environmental investigation of Hot Dry Rock (HDR) geothermal development was conducted at Fenton Hill, New Mexico, during 1976-1979. Activities at the Fenton Hill Site included an evaluation of baseline data for biotic and abiotic ecosystem components. Identification of contaminants produced by HDR processes that had the potential for reaching the surrounding environment is also discussed. Three dominant vegetative communities were identified in the vicinity of the site. These included grass-forb, aspen, and mixed conifer communities. The grass-forb area was identified as having the highest number of species encountered, with Phleum pratense and Dactylis glomerata being the dominant grass species. Frequency of occurrence and mean coverage values are also given for other species in the three main vegetative complexes. Live trapping of small mammals was conducted to determine species composition, densities, population, and diversity estimates for this component of the ecosystem. The data indicate that Peromyscus maniculatus was the dominant species across all trapping sites during the study. Comparisons of relative density of small mammals among the various trapping sites show the grass-forb vegetative community to have had the highest overall density. Comparisons of small mammal diversity for the three main vegetative complexes indicate that the aspen habitat had the highest diversity and the grass-forb habitat had the lowest. Analyses of waste waters from the closed circulation loop indicate that several trace contaminants (e.g., arsenic, cadmium, fluoride, boron, and lithium) were present at concentrations greater than those reported for surface waters of the region.

  19. 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

    2016-12-01

    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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, Carmen S.D. [LSRE - Laboratory of Separation and Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, R. Dr. Roberto Frias, s/n, 4200-465 Porto (Portugal); Madeira, Luis M. [LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, R. Dr. Roberto Frias, s/n, 4200-465 Porto (Portugal); Boaventura, Rui A.R., E-mail: bventura@fe.up.pt [LSRE - Laboratory of Separation and Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, R. Dr. Roberto Frias, s/n, 4200-465 Porto (Portugal)

    2009-12-30

    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{sub 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.

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

    International Nuclear Information System (INIS)

    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

  2. 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.

  3. 利用固体类Fenton试剂降解五氯酚的探讨%Decontamination of Pentachlorophenol Using Solid Fenton-like Reagents

    Institute of Scientific and Technical Information of China (English)

    杨冰; Pignatello Joseph J; 曲东

    2015-01-01

    In this study, four types of solid peroxides(calcium peroxide, CP;sodium perborate, SPB;sodium percarbonate, SPC;urea hydro-gen peroxide, UHP), H2O2, and two iron sources[Fe3(PO4)2 and FeSO4] were used to investigate pentachlorophenol(PCP)degradation in sil-ica sand slurries by Fenton-like reactions in incubation experiment. The main factors influencing the effectiveness and sustainability of ac-tive components of Fenton-like reagents were explored. Adding CP, SPB or SPC quickly increased solution pH to 10~12 and significantly inhibited Fe(Ⅱ)effectiveness. However, H2O2 or UHP showed little effect on solution pH. The rate of PCP degradation was 22.0%, 14.6%, 17.3%, 86.5%and 83.8%, respectively, for CP, SPB, SPC, UHP and H2O2 with FeSO4 as Fe(Ⅱ)source in 24 hours, and no obvious further PCP degradation was observed from 24 to 48 hours. For treatments with Fe3(PO4)2 as a steady Fe(Ⅱ)source, however, PCP showed contin-uous degradation during 20 d experimental period. The PCP degradation rate on the 20th day was 30.1%, 13.6%, 8.6%and 37.0%, for CP, SPB, SPC and UHP, respectively. Applying H2O2 resulted in 55.6%degradation of PCP in 16 days in Fe3(PO4)2 Fenton reaction. The pre-sent results show that pH buffer is required for a better decontamination performance when using alkaline-inducing solid peroxides(CP, SPB and SPC)as Fenton-like reagents. UHP might be an alternative for H2O2. Solid Fenton-like reagents significantly extend active compo-nents′life time from less than 24 hours to more than 20 days, thus possessing greater potential for soil contamination remediation.%采用四种固体过氧化物(过氧化钙,CP;过硼酸钠,SPB;过碳酸钠,SPC;过氧化尿素,UHP)以及 H2O2和两种铁源[(Fe3(PO4)2和FeSO4],通过室内模拟试验,研究不同过氧化物和Fe(Ⅱ)源组合构成的(类)Fenton反应对石英砂中五氯酚(PCP)的降解能力,探讨了影响类Fenton试剂活性成分有效性和持续性的

  4. Heterogeneous photo-Fenton degradation of acid red B over Fe2O3 supported on activated carbon fiber

    International Nuclear Information System (INIS)

    Highlights: • Fe2O3 with small particle size was highly dispersed on activated carbon fiber. • Fe2O3/ACF exhibited higher photo-Fenton activity toward ARB degradation. • Fe2O3/ACF has an excellent long-term stability without obvious deactivation. - Abstract: Fe2O3 supported on activated carbon fiber (Fe2O3/ACF) was prepared via an impregnation method and characterized by X-ray diffraction, scanning electron microscopy and BET analysis. The results indicated that Fe2O3 with small particle size was highly dispersed on the surface of the ACF and the introduction of Fe2O3 did not change the ACF pore structure. Fe2O3/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 CO2 and H2O. Moreover, Fe2O3/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 Fe2O3/ACF had good long-term stability

  5. Application of iron electrode corrosion enhanced electrokinetic-Fenton oxidation to remediate diesel contaminated soils: A laboratory feasibility study

    Science.gov (United States)

    Tsai, Tzai-Tang; Sah, Jygau; Kao, Chih-Ming

    2010-01-01

    SummaryDiesel soil contamination on gas stations or refinery plants is a worldwide environmental problem. The main objectives of this study were to (1) evaluate the efficiency of electrokinetic (EK) by using different electrode materials (graphite and iron rods) and electrolytes (tap water, 0.01 M NaCl, and 0.1 M NaCl) on the remediation of diesel contaminated soils, and (2) evaluate the feasibility of total petroleum hydrocarbon-diesel (TPH-D) reducing in soils via EK-Fenton oxidation enhanced by corroded iron electrode. The EK and EK-Fenton experiments were conducted in batch and sand box experiments, respectively. Batch experiments reveal that the most appropriate electrolyte was 0.1 M NaCl when iron electrode was used in the EK system. Sand box experiments indicate that the TPH-D concentration dropped from 10,000 to 300 mg kg -1 when amorphous iron/total iron (Fe o/Fe t) ratio increased from 0.1 to 0.33, with the addition of 8% of H 2O 2 and 0.1 M NaCl after 60 days of EK-Fenton operation. Electrokinetically enhanced oxidation with the presence of both H 2O 2 and Fe 3O 4 (iron electrode corrosion) resulted in higher TPH-D removal efficiency (97%) compared to the efficiencies observed from EK (55%) or Fenton oxidation (27%) alone. This demonstrates that EK-Fenton oxidation catalyzed by iron electrode corrosion is a valuable direction to efficiently and effectively remediate diesel contaminated soils.

  6. 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.

  7. Rapid degradation of methylene blue in a novel heterogeneous Fe3O4 @rGO@TiO2-catalyzed photo-Fenton system

    Science.gov (United States)

    Yang, Xiaoling; Chen, Wei; Huang, Jianfei; Zhou, Ying; Zhu, Yihua; Li, Chunzhong

    2015-05-01

    Herein, a ternary nanocomposite with TiO2 nanoparticles anchored on reduced graphene oxide (rGO)-encapsulated Fe3O4 spheres (Fe3O4@rGO@TiO2) is presented as a high efficient heterogeneous catalyst for photo-Fenton degradation of recalcitrant pollutants under neutral pH. Fe3O4@rGO@TiO2 was synthesized by depositing TiO2 nanoparticles on the surface of the Fe3O4 spheres wrapped by graphene oxide (GO) which was obtained by an electrostatic layer-by-layer method. This as-prepared catalyst reflected good ferromagnetism and superior stability which makes it convenient to be separated and recycled. Due to the synergic effects between the different components composed the catalyst, swift reduction of Fe3+ can be achieved to regenerate Fe2+. Fe3O4@rGO@TiO2 exhibited enhancing catalytic activity for the degradation of azo-dyes compared with Fe3O4, Fe3O4@SiO2@TiO2 or SiO2@rGO@TiO2, further conforming the rapid redox reaction between Fe2+ and Fe3+. All these merits indicate that the composite catalyst possesses great potential for visible-light driven destruction of organic compounds.

  8. Heterogeneous sono-Fenton-like process using nanostructured pyrite prepared by Ar glow discharge plasma for treatment of a textile dye.

    Science.gov (United States)

    Khataee, Alireza; Gholami, Peyman; Vahid, Behrouz

    2016-03-01

    The plasma-treated pyrite (PTP) nanostructures were prepared from natural pyrite (NP) utilizing argon plasma due to its sputtering and cleaning effects resulting in more active surface area. The NP and PTP were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) and scanning electron microscopy (SEM) methods. The performance of the PTP was greater than NP for treatment of Reactive Red 84 (RR84) by the heterogeneous sono-Fenton process. The optimum amounts of main operational parameters were obtained as PTP of 4 g/L, initial dye concentration of 10 mg/L, pH of 5, and ultrasonic power of 300 W after 120 min of reaction time. Also, the effects of enhancers, and inorganic salts and t-butanol as hydroxyl radical scavengers on the degradation efficiency were investigated. Gas chromatography-mass spectroscopy analysis (GC-MS) was applied for detection of some degradation intermediates. Environmentally friendly plasma modification of the NP, in situ production of H2O2 and OH radicals, low leached iron concentration and repeated reusability at the milder pH are the significant benefits of the PTP utilization. PMID:26585001

  9. Vanillic and syringic acids from biomass burning: Behaviour during Fenton-like oxidation in atmospheric aqueous phase and in the absence of light.

    Science.gov (United States)

    Santos, Gabriela T A D; Santos, Patrícia S M; Duarte, Armando C

    2016-08-01

    Biomass combustion is a threat to the environment since it emits to the atmosphere organic compounds, which may react and originate others more aggressive. This work studied the behaviours of vanillic and syringic acids, small aromatic tracers of biomass burning, during Fenton-like oxidation in aqueous phase and absence of light. For both compounds, the extent of oxidation increased with pH decrease from neutral to acid in atmospheric waters, but for vanillic acid the neutral pH was not able of promoting the oxidation. With the oxidation of both acids were formed chromophoric compounds, and the formation rate increased with the degree of electron-donator substituents in benzene ring. The initial and produced compounds were not totally degraded up to 24h of reaction at pH 4.5, suggesting that the night period may be not sufficient for their full degradation in atmospheric waters. The major compounds formed were the 3,4-dihydroxybenzoic acid for vanillic acid, and the 1,4-dihydroxy-2,6-dimethoxybenzene for syringic acid. These findings suggest the occurrence of an ipso attack by the hydroxyl radical preferential to the methoxy and carboxyl groups of vanillic and syringic acids, respectively. It is important to highlight that for both aromatic acids the main compounds produced are also small aromatic compounds. PMID:27085101

  10. Catalytic degradation of recalcitrant pollutants by Fenton-like process using polyacrylonitrile-supported iron (II) phthalocyanine nanofibers: Intermediates and pathway.

    Science.gov (United States)

    Zhu, Zhexin; Chen, Yi; Gu, Yan; Wu, Fei; Lu, Wangyang; Xu, Tiefeng; Chen, Wenxing

    2016-04-15

    Iron (II) phthalocyanine (FePc) molecules were isolated in polyacrylonitrile (PAN) nanofibers by electrospinning to prevent the formation of dimers and oligomers. Carbamazepine (CBZ) and Rhodamine B (RhB) degradation was investigated during a Fenton-like process with FePc/PAN nanofibers. Classical quenching tests with isopropanol and electron paramagnetic resonance tests with 5,5-dimethyl-pyrroline-oxide as spin-trapping agent were performed to determine the formation of active species during hydrogen peroxide (H2O2) decomposition by FePc/PAN nanofibers. After eight recycles for CBZ degradation over the FePc/PAN nanofibers/H2O2 system, the removal ratios of CBZ remained at 99%. Seven by-products of RhB and twelve intermediates of CBZ were identified using ultra-performance liquid chromatography and high-resolution mass spectrometry. Pathways of CBZ and RhB degradation were proposed based on the identified intermediates. As the reaction proceeded, all CBZ and RhB aromatic nucleus intermediates decreased and were transformed to small acids, but also to potentially toxic epoxide-containing intermediates and acridine, because of the powerful oxidation ability of •OH in the catalytic system. PMID:26949842

  11. A parametric study on the decolorization and mineralization of C.I. Reactive Red 141 in water by heterogeneous Fenton-like oxidation over FeZSM-5 zeolite.

    Science.gov (United States)

    Yaman, Ceyda; Gündüz, Gönül

    2015-01-01

    In this study, the heterogeneous Fenton-like degradation of Reactive Red 141 (RR141) in water was investigated over iron containing ZSM-5 zeolite (Si/Al = 42) prepared by ion-exchange (FeZSM-5 (42)). The catalyst was characterized by XRD, SEM, FTIR, TPR, and ICP-AES measurements. The effects of the initial concentrations of the dye and H2O2, the initial pH of the solution, catalyst loading, and the reaction temperature were investigated on heterogeneous Fenton-like degradation of RR141. The reduction of the solution initial pH from ca. 7.0 to ca. 3.5 had a positive effect on color removal. A complete color removal was achieved with all the H2O2 concentrations in the range of 0.007 - 0.067 M over the FeZSM-5 (42) catalyst after 2 h of reaction. The COD reduction increased from 52% to 81% with an increase in the amount of the catalyst. The COD reduction was affected positively with the increase in temperature from 298 K through 313 K to 323 K and then to 333 K. The initial decolorization rate was described by the equation: -rA0 = 9.4*10(4) e(-38.8/RT) CRR141,0 CH2O2,0 (0.184) with an H2O2 concentration range of 0.007 M - 0.033 M (where R is in kJ/mol).

  12. A novel Electro-Fenton-Like system using PW{sub 11}O{sub 39}Fe(III)(H{sub 2}O){sup 4-} as an electrocatalyst for wastewater treatment

    Energy Technology Data Exchange (ETDEWEB)

    Wang Chongtai [School of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, Hainan Province (China); Hua Yingjie, E-mail: 521000hua282@sina.co [School of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158, Hainan Province (China); Tong Yexiang [Institute of Optoelectronic and Functional Composite Materials, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China)

    2010-09-01

    A novel Electro-Fenton-Like (EFL) system was developed using the Keggin-type iron-substituted heteropolytungstate anion PW{sub 11}O{sub 39}Fe(III)(H{sub 2}O){sup 4-} to substitute for Fe{sup 3+} in the conventional Electro-Fenton (EF) system for treatment of water polluted with organic compounds. The EFL system overcomes the drawback of low pH in conventional EF approaches and can be directly applied to neutral water treatment without any pH adjustment. Experimental results for dimethylphthalate (DMP) revealed complete degradation in <80 min in pH 6.86 solution containing 0.1 mM DMP at a potential of -0.5 V and O{sub 2} flow rate of 60 mL min{sup -1}. Total organic carbon removal of {approx}56% was achieved at 120 min. Comparison with conventional EF oxidation revealed better efficiency of the present system for DMP degradation, suggesting its potential in treatment of water and wastewater with a relaxed pH requirement. The cumulative H{sub 2}O{sub 2} concentration generated in situ at the electrode was monitored and the observed degradation rate constants k{sub obs} were determined for different initial DMP concentrations. The ligand exchange reaction of PW{sub 11}O{sub 39}Fe(III)(H{sub 2}O){sup 4-} with H{sub 2}O{sub 2} and the electron transfer resulting in hydroxyl radicals were examined using HPLC and electrochemical impedance spectroscopy. An electrocatalytic model involving inner-sphere electron transfer and a reaction mechanism for PW{sub 11}O{sub 39}Fe(III)(H{sub 2}O){sup 4-} electrocatalytic reduction of H{sub 2}O{sub 2} are proposed.

  13. Pretreatment of 2,4-dinitroanisole (DNAN) producing wastewater using a combined zero-valent iron (ZVI) reduction and Fenton oxidation process.

    Science.gov (United States)

    Shen, Jinyou; Ou, Changjin; Zhou, Zongyuan; Chen, Jun; Fang, Kexiong; Sun, Xiuyun; Li, Jiansheng; Zhou, Lin; Wang, Lianjun

    2013-09-15

    A combined zero-valent iron (ZVI) reduction and Fenton oxidation process was tested for the pretreatment of 2,4-dinitroanisole (DNAN) producing wastewater. Operating conditions were optimized and overall performance of the combined process was evaluated. For ZVI process, almost complete reduction of nitroaromatic compounds was observed at empty bed contact time (EBCT) of 8h. For Fenton process, the optimal pH, H₂O₂ to Fe(II) molar ratio, H₂O₂ dosage and hydraulic retention time (HRT) were found to be 3.0, 15, 0.216 mol/L and 5h, respectively. After pretreatment by the combined ZVI-Fenton process under the optimal conditions, aromatic organic compound removal was as high as 77.2%, while the majority of COD remained to be further treated by sequent biological process. The combined anaerobic-aerobic process consisted of an anaerobic baffled reactor (ABR) and a moving-bed biofilm reactor (MBBR) was operated for 3 months, fed with ZVI-Fenton effluent. The results revealed that the coupled ZVI-Fenton-ABR-MBBR system was significantly efficient in terms of correcting the effluent's main parameters of relevance, mainly aromatic compounds concentration, COD concentration, color and acute toxicity. These results indicate that the combined ZVI-Fenton process offers bright prospects for the pretreatment of wastewater containing nitroaromatic compounds. PMID:23892166

  14. Inhibition of hydroxyl radical reaction with aromatics by dissolved natural organic matter

    Science.gov (United States)

    Lindsey, M.E.; Tarr, M.A.

    2000-01-01

    Reaction of aromatic compounds with hydroxyl radical is inhibited by dissolved natural organic matter (NOM). The degree of inhibition is significantly greater than that expected based on a simple model in which aromatic compound molecules bound to NOM are considered to be unreactive. In this study, hydroxyl radical was produced at steady-state concentrations using Fenton chemistry (H2O2 + Fe2+ ??? Fe3+ + HO- + HO??). Suwannee River fulvic acid and humic acid were used as NOM. The most likely mechanism for the observed inhibition is that hydroxyl radical formation occurs in microenvironmental sites remote from the aromatic compounds. In addition to changes in kinetics, pyrene hydroxyl radical reaction also exhibited a mechanistic change in the presence of fulvic acid. The mechanism changed from a reaction that was apparently firstorder in pyrene to one that was apparently secondorder in pyrene, indicating that pyrene self-reaction may have become the dominant mechanism in the presence of fulvic acid. Dissolved NOM causes significant changes in the rate and mechanism of hydroxyl radical degradation of aromatic compounds. Consequently, literature rate constants measured in pure water will not be useful for predicting the degradation of pollutants in environmental systems. The kinetic and mechanistic information in this study will be useful for developing improved degradation methods involving Fenton chemistry.Reaction of aromatic compounds with hydroxyl radical is inhibited by dissolved natural organic matter (NOM). The degree of inhibition is significantly greater than that expected based on a simple model in which aromatic compounds molecules bounds to NOM are considered to be unreactive. In this study, hydroxyl radical was produced at steady-state concentrations using Fenton chemistry (H2O2 + Fe2+ ??? Fe3+ + HO- + HO??). Suwannee River fulvic acid and humic acid were used as NOM. The most likely mechanisms for the observed inhibition is that hydroxyl radical

  15. Water quality in the vicinity of Fenton Hill: Progress report, 1983 and 1984

    Energy Technology Data Exchange (ETDEWEB)

    Purtymun, W.D.; Ferenbaugh, R.W.; Becker, N.M.; Williams, M.C.; Maes, M.

    1987-01-01

    Water quality data have been collected since 1974 from established surface and groundwater stations at and in the vicinity of Fenton Hill (Hot Dry Rock Geothermal Demonstration Site) located in the Jemez Mountains. This is part of a continued program of environmental studies. There has been a slight variation in chemical quality of water from the surface and groundwater stations; however, these variations are within normal seasonal fluctuations. Water supply at the site is pumped from the aquifer in the Abiquiu Tuff. Cumulative production from 1976 through 1984 has been 41.5 x 10/sup 6/ gal. The water level in the supply well declined from 365 ft in 1976 to 379 ft in 1984.

  16. Fighting Fenton Chemistry: A Highly Active Iron(III) Tetracarbene Complex in Epoxidation Catalysis.

    Science.gov (United States)

    Kück, Jens W; Anneser, Markus R; Hofmann, Benjamin; Pöthig, Alexander; Cokoja, Mirza; Kühn, Fritz E

    2015-12-01

    Organometallic Fe complexes with exceptionally high activities in homogeneous epoxidation catalysis are reported. The compounds display Fe(II) and Fe(III) oxidation states and bear a tetracarbene ligand. The more active catalyst exhibits activities up to 183 000 turnovers per hour at room temperature and turnover numbers of up to 4300 at -30 °C. For the Fe(III) complex, a decreased Fenton-type reactivity is observed compared with Fe(II) catalysts reported previously as indicated by a substantially lower H2 O2 decomposition and higher (initial) turnover frequencies. The dependence of the catalyst performance on the catalyst loading, substrate, water addition, and the oxidant is investigated. Under all applied conditions, the advantageous nature of the use of the Fe(III) complex is evident.

  17. 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.

  18. Geological structures from televiewer logs of GT-2, Fenton Hill, New Mexico: Part 2, Rectification

    Energy Technology Data Exchange (ETDEWEB)

    Burns, K.L.

    1987-08-01

    Televiewer logs from drill hole GT-2 at the Fenton Hill, New Mexico, Hot Dry Rock Site, have been rectified by conversion of structural traces on the scanner imagery to geographic location and orientation. The rectification method was direct inversion that consisted of mapping from the image to the wellbore, inverting the trace on the wellbore for principal points, and rotating from wellbore to geographic coordinates. From the test imagery of GT-2, 733 structures (fractures and foliations) were measured, compared with 42 structures from recovered core. The 733 new measurements listed in this report are a unique and unrepeatable collection of structural information from the Precambrian basement of northern New Mexico. This direct inversion method is accurate where the magnetic field vector is constant and the tool is centered and aligned in a circular wellbore. In other cases this method yields only approximate results.

  19. Revisiting Fenton Hill Phase I reservoir creation and stimulation mechanisms through the GTO code comparison effort

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Pengcheng; Mcclure, Mark; Shiozawa, Sogo; White, Mark D.

    2016-06-27

    A series of experiments performed at the Fenton Hill hot dry rock site after stage 2 drilling of Phase I reservoir provided intriguing field observations on the reservoir’s responses to injection and venting under various conditions. Two teams participating in the US DOE Geothermal Technologies Office (GTO)’s Code Comparison Study (CCS) used different numerical codes to model these five experiments with the objective of inferring the hydraulic stimulation mechanism involved. The codes used by the two teams are based on different numerical principles, and the assumptions made were also different, due to intrinsic limitations in the codes and the modelers’ personal interpretations of the field observations. Both sets of models were able to produce the most important field observations and both found that it was the combination of the vertical gradient of the fracture opening pressure, injection volume, and the use/absence of proppant that yielded the different outcomes of the five experiments.

  20. Solar photo-Fenton treatment of chip board production waste water

    Energy Technology Data Exchange (ETDEWEB)

    Machado, A.E. da H.; Xavier, T.P.; Souza, D.R. de; Miranda, J.A. de; Duarte, E.T.F.M.; Ruggiero, R. [Universidade Federal de Uberlandia, Minas Gerais (Brazil). Lab. de Fotoquimica; Oliveira, L. de; Sattler, C. [Deutsches Zentrum fuer Luft- und Raumfahrt e.V., Koeln Porz (Germany)

    2004-11-01

    In a joint project the Universidade Federal de Uberlandia and the German Aerospace Center are developing solar water treatment technologies for industrial applications. Wastewater from chip-board production is difficult to detoxify by standard processes. Different advanced oxidation processes using solar light were tested on this effluent. In opposition to TiO{sub 2} treatment, the application of the photo-Fenton process using a compound parabolic collector (CPC) type solar reactor shows excellent results, with a reduction in the COD higher than 70% with the application of about 800 kJ m{sup -2} of UVA radiation. HPLC analysis shows an efficient degradation of the organic matter present in the effluent (formaldehyde, melamine, urea, wood extractives, lignin and urea/formaldehyde and melamine/formaldehyde resins fragments) prior to their complete disappearance. (Author)

  1. Hot Dry Rock Project modification and expansion, Fenton Hill, Sandoval County, New Mexico: Environmental assessment

    Energy Technology Data Exchange (ETDEWEB)

    1979-09-01

    This environmental assessment (EA) addresses the modification and expansion of the ongoing Hot Dry Rock Project at Fenton Hill, New Mexico. Modifications to the Project include the upgrading and improvement of the hot dry rock (HDR) heat transfer system and the onsite support facilities. At least one new heat extraction well will be drilled to accommodate a large thermal loop experiment. The existing wells will be redrilled to greater depth. Expansion of the Project includes the construction and operation of heat utilization facilities (that is, 60 kW electric generator and greenhouse), wellbore equipment test station, large-capacity water supply and storage system, water treatment facility, and additional seismic monitoring stations. This EA addresses the potential environmental impacts of the total facility as expanded to accommodate the large thermal loop and heat utilization experiments.

  2. Avaliação da microfiltração para remoção do lodo gerado no processo oxidativo avançado empregando o reagente de Fenton no tratamento de lixiviado de aterro sanitário Evaluation of microfiltration for removal of sludge generated in advanced oxidation process by Fenton reagent in treatment of landfill leachate

    Directory of Open Access Journals (Sweden)

    Wagner Guadagnin Moravia

    2011-12-01

    Full Text Available Uma alternativa atrativa para o tratamento de lixiviado de aterro sanitário são os processos oxidativos avançados empregando o reagente de Fenton (POA/Fenton. No entanto, a aplicação do POA/Fenton é limitada pela geração de lodo no processo. Esse lodo possui elevada concentração de ferro, o que torna necessária sua separação do efluente tratado. O objetivo desse trabalho foi avaliar a microfiltração para a remoção de lodo gerado no POA/Fenton. A pesquisa foi desenvolvida em unidade de bancada. O POA/Fenton apresentou elevada eficiência na remoção de matéria orgânica (75% e cor real (95%. O processo de microfiltração foi eficiente na separação do lodo gerado, o qual apresentou baixa sedimentabilidade, dificultando sua separação por sedimentação, além de ter contribuído para a remoção de outros poluentes.Advanced oxidation processes using Fenton's reagent (AOP/Fenton are an attractive alternative for landfill leachate treatment. However, the implementation of the AOP/Fenton is limited by the generation of sludge in the process. The sludge has a high iron concentration, which needs its separation from the treated effluent. The aim of this study was to evaluate the microfiltration for sludge removal from an AOP/Fenton. The work was conducted in bench scale. The advanced oxidation process showed high efficiency in removing organic matter (75% and true color (95%. The microfiltration was effective in separating the sludge, which showed low settling hindering their separation by sedimentation, and has contributed to the removal of other pollutants.

  3. Study on Degradation of Musty-earthy Odors by Heterogeneous UV/Fenton Photocatalysis%非均相UV/Fenton光催化降解土霉异味研究

    Institute of Scientific and Technical Information of China (English)

    刘立明; 李林; 闪锟; 黄应平; 宋立荣

    2012-01-01

    [目的]探索非均相UV/Fenton光催化降解土霉异味的效果.[方法]利用离子交换方法将Fe2+负载在NaY分子筛载体上,制得催化剂FeY.在不同紫外波长照射下,利用Fenton反应降解2种土霉异味物质2-甲基异莰醇(MIB)和土腥素(Geosmin),优化pH和H2O2等降解条件,并将MIB和Geosmin添加到东湖本底湖水中进行降解.[结果]FeY的负载量为352.8 mg/g,Fe2+脱附率为5.7%.在FeY为28 mg/L,pH 6.5,H2O2 20 mg/L和反应60min的试验条件下,非均相UVB/Fenton体系对MIB和Geosmin的降解率分别为80.2%和84.9%.在UVA、UVB和UVC紫外光(波长分别为365、312和256 nm)条件下Photo-Fenton体系对MIB和Geosmin的降解率,随着紫外波长的降低而增大,且Geosmin降解速率常数高于MIB.湖泊水样中加入MIB和Geosmin降解表明,降解效率明显低于纯水样品.[结论]该研究制得的催化剂应用于非均相光催化体系,不仅可循环使用,而且还可扩大反应体系的pH应用范围.%[Objective] The study aimed to explore the effects of the heterogeneous UV/Fenton photocatalysis on the degradation of the musty-earthy odors. [ Result] By using ion exchange method, the Fe2+ was loaded on the NaY molecular sieve carrier to prepare the catalyst FeY. Under the radiation of different ultraviolet wavelengths, 2 musty-earthy odor materials of 2-Methylisobomeol ( MIB) and trans-1, 10-dimethyl-trans-9-decalol (Geosmin) were degraded by using Fenton reaction, the degradation conditions such as pH and H2O2 were optimized and the MIB and Geosmin were added to the bottom of East Lake for the degradation. [ Conclusion] The FeY loading amount was 352.8 mg/g and the Fe2+ desorption rate was 5. 7%. The heterogeneous UV/Fenton system had the degradation rate of 80. 2% and 84. 9% resp. On MIB and Geosmin under the test conditions as FeY of 28 mg, pH of 6.5, H2O2 of 20 mg/L and reaction time of 60 min. Under the UVA, UVB and UVC wavelengths of 365 ,312 and 256 nm, resp. , the

  4. 铁炭微电解法、Fenton氧化法处理印染废水的效果比较%Comparison of Iron-carbon microelectrolysis and Fenton oxidation on treatment of dyeing wastewater

    Institute of Scientific and Technical Information of China (English)

    丁绍兰; 汪晶; 杜虎

    2013-01-01

    [目的]印染废水具有浓度高、色度高、成分复杂、难降解的特点,比较了铁炭微电解法和Fenton氧化法处理印染废水的效果.[方法]以取自陕西咸阳第二印染厂的综合废水为供试材料,通过单因素试验,分别对铁炭微电解法和Fenton氧化法处理印染废水的最佳条件进行了研究,并对二者的处理效果进行了比较.[结果]在处理印染废水时,铁炭微电解法的最佳反应条件为:停留时间30 min,进水pH=3~4,铁炭体积比1∶1,此时色度去除率达到80%,COD去除率达到60%;Fenton氧化法的最佳反应条件为:pH=3,停留时间45 min,H2O2和FeSO4用量分别为20,25 mL/L,H2O2分3次加入,此条件下色度去除率达到79%,COD去除率达到80%.[结论]铁炭微电解法和Fenton氧化法对印染废水均有较好的处理效果,可考虑将两者联合运用,以进一步提高处理效果.%[Objective] Dyestuff wastewater is a typical kind of biorefractory wastewater with high concentration, high chroma,complicated components and low degradability. [Method] Dyeing wastewater from the Second Printing and Dyeing Mill of Xianyang,Shaanxi was chosen as experimental material to study the optimal conditions of for Iron-carbon microelectrolysis and Fenton oxidation using the single-factor experiments. The treatment effects of the two methods were compared as well. [Result] In disposing printing and dyeing waste water,optimum reaction conditions of Iron-carbon microelectrolysis were as follows:exposure time was 30 min,pH value was 3 -4, volume ratio of iron to carbon was l,and chroma and COD removal efficiency were 80% and 60%, respectively. Optimum reaction conditions of Fenton oxidation were as follows :pH value was 3, exposure time was 45 minutes, the dosage of hydrogen peroxide was 20 mL/L and ferrous sulphate was 25 mL/L, the hydrogen peroxide was added in the reaction system three times, and chroma and COD removal efficiency were 79% and 80%, respectively

  5. Ferrous ion-EDTA-stimulated phospholipid peroxidation. A reaction changing from alkoxyl-radical- to hydroxyl-radical-dependent initiation.

    Science.gov (United States)

    Gutteridge, J M

    1984-01-01

    The stimulatory effect of ferrous salts on the peroxidation of phospholipids can be enhanced by EDTA when the concentration of Fe2+ in the reaction is greater than that of EDTA. Hydroxyl-radical scavengers do not inhibit peroxidation until the concentrations of Fe2+ and EDTA in the reaction are equal. Lipid peroxidation is then substantially initiated by hydroxyl radicals derived from a Fenton-type reaction requiring hydrogen peroxide. Superoxide radicals appear to play some role in the formation of initiating species. PMID:6441569

  6. [Study on treatment of methylene blue wastewater by fly ash adsorption-Fenton and thermal regeneration].

    Science.gov (United States)

    Bai, Yu-Jie; Zhang, Ai-Li; Zhou, Ji-Ti

    2012-07-01

    The physicochemical properties of water-washed fly ash (FA) and acid modified fly ash (M-FA) were investigated. The adsorption of methylene blue by FA and M-FA were studied by batch experiments. Two methods, Fenton-drive oxidation regeneration and thermal regeneration, were used for regeneration of the used FA and M-FA. The result showed that the rate of adsorption process followed the second order kinetics and the adsorption followed Langmuir isotherms. The adsorption equilibrium time was 30 min, and the equilibrium adsorption capacity of FA and M-FA were 4.22 mg x g(-1) and 5.98 mg x g(-1) respectively. The adsorption capability of M-FA was higher than that of FA. In the range of pH 2-12, the adsorption capacity of M-FA increased with the increase of pH, whereas the adsorption capacity of FA decreased slowly until the pH 8 and then increased. Electrostatic adsorption was the major factor on the adsorption capacity. Around 61% and 55% percentage regeneration (PR) were obtained for FA and M-FA respectively when 78.4 mmol x L(-1) H2O2 and 0.72 mmol x L(-1) Fe2+ were used. When the condition of thermal regeneration was 400 degrees C and 2 h, a positive correlation can be found between the PRs of FA and regeneration times, the PRs were 102%, 104% and 107% in three cycles of adsorption-thermal regeneration process. However a negative correlation can be found between the PRs of M-FA and regeneration times, the PRs were 82%, 75% and 74% in three cycles of adsorption-thermal regeneration process. The PR of FA was higher than that of M-FA, and thermal regeneration was superior to Fenton-drive regeneration.

  7. 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.

  8. Nanoscale zero-valent iron/AC as heterogeneous Fenton catalysts in three-dimensional electrode system.

    Science.gov (United States)

    Zhang, Chao; Zhou, Lei; Yang, Jie; Yu, Xinmin; Jiang, Yonghai; Zhou, Minghua

    2014-01-01

    In the present work, nanoscale zero-valent iron/activated carbon (NZVI/AC) was investigated as heterogeneous Fenton catalyst in three-dimensional (3D) electrode system for methyl orange (MO) degradation. Some important operating parameters such as cathodic potential, pH, and O₂ flow rate were investigated, exhibiting good decolorization. The mineralization of MO was significantly improved by 20-35% compared to two-dimensional (2D) AC system at the optimum conditions. Although the TOC removal of AC was higher than NZVI/AC due to its good adsorption capacity initially, heterogeneous Fenton catalysis played a more and more important roles in the following test. After eight runs, NZVI/AC still exhibited excellent catalytic properties with low iron leaching. Further, a relatively comprehensive mechanism of NZVI/AC as particle electrodes in 3D system was proposed.

  9. Evaluation of Electro-Fenton Process Performance for COD and Reactive Blue 19 Removal from Aqueous Solution

    OpenAIRE

    Mohammad Malakootian; Mahdi Asadi; Amir Hossein Mahvi

    2013-01-01

    Background and Objectives: Synthetic dyes represent one of the largest groups of pollutants in wastewater of dying industries. Discharging these wastewaters into receiving streams not only affects the aesthetic but also reduces photosynthetic activity. Electrochemical advanced oxidation processes such as Electro-Fenton process are low operational and have high mineralization degree of pollutants. In this study, we investigated affective factors in this process to determine the optimum conditi...

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

    International Nuclear Information System (INIS)

    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 H2O2 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 H2O2. The Fourier transformation infrared (FTIR) spectroscopy shows that the peak intensity of hydroxyl groups on the treated felt is increased with the H2O2 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

  11. 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.

  12. Abbau von epsilon-Caprolactam aus Abluftwäscherlaugen mittels Licht verstärkter Fenton-Reaktion

    OpenAIRE

    Heck, Edmund; Jung, Christian; de Oliveira, Lamark; Olwig, Ralf; Säck, Jan-Peter; Sattler, Christian; Schäfer, Thomas; Senholdt, Marion; Weskott, Klaus; Zinner, Dania

    2009-01-01

    Caprolactam-haltige Wässer aus Abluftwäschern der Veredlung von Nylongewebe können mittels der Licht verstärkten Fenton-Reaktion gereinigt und für die Kreislaufführung aufbereitet werden. Der Abbauweg des Caprolactams wurde untersucht, um die rasche Eliminierung zu erklären und um die Zwischenprodukte bis zur Mineralisierung zu identifizieren.

  13. Enhancement of enzymatic saccharification of corn stover with sequential Fenton pretreatment and dilute NaOH extraction.

    Science.gov (United States)

    He, Yu-Cai; Ding, Yun; Xue, Yu-Feng; Yang, Bin; Liu, Feng; Wang, Cheng; Zhu, Zheng-Zhong; Qing, Qing; Wu, Hao; Zhu, Cheng; Tao, Zhi-Cheng; Zhang, Dan-Ping

    2015-10-01

    In this study, an effective method by the sequential Fenton pretreatment and dilute NaOH extraction (FT-AE) was chosen for pretreating corn stover. Before dilute NaOH (0.75 wt%) extraction at 90 °C for 1h, Fenton reagent (0.95 g/L of FeSO4 and 29.8 g/L of H2O2) was employed to pretreat CS at a solid/liquid ratio of 1/20 (w/w) at 35 °C for 30 min. The changes in the cellulose structural characteristics (porosity, morphology, and crystallinity) of the pretreated solid residue were correlated with the enhancement of enzymatic saccharification. After being enzymatically hydrolyzed for 72 h, the reducing sugars and glucose from the hydrolysis of 60 g/L FT-AE-CS pretreated could be obtained at 40.96 and 23.61 g/L, respectively. Finally, the recovered hydrolyzates containing glucose had no inhibitory effects on the ethanol fermenting microorganism. In conclusion, the sequential Fenton pretreatment and dilute NaOH extraction has high potential application in future.

  14. Oxalate enhanced mechanism of hydroxyl-Fe-pillared bentonite during the degradation of Orange II by UV-Fenton process.

    Science.gov (United States)

    Chen, Jianxin; Zhu, Lizhong

    2011-01-30

    An enhanced method of hydroxyl-Fe-pillared bentonite (H-Fe-P-B) during the degradation of Orange II was studied to provide novel insight to interactions of degradation intermediates with heterogeneous catalyst in UV-Fenton system. Based on the degradation mechanism of Orange II, oxalate enhanced mechanism of H-Fe-P-B in heterogeneous UV-Fenton system was developed. The results showed that additional oxalate could increase the Fe leaching of H-Fe-P-B during heterogeneous UV-Fenton process, which led to higher mineralization efficiency of Orange II and lower energy consumption of treatment. When the concentrations of additional sodium oxalate increased up to 0.1 mmol L(-1), 0.2 mmol L(-1) and 0.4 mmol L(-1), the rate of Orange II degradation could increase 30%, 46% and 63%, respectively. The iron ions leached from catalyst could be adsorbed back to the catalyst again after the organic intermediates were mineralized completely. Then the catalyst of H-Fe-P-B could be reused and additional pollution caused by iron ions could be avoided.

  15. Optimisation of decolourisation and degradation of Reactive Black 5 dye under electro-Fenton process using Fe alginate gel beads.

    Science.gov (United States)

    Iglesias, O; Fernández de Dios, M A; Rosales, E; Pazos, M; Sanromán, M A

    2013-04-01

    The aim of this work was to improve the ability of the electro-Fenton process using Fe alginate gel beads for the remediation of wastewater contaminated with synthetic dyes and using a model diazo dye such as Reactive Black 5 (RB5). Batch experiments were conducted to study the effects of main parameters, such as voltage, pH and iron concentration. Dye decolourisation, reduction of chemical oxygen demand (COD) and energy consumption were studied. Central composite face-centred experimental design matrix and response surface methodology were applied to design the experiments and to evaluate the interactive effects of the three studied parameters. A total of 20 experimental runs were set, and the kinetic data were analysed using first-order and second-order models. In all cases, the experimental data were fitted to the empirical second-order model with a suitable degree for the maximum decolourisation of RB5, COD reduction and energy consumption by electro-Fenton-Fe alginate gel beads treatment. Working with the obtained empirical model, the optimisation of the process was carried out. The second-order polynomial regression model suggests that the optimum conditions for attaining maximum decolourisation, COD reduction and energy consumption are voltage, 5.69 V; pH 2.24 and iron concentration, 2.68 mM. Moreover, the fixation of iron on alginate beads suggests that the degradation process can be developed under this electro-Fenton process in repeated batches and in a continuous mode.

  16. Tubular carbon nanotube-based gas diffusion electrode removes persistent organic pollutants by a cyclic adsorption - Electro-Fenton process.

    Science.gov (United States)

    Roth, Hannah; Gendel, Youri; Buzatu, Pompilia; David, Oana; Wessling, Matthias

    2016-04-15

    We report a novel tubular electrochemical cell which is operated in a cyclic adsorption - electro-Fenton process and by this means overcomes the drawbacks of the traditional electro-Fenton process. A microtube made only of multi-walled carbon nanotubes (MWCNT) functions as a gas diffusion electrode (GDE) and highly porous adsorber. In the process, the pollutants were first removed electroless from the wastewater by adsorption on the MWCNT-GDE. Subsequently, the pollutants are electrochemically degraded in a defined volume of electrolyte solution using the electro-Fenton process. Oxygen was supplied into the lumen of the saturated microtubular GDE which was surrounded by a cylindrical anode made of Ti-felt coated with Pt/IrO2 catalysts. For the proof of concept the model pollutant Acid Red 14 (AR14), an azo dye, was used. The decomposition of AR14 was studied at different applied current densities and initial concentrations of ferrous iron in the electrolyte solution. At optimal conditions, complete regeneration of the adsorption capacity of the MWCNT-GDE, complete decolorization and TOC and COD removal rates of 50% and 70% were achieved, respectively. The MWCNT-GDE is regenerated and again available for adsorption. This approach allows water treatment independent of its composition, thus does not require any addition of chemicals to the wastewater. PMID:26775104

  17. Sono-Fenton process for metronidazole degradation in aqueous solution: Effect of acoustic cavitation and peroxydisulfate anion.

    Science.gov (United States)

    Ammar, Hafedh Belhadj

    2016-11-01

    The present work investigates the application of an improved treatment approach based on the ultrasound irradiation as clean technology driven Fenton in the presence of peroxydisulfate anion (S2O8(2-)) for the removal of metronidazole (MTZ) from aqueous solution. The sono-generation of sulfate radicals (SO4(-)) as a stronger oxidizing agent from S2O8(2-) (redox potential of 2.6V) has improved the degradation of MTZ. However, no studies have focused on the removal of MTZ using peroxydisulfate anion under sono-Fenton process. The MTZ concentration measurement during the processing allowed the evaluation of the kinetics of organic matter decay. The results have shown that the degradation of MTZ dependent on Fe(2+)/H2O2 molar ratio, temperature and S2O8(2-) concentration. The MTZ concentration decay follows pseudo first-order kinetics, within the range studied. Sono-Fenton process using low iron and hydrogen peroxide doses was proved to be an efficient method for the elimination of MTZ with high degradation rates. At optimum conditions, 96% of MTZ removal was achieved at 60°C in the presence of 1mM of S2O8(2-). PMID:27245967

  18. Performance evaluation of a photo-Fenton process applied to pollutant removal from textile effluents in a batch system.

    Science.gov (United States)

    Módenes, A N; Espinoza-Quiñones, F R; Manenti, D R; Borba, F H; Palácio, S M; Colombo, A

    2012-08-15

    In this work, the performance of a photo-Fenton process-based textile effluent treatment was investigated using both solar and artificial light sources. A full 3(3) factorial experimental design was applied for the optimisation with respect to three parameters: initial pH, amounts of Fe(2+) (0.01-0.09 g L(-1)) and H(2)O(2) (1-7 g L(-1)). The photo-Fenton process response was evaluated on the basis of chemical oxygen demand (COD) removal and decolourisation. The optimum conditions of the photo-Fenton process were attained at concentration values of 0.05 g Fe(2+) L(-1) and 6.0 g H(2)O(2) L(-1) and pH 3, for both solar and artificial light sources. The effects of initial pH, and Fe(2+) and H(2)O(2) concentrations were evaluated. From the monitoring of TOC, COD, turbidity and decolourisation over time, the progress of the mineralisation of dyes was analysed, forming nitrate, ammonia nitrogen and nitrite. Low amounts of residual peroxide and iron, which were below the limit allowed by Brazilian environmental legislation, were attained after 360 min of irradiation time for both artificial and solar sources. An operational cost of US$ 6.85 per m(3) of treated effluent was estimated using solar irradiation.

  19. Treatment of crystallized-fruit wastewater by UV-A LED photo-Fenton and coagulation-flocculation.

    Science.gov (United States)

    Rodríguez-Chueca, Jorge; Amor, Carlos; Fernandes, José R; Tavares, Pedro B; Lucas, Marco S; Peres, José A

    2016-02-01

    This work reports the treatment of crystallized-fruit effluents, characterized by a very low biodegradability (BOD5/COD UV-A LED photo-Fenton process. Firstly, a Box-Behnken design of Response Surface Methodology was applied to achieve the optimal conditions for the UV-A LED photo-Fenton process, trying to maximize the efficiency by saving chemicals and time. Under the optimal conditions ([H2O2] = 5459 mg/L; [Fe(3+)] = 286 mg/L; time >180 min), a COD removal of 45, 64 and 74% was achieved after 360 min, using an irradiance of 23, 70 and 85 W/m(2) respectively. Then a combination of UV-A LED photo-Fenton with coagulation-flocculation-decantation attained a higher COD removal (80%), as well as almost total removal of turbidity (99%) and total suspended solids (95%). Subsequent biodegradability of treated effluents increased, allowing the application of a biological treatment step after the photochemical/CFD with 85 W/m(2).

  20. Fate of thiabendazole through the treatment of a simulated agro-food industrial effluent by combined MBR/Fenton processes at μg/L scale.

    Science.gov (United States)

    Sánchez Peréz, J A; Carra, I; Sirtori, C; Agüera, A; Esteban, B

    2014-03-15

    This study has been carried out to assess the performance of a combined system consisting of a membrane bioreactor (MBR) followed by an advanced oxidation process (Fenton/Photo-Fenton) for removing the fungicide thiabendazole (TBZ) in a simulated agro-food industrial wastewater. Previous studies have shown the presence of TBZ in the effluent of an agro-food industry treated by activated sludge in a sequencing batch reactor (SBR), thus reinforcing the need for alternative treatments for removal. In this study, a simulated agro-food industry effluent was enriched with 100 μg L(-1) TBZ and treated by combined MBR/Fenton and MBR/solar photo-Fenton systems. Samples were directly injected into a highly sensitive liquid chromatography-triple quadrupole-linear ion trap-mass spectrometer (LC-QqLiT-MS/MS) analytical system to monitor the degradation of TBZ even at low concentration levels (ng L(-1)). Results showed that the biological treatment applied was not effective in TBZ degradation, which remained almost unaltered; although most dissolved organic matter was biodegraded effectively. Fenton and solar photo-Fenton, were assayed as tertiary treatments. The experiments were run without any pH adjustment by using an iron dosage strategy in the presence of excess hydrogen peroxide. Both treatments resulted in a total degradation of TBZ, obtaining more than 99% removal in both cases. To assure the total elimination of contaminants in the treated waters, transformation products (TPs) of TBZ generated during Fenton degradation experiments were identified and monitored by liquid chromatography-quadrupole time-of-flight mass spectrometry (LC-QTOF-MS/MS). Up to four TPs could be identified. Two of them corresponded to mono-hydroxylated derivatives, typically generated under hydroxyl radicals driven processes. The other two corresponded with the hydrolysis of the TBZ molecule to yield benzoimidazole and thiazole-4-carboxamidine. All of them were also degraded during the

  1. Degradation of 32 emergent contaminants by UV and neutral photo-fenton in domestic wastewater effluent previously treated by activated sludge.

    Science.gov (United States)

    De la Cruz, N; Giménez, J; Esplugas, S; Grandjean, D; de Alencastro, L F; Pulgarín, C

    2012-04-15

    This study focuses on the removal of 32 selected micropollutants (pharmaceuticals, corrosion inhibitors and biocides/pesticides) found in an effluent coming from a municipal wastewater treatment plant (MWTP) based on activated sludge. Dissolved organic matter was present, with an initial total organic carbon of 15.9 mg L(-1), and a real global quantity of micropollutants of 29.5 μg L(-1). The treatments tested on the micropollutants removal were: UV-light emitting at 254 nm (UV(254)) alone, dark Fenton (Fe(2+,3+)/H(2)O(2)) and photo-Fenton (Fe(2+,3+)/H(2)O(2)/light). Different irradiation sources were used for the photo-Fenton experiences: UV(254) and simulated sunlight. Iron and H(2)O(2) concentrations were also changed in photo-Fenton experiences in order to evaluate its influence on the degradation. All the experiments were developed at natural pH, near neutral. Photo-Fenton treatments employing UV(254), 50 mg L(-1) of H(2)O(2), with and without adding iron (5 mg L(-1) of Fe(2+) added or 1.48 mg L(-1) of total iron already present) gave the best results. Global percentages of micropollutants removal achieved were 98 and a 97% respectively, after 30 min of treatments. As the H(2)O(2) concentration increased (10, 25 and 50 mg L(-1)), best degradations were observed. UV(254), Fenton, and photo-Fenton under simulated sunlight gave less promising results with lower percentages of removal. The highlight of this paper is to point out the possibility of the micropollutants degradation in spite the presence of DOM in much higher concentrations. PMID:22305640

  2. Fate of thiabendazole through the treatment of a simulated agro-food industrial effluent by combined MBR/Fenton processes at μg/L scale.

    Science.gov (United States)

    Sánchez Peréz, J A; Carra, I; Sirtori, C; Agüera, A; Esteban, B

    2014-03-15

    This study has been carried out to assess the performance of a combined system consisting of a membrane bioreactor (MBR) followed by an advanced oxidation process (Fenton/Photo-Fenton) for removing the fungicide thiabendazole (TBZ) in a simulated agro-food industrial wastewater. Previous studies have shown the presence of TBZ in the effluent of an agro-food industry treated by activated sludge in a sequencing batch reactor (SBR), thus reinforcing the need for alternative treatments for removal. In this study, a simulated agro-food industry effluent was enriched with 100 μg L(-1) TBZ and treated by combined MBR/Fenton and MBR/solar photo-Fenton systems. Samples were directly injected into a highly sensitive liquid chromatography-triple quadrupole-linear ion trap-mass spectrometer (LC-QqLiT-MS/MS) analytical system to monitor the degradation of TBZ even at low concentration levels (ng L(-1)). Results showed that the biological treatment applied was not effective in TBZ degradation, which remained almost unaltered; although most dissolved organic matter was biodegraded effectively. Fenton and solar photo-Fenton, were assayed as tertiary treatments. The experiments were run without any pH adjustment by using an iron dosage strategy in the presence of excess hydrogen peroxide. Both treatments resulted in a total degradation of TBZ, obtaining more than 99% removal in both cases. To assure the total elimination of contaminants in the treated waters, transformation products (TPs) of TBZ generated during Fenton degradation experiments were identified and monitored by liquid chromatography-quadrupole time-of-flight mass spectrometry (LC-QTOF-MS/MS). Up to four TPs could be identified. Two of them corresponded to mono-hydroxylated derivatives, typically generated under hydroxyl radicals driven processes. The other two corresponded with the hydrolysis of the TBZ molecule to yield benzoimidazole and thiazole-4-carboxamidine. All of them were also degraded during the

  3. Experimental Design of Photo-Fenton Reactions for the Treatment of Car Wash Wastewater Effluents by Response Surface Methodological Analysis

    OpenAIRE

    Tony, Maha A.; Zeinab Bedri

    2014-01-01

    Establishing a treatment process for practical and economic disposal of car wash wastewater has become an urgent environmental concern. Photo-Fenton’s process as one of the advanced oxidation processes is a potentially useful oxidation process in treating such wastewater. Lab-scale experiments with UV source, coupled with Fenton’s reagent, showed that hydrocarbon oil is degradable through such a process. The feasibility of photo-Fenton’s process to treat wastewater from a car wash is investig...

  4. Ex Vivo Antioxidant Activity of Selected Medicinal Plants against Fenton Reaction-Mediated Oxidation of Biological Lipid Substrates

    OpenAIRE

    Namratha Pai Kotebagilu; Vanitha Reddy Palvai; Asna Urooj

    2015-01-01

    Free radical-mediated oxidation is often linked to various degenerative diseases. Biological substrates with lipids as major components are susceptible to oxygen-derived lipid peroxidation due to their composition. Lipid peroxide products act as biomarkers in evaluating the antioxidant potential of various plants and functional foods. The study focused on evaluation of the antioxidant potential of two extracts (methanol and 80% methanol) of four medicinal plants, Andrographis paniculata, Cost...

  5. Avaliação da microfiltração para remoção do lodo gerado no processo oxidativo avançado empregando o reagente de Fenton no tratamento de lixiviado de aterro sanitário Evaluation of microfiltration for removal of sludge generated in advanced oxidation process by Fenton reagent in treatment of landfill leachate

    OpenAIRE

    Wagner Guadagnin Moravia; Liséte Celina Lange; Míriam Cristina Santos Amaral

    2011-01-01

    Uma alternativa atrativa para o tratamento de lixiviado de aterro sanitário são os processos oxidativos avançados empregando o reagente de Fenton (POA/Fenton). No entanto, a aplicação do POA/Fenton é limitada pela geração de lodo no processo. Esse lodo possui elevada concentração de ferro, o que torna necessária sua separação do efluente tratado. O objetivo desse trabalho foi avaliar a microfiltração para a remoção de lodo gerado no POA/Fenton. A pesquisa foi desenvolvida em unidade de bancad...

  6. Electro-Fenton treatment of mature landfill leachate in a continuous flow reactor

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Hui, E-mail: eeng@whu.edu.cn [Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, P.O. Box C319, Luoyu Road 129, Wuhan 430079 (China); Ran, Xiaoni; Wu, Xiaogang [Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, P.O. Box C319, Luoyu Road 129, Wuhan 430079 (China)

    2012-11-30

    Highlights: Black-Right-Pointing-Pointer CSTR mode was used for COD removal of landfill leachate by Fered-Fenton process. Black-Right-Pointing-Pointer The complete mixing condition in the CSTR was verified. Black-Right-Pointing-Pointer A modified pseudo-first order kinetic model was developed. Black-Right-Pointing-Pointer The effects of important parameters on COD removal were investigated. Black-Right-Pointing-Pointer The organic components before and after treatment were determined by GC-MS. - Abstract: The treatment of mature landfill leachate by EF-Fere (also called Fered-Fenton) method was carried out in a continuous stirred tank reactor (CSTR) using Ti/RuO{sub 2}-IrO{sub 2}-SnO{sub 2}-TiO{sub 2} mesh anodes and Ti mesh cathodes. The effects of important parameters, including initial pH, inter-electrode gap, H{sub 2}O{sub 2} to Fe{sup 2+} molar ratio, H{sub 2}O{sub 2} dosage and hydraulic retention time, on COD removal were investigated. The results showed that the complete mixing condition was fulfilled in the electrochemical reactor employed in this study and COD removal followed a modified pseudo-first order kinetic model. The COD removal efficiency increased with the decrease of H{sub 2}O{sub 2} to Fe{sup 2+} molar ratio and hydraulic retention time. There existed an optimal inter-electrode gap or H{sub 2}O{sub 2} dosage so that the highest COD removal was achieved. Nearly the same COD removal was obtained at initial pH 3 and 5, but the steady state was quickly achieved at initial pH 3. The organic pollutants in the leachate were analyzed through a gas chromatography coupled with mass spectrometry (GC-MS) system. About 73 organics were detected in the leachate, and 52 of which were completely removed after EF-Fere process.

  7. High performance of nanoscaled Fe2O3 catalyzing UV-Fenton under neutral condition with a low stoichiometry of H2O2: Kinetic study and mechanism

    DEFF Research Database (Denmark)

    Wang, Yong; Sun, Yunkai; Li, Weiguang;

    2015-01-01

    radical), O21 (singlet oxygen) and O2- (superoxide radical) showed HO, O21 and O2- participated in nano-Fe2O3 catalyzing UV-Fenton. Presence of oxygen could greatly enhance the degradation rate compared with the case of bubbling nitrogen, and a possible mechanism of catechol oxidation in nano-Fe2O3......Kinetics and mechanism of nano-Fe2O3 catalyzing UV-Fenton were investigated in this study with catechol as model pollutant. This type of heterogeneous UV-Fenton was proven to be characteristic of a wide pH range from mildly acidic to slightly alkaline and low H2O2 requirement accompanied with H2O2...... catalyzing UV-Fenton was proposed. At last, reusability and stability of nano-Fe2O3 were evaluated in six repeated runs. This study will provide some deep understanding of nano-Fe2O3 catalyzing UV-Fenton with respect to technical advantage and oxidation mechanism. [All rights reserved Elsevier]....

  8. Fenton试剂强化微电解工艺预处理中纤板热磨废水%Micro-electrolysis treatment for hot, grinding wastewater from MDF production using Fenton's reagent

    Institute of Scientific and Technical Information of China (English)

    张文妍; 李凡; 孙盼华; 张齐生

    2011-01-01

    The hot, grinding wastewater from medium density fiberboard (MDF) production contains high concentrated toxic oranic maters. It is not fit for biochemical treatment even after pretreatment of micro-electrolysis. Fenton's reagent method was employed to improve the former micro-electrolysis treatment by means of jar test. Optimal parameters of the Fenton process were determined as 0.05-0.10 of [Fe2+]/[H2O2] with 1 h reaction time. When Fenton treated effluent was controlled at pH 8.5, the sedimentation process further removed pollutants, and the chemical oxygen demand (COD) concentration of the former micro-electrolysis treatment effluent was reduced from 14 000 mg· L-1 to about 3 500 mg·L-1 . GC-MS analysis indicated that the combined process of micro-electrolysis and Fenton oxidation broke almost all of the monocyclic terpene bonds in the wastewater, oxidizing them to esters, alcohols, and ketones with a lower carbon number. However, for double ring terpense the combined process only broke some of the bonds. These obtained results evidenced the efficiency of the combined process to the hot, grinding wastewater pretreatment and should contribute to further studies of MDF wastewater treatment. [Ch, 5 fig. 1 tab. 13 ref.]%研究了Fenton试剂强化微电解工艺预处理中纤板热磨废水的效果.结果表明,保持废水中亚铁离子(Fe2+)和过氧化氢(H2O2)的摩尔比为0.05~0.10,反应30 min后将废水pH值调到8.5,可进一步将微电解出水的化学需氧量值从14 000 mg·L-1降低到3 500mg·L-1左右,大幅提升了预处理的效果,并为后续的生化处理提供良好的基础.另外,对热磨废水和最终出水进行了气相色谱/质谱联用技术(GC-MS)分析,结果显示,微电解-Fenton氧化工艺的氧化能力可以打开所有热磨废水中单环萜烯的键,将它们氧化成低碳原子的酯类、醇类和酮类化合物,但还不足以将废水中所有双环萜烯的键打开.图5表1参13

  9. Aquatic toxicity of dyes before and after photo-Fenton treatment.

    Science.gov (United States)

    de Luna, Luis A V; da Silva, Thiago H G; Nogueira, Raquel F Pupo; Kummrow, Fábio; Umbuzeiro, Gisela A

    2014-07-15

    This study evaluated the ecotoxicity of five dyes to freshwater organisms before and during their photo-Fenton degradation. EC50 (48h) of the five tested dyes ranged from of 6.9 to >1000mgL(-1) for Daphnia similis. In the chronic tests IC50 (72h) varied from 65 to >100mgL(-1) for Pseudokirchneriella subcapitata and IC50 (8 days) from 0.5 to 410mgL(-1) for Ceriodaphnia dubia. Toxicity tests revealed that although the applied treatment was effective for decolorization of the dye, the partial mineralization may be responsible for the presence of degradation products which can be either more toxic than the original dye, as is the case of Vat Green 3 and Reactive Black 5, lead to initially toxic products which may be further degraded to non toxic products (acid Orange 7 and Food Red 17), or generate non toxic products as in the case of Food Yellow 3. The results highlighted the importance of assessing both acute and chronic toxicity tests of treated sample before effluent discharge.

  10. Water quality in the vicinity of Fenton Hill, 1985 and 1986: Progress report

    Energy Technology Data Exchange (ETDEWEB)

    Purtymun, W.D.; Ferenbaugh, R.W.; Williams, M.C.; Maes, M.N.

    1988-03-01

    Water quality data have been collected since 1974 from established surface and groundwater stations at and in the vicinity of Fenton Hill (Hot Dry Rock Geothermal Demonstration Site) located in the Jemez Mountains. This is part of a continuing program of environmental studies. Data on chemical quality of water were determined for samples collected from 13 surface water and 19 groundwater stations in 1985 and 1986. There were slight variations in the chemical quality of the ground and surface water in 1985 and 1986 as compared with previous analyses; however, these variations are within normal seasonal fluctuations. Chemical uptake in soil, roots, and foliage is monitored in the canyon, which receives intermittent effluent release of water from tests in the geothermal circulation loop and occasional fluids from drilling operations. The chemical concentrations found in soil, roots, and vegetation as the result of effluent release have shown a decrease in concentration down-canyon and also have decreased in concentration with time since the larger releases that took place in the late 1970s and early 1980s. 18 refs., 7 figs., 9 tabs.

  11. Electro-Fenton treatment of mature landfill leachate in a continuous flow reactor.

    Science.gov (United States)

    Zhang, Hui; Ran, Xiaoni; Wu, Xiaogang

    2012-11-30

    The treatment of mature landfill leachate by EF-Fere (also called Fered-Fenton) method was carried out in a continuous stirred tank reactor (CSTR) using Ti/RuO(2)-IrO(2)-SnO(2)-TiO(2) mesh anodes and Ti mesh cathodes. The effects of important parameters, including initial pH, inter-electrode gap, H(2)O(2) to Fe(2+) molar ratio, H(2)O(2) dosage and hydraulic retention time, on COD removal were investigated. The results showed that the complete mixing condition was fulfilled in the electrochemical reactor employed in this study and COD removal followed a modified pseudo-first order kinetic model. The COD removal efficiency increased with the decrease of H(2)O(2) to Fe(2+) molar ratio and hydraulic retention time. There existed an optimal inter-electrode gap or H(2)O(2) dosage so that the highest COD removal was achieved. Nearly the same COD removal was obtained at initial pH 3 and 5, but the steady state was quickly achieved at initial pH 3. The organic pollutants in the leachate were analyzed through a gas chromatography coupled with mass spectrometry (GC-MS) system. About 73 organics were detected in the leachate, and 52 of which were completely removed after EF-Fere process.

  12. Degradation of phenol with using of Fenton-like Processes from water

    Directory of Open Access Journals (Sweden)

    Ahmad Reza Yazdanbakhsh

    2015-08-01

    Full Text Available Phenol is one of the serious pollutants from the chemical and petrochemical industries. This pollutant due to its convoluted structure is resistant to biodegradation. One of the methods that are useful to remove this pollutant is advanced oxidation (AOP. A laboratory scale study was done on a synthetic wastewater containing phenol. All experiments were done in batch conditions and effect of variables pH, amount of hydrogen peroxide, iron dosage, contact time and an initial concentration on the phenol removal were tested. The remaining phenol concentration was evaluated using the DR-5000 device. In order to effect of these parameters, the experiment was performance at pH 2 to 6, 5 to 45 ml/ml of peroxide, and time of 5 to 60 minutes with 2 to 15 g/ml iron (Fe˚. The optimum pH, the ratio of hydrogen, Fe˚and time were 3, 15 ml, 8g and 5 minutes respectively. Chemical oxygen demand (COD index was chosen as the parameter for evaluation in this study. Result showed that mineralization of phenol was not complete. The COD removal efficiency was obtained 71%. According to the results of this study, Fenton-like process can be used for conversion organic resistant compounds to other compounds with lower toxicity.

  13. 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.

  14. Degradation of hydroxycinnamic acid mixtures in aqueous sucrose solutions by the Fenton process.

    Science.gov (United States)

    Nguyen, Danny M T; Zhang, Zhanying; Doherty, William O S

    2015-02-11

    The degradation efficiencies and behaviors of caffeic acid (CaA), p-coumaric acid (pCoA), and ferulic acid (FeA) in aqueous sucrose solutions containing the mixture of these hydroxycinnamic acids (HCAs) were studied by the Fenton oxidation process. Central composite design and multiresponse surface methodology were used to evaluate and optimize the interactive effects of process parameters. Four quadratic polynomial models were developed for the degradation of each individual acid in the mixture and the total HCAs degraded. Sucrose was the most influential parameter that significantly affected the total amount of HCA degraded. Under the conditions studied there was a analysis showed goodness of fit between the experimental results and the predicted values. The degradation behavior of CaA differed from those of pCoA and FeA, where further CaA degradation is observed at increasing sucrose and decreasing solution pH. The differences (established using UV/vis and ATR-FTIR spectroscopy) were because, unlike the other acids, CaA formed a complex with Fe(III) or with Fe(III) hydrogen-bonded to sucrose and coprecipitated with lepidocrocite, an iron oxyhydroxide. PMID:25585639

  15. Optimization of photo-Fenton process parameters on carbofuran degradation using central composite design.

    Science.gov (United States)

    Lu, Li A; Ma, Ying S; Daverey, Achlesh; Lin, Jih G

    2012-01-01

    Carbofuran, one of the most toxic and biorefractory carbamate compounds, is widely used in insecticides in Taiwan (9-18% of total insecticides production per year). In the present study, a central composite design experiment was used to study the effect of photo-Fenton treatment on carbofuran solution and to optimize the process variables such as carbofuran concentration (1-100 mg L(-1)), H(2)O(2) dosage rate (0.25-6 mg L(-1) min(-1)) and Fe(3+) dosage (1-50 mg L(-1)), which influenced the efficiency of carbofuran degradation and mineralization. The results indicated that all the variables investigated in this study had significant roles in the degradation and mineralization of carbofuran in solution. The carbofuran degradation and mineralization efficiencies were increased with increase in H(2)O(2) dosage rate and Fe(3+) dosage, and with decrease in carbofuran concentration. Furthermore, optimum values of both H(2)O(2) dosage rate and Fe(3+) dosage were found to shift to higher values as carbofuran concentration increased. Based on the model obtained in this study, optimum H(2)O(2) dosage rate and Fe(3+) dosage were found to be 4 mg L(-1) min(-1) and 20 mg L(-1), respectively, for 51 mg L(-1) of carbofuran concentration. Under these conditions, carbofuran was completely removed within 30 min and coupled with 78% mineralization at the end of experiment.

  16. Sono-advanced Fenton decolorization of azo dye Orange G: Analysis of synergistic effect and mechanisms.

    Science.gov (United States)

    Cai, Meiqiang; Su, Jie; Lian, Guanghu; Wei, Xiaoqin; Dong, Chunying; Zhang, Haojie; Jin, Micong; Wei, Zongsu

    2016-07-01

    In this study, a successful decolorization of Orange G was achieved by means of coupling zero valent iron (ZVI), H2O2 and ultrasound (US) under acidic pH conditions. The synergistic effect and characterization of potential roles of the factors including ZVI, tert-Butanol as radical scavenger, dissolved ferrous ions and H2O2 generated from sonication were evaluated in this sono-advanced Fenton process (SAFP) system. A clear synergy was evident in terms of decolorization rate and the TOC removal as the input of US enhanced the activity of the Fe(0)/H2O2 system. The results suggested that the ZVI was potential replacement for the Fe(2+) ion. This remarkable activity was attributed to the capacity of Fe(2+) formed and reduction of sonic-dissolved Fe(2+) concentration by the formation of {Fe·Fe(2+)}. The modification of the condition of H2O2 addition such as the dosage and input method showed significant variations in terms of decolorization rate. This result indicated that the optimal external addition of H2O2 and input method is a limited factor of decolorization rate due to its comparatively insufficient generated by ultrasound. PMID:26964940

  17. [Modification of activated carbon fiber for electro-Fenton degradation of phenol].

    Science.gov (United States)

    Ma, Nan; Tian, Yao-Jin; Yang, Guang-Ping; Xie, Xin-Yuan

    2014-07-01

    Microwave-modified activated carbon fiber (ACF-1), nitric acid-modified activated carbon fiber (ACF-2), phosphoric acid-modified activated carbon fiber (ACF-3) and ammonia-modified activated carbon fiber (ACF-4) were successfully fabricated. The electro-Fenton catalytic activities of modified activated carbon fiber were evaluated using phenol as a model pollutant. H2O2 formation, COD removal efficiency and phenol removal efficiency were investigated compared with the unmodified activated carbon fiber (ACF-0). Results indicated that ACF-1 showed the best adsorption and electrocatalytic activity. Modification was in favor of the formation of H2O2. The performance of different systems on phenol degradation and COD removal were ACF-1 > ACF-3 > ACF-4 > ACF-2 > ACF-0 and ACF-1 > ACF-4 > ACF-3 > ACF-2 > ACF-0, respectively, which confirmed that electrocatalytic activities of modified activated carbon fiber were better than the unmodified. In addition, phenol intermediates were not the same while using different modified activated carbon fibers.

  18. Pd/RGO modified carbon felt cathode for electro-Fenton removing of EDTA-Ni.

    Science.gov (United States)

    Zhang, Zhen; Zhang, Junya; Ye, Xiaokun; Hu, Yongyou; Chen, Yuancai

    2016-01-01

    Ethylenediaminetetraacetic acid (EDTA) forms stable complexes with toxic metals such as nickel due to its strong chelation. The electro-Fenton (EF) process using a cathode made from palladium (Pd), reduced graphene oxide (RGO) and carbon felt, fed with air, exhibited high activities and stability for the removal of 10 mg L(-1) EDTA-Ni solution. Pd/RGO catalyst was prepared by one-pot synthesis; the scanning electron microscopy and X-ray diffraction analysis indicated nanoparticles and RGO were well distributed on carbon felt, forming three dimensional architecture with both large macropores and a mesoporous structure. The cyclic voltammetric results showed that the presence of RGO in Pd/RGO/carbon felt significantly increased the current response of two-electron reduction of O2 (0.45 V). The key factors influencing the removal efficiency of EDTA-Ni, such as pH, current and Fe(2+) concentration, were investigated. Under the optimum conditions, the removal efficiency of EDTA-Ni reached 83.8% after 100 min EF treatment. Mechanism analysis indicated that the introduction of RGO in Pd/RGO/carbon felt significantly enhanced the electrocatalytic activities by inducing •OH in the EF process; direct H2O2 oxidation still accounted for a large amount of EDTA-Ni removal efficiency. PMID:27508368

  19. A Comparison of Central Composite Design and Taguchi Method for Optimizing Fenton Process

    Directory of Open Access Journals (Sweden)

    Anam Asghar

    2014-01-01

    Full Text Available In the present study, a comparison of central composite design (CCD and Taguchi method was established for Fenton oxidation. Dyeini, Dye : Fe+2, H2O2 : Fe+2, and pH were identified control variables while COD and decolorization efficiency were selected responses. L9 orthogonal array and face-centered CCD were used for the experimental design. Maximum 99% decolorization and 80% COD removal efficiency were obtained under optimum conditions. R squared values of 0.97 and 0.95 for CCD and Taguchi method, respectively, indicate that both models are statistically significant and are in well agreement with each other. Furthermore, Prob > F less than 0.0500 and ANOVA results indicate the good fitting of selected model with experimental results. Nevertheless, possibility of ranking of input variables in terms of percent contribution to the response value has made Taguchi method a suitable approach for scrutinizing the operating parameters. For present case, pH with percent contribution of 87.62% and 66.2% was ranked as the most contributing and significant factor. This finding of Taguchi method was also verified by 3D contour plots of CCD. Therefore, from this comparative study, it is concluded that Taguchi method with 9 experimental runs and simple interaction plots is a suitable alternative to CCD for several chemical engineering applications.

  20. Degradation of enoxacin antibiotic by the electro-Fenton process: Optimization, biodegradability improvement and degradation mechanism.

    Science.gov (United States)

    Annabi, Cyrine; Fourcade, Florence; Soutrel, Isabelle; Geneste, Florence; Floner, Didier; Bellakhal, Nizar; Amrane, Abdeltif

    2016-01-01

    This study aims to investigate the effectiveness of the electro-Fenton process on the removal of a second generation of fluoroquinolone, enoxacin. The electrochemical reactor involved a carbon-felt cathode and a platinum anode. The influence of some experimental parameters, namely the initial enoxacin concentration, the applied current intensity and the Fe(II) amount, was examined. The degradation of the target molecule was accompanied by an increase of the biodegradability, assessed from the BOD5 on COD ratio, which increased from 0 before treatment until 0.5 after 180 min of electrolysis at 50 mg L(-1) initial enoxacin concentration, 0.2 mmol L(-1) Fe(II) concentration and 300 mA applied current intensity. TOC and COD time-courses were also evaluated during electrolysis and reached maximum residual yields of 54% and 43% after 120 min of treatment, respectively. Moreover, a simultaneous generation of inorganic ions (fluorides, ammonium and nitrates) were observed and 3 short chain carboxylic acids (formic, acetic and oxalic acids) were identified and monitored during 180 min of electrolysis. By-products were identified according to UPLC-MS/MS results and a degradation pathway was proposed. PMID:26413803

  1. Aquatic toxicity of dyes before and after photo-Fenton treatment.

    Science.gov (United States)

    de Luna, Luis A V; da Silva, Thiago H G; Nogueira, Raquel F Pupo; Kummrow, Fábio; Umbuzeiro, Gisela A

    2014-07-15

    This study evaluated the ecotoxicity of five dyes to freshwater organisms before and during their photo-Fenton degradation. EC50 (48h) of the five tested dyes ranged from of 6.9 to >1000mgL(-1) for Daphnia similis. In the chronic tests IC50 (72h) varied from 65 to >100mgL(-1) for Pseudokirchneriella subcapitata and IC50 (8 days) from 0.5 to 410mgL(-1) for Ceriodaphnia dubia. Toxicity tests revealed that although the applied treatment was effective for decolorization of the dye, the partial mineralization may be responsible for the presence of degradation products which can be either more toxic than the original dye, as is the case of Vat Green 3 and Reactive Black 5, lead to initially toxic products which may be further degraded to non toxic products (acid Orange 7 and Food Red 17), or generate non toxic products as in the case of Food Yellow 3. The results highlighted the importance of assessing both acute and chronic toxicity tests of treated sample before effluent discharge. PMID:24910910

  2. Reduction of COD in wastewater from an organized tannery industrial region by Electro-Fenton process

    Energy Technology Data Exchange (ETDEWEB)

    Kurt, Ugur [Yildiz Technical University, Environmental Engineering Department, 34349 Istanbul (Turkey)]. E-mail: ukurt@yildiz.edu.tr; Apaydin, Omer [Yildiz Technical University, Environmental Engineering Department, 34349 Istanbul (Turkey)]. E-mail: apaydin@yildiz.edu.tr; Gonullu, M. Talha [Yildiz Technical University, Environmental Engineering Department, 34349 Istanbul (Turkey)]. E-mail: gonul@yildiz.edu.tr

    2007-05-08

    Advanced oxidation processes (AOPs) have led the way in the treatment of aqueous waste and are rapidly becoming the chosen technology for many applications. In this paper, COD reduction potential of leather tanning industry wastewaters by Electro-Fenton (EF) oxidation, as one of the AOPs, was experimentally evaluated. The wastewater sample was taken from an outlet of an equalization basin in a common treatment plant of an organized tannery industrial region in Istanbul, Turkey. Treatment of the wastewater was carried out by an electrochemical batch reactor equipped with two iron electrodes, which were connected parallel to each other. The oxidation process was studied for optimization of H{sub 2}O{sub 2} and the electricity consumptions were observed at different contact times under different pH conditions (3.0, 5.0 and 7.2). In each case, electricity consumption for decreased COD mass was estimated. In this process, COD was reduced by 60-70% within 10 min. By taking into consideration the local sewerage discharge limit, applicability of EF process for the tannery wastewaters was evaluated.

  3. Minimization of organic content in simulated industrial wastewater by Fenton type processes: a case study.

    Science.gov (United States)

    Grcić, Ivana; Vujević, Dinko; Sepcić, Josip; Koprivanac, Natalija

    2009-10-30

    Pre-treatment of simulated industrial wastewaters (SIM1, SIM2 and SIM3) containing organic and inorganic compounds (1,2-dichloroethane, sodium formate, sodium hydrogen carbonate, sodium carbonate and sodium chloride) by oxidative degradation using homogeneous Fenton type processes (Fe2+/H2O2 and Fe3+/H2O2) has been evaluated. The effects of initial Fe2+ and Fe3+ concentrations, [Fe2+/3+], type of iron salt (ferrous sulfate vs. ferric chloride), initial hydrogen peroxide concentration, [H2O2], on mineralization extent, i.e., total organic content (TOC) removal, were studied. Response surface methodology (RSM), particularly Box-Behnken design (BBD) was used as modelling tool, and obtained predictive function was used to optimize the overall process by the means of desirability function approach (DFA). Up to 94% of initial TOC was removed after 120 min. Ferrous sulfate was found to be the most appropriate reagent, and the optimal doses of Fe2+ and H2O2 for reducing the pollutant content, in terms of final TOC and sludge production were assessed. PMID:19525062

  4. Degradation of sulfonamides in aqueous solution by membrane anodic fenton treatment.

    Science.gov (United States)

    Neafsey, Katherine; Zeng, Xia; Lemley, Ann T

    2010-01-27

    Two agricultural antibiotics used heavily in agriculture, sulfamethazine and sulfadiazine, were degraded in an aqueous system by anodic Fenton treatment (AFT), an advanced oxidation technique that has been shown to be effective in degrading various pesticides but has not been applied to antibiotics. The effects of the H(2)O(2)/Fe(2+) ratio, Fe(2+) delivery rate, and initial contaminant concentration on the degradation of sulfamethazine by AFT were determined. The optimal H(2)O(2)/Fe(2+) ratio was determined to be 10:1, and the optimal Fe(2+) delivery rate was found to be between 38.9 and 54.4 microM min(-1). Under these conditions, sulfamethazine was completely degraded within 10 min at a range of concentrations (18-250 microM) commonly found in manure lagoons, contaminated rivers, and groundwater. Using the same optimal conditions, the effect of pH on the degradation of sulfadiazine by AFT was analyzed, and 100 microM sulfadiazine was degraded within 6-8 min of treatment at a range of pH values (3.1-7.1) that could potentially be found in aquatic environments. Degradation products and pathways were proposed for both compounds, and it was inferred that AFT degradation products of sulfadiazine and sulfamethazine are unlikely to retain the bacteriostatic properties of their parent compounds. An aquatic toxicity test employing Lemna gibba confirmed that AFT removes the bacteriostatic properties of sulfamethazine and sulfadiazine during degradation. PMID:20028131

  5. Applicability of Fenton Process for Treatment of Industrial Effluents: A Review

    Directory of Open Access Journals (Sweden)

    Mehali Mehta

    2014-12-01

    Full Text Available Wastewater and effluent treatment has undergone innovative changes over the years. Traditional wastewater treatment has yielded to modern and path-breaking procedures which are more efficient and effective. The world of difficulties and unknown has opened new avenues and paths to highly feasible effluent treatment procedures, so the vigorous importance of advanced oxidation procedures. This review paper will delineate the increasing importance of various advanced oxidation processes including Fenton treatment for wastewater. Advanced oxidation processes (AOP’s, which involve and includes the in-situ generation of highly potent chemical oxidants such as the hydroxyl radical, have emerged as an important avenue of technologies to accelerate the non-selective oxidation and thus the destruction of a wide range of non-degradable organic contaminants in wastewater which cannot be eliminated biologically. Advanced oxidation processes (AOP are technologies based on the generation of highly reactive species, the hydroxyl radicals, used in oxidative degradation procedures for organic compounds dissolved or dispersed in aquatic media. These processes are promising alternatives for decontamination of media containing dissolved recalcitrant organic substances, which would not be efficiently removed by conventional methods.

  6. Solar photo-Fenton like using persulphate for carbamazepine removal from domestic wastewater.

    Science.gov (United States)

    Ahmed, Moussa Mahdi; Chiron, Serge

    2014-01-01

    This work aimed at decontaminating biologically treated domestic wastewater effluent from pharmaceutical residues by using sulphate radical based homogeneous photo-Fenton involving persulphate (PS) as an oxidant, ferrous iron (Fe(II)) as a catalyst and simulated solar irradiation as a light source. This is the first time that the beneficiary use of solar energy in PS/Fe(II)/UV-Vis system was evaluated by using carbamazepine (CBZ) as a probe compound. In wastewater, CBZ was fully degraded in 30 min for an initial CBZ concentration of 50 μM and an optimal PS:Fe(II) molar ratio of 2:1 thanks to the high selectivity in reactivity of the sulphate radical limiting scavenging effects of organic matter and inorganic ions. Seventeen by-products were identified using liquid chromatography-high resolution-mass spectrometry allowing for the establishment of degradation pathways. CBZ first underwent degradation through one electron transfer oxidation processes due to sulphate radical reactivity followed by hydroxylation processes through hydroxyl radical formed by Fe(III) photoreduction. The sequential generation of sulphate radical and hydroxyl radical has made PS/Fe(II)/UV-Vis a kinetically effective process in removing CBZ from wastewater without the accumulation of toxic intermediates and opens new remediation strategies for tertiary treatment in domestic wastewater treatment plants. PMID:24095595

  7. Reduction of COD in wastewater from an organized tannery industrial region by Electro-Fenton process

    International Nuclear Information System (INIS)

    Advanced oxidation processes (AOPs) have led the way in the treatment of aqueous waste and are rapidly becoming the chosen technology for many applications. In this paper, COD reduction potential of leather tanning industry wastewaters by Electro-Fenton (EF) oxidation, as one of the AOPs, was experimentally evaluated. The wastewater sample was taken from an outlet of an equalization basin in a common treatment plant of an organized tannery industrial region in Istanbul, Turkey. Treatment of the wastewater was carried out by an electrochemical batch reactor equipped with two iron electrodes, which were connected parallel to each other. The oxidation process was studied for optimization of H2O2 and the electricity consumptions were observed at different contact times under different pH conditions (3.0, 5.0 and 7.2). In each case, electricity consumption for decreased COD mass was estimated. In this process, COD was reduced by 60-70% within 10 min. By taking into consideration the local sewerage discharge limit, applicability of EF process for the tannery wastewaters was evaluated

  8. Removal of organic pollutants in tannery wastewater from wet-blue fur processing by integrated Anoxic/Oxic (A/O) and Fenton: Process optimization

    DEFF Research Database (Denmark)

    Wang, Yong; Li, Weiguang; Angelidaki, Irini;

    2014-01-01

    the highest COD removal of 55.87%. GC-MS analysis was carried out to observe the change of organic composition during Fenton oxidation, and most of the residual organic pollutants resistant to Fenton treatment belonged to organosilanes and saturated alkanes. This study will provide useful information......Treatment of tannery wastewater has been a challenge in remediation of aquatic environment in developing countries. Removal of organic pollutants in tannery wastewater from wet-blue fur processing was studied using integrated processes of Anoxic/Oxic and Fenton. Analysis of COD composition based...... performance than anaerobic degradation. Effect of hydraulic retention time on A/O performance in terms of COD removal efficiency was evaluated, excess HRT like 60h would reduce the effluent quality, and the appropriate organic load rate was at least up to 0.8kgCODm-3d-1 with corresponding COD removal of about...

  9. Nanocasted synthesis of magnetic mesoporous iron cerium bimetal oxides (MMIC) as an efficient heterogeneous Fenton-like catalyst for oxidation of arsenite

    International Nuclear Information System (INIS)

    Highlights: • MMIC with large surface area and pore volume was synthesized via the hard template. • MMIC could be easily separated from aqueous solution with an external magnetic field. • MMIC presented excellent catalytic activity for the oxidation of As(III). • As(III) was mainly oxidized by surface-bound ·OHads and free ·OHfree radicals. • MMIC played a dual function role for the arsenic removal in aqueous solution. - Abstract: Magnetic mesoporous iron cerium bimetal oxides (MMIC) with large surface area and pore volume was synthesized via the hard template approach. This obtained MMIC was easily separated from aqueous solution with an external magnetic field and was proposed as a heterogeneous Fenton-like catalyst for oxidation of As(III). The MMIC presented excellent catalytic activity for the oxidation of As(III), achieving almost complete oxidation of 1000 ppb As(III) after 60 min and complete removal of arsenic species after 180 min with reaction conditions of 0.4 g/L catalyst, pH of 3.0 and 0.4 mM H2O2. Kinetics analysis showed that arsenic removal followed the pseudo-first order, and the pseudo-first-order rate constants increased from 0.0014 min−1 to 0.0548 min−1 as the H2O2 concentration increased from 0.04 mM to 0.4 mM. On the basis of the effects of XPS analysis and reactive oxidizing species, As(III) in aqueous solution was mainly oxidized by ·OH radicals, including the surface-bound ·OHads generated on the MMIC surface which were involved in ≡Fe2+ and ≡Ce3+, and free ·OHfree generation by soluble iron ions which were released from the MMIC into the bulk solution, and the generated As(V) was finally removed by MMIC through adsorption

  10. Oxidation of disinfectants with Cl-substituted structure by a Fenton-like system Cu(2+)/H2O2 and analysis on their structure-reactivity relationship.

    Science.gov (United States)

    Peng, Jianbiao; Li, Jianhua; Shi, Huanhuan; Wang, Zunyao; Gao, Shixiang

    2016-01-01

    As widely used chemicals intended to protect human being from infection of microorganisms, disinfectants are ubiquitous in the environment. Among them chlorine-substituted phenol is a basic structure in many disinfectant molecules. Removal of these pollutants from wastewater is of great concern. The oxidative degradation of antimicrobial agents such as triclosan, chlorofene, and dichlorofene by a Fenton-like system Cu(2+)/H2O2 was examined. Reaction conditions such as temperature, initial concentrations of H2O2 and Cu(2+), and pH were optimized using triclosan as a representative. The degradation kinetics of the above disinfectants followed pseudo-first-order kinetics under the investigated conditions. Fourteen chlorophenols (CPs) with different chlorine substitution were also studied to evaluate the influence of molecular structure on the degradation process in the Cu(2+)/H2O2 system. Fourteen structure-related parameters were calculated using Gaussian 09 program. A quantitative structure-activity relationship (QSAR) model was established using SPSS software with measured rate constant (k) as dependent variable and calculated molecular descriptors as independent variables. A three-parameter model including energy of HOMO (E homo), molar heat capacity at constant volume (Cv(θ)), and the most positive net charge of hydrogen atoms (qH(+)) was selected for k prediction, with correlation coefficient R(2) = 0.878. Analyses of the model demonstrated that the Cv(θ) was the most significant factor affecting the k of chlorophenols. Variance analysis and standard t-value test were used to validate the model. PMID:26408114

  11. A DFT Study Toward the Reaction Mechanisms of TNT With Hydroxyl Radicals for Advanced Oxidation Processes.

    Science.gov (United States)

    He, Xi; Zeng, Qun; Zhou, Yang; Zeng, Qingxuan; Wei, Xianfeng; Zhang, Chaoyang

    2016-05-26

    The degradation pathway of environmental contaminant 2,4,6-trinitrotoluene (TNT) was investigated computationally at the SMD(Pauling)/M06-2X/6-311+G(d,p) level of theory. The dominant decomposition pathway of TNT → 4,6-dinitro-o-cresol → 4,6-dinitro-2-hydroxybenzylalcohol → 4,6-dinitro-2-hydroxybenzaldehyde was provided, and the corresponding predicted products and their distributions are in a good agreement with available experimental data on TNT degradation by Fenton reaction. It was shown that the mechanism of addition-elimination is crucial for this stage of the reaction. The reaction of H atom abstraction is a minor competing pathway. The details on transition states, intermediate radicals, and free energy surfaces for all proposed reactions are given and make up for a lack of experimental knowledge. PMID:27135259

  12. Characterization of dissolved organic matter in landfill leachate during the combined treatment process of air stripping, Fenton, SBR and coagulation

    Energy Technology Data Exchange (ETDEWEB)

    Liu, ZhiPing, E-mail: liulqs@163.com [Key Laboratory of Three Gorges Reservoir Region’s Eco-Environment, Ministry of Education, Chongqing University, Chongqing 400045 (China); Faculty of Urban Construction and Environmental Engineering, Chongqing University, Chongqing 400020 (China); Wu, WenHui; Shi, Ping [Faculty of Urban Construction and Environmental Engineering, Chongqing University, Chongqing 400020 (China); Guo, JinSong [Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 400045 (China); Cheng, Jin [Faculty of Urban Construction and Environmental Engineering, Chongqing University, Chongqing 400020 (China)

    2015-07-15

    Highlights: • DOM fractions spectra analysis during the whole treatment process. • Efficient method was achieved to remove organic matters in landfill leachate. • Molecular weight distribution and fractions were discussed. - Abstract: A combined treatment process of air stripping + Fenton + sequencing batch reactor (SBR)+ coagulation was performed to remove the pollutants in landfill leachate. Molecular weight (MW) distribution and fractions of dissolved organic matter (DOM) were discussed to study the characteristics. The experiment showed that the removal rate of chemical oxygen demand (COD), five day biological oxygen demand (BOD{sub 5}) and ammonia nitrogen (NH{sub 3}−N) by the combined process were 92.8%, 87.8% and 98.0%, respectively. Humic acid (HA) and fulvic acid (FA) were the main fractions in raw leachate with 81.8% of the total COD concentration, while hydrophilic organic matter (HyI) was the dominant fraction in the final effluent of the combined process with 63.5% of the total COD concentration. After the combined treatment process, the removal rate of DOM and fractions HA, FA, HyI were 91.9%, 97.1%, 95.8% and 71.7%, respectively. Organic matters of MW < 2 k and MW > 100 k were removed with 90.5% and 97.9% COD concentration after the treatment. The ultraviolet–visible spectra (UV–vis), Fourier transform infrared spectra (FTIR) and three-dimensional excitation-emission matrices spectra (EEMs) indicated that benzene materials and phenol compounds were preferentially removed in air stripping. High MW matters, aromatic rings, conjugated moieties and some functional groups were mainly removed by Fenton. While small MW fractions, carboxylic acids, alcohols and protein-like materials were preferentially biodegraded via SBR. Fulvic-like and humic-like materials were mainly destroyed via Fenton oxidation and coagulation.

  13. Evaluación del método Fenton para tratamientos de aguas industriales en ingeniería

    OpenAIRE

    Avendaño P., Gerardo; Reyes G., Maritza

    2012-01-01

    Por parte de los sectores industrial y académico, existe un gran interés en el uso de alternativas económicas que posibiliten una degradación efectiva de la carga contaminante de las aguas residuales, sin producir efectos colaterales que trasladan el problema pero no lo resuelven. El método Fenton es un tratamiento químico para vertimientos industriales que se presenta en esta investigación como una nueva alternativa para el tratamiento de vertimientos industriales med...

  14. Synthesis for Magnetic Mesoporous Fe3O4-SiO2 Composites and Heterogeneous Fenton Degradation of Methyl Blue

    Science.gov (United States)

    Xie, Huanling; Zhang, Tengyun

    2014-12-01

    In this work, we presented a facile, one-step preparation for magnetic mesoporous Fe3O4-SiO2 composites under closely neutral conditions by an evaporation-induced self-assembly (EISA) and adding 1,3,5-TMB as co-solvent approach. The resulting samples were characterized by X-ray diffraction, N2 adsorption measurement, FT-IR and SEM. Magnetic mesoporous composites and H2O2 form heterogeneous Fenton in order to removal methylene blue as the dye wastewater model object. The catalysts showed high catalytic activity and stability in the decolorization of methlye blue.

  15. Fe(III/TiO2-Montmorillonite Photocatalyst in Photo-Fenton-Like Degradation of Methylene Blue

    Directory of Open Access Journals (Sweden)

    Is Fatimah

    2015-01-01

    Full Text Available A photodegradation process of methylene blue (MB in aqueous solution using Fe(III/TiO2-montmorillonite photocatalyst is presented. The photocatalyst material was prepared using Indonesian natural montmorillonite in TiO2 pillarization process followed by Fe(III ion exchange. Kinetic study on MB degradation was conducted and evaluated by three kinetic models: the pseudo-first- and second-order equations and the Elovich equation. From the results, it is concluded that the degradation under the photo-Fenton-like process utilizing Fe(III/TiO2-montmorillonite photocatalyst conformed to the Elovich kinetic model.

  16. Fenton treatment of olive oil mill wastewater--applicability of the method and parameters effects on the degradation process

    Institute of Scientific and Technical Information of China (English)

    Bensalah Nasr; Bedoui Ahmed; Gadri Abdellatif

    2004-01-01

    The low biodegradability of polyphenolic compounds typically found in olive processing indicated that biological treatment is not always successful in the treatment of olive oil mill wastewater in term of COD removal. In this study the results of investigations on the applicability of Fenton's reagent in the treatment of this effluent were discussed. The efficiency of this method was determined. 86 % of removal COD was obtained using 5 mol H2O2 and 0.4 mol Fe2+ per liter of crude OMW. The main parameters that govern the complex reactive system, i.e., time, pH, [H2O2] and [Fe(II)] have been studied.

  17. Application of SBA-15 in Adsorption-Fenton Oxidation Process for Simultaneous Remediation of Dehp and As(iii)

    Science.gov (United States)

    Latorre, I.; Hwang, S.

    2013-12-01

    Di-2-ethylhexyl phthalate (DEHP) has been widely used as plasticizer in the manufacturing of polymeric materials to enhance flexibility, transparency and softness, particularly, in polyvinyl chloride (PVC) production. Several studies elucidated that DEHP could be linked to hepatocellular tumors and pre-term birth and may be a developmental and reproductive toxicant. Arsenic (As) contamination has been widespread in the environment and because of its toxicity and prevalence in nature; it also has become a significant environmental health concern. Most solid waste materials containing DEHP and As(III) are disposed of in landfills and may migrate to groundwater and soil environments representing a threat to human receptors. Therefore, the application of adsorption-Fenton oxidation process with Fe adsorbed to SBA-15 matrix was assessed for simultaneous remediation of DEHP and As(III). Three sequences were run to assess the regeneration efficiency of the SBA-15. A response surface methodology was employed to optimize adsorption and Fenton regeneration. Adsorption optimization was evaluated with regard to SBA-15 doses and the extent of As(III) and Fe concentrations. Optimization of Fenton regeneration, in addition, assessed initial H2O2 concentration. Global optimization for maximum reduction of DEHP and As(III) was performed by D-Optimal. Highest adsorption of DEHP (90-95%) and As (40-95%) into the SBA-15 was predicted at 1.16 mM Fe, 18.74 mg SBA-15 and 3.71 mg/L As(III). Highest reduction of As (78-99%) and DEHP (90-97%) was predicted with 0.50 mM Fe, 22 mg SBA-15, 3.02 mg/L As(III) and 22.50 mM H2O2. Global optimal treatments were validated and SBA-15 regenerated material was characterized via SEM and XPS. The efficiency of DEHP and As(III) remediation by adsorption-Fenton oxidation process, applying optimal treatment combinations, was evaluated using leachate from a lab scale bioreactor monofill (i.e., filled with PVC materials). Capability of As(III) and DEHP

  18. 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

  19. Electrochemically assisted Fenton reaction : reaction of hydroxyl radicals with xenobiotics followed by on-line analysis with high-performance liquid chromatography/tandem mass spectrometry

    NARCIS (Netherlands)

    Jurva, U; Wikstrom, HV; Bruins, AP

    2002-01-01

    Oxygen radicals are generated in vivo by various processes, often as toxic intermediates in different metabolic transformations, and have been shown to play an important role for a large number of diseases. In this article we introduce an electrochemical flow-through system that allows generation of

  20. 煤渣-Fenton联用工艺处理偶氮染料废水的研究%Investigation on Combination of Coal Cinders and Fenton Processes for Azo Dye Wastewater Treatment

    Institute of Scientific and Technical Information of China (English)

    高丽娟; 商志娟; 王进岗; 姜程程; 申婷婷; 王西奎

    2016-01-01

    本研究采用Fenton法与煤渣吸附联合工艺对偶氮染料废水直接黑19进行了处理,通过优化煤渣对偶氮染料废水的吸附条件与Fenton工艺对偶氮染料降解条件,构建两种联合工艺煤渣-Fenton/Fenton-煤渣对偶氮染料废水进行处理。研究结果表明,先进行煤渣吸附后进行Fenton氧化的联合工艺煤渣-Fenton可有效降解偶氮染料废水,脱色率可达99.6%,总有机碳( Total Organic Carbon, TOC)去除率可达72.7%。%Combination process of coal cinders and Fenton was applied for the treatment of azo dye wastewater of Direct Black 19. The investigations were mainly involved in the following aspects:the optimum conditions for coal cinders process and Fenton process, the combined process of coal cinders-Fenton/Fenton-coal cinders for the treatment of azo dye. The results showed that the coal cinders-Fenton was an effective way for Direct Black 19 removal. It was investigated that the decolorization of Direct Black 19 was 99. 6% and TOC removal efficiency was up to 72. 7%.

  1. Use of Fenton reagent combined with humic acids for the removal of PFOA from contaminated water.

    Science.gov (United States)

    Santos, Aurora; Rodríguez, Sergio; Pardo, Fernando; Romero, Arturo

    2016-09-01

    Perfluorinated compounds (PFCs) are receiving significant attention due to its global distribution, high persistence, and bioaccumulation properties. Among them, perfluorooctanoic acid (PFOA) is one of the most commonly found in the environment. The strong bond C-F in PFOA is extremely difficult to degrade, therefore advanced oxidation processes (AOPs) at room temperature and pressure are not able to oxidize them, as was noticed here using Fenton like reagent (FR) or persulfate (PS) at 25°C. On the contrary, by using persulfate activated by heat (100mM and T=70°C) a complete defluorination of PFOA 0.1mM was noticed after 18h, with a sequential degradation mechanism of losing one CF2 unit from PFOA and its intermediates (perfluoroheptanoic acid (PFHpA), perfluorohexanoic acid (PFHxA), perfluoropentanoic acid (PFPA) and perfluorobutanoic acid (PFBA)). Since this thermal treatment is not usually desirable from an economical point of view, alternative process has been tested. For this scope, a hybrid process is proposed in this work, by adding humic acid, HA, (600mgL(-1)) and FR, (165mM in H2O2 and 3mM in Fe(3+)) to the 0.1mM PFOA solution. It was found that the HA was oxidized by FR. PFOA was entrapped quantitatively and irreversibly during HA oxidation, resulting PFOA non-available to the aqueous phase. Oxidized HA with PFOA entrapped precipitates. Both, the leftover Fe(III) acting as a coagulant and neutral pH enhance the separation of this solid phase. The precipitation noticed by adding HA to the PFOA solution in absence of FR was negligible. PMID:26412418

  2. Enhanced bioremediation of oil contaminated soil by graded modified Fenton oxidation

    Institute of Scientific and Technical Information of China (English)

    Jinlan Xu; Lei Xin; Tinglin Huang; Kun Chang

    2011-01-01

    Graded modified Fenton's (MF) oxidation is a strategy in which H2O2 is added intermittently to prevent a sharp temperature increase and undesired soil sterilization at soil circumneutral pH versus adding the same amount of H2O2 continuously.The primary objective of the present study was to investigate whether a mild MF pre-oxidation such as a stepwise addition of H2O2 can prevent sterilization and achieve a maximum degradation of tank oil in soil.Optimization experiments of graded MF oxidation were conducted using citric acid,oxalic acid and SOLV-X as iron chelators under different frequencies of H2O2 addition.The results indicated that the activity order of iron chelates decreased as:citric acid (51%) > SOLV-X (44%) > oxalic acid (9%),and citric acid was found to be an optimized iron chelating agent of graded MF oxidation.Three-time addition of H2O2 was found to be favorable and economical due to decreasing total petroleum hydrocarbon removal from three time addition (51%) to five time addition (59%).Biological experiments were conducted after graded MF oxidation of tank oil completed under optimum conditions mentioned above.After graded oxidation,substantially higher increase (31%) in microbial activity was observed with excessive H2O2 (1470 mmol,/L,the mol ratio of H2O2:Fe2+ was 210:1)than that of non-oxidized soil.Removal efficiency of tank oil was up to 93% after four weeks.Especially,the oil fraction (C10-C40) became more biodagradable after graded MF oxidation than its absence.Therefore,graded MF oxidation is a mild pretreatment to achieve an effective bioremediation of oil contaminated soil.

  3. Use of Fenton reagent combined with humic acids for the removal of PFOA from contaminated water.

    Science.gov (United States)

    Santos, Aurora; Rodríguez, Sergio; Pardo, Fernando; Romero, Arturo

    2016-09-01

    Perfluorinated compounds (PFCs) are receiving significant attention due to its global distribution, high persistence, and bioaccumulation properties. Among them, perfluorooctanoic acid (PFOA) is one of the most commonly found in the environment. The strong bond C-F in PFOA is extremely difficult to degrade, therefore advanced oxidation processes (AOPs) at room temperature and pressure are not able to oxidize them, as was noticed here using Fenton like reagent (FR) or persulfate (PS) at 25°C. On the contrary, by using persulfate activated by heat (100mM and T=70°C) a complete defluorination of PFOA 0.1mM was noticed after 18h, with a sequential degradation mechanism of losing one CF2 unit from PFOA and its intermediates (perfluoroheptanoic acid (PFHpA), perfluorohexanoic acid (PFHxA), perfluoropentanoic acid (PFPA) and perfluorobutanoic acid (PFBA)). Since this thermal treatment is not usually desirable from an economical point of view, alternative process has been tested. For this scope, a hybrid process is proposed in this work, by adding humic acid, HA, (600mgL(-1)) and FR, (165mM in H2O2 and 3mM in Fe(3+)) to the 0.1mM PFOA solution. It was found that the HA was oxidized by FR. PFOA was entrapped quantitatively and irreversibly during HA oxidation, resulting PFOA non-available to the aqueous phase. Oxidized HA with PFOA entrapped precipitates. Both, the leftover Fe(III) acting as a coagulant and neutral pH enhance the separation of this solid phase. The precipitation noticed by adding HA to the PFOA solution in absence of FR was negligible.

  4. Humic Acid Degradation via Solar Photo-Fenton Process in Aqueous Environment

    Directory of Open Access Journals (Sweden)

    Seyed Ali Sajjadi

    2015-08-01

    Full Text Available Control of mutagenic and carcinogenic disinfection by-products, particularly Trihalomethanes (THMs and Halo Acetic Acids (HAAs in water treatment process is critical, due to their adverse effects on human health. Generally, reducing the toxicity of these by-products hinges on prior removal of the precursor materials, such as Humic Acid (HA in drinking water. This study was conducted to investigate the role of some parameters that could affect the removal of HA, including HA (5 and 10 ppm and H2O2 (20, 40, 60, and 80 ppm initial concentrations, Iron (II, sulfate heptahydrate dosage (4, 8, 12, and 16 ppm, pH (2, 3, 4 and 5, Oxidation time (5, 10, 15 and 30 min, and Sunlight levels (322±13 kWm-2. To accelerate the process of HA removal, the Solar Photo-Fenton (SPF process was employed by direct irradiation of converged sunlight in a Parabolic Trough Collectors (PTC, with 3m2 effective area. HA levels were measured via quantifying Dissolved Organic Carbon (DOC concentrations by means of a TOC Analyzer method. The results showed that the SPF process is under control of the Fe & H2O2 ratio, the Fe2+ dosage and especially the pH quantity. In optimal condition, (pH: 4, oxidation time: 30min, initial HA levels: 50 ppm, H2O2 concentrations: 20 ppm Fe+2 levels: 4 ppm, the study found more than 98% DOC removal. In conclusion, the SPF, as an economically effective technique, could be applied for the removal of HA in aqueous environments.

  5. How do Enzymes Utilize Reactive OH Radicals? Lessons from Nonheme HppE and Fenton Systems.

    Science.gov (United States)

    Wang, Binju; Lu, Jiarui; Dubey, Kshatresh Dutta; Dong, Geng; Lai, Wenzhen; Shaik, Sason

    2016-07-13

    The iron(IV)-oxo (ferryl) intermediate has been amply established as the principal oxidant in nonheme enzymes and the key player in C-H bond activations and functionalizations. In contrast to this status, our present QM/MM calculations of the mechanism of fosfomycin biosynthesis (a broad range antibiotic) by the nonheme HppE enzyme rule out the iron(IV)-oxo as the reactive species in the hydrogen abstraction (H-abstraction) step of the pro-R hydrogen from the (S)-2-hydroxypropylphosphonic substrate. Moreover, the study reveals that the ferryl species is bypassed in HppE, while the actual oxidant is an HO(•) radical hydrogen-bonded to a ferric-hydroxo complex, resulting via the homolytic dissociation of the hydrogen peroxide complex, Fe(II)-H2O2. The computed energy barrier of this pathway is 12.0 kcal/mol, in fair agreement with the experimental datum of 9.8 kcal/mol. An alternative mechanism involves the iron-complexed hydroxyl radical (Fe(III)-(HO(•))) that is obtained by protonation of the iron(IV)-oxo group via the O-H group of the substrate. The barrier for this pathway, 23.0 kcal/mol, is higher than the one in the first mechanism. In both mechanisms, the HO(•) radical is highly selective; its H-abstraction leading to the final cis-fosfomycin product. It appears that HppE is prone to usage of HO(•) radicals for C-H bond activation, because the ferryl oxidant requires a specific H-abstraction trajectory (∠FeOH ∼ 180°) that cannot be met for intramolecular H-abstraction. Thus, this work broadens the landscape of nonheme iron enzymes and makes a connection to Fenton chemistry, with implications on new potential biocatalysts that may harness hydroxyl radicals for C-H bond functionalizations. PMID:27309496

  6. Multistage treatment system for raw leachate from sanitary landfill combining biological nitrification-denitrification/solar photo-Fenton/biological processes, at a scale close to industrial--biodegradability enhancement and evolution profile of trace pollutants.

    Science.gov (United States)

    Silva, Tânia F C V; Silva, M Elisabete F; Cunha-Queda, A Cristina; Fonseca, Amélia; Saraiva, Isabel; Sousa, M A; Gonçalves, C; Alpendurada, M F; Boaventura, Rui A R; Vilar, Vítor J P

    2013-10-15

    A multistage treatment system, at a scale close to the industrial, was designed for the treatment of a mature raw landfill leachate, including: a) an activated sludge biological oxidation (ASBO), under aerobic and anoxic conditions; b) a solar photo-Fenton process, enhancing the bio-treated leachate biodegradability, with and without sludge removal after acidification; and c) a final polishing step, with further ASBO. The raw leachate was characterized by a high concentration of humic substances (HS) (1211 mg CHS/L), representing 39% of the dissolved organic carbon (DOC) content, and a high nitrogen content, mainly in the form of ammonium nitrogen (>3.8 g NH4(+)-N/L). In the first biological oxidation step, a 95% removal of total nitrogen and a 39% mineralization in terms of DOC were achieved, remaining only the recalcitrant fraction, mainly attributed to HS (57% of DOC). Under aerobic conditions, the highest nitrification rate obtained was 8.2 mg NH4(+)-N/h/g of volatile suspended solids (VSS), and under anoxic conditions, the maximum denitrification rate obtained was 5.8 mg (NO2(-)-N + NO3(-)-N)/h/g VSS, with a C/N consumption ratio of 2.4 mg CH3OH/mg (NO2(-)-N + NO3(-)-N). The precipitation of humic acids (37% of HS) after acidification of the bio-treated leachate corresponds to a 96% DOC abatement. The amount of UV energy and H2O2 consumption during the photo-Fenton reaction was 30% higher in the experiment without sludge removal and, consequently, the reaction velocity was 30% lower. The phototreatment process led to the depletion of HS >80%, of low-molecular-weight carboxylate anions >70% and other organic micropollutants, thus resulting in a total biodegradability increase of >70%. The second biological oxidation allowed to obtain a final treated leachate in compliance with legal discharge limits regarding water bodies (with the exception of sulfate ions), considering the experiment without sludge. Finally, the high efficiency of the overall treatment

  7. Fenton氧化工艺在处理炼化废水中苯酚的应用研究%Study on Treatment of Phenol in Petroleum Refining Industry Wastewater by Fenton Reagent

    Institute of Scientific and Technical Information of China (English)

    李锐

    2014-01-01

    通过正交实验和单因素实验探索了Fenton氧化炼化废水中苯酚的最佳工艺条件。实验结果表明,Fenton试剂处理苯酚废水时,各影响因素的作用大小顺序是:pH>反应温度>H2O2投加量>反应时间>FeSO4·7H2O投加量;最佳氧化反应条件为:pH=3.5,反应温度为20℃,H2O2投加量为12 mL·L-1,反应时间为30min,FeSO4·7H2O投加量为450 mg·L-1,此时废水中苯酚的去除率为89.26%,残余苯酚含量为11.76 mg·L-1。因此,用Fenton氧化法处理含苯酚废水是一种非常有效的方法。%Removal of phenol in petroleum refining industry wastewater by Fenton reagent oxidation was examined. The optimal operating conditions were determined by orthogonal experiments and single factor experiments.The ex-periment results indicated that the order of effects was pH>reaction temperature>H2 O2 dosage >reaction time>FeSO4 7H2O dosage.After 30min,the removal rate of phenol in petroleum refining industry wastewater reaches 89.26% and the residual phenol in wastewater is 11.76 mg·L-1 when pH value is 3.5,temperature is 20 ℃, H2 O2 and FeSO4 dosage is 12 mL·L-1 and 450mg/L,respectively.So it is a very effective way to treat petroleum refining industry wastewater containing phenol using Fenton method.

  8. Manganese functionalized silicate nanoparticles as a fenton-type catalyst for water purification by advanced oxidation processes (AOP)

    Energy Technology Data Exchange (ETDEWEB)

    Tusar, Natasa Novak [National Institute of Chemistry, Ljubljana (Slovenia); University of Nova Gorica, Nova Gorica (Slovenia); Maucec, Darja; Rangus, Mojca; Mazaj, Matjaz; Cotman, Magda; Pintar, Albin; Kaucic, Venceslav [National Institute of Chemistry, Ljubljana (Slovenia); Arcon, Iztok [University of Nova Gorica, Nova Gorica (Slovenia)

    2012-02-22

    Wet hydrogen peroxide catalytic oxidation (WHPCO) is one of the most important industrially applicable advanced oxidation processes (AOPs) for the decomposition of organic pollutants in water. It is demonstrated that manganese functionalized silicate nanoparticles with interparticle porosity act as a superior Fenton-type nanocatalyst in WHPCO as they can decompose 80% of a test organic compound in 30 minutes at neutral pH and room temperature. By using X-ray absorption spectroscopic techniques it is also shown that the superior activity of the nanocatalyst can be attributed uniquely to framework manganese, which decomposes H{sub 2}O{sub 2} to reactive hydroxyls and, unlike manganese in Mn{sub 3}O{sub 4} or Mn{sub 2}O{sub 3} nanoparticles, does not promote the simultaneous decomposition of hydrogen peroxide. The presented material thus introduces a new family of Fenton nanocatalysts, which are environmentally friendly, cost-effective, and possess superior efficiency for the decomposition of H{sub 2}O{sub 2} to reactive hydroxyls (AOP), which in turn readily decompose organic pollutants dissolved in water. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Heterogeneous photo-Fenton degradation of polyacrylamide in aqueous solution over Fe(III)-SiO2 catalyst

    International Nuclear Information System (INIS)

    This article presents preparation, characterization and evaluation of heterogeneous Fe(III)-SiO2 catalysts for the photo-Fenton degradation of polyacrylamide (PAM) in aqueous solution. Fe(III)-SiO2 catalysts are prepared by impregnation method with two iron salts as precursors, namely Fe(NO3)3 and FeSO4, and are characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. The irradiated Fe(III)-SiO2 is complexed with 1,10-phenanthroline, then is measured by UV-vis-diffuse reflectance spectroscopy (UV-vis-DRS) and XPS to confirm the oxidation state of Fe in solid state. By investigating the photo-Fenton degradation of PAM in aqueous solution, the results indicate that Fe(III)-SiO2 catalysts exhibit an excellent photocatalytic activity in the degradation of PAM. Moreover, the precursor species and the OH-/Fe mole ratio affect the photocatalytic activity of Fe(III)-SiO2 catalysts to a certain extent. Finally, the amount of Fe ions leaching from the Fe(III)-SiO2 catalysts is much low

  10. Effect of different carriers and operating parameters on degradation of flax wastewater by fluidized-bed Fenton process.

    Science.gov (United States)

    Chen, Mengtian; Ren, Hongqiang; Ding, Lili; Gao, Baotian

    2015-01-01

    This investigation evaluates the effectiveness of a fluidized-bed Fenton process in treating flax wastewater. Flax wastewater was taken from a paper-making factory in a secondary sedimentation tank effluent of a paper-making factory in Hebei. The performance of three carriers (SiO2, Al2O3, Fe2O3) used in the r