RESUMEN
This work reports the first investigation on the use of EDDS as chelating agent in photoelectro-Fenton (PEF) treatment of water at near-neutral pH. As a case study, the removal of the antidepressant fluoxetine was optimized, using an electrochemical cell composed of an IrO2-based anode an air-diffusion cathode for in-situ H2O2 production. Electrolytic trials at constant current were made in ultrapure water with different electrolytes, as well as in urban wastewater (secondary effluent) at pH 7.2. PEF with Fe(III)-EDDS (1:1) complex as catalyst outperformed electro-Fenton and PEF processes with uncomplexed Fe(II) or Fe(III). This can be explained by: (i) the larger solubilization of iron ions during the trials, favoring the production of â¢OH from Fenton-like reactions between H2O2 and Fe(II)-EDDS or Fe(III)-EDDS, and (ii) the occurrence of Fe(II) regeneration from Fe(III)-EDDS photoreduction, which was more efficient than conventional photo-Fenton reaction with uncomplexed Fe(III). The greatest drug concentration decays were achieved at low pH, using only 0.10â¯mM Fe(III)-EDDS, although complete removal in wastewater was feasible only with 0.20â¯mM Fe(III)-EDDS due to the greater formation of â¢OH. The effect of the applied current and anode nature was rather insignificant. A progressive destruction of the catalytic complex was unveiled, whereupon the mineralization mainly progressed thanks to the action of â¢OH adsorbed on the anode surface. Despite the incomplete mineralization using BDD as the anode, a remarkable toxicity decrease was determined. Fluoxetine degradation yielded F- and NO3- ions, along with several aromatic intermediates. These included two chloro-organics, as a result of the anodic oxidation of Cl- to active chlorine. A detailed mechanism for the Fe(III)-EDDS-catalyzed PEF treatment of fluoxetine in urban wastewater is finally proposed.
Asunto(s)
Aguas Residuales , Contaminantes Químicos del Agua , Electrodos , Compuestos Férricos , Peróxido de Hidrógeno , Hierro , Oxidación-ReducciónRESUMEN
The treatment of olive oil mill wastewater (OOMW) by novel sequential processes involving electrocoagulation (EC) followed by electro-Fenton (EF) or photoelectro-Fenton (PEF) under UVA irradiation has been studied using a boron-doped diamond anode and an air-diffusion cathode for H2O2 electrogeneration. Their performance was monitored from the removal of total organic carbon (TOC), chemical oxygen demand, turbidity, total solids and total nitrogen, as well as from the energy consumption. Preliminary EC assays were performed with one pair of electrodes made of Al, Fe, AISI 304 or AISI 316L. The Fe/Fe cell showed the best performance, yielding 40% TOC decay in 20â¯min. Subsequent EF or PEF at natural pH 7.2 performed similarly, whereas PEF became superior at pH 3.0 due to the action of UVA photons. Comparison between EC/PEF and single EF or PEF at pH 3.0 and 25â¯mA cm-2 with 0.50â¯mM Fe2+ revealed the positive outcome of the sequential process, attaining 97.1% TOC abatement after 600â¯min. GC-MS analysis of the raw wastewater allowed identifying 18 cyclic and 27 aliphatic compounds, most of which could not be removed by EC. The final solutions in EC/EF and EC/PEF contained a large plethora of persistent long-chain aliphatic acids and alkanes.
RESUMEN
The electrochemical degradation of tetracaine hydrochloride has been studied in urban wastewater. Treatments in simulated matrix with similar ionic composition as well as in 0.050 M Na2SO4 were comparatively performed. The cell contained an air-diffusion cathode for H2O2 electrogeneration and an anode selected among active Pt, IrO2-based and RuO2-based materials and non-active boron-doped diamond (BDD). Electrochemical oxidation with electrogenerated H2O2 (EO-H2O2), electro-Fenton (EF) and photoelectro-Fenton (PEF) were comparatively assessed at pH 3.0 and constant current density. The pharmaceutical and its byproducts were oxidized by OH formed from water oxidation at the anode surface and in the bulk from Fenton's reaction, which occurred upon addition of 0.50 mM Fe2+ in all media, along with active chlorine originated from the anodic oxidation of Cl- contained in the simulated matrix and urban wastewater. The PEF process was the most powerful treatment regardless of the electrolyte composition, owing to the additional photolysis of intermediates by UVA radiation. The use of BDD led to greater mineralization compared to other anodes, being feasible the total removal of all organics from urban wastewater by PEF at long electrolysis time. Chlorinated products were largely recalcitrant when Pt, IrO2-based or RuO2-based anodes were used, whereas they were effectively destroyed by BDD(OH). Tetracaine decay always obeyed a pseudo-first-order kinetics, being slightly faster with the RuO2-based anode in Cl- media because of the higher amounts of active chlorine produced. Total nitrogen and concentrations of NH4+, NO3-, ClO3-, ClO4- and active chlorine were determined to clarify the behavior of the different electrodes in PEF. Eight intermediates were identified by GC-MS and fumaric and oxalic acids were quantified as final carboxylic acids by ion-exclusion HPLC, allowing the proposal of a plausible reaction sequence for tetracaine mineralization by PEF in Cl--containing medium.
Asunto(s)
Tetracaína/análisis , Aguas Residuales/química , Contaminantes Químicos del Agua/análisis , Purificación del Agua/métodos , Boro/química , Cloro/análisis , Técnicas Electroquímicas , Peróxido de Hidrógeno/química , Hierro/química , Cinética , Nitrógeno/análisis , Oxidación-Reducción , Fotólisis , Tetracaína/química , Rayos Ultravioleta , Contaminantes Químicos del Agua/químicaRESUMEN
The degradation of 4-hydroxyphenylacetic acid, a ubiquitous component of olive oil mill wastewater (OOMW), has been studied by anodic oxidation with electrogenerated H2O2 (AO-H2O2), electro-Fenton (EF) and photoelectro-Fenton (PEF). Experiments were performed in either a 0.050M Na2SO4 solution or a real OOMW at pH 3.0, using a cell with a boron-doped diamond (BDD) anode and an air-diffusion cathode for H2O2 generation. Hydroxyl radicals formed at the BDD surface from water oxidation in all processes and/or in the bulk from Fenton's reaction between added Fe2+ and generated H2O2 in EF and PEF were the main oxidants. In both matrices, the oxidation ability of the processes increased in the order AO-H2O2Asunto(s)
Boro/química
, Residuos Industriales/análisis
, Aceite de Oliva/química
, Fenilacetatos/química
, Sulfatos/química
, Aguas Residuales/análisis
, Diamante
, Técnicas Electroquímicas
, Electrodos
, Compuestos Ferrosos/química
, Peróxido de Hidrógeno/química
, Hierro
, Cinética
, Oxidación-Reducción
RESUMEN
Acidic solutions of trans-cinnamic acid at pH 3.0 have been comparatively treated by anodic oxidation with electrogenerated H2O2 (AO-H2O2), electro-Fenton (EF), and photoelectro-Fenton (PEF). The electrolytic experiments were carried out with a boron-doped diamond (BDD)/air-diffusion cell. The substrate was very slowly abated by AO-H2O2 because of its low reaction rate with oxidizing â¢OH produced from water discharge at the BDD anode. In contrast, its removal was very rapid and at similar rate by EF and PEF due to the additional oxidation by â¢OH in the bulk, formed from Fenton's reaction between cathodically generated H2O2 and added Fe2+. The AO-H2O2 treatment yielded the lowest mineralization. The EF process led to persistent final products like Fe(III) complexes, which were quickly photolyzed upon UVA irradiation in PEF to give an almost total mineralization with 98 % total organic carbon removal. The effect of current density and substrate concentration on all the mineralization processes was examined. Gas chromatography-mass spectrometry (GC-MS) analysis of electrolyzed solutions allowed identifying five primary aromatics and one heteroaromatic molecule, whereas final carboxylic acids like fumaric, acetic, and oxalic were quantified by ion exclusion high-performance liquid chromatography (HPLC). From all the products detected, a degradation route for trans-cinnamic acid is proposed.
Asunto(s)
Cinamatos , Técnicas Electroquímicas/métodos , Cinamatos/análisis , Cinamatos/química , Electrodos , Cromatografía de Gases y Espectrometría de Masas , Peróxido de Hidrógeno , Cinética , Oxidación-ReducciónRESUMEN
Solutions of 100 mL with 1.20 mM of salicylic acid (SA), 4-aminosalicylic acid (4-ASA) or 5-aminosalicylic acid (5-ASA) have been comparatively degraded by anodic oxidation with electrogenerated H2O2 (AO-H2O2), electro-Fenton (EF) and photoelectro-Fenton (PEF). Trials were carried out with a stirred tank reactor with a BDD anode and an air-diffusion cathode for continuous H2O2 production. A marked influence of the functional groups of the drugs was observed in their decay kinetics, increasing in the order SA < 5-ASA < 4-ASA in AO-H2O2 and 5-ASA < SA < 4-ASA in EF and PEF, due to the different attack of OH generated at the BDD surface and in the bulk from Fenton's reaction, respectively. This effect was clearly observed when varying the current density between 16.7 and 100 mA cm(-2). The relative mineralization power of the processes always followed the sequence: AO-H2O2 < EF < PEF. The three drugs underwent analogous mineralization abatement up to 88% by AO-H2O2 at 100 mA cm(-2). The mineralization rate in EF and PEF grew in the order: 4-ASA < 5-ASA < SA. The most powerful process was PEF, attaining >98% mineralization for all the drugs at 100 mA cm(-2). Oxalic and oxamic acids were detected as final short-linear aliphatic carboxylic acids by ion-exclusion HPLC, allowing the fast photolysis of their Fe(III) complexes by UVA light to justify the high power of PEF.
Asunto(s)
Ácidos Aminosalicílicos/química , Ácidos Carboxílicos/análisis , Peróxido de Hidrógeno/química , Ácido Oxálico/análisis , Ácido Oxámico/análisis , Ácido Salicílico/química , Aguas Residuales/química , Contaminantes Químicos del Agua/química , Cromatografía Líquida de Alta Presión , Electrodos , Hierro/química , Cinética , Oxidación-Reducción , Fotólisis , Aguas Residuales/análisisRESUMEN
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.
RESUMEN
The degradation of 2.5L of Allura Red AC solutions in sulfate medium containing 0.50mM Fe(2+) has been studied by solar photoelectro-Fenton (SPEF) using a flow plant equipped with a Pt/air-diffusion cell and a solar photoreactor. Comparative electro-Fenton treatment yielded rapid total decolorization but poor mineralization, since most products were slowly destroyed by OH formed from Fenton's reaction between Fe(2+) and H2O2 generated at the air-diffusion cathode. In contrast, the potent action of UV radiation from sunlight in SPEF allowed the rapid photolysis of recalcitrant intermediates, thus giving rise to a quick mineralization. Sulfate and nitrate ions, along with a large proportion of volatile N-derivatives, were always released. The increase in current density and decrease in azo dye concentration accelerated the decolorization and mineralization in SPEF, although lower current efficiency and greater specific energy consumption were obtained. The most cost-effective SPEF treatment was found for 460 mg L(-1) azo dye in 0.05 M Na2SO4 at 50 mA cm(-2), which yielded 95% mineralization with 81% current efficiency and 8.50 kW h m(-3). No significant effect of sulfate concentration was found. Up to 16 aromatic intermediates and 11 short-chain carboxylic acids, including oxalic and oxamic as the most persistent ones, were detected by GC-MS and HPLC. The large oxidation ability of SPEF can be explained by the quick photolysis of Fe(III)-oxalate complexes and other undetected intermediates.
Asunto(s)
Compuestos Azo/química , Compuestos Férricos/química , Fotólisis , Eliminación de Residuos Líquidos/métodos , Colorantes , Electrodos , Peróxido de Hidrógeno , Hierro , Oxidación-Reducción , Luz Solar , Rayos UltravioletaRESUMEN
The mineralization of sulfanilamide solutions at pH 3.0 was comparatively studied by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF) using a 2.5 L pre-pilot plant containing a Pt/air-diffusion cell coupled with a solar photoreactor. Organics were primordially oxidized by hydroxyl radical (OH) formed from Fenton's reaction between H2O2 generated at the cathode and added Fe(2+) and/or under the action of sunlight. A mineralization up to 94% was achieved using SPEF, whereas EF yielded much poorer degradation. The effect of current density and Fe(2+) and drug concentrations on the degradation rate, mineralization current efficiency and energy cost per unit DOC mass of EF and/or SPEF was examined. The sulfanilamide decay always followed a pseudo first-order kinetics, being more rapid in SPEF due to the additional generation of OH induced by sunlight on Fe(III) species. Catechol, resorcinol, hydroquinone and p-benzoquinone were identified as aromatic intermediates. The final solutions treated by EF contained Fe(III) complexes of maleic, fumaric, oxamic and mainly oxalic acids, which are hardly destroyed by OH. The quick photolysis of Fe(III)-oxalate complexes by sunlight explains the higher oxidation ability of SPEF. The N content of sulfanilamide was mainly mineralized as NH4⺠ion and in much lesser extent as NO3â» ion, whereas most of its initial S was converted into SO4²â» ion.
Asunto(s)
Aire , Peróxido de Hidrógeno/química , Hierro/química , Platino (Metal)/química , Sulfanilamidas/química , Difusión , Técnicas Electroquímicas , Electrodos , Restauración y Remediación Ambiental , Compuestos Férricos/química , Concentración de Iones de Hidrógeno , Radical Hidroxilo/química , Cinética , Oxidación-Reducción , Fotólisis , Proyectos Piloto , Sulfanilamida , Luz Solar , Contaminantes Químicos del Agua/químicaRESUMEN
The electrochemical incineration of omeprazole, a widely prescribed gastrointestinal drug which is detected in natural waters, has been studied in a phosphate buffer of pH 7.0 by anodic oxidation with electrogenerated H(2)O(2) (AO-H(2)O(2)) operating at constant current density (j). The experiments were carried out in a cell equipped with either a Pt or a boron-doped diamond (BDD) anode and an air-diffusion cathode to continuously produce H(2)O(2). In these systems, organics are mainly oxidized by hydroxyl radicals formed at the Pt or BDD surface from water oxidation. A partial total organic carbon (TOC) abatement close to 78% for omeprazole was achieved by AO-H(2)O(2) with a BDD anode after consumption of 18 Ah L(-1) at 100 mA cm(-2), whereas the alternative use of Pt did not allow mineralizing the drug. However, the drug was totally removed using both anodes, although it decayed more rapidly using BDD. In this latter system, increasing j accelerated the degradation process, but lowering the mineralization current efficiency. Greater drug content also enhanced the degradation rate with higher mineralization degree and current efficiency. The kinetics for omeprazole decay always followed a pseudo-first-order reaction and its rate constant increased with increasing j and with decreasing its concentration. Seven heteroaromatic intermediates and four hydroxylated derivatives were detected by LC-MS, while nine short-linear carboxylic acids were identified and quantified by ion-exclusion HPLC. These acids were largely accumulated using Pt and rapidly removed using BDD, thus explaining the partial mineralization of omeprazole achieved by AO-H(2)O(2) with the latter anode. The release of inorganic ions such as NO(3)(-), NH(4)(+) and SO(4)(2-) was followed by ionic chromatography. A plausible reaction sequence for omeprazole mineralization involving all intermediates detected is proposed.
Asunto(s)
Boro/química , Diamante/química , Electroquímica/métodos , Incineración/métodos , Omeprazol/aislamiento & purificación , Platino (Metal)/química , Agua/química , Aire , Carbono/análisis , Ácidos Carboxílicos/análisis , Difusión , Electricidad , Electrodos , Peróxido de Hidrógeno/química , Iones , Cinética , Minerales/química , Nitrógeno/análisis , Omeprazol/análisis , Omeprazol/química , Compuestos Orgánicos/análisis , Oxidación-Reducción , Soluciones , Sulfatos/análisis , Factores de TiempoRESUMEN
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.
Asunto(s)
Boro/química , Electrones , Peróxido de Hidrógeno/química , Hierro/química , Ácidos Sulfanílicos/química , Aire , Difusión , Electrodos , Iones/química , Cinética , Nitrógeno/química , Procesos Fotoquímicos , Factores de TiempoRESUMEN
The mineralization of flumequine, an antimicrobial agent belonging to the first generation of synthetic fluoroquinolones which is detected in natural waters, has been studied by electrochemical advanced oxidation processes (EAOPs) like electro-Fenton (EF) and photoelectro-Fenton (PEF) with UVA light. The experiments were performed in a cell containing a boron-doped diamond (BDD) anode and an air-diffusion cathode to generate H(2)O(2) at constant current. The Fe(2+) ion added to the medium increased the solubility of the drug by the formation of a complex of intense orange colour and also reacted with electrogenerated H(2)O(2) to form hydroxyl radical from Fenton reaction. Oxidant hydroxyl radicals at the BDD surface were produced from water oxidation. A partial mineralization of flumequine in a solution near to saturation with optimum 2.0mM Fe(2+) at pH 3.0 was achieved by EF. The PEF process was more powerful, giving an almost total mineralization with 94-96% total organic carbon removal. Increasing current accelerated both treatments, but with decreasing mineralization current efficiency. Comparative treatments using a real wastewater matrix led to similar degradation degrees. The kinetics for flumequine decay always followed a pseudo-first-order reaction and its rate constant, similar for both EAOPs, raised with increasing current. Generated carboxylic acids like malonic, formic, oxalic and oxamic acids were quantified by ion-exclusion HPLC. Fe(III)-oxalate and Fe(III)-oxamate complexes were the most persistent by-products under EF conditions and their quicker photolysis by UVA light explains the higher oxidation power of PEF. The release of inorganic ions such as F(-), NO(3)(-) and in lesser extent NH(4)(+) was followed by ionic chromatography.
Asunto(s)
Técnicas Electroquímicas/métodos , Fluoroquinolonas/química , Peróxido de Hidrógeno/química , Hierro/química , Procesos Fotoquímicos , Rayos Ultravioleta , Contaminantes Químicos del Agua/química , Purificación del Agua/métodos , Cromatografía por Intercambio Iónico , Estructura Molecular , Oxidación-ReducciónRESUMEN
The anodic oxidation of sulfanilic acid solutions has been studied in acidic medium using a divided cell with a boron-doped diamond (BDD) anode and a stainless steel cathode. Overall mineralization was achieved under all experimental conditions tested due to the efficient destruction of sulfanilic acid and all its by-products with hydroxyl radicals generated at the BDD anode from water oxidation. The alternative use of an undivided cell with the same electrodes gave rise to the coating of the cathode with polymeric compounds, thus preventing the complete electrochemical incineration of sulfanilic acid. The solutions treated in the anodic compartment of the divided cell were degraded at similar rate under pH regulation within the pH interval 2.0-6.0. The mineralization current efficiency was enhanced when the applied current decreased and the initial substrate concentration increased. The decay of sulfanilic acid was followed by reversed-phase HPLC, showing a pseudo first-order kinetics. Hydroquinone and p-benzoquinone were identified as aromatic intermediates by gas chromatography-mass spectrometry and/or reversed-phase HPLC. Maleic, acetic, formic, oxalic and oxamic acids were detected as generated carboxylic acids by ion-exclusion HPLC. Ionic chromatographic analysis of electrolyzed solutions revealed that the N content of sulfanilic acid was mainly released as NH(4)(+) ion and in much smaller proportion as NO(3)(-) ion.
Asunto(s)
Boro/química , Diamante/química , Electrodos , Ácidos Sulfanílicos/química , Eliminación de Residuos Líquidos , Contaminantes Químicos del Agua/química , Cromatografía Liquida , Técnicas Electroquímicas , Cromatografía de Gases y Espectrometría de Masas , Concentración de Iones de Hidrógeno , Oxidación-Reducción , Acero Inoxidable/químicaRESUMEN
The degradation of the beta-blockers atenolol, metoprolol tartrate and propranolol hydrochloride was studied by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF). Solutions of 10 L of 100 mg L⻹ of total organic carbon of each drug in 0.1 M Na2SO4 with 0.5 mM Fe²âº of pH 3.0 were treated in a recirculation flow plant with an electrochemical reactor coupled with a solar compound parabolic collector. Single Pt/carbon felt (CF) and boron-doped diamond (BDD)/air-diffusion electrode (ADE) cells and combined Pt/ADE-Pt/CF and BDD/ADE-Pt/CF cells were used. SPEF treatments were more potent with the latter cell, yielding 95-97% mineralization with 100% of maximum current efficiency and energy consumptions of about 0.250 kWh g TOC⻹. However, the Pt/ADE-Pt/CF cell gave much lower energy consumptions of about 0.080 kWh g TOC⻹ with slightly lower mineralization of 88-93%, then being more useful for its possible application at industrial level. The EF method led to a poorer mineralization and was more potent using the combined cells by the additional production of hydroxyl radicals (â¢OH) from Fenton's reaction from the fast Fe²âº regeneration at the CF cathode. Organics were also more rapidly destroyed at BDD than at Pt anode. The decay kinetics of beta-blockers always followed a pseudo first-order reaction, although in SPEF, it was accelerated by the additional production of â¢OH from the action of UV light of solar irradiation. Aromatic intermediates were also destroyed by hydroxyl radicals. Ultimate carboxylic acids like oxalic and oxamic remained in the treated solutions by EF, but their Fe(III) complexes were photolyzed by solar irradiation in SPEF, thus explaining its higher oxidation power. NO3â» was the predominant inorganic ion lost in EF, whereas the SPEF process favored the production of NH4⺠ion and volatile N-derivatives.
Asunto(s)
Antagonistas Adrenérgicos beta/química , Electroquímica/métodos , Peróxido de Hidrógeno/química , Hierro/química , Fotoquímica/métodos , Contaminantes Químicos del Agua/química , Purificación del Agua/métodos , Atenolol/química , Boro/química , Carbono/química , Diamante/química , Compuestos Férricos/química , Cinética , Metoprolol/química , Nitratos/química , Compuestos de Nitrógeno , Oxidación-Reducción , Platino (Metal)/química , Propranolol/química , Compuestos de Amonio Cuaternario/química , Luz SolarRESUMEN
Solutions of about 0.25 mM of the ß-blocker metoprolol tartrate (100 mg L(-1) total organic carbon) with 0.5 mM Fe(2+) in the presence and absence of 0.1 mM Cu(2+) of pH 3.0 have been comparatively degraded under electro-Fenton (EF) and photoelectro-Fenton (PEF) conditions. The electrolyses were carried out with two systems: (i) a single cell with a boron-doped diamond (BDD) anode and an air-diffusion cathode (ADE) for H(2)O(2) electrogeneration and (ii) a combined cell with a BDD/ADE pair coupled with a Pt/carbon felt (CF) cell. Overall mineralization was reached in all PEF treatments using both systems due to the efficient production of hydroxyl radical ((â¢)OH) from Fenton's reaction induced by UVA light and the quick photolysis of Fe(III) carboxylate complexes formed. In EF, the combined cell was much more potent than the single one by the larger (â¢)OH generation from the continuous Fe(2+) regeneration at the CF cathode, accelerating the oxidation of organics. However, almost total mineralization in EF was feasible using the combined cell in the presence of 0.1 mM Cu(2+), because of the parallel quick oxidation of Cu(II) carboxylate complexes by (â¢)OH. Metoprolol decay always followed a pseudo-first-order reaction. Aromatic products related to consecutive hydroxylation/oxidation reactions of metoprolol were detected by gas chromatography-mass spectrometry. The evolution of the aromatic 4-(2-methoxyethyl)phenol and generated carboxylic acids was followed by HPLC. The degradation rate and mineralization degree of metoprolol tartrate were limited by the removal of Fe(III) and Cu(II) complexes of ultimate carboxylic acids such as formic, oxalic, and oxamic. NH(4)(+) ion and to a lesser extent NO(3)(-) ion were released in all treatments, being quantified by ionic chromatography.
Asunto(s)
Peróxido de Hidrógeno/química , Radical Hidroxilo/química , Hierro/química , Metoprolol/análogos & derivados , Metoprolol/química , Contaminantes Químicos del Agua/química , Boro/química , Diamante/química , Electroquímica/métodos , Electrodos , Electrólisis/métodos , Compuestos Férricos/química , Cromatografía de Gases y Espectrometría de Masas/métodos , Oxidación-Reducción , Fotoquímica/métodos , Platino (Metal)/química , Eliminación de Residuos Líquidos/métodosRESUMEN
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(2)O(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 (OH) formed from Fenton's reaction between added Fe(2+) and electrogenerated H(2)O(2). The PEF treatment in Pt/ADE-Pt/CF system yields almost total mineralization because OH production is enhanced by Fe(2+) regeneration from Fe(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(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(4)(+) and NO(3)(-) ions are released to the medium. A reaction sequence for propranolol hydrochloride mineralization is proposed.
Asunto(s)
Antagonistas Adrenérgicos beta/química , Electroquímica/métodos , Peróxido de Hidrógeno/química , Hierro/química , Fotoquímica/métodos , Propranolol/química , Oxidación-Reducción , Rayos UltravioletaRESUMEN
The treatment of enrofloxacin synthetic wastewaters using conductive-diamond electrochemical oxidation (CDEO), ozonation and Fenton oxidation has been studied. Results show that the three technologies can reduce the organic content of enrofloxacin synthetic wastewaters but with different performances. CDEO was the most efficient technology in terms of mineralization but not on COD removal, which was more efficiently achieved by ozonation. This indicates that ozonation is efficient in the breakage of the complex molecules but not on the removal of final carboxylic acids. The high initial efficiency in terms of oxidant-use obtained by Fenton oxidation evidences that it is very efficient in the removal of the enrofloxacin, although it rapidly leads to the formation of refractory compounds to the treatment. This indicates the significance of other oxidation mechanisms (e.g. coagulation) that enhance the results obtained by the expected hydroxyl-mediated oxidation. Ammonium ions were the primary product species in CDEO and nitrate ions in ozonation, whereas Fenton effluents contained similar amounts of both nitrogen ionic species.
Asunto(s)
Diamante/química , Conductividad Eléctrica , Técnicas Electroquímicas , Fluoroquinolonas/química , Peróxido de Hidrógeno/química , Hierro/química , Ozono/química , Carbono/química , Carbono/aislamiento & purificación , Enrofloxacina , Nitrógeno/química , Oxidantes/química , Oxidación-Reducción , Factores de TiempoRESUMEN
Electrochemical advanced oxidation processes (EAOPs) are environmentally friendly methods based on the destruction of organic pollutants in wastewaters with in situ electrogenerated hydroxyl radical. This species is formed in anodic oxidation (AO) from water oxidation at the anode and in indirect electro-oxidation methods like electro-Fenton (EF) and photoelectro-Fenton (PEF) also from reaction between catalytic Fe2+ and H2O2 continuously produced at the O2-diffusion cathode. The PEF method involves the irradiation of the treated solution with UVA light to enhance the photolysis of organics including Fe(III) complexes. In this work, the oxidation power of such EAOPs to decontaminate synthetic wastewaters of the biocide chloroxylenol (4-chloro-3,5-dimethylphenol) at pH 3.0 is comparatively examined with an undivided electrolytic cell containing a Pt or boron-doped diamond (BDD) anode and a stainless steel or O2-diffusion cathode. The initial chlorine is released as Cl(-) ion, which remains stable in the medium using Pt or is oxidized to Cl2 on BDD. The biocide solutions can be completely decontaminated using AO with a BDD anode, as well as PEF with a Pt or BDD anode. The PEF procedure with a BDD anode is the most powerful method leading to total mineralization in about 300 min, practically independent of current density. When current density rises, the degradation rate of processes increases, but they become less efficient due to the larger enhancement of waste reactions of oxidants. Chloroxylenol is much more rapidly removed in EF and PEF than in AO. 2,6-dimethylhydroquinone, 2,6-dimethyl-p-benzoquinone and 3,5-dimethyl-2-hydroxy-p-benzoquinone are identified as aromatic by-products, and maleic, malonic, pyruvic, acetic and oxalic acids are found as generated carboxylic acids. A general pathway for chloroxylenol mineralization by all EAOPs including the above by-products is proposed.
Asunto(s)
Desinfectantes/química , Electroquímica/métodos , Restauración y Remediación Ambiental/métodos , Minerales/química , Xilenos/química , Oxidación-ReducciónRESUMEN
Solutions containing 164 mg L(-1) salicylic acid of pH 3.0 have been degraded by electrochemical advanced oxidation processes such as anodic oxidation, anodic oxidation with electrogenerated H(2)O(2), electro-Fenton, photoelectro-Fenton and solar photoelectro-Fenton at constant current density. Their oxidation power has been comparatively studied in a one-compartment cell with a Pt or boron-doped diamond (BDD) anode and a graphite or O(2)-diffusion cathode. In the three latter procedures, 0.5mM Fe(2+) is added to the solution to form hydroxyl radical (()OH) from Fenton's reaction between Fe(2+) and H(2)O(2) generated at the O(2)-diffusion cathode. Total mineralization is attained for all methods with BDD and for photoelectro-Fenton and solar photoelectro-Fenton with Pt. The poor decontamination achieved in anodic oxidation and electro-Fenton with Pt is explained by the slow removal of most pollutants by ()OH formed from water oxidation at the Pt anode in comparison to their quick destruction with ()OH produced at BDD. ()OH generated from Fenton's reaction oxidizes rapidly all aromatic pollutants, but it cannot destroy final Fe(III)-oxalate complexes. Solar photoelectro-Fenton treatments always yield quicker degradation rate due to the very fast photodecarboxylation of these complexes by UVA irradiation supplied by solar light. The effect of current density on the degradation rate, efficiency and energy cost of all methods is examined. The salicylic acid decay always follows a pseudo-first-order kinetics. 2,3-Dihydroxybenzoic, 2,5-dihydroxybenzoic, 2,6-dihydroxybenzoic, alpha-ketoglutaric, glycolic, glyoxylic, maleic, fumaric, malic, tartronic and oxalic acids are detected as oxidation products. A general reaction sequence for salicylic acid mineralization considering all these intermediates is proposed.
Asunto(s)
Ácido Salicílico/química , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua/química , Boro/química , Diamante/química , Electrodos , Electrólisis , Grafito/química , Peróxido de Hidrógeno/química , Concentración de Iones de Hidrógeno , Residuos Industriales , Hierro/química , Oxidación-Reducción , Platino (Metal)/químicaRESUMEN
Acidic aqueous solutions of clofibric acid (2-(4-chlorophenoxy)-2-methylpropionic acid), the bioactive metabolite of various lipid-regulating drugs, have been degraded by indirect electrooxidation methods such as electro-Fenton and photoelectro-Fenton with Fe(2+) as catalyst using an undivided electrolytic cell with a Pt anode and an O(2)-diffusion cathode able to electrogenerate H(2)O(2). At pH 3.0 about 80% of mineralization is achieved with the electro-Fenton method due to the efficient production of oxidant hydroxyl radical from Fenton's reaction between Fe(2+) and H(2)O(2), but stable Fe(3+) complexes are formed. The photoelectro-Fenton method favors the photodecomposition of these species under UVA irradiation, reaching more than 96% of decontamination. The mineralization current efficiency increases with rising metabolite concentration up to saturation and with decreasing current density. The photoelectro-Fenton method is then viable for treating acidic wastewaters containing this pollutant. Comparative degradation by anodic oxidation (without Fe(2+)) yields poor decontamination. Chloride ion is released during all degradation processes. The decay kinetics of clofibric acid always follows a pseudo-first-order reaction, with a similar rate constant in electro-Fenton and photoelectro-Fenton that increases with rising current density, but decreases at greater metabolite concentration. 4-Chlorophenol, 4-chlorocatechol, 4-chlororesorcinol, hydroquinone, p-benzoquinone and 1,2,4-benzenetriol, along with carboxylic acids such as 2-hydroxyisobutyric, tartronic, maleic, fumaric, formic and oxalic, are detected as intermediates. The ultimate product is oxalic acid, which forms very stable Fe(3+)-oxalato complexes under electro-Fenton conditions. These complexes are efficiently photodecarboxylated in photoelectro-Fenton under the action of UVA light.