Examinando por Materia "Effluents"

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    Ítem
    Efficient treatment for textile wastewater through sequential electrocoagulation, electrochemical oxidation and adsorption processes: Optimization and toxicity assessment
    (Elsevier BV, 2020-01-01) GilPavas E.; Dobrosz-Gómez I.; Gómez-García M.-Á.; GilPavas E.; Dobrosz-Gómez I.; Gómez-García M.-Á.; Universidad EAFIT. Departamento de Ingeniería de Procesos; Procesos Ambientales (GIPAB)
    In this work, the sequential Electrocoagulation + Electro-oxidation + Activated carbon adsorption (EC + EO + AC) process was studied as an alternative for the treatment of an industrial textile wastewater (TWW) issuing from a manufacturing company located in Medellín (Colombia). The EC's and EO's operational conditions were optimized using a Box-Behnken experimental design, the Response Surface Methodology and a constrained nonlinear optimization algorithm in terms of organic matter degradation efficiency. The best performance for EC (i. e., dye removal = 94%, COD and TOC degradation of 45 and 40%, respectively) was obtained using Fe anode and Boron Doped Diamond (BDD) cathode, with current density, jEC, equals to 5 mA/cm2, pH = 9.3, 60 RPM and 10 min of electrolysis. After EC treatment, the effluent biodegradability (evaluated as the BOD5/COD ratio) increases from 0.14 to 0.23. Regrettably, EC was not effective for the removal of acute toxicity to Artemia salina since the treated effluent remained very toxic (100%). The treatment of EC's effluent by EO enhanced organic pollutant removal. For EC + EO sequential process, EO optimal operational conditions (jEO = 10 mA/cm2, pH = 3, 240 RPM, BDD as anode and Fe as cathode) allowed reduction of 100% of color, 88% of COD and 79% of TOC after 30 min of electrolysis. Moreover, the BOD5/COD ratio increased from 0.23 to 0.58; however, the treated effluent remained very toxic to the Artemia salina. Consequently, an activated carbon adsorption step was included to complete the treatment process. Thus, by coupling the EC + EO + AC process, effluent's acute toxicity decreased completely. From molecular weight distribution analysis, it was concluded that EC + EO was efficient in eliminating low molecular weight (< 5 kDa) compounds. Finally, the operation cost, which includes chemical reagents, electrodes, energy consumption, and sludge disposal, for the EC + EO + AC sequential process was estimated in 3.83 USD /m3. © 2020 Elsevier B.V.
  • No hay miniatura disponible
    Ítem
    Efficient treatment for textile wastewater through sequential electrocoagulation, electrochemical oxidation and adsorption processes: Optimization and toxicity assessment
    (Elsevier BV, 2020-01-01) GilPavas E.; Dobrosz-Gómez I.; Gómez-García M.-Á.; Universidad EAFIT. Departamento de Ingeniería de Procesos; Desarrollo y Diseño de Procesos
    In this work, the sequential Electrocoagulation + Electro-oxidation + Activated carbon adsorption (EC + EO + AC) process was studied as an alternative for the treatment of an industrial textile wastewater (TWW) issuing from a manufacturing company located in Medellín (Colombia). The EC's and EO's operational conditions were optimized using a Box-Behnken experimental design, the Response Surface Methodology and a constrained nonlinear optimization algorithm in terms of organic matter degradation efficiency. The best performance for EC (i. e., dye removal = 94%, COD and TOC degradation of 45 and 40%, respectively) was obtained using Fe anode and Boron Doped Diamond (BDD) cathode, with current density, jEC, equals to 5 mA/cm2, pH = 9.3, 60 RPM and 10 min of electrolysis. After EC treatment, the effluent biodegradability (evaluated as the BOD5/COD ratio) increases from 0.14 to 0.23. Regrettably, EC was not effective for the removal of acute toxicity to Artemia salina since the treated effluent remained very toxic (100%). The treatment of EC's effluent by EO enhanced organic pollutant removal. For EC + EO sequential process, EO optimal operational conditions (jEO = 10 mA/cm2, pH = 3, 240 RPM, BDD as anode and Fe as cathode) allowed reduction of 100% of color, 88% of COD and 79% of TOC after 30 min of electrolysis. Moreover, the BOD5/COD ratio increased from 0.23 to 0.58; however, the treated effluent remained very toxic to the Artemia salina. Consequently, an activated carbon adsorption step was included to complete the treatment process. Thus, by coupling the EC + EO + AC process, effluent's acute toxicity decreased completely. From molecular weight distribution analysis, it was concluded that EC + EO was efficient in eliminating low molecular weight (< 5 kDa) compounds. Finally, the operation cost, which includes chemical reagents, electrodes, energy consumption, and sludge disposal, for the EC + EO + AC sequential process was estimated in 3.83 USD /m3. © 2020 Elsevier B.V.
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    Ítem
    Mineralization of cyanide originating from gold leaching effluent using electro-oxidation: multi-objective optimization and kinetic study
    (SPRINGER, 2020-01-01) Dobrosz-Gómez I.; Gómez García M.Á.; Gaviria G.H.; GilPavas E.; Universidad EAFIT. Departamento de Ingeniería de Procesos; Desarrollo y Diseño de Procesos
    Abstract: This study examines the electro-oxidation (EO) of cyanide originating from an industrial plant´s gold leaching effluent. Experiments were carried out in a laboratory-scale batch cell reactor. Monopolar configuration of electrodes consisting of graphite (anode) and aluminum (cathode) was employed, operating in galvanostatic mode. Response Surface Methodology (RSM), based on a Box–Behnken experimental Design (BBD), was used to optimize the EO operational conditions. Three independent process variables were considered: initial cyanide concentration ([CN-]0 = 1000–2000 mg L-1), current density (J =7–107 mA cm-2), and stirring velocity (? = 250–750 rpm). The cyanide conversion (XCN-), Chemical Oxygen Demand (COD) removal percentage (%RCOD), and specific Energy Consumption per unit mass of removed cyanide (EC) were analyzed as response variables. Multi-objective optimization let to establish the most effective EO conditions ([CN-]0 = 1000 mg L-1, J = 100 mA cm-2 and ? = 750 rpm). The experimental data (XCN-, %RCOD, and EC) were fitted to second-order polynomial models with adjusted correlation coefficients (Radj2) of ca. 98, 99 and 87%, respectively. The kinetic analysis, performed at optimal EO operational conditions, allowed determination of time required to meet Colombian permissible discharge limits. The predictive capacity of kinetic expressions was verified against experimental data obtained for gold leaching effluent. Total cyanide removal and 96% of COD reduction were obtained, requiring EC of 71.33 kWh kg-1 and 180 min. The BOD5 (biological oxygen demand)/COD ratio increased from 4.52 × 10-4 to 0.5573, confirming effluent biodegradability after EO treatment. Graphic Abstract: [Figure not available: see fulltext.]The variation of cyanide (CN-), cyanate (CNO-) and ammonium (NH4 +) ions concentrations vs. time at alkaline conditions. EO operational conditions: [CN-]0 = 1000 mg/L, J = 100 mA/cm2 , ? = 750 rpm, [NaCl] = 0.15 M and pH 11.1. © 2020, Springer Nature B.V.
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    Ítem
    Mineralization of cyanide originating from gold leaching effluent using electro-oxidation: multi-objective optimization and kinetic study
    (SPRINGER, 2020-01-01) Dobrosz-Gómez I.; Gómez García M.Á.; Gaviria G.H.; GilPavas E.; Dobrosz-Gómez I.; Gómez García M.Á.; Gaviria G.H.; GilPavas E.; Universidad EAFIT. Departamento de Ingeniería de Procesos; Procesos Ambientales (GIPAB)
    Abstract: This study examines the electro-oxidation (EO) of cyanide originating from an industrial plant´s gold leaching effluent. Experiments were carried out in a laboratory-scale batch cell reactor. Monopolar configuration of electrodes consisting of graphite (anode) and aluminum (cathode) was employed, operating in galvanostatic mode. Response Surface Methodology (RSM), based on a Box–Behnken experimental Design (BBD), was used to optimize the EO operational conditions. Three independent process variables were considered: initial cyanide concentration ([CN-]0 = 1000–2000 mg L-1), current density (J =7–107 mA cm-2), and stirring velocity (? = 250–750 rpm). The cyanide conversion (XCN-), Chemical Oxygen Demand (COD) removal percentage (%RCOD), and specific Energy Consumption per unit mass of removed cyanide (EC) were analyzed as response variables. Multi-objective optimization let to establish the most effective EO conditions ([CN-]0 = 1000 mg L-1, J = 100 mA cm-2 and ? = 750 rpm). The experimental data (XCN-, %RCOD, and EC) were fitted to second-order polynomial models with adjusted correlation coefficients (Radj2) of ca. 98, 99 and 87%, respectively. The kinetic analysis, performed at optimal EO operational conditions, allowed determination of time required to meet Colombian permissible discharge limits. The predictive capacity of kinetic expressions was verified against experimental data obtained for gold leaching effluent. Total cyanide removal and 96% of COD reduction were obtained, requiring EC of 71.33 kWh kg-1 and 180 min. The BOD5 (biological oxygen demand)/COD ratio increased from 4.52 × 10-4 to 0.5573, confirming effluent biodegradability after EO treatment. Graphic Abstract: [Figure not available: see fulltext.]The variation of cyanide (CN-), cyanate (CNO-) and ammonium (NH4 +) ions concentrations vs. time at alkaline conditions. EO operational conditions: [CN-]0 = 1000 mg/L, J = 100 mA/cm2 , ? = 750 rpm, [NaCl] = 0.15 M and pH 11.1. © 2020, Springer Nature B.V.
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    Multifactorial optimization of the decolorisation parameters of wastewaters resulting from dyeing flowers.
    (IWA PUBLISHING, 2009-01-01) Gil Pavas, Edison; Angel Gomez-Garcia, Miguel; Gil Pavas, Edison; Angel Gomez-Garcia, Miguel; Universidad EAFIT. Departamento de Ingeniería de Procesos; Procesos Ambientales (GIPAB)
    This work deals with the treatment of the wastewaters resulting from the process of dyeing flowers. In some local cases for growing flowers near to Medellin (Colombia), wastewater color was found to be one of the main problems in meeting local effluent standards. Wastewaters were treated by photodegradation process (which includes photocatalysis) to achieve the degradation of dyes mixture and organic matter in the wastewater. A multifactorial experimental design was proposed, including as experimental factors the following variables: pH, and the concentration of both catalyst (TiO(2)) and hydrogen peroxide (H(2)O(2)). According to the obtained results, at the optimized variables values, it is possible to reach a 99% reduction of dyes, a 76.9% of mineralization (TOC) and a final biodegradability of 0.834. Kinetic analysis allows proposing a pseudo first order reaction for the reduction, the mineralization, and the biodegradation processes.
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    Ítem
    Optimization and toxicity assessment of a combined electrocoagulation, H2O2/Fe2+/UV and activated carbon adsorption for textile wastewater treatment
    (Elsevier, 2019-02-15) GilPavas, E; Dobrosz-Gomez, I; Gomez-Garcia, MA; GilPavas, E; Dobrosz-Gomez, I; Gomez-Garcia, MA; Universidad EAFIT. Departamento de Ingeniería de Procesos; Procesos Ambientales (GIPAB)
    In this study, the potential application of sequential Electrocoagulation + Fenton (F) or Photo-Fenton (PF) + Active carbon adsorption (EC + F/PF + AC) processes were analyzed as alternatives for the treatment of an industrial textile wastewater resulting from an industrial facility located in Medellín (Colombia). In order to maximize the organic matter degradation, each step of the treatment was optimized using the Response Surface Methodology. At first, the optimal performance of EC was achieved with Fe electrodes operating at pH = 7, jEC = 10 mA/cm2 and 60 rpm, during 10 min of electrolysis. At these conditions, EC let to remove 94% of the dye's color, 56% of the COD and 54% of the TOC. Next, sequentially applied Fenton or photo-Fenton process (i.e., EC + F/PF), operating at the optimized conditions (pH = 4.3, [Fe2+] = 1.1 mM, [H2O2] = 9.7 mM, stirring velocity = 100 rpm and reaction time = 60 min.), improved the quality of the treated effluent. The EC + F let to achieve total color reduction, as well as COD and TOC removals of 72 and 75%, respectively. The EC + PF reached 100% of color, 76% of COD and 78% of TOC reductions. The EC + F/PF processes were more efficient than EC in elimination of low molecular weight (<5 kDa) compounds from wastewater. Moreover, the BOD5/COD ratio increased from 0.21 to 0.42 and from 0.21 to 0.46 using EC + F and EC + PF processes, respectively. However, EC + F/PF were not fully effective for the removal of acute toxicity to Artemia salina: 20% and 60% of reduction in toxicity using EC + F and EC + PF, respectively, comparing to very toxic (100%) raw textile wastewater. Thus, activated carbon adsorption was applied as an additional step to complete the treatment. After AC adsorption, the acute toxicity decreased to 10% and 0% using EC + F and EC + PF, respectively. The total operational costs, including chemical reagents, electrodes, energy consumption and sludge disposal, were of 1.65 USD/m3 and 2.3 USD/m3 for EC + F and EC + PF, respectively. © 2018 Elsevier B.V.
  • No hay miniatura disponible
    Ítem
    Optimization and toxicity assessment of a combined electrocoagulation, H2O2/Fe2+/UV and activated carbon adsorption for textile wastewater treatment
    (Elsevier, 2019-02-15) GilPavas, E; Dobrosz-Gomez, I; Gomez-Garcia, MA; Universidad EAFIT. Departamento de Ingeniería de Procesos; Desarrollo y Diseño de Procesos
    In this study, the potential application of sequential Electrocoagulation + Fenton (F) or Photo-Fenton (PF) + Active carbon adsorption (EC + F/PF + AC) processes were analyzed as alternatives for the treatment of an industrial textile wastewater resulting from an industrial facility located in Medellín (Colombia). In order to maximize the organic matter degradation, each step of the treatment was optimized using the Response Surface Methodology. At first, the optimal performance of EC was achieved with Fe electrodes operating at pH = 7, jEC = 10 mA/cm2 and 60 rpm, during 10 min of electrolysis. At these conditions, EC let to remove 94% of the dye's color, 56% of the COD and 54% of the TOC. Next, sequentially applied Fenton or photo-Fenton process (i.e., EC + F/PF), operating at the optimized conditions (pH = 4.3, [Fe2+] = 1.1 mM, [H2O2] = 9.7 mM, stirring velocity = 100 rpm and reaction time = 60 min.), improved the quality of the treated effluent. The EC + F let to achieve total color reduction, as well as COD and TOC removals of 72 and 75%, respectively. The EC + PF reached 100% of color, 76% of COD and 78% of TOC reductions. The EC + F/PF processes were more efficient than EC in elimination of low molecular weight (<5 kDa) compounds from wastewater. Moreover, the BOD5/COD ratio increased from 0.21 to 0.42 and from 0.21 to 0.46 using EC + F and EC + PF processes, respectively. However, EC + F/PF were not fully effective for the removal of acute toxicity to Artemia salina: 20% and 60% of reduction in toxicity using EC + F and EC + PF, respectively, comparing to very toxic (100%) raw textile wastewater. Thus, activated carbon adsorption was applied as an additional step to complete the treatment. After AC adsorption, the acute toxicity decreased to 10% and 0% using EC + F and EC + PF, respectively. The total operational costs, including chemical reagents, electrodes, energy consumption and sludge disposal, were of 1.65 USD/m3 and 2.3 USD/m3 for EC + F and EC + PF, respectively. © 2018 Elsevier B.V.
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    Ítem
    Statistical optimization of industrial textile wastewater treatment by electrochemical methods
    (SPRINGER, 2014-12-01) GilPavas, Edison; Medina, Jose; Dobrosz-Gomez, Izabela; Angel Gomez-Garcia, Miguel; GilPavas, Edison; Medina, Jose; Dobrosz-Gomez, Izabela; Angel Gomez-Garcia, Miguel; Universidad EAFIT. Departamento de Ingeniería de Procesos; Procesos Ambientales (GIPAB)
    In this work, the Box–Behnken experimental design and the surface response methodology were applied for the optimization of the operational conditions of the electro-catalytic degradation of wastewaters, resulting from a local textile industry. The experiments were carried out in a laboratory scale batch cell reactor, with monopolar configuration, and electrodes made of boron-doped diamond (anode) and titanium (cathode). The multifactorial experimental design included the following variables: current density (i: 5–10 ?mA/cm2), pH (3–7), and submerged cathode area (CA: 8–24 ?cm2). To determine the process efficiency, the degradation percentage of: the chemical oxygen demand (%DCOD), the total organic carbon (%DTOC) and the color (%DC) were defined as response variables. The following optimal conditions for the electro-oxidation (EO) process were obtained: i ?= ?10 ?mA/cm2, pH = 3 and CA ?= ?16 ?cm2, reaching ca. 92 ?% of DC, 37 ?% of DCOD and 31 ?% of DTOC. The electro-Fenton (EF) and photo-electro-Fenton (PEF) processes were also evaluated at EO optimal conditions. For the EF process, with addition of iron (0.3 ?mM), the %DC, %DCOD and %DTOC was enhanced to 95, 52 and 45 ?%, respectively. For the PEF process (UV ?= ?365 ?nm), it was possible to reach 98 ?%DC, 56 ?%DCOD and 48 ?%DTOC. © 2014, Springer Science+Business Media Dordrecht.