RESUMO
A treatment unit packed by granular adsorbent of Fe-Mn binary oxide incorporated into diatomite (FMBO(1:1)-diatomite) was studied to remove arsenic from anaerobic groundwater without any pre-treatment or post-treatment. The raw anaerobic groundwater containing 35-45 microg/L of arsenic was collected from suburb of Beijing. Arsenic (III) constituted roughly 60%-80% of the total arsenic content. Approximately 7,000 bed volumes (ratio of effluent volume to adsorbent volume) treated water with arsenic concentration below 10 microg/L were produced in the operation period of four months. The regeneration of FMBO (1:1)-diatomite had been operated for 15 times. In the first stage, the regeneration process significantly improved the adsorption capacity of FMBO (1:1)-diatomite. With increased loading amount of Fe-Mn binary oxide, the adsorption capacity for arsenic decreased 20%-40%. Iron and manganese in anaerobic groundwater were oxidized and adsorptive filtrated by FMBO (1:1)-diatomite efficiently. The final concentrations of iron and manganese in effluents were nearly zero. The continued safe performance of the treatment units proved that adsorbent FMBO (1:1)-diatomite had high oxidation ability and exhibited strong adsorptive filtration.
Assuntos
Arsênio/química , Terra de Diatomáceas/química , Compostos Férricos/química , Água Doce/química , Compostos de Manganês/química , Óxidos/química , Poluentes Químicos da Água/química , Purificação da Água/métodos , Adsorção , Microscopia Eletrônica de VarreduraRESUMO
A novel photoanode was prepared by immobilizing TiO(2) film onto activated carbon fibers (TiO(2)/ACF) using liquid phase deposition (LPD) to study the electro-photocatalytic (EPC) degradation of organic compounds exemplified by an azo-dye, namely, Acid Orange II (AOII). Results demonstrated that by applying a 0.5 V bias (vs. SCE) across the TiO(2)/ACF electrode, the AOII degradation rate was increased significantly compared to that of photocatalytic (PC) oxidation. The application of an electric field promotes the separation of photogenerated electrons and holes as confirmed by electrochemical impedance spectroscopy (EIS) measurements. The structural and surface morphology of the TiO(2)/ACF electrode was characterized by field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD). SEM images showed that TiO(2) was deposited on almost every carbon fiber with an average thickness of about 200 nm with the inner space between neighboring fibers being maintained unfilled. The morphological features of the photo-anode facilitated the passage of solution as well as UV light through the felt-form electrode and created a three-dimensional environment favorable to EPC oxidation. Both the large outer surface area of the 3D electrode and the good organic adsorption capacity of the ACF support promoted high contact efficiency between AOII and TiO(2) surface. Anatase was the major crystalline TiO(2) deposited. UV-vis spectrophotometry, TOC (total organic carbon) analysis, and HPLC technique were used to monitor the concentration change of AOII and intermediates as to gain insight into the EPC degradation of AOII using the TiO(2)/ACF electrode.
Assuntos
Compostos Azo/química , Carbono/química , Naftalenos/química , Titânio/química , Poluentes Químicos da Água/química , Purificação da Água/métodos , Adsorção , Fibra de Carbono , Impedância Elétrica , Técnicas Eletroquímicas , Eletrodos , Microscopia Eletrônica de Varredura , Oxirredução , Processos Fotoquímicos , Difração de Raios XRESUMO
The Pd/Sn-modified activated carbon fiber (ACF) electrodes were successfully prepared by the impregnation of Pd2+ and Sn2+ ions onto ACF, and their electrocatalytic reduction capacity for nitrate ions in water was evaluated in a batch experiment. The electrode was characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), X-ray photoelectron spectrum (XPS) and temperature programmed reduction (TPR). The capacity for nitrate reduction depending on Sn content on the electrode and the pH of electrolyte was discussed at length. The results showed that at an applied current density of 1.11 mA cm(-2), nitrate ions in water (solution volume: 400 mL) were reduced from 110 to 3.4 mg L(-1) after 240 min with consecutive change of intermediate nitrite. Ammonium ions and nitrogen were formed as the main final products. The amount of other possible gaseous products (including NO and N2O) was trace. With the increase of Sn content on the Pd/Sn-modified ACF electrode, the activity for nitrate reduction went up to reach a maximum (at Pd/Sn = 4) and then decreased, while the selectivity to N2 was depressed. Higher pH value of electrolyte exhibited more suppression effect on the reduction of nitrite than that of nitrate. However, no significant influence on the final ammonia formation was observed. Additionally, Cu ion in water was found to cover the active sites of the electrode to make the electrode deactivated.
Assuntos
Carbono/química , Eletrodos , Nitratos/química , Paládio/química , Estanho/química , Poluentes Químicos da Água/isolamento & purificação , Catálise , Concentração de Íons de Hidrogênio , Microscopia Eletrônica , Oxirredução , Difração de Raios XRESUMO
A novel technology which combined electrochemical process catalyzed by manganese mineral with electro-assisted coagulation process was proposed in this study. The mineralization of organic pollutant from simulated dye wastewater containing an azo dye Acid Red B (ARB) was experimentally investigated using this method. It was found that the manganese mineral could catalyze the electrochemical process dramatically. The TOC removal percentage of electrochemical treatment catalyzed by manganese mineral was 43.6% while the TOC removal percentage of the process using the manganese mineral alone and using the electrolysis alone were 9.3% and 20.8%, respectively. Moreover, it was found that combined electroxidation with electro-assisted coagulation process could more effectively eliminate ARB. After a period of 180 min electrooxidation and 300 min electroreduction, almost 66.9% of TOC was removed, and the dissolved Mn2+ could be effectivly removed. The effects of the order of oxidation and reduction, the proper ratio electrooxidation/reduction time, and current density on the removal efficiency were investigated in detail. In addition, a proposed mechanism of manganese-mineral-catalyzed electrooxidation-reduction process was discussed in this paper.
Assuntos
Corantes/química , Eletroquímica/instrumentação , Manganês/química , Poluentes Químicos da Água/química , Cinética , OxirreduçãoRESUMO
Ferrate is an excellent water treatment agent for its multi-functions in oxidation, disinfection, coagulation and adsorption, but its coagulation ability depends on its dosage and is after its oxidation. This paper focuses on preparing a new kind of ferrate combined with alum to enhance its coagulation function for water purification. An effective electrolysis reactor was designed and employed in the test. Some key parameters in the process of electrolysis concerning the preparation efficiency, such as the current density, temperature and alkalinity were also investigated. The proper conditions for ferrate-alum preparation were determined. Under the condition of 5 V given voltage, 6 h electrolyzing interval, below 2% alum concentration (in weight), a combined liquid ferrate-alum products was successfully prepared, which contained 0.0294 mol/L FeO4(2-) and 0.0302 mol/L total soluble ferron with 2% Al2O3. There was no insoluble ferron produced by controlling an optimum electrochemical condition.
Assuntos
Ferro/química , Purificação da Água/métodos , Compostos de Alúmen/química , Eletroquímica , OxirreduçãoRESUMO
A combined bioelectrochemical and sulfur autotrophic denitrification system (CBSAD) was evaluated to treat a groundwater with nitrate contamination (20.9-22.0mgNO(3)(-)-N/L). The reactor was operated continuously for several months with groundwater to maximize treatment efficiency under different hydraulic retention times (HRT) and electric currents. The denitrification rate of sulfur autotrophic part followed a half-order kinetics model. Moreover, the removal efficiency of bioelectrochemical part depended on the electric current. The reactor could be operated efficiently at the HRT ranged from 4.2 to 2.1h (corresponding nitrogen volume-loading rates varied from 0.12 to 0.24 kg N/m(3)d; and optimum current ranged from 30 to 1000 mA), and the NO(3)(-)-N removal rate ranged from 95% to 100% without NO(3)(-)-N accumulation. The pH of effluent was satisfactorily adjusted by bioelectrochemical part, and the sulfate concentration of effluent was lower than 250 mg/L, meeting the drinking water standard of China EPA.
Assuntos
Bactérias Anaeróbias/metabolismo , Reatores Biológicos/microbiologia , Eletroquímica/instrumentação , Nitratos/metabolismo , Enxofre/metabolismo , Poluentes Químicos da Água/metabolismo , Purificação da Água/instrumentação , Processos Autotróficos/fisiologia , Simulação por Computador , Desenho de Equipamento , Análise de Falha de Equipamento , Modelos Biológicos , Nitratos/isolamento & purificação , Enxofre/isolamento & purificação , Integração de SistemasRESUMO
Algae in waters often bring about influence in drinking water supplies. In this study, an electrochemical tube employing titanium coated with RuO2 as anode was constructed for inactivation of cyanobacteria (often called bluegreen algae) Microcystis aeruginosa. Suspensions containing M. aeruginosa (2-4 x 10(9) L(-1)) were exposed to current densities ranging from 1 to 10 mA cm(-2) in a detention time of 52 min. The variations of cell density, chlorophyll-a, optical density, pH, and conductivity were examined during the treatment. After 3.5 min the population of M. aeruginosa dropped rapidly and was reduced from 3 x 10(9) to 0.6 x 10(9) L(-1) after 52 min at current densities from 5 to 10 mA cm(-2). The cell density and optical density of M. aeruginosa decreased proportionally to the current density and the detention time. Scanning electron microscopy investigation of algae revealed surface damage and apparent leakage of intracellular contents after electrochemical cycling process. Due to the damage of cells, the chlorophyll-a released from the cells was degraded by electrochemical oxidation. The removal rate of chlorophyll-a could reach 96% at the current density of 10 mA cm(-2). Electrochemical treatment caused minor variation of pH values and conductivity of the suspensions. After electrochemical cycling processes, the optical density at 680 nm of algal cell suspensions remained below 0.1 after 6 days, and it showed that cells had no potential to survive and grow. The results implicated that the inactivation of M. aeruginosa was successfully performed by the electrochemical treatment, and it made the algal cells lose ability to survive, demonstrating the potential of such an alternative process for efficient water purification.
Assuntos
Eletroquímica/métodos , Viabilidade Microbiana , Microcystis/química , Compostos de Rutênio/química , Titânio/química , Purificação da Água/métodos , Análise de Variância , Clorofila/química , Clorofila A , Condutividade Elétrica , Eletrodos , Concentração de Íons de Hidrogênio , Microcystis/ultraestrutura , Microscopia Eletrônica de VarreduraRESUMO
Triolein is successfully embedded into cellulose acetate (CA) by phase inversion. This prepared flat membrane can effectively remove trace lipophilic organic pollutants from water. Structure of hybrid membrane is mainly observed by scanning electron microscope (SEM). Triolein dispersion by mechanical rabbling and ultrasound are investigated. Ultrasound can more effectively strengthen triolein dispersion than mechanical rabbling. Effect of casting membrane temperature (room temperature, 0 degrees C) shows low temperature can help to forming smaller triolein droplets. In addition, interaction between triolein and CA belongs to physical mixing by the observation of FT-IR, accordingly triolein structure is not changed and adsorptive capacity for persistent organic pollutants is not affected. Triolein in hexane is analyzed by fluorometric measure. The results show that triolein is completely embedded into membrane, so it is impossible that triolein leaks into water in the process of the adsorption.
Assuntos
Celulose/análogos & derivados , Filtros Microporos , Trioleína/química , Poluentes Químicos da Água/química , Adsorção , Celulose/química , Monitoramento Ambiental , Membranas Artificiais , Filtros Microporos/normas , Trioleína/análise , Purificação da Água/métodosRESUMO
In this paper, an applicable swept pulsed equipment was developed to treat the domestic wastewater and the effect of swept pulsed electromagnetic field on disinfection was studied. It was found that the effect was obvious and the disinfection performance of electromagnetic field was increased with the increasing of the pH, the temperature, the treatment time and the bactericidal concentration. The experimental results showed that the amounts of total bacterium and coliform per milliliter were decreased from 7.2 x 10(6) to 2.2 x 10(4) and from 9.2 x 10(5) to 3.5 x 10(4) respectively after the treatment period of 4 h when the temperature was 25 degrees C and pH 9.0. Corresponding, the removal efficiency of total bacterium were 99.7% and 96.2%.