boron and sodium-sulfate

In this work, the combination of biological and electrochemical processes to mineralize oxyfluorfen has been studied. First, an acclimatized mixed-culture biological treatment was used to degrade the biodegradable fraction of the pesticide, reaching up to 90% removal. After that, the non-biodegraded fraction was oxidised by electrolysis using boron-doped diamond as the anode. The results showed that the electrochemical technique was able to completely mineralize the residual pollutants. The study of the influence of the supporting electrolyte on the electrochemical process showed that the trace mineral solution used in the biological treatment was enough to completely mineralize the oxyfluorfen, resulting in total organic carbon removal rates that were well-fitted by a first-order model with a kinetic constant of 0.91 h

Topics: Bioreactors; Boron; Diamond; Electrodes; Electrolysis; Halogenated Diphenyl Ethers; Kinetics; Oxidation-Reduction; Pesticides; Sulfates; Waste Disposal, Fluid; Water Pollutants, Chemical

In this work, ecotoxicological bioassays based on Lactuca sativa seeds and bioluminescent bacterium (Vibrio fischeri) have been carried out in order to quantify the toxicity of Norfloxacin (NOR) and sodium sulfate solutions, before and after treating them using electrochemical advanced oxidation. The effect of some process variables (anode material, reactor configuration and applied current) on the toxicity evolution of the treated solution has been studied. A NOR solution shows an EC

Topics: Aliivibrio fischeri; Boron; Ceramics; Diamond; Ecotoxicology; Electrochemical Techniques; Electrodes; Lactuca; Norfloxacin; Oxidation-Reduction; Sulfates; Water Pollutants, Chemical; Water Purification

This work reported a comparative study on the electrochemical incineration of nitrilotriacetic acid (NTA) in the presence of different supporting electrolytes (Na2SO4 and NaCl). Galvanostatic electrolyses were conducted in an undivided electrochemical cell containing boron-doped diamond (BDD) anode and platinum cathode. Initial solution pH, flow rate, applied current density, and supporting electrolyte concentration were selected as variables, besides the mineralization efficiency of NTA that was selected as response. Central composite rotatable design and response surface methodology were employed here to examine the statistical significance of the selected variables, as well as to determine the optimal conditions of the degradation process. Under the same operating conditions, two regression models were thus constructed to illustrate the differing impact of supporting electrolytes in BDD anode cells. The kinetics for NTA degradation followed different reaction orders for the two scenarios (in the absence and presence of NaCl), indicating the complex interaction between hydroxyl radicals and active chlorine. Despite this, the experimental results demonstrated that effective mineralization of NTA might also be achieved in the presence of chlorides (of lower concentrations). Besides, in the case of chlorides, the average mass transfer coefficient of the system was found to be strongly dependent on the initial solution pH. Lastly, a plausible reaction sequence concerning the electrolytic oxidation of NTA in chloride media was also proposed.

Topics: Boron; Diamond; Electrodes; Electrolytes; Incineration; Nitrilotriacetic Acid; Oxidation-Reduction; Platinum; Sodium Chloride; Sulfates

Uric acid (UA) is one of the principal effluents of urine wastewaters, widely used in agriculture as fertilizer, which is potentially dangerous and biorefractory. Hence, the degradation of UA (2,6,8-trihydroxy purine) in aqueous solution of pH 3.0 has been studied by conductive-diamond electrochemical oxidation. Hydroxyl radicals formed from water oxidation at the surface of boron-doped diamond anodes were the main oxidizing agents. Effects of current density and supporting electrolyte on the degradation rate and process efficiency are assessed. Results show that the increase of current density from 20 to 60 mA cm(-2) leads to a decrease in the efficiency of the electrochemical process. In addition, the best degradation occurred in the presence of NaCl as conductive electrolyte. Interestingly, an almost total mineralization of 50 ppm UA was obtained when anodic oxidation was performed at low current densities (20 mA cm(-2)) and in the presence of NaCl. This result confirmed that the electrolysis using diamond anodes is a very interesting technology for the treatment of UA. The identification of UA transformation products was performed by high-performance liquid chromatography (HPLC). HPLC analysis of treated solutions revealed that oxalic acid and urea were the two intermediates found. Oxalic acid was the most persistent product. Based on detected intermediates and bibliographic research, a mechanism of UA mineralization by anodic oxidation has been proposed. Ionic chromatography analysis confirmed the release of [Formula: see text] and [Formula: see text] ions during UA mineralization.

Topics: Boron; Diamond; Electrochemistry; Electrodes; Electrolysis; Kinetics; Sodium Chloride; Sulfates; Uric Acid; Waste Disposal, Fluid; Water Pollutants, Chemical

The anodic oxidation of tetracycline was performed in an up-flow reactor, operating in batch mode with recirculation, using as anode a boron-doped diamond electrode. The influence on the degradation rate of solution initial pH (2 to 12), applied current intensity (25 to 300 A m(-2)) and type of electrolyte (sodium sulphate or sodium chloride) were investigated. For the assays run at equal current density, with sodium sulphate as electrolyte, the solution's initial pH of 2 presented the highest absorbance and chemical oxygen demand removals. Regarding the influence of current density, for equal charge passed, the organic load removal rate decreased with the increase in applied current. When sodium sulphate was used as an electrolyte, high-performance liquid chromatography (HPLC) results have shown an almost complete removal of tetracycline after a 2-h assay. HPLC results have also shown the presence of oxamic acid as one of the intermediates of tetracycline anodic oxidation. The complete removal of tetracycline was much faster in the presence of chloride ions that promoted the complete degradation of this antibiotic in 30 min. However, in the presence of chloride ions, the tetracycline mineralization is slower, as observed by the lower organic carbon removal rate when compared to that of the tetracycline degradation in the presence of sulphate.

Topics: Anti-Bacterial Agents; Biological Oxygen Demand Analysis; Boron; Chromatography, High Pressure Liquid; Diamond; Electrodes; Hydrogen-Ion Concentration; Oxidation-Reduction; Sodium Chloride; Sulfates; Tetracycline; Water Pollutants, Chemical; Water Purification

Anodic oxidation of bisphenol A (BPA), a representative endocrine disrupting chemical, was carried out using boron-doped diamond (BDD) electrode at galvanostatic mode. The electro-oxidation behavior of BPA at BDD electrode was investigated by means of cyclic voltammetric technique. The extent of degradation and mineralization of BPA were monitored by HPLC and total organic carbon (TOC) value, respectively. The results obtained, indicate that the BPA removal at BDD depends on the applied current density (Iappl), initial concentration of BPA, pH of electrolyte and supporting medium. Galvanostatic electrolysis at BDD anode cause concomitant generation of hydroxyl radical that leads to the BPA destruction. The kinetics for the BPA degradation follows a pseudo-first order reaction with a higher rate constant 12.8x10(-5) s(-1) for higher Iappl value 35.7 mA cm(-2), indicating that the oxidation reaction is limited by Iappl control. Complete mineralization of BPA was achieved regardless of the variables and accordingly the mineralization current efficiency was calculated from the TOC removal measurements. Considering global oxidation process, the effect of supporting electrolytes has been discussed in terms of the electro generated inorganic oxidants. The better performance of BDD anode was proved on a comparative study with Pt and glassy carbon under similar experimental conditions. A possible reaction mechanism for BPA degradation involving three main aromatic intermediates, identified by GC-MS analysis, was proposed.

Topics: Benzhydryl Compounds; Boron; Diamond; Electrodes; Electrolysis; Hydrogen-Ion Concentration; Kinetics; Nitrates; Oxidation-Reduction; Phenols; Sodium Chloride; Sulfates; Waste Disposal, Fluid; Water Pollutants, Chemical; Water Purification