Publications by authors named "Bensalah Nasr"

Vanadium oxide-based compounds have attracted significant interest as battery materials, especially in aqueous Zn-ion batteries, due to favorable properties and compatibility in Zn-ion systems. In a simple hydrothermal method with moderate conditions, a novel vanadium oxide compound has been synthesized using ammonium metavanadate with oxalic acid as a reducing agent. Various characterization techniques confirmed the formation of layered VO(HO) nanoplatelets with a tetragonal crystal structure.

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The purpose of this study is the synthesis of α-MnO-based cathode materials for rechargeable aqueous zinc ion batteries by hydrothermal method using KMnO and MnSO as starting materials. The aim is to improve the understanding of Zn insertion/de-insertion mechanisms. The as-prepared solid compounds were characterized by spectroscopy and microscopy techniques.

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In this work, new electrochemical sensors based on the modification of glassy carbon electrode (GCE) with multiwalled carbon nanotubes (MWCNTs)-rare metal oxides (REMO) nanocomposites were fabricated by drop-to-drop method of MWCNTs-REMO dispersion in ethanol. REMO nanoparticles were synthesized by precipitation followed by hydrothermal treatment at 180 °C in absence and presence of Triton X-100 surfactant. Cyclic voltammetry (CV) analysis using MWCNTs-CeO@GCE and MWCNTs-YbO@GCE sensors were used for the analysis of sulfisoxazole (SFX) drug in water samples.

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Silicon and silicon nitride (SiN) are some of the most appealing candidates as anode materials for LIBs (Li-ion battery) due to their favorable characteristics: low cost, abundance of Si, and high theoretical capacity. However, these materials have their own set of challenges that need to be addressed for practical applications. A thin film consisting of silicon nitride-coated silicon on a copper current collector (SiN@Si@Cu) has been prepared in this work via RF magnetron sputtering (Radio Frequency magnetron sputtering).

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In this work, the degradation of hydroxychloroquine (HCQ) drug in aqueous solution by electrochemical advanced oxidation processes including electrochemical oxidation (EO) using boron doped diamond (BDD) and its combination with UV irradiation (photo-assisted electrochemical oxidation, PEO) and sonication (sono-assisted electrochemical oxidation, SEO) was investigated. EO using BDD anode achieved the complete depletion of HCQ from aqueous solutions in regardless of HCQ concentration, current density, and initial pH value. The decay of HCQ was more rapid than total organic carbon (TOC) indicating that the degradation of HCQ by EO using BDD anode involves successive steps leading to the formation of organic intermediates that end to mineralize.

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In this work, the degradation of chloroquine (CLQ), an antiviral and antimalarial drug, using electro-Fenton oxidation was investigated. Due to the importance of hydrogen peroxide (HO) generation during electro-Fenton oxidation, effects of pH, current density, molecular oxygen (O) flow rate, and anode material on HO generation were evaluated. HO generation was enhanced by increasing the current density up to 60 mA/cm and the O flow rate up to 80 mL/min at pH 3.

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In the present work, electrochemical technology was used simultaneously for the deactivation of microorganisms and the destruction of micro-pollutants contained in synthetic urine wastewaters. Microorganisms () were added to synthetic urine wastewaters to mimic secondary treated sewage wastewaters. Different anode materials were employed including boron-doped diamond (BDD), dimensionally stable anode (DSA: IrO and RuO) and platinum (Pt).

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In this work, the treatment of 4-nitrophenol (NP) in water by ozonation, electrolysis, electro-peroxone (EP), and photo-electro-peroxone (PEP) processes was investigated. PEP process is based on the combination of ozonation, UV irradiation, and electrolysis using a carbon felt cathode and a boron-doped diamond (BDD) anode. In this process, HO is electrochemically generated from reduction of O in the ozone generator effluent at a carbon felt cathode.

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In this work, the contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using boron-doped diamond (BDD) anodes was investigated in different electrolytes. A complete mineralization of cyanuric acid was obtained in NaCl; however lower degrees of mineralization of 70% and 40% were obtained in Na2SO4 and NaClO4, respectively. This can be explained by the nature of the oxidants electrogenerated in each electrolyte.

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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.

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In this work, the electrochemical oxidation of synthetic urine by anodic oxidation using boron-doped diamond as anode and stainless steel as cathode was investigated. Results show that complete depletion of chemical oxygen demand (COD) and total organic carbon (TOC) can be attained regardless of the current density applied in the range 20-100 mA cm(-2). Oxalic and oxamic acids, and, in lower concentrations, creatol and guanidine were identified as the main intermediates.

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In this work, chemical oxidation of mesotrione herbicide by Fenton process in acidic medium (pH 3.5) was investigated. Total disappearance of mesotrione and up to 95% removal of total organic carbon (TOC) were achieved by Fenton's reagent under optimized initial concentrations of hydrogen peroxide (H(2)O(2)) and ferrous iron (Fe(2+)) at pH 3.

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Synthetic aqueous wastes polluted with Congo Red (CR) have been treated by two advanced oxidation processes: electrochemical oxidation on boron doped diamond anodes (BDD-EO) and ozonation under alkaline conditions. For same concentrations, galvanostatic electrolyses have led to total COD and TOC removals but ozonation process can reach only 85% and 81% of COD and TOC removals, respectively. UV-vis qualitative analyses have shown different behaviors of CR molecules towards ozonation and electrochemical oxidation.

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In this work, the electrochemical oxidation of pyrogallol (1,2,3-trihydroxybenzene) on boron-doped diamond anodes has been studied. The voltammetric results showed that pyrogallol oxidation takes place in the same potential region as that of phenol where the supporting electrolyte is stable. Synthetic wastewaters containing pyrogallol have been treated in a bench-scale electrolysis plant.

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The electrochemical oxidation of aqueous wastes polluted with hydroquinone, resorcinol, or catechol on boron-doped diamond electrodes has been studied. The complete mineralization of the organic waste has been obtained independently of the nature of each isomer. No aromatic intermediates were found during the treatment, and solely aliphatic intermediates (carboxylic acids C4 and C2, mainly) were detected in the three cases.

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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.

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