Performance Investigation of Electrochemical Assisted HClO/Fe2+ Process For The Treatment of Landfill Leachate

The feasibility of removal of COD and ammonia nitrogen (NH4+-N) from landfill leachate by electrochemical assisted HClO/Fe2+ process is demonstrated for the first time. The performance of active chlorine generation at the anode was evaluated in Na2SO4/NaCl media, and a higher amount of active chlorine was produced at greater chloride concentration and higher current density. The probe experiments confirmed the coexistence of hydroxyl radical (·OH) and Fe(IV)-oxo complex (FeIVO2+) in the HClO/Fe2+ system. The influence of initial pH, Fe2+ concentration and applied current density on COD and NH4+-N abatement was elaborately investigated. The optimum pH was found to be 3.0, and the proper increase in Fe2+ dosage and current density resulted in higher COD removal due to the accelerated accumulation of ·OH and FeIVO2+ in the bulk liquid phase. Whereas, the NH4+-N oxidation was significantly affected by the applied current density because of the effective active chlorine generation at high current, but was nearly independent of Fe2+ concentration. The reaction mechanism of electrochemical assisted HClO/Fe2+ treatment of landfill leachate was finally proposed. The powerful ·OH and FeIVO2+, in concomitance with active chlorine and M(·OH) were responsible for COD abatement and active chlorine played a key role in NH4+-N oxidation. The proposed electrochemical assisted HClO/Fe2+ process is a promising alternative for the treatment of refractory landfill leachate.

Excellent Properties of Ni-15 wt.% W Alloy Electrodeposited from a Low-Temperature Pyrophosphate System

Electrodeposited Ni-W alloy coatings are considered to be one of the most suitable candidate coatings to replace carcinogenic hexavalent chromium coatings. In this work, Ni-W alloys are electrodeposited from pyrophosphate baths containing different concentrations of Na2WO4 2H2O (CW) at 40 °C. Both CW and the applied current density can affect the W content in the coatings. The effect of CW becomes weaker with the increased current density. The Ni-W alloys with 15 ± 5 wt.% W (Ni-15 wt.% W) are obtained from the bath containing 40 g L−1 CW at a high current of 8 A dm−2. The microhardness, corrosion resistance and hydrogen evolution reaction (HER) are measured with a microhardness tester and an electrochemical workstation. The modified properties are studied by heat treatment from 200 to 700 °C. The highest microhardness of 895.62 HV and the better HER property is presented after heat treatment at 400 °C, while the best corrosion resistance in 3.5 wt.% NaCl solution appears at 600 °C.

Electrochemical oxidation and electroanalysis of paracetamol on a boron-doped diamond anode material in aqueous electrolytes

Electrochemical oxidation of paracetamol on boron-doped diamond (BDD) anode has been studied by cyclic voltammetry and preparative electrolysis. Quantification of paracetamol during electrolysis has been mainly realized by differential pulse voltammetry technique in the Britton-Robinson buffer solutions used as the supporting electrolyte. Various parameters such as current intensity, nature of the supporting electrolyte, temperature, and initial concentration of paracetamol have been investigated. The electrochemical characterization by the outer sphere Fe(III)/Fe(II) redox couple has also been performed, showing the metallic character of BDD electrode. The obtained linear dependency of the oxidation peak current intensity and paracetamol concentration indicates that BDD electrode can be used as an electrochemical sensor for the detection and quantification of paracetamol. The investi­gation of paracetamol degradation during preparative electrolysis showed that: (i) the degradation rate of paracetamol increases with increase of current intensity applied; (ii) for the initial concentrations of 10, 6 and 1 mM of paracetamol, its oxidation rate reaches 60, 78 and 99 % respectively, after 1 h of electrolysis in 0.3 M H2SO4 (pH 0.6) at applied current density of 70 mA cm-2; (iii) at temperatures of electrolyte solution of 28, 55 and 75 °C, paracetamol oxidation rate reached 85, 92 and 97 % respectively, after 2 h at applied current density of 70 mA cm2. From the investigation of the effect of pH value of electrolyte solution, it appears that oxidation of paracetamol is more favorable in acidic solution at pH 3 than solutions of higher pH values.

Methiocarb Degradation by Electro-Fenton: Ecotoxicological Evaluation

This paper studies the degradation of methiocarb, a highly hazardous pesticide found in waters and wastewaters, through an electro-Fenton process, using a boron-doped diamond anode and a carbon felt cathode; and evaluates its potential to reduce toxicity towards the model organism Daphnia magna. The influence of applied current density and type and concentration of added iron source, Fe2(SO4)3·5H2O or FeCl3·6H2O, is assessed in the degradation experiments of methiocarb aqueous solutions. The experimental results show that electro-Fenton can be successfully used to degrade methiocarb and to reduce its high toxicity towards D. magna. Total methiocarb removal is achieved at the applied electric charge of 90 C, and a 450× reduction in the acute toxicity towards D. magna, on average, from approximately 900 toxic units to 2 toxic units, is observed at the end of the experiments. No significant differences are found between the two iron sources studied. At the lowest applied anodic current density, 12.5 A m−2, an increase in iron concentration led to lower methiocarb removal rates, but the opposite is found at the highest applied current densities. The highest organic carbon removal is obtained at the lowest applied current density and added iron concentration.

Dynamics of chiral solitons driven by polarized currents in monoaxial helimagnets

Chiral solitons are one dimensional localized magnetic structures that are metastable in some ferromagnetic systems with Dzyaloshinskii–Moriya interactions and/or uniaxial magnetic anisotropy. Though topological textures in general provide a very interesting playground for new spintronics phenomena, how to properly create and control single chiral solitons is still unclear. We show here that chiral solitons in monoaxial helimagnets, characterized by a uniaxial Dzyaloshinskii–Moriya interaction, can be stabilized with external magnetic fields. Once created, the soliton moves steadily in response to a polarized electric current, provided the induced spin-transfer torque has a dissipative (nonadiabatic) component. The structure of the soliton depends on the applied current density in such a way that steady motion exists only if the applied current density is lower than a critical value, beyond which the soliton is no longer stable.

Ecotoxicological Evaluation of Methiocarb Electrochemical Oxidation

The ecotoxicity of methiocarb aqueous solutions treated by electrochemical oxidation was evaluated utilizing the model organism Daphnia magna. The electrodegradation experiments were performed using a boron-doped diamond anode and the influence of the applied current density and the supporting electrolyte (NaCl or Na2SO4) on methiocarb degradation and toxicity reduction were assessed. Electrooxidation treatment presented a remarkable efficiency in methiocarb complete degradation and a high potential for reducing the undesirable ecological effects of this priority substance. The reaction rate followed first-order kinetics in both electrolytes, being more favorable in a chloride medium. In fact, the presence of chloride increased the methiocarb removal rate and toxicity reduction and favored nitrogen removal. A 200× reduction in the acute toxicity towards D. magna, from 370.9 to 1.6 toxic units, was observed for the solutions prepared with NaCl after 5 h treatment at 100 A m−2. An increase in the applied current density led to an increase in toxicity towards D. magna of the treated solutions. At optimized experimental conditions, electrooxidation offers a suitable solution for the treatment and elimination of undesirable ecological effects of methiocarb contaminated industrial or agricultural wastewaters, ensuring that this highly hazardous pesticide is not transferred to the aquatic environment.

Electrodeposition of Photocatalytic Sn–Ni Matrix Composite Coatings Embedded with Doped TiO2 Particles

Direct current electrodeposited Sn–Ni/TiO2 nanostructured coatings were produced by embedding two different doped types of TiO2 particles within the alloy matrix, a commercially available doped carbon-based and doped N,S-TiO2 particles. The structural characteristics of the composite coatings have been correlated with the effect of loading, type of particles in the electrolytic bath, and the applied current density. Regardless of the type of doped particles TiO2, increasing values of applied current density resulted in a reduction of the co-deposition percentage of TiO2 particles and an increase of Tin content into the alloy matrix. The application of low current density values accompanied by a high load of particles in the bath led to the highest codeposition percentage (~3.25 wt.%) achieved in the case of embedding N,S-TiO2 particles. X-ray diffraction data demonstrated that in composite coatings the incorporation of the different types of TiO2 particles in the alloy metal matrix modified significantly the nano-crystalline structure in comparison with the pure coatings. The best photocatalytic behavior under visible irradiation was revealed for the composite coatings with the highest co-deposition percentage of doped N,S-TiO2 particles, that also exhibited enhanced wear resistance and slightly reduced microhardness compared to pure ones.

Electro-Absorbers: A Comparison on Their Performance with Jet-Absorbers and Absorption Columns

This work focuses on the removal of perchloroethylene (PCE) from gaseous streams using absorbers connected with electrolyzers. Two types of absorption devices (jet absorber and absorption column) were compared. In addition, it has been evaluated the different by-products generated when a simultaneous electrolysis with diamond anodes is carried out. PCE was not mineralized, but it was transformed into phosgene that mainly derivates into carbon tetrachloride. Trichloroacetic acid was also formed, but in much lower amounts. Results showed a more efficient absorption of PCE in the packed column, which it is associated to the higher gas–liquid contact surface. Jet absorber seems to favor the production of carbon tetrachloride in gaseous phase, whereas the packed column promotes a higher concentration of trichloroacetic acid in liquid. It was also evaluated the scale up of the electrolytic stage of these electro-absorption devices by using a stack with five perforated electrode packages instead of a single cell. Clarification of the effect of the applied current density on the speciation attained after the electrolysis of the absorbent has been attempted. Experiments reveal similar results in terms of PCE removal and a reduced generation of gaseous intermediates at lower current densities.