Tracing the impact of CO2 on the electrochemical and charge-discharge behavior for Al-Mg alloy in KOH and LiOH electrolytes for battery applications.

For the first time, it has been found that the electrochemical performance of the Al-Mg alloy as an anode in alkaline batteries has been markedly enhanced in the presence of CO2 and LiOH as an electrolyte. This work compares the electrochemical performance of an Al-Mg alloy used as an anode in Al-air batteries in KOH and LiOH solutions, both with and without CO2. Potentiodynamic polarization (Tafel), charging-discharging (galvanostatic) experiments, and electrochemical impedance spectroscopy (EIS) are used. X-ray diffraction spectroscopy (XRD) and a scanning electron microscope (SEM) outfitted with an energetic-dispersive X-ray spectroscope (EDX) were utilized for the investigation of the products on the corroded surface of the electrode. Findings revealed that the examined electrode's density of corrosion current (icorr.) density in pure LiOH is significantly lower than in pure KOH (1 M). Nevertheless, in the two CO2-containing solutions investigated, icorr. significantly decreased. The corrosion rate of the examined alloy in the two studied basic solutions with and without CO2 drops in the following order: KOH > LiOH > KOH + CO2 > LiOH + CO2. The obtained results from galvanostatic charge-discharge measurements showed excellent performance of the battery in both LiOH and KOH containing CO2. The electrochemical findings and the XRD, SEM, and EDX results illustrations are in good accordance.

The passivity breakdown of zinc antimony alloy as an anode in the alkaline batteries.

Zn is utilized as an anode in alkaline batteries because of its propensity to produce a passive colloidal layer on its surface. Then the surface should be reactivated in the passive region. Therefore, the passive state on the surface can be significantly hindered by utilizing a tiny percentage of Sb alloyed with Zn. Accordingly, the effect of minor Sb alloying with Zn on the performance of anodic dissolution and passivation in concentrated alkaline media (6 M KOH, which is used in the batteries) was studied using potentiodynamic and potentiostatic techniques. Besides, the passive layers formed at various anodic potentials were characterized utilizing scanning electron microscopy (SEM) and X-ray diffraction (XRD). The data of potentiodynamic measurements exhibited the active-passive transition curve of all studied specimens. All obtained results revealed that passivation is gradually hindered with increasing Sb content in the alloy, and less passivity was obtained at 1% Sb. Along this, a dramatic rise in current density at a particular positive potential (+ 2.0 V vs. SCE) to markedly higher values only of the electrodes containing Sb is observed.

Enhanced Nitrate Ions Remediation Using Fe0 Nanoparticles from Underground Water: Synthesis, Characterizations, and Performance under Optimizing Conditions.

The presence of nitrates in water in large amounts is one of the most dangerous health issues. The greatest risk posed by nitrates is hemoglobin oxidation, which results in Methemoglobin in the human body, resulting in Methemoglobinemia. There are many ways to eliminate nitrates from underground water. One of the most effective and selective methods is using zero-valent iron (ZVI) nanoparticles. ZVI nanoparticles can be easily synthesized by reducing ferric or ferrous ions using sodium borohydride. The prepared ZVI nanoparticles were examined by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), electron microscopy (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area, and zeta potential. We aim to eliminate or reduce the nitrates in water to be at the acceptable range, according to the world health organization (WHO), of 10.0 mg/L. Nitrate concentration in water after and before treatment is measured using the UV scanning method at 220 nm wavelength for the synthetic contaminated water and electrochemical method for the naturally contaminated water. The conditions were optimized for obtaining an efficient removing process. The removal efficiency reaches about 91% at the optimized conditions.

Removal of the Harmful Nitrate Anions from Potable Water Using Different Methods and Materials, including Zero-Valent Iron.

Drinking water containing nitrate ions at a higher concentration level of more than 10 mg/L, according to the World Health Organization (WHO), poses a considerable peril to humans. This danger lies in its reduction of nitrite ions. These ions cause methemoglobinemia during the oxidation of hemoglobin into methemoglobin. Many protocols can be applied to the remediation of nitrate ions from hydra solutions such as Zn metal and amino sulfonic acid. Furthermore, the electrochemical process is a potent protocol that is useful for this purpose. Designing varying parameters, such as the type of cathodic electrode (Sn, Al, Fe, Cu), the type of electrolyte, and its concentration, temperature, pH, and current density, can give the best conditions to eliminate the nitrate as a pollutant. Moreover, the use of accessible, functional, and inexpensive adsorbents such as granular ferric hydroxide, modified zeolite, rice chaff, chitosan, perlite, red mud, and activated carbon are considered a possible approach for nitrate removal. Additionally, biological denitrification is considered one of the most promising methodologies attributable to its outstanding performance. Among these powerful methods and materials exist zero-valent iron (ZVI), which is used effectively in the deletion process of nitrate ions. Non-precious synthesis pathways are utilized to reduce the Fe2+ or Fe3+ ions by borohydride to obtain ZVI. The structural and morphological characteristics of ZVI are elucidated using UV-Vis spectroscopy, zeta potential, XRD, FE-SEM, and TEM. The adsorptive properties are estimated through batch experiments, which are achieved to control the feasibility of ZVI as an adsorbent under the effects of Fe0 dose, concentration of NO3- ions, and pH. The obtained literature findings recommend that ZVI is an appropriate applicant adsorbent for the remediation of nitrate ions.

Electrodeposition and Growth of Iron from an Ethylene Glycol Solution.

The electrochemical reduction of iron (III) ions into zero-valent iron from a solution of ethylene glycol was accomplished. The kinetics and mechanism of the electroreduction process were investigated by cyclic and linear polarization techniques. The influence of temperature, potential sweep rate, and concentration of iron (III) ions on the electroreduction process was also studied. The observed values of effective activation energy revealed that the investigated electroreduction process is accompanied by mixed kinetics control. Moreover, the results of SEM and X-ray diffraction analysis confirmed the deposition of thin Fe films under the optimized conditions.

Investigation of the Electrochemical Reduction Process of the Molybdate Ions in the Tartaric Electrolytes.

The electrochemical reduction of molybdate ions in tartaric electrolyte has been investigated in this work. Kinetics and mechanism of the electrochemical process have been studied by cyclic and linear voltammetric polarization methods. The effect of the temperature, the rate of potential-scanning and the concentration of the molybdate ions on the electrochemical process has been also studied. By estimating the effective activation energy, it was revealed that the electroreduction process is accompanied by mixing kinetics control.