Improvement of the magnesium battery electrolyte properties through gamma irradiation of nano polymer electrolytes doped with magnesium oxide nanoparticles

Nanocomposite polymer electrolytes (NCPE) were prepared using nano polyethylene oxide PEO doped with Magnesium (Mg) salts. Gamma irradiation was utilized to improve the PEO‐Mg salts particle sizes. Consequently, Magnesium Oxide (MgO) nanoparticles were prepared by green synthesis and incorporated into PEO‐Mg salts to improve their properties toward magnesium battery electrolyte applications. The prepared samples were examined before and after exposures to the radiation doses. Dynamic light scattering (DLS) indicated the particles size of the synthesized nano polymer‐Mg salts and MgO nanoparticles. Fourier transform infra‐red (FTIR) spectroscopic measurements, transmission electron microscopy (TEM), electrical conductivity, electrochemical properties, and thermal stability of the samples were determined. FTIR indicated the interaction between PEO with Mg salts and MgO nanoparticles which confirmed the structure. The TEM results showed a spherical nanoparticles of MgO and a good dispersion of MgO in PEO matrix. It was found that the irradiation dose 70 kGy gave the best results for the nano polymer‐Mg salts (13 nm). The electrical conductivity (σ) evaluated for NCPE, was more than three orders of magnitude of pure PEO. The liquid NCPE of 20 mL MgO NPs at 100 kGy exhibited a maximum conductivity of 3.63 × 10^–3 Scm^?1 at room temperature. The increase in temperature caused a slight effect on conductivity, 4.85 × 10^–3 Scm^?1 at temperature 250°C, at the same concentration. While un‐irradiated sample of 30 mL MgO NPs (σ) reached to 3.8 × 10^?3 Scm^?1 then became 5.03 × 10^?3 Scm^?1 by increasing temperature. From the cyclic voltammetry results, the polymer electrolytes containing MgO filler, 20 and 30 mL, for irradiated and un‐irradiated samples, respectively exhibited wider electrochemical stability window than the others due to the appearance of Mg deposition/desolution peak in CV curve showed that magnesium effectively migrating through electrolytes. Thermogravimetric analysis (TGA) was enhanced by adding Mg salts electrolyte and also MgO nanoparticles to PEO. J. VINYL ADDIT. TECHNOL., 25:243–254, 2019. © 2018 Society of Plastics Engineers     

Influences of Mn doping on the microstructural,semiconducting, and optoelectronic properties of HgO nanostructure films

Mn-doped HgO nanostructured thin films (Hg_1-xMn_xO) have been prepared using electron beam evaporation technique on Corning glass (1022) substrate at room temperature with different concentrations x = 0, 0.015, 0.05, 0.1, 0.15, and 0.2. The microstructural, morphological, semiconducting, and optoelectronic properties of the films have been investigated. The X-ray diffraction spectra suggest a hexagonal wurtzite type structure with lattice parameters decreased with increasing Mn content. It was found that the average particle size of the films decreases with increasing Mn doping which is confirmed by FE-SEM and AFM micrographs. The optical band gap of the investigated Mn-doped HgO nanocrystalline films is determined from the absorption coefficient and found to increase with the increase of Mn concentration which is attributed to the sp-d exchange interaction and/or the quantum confinement effect. The refractive index and extinction coefficient of the Mn-doped HgO films are also reported. The refractive index dispersion n(λ) is analyzed by single-effective-oscillator dispersion model proposed by the Wemple–DiDomenico (WDD). The oscillator parameters were estimated. The obtained dispersion values are suitable for the design of optoelectronic devices.     

Mechanical properties of gamma‐irradiated styrene‐butadiene rubber/acid‐treated vermiculite clay/maleic anhydride nanocomposites

Nanoparticle vermiculite (VMT) clay was prepared by treatment with hydrochloric acid. Styrene‐butadiene rubber (SBR) nanocomposites were prepared by mixing different contents (2.5, 5, 7.5, and 10 phr) of untreated (VMT) and acid‐treated (DVMT) vermiculite clay, respectively. In addition, different contents (3, 7, and 10 phr) of maleic anhydride (MA) as compatibilizer were mixed via direct melt compounding in internal mixer. The effect of gamma irradiation, VMT clay, and MA contents on the mechanical properties was studied. The acid‐treated VMT clay was characterized by x‐ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared (FT‐IR) spectroscopy. Meanwhile, the SBR/VMT composites, SBR/DVMT, and SBR/DVMT/MA nanocomposites were characterized via crosslinking density and tensile mechanical testing and FT‐IR spectroscopic analysis. The results indicated that good yield of nanoparticle vermiculite was achieved when the acid treatment was carried out for 120 h. In addition, the results showed that the presence of DVMT clay improved the chemical bonding in the SBR nanocomposites and hence their mechanical properties. The highest improvement was obtained when the contents of DVMT clay, MA, and irradiation dose were 10 phr, 3 phr, and 100 kGy, respectively. POLYM. ENG. SCI., 59:355–364, 2019. © 2018 Society of Plastics Engineers     

Preparation of Electrolytic Quasi-Solid-State Nanofibers for Dye-Sensitized Solar Cells

JOM - Nanofibers were prepared from a poly(acrylonitrile-co-vinyl acetate) [P(AN-co-VAC)]/polyvinylidene fluoride (PVDF) blend and used as a quasi-solid (QS) electrolyte for dye-sensitized solar...     

On thermoelectric materials with memory-dependent derivative and subjected to a moving heat source

We develop a model of generalized thermoelasticity with memory-dependent derivative (MDD) heat conduction law for a thermoelectric half-space. Some urgent theories take after as most remote point cases. The Laplace transform and state-space procedures are utilized to urge the overall account for any arrangement of limit conditions. The general solution acquired is connected to the particular issue of a half-space exposed to a uniform magnetic field, a moving heat source with consistent speed and ramp-type heating. The inverse Laplace transforms are registered numerically. The impacts of various estimations of the figure-of-merit quantity, heat source speed, MDD parameters, the magnetic number and the ramping time parameter are thought about.

     

Development of novel amisulpride-loaded solid self-nanoemulsifying tablets: preparation and pharmacokinetic evaluation in rabbits

Objective: The current investigation is focused on the formulation and in vivo evaluation of optimized solid self-nanoemulsifying drug delivery systems (S-SNEDDS) of amisulpride (AMS) for improving its oral dissolution and bioavailability.

Methods: Liquid SNEDDS (L-SNEDDS) composed of Capryol? 90 (oil), Cremophor^® RH40 (surfactant), and Transcutol^® HP (co-surfactant) were transformed to solid systems via physical adsorption onto magnesium aluminometasilicate (Neusilin US2). Micromeretic studies and solid-state characterization of formulated S-SNEDDS were carried out, followed by tableting, tablet evaluation, and pharmacokinetic studies in rabbits.

Results: Micromeretic properties and solid-state characterization proved satisfactory flow properties with AMS present in a completely amorphous state. Formulated self-nanoemulsifying tablets revealed significant improvement in AMS dissolution compared with either directly compressed or commercial AMS tablets. In vivo pharmacokinetic study in rabbits emphasized significant improvements in t_max, AUC_(0–12), and AUC_(0–∞) at p?<?.05 with 1.26-folds improvement in relative bioavailability from the optimized self-nanoemulsifying tablets compared with the commercial product.

Conclusions: S-SNEDDS can be a very useful approach for providing patient acceptable dosage forms with improved oral dissolution and biovailability.     

Characterisation of manganese dioxides II. Kinetics of Interaction with Manganese (II) Ions in Aqueous Solution

The interaction between MnO₂ (I.C.S. No. 5), in the Na⁺ form and ⁵⁴Mn²⁺-labelled solution at pH 6 involves: a rapid process assumed to be Na⁺/Mn²⁺ ion-exchange and a slower process assumed to involve the exchange between Mn²⁺ ions in solution and Mn ions in a surface phase. The activation parameters ΔH^# and ΔS^# were found to be 52 and 83 kJ mol^?1 and ?130 and ?63 J mol^?1 for the two processes respectively. Exposing the solid to a flux of moderated neutrons had no effect on the rate of the second process. The exchange of Mn ions from the solid to the solution was demonstrated using ⁵⁶Mn-labelled solid and inactive Mn²⁺ solution. There was evidence of a still slower process.     

Separation of a compound effective against Biomphalaria alexandrina snails from the filtrate of Penicillium janthinellum

Biomphalaria alexandrina snails, as intermediate hosts of schistosomiasis, play a central role in dissemination of the disease. Control of these snails by chemical molluscicides adversely affects the aquatic environment, causing toxic and carcinogenic effects on non-target organisms. Searching for promising substances from biological origin becomes an urgent need to overcome these drawbacks. Screening tests were carried out on 236 fungal genera isolated from the habitat of freshwater snails in four Egyptian governorates. Twenty species were effective against B. alexandrina snails, but the most potent was Penicillium janthinellum as the value of LC₅₀ was 1.03%. Chemical analyses of this filtrate resulted in the separation of a compound effective against snails; it was identified as methyl gallate. Protein electrophoresis showed that both fungal filtrate and methyl gallate affect the protein pattern of snails’ haemolymph. Little or no mortality of Daphnia pulex individuals was observed after their exposure to sub lethal concentrations of each treatment.     

Improving the throwing power of acidic zinc sulfate electroplating baths

The effect of some plating parameters, such as Zn²⁺ ion concentration, pH, current density, temperature and duration on the throwing power, as well as on the throwing index of acidic zinc sulfate baths has been investigated. The addition of p‐anisidine (PA) and/or sodium dodecylbenzenesulfonate (DBS) has been examined as a possible means of improving the uniformity of deposit distribution. The additives cause a substantial increase in the overpotential for the reduction of Zn²⁺ ions and consequently improve the throwing power of the baths. The throwing power increases by a factor of four in the presence of DBS and a factor of one‐and‐a‐half in the presence of PA. The inhibition of zinc reduction was assumed to occur via adsorption of the PA or DBS molecules on the cathode surface and the adsorption followed the Langmuir adsorption isotherm. The surface morphology of the zinc plated with and without the additives was examined by using scanning electron microscopy (SEM). © 2000 Society of Chemical Industry     

Electroplating of cobalt from aqueous citrate baths

Electroplating of cobalt onto steel substrates from citrate baths has been investigated under different conditions of bath composition, current density, pH and temperature. A detailed study has been made of the influence of these variables on the potentiodynamic cathodic polarization curves, cathodic current efficiency and the throwing power as well as the throwing index of these baths. The optimum bath composition has been established and it contains: CoSO₄.7H₂O (0·36 mol dm⁻³) trisodium citrate (0·19 mol dm⁻³) and citric acid (0·1 mol dm⁻³) at pH 5·0. The microhardness of cobalt electrodeposited from citrate baths is high and it may be, under certain conditions, two or three times higher than that reported for cobalt electrodeposited from other different baths. The surface morphology of the as-plated cobalt was investigated by using scanning electron microscopy (SEM) while the structure was studied by using X-ray diffraction analysis and anodic stripping voltammetry (ASV) techniques. © 1998 Society of Chemical Industry