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Gold is one of the precious metals with multiple uses, whose deposits are much smaller than the global production needs. Therefore, extracting maximum gold quantities from industrial diluted solutions is a must. Am-L-GA is a new material, obtained by an Amberlite XAD7-type commercial resin, functionalized through saturation with L-glutamic acid, whose adsorption capacity has been proved to be higher than those of other materials utilized for gold adsorption. In this context, this article presents the results of a factorial design experiment for optimizing the gold recovery from residual solutions resulting from the electronics industry using Am-L-GA. Firstly, the material was characterized using atomic force microscopy (AFM), to emphasize the material’s characteristics, essential for the adsorption quality. Then, the study showed that among the parameters taken into account in the analysis (pH, temperature, initial gold concentration, and contact time), the initial gold concentration in the solution plays a determinant role in the removal process and the contact time has a slightly positive effect, whereas the pH and temperature do not influence the adsorption capacity. The maximum adsorption capacity of 29.27 mg/L was obtained by optimizing the adsorption process, with the control factors having the following values: contact time ~106 min, initial Au(III) concentration of ~164 mg/L, pH = 4, and temperature of 25 °C. It is highlighted that the factorial design method is an excellent instrument to determine the effects of different factors influencing the adsorption process. The method can be applied for any adsorption process if it is necessary to reduce the number of experiments, to diminish the resources or time consumption, or for expanding the investigation domain above the experimental limits.

Hybrid materials based on montmorillonite functionalized with LaMnO3 perovskitic structures were obtained for the first time by ultrasonic method with sonotrode immersed in the reaction medium, followed by heat treatment at a temperature of 600 °C. The clay mineral montmorillonite (Mmt), sodium montmorillonite (Mmt-Na+) and functionalized material (Mmt-LMO) were characterized by X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM/Edx) techniques. The XRD patterns of Mmt-LMO composites show both the presence of the perovskitic phase with orthorhombic structure, and a mixture of aluminosilicates, corresponding to the montmorillonite clay minerals. The (Mmt), (Mmt-Na+) minerals and (Mmt-LMO) hybrid material were used to manufacture modified electrodes whose catalytic properties for the oxygen and hydrogen evolution reactions were investigated in alkaline medium. Based on electrochemical experimental results, some of these electrodes are catalytically active toward the hydrogen evolution reaction and the more performant ones were investigated further and it was found that the electrode modified with the composition containing 6 mg LaMnO3 functionalized montmorillonite and 10 µL Nafion solutions have the best electrocatalytic properties. At the current density of −10 mA/cm2 the electrode exhibits an over potentialfor hydrogen evolution of −0.48 V and its Tafel slope was measured to be 70 mV/dec. This study complements the extant scientific knowledge relevant to the water splitting domain.

In this study series of CdxZn1-xS solid solutions with different amounts of Cd and Zn were synthesized by the hydrothermal treatment of aqueous solutions containing CdCl2, Na2S ? 9H2O and ZnSO4 ? 7H2O. The aim was to examine the influence of Zn concentration and processing conditions (hydrothermal temperature and duration) on the structure of the obtained powders and their photocatalytic activity (in water splitting process). The obtained photocatalysts (with and without Pd co-catalyst) were analysed by X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), ultraviolet-visible spectroscopy (UV-VIS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) method and gas chromatography (GC). The XRD results confirmed the crystallinity of the compounds and transition from hexagonal to cubic phase with increasing Zn content. Complete transformation from hexagonal to cubic phase did not take place, and both phases were present in almost all samples. BET analysis showed the importance of the pore distribution and pore size, especially in the case of photocatalysts with different duration treatment. GC measurements of the photocatalysts without and with Pd co-catalyst confirmed the production of hydrogen for all tested compounds. The best photocatalytic performance was achieved by the sample Zn50230/72-Pd prepared at 230?C, for 72 hours, with 50% Zn and in the presence of Pd co-catalyst. The synthesis implied neither stabilizer nor organic compound.

Intriguing micro-currents in the graphenic oxide flakes obtained from the cracked fullerenes ozopolymers were predicted from their Raman spectra. They are interpreted with the aid of the bondonic theory combined with the inverse information for the quantum observed vs. quantum free evolution ratio, respectively. The peculiar quantum dots of the bondonic propagation in these nanoscopic systems may suggest the potentially critical phenomenology of phase transition, and possible local superconductivity by passing from the C60 derivative graphenic oxide to the C70 based compound. These results may have an impact on the future design of the graphene-based semiconductors, of the quantum graphenic gates, as well as on and the integrated graphenic microcircuits in the generic new field of graphentronics.

Ni11□(HPO3)8(OH)6 nanorods were the focus of three different studies. First, the thermal behaviour of the material was investigated and it outlined a good thermal stability up to 400 °C. Second, a comparative electrochemical study concerning the OER performance in alkaline medium of several graphite electrodes modified with the nickel phosphite was performed. The most promising electrodes were further characterised electrochemically and the electrode modified with Nafion solution and 5 mg Ni11□(HPO3)8(OH)6 exhibited the smallest overpotential value at the 10 mA cm−2 anodic current density (0.59 V), as well as the smallest Tafel slope (0.081 V dec−1). Furthermore, the constant potential electrolysis test revealed that this electrode is fairly stable within a time span of 300 min. Third, the capacity of Ni11□ (HPO3)8(OH)6 nanorods to remove MB and RhB were investigated under simulated visible light irradiation and positive results were obtained for the application as visible-light active photocatalyst. All this together corroborated with the eco-friendly nature of the materials, reinforces the fact that the phosphite type compound is a promising candidate for the design of new multifunctional and advanced materials.

The aim of this study is the enhancement of the electrical properties of thin films obtained from silver nanowires (AgNWs) deposited on a flexible polyethylene terephthalate (PET) support. First, AgNWs were obtained by the “polyol” liquid phase synthesis method in the presence of chloride ions. After purification, the AgNWs were successively deposited on a flexible support of PET by doctor blade method. To improve the adhesion of the AgNWs coating to the substrate, thin films of polymethyl methacrylate (PMMA) were interposed between the layer of AgNWs and PET substrate. The properties of the thin films have been studied depending on the number of AgNWs layers and heat treatment procedure. Characterization of pure AgNWs as well as of AgNWs/PMMA/PET structures has been carried out by x-ray diffraction, scanning electron microscopy, energy-dispersive x-ray analysis, transmission electron microscopy, UV–Vis spectroscopy, and scanning probe microscopy. The sheet resistance of the transparent conducting...