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Aggressive industrial development over the last century involved different heavy metals being used, including high quantities of molybdenum, which need to be treated before discharge in industrial waters. Molybdenum’s market price and industrial applicability make its recovery a big challenge. In the present study the possibility to recover molybdenum ions from aqueous solutions by adsorption on a composite material based on silica matrix and iron oxides—SiO2FexOy—was evaluated. Tests were performed in order to determine the influence of adsorbent material dose, initial solution pH, contact time and temperature over adsorption capacity of synthesized adsorbent material. For better understanding of the adsorption process, the obtained experimental data were modelled using Langmuir, Freundlich and Sips adsorption isotherms. Based on the obtained data, it can proved that the Sips isotherm was describing with better orderliness the studied process, obtaining a maximum adsorption capacity of 10.95 mg MoO42− for each gram of material. By modelling the studied adsorption process, it was proven that the pseudo-second order model is accurately describing the adsorption process. By fitting experimental data with Weber-Morris model, it was proven that MoO42− adsorption is a complex process, occurring in two different steps, one controlled by diffusion and the second one controlled by mass transfer. Further, studies were performed in order to determine the optimum pH value needed to obtain maximum adsorption capacity, but also to determine which are the adsorbed species. From pH and desorption studies, it was proven that molybdate adsorption is a physical process. In order to establish the adsorption mechanism, the thermodynamic parameters (ΔG0, ΔH0 and ΔS0) were determined.

Herein, we present the investigation of catalytical and fluorescence properties for Ni11(HPO3)8(OH)6 materials obtained through a hydrothermal approach. As part of the constant search for new materials that are both cost effective and electrocatalytically active for the oxygen evolution reaction (OER) in alkaline medium, the present study involves several graphite electrodes modified with Ni11(HPO3)8(OH)6 mixed with reduced graphene oxide (rGO) and carbon black. The experimental results obtained in 0.1 mol L–1 KOH electrolyte solution show the electrode modified with rGO, 5 mg carbon black and 1 mg nickel phosphite as displaying the highest current density. This performance can be attributed to the synergistic effect between nickel phosphite and the carbon materials. Investigation of the electrode’s OER performance in 0.1 mol L–1 KOH solution revealed a Tafel slope value of just 46 mV dec–1. By increasing the concentration to 0.5 and 1 mol L–1, this value increased as well, but there was a significant decrease in overpotential. Fluorescence properties were analyzed for the first time at the excitation length of 344 nm, and the observed strong and multiple emissions are described.

This study aimed to evaluate the comparative biological effects of Polygonum aviculare L. herba (PAH) extract and quercetin-entrapped liposomes on doxorubicin (Doxo)-induced toxicity in HUVECs. HUVECs were treated with two formulations of liposomes loaded with PAH extract (L5 and L6) and two formulations of liposomes loaded with quercetin (L3 prepared with phosphatidylcholine and L4 prepared with phosphatidylserine). The results obtained with atomic force microscopy, zeta potential and entrapment liposome efficiency confirmed the interactions of the liposomes with PAH or free quercetin and a controlled release of flavonoids entrapped in all the liposomes. Doxo decreased the cell viability and induced oxidative stress, inflammation, DNA lesions and apoptosis in parallel with the activation of Nrf2 and NF-kB. Free quercetin, L3 and L4 inhibited the oxidative stress and inflammation and reduced apoptosis, particularly L3. Additionally, these compounds diminished the Nrf2 and NF-kB expressions and DNA lesions, principally L4. PAH extract, L5 and L6 exerted antioxidant and anti-inflammatory activities, reduced γH2AX formation and inhibited extrinsic apoptosis and transcription factors activation but to a lesser extent. The loading of quercetin in liposomes increased the cell viability and exerted better endothelial protection compared to free quercetin, especially L3. The liposomes with PAH extract had moderate efficiency, mainly due to the antioxidant and anti-inflammatory effects and the inhibition of extrinsic apoptosis.

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.

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...