Effect of Plasma pretreatment and Graphene oxide ratios on the transport properties of PVA/PVP membranes for fuel cells.

In this study, a novel proton-conducting polymer electrolyte membrane based on a mixture of polyvinyl alcohol (PVA)/polyvinyl pyrrolidone (PVP) (1:1) mixed with different ratios of graphene oxide (GO) and plasma-treated was successfully synthesized. Dielectric barrier dielectric (DBD) plasma was used to treat the prepared samples at various dose rates (2, 4, 6, 7, 8, and 9 min) and at fixed power input (2 kV, 50 kHz). The treated samples (PVA/PVP:GO wt%) were soaked in a solution of styrene and tetrahydrofuran (70:30 wt%) with 5 × 10-3 g of benzoyl peroxide as an initiator in an oven at 60 °C for 12 h and then sulfonated to create protonic membranes (PVA/PVP-g-PSSA:GO). The impacts of graphene oxide (GO) on the physical, chemical, and electrochemical properties of plasma-treated PVA/PVP-g-PSSA:x wt% GO membranes (x = 0, 0.1, 0.2, and 0.3) were investigated using different techniques. SEM results showed a better dispersion of nanocomposite-prepared membranes; whereas the AFM results showed an increase in total roughness with increasing the content of GO. FTIR spectra provide more information about the structural variation arising from the grafting and sulfonation processes to confirm their occurrence. The X-ray diffraction pattern showed that the PVA/PVP-g-PSSA:x wt% GO composite is semi-crystalline. As the level of GO mixing rises, the crystallinity of the mixes decreases. According to the TGA curve, the PVA/PVP-g-PSSA:x wt% GO membranes are chemically stable up to 180 °C which is suitable for proton exchange membrane fuel cells. Water uptake (WU) was also measured and found to decrease from 87.6 to 63.3% at equilibrium with increasing GO content. Ion exchange capacity (IEC) was calculated, and the maximum IEC value was 1.91 meq/g for the PVA/PVP-g-PSSA: 0.3 wt% GO composite membrane. At room temperature, the maximum proton conductivity was 98.9 mS/cm for PVA/PVP-g-PSSA: 0.3 wt% GO membrane. In addition, the same sample recorded a methanol permeability of 1.03 × 10-7 cm2/s, which is much less than that of Nafion NR-212 (1.63 × 10-6 cm2/s). These results imply potential applications for modified polyelectrolytic membranes in fuel cell technology.

Textural properties and adsorption behavior of Zn-Mg-Al layered double hydroxide upon crystal violet dye removal as a low cost, effective, and recyclable adsorbent.

The preparation of adsorbents plays a vital role in the adsorption method. In particular, many adsorbents with high specific surface areas and unique shapes are essential for the adsorption strategy. A Zn-Mg-Al/layer double hydroxide (LDH) was designed in this study using a simple co-precipitation process. Adsorbent based on Zn-Mg-Al/LDH was used to remove crystal violet (CV) from the wastewater. The impacts of the initial dye concentration, pH, and temperature on CV adsorption performance were systematically examined. The adsorbents were analyzed both before and after adsorption using FTIR, XRD, and SEM. The roughness parameters and surface morphologies of the produced LDH were estimated using 3D SEM images. Under the best conditions (dose of adsorbent = 0.07 g and pH = 9), the maximum adsorption capacity has been achieved. Adsorption kinetics studies revealed that the reaction that led to the adsorption of CV dye onto Zn-Mg-Al/LDH was a pseudo-second-order model. Additionally, intraparticle diffusion suggests that Zn-Mg-Al/LDH has a fast diffusion constant for CV molecules (0.251 mg/(g min1/2)). Furthermore, as predicted by the Langmuir model, the maximal Zn-Mg-Al/LDH adsorption capacity of CV was 64.80 mg/g. The CV dimensionless separation factor (RL) onto Zn-Mg-Al/LDH was 0.769, indicating that adsorption was favorable. The effect of temperature was performed at 25, 35, and 45 °C in order to establish the thermodynamic parameters ∆Ho, ∆So, and ∆Go. The computed values indicated exothermic and spontaneous adsorption processes. The study presented here might be used to develop new adsorbents with enhanced adsorption capabilities for the purpose of protecting the water environment.

Methanol electro oxidation on Ni-Pt-CrO/CNFs composite: morphology, structural, and electrochemical characterization.

In this work, prepared nanoparticle samples of Ni1-xCrx with a fixed ratio of platinum (3%) were synthesized and loaded onto carbon nanofibers, which were produced by an electrospinning technique and carbonized at 900 °C for 7 h in an argon atmosphere. A variety of analysis techniques were applied to examine the stoichiometry, structure, surface morphology, and electrochemical activity. The carbonization process produces carbon nanofibers decorated with metal nanoparticles. Typical fibre diameters are 250-520 nm. The fibre morphologies of the treated samples don't exhibit any overt alterations. A study of the samples' methanol electrocatalytic capabilities was conducted. Cyclic voltammetry, chronoamperometry, and electrochemical impedance measurements were used to investigate catalytic performance and electrode stability as a function of electrolyte concentration, scan rate, and reaction time. The electrooxidation reaction's activation energy is increased, and the electrode's stability is increased, when Cr is added to Ni. In sample C3, the maximum current density (JPE) was 170.3 mA/cm2 at 0.8 V with an onset potential of 0.352 V. Utilizing our electrocatalysts, the electrooxidation of methanol involves a mix of kinetic and diffusion control limiting reactions. This study has shown how to fabricate a powerful Ni-Pt-Cr-based methanol electrooxidation catalyst using a novel approach.

Valorization of spent double substituted Co-Ni-Zn-Fe LDH wastewater nanoadsorbent as methanol electro-oxidation catalyst.

Finding suitable non-expensive electrocatalyst materials for methanol oxidation is a significant challenge. Waste valorization of spent wastewater nanoadsorbents is a promising route toward achieving circular economy guidelines. In this study, the residual of layered double hydroxide (LDH) can be used as an electrocatalyst in direct methanol fuel cells as a novel approach. The Co-Ni-Zn-Fe LDH was prepared by the co-precipitation method followed by the adsorption of methyl orange (MO). Moreover, the spent adsorbent was calcined at different temperatures (200, 400, and 600 °C) to be converted to the corresponding mixed metal oxides (MMO). The prepared samples were characterized using XRD, FTIR, HRTEM, zeta potential, and hydrodynamic size measurements. The spent adsorbent was tested as an electro-catalyst for direct methanol electro-oxidation. The spent LDH/MO adsorbent showed a maximum current density of 6.66 mA/cm2 at a 50 mV/s scan rate and a 1 M methanol concentration. The spent MMO/MO adsorbent showed a maximum current density of 8.40 mA/cm2 at a 200 °C calcination temperature, 50 mV/s scan rate, and a 3 M methanol concentration. Both samples show reasonable stability over time, as indicated by the chronoamperometric response. Further nanoengineering of used nanoadsorbents could be a promising path to repurposing these wastes as electro-oxidation catalysts.

Radiation effect on positronium formation in solid state nuclear track detector.

The effect of alpha-particles on CR-39, a material used in solid state nuclear track detectors (SSNTDs), has been investigated using the positron annihilation lifetime (PAL) technique. The samples were irradiated using a (238)Pu alpha-source of energy ranging from 1 to 5 MeV and with different doses ranging from 0 to 57.87 mGy. The ortho-positronium (o-Ps) lifetime, tau(3), shows a slight increase as the irradiation dose increases, while a rapid change in the o-Ps intensity, I(3) at 10 mGy was found. In addition, the PAL parameters (tau(3), I(3)) have been studied as a function of the energy of alpha-particles. The obtained results indicate that the o-Ps lifetime increases slightly with increasing energy of the alpha-particle. On the other hand, the o-Ps intensity decreases exponentially with increasing alpha-particle energy, plateaus, and finally increases. The data show that the track diameter increases with decreasing energy of the alpha-particle, while the track density increases with increasing the irradiation dose. A correlation between the track diameter and the o-Ps hole diameter was observed.