Facile synthesis of polyoxometalate-based composite with doped ternary NiCoFe cations as electrocatalyst for oxygen evolution reaction

The construction of efficient and low-cost electrocatalysts for oxygen evolution reactions (OER) to replace precious catalysts is a necessity to achieve economic production of hydrogen. Herein, we report an efficient tri-metallic electrocatalysts for the OER that is prepared by incorporate nickel, cobalt and iron cations on Triton X-100/phosphotungstic acid organic-inorganic composite without utilize any binders or energy consumer procedure. Considering to the synergy effect of simultaneous absorption of NiCoFe cations on composite substrate, the as-made tri-metallic catalyst exhibits excellent OER activity with a small overpotential of 210 and 330 mV at a current density of 10 and 100 mA cm^?2, respectively. Moreover, remarkable trends in electrocatalytic activity of mono-, bi- and tri-metallic electrocatalysts at low (10 mA) and high (100 mA) current density are observed. In addition, this new families of non-precious metal catalyst shows long-term durability in 1 M KOH.     

Introducing a new classification of soft rocks based on the main geological and engineering aspects

Bulletin of Engineering Geology and the Environment - Soft rock masses represent a significant percentage of rock material on the earth’s crust. The engineering properties of these rocks are...     

Sonification and interaction design in computer games for visually impaired individuals

Multimedia Tools and Applications - Video games are changing how we interact and communicate with each other. They can provide an authentic and collaborative platform for building new communities...     

Influence of Ni/Co binders and Mo2C on the microstructure evolution and mechanical properties of (Ti0.93W0.07)C–based cermets

In this research, solid–solution powder of (Ti_0.93W_0.07)C was synthesized by high–energy ball mill method followed by carbothermal reduction process. Subsequently, the acquired powder was blended with Ni/Co and Mo₂C secondary carbide, and sintered under the optimized temperature (1510?°C) for 1?h to produce the modulated cermets. A typical core–rim structure formation with solid–solution phases was confirmed by backscattered electrons studies using a Field Emission electron scanning microscope. The hardness of the synthesized cermets was enhanced by increasing the specific amount of Mo₂C. The acquired results demonstrate that the binder type has a prominent influence on the microstructure and hardness of the prepared cermets. The hardness of (Ti_0.93W_0.07)C–xMo₂C–Ni cermet increased ~ 9%, when nickel was partially substituted by cobalt.     

Impregnated active layer combustion synthesis of nano MgFe2O4 using green template

Nano-Magnesium ferrite (MgFe₂O₄) powders have been prepared by a modified combustion synthesis method named impregnated active layer combustion (IALC). The effects of five important parameters such as main fuel to oxidizer ratio (F/O), main fuel type, added fuel type, template type and main fuel (Added F/MF) to the added fuel ratio have been studied using Taguchi design. Xylitol, D-mannitol, ethylene diamine tetra acetic acid (EDTA) and diethylene triamine penta acetic acid (DTPA) were used as fuels. Besides, waste newspaper and Platanus orientalis leaf (POL) were used as new green templates. Samples were characterized by XRD, XRF, SEM, TEM, BET and VSM analyses. Results showed that the average crystallite size of the sample prepared under optimized condition (mixture of Xylitol and DTPA as fuel, POL as template, and Added F/MF ratio of 0.75) was 17.66?nm. The result was confirmed by TEM. The saturated magnetization of the optimum sample was 21?emu/g and the specific surface area was 15.377?m²/g.     

Synthesis of High‐Performance Pebax®‐1074/DD3R Mixed‐Matrix Membranes for CO2/CH4 Separation

This work deals with the incorporation of deca‐dodecasil 3 rhombohedral (DD3R) zeolite as an inorganic filler into the Pebax®‐1074‐based polymer matrix to enhance the performance of the pure polymeric membrane in CO₂/CH₄ separation. The membranes were fabricated with different concentrations of DD3R. Separation performances of the membranes were investigated at various feed pressures and temperatures. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC) analysis of the prepared membranes were performed. In the best case, selectivity for CO₂/CH₄ separation was improved, while the permeability decreased. Membranes with 1 and 5 wt % DD3R were located in the acceptable region beyond the Robeson plot (1991) for CO₂/CH₄ gas pairs.     

Multilayer assembly of ionic starches on old corrugated container recycled cellulosic fibers

In this study, old corrugated container recycled fibers were treated with polyelectrolyte multilayers consisting of biopolymer cationic starch with two degrees of substitution (DS) each in combination with one anionic starch. Pulp zeta potential, paper strength and the thin layer ellipsometry technique were applied to examine the influence of cationic starch DS on the formation of polyelectrolyte multilayers. The results indicated a significant interaction between the DS of cationic starch and the number of ionic starch layers formed. When low‐DS cationic starch was used, the pulp zeta potential and the paper strength increased significantly in assembling the first cationic layer. However, in depositing high‐DS cationic starch a greater zeta potential and a stronger influence on the paper strength were observed with a larger number of starch layers. This was confirmed by thin layer ellipsometry when a greater thickness of multilayers was achieved by employing high‐DS cationic starch to form a higher number of layers. © 2017 Society of Chemical Industry     

The effects of processing parameters on the morphology of PLA/PEG melt electrospun fibers

Electrospinning of a polymer melt is an ideal technique to produce highly porous nanofibrous or microfibrous scaffolds appropriate for biomedical applications. In recent decades, melt electrospinning has been known as an eco‐friendly procedure as it eliminates the cytotoxic effects of the solvents used in solution electrospinning. In this work, the effects of spinning conditions such as temperature, applied voltage, nozzle to collector distance and collector type as well as polyethylene glycol (PEG) concentration on the diameter of melt electrospun polylactic acid (PLA)/PEG fibers were studied. The thermal stability of PLA/PEG blends was monitored through TGA and rheometry. Morphological investigations were carried out via optical and scanning electron microscopy. Based on the results, blends were almost stable over the temperature range of melt electrospinning (170 ? 230 °C) and a short spinning time of 5 min. To obtain non‐woven meshes with uniform fiber morphologies, experimental parameters were optimized using ANOVA. While increasing the temperature, applied voltage and PEG content resulted in thinner fibers, PEG concentration was the most influential factor on the fiber diameter. In addition, a nozzle to collector distance of 10 cm was found to be the most suitable for preparing uniform non‐woven PLA/PEG meshes. At higher PEG concentrations, alterations in the collector distance did not affect the uniformity of fibers, although at lower distances vigorous bending instabilities due to polarity augmentation and viscosity reduction resulted in curly fibrous meshes. Finally, the finest and submicron scale fibers were obtained through melt electrospinning of PLA/PEG (70/30) blend collected on a metallic frame. © 2017 Society of Chemical Industry     

Effect of matrix−nanoparticle supramolecular interactions on the morphology and mechanical properties of polymer foams

In this study, we report the fabrication of supramolecular polymer nanocomposite foams with a uniform cell structure, high cell density and high expansion ratio using a soft matrix of poly(methyl acrylate‐co‐2‐hydroxyethyl methacrylate) and silica nanoparticle fillers, both functionalized with ureido‐pyrimidinone (UPy) supramolecular groups. Microcellular structures were formed using a batch foaming process at 90 °C under a 9 MPa nitrogen atmosphere. Nanocomposites were characterized and compared before and after the foaming process to investigate the effect of supramolecular interactions on the thermomechanical properties and morphology of the foams. TEM images revealed that while strong inter‐filler supramolecular interactions do not have a positive effect on their dispersion state, matrix?filler interactions derived from hydrogen bonding UPy motifs result in a rather uniform distribution of nanoparticles. Competing filler?filler and matrix?filler supramolecular interactions can be balanced and optimized by adjusting UPy populations along the chains and on the surface of nanoparticles. At a given chain functionality, increasing the nanoparticle loading up to an optimum concentration improves the mechanical properties and formability of the system. Above such concentration strong interactions between fillers, which are not compensated by the matrix, result in large aggregates and consequently undermine the material performance. Supramolecular polymer foams illustrate a similar thermal and viscoelastic behavior to that of neat samples but after foaming, due to the formation of a cellular structure and rearrangement or dissociation of UPy dimers under the foaming conditions, the elastic modulus is reduced. © 2018 Society of Chemical Industry     

Hydrolytic degradation of poly(l‐lactic acid)/poly(methyl methacrylate) blends

The hydrolytic degradation of poly(l ‐lactic acid)/poly(methyl methacrylate) (PLLA/PMMA) blends was carried out by the immersion of thin films in buffer solutions (pH = 7.24) in a shaking water bath at 60 °C for 38 days. The PLA/PMMA blends (0/100; 30/70; 50/50; 70/30; 100/0) were obtained by melt blending using a Brabender internal mixer and shaped into thin films of about 150 µm in thickness. Considering that PMMA does not undergo hydrolytic degradation, that of PLLA was followed via evolution of PLA molecular weight (recorded by size exclusion chromatography), thermal parameters (differential scanning calorimetry (DSC)) and morphology of the films (scanning transmission electron microscopy). The results reveal a completely different degradation pathway of the blends depending on the polymethacrylate/polyester weight ratio. DSC data suggest that, during hydrolysis at higher PMMA content, the polyester amorphous chains, more sensitive to water, are degraded before being able to crystallize, while at higher PLLA content, the crystallization is favoured leading to a sample more resistant to hydrolysis. In other words, and quite unexpectedly, increasing the content of water‐sensitive PLLA in the PLLA/PMMA blends does not mean de facto faster hydrolytic degradation of the resulting materials. © 2018 Society of Chemical Industry