Novel colloidal nanofiber electrolytes from PVA‐organoclay/poly(MA‐alt‐MVE), and their NaOH and Ag‐carrying polymer complexes

Novel multifunctional polymer nanofiber electrolytes with covalence crosslinked structures from various solution blends of reactive intercalated poly(vinyl alcohol)/octadecylamine montmorillonite (as a matrix polymer), poly(maleic anhydride‐alt‐methyl vinyl ether) (as a partner polymer) and their NaOH‐absorbing and Ag‐carrying polymer complexes were fabricated via electrospinning. Chemical, physical, morphological, and electrical properties of nanofiber structures were investigated by FTIR, XRD, SEM, and electrical analysis methods. Ag precursors in fiber composites significantly improved phase separation processing, fiber morphologies, diameter distributions, and electrical properties of the fibers. In situ generation of Ag nanoparticles and their distribution on nanofiber surfaces during fiber formation occurred via complex formation between silver cations and electronegative functional groups from both matrix and partner polymers as stabilizing/reducing agents. Electrical resistance and conductivity strongly depended on matrix/partner polymer ratios and absorption time of NaOH solution on nanofibers. Addition of NaOH changed the electrical properties of fiber structures from almost dielectric state to excellent conductivity form. The fabricated unique nanofiber electrolytes are promising candidates for applications in power and fuel cell nanotechnology, electrochemical, and bioengineering processes as reactive semiconductive platforms. POLYM. ENG. SCI., 56:204–213, 2016. © 2015 Society of Plastics Engineers     

Pt nanoparticles synthesized with new surfactants: improvement in C1–C3 alcohol oxidation catalytic activity

Platinum electrocatalysts were prepared using PtCl₄ as a starting material and 1-decylamine, N,N-dimethyldecylamine, 1-dodecylamine, N,N-dimethyldodecylamine, 1-hexadecylamine, and 1-octadecylamine as surfactants. These surfactants were used for the first time in this synthesis to determine whether the primary and/or tertiary structure and/or chain length of the surfactants, affects the size and/or activity of the catalysts in C₁–C₃ alcohol electro-oxidation reactions. Electrochemical measurements (cyclic voltammetry and chronoamperometry) indicated that the highest electrocatalytic performance was observed for the Pt nanocatalysts that were stabilized by N,N-dimethyldecylamine, and this has a tertiary amine structure with a short chain length (R = C₁₀H₂₁). The high performance may be due to the high electrochemical surface area, Pt(0)/Pt(IV) ratio, %Pt utility, and roughness factor (R _f). X-ray photoelectron spectroscopy, X-ray diffraction, atomic force microscopy, and transmission electron microscopy were used to determine the parameters that affect the catalytic activities.     

Hybrid dual-curable cyanate ester/boron phosphate composites via sequential thiol-ene photopolymerization and thermal polymerization

The aim of this study was to improve hybrid dual-curable cyanate ester/boron phosphate composites via sequential thiol-ene photopolymerization and thermal polymerization for high performance applications such as aerospace and electronic devices. A novel 2,2′-diallylbisphenol A dicyanate ester (DA-BADCy) which is the allyl group containing cyanate ester was synthesized and characterized. DA-BADCy, silicon containing monofunctional thiol compound, trifunctional thiol compound and boron phosphate were cured using both ultraviolet (UV) and thermal methods. Using thiol-ene system, cyanate ester formulations, which are normally prepared at high temperatures, were prepared at room temperature. This study maintains ease of application for cyanate esters. Thermal stability, flammability and thermal conductivity of the samples were evaluated by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), limiting oxygen index (LOI) and laser flash method, respectively. The samples were characterized with the following analysis; gel content, water absorption capacity and stress–strain test. Hydrophobicity of the samples was determined by the contact angle measurements. Moreover, the surface morphology of the samples was investigated by a scanning electron microscopy (SEM–EDS). The obtained results prove that the composites have good thermal and mechanical properties and with the help of easier preparation techniques, they can be used in many applications such as aerospace, electronic devices, materials engineering.     

Electrical characterization of the boron trifluoride doped poly(3‐aminoacetophenone)/p‐Si junction

Electrical and interface state properties of the borontrifluoride doped poly(3‐aminoacetophenone)/p‐Si junction have been investigated by current‐voltage and impedance spectroscopy methods. Al/p‐Si/P₃APBF₃/Aldiode indicates a nonideal behavior with electrical parameters (n = 3.53, ?_B = 0.82 eV, and R_s = 1.48 kΩ), which result from the interfacial layer, series resistance, and resistance of the organic semiconductor. The obtained barrier height value of the Al/p‐Si/P₃APBF₃/Aldiode is higher than that of the conventional Al/p‐Si (?_B = 0.58 eV) Schottky diode. The interface state density of the diode was of the order of 1.05× 10¹² eV^?1 cm^?2. It is evaluated that the barrier height and interface state density values of the diode are modified using the boron trifluoride doped poly (3‐aminoacetophenone) organic semiconductor. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers     

The Hydroloysis of ammonia borane by using Amberlyst-15 supported catalysts for hydrogen generation

Resin catalysts have the advantage of having various properties and long lifetime due to their ability to be regenerated easily, which makes them attractive supports. In this paper, a comparative study was conducted to optimize the dehydrogenation reaction condition using two different types of support materials: alumina (Al₂O₃), and Amberlyst-15 and to improve the catalytic activity as well as preparing an efficient and low-cost system for practical application, ruthenium metal catalyst was incorporated on Amberlyst-15 resin (a sulfonic acid type based upon a styrene-divinylbenzene copolymer) to release H₂ via hydrolytic dehydrogenation of ammonia borane. Using ruthenium (Ru) catalysts based on Amberlyst-15 support material and comparing the results with Al₂O₃ as the common supporting material is considered to be studied for the first time. The effect of temperature (20–50 °C), the initial ammonia borane concentration (0.05–0.5 %wt), and catalyst amount (0.2–0.5 g) on the produced H₂ yield was also investigated. Ru@Amberlyst-15 nanoparticle was discovered to be an effective catalyst for hydrogen evolution via the hydrolysis of ammonia borane with a turnover frequency value (TOF) of 343.3 min^?1, while Ru@Al₂O₃ yielded a TOF of 87.5 min^?1 at the room temperature. Therefore, it can be concluded that the Amberlyst-15 supporting effect on ruthenium metal leads an increase in the hydrogen production rate.     

Preparation of N‐doped graphene powders by cyclic voltammetry and a potential application of them: Anode materials of Li‐ion batteries

Nowadays, doped graphenes are attracting much interest in the field of Li‐ion batteries since it shows higher specific capacity than widely used graphite. However, synthesis methods of doped graphenes have secondary processes that requires much energy. In this study, in situ synthesis of N‐doped graphene powders by using of cyclic voltammetric method from starting a graphite rod in nitric acid solution has been discussed for the first time in the literature. The N‐including functional groups such as nitro groups, pyrrolic N, and pyridinic N have been selectively prepared as changing scanned potential ranges in cyclic voltammetry. The electrochemical performance as anode material in Li‐ion batteries has also been covered within this study. N‐doped graphene powders have been characterized by electrochemical, spectroscopic, and microscopic methods. According to the X‐ray photoelectron spectroscopy and Raman results, N‐doped graphene powders have approximately 16 to 18 graphene rings in their main structure. The electrochemical analysis of graphene powders synthesized at different potential ranges showed that the highest capacity was obtained 438 mAh/g after 10 cycles by using current density of 50 mA/g at N‐GP4. Furthermore, the sample having higher defect size shows better specific capacity. However, the more stable structure due to oxygen content and less defect size improves the rate capabilities, and thus, the results obtained at high current density indicated that the remaining capacity of N‐GP1 was higher than the others.     

Synthesis of polymer supported Ni (II)-Schiff Base complex and its usage as a catalyst in sodium borohydride hydrolysis

Influence of using as catalysis, Ni-Schiff Base complex which we previously synthesized [1] used to support with amberzyme oxirane resin (A.O.R.) polymer for increasing the catalytic activity in NaBH₄ hydrolysis reaction, to hydrogen generation was studied. The prepared catalyst was characterized by using SEM, XRD, BET, FT-IR analyze technique. Polymer supported Ni-Schiff Base complex catalyzed NaBH₄ hydrolysis reaction was investigated depending on concentration of NaBH₄, concentration of NaOH, temperature, percentage of Ni complex in total polymer supported Ni-Schiff Base complex and amount of catalyst factors. The maximum hydrogen production rate from hydrolysis of sodium borohydride with nickel-based complex catalyst compared to the pure nickel catalyst is increased from 772 mL H₂·g^?1 cat.·min^?1 to 2240 mL H₂ g^?1 cat.·min^?1 [1], and with supported amberzyme oxirane resin polymer this nickel based complex catalyst was increased to 13000 mL H₂·g^?1 cat.·min^?1 at 30 °C. The activation energy of complex catalyzed NaBH₄ hydrolysis reaction was found as 25.377 kJ/mol. This work also includes kinetic information for the hydrolysis of NaBH₄.     

Developing microencapsulated 12‐hydroxystearic acid (HSA) for phase change material use

Phase change materials (PCM) have an increasingly more important role as a thermal energy storage (TES) media. However, leakage problem of PCM causes limitation during their integration in TES systems. Therefore, the encapsulation of PCMs is attracting research interest to extend usage of PCMs in real TES applications in recent years. In this study, hydroxystearic acid (HSA) was encapsulated with polymethyl methacrylate (PMMA) and different PMMA comonomer shells via emulsion polymerization method for the first time in literature. HSA with high melting temperature range (74–78°C) can widen the scope of using PCMs, and the encapsulated form can make it more versatile. The chemical structures, morphologies, and thermophysical properties of capsules were determined by FT‐IR, SEM, DSC, TGA, and thermal infrared camera. Among the produced HSA capsule candidates, PMMA‐HEMA is the most promising with latent heat of 48.5 J/g with melting range of 47 to 85°C. SEM analysis indicated that the capsules have spherical shape with compact surface at nano‐micro (100–440 nm) size range; however, some capsules exhibited agglomeration.     

Calculations of neutron-induced production cross-sections of W up to 20 MeV

Neutron-induced cross-sections for the stable isotopes ^{180,182,183,184,186}W in the energy region up to 20 MeV have been calculated. Calculations were made with the codes CEM03.01 and ALICE/ASH, using the following models: the Dubna version of the intranuclear cascade model for the cascade stage of interaction; the hybrid, the geometry dependent hybrid and the exciton model for the pre-equilibrium component; the Hauser–Feshbach and the Weisskopf–Ewing statistical models for the equilibrium component. Effects of some important model parameters such as level density parameter and pairing correction were investigated. Calculated cross-sections were compared with available experimental data in the literature and with ENDF/B-VI T = 300 K and JENDL-3.3 T = 300 K evaluated data libraries.     

The investigation of the neutron emission spectra of Th and U for neutron incident energy from 2 to 18 MeV

In this study, experimental neutron-emission spectra produced by (n, xn) reactions on nuclei ²³²Th have been compared with experimental ²³⁸U(n, xn) neutron-emission spectra from 2 to 18 MeV. Angle-integrated cross-sections in neutron induced reactions on targets ²³⁸U have been calculated at the bombarding energies from 2 to 18 MeV. In the calculations, the geometry dependent hybrid model and the cascade exciton model including the effects of pre-equilibrium have been used. In addition, we have described how multiple pre-equilibrium emissions can be included in the Feshbach–Kerman-Koonin (FKK) fully quantum-mechanical theory. By analyzing (n, xn) reaction on ²³⁸U with the incident energy from 2 to 18 MeV, the importance of multiple pre-equilibrium emission can be seen clearly. All calculated results have been compared with experimental data. The obtained results have been discussed and compared with the available experimental data and found agreement with each other.