Preparation and Characterization of PVA/PVP Nanofibers as Promising Materials for Wound Dressing

The PVA/PVP, PVA/PVP with 5% and 10% chitosan and PVA/PVP-Iodine fibers were produced via electrospinning technique. Their morphological and chemical characteristics were examined with SEM, TGA, FT-IR, viscometer and four-point probe conductivity measurement apparatus. The addition of chitosan increased the viscosity and the electrical conductivity of the polymer. The increase chitosan contents resulted in the diameters of the fibers smaller than expected. This was attributed to the increase in the viscosity of the solution and the electrical conductivity of the resulting fibers. The DSC results show that iodine was efficiently cross-linked with the polymer, forming an amorphous structure.     

EFFECT OF INITIAL MOISTURE CONTENT ON THE THIN LAYER DRYING CHARACTERISTICS OF HAZELNUTS DURING ROASTING

ABSTRACT

Effect of initial moisture content on the thin layer drying characteristics of hazelnuts during roasting was described for a temperature range of 100-160°C, using several thin layer equations. The effective diffusivity varied from 2.8×10^?7 to 21.5×10^?7m²/s over the temperature and moisture range. Temperature dependence of the diffusivity coefficient was described by Arrhenius-type relationship. The activation energy for moisture diffusion was found to be 2703 kJ/kg, 2289 kJ/kg and 2030 kJ/kg for the initial moisture content of 12.3% db, 6.14% db, and 2.41% db, respectively. Two-term equation gave better predictions than Henderson and Pabis and Thompson equations, and satisfactorily described thin layer drying characteristics of hazelnut roasting. A generalised mathematical model with the linear temperature dependence for moistured, non-treated and pre-dried hazelnuts were also developed.     

Highly Efficient Room Temperature Synthesis of Silver‐Doped Zinc Oxide (ZnO:Ag) Nanoparticles: Structural,Optical, and Photocatalytic Properties

Synthesis of silver‐doped zinc oxide (ZnO:Ag) nanoparticles through precipitation method has been reported. The synthesis was conducted at room temperature and no subsequent thermal treatment was applied. ZnO nanoparticles were characterized by X‐ray diffraction (XRD), transmission electron microscopy (TEM), X‐ray photoelectron spectroscopy (XPS), fourier transmission infrared spectroscopy (FTIR), and ultraviolet‐visible (UV–Vis) spectroscopy. Detailed crystallographic investigation was accomplished through Rietveld refinement. The effect of silver content on structural and optical properties of resultant ZnO nanoparticles has been reported. It was found that silver doping results in positional shifts for the XRD peaks and the absorption band edge of ZnO. These were attributed to the substitutional incorporation of Ag⁺ ions into Zn²⁺ sites within the ZnO crystal. In addition, higher silver incorporation resulted in smaller size for ZnO nanoparticles. The photocatalytic activity of the ZnO:Ag nanoparticles was also determined by methylene orange (MO) degradation studies and compared to that of undoped ZnO. Improved photocatalytic activity was obtained for ZnO:Ag nanoparticles. It has been shown that an optimum amount of silver dopant is required to obtain maximum photocatalytic activity.     

Effects of Nanoparticles on Film Properties of Waterborne Acrylic Emulsions

Waterborne acrylic emulsion was obtained by using methyl methacrylate, ethyl and butyl acrylate monomers. Emulsions containing nanoparticles were prepared by blending the stable dispersions containing SiO₂ or MMT nanoparticles. The films were prepared from emulsions and coating tests were applied. The physical properties of prepared emulsions are better than the commercial emulsions. The addition of the nanoparticles especially SiO₂ have positive effect on the resistance to environmental conditions of emulsions. Waterborne acrylic emulsions containing nanoparticles prepared in this study can be used in the manufacturing of the semi-lustrous emulsion type nano paint with low cost, high performance and environmentally friendly.     

Physical and Mechanical Properties of Iron Powder Filled Polystyrene Composites

This article reports on an experimental study of the physical and mechanical properties of Polystyrene (PS) and Fe-PS polymer composites containing 5, 10, and 15 vol.% of Fe powder. After mixing Fe powder and PS in a twin-screw extruder, an injection-molding machine was used to prepare unfilled PS and Fe-PS polymer composite samples. After that, the material properties were experimentally determined for each sample. The investigated material properties included the modulus of elasticity, yield and tensile strength, % elongation, Izod impact strength (notched), hardness (Shore D), melt flow index (MFI), heat deflection temperature (HDT), Vicat softening point, and glass transition temperature (T _g ). The results indicated that, compared to the unfilled PS, an addition of Fe into PS decreases the yield and tensile strength, % elongation, and Izod impact strength. Furthermore, it was determined that the Fe particles increase the modulus of elasticity, hardness, MFI, Vicat softening point, and HDT values.     

Application of adaptive neuro-fuzzy interference system on biosorption of malachite green using fir (Abies nordmanniana) cones biomass

Removal of malachite green (MG) onto fir (Abies nordmanniana) cones biomass (FCB) as a lingo-cellulosic-based structure material was investigated in the present study. Characterization of FCB was performed using Fourier transform infra red and scanning electron microscobe analyses. Several parameters (biomass dose and particle size, dye concentration, temperature, and pH) were investigated to determine optimal working conditions. Subsequently, FCB yelded a q_e of 2.2?mg/g for 50?g/L FCB, in an MG solution of 110?mg/L, pH 3.3, at a temperature of 21?°C, on a 0.2-0.4?mm fraction powder after 146?h of contact. Adaptive neuro-fuzzy interference system modeling was applied to experimental data and results showed that predicted model fitted experimental data with R² = 0.994. In a nutshell, it can be concluded that FCB shows good potential for treating MG contaminated waters.     

Phase Transfer Catalysis with Quaternary Ammonium Type Gemini Surfactants: <Emphasis Type="Italic">O</Emphasis>-Alkylation of Isovanillin

In this paper, O-alkylation of isovanillin with unusual phase transfer catalysts alkandiyl-α,ω-bis(dimethylalkylammonium bromide) dimeric surfactants (also known as gemini surfactants) is described. Some dimeric surfactants with simple hydrophobic alkyl chains and others with hydrophobic alkyl chains containing ester functionalities with different lengths were synthesized and characterized in our laboratory. The alkylation of isovanillin with alkyl halide was successively carried out in the presence of potassium carbonate and a phase transfer catalyst in tetrahydrofuran. The same reactions were also performed with both the traditional phase transfer catalyst tetrabutylammonium bromide and without any catalyst. The results were compared with those of dimeric surfactants. Consequently, it was expressed that alkandiyl-α,ω-bis(dimethylalkylammonium bromide) dimeric surfactants successively exhibit the character of phase transfer catalysts through environmentally friendly procedures under mild conditions. The most significant feature of this work is that dimeric surfactants have been determined to act as phase transfer agents.     

Preparation and properties of selective polyurethane films and their use for the development of biomedical dopamine sensor

Polyurethane films were synthesized by 3,4-divanillyltetrahydrofuran and different diisocyanates. These prepared polyurethanes were characterized by FT-IR, DSC, DTA, and TGA techniques. For the amperometric applications, synthesized polyurethanes exhibited suitable T_g (°C), good thermal stability and good adhesive properties. In addition, because of their interesting film properties, attempts were made to prepare dopamine-sensing electrode. For this reason, selectivity of film-coated electrodes obtained from the chemically prepared polyurethanes toward electroactive and nonelectroactive species were examined by means of DPV technique. From the electrochemical results obtained, it has been demonstrated that the PU-1-coated electrode can be used for the development of biomedical sensor.     

Photocrosslinked biobased phase change material for thermal energy storage

A series of novel photocrosslinked biobased shape‐stabilized phase change materials (PCMs) based on octadecanol, eicosanol and docosanol have been prepared by UV technique for the purpose of thermal energy storage applications. Epoxidized soybean oil was reacted with acrylic acid to form acrylated soybean oil (ASO). The structure and composition, cross‐section morphology, thermal stability performances and phase change behaviors of ASO and UV‐cured PCMs were examined by using Attenuated total reflection fourier transform infrared spectroscopy, thermogravimetric analysis system (TGA), scanning electron microscopy, and differential scanning calorimetry. The results indicate that the UV‐cured biobased PCMs possess perfect phase change properties and a suitable working temperature range. The heating process phase change enthalpy is measured between 30 and 68 J/g, and the freezing process phase change enthalpy is found between 18 and 70 J/g. The decomposition of UV‐cured PCMs started at 260 °C and reached a maximum of 430 °C. All the biobased UV‐cured PCMs improved latent heat storage capacity in comparison with the pristine ASO sample. With the obtained results we conclude that, these materials promise a great potential in thermal energy storage applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43757.     

Stabilized electrospinning of heat stimuli/in situ crosslinkable nanofibers and their self‐same nanocomposites

We present a strategy for stabilizing the morphological integrity of electrospun polymeric nanofibers by heat stimuli in situ crosslinking. Amorphous polymer nanofibers, such as polystyrene (PS) and its co‐polymers tend to lose their fiber morphology during processing at temperatures above their glass transition temperature (T_g) typically bound to happen in nanocomposite/structural composite applications. As an answer to this problem, incorporation of the crosslinking agents, phthalic anhydride (PA) and tributylamine (TBA), into the electrospinning polymer solution functionalized by glycidylmethacrylate (GMA) copolymerization, namely P(St‐co‐GMA), is demonstrated. Despite the presence of the crosslinker molecules, the electrospinning polymer solution is stable and its viscosity remains unaffected below 60 °C. Crosslinking reaction stands‐by and can be thermally stimulated during post‐processing of the electrospun P(St‐co‐GMA)/PA‐TBA fiber mat at intermediate temperatures (below the T_g). This strategy enables the preservation of the nanofiber morphology during subsequent high temperature processing. The crosslinking event leads to an increase in T_g of the base polymer by 30 °C depending on degree of crosslinking. Crosslinked nanofibers are able to maintain their nanofibrous morphology above the T_g and upon exposure to organic solvents. In situ crosslinking in epoxy matrix is also reported as an example of high temperature demanding application/processing. Finally, a self‐same fibrous nanocomposite is demonstrated by dual electrospinning of P(St‐co‐GMA) and stabilized P(St‐co‐GMA)/PA‐TBA, forming an intermingled nanofibrous mat, followed by a heating cycle. The product is a composite of crosslinked P(St‐co‐GMA)/PA‐TBA fibers fused by P(St‐co‐GMA) matrix. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44090.