The effects of processing parameters on formation of nano-spinel (MgAl2O4) from LiCl moltensalt

Nano-MgAl₂O₄ particles were successfully synthesized at 850 °C using the molten-salt method, and the effects of processing parameters, such as temperature, holding time and amount of salt on the crystallization of MgAl₂O₄ were investigated. Nano-alumina, magnesia and lithium chloride were used as starting materials. LiCl molten salt provided a liquid medium for reaction of Al₂O₃ and MgO to form MgAl₂O₄. The results demonstrated that MgAl₂O₄ started to form at about 650 °C and that, after the temperature was increased to 1000 °C, the amounts of MgAl₂O₄ in the resultant powders increased with a concomitant decrease in Al₂O₃ and MgO contents. After washing with hot-distilled water, the samples heated for 3 h at 850 °C were single-phase MgAl₂O₄ with 30–50 nm particle size. Furthermore, the synthesized MgAl₂O₄ particles retained the size and morphology of the Al₂O₃ powders, which indicated that a template formation mechanism dominated the formation of MgAl₂O₄ by molten-salt method.     

Siloxane‐based segmented poly(urethane‐urea) elastomer: Synthesis and characterization

A series of segmented poly(urethane‐urea) block copolymers were synthesized with varying proportions of polydimethylsiloxane diols in combination with polytetramethylene ether glycol (PTMG) using 4,4'‐methylenediphenyl diisocyanate followed by chain extension with a (50:50 mol %) mixture of 4,4'‐methylene‐bis(3‐chloro‐2,6‐diethylaniline) (M‐CDEA) and 1,4‐butanediol (BD). The molecular structures of polydimethylsiloxane urethane‐ureas were characterized by ATR‐FTIR and ¹H‐NMR spectroscopic techniques. Distribution of siloxane domain and its influence on surface roughness were investigated by scanning electron microscopy (SEM) and atomic forced microscopy (AFM), respectively. The mechanical and thermal properties of the elastomers were studied by thermogravimetric analysis, dynamical mechanical thermal analysis, and tensile measurement. The results showed that by incorporation of polydimethylsiloxane diol and M‐CDEA chain extender in polyurethane formulation, some improvements in thermal stability, fire resistance and surface hydrophilicity were achieved. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1743–1751, 2013     

Characterization of Ag(I), Co(II) and Cu(II) removal process from aqueous solutions using dolomite powder

Dolomite, a natural adsorbent, was used for removal of Ag(I), Cu(II) and Co(II) from aqueous solutions. Adsorption parameters including pH, temperature and contact time have been investigated to obtain adsorption mechanism. The results of experiments showed that adsorption of the metal ions increased by increasing pH values up to 5.5. The adsorption process was initially fast. Equilibrium isotherm data were analyzed using Langmuir, Freundlich and Dubinin-Radushkevich isotherm models. Maximum adsorption capacity of Ag(I), Cu(II) and Co(II) was 1.34, 1.63 and 2.84 mg/g at 20 oC, respectively. Kinetic models including Lagergren first-order and pseudo-second-order were used to test kinetic data. The results showed that pseudo-second-order has good agreement with experimental data. Thermodynamic parameters of the process were also investigated at different temperatures. The negative values of Gibbs free energy and enthalpy changes for Ag(I), Cu(II) and Co(II) indicated the spontaneous and exothermic nature of the adsorption process.     

The adsorption of malachite green (MG) as a cationic dye onto functionalized multi walled carbon nanotubes

Synthetic dyes are widely used by several industries to color their products. The discharge of colored wastewater into the hydrosphere causes serious environmental problems. We used functionalized multi wall carbon nanotubes as an adsorbent for the adsorption of cationic dye, malachite green, from aqueous solution. Based on information provided by the Iranian Research Institute of Petroleum Industry, carbon nanotubes are produced using a chemical vapor deposition (CVD) technique. These as-received MWCNTs were functionalized by acid treatment. The remaining dye concentration was read by UV-visible absorption spectroscopy at maximum adsorption wavelength. The effect of different operational parameters such as contact time, pH of solution, adsorbent dose and initial dye concentration were studied. The results showed that by increasing of contact time, pH and adsorbent dose the removal of dye increased, but by increasing initial dye concentration, the removal efficiency decreased. Adsorption isotherms and kinetics behavior of f-MWCNTs for removal of malachite green was analyzed, and fitted to various existing models. The experimental data were well correlated with the Langmuir isotherm with a maximum adsorption capacity (q _m ) and regression coefficient (R²) of 142.85 mg/g and 0.997, respectively. The results of this study indicate that functionalized multi wall carbon nanotubes can be used as an effective adsorbent for the removal of dyes.     

Accuracy enhancement of thermal dispersion model in prediction of convective heat transfer for nanofluids considering the effects of particle migration

A thermal dispersion model is utilized for simulation of convective heat transfer of water-TiO₂ nanofluid for laminar flow in circular tube. Concentration distribution at cross section of the tube was obtained considering the effects of particle migration, and this concentration distribution was applied in the numerical solution. Numerical solution was done at Reynolds numbers of 500 to 2000 and mean concentrations of 0.5 to 3%. Meanwhile, an experimental study was conducted to investigate the accuracy of the results obtained from the numerical solution. Non-uniformity of the concentration distribution increases with raising mean concentration and Reynolds number. Thereby, for mean concentration of 3%, at Reynolds numbers of 500 and 2000, the concentration from wall to center of the tube increases 2.6 and 30.9%, respectively. In the dispersion model, application of non-uniform concentration distribution improves the accuracy in prediction of the convective heat transfer coefficient in comparison with applying uniform concentration.     

Synthesis and characterization of modified ZSM-5 nanozeolite and their applications in adsorption of Acridine Orange dye from aqueous solution

In this research, a novel method was reported for the synthesis of ZSM-5 nanozeolite. The ZSM-5 nanozeolite was modified by transition metals such as nickel, copper and iron. These nanozeolites were characterized using X-ray diffraction, scanning electronic microscopy, Fourier transform infrared and Energy-dispersive X-ray techniques. The synthesized Fe-ZSM-5 nanozeolite has been smaller average particle size than the other nanozeolites. Adsorption behavior of Acridine Orange (AO) onto nanozeolites has been studied in an aqueous medium using UV–VIS technique. The modified nanozeolites have more adsorption efficiency compared to the unmodified ZSM-5 nanozeolite for AO removal. Also, Fe-ZSM-5 nanozeolite was shown higher adsorption efficiency of AO than the other synthesized nanozeolites. Adsorption isotherms were fitted with the Langmuir, Freundlich and D–R models. The kinetic data were investigated using pseudo-first order and pseudo-second order models. The adsorption kinetics of AO on Fe-ZSM-5 nanozeolitewell matched with pseudo-second order kinetic model.     

Solid-phase electrochemical reduction of graphene oxide films in alkaline solution

Graphene oxide (GO) film was evaporated onto graphite and used as an electrode to produce electrochemically reduced graphene oxide (ERGO) films by electrochemical reduction in 6 M KOH solution through voltammetric cycling. Fourier transformed infrared and Raman spectroscopy confirmed the presence of ERGO. Electrochemical impedance spectroscopy characterization of ERGO and GO films in ferrocyanide/ferricyanide redox couple with 0.1 M KCl supporting electrolyte gave results that are in accordance with previous reports. Based on the EIS results, ERGO shows higher capacitance and lower charge transfer resistance compared to GO.     

Static and dynamic mechanical properties of a kenaf fiber–wood flour/polypropylene hybrid composite

A natural fiber hybrid composite containing equal proportions of kenaf fibers (KFs) and wood flour (WF) as the reinforcements and polypropylene (PP) as the polymer matrix was prepared, and its static and dynamic mechanical properties were compared with KF/PP and WF/PP composites. Static tensile and flexural tests and dynamic mechanical analysis (DMA) were carried out. The hybrid composite exhibited tensile and flexural moduli and strength values closer to those of the KF composite, which indicated a higher reinforcing efficiency of KFs compared with WF. DMA revealed that although the glass‐transition temperature remained unchanged by the replacement of half of the WF by KFs, the α‐transition temperature of the hybrid composite was identical to that of WF composite. The magnitudes of both the α and β (glass) transitions of the hybrid composite were comparable to that of the WF/PP composite. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 665–672, 2005     

Production of hyaluronic‐acid‐based cell‐enclosing microparticles and microcapsules via enzymatic reaction using a microfluidic system

This article describes the preparation of cell‐enclosing hyaluronic acid (HA) microparticles with solid core and microcapsules with liquid core through cell‐friendly horseradish peroxidase (HRP)‐catalyzed hydrogelation. The spherical vehicles were made from HA derivative possessing phenolic hydroxyl moieties (HA‐Ph) cross‐linkable through the enzymatic reaction by extruding cell‐suspending HA‐Ph aqueous solution containing HRP from a needle of 180 μm in inner diameter into the ambient coaxial flow of liquid paraffin containing H₂O₂ in a microtubule of 600 μm in diameter. By altering the flow rate of liquid paraffin, the diameters of gelatin and HA‐Ph microparticles were varied in the range of 120–220 μm and 100–300 μm, respectively. The viability of the enclosed human hepatoma HepG2 cells in the HA‐Ph microparticles of 180 μm in diameter was 94.2 ± 2.3%. The growth of the enclosed HepG2 cells was enhanced by decreasing the HRP concentration. The microcapsules of 200 μm in diameter were obtained by extruding HA‐Ph aqueous solution containing thermally liquefiable cell‐enclosing gelatin microparticles of 150 μm in diameter using the same microfluidic system. The enclosed cells grew and filled the cavity within 10 days. Spherical tissues covered with a heterogeneous cell layer were obtained by degrading the microcapsule membrane using hyaluronidase after covering the surface with a heterogeneous cell layer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43107.     

A novel stimuli-responsive magnetic hydrogel based on nature-inspired tragacanth gum for chemo/hyperthermia treatment of cancerous cells

Journal of Polymer Research - Derivatives of formyl pyrazole were synthesized by the reaction of acetophenone, 4-methyl acetophenone, 3-acetyl furan, 3-acetyl thiophen and phenyl hydrazine...