Synthesis and architecture study of a reactive polybutadiene polyamine as a toughening agent for epoxy resin

In this study, a novel reactive toughener for the epoxy resin was developed and compared with traditional hydroxyl‐terminated polybutadiene (HTPB). For this purpose, the highly reactive aliphatic amine‐terminated polybutadiene (ATPB) was synthesized at ambient conditions by nucleophilic substitution amination. The characterizations of the product were provided by Fourier transform infrared and ¹H NMR spectroscopy. According to the mechanical test results, incorporation of ATPB into epoxy networks can significantly toughen the epoxy matrix. The addition of 10 phr ATPB increased the critical stress intensity factor (K_IC) and critical strain energy release rate (G_IC) of the epoxy from 0.85 to 2.16 MPa m^1/2 and from 0.38 to 3.02 kJ m^?2, respectively. Furthermore, unlike HTPB, the presence of the ATPB did not deteriorate the tensile strength of the matrix. The toughening and failure mechanisms were discussed based on the epoxy network morphological characteristics. The reduction in cross‐linking density and glass transition temperature of the epoxy system upon modification with liquid rubbers was confirmed by dynamic mechanical analysis. This article opens up the possibility of utilizing reactive flexible diamines with polybutadiene backbone as effective toughening agents for thermoset polymers. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44061.     

Optimization of the Length of Silicon Nanowires Prepared from MACE Method Using Gene Expression Programming and Genetic Algorithm

Silicon - Metal-assisted chemical etching (MACE) of silicon is used in this study to fabricate silicon nanowire arrays (SiNWs) of different length. This method was modeled using gene expression...     

Direct and Residual Effects of Water Deficit Stress,Different Sources of Silicon and Plant-Growth Promoting Bacteria on Silicon Fractions in the Soil

Silicon - Silicon (Si) and plant growth promoting bacteria (PGPB) can effectively reduce the negative effects of water deficit stress and augment plant growth. Few studies have simultaneously...     

The morphology and gas‐separation performance of membranes comprising multiwalled carbon nanotubes/polysulfone–Kapton

The development of desirable chemical structures and properties in nanocomposite membranes involve steps that need to be carefully designed and controlled. This study investigates the effect of adding multiwalled nanotubes (MWNT) on a Kapton–polysulfone composite membrane on the separation of various gas pairs. Data from Fourier transform infrared spectroscopy and scanning electron microscopy confirm that some studies on the Kapton–polysulfone blends are miscible on the molecular level. In fact, the results indicate that the chemical structure of the blend components, the Kapton–polysulfone blend compositions, and the carbon nanotubes play important roles in the transport properties of the resulting membranes. The results of gas permeability tests for the synthesized membranes specify that using a higher percentage of polysulfone (PSF) in blends resulted in membranes with higher ideal selectivity and permeability. Although the addition of nanotubes can increase the permeability of gases, it decreases gas pair selectivity. Furthermore, these outcomes suggest that Kapton–PSF membranes with higher PSF are special candidates for CO₂/CH₄ separation compared to CO₂/N₂ and O₂/N₂ separation. High CH₄, CO₂, N₂, and O₂ permeabilities of 0.35, 6.2, 0.34, and 1.15 bar, respectively, are obtained for the developed Kapton–PSF membranes (25/75%) with the highest percentage of carbon nanotubes (8%), whose values are the highest among all the resultant membranes. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43839.     

A three-chamber electrochemical cell facilitated biogas upgrading and high-purity oxygen production

Journal of Applied Electrochemistry - Anion exchange membrane (AEM)-equipped electrochemical cells can be used for removing the carbon dioxide (CO2) from biogas, thereby upgrading its energy...     

A new nickel metal organic framework (Ni-MOF) porous nanostructure as a potential novel electrochemical sensor for detecting glucose

Journal of Porous Materials - A Ni-MOF-based novel electrochemical sensor was synthesized with high surface area of 1381 m2/g, significant porosity of 1.14–9.6 nm and average...     

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...     

The effect of fluorine content on the mechanical properties of poly (?-caprolactone)/nano-fluoridated hydroxyapatite scaffold for bone-tissue engineering

In this study, the effect of fluorine content on the mechanical properties of the novel poly (?-caprolactone)/nano-fluoridated hydroxyapatite nanocomposite scaffolds was investigated. Poly (?-caprolactone)/nano-fluoridated hydroxyapatite (PCL-FHA) scaffolds were produced by solvent casting/particulate leaching method. The fluoridated hydroxyapatite nanopowders had a chemical composition of Ca₁₀(PO₄)₆OH_2−xF_x (where x values were selected equal to 0.5, 1, 1.5 and 2.0). Various weight percentages (10, 20, 30 and 40) of the FHA were added to the PCL. Sodium chloride (NaCl) particles having diameter of 300-500 μm were used as porogen. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) were used to identify the phase structure and functional groups of obtained scaffolds. Mechanical properties of the prepared scaffolds were also determined. Results showed that the compressive strength of scaffolds increases with decreasing the weight percent of fluorine in FHA.     

Fractional factorial design for the optimization of supercritical carbon dioxide extraction of La, Ce and Sm ions from a solid matrix using bis(2,4,4-trimethylpentyl)dithiophosphinic acid + tributylphosphate

In this study, La³⁺, Ce³⁺ and Sm³⁺ were removed from a solid matrix using supercritical CO₂ which contained bis(2,4,4-trimethylpentyl)dithiophosphinic acid (Cyanex 301) as a chelating agent and tributylphosphate (TBP) as a co-extractant. The fractional factorial design, 2⁵⁻¹, was employed to optimize the SFE of these ions from spiked filter paper matrices. Effect of five experimental factors: amount of Cyanex 301, flow rate, temperature, pressure and amount of TBP and each factor at two levels on the SFE of these ions were studied and optimized. The results showed that these ions could be quantitatively extracted from the solid matrix at amount of Cyanex 301 of 0.14 g, flow rate of 4 ml min⁻¹, 313 K, 250 bar and amount of TBP of 30 μl. Finally, by employing a regression analysis a model was proposed. Results showed that obtained recoveries are similar to those predicted by the model.     

Dehydrogenation of isobutane over Sn/Pt/Na-ZSM-5 catalysts: The effect of SiO<Subscript>2</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> ratio,amount and distribution of Pt nanoparticles on the catalytic behavior

Sn/Pt/Na-ZSM-5 was used as catalyst for the dehydrogenation of isobutane, and the effect of SiO₂/Al₂O₃ ratio and the dispersion of Pt nanoparticles on the conversion and product selectivity were studied under atmospheric pressure at 848 K. The catalysts were characterized by various techniques such as H₂ chemisorption, TEM, SEM, EDX, XRD, FT-IR, TG/DTG, elemental analysis by XRF and ICP techniques. Higher dispersion of Pt nanoparticles in the catalyst with SiO₂/Al₂O₃ ratio of 40 resulted in higher selectivity for isobutene.