Micellar Growth in Cetylpyridinium Chloride/Alcohol System: Role of Long Chain Alcohol,Electrolyte and Surfactant Head Group

The microstructural transition of aqueous 0.1 M cetylpyridinium chloride (CPC) in the combined presence of salt KBr and long chain alcohol (C₉OH-C₁₂OH) has been studied as a function of alcohol concentration, electrolyte concentration and temperature. The viscosity of the CPC/KBr micellar system showed a peaked behavior with alcohol concentration (C ₀), due to alcohol induced structural transition, which was confirmed by dynamic light scattering (DLS) and rheological analysis. Besides C ₀, the chain length of alcohol (n) was found to show a remarkable effect on the micellization behavior of CPC/KBr system. It was observed that the ability of alcohol to induce micelle growth diminishes with n, which was well supported by viscosity, rheology and DLS measurements. To examine the effect of the electrolyte on the micellar growth, the salt concentration was varied from 0.05 to 0.15 M and it was observed that with increase in [KBr], the peak position shifts towards lower C ₀. The effect of temperature on the micellar system showed interesting phase behavior for CPC/KBr/Decanol. The system exhibited a closed solubility loop with an upper critical solution temperature (UCST) > the lower critical solution temperature (LCST), reminiscence of nicotine-water system. The role of surfactant head group on the structural evolution was revealed by comparing the present results with our previous report for similar micellar system, CTAB/KBr/long chain alcohol.     

Modeling of single-lap composite adhesive joints under mechanical and thermal loads

Two-dimensional (plane-stress and plane-strain) theoretical models are presented for stress analysis of adhesively bonded single-lap composite joints subjected to either thermal or mechanical loading or a combination thereof. The joints consist of similar/dissimilar orthotropic or isotropic adherends and an isotropic adhesive interlayer. The governing differential equation of the problem is obtained using a variational method which minimizes the complementary strain energy in the bonded assembly. In this formulation, through-thickness variation of shear and peel stresses in the interlayer is considered. Both shear and normal traction-free boundary conditions are exactly satisfied. Peel and shear stresses obtained from plane-strain analytical models considering a homogeneous adhesive interlayer are in close agreement with those of the finite element predictions. A systematic parametric study is also conducted to identify an ideal set of geometric and material parameters for the optimal design of single-lap composite joints.     

Experimental study of paddy drying in a vortex chamber

The intensification of interfacial mass, heat, and momentum transfer makes vortex chambers potentially interesting for the efficient drying of paddy, allowing shorter drying times and/or more compact equipment. The presence of a shell introduces particular challenges. Intraparticle diffusion limitations are strong and may reduce the advantage from intensified interfacial mass and heat transfer and the efficiency of air usage. Furthermore, high shear and normal stresses in the fast rotating particle bed may cause damage to the paddy shell, posing problems for transport and storage. With these specific aspects in mind, the use of vortex chambers for paddy drying is experimentally evaluated.     

Polyacrylonitrile solution homogeneity study by dynamic shear rheology and the effect on the carbon fiber tensile strength

Poly(acrylonitrile‐co‐methacrylic acid) (PAN‐co‐MAA)/N,N‐dimethylformamide (DMF) solutions were prepared and dynamic shear rheology of these solutions were investigated. With increasing stirring time up to 72 h at 70°C, the polymer solution became less elastic (more liquid‐like) with a ～60% reduction in the zero‐shear viscosity. Relaxation spectra of the PAN‐co‐MAA/DMF solutions yield a decrease in relaxation time (disentanglement time, τ_d), corresponding to an about 8% decrease in viscosity average molecular weight. The log‐log plot of G′ (storage modulus) versus G″ (loss modulus) exhibited an increase in slope as a function of stirring time, suggesting that the molecular level solution homogeneity increased. In order to study the effect of solution homogeneity on the resulting carbon fiber tensile strength, multiple PAN‐co‐MAA/DMF solutions were prepared, and the precursor fibers were processed using gel‐spinning, followed by continuous stabilization and carbonization. The rheological properties of each solution were also measured and correlated with the tensile strength values of the carbon fibers. It was observed that with increasing the slope of the G′ versus G″ log‐log plot from 1.471 to 1.552, and reducing interfilament fiber friction during precursor fiber drawing through the addition of a fiber washing step prior to fiber drawing, the carbon fiber strength was improved (from 3.7 to 5.8 GPa). This suggests that along with precursor fiber manufacturing and carbonization, the solution homogeneity is also very important to obtain high strength carbon fiber. POLYM. ENG. SCI., 56:361–370, 2016. © 2016 Society of Plastics Engineers     

A Review on Wear and Friction Performance of Carbon–Carbon Composites at High Temperature

Carbon–carbon (C/C) composite is one of the best ceramic matrix composite due to its high mechanical properties and applications at control environments in various sectors. Carbon–carbon composite is made of woven carbon fibers; carbonaceous polymers and hydrocarbons are used as matrix precursors. These composites generally have densities <2.0 g/cm³ even after densification. C/C composites have good frictional properties and thermal conductivity at high temperature. Also C/C composite can be used as brake pads in high‐speed vehicles. In spite of various applications, C/C composites are very much prone to oxidation at high temperature. Therefore, C/C composites must be protected from oxidation for the use at high temperature.     

Aqueous Slip Casting of Transparent Aluminum Oxynitride

Highly transparent Aluminum oxynitride (AlON) body has been produced using aqueous slip casting technique. High‐purity alumina and AlN were used as raw materials for the synthesis of single‐phase AlON powder. As‐synthesized AlON powder was surface modified to enable the AlON powders resistant to hydrolysis in water during aqueous slip casting. High solid loaded aqueous AlON slip was prepared for casting followed by drying and sintering to produce transparent AlON. Phase formation and stability was characterized by XRD, pH, and viscosity measurements. AlON powders before and after surface treatments were characterized. Sintered transparent AlON samples were characterized for their mechanical, microstructural, and optical properties. Sintered and polished AlON produced in this study has shown inline transparency up to 80% between 0.22 and 6 μm wavelength region.     

Minocycline Loaded Hybrid Composites Nanoparticles for Mesenchymal Stem Cells Differentiation into Osteogenesis

Bone transplants are used to treat fractures and increase new tissue development in bone tissue engineering. Grafting of massive implantations showing slow curing rate and results in cell death for poor vascularization. The potentials of biocomposite scaffolds to mimic extracellular matrix (ECM) and including new biomaterials could produce a better substitute for new bone tissue formation. A purpose of this study is to analyze polycaprolactone/silk fibroin/hyaluronic acid/minocycline hydrochloride (PCL/SF/HA/MH) nanoparticles initiate human mesenchymal stem cells (MSCs) proliferation and differentiation into osteogenesis. Electrospraying technique was used to develop PCL, PCL/SF, PCL/SF/HA and PCL/SF/HA/MH hybrid biocomposite nanoparticles and characterization was analyzed by field emission scanning electron microscope (FESEM), contact angle and Fourier transform infrared spectroscopy (FT-IR). The obtained results proved that the particle diameter and water contact angle obtained around 0.54 ± 0.12 to 3.2 ± 0.18 µm and 43.93 ± 10.8° to 133.1 ± 12.4° respectively. The cell proliferation and cell-nanoparticle interactions analyzed using (3-(4,5-dimethyl thiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium inner salt) MTS assay (Promega, Madison, WI, USA), FESEM for cell morphology and 5-Chloromethylfluorescein diacetate (CMFDA) dye for imaging live cells. Osteogenic differentiation was proved by expression of osteocalcin, alkaline phosphatase activity (ALP) and mineralization was confirmed by using alizarin red (ARS). The quantity of cells was considerably increased in PCL/SF/HA/MH nanoparticles when compare to all other biocomposite nanoparticles and the cell interaction was observed more on PCL/SF/HA/MH nanoparticles. The electrosprayed PCL/SF/HA/MH biocomposite nanoparticle significantly initiated increased cell proliferation, osteogenic differentiation and mineralization, which provide huge potential for bone tissue engineering.     

Effect of flow rate and temperature on crystallization kinetics,crystallinity index,and elastic modulus of PEEK

Dynamic, in situ wide angle X-ray scattering (WAXS) studies of the melt crystallization of injection-molded poly(ether ether ketone) (PEEK) have been carried out using an X-ray diffractometer and a position-sensitive detector. A test cell has been fabricated to fit inside the diffractometer and yet work as a complete injection molding apparatus. The rate of crystallization has been shown to increase with decreasing crystallization temperature and/or increasing flow rate in the mold. The crystallization rate decreases dramatically with increase in melt soak time at 400°C. The crystallinity index, which affects the stiffness, toughness, and fracture behavior of PEEK, has been measured under various processing conditions, by wide angle X-ray scattering, so as to optimize the process parameters: molding time, mold temperature, melt temperature, soak time at melt temperature, and flow rate. It has been shown that the crystallinity and hence the elastic modulus increase with increase in crystallization temperature and/or flow rate. Chain orientation has been shown to be absent in the bulk of the injection-molded specimens under normal molding conditions.