Cyanoethylation of Hydroxyethyl Cellulose: Preparation and Characterization

Commercial hydroxyethyl cellulose (HEC) was cyanoethylated with acrylonitrile in nonaqueous medium in the presence of sodium hydroxide under a variety of conditions. Variables studied included the amount of acrylonitrile and the reaction temperature. The reaction was proved by NMR and its extent was measured by determining the nitrogen content. The physical properties of the obtained derivatives—i.e., the electric properties and the apparent viscosity at various rates of shear—were investigated. It was found that the extent of reaction was increased by increasing the amount of acrylonitrile as well as the reaction temperature. The products were water soluble and their apparent viscosity increased with increasing nitrogen content. The same holds true for the dielectric constant and dielectric loss.     

Effect of filler dispersion degree on the Joule heating stimulated recovery behaviour of nanocomposites

Composites based on highly branched ethylene-1-octene copolymer (EOC) and carbon black (CB) with different dispersion degree of CB were prepared. The method of the online measured electrical conductance/resistance was used to monitor the change of the electrical conductance/resistance of the composites during the preparation processes, i.e. mixing and cross-linking. It was found that the kinetics of thermally stimulated shape-memory recovery of CB filled EOC is strongly influenced by the filler dispersion degree, which actually affects the heat transfer in the composites. Using a special arrangement of experiments the Joule heating stimulated shape-memory behaviour was quantified. CB dispersion degree and related electrical resistivity determine the extent of the Joule heating stimulated shape-memory behaviour. Composite collected at the maximum in the online measured conductance–time characteristics showed the best shape-memory effect owing to the highest electrical conductivity in the solid state. The CB filled EOC showed a negative thermal coefficient of resistivity (NTC) effect, which accelerates the temperature increase and shape-memory recovery of the composites when applying a voltage.     

STEM nanoanalysis of Au/Pt/Ti-Si3N4 interfacial defects and reactions during local stress of SiGe HBTs

Nanoscaled materials are attractive building blocks for hierarchical assembly of functional nanodevices, which exhibit diverse performances and simultaneous functions. We innovatively fabricated semiconductor nano-probes of tapered ZnS nanowires through melting and solidifying by electro-thermal process; and then, as-prepared nano-probes can manipulate nanomaterials including semiconductor/metal nanowires and nanoparticles through sufficiently electrostatic force to the desired location without structurally and functionally damage. With some advantages of high precision and large domain, we can move and position and interconnect individual nanowires for contracting nanodevices. Interestingly, by the manipulating technique, the nanodevice made of three vertically interconnecting nanowires, i.e., diode, was realized and showed an excellent electrical property. This technique may be useful to fabricate electronic devices based on the nanowires' moving, positioning, and interconnecting and may overcome fundamental limitations of conventional mechanical fabrication.     

Bond Strength of a Silicone Soft Lining Material to Poly(methyl methacrylate) Resin Treated with Maleic Anhydride and its Terpolymers

This study investigated the effectiveness of surface treatment of Poly (methyl methacrylate) (PMMA) denture base resin on tensile bond strength between PMMA/silicone-based soft liner. A total of 25 specimens were fabricated and assigned into five groups (n = 5). The surfaces of PMMA were treated with maleic anhydride, maleic anhydride-styrene-vinyl-acetate, n-butylmaleate-styrene-vinyl-acetate, or n-pentamaleate-styrene-vinyl-acetate prior to Primo adhesive primer application and silicone liner placement. The Primo adhesive primer on applied group untreated dentuse base resin served as control. The tensile test was performed using a universal testing machine. Fractured surfaces were observed under Scanning Electron Microscopy (SEM) and spectroscopic interpretation of the interfaces was done by Fourier Transform Infrared (FTIR). Test results showed that surface treatment increased interfacial strength giving the highest value for n-butylmaleate-styrene-vinyl acetate treated group. SEM micrographs revealed that the specimens with n-butylmaleate-styrene-vinyl-acetate and n-penta maleate-styrene-vinyl-acetate terpolymers underwent cohesive failure. FTIR analysis indicated secondary interactions such as hydrogen bonding, possibly on acrylic resin surfaces, caused by the use of maleic anhydride and its terpolymers, and the adhesive.     

Modeling reaction kinetics of rigid polyurethane foaming process

A theoretical model was developed to simulate the polyurethane foaming process for a rigid foam. In the model, multiple ordinary differential equations were solved by MATLAB and the model was able to predict temperature profiles by inputting foam recipe information. This initial study on foam modeling focusses on reaction kinetic parameters that were fitted to experimental temperature data as a function of time. The modeling was able to accurately model temperature profiles of single‐polyol polyurethane formulations and was able to accurately predict temperature profiles of mixtures based on pure component kinetic parameters. A primary goal of this work is to expedite the ability to develop new foam formulations by simulation—especially for incorporation of new bio‐based polyols into formulations. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1131‐1138, 2013     

Online monitoring of diallyldimethylammonium chloride polymerization

Diallyldimethylammonium chloride, which is an acidic salt with numerous applications, was polymerized in water at three different monomer concentrations and at three different pHs which the monomer is in charged form. Reactions were investigated by the automatic continuous online monitoring of polymerization technique. Conversion, molecular weight, and reduced viscosity were monitored. The reaction is found to be second‐order with respect to monomer. Rate constants and molecular weights tend to increase with pH and concentration. POLYM. ENG. SCI., 54:1350–1356, 2014. © 2013 Society of Plastics Engineers     

Morphology, rheology and dynamic mechanical properties of PP/EVA/clay nanocomposites

This paper reports on morphology, rheology and dynamic mechanical properties of polypropylene (PP)/ethylene vinyl acetate (EVA) copolymer/clay nanocomposite system prepared via a single step melt compounding process using a twin screw micro-compounder. Scanning electron microscopic (SEM) investigations revealed that the dispersed phase droplet size was reduced with incorporation of an organo-modified montmorillonite (OMMT). This reduction was more significant in presence of a maleated PP (PP-g-MAH) used as compatibilizer. Phase inversion in the compatibilized blends caused a further decrease in PP droplet size. The OMMT gallery spacing was higher in nanocomposites with EVA as matrix which could be attributed to higher tendency of OMMT nanoparticles towards EVA rather than PP. This enhanced tendency was confirmed by rheological analysis too. Transmission electron microscopy (TEM) results also showed that the majority of OMMT nanoparticles were localized on the interface and within EVA droplets. According to dynamic mechanical analysis, the compatibilized nanocomposites showed higher storage and loss moduli due to better dispersion of OMMT layers. The modulus enhancement of nanocomposites as a function of OMMT volume fraction was modeled by Halpin-Tsai’s-Nielsen expression of modulus for nanocomposites. The results of modeling suggested that the aspect ratio of the intercalated OMMT, in the form of Einstein coefficient (K _E), plays a determining role in the modulus enhancement of nanocomposites.