Effect of Porosity on Structure,Young's Modulus,and Thermal Conductivity of SiC Foams by Direct Foaming and Gelcasting

The study demonstrates the aqueous processing of solid‐state‐sintered SiC foams by gelcasting technique. Aside from increasing strength of green bodies, gelcasting monomers were the source of carbon additive which helped in sintering of SiC foams. Sintered foams with the relative density (RD) between 0.44 and 0.11 were processed by direct foaming of SiC slurries followed by gelcasting and sintering. Structural analysis by X‐ray tomography showed the presence of spherical pores with bimodal pore size distribution and the proportion of large size cell and their interconnectivity increased in low RD foams. SEM study revealed that decreased RD resulted in gradual changes in the strut microstructure from the grains with faceted interface to smooth interfaced grains. The analysis of changes in Young's modulus and thermal conductivity with RD were in agreement with the Ashby model for open cell foams.     

Contribution of organomodified clay on hybrid microstructures and properties of epoxidized natural rubber‐based nanocomposites

Influence of organic modifying agent of clay on dispersion, distribution, hybrid microstructure formation, and associated performance properties of epoxidized natural rubber‐based composites was evaluated. Binary and ternary composites of carbon black (CB) and two organomodified layered silicates (i.e., nanomer I30E and Cloisite 30B) were prepared and characterized based on small angle X‐ray scattering, transmission electron microscopy, hydrodynamic swelling, tensile measurement, and dynamic mechanical analyses. Greater extent of exfoliation and “nanounit” formation was noted in ternary composites containing nanomer I30E, which was reflected in higher interfacial roughness (d_s = 2.82) and lower radius of gyration (R_g = 205 Å). Morphological observations suggested higher nanomer I30E–CB interactions than that of Cloisite 30B–CB. The interplatelet distance in Cloisite 30B (d = 1.83 nm) stacks was lower than that of nanomer I30E (d = 2.26 nm). These two factors jointly contributed in higher breakdown of nanomer I30E stacks by CB than that of Cloisite 30B stacks. Greater exfoliation and nanounit formation in I30E–CB‐filled nanocomposite was also reflected in increased degree of crosslinking (n = 20 × 10^?5%), tensile modulus/strength, half height width of damping peak (20.3°C), and filler effectiveness (C = 0.33). POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Size Distribution and Morphology of Liposome Aerosols Generated By Two Methodologies

Pulmonary delivery of sustained release formulations needs drug encapsulation in a suitable matrix, as well as the generation of aerosols with high lung penetration and suitable release characteristics. Nanometer sized liposomes offer the potential for biocompatibility, controlled release and easy internalization in the lung. For uniform dose delivery and drug release kinetics, it is of interest to understand generation techniques to obtain aerosols containing nearly monodispered nanometer sized dry particles. Two aerosolization techniques, air-jet atomization and electrohydrodynamic atomization (EHDA) were studied to identify conditions under which the inclusion of one-liposome-per-drop could be achieved. In air-jet atomization, low lipid concentrations resulted in a unimodal aerosol with a median mobility diameter of 94 (± 3.5) nm, while higher concentrations led to larger median diameters, implying possible inclusion of multiple liposomes per drop. In EHDA, tuning drop sizes in the range of 130 to 200 nm, as well as the use of high lipid concentrations, resulted in a bimodal aerosol distribution, with peaks at 35 and 100 nm mobility diameters. TEM images of the liposome aerosol from EDHA showed fused liposomes, resulting in cylindrical structures with different physical diameters. It was hypothesized that deformation of liposomes to cylindrical structures in the micro-capillary liquid tip of the electrospray, and interactions along the axial or cross sectional surfaces led to dry particles with different mobility sizes.     

Kinetics of the enzymatic degradation of poly(vinyl acetate) in solution

The enzymatic degradability of poly(vinyl acetate) was investigated in toluene solutions at various temperatures with hog pancreas lipase. The polymer degraded by specific scission to yield oligomeric products with a molecular weight of 700. Continuous distribution kinetics were used to determine the rate coefficients. The variation of the rate coefficients with the temperature indicated an optimum at 55°C. The p‐toluene sulfonic acid catalyzed degradation of poly(vinyl acetate) was also investigated. The degradation mechanism was random chain scission, and the energy of activation for degradation was determined from the variation of the rate coefficients with the temperature. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2579–2582, 2003     

Degradation profiles of polyester–urethane (hydroxylated polyester/diphenylmethane diisocyanate) and polyester–melamine (hydroxylated polyester/hexamethoxymethylmelamine) coatings: An accelerated weathering study

The successful material performance of coatings depends on the environmental conditions to which they are exposed. The effects of the diol structure and acetoacetylation on the weathering degradation of hydroxylated polyester (HP)/hexamethoxymethylmelamine and HP/diphenylmethane diisocyanate clear coatings were studied. The acetoacetylation of HPs led to better performance for higher application solids than the acetoacetylation of their base counterparts. Weathering degradation profiles were investigated with dynamic mechanical thermal analysis, scanning electron microscopy, and X‐ray photoelectron spectroscopy. The structural variations of the building blocks and acetoacetylation were found to be important for enhancing the stability of coatings at higher application solids. Polyester–urethane coatings were more stable toward weathering than polyester–melamine coatings. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1069–1081, 2005     

A numerical model to predict the powder–binder separation during micro-powder injection molding

The micro-powder injection molding (micro-PIM) process has the potential to bridge the gap between the design and manufacturing of micro-components that are often used in small and handy devices. Numerical modeling helps to analyze and overcome various difficulties of micro-PIM. In the present work, a numerical model is developed to predict the powder–binder separation (a common defect in PIM and especially severe in micro-PIM) during the injection of an alumina feedstock. A powder–binder separation criterion is proposed dealing with applied injection pressure and friction force between the powder and binder. An indirect comparison of feedstock travel time between two locations is used to validate the model. The predicted segregation from the simulated result is supported by a qualitative experimental measurement. The developed model can be used to optimize injection parameters to get a defect-free product.     

Angular absorptance and thermal degradation analysis of TiB2/Ti(B,N)/SiON/SiO2 multilayer solar absorber coating

Multilayer solar selective absorber coatings have been developed in the last few decades. The thermal stability in terms of microstructure gives an insightful understanding of the optical properties of such coatings. In this context, we extensively utilized transmission electron microscopy (TEM) analysis to establish the thermal stability of TiB₂/Ti(B,N)/SiON/SiO₂ coating, under thermal cycling/continuous heating to 500°C in vacuum for 250 h. In particular, this work reports the variation in the solar absorptance of TiB₂/Ti(B,N)/SiON/SiO₂ coating with different angles of incidence of the solar radiation. Extensive analysis using the TEM technique reveals the presence of oxide interlayers that act as diffusion barrier layers to enhance the thermal stability of the coating. Computational simulation using SCOUT software validates the measured reflectance spectrum of the developed multilayer coating. The minor changes in absorptance and emissivity after heat treatment in vacuum at 500°C, together with high solar absorptance over a broad angular variation, establish the potential application of TiB₂/Ti(B,N)/SiON/SiO₂ as a selective coating in concentrated solar power systems.     

Metal hollow sphere electrocatalysts

Metal micro-/nano hollow spheres have been widely applied in numerous fields during the last decade. This review will only focus on the synthetic strategies to synthesize hollow spherical structures in the enhancement of their electrocatalytic activity, especially the metal hollow spherical materials. We present a comprehensive overview of synthetic strategies for metal hollow spherical structures which have been approached specifically in electrochemical reactions. These synthetic methods are mainly categorized as hard templates, soft templates, sacrificial templates and without templates. The review further includes electrocatalytic approaches of hollow spherical metals in different electrochemical processes, especially the methanol electro-oxidation reaction for methanol fuel cell application and hydrogen and oxygen evolution reactions in water electrolyzer, as metal hollow spherical materials are especially applied in these specific reactions.     

Hybrid coatings from novel silane-modified glycidyl carbamate resins and amine crosslinkers

Organic–inorganic hybrid coatings were prepared using silane-modified glycidyl carbamate resins and different amine crosslinkers via the sol–gel process. Two different silane-modified glycidyl carbamate resins with 33% and 20% silane modification were prepared. The synthesized resins were crosslinked with amine crosslinkers such as Amicure PACM, Ancamide 805, Ancamide 2050, Ancamide 2353, Epicure 3164, Jeffamine D-400, etc., at different epoxy to amine equivalent ratios. The formulated hybrid coatings were cured at laboratory temperature and humidity for more than 20 days and subjected to different tests. The hybrid coatings were analyzed using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) during network maturation. Post-cured coatings were also analyzed to understand the effect of structural variables on the coatings thermal properties. Mechanical testing of the post-cured coatings such as König pendulum hardness, crosshatch adhesion and impact resistance were also evaluated. Solvent resistance of the coatings was evaluated by of testing the methyl ethyl ketone (MEK) double rub resistance. Atomic force microscopy (AFM) was used to characterize the surface topography of the hybrid coatings. Finally, structure–property correlations were given based on the observed results.