The control of abnormal grain growth in low-voltage SnO2 varistors by microseed addition

In this research, the addition effects of three different quantities of micron-sized seeds (microseeds) to a SnO₂ varistor prepared from nanomaterials on the microstructure and electrical properties were studied. Moreover, surge-withstanding capability of low-voltage SnO₂ varistors was investigated. The X-ray diffraction pattern disclosed a single phase SnO₂ for microseed grains. The morphological features of samples were characterized using scanning electron microscopy. The abnormal distribution of grain size with elongated grains of SnO₂ in fine grains matrix was observed in sintered samples without microseeds. The low content of microseed addition (0.3 wt%) had not controlled abnormal grain growth, however, it increased mean grain size to 37 µm. Although the high content of microseeds (7.5 wt%) stopped abnormal grain growth, it had a negative effect on relative density and mean grain size. The normal grain size distribution with maximum mean grain size (45 µm) was obtained in samples containing 1.5 wt% microseeds. These samples showed the lowest breakdown field (240 V/cm) and the highest surge-withstanding capability (1.5 kA/cm²). Furthermore, the standard deviation of the electrical parameters of these samples was improved due to normal grain-size distribution.     

Synthesis and characterization of exfoliated poly(styrene‐co‐methyl methacrylate) nanocomposite via miniemulsion atom transfer radical polymerization: an activators generated by electron transfer approach

Exfoliated poly(styrene‐co‐methyl methacrylate) nanocomposites were synthesized using activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP). Miniemulsion polymerization was used for its abundant advantages to encapsulate inorganic materials and eliminate organic solvents from products for environmentally friendly purposes. Cetyltrimethylammonium bromide (CTAB) as a cationic surfactant, which is an effective surfactant at higher temperatures, was used to stabilize the miniemulsion system. Successful miniemulsion AGET ATRP was carried out by using 4,4'‐dinonyl‐2,2'‐bipyridine (dNbPy) as a hydrophobic ligand. Formation of monodispersed droplets and particles with sizes in the range of 200nm was examined by dynamic light scattering (DLS). Conversion and molecular weight study were also carried out using gravimetry and gel permeation chromatography, respectively. By adding clay content, a decrease in the conversion and molecular weight of the nanocomposites are observed. However, an increase in the PDI values of nanocomposites was observed by the addition of nanoclay content. Thermogravimetric analysis results demonstrate that thermal stability of all the nanocomposites in comparison with the neat copolymer increases. Differential scanning calorimetry results show that T_g decreases by increasing clay content. Monodisperse distribution of spherical shape particles with sizes in the range of ∼ 200 nm was demonstrated by using scanning electron microscopy images of nanocomposite containing 1 wt% of nanoclay, which is more compiled with DLS results. Transmission electron microscopy results shows well‐dispersed exfoliated clay layers in the polymer matrix of PSMNM 1, which is coincidence with X‐ray diffraction data. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Preparation of tailor‐made polystyrene nanocomposite with mixed clay‐anchored and free chains via atom transfer radical polymerization

Tailor‐made polystyrene nanocomposite with mixed free and clay‐attached polystyrene chains was synthesized using atom transfer radical polymerization. Vinylbenzyl trimethylammonium chloride having a double bond, which could be incorporated into polystyrene chains by a grafting through process, was used as a nanoclay modifier. Conversion and molecular weight evaluation was carried out using gas chromatography and gel permeation chromatography, respectively. The thermogravimetric analysis results confirmed the elevated thermal stability of the nanocomposites in comparison with the neat polystyrene sample. Additionally, the T_g increases by clay loading was confirmed by differential scanning calorimetry (DSC). The difference in the degradation temperature of C? Br bond in attached and free polystyrene chains was well revealed in DSC thermograms. Finally, a lower clay loading resulted in an exfoliated structure as proved by X‐ray diffraction and transmission electron microscopy results. © 2010 American Institute of Chemical Engineers AIChE J, 2011     

Investigation of effective dimensionless numbers on initiation of instability in combustion of moisty organic dust简

In this work, the effect of various effective dimensionless numbers and moisture contents on initiation of instability in combustion of moisty organic dust is calculated. To have reliable model, effect of thermal radiation is taken into account. One- dimensional flame structure is divided into three zones： preheat zone, reaction zone and post-flame zone. To investigate pulsating characteristics of flame, governing equations are rewritten in dimensionless space-time （（, r/, ~） coordinates. By solving these newly achieved governing equations and combining them, which is completely discussed in body of article, a new expression is obtained. By solving this equation, it is possible to predict initiation of instability in organic dust flame. According to the obtained results by increasing Lewis number, threshold of instability happens sooner. On the other hand, pulsating is postponed by increasing Damk6hler number, pyrolysis temperature or moisture content. Also, by considering thermal radiation effect, burning velocity predicted by our model is closer to experimental results.     

Efficient Synthesis of α-Monoglycerides via Solventless Condensation of Fatty Acids with Glycerol Carbonate

Highly pure α-monoglycerides (5a–e) were successfully prepared in high yields by the condensation of fatty acids such as lauric, myristic, palmitic, stearic and oleic (2a–e) with glycerol carbonate (4-hydroxymethyl-1,3-dioxolan-2-one) (1) in the presence of triethylamine as catalyst. Reaction conditions and spectroscopic identification of products will be presented in this article.     

Kinetic study of styrene atom transfer radical polymerization from hydroxyl groups of graphene nanoplatelets: Heterogeneities in chains and graft densities

Confinement effect of graphene nanoplatelets on the kinetics of styrene atom transfer radical polymerization was studied by a “grafting from” reaction. Graphene oxide was modified by different amounts of (3‐aminopropyl) triethoxysilane and then alpha‐bromoisobutyryl bromide from the hydroxyl groups. Polymerization of styrene in the presence of modified graphene and free initiator, ethyl alpha‐bromoisobutyrate, was accomplished at 110°C. Then, effect of various graft densities and different graphene loadings on the heterogeneous graft and free polystyrene chains characteristics and also kinetics of polymerization was studied by gas and gel permeation chromatographies. Efficiency of grafting reactions along with the graft contents was studied by X‐ray photoelectron spectroscopy, elemental analysis, and thermogravimetric analysis. Confinement effects of graphene on the relaxation behavior of polystyrene chains and also morphology of the graphenes were studied by differential scanning calorimetry and transmission electron microscopy, respectively. POLYM. ENG. SCI., 55:1720–1732, 2015. © 2014 Society of Plastics Engineers     

Evolution of vinyl chloride conversion below critical micelle concentration: A response surface analysis

Utilizing response surface methodology, the conversion of vinyl chloride monomer (VCM) was monitored when the polymerization temperature, the type of surfactant, and the weight ratio of water‐to‐monomer (W/M) were taken as the emulsion polymerization variables. Because the homogeneous nucleation was found to be the dominant mechanism in VCM emulsion polymerization, irrespective of the surfactant concentration, the whole experiments have been carried out below critical micelle concentration of the used surfactants. Among all the studied variables, the polymerization temperature appeared as the most effective parameter; moreover, its interactive effect with W/M caused different trends in the alteration of final conversion being observed. Also, depending on the reaction temperature, the VCM conversion would be affected by the type of the surfactant used. Contrarily, simultaneous change in the type of surfactant and W/M revealed an insignificant effect on the evolution of VCM conversion. The optimization of final conversion of VCM was also accessible through contour plots of response surface methodology. It is worth noting that, taking a conventional approach into consideration, the alteration of VCM conversion seemed to be a monotonic function of temperature. J. VINYL ADDIT. TECHNOL., 21:157–165, 2015. © 2014 Society of Plastics Engineers     

Synthesis,Characterization, and Bioactivity Evaluation of Amorphous and Crystallized 58S Bioglass Nanopowders

The aim of this work was synthesis and characterization of amorphous and crystallized 58S nanopowders produced via sol‐gel method. According to the thermal analysis, the nanopowders were heat‐treated at 600°C and 1100°C. X‐ray diffraction results revealed that the phases of Wollastonite and tricalcium phosphate were formed at 1100°C. The in vitro tests showed that hydroxyl carbonate apatite was precipitated on both crystallized and amorphous nanopowders, while amorphous nanopowder showed a higher bioactivity than that of crystallized nanopowder. In contrast, mechanical properties of crystallized specimen were higher than those of amorphous specimen.