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Epoxy Blends (epoxy + blend)
Selected AbstractsPreparation and properties of dynamically cured PP/MAH- g -EVA/epoxy blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009Xueliang Jiang Abstract A method concerning with the simultaneous reinforcing and toughening of polypropylene (PP) was reported. Dynamical cure of the epoxy resin with 2-ethylene-4-methane-imidazole (EMI-2,4) was successfully applied in the PP/maleic anhydride-grafted ethylene-vinyl acetate copolymer (MAH- g -EVA), and the obtained blends named as dynamically cured PP/MAH- g -EVA/epoxy blends. The stiffness and toughness of the blends are in a good balance, and the smaller size of epoxy particle in the PP/MAH- g -EVA/epoxy blends shows that MAH- g -EVA was also used as a compatibilizer. The structure of the dynamically cured PP/MAH- g -EVA/epoxy blends is the embedding of the epoxy particles by the MAH- g -EVA. The cured epoxy particles as organic filler increases the stiffness of the PP/MAH- g -EVA blends, and the improvement in the toughness is attributed to the embedded structure. The tensile strength and flexural modulus of the blends increase with increasing the epoxy resin content, and the impact strength reaches a maximum of 258 J/m at the epoxy resin content of 10 wt %. DSC analysis shows that the epoxy particles in the dynamically cured PP/MAH- g -EVA/epoxy blends could have contained embedded MAH- g -EVA, decreasing the nucleating effect of the epoxy resin. Thermogravimetric results show the addition of epoxy resin could improve the thermal stability of PP, the dynamically cured PP/MAH- g -EVA/epoxy stability compared with the pure PP. Wide-angle x-ray diffraction analysis shows that the dynamical cure and compatibilization do not disturb the crystalline structure of PP in the blends. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Fire-resistant cyanate ester,epoxy blendsFIRE AND MATERIALS, Issue 4 2003Richard N. Walters Abstract The cure chemistry, thermal stability and fire behaviour of a series of fire-resistant cyanate ester,epoxy blends were examined. The dicyanate and diepoxide of 1, 1-dichloro-2, 2-bis(4-hydroxyphenyl)ethylene (bisphenol-C, BPC) were combined in various molar ratios and the reaction chemistry was monitored using Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). The fire behaviour of the BPC cyanate,epoxy blends was studied in flaming and non-flaming combustion, using OSU calorimetry and pyrolysis-combustion flow calorimetry (PCFC), respectively. Published in 2003 by John Wiley & Sons, Ltd. [source] Simultaneously improved toughness and dielectric properties of epoxy/core-shell particle blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Weitao Wan Abstract Epoxy/core-shell particle blends were prepared using a diglycidylether of bisphenol A epoxy and acrylics-type core-shell particles. The impact strength of the blends was tested, and the result showed that the epoxy was greatly toughened with optimum core-shell particle content. Meanwhile, the dielectric properties of both epoxy and its blends were investigated using a broadband dielectric analyzer. It was found that the dielectric constant of the epoxy blends with lower core-shell particle content were less than that of the epoxy in the investigated frequency range, while the dielectric loss was less than that of the neat epoxy over a low frequency range, even for the epoxy blends with the optimum core-shell particle content. The dielectric breakdown strength of the epoxy blends at room and cryogenic temperature were also investigated. To identify the primary relationship of the above properties and structure of the epoxy blends, the microstructure of the core-shell particle and the morphology of the samples were observed by transmission electron microscopy and scanning electron microscopy. It was considered that these epoxy/core-shell particle blends with improved toughness and desirable dielectric properties could have a potential application in the insulation of electronic packaging system. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Effect of Biodegradable Epoxidized Castor Oil on Physicochemical and Mechanical Properties of Epoxy ResinsMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 15 2004Soo-Jin Park Abstract Summary: Biobased epoxy materials were prepared from diglycidyl ether of bisphenol A (DGEBA) and epoxidized castor oil (ECO) initiated by a latent thermal catalyst. The physicochemical and mechanical interfacial properties of the DGEBA/ECO blends were investigated. As a result, the thermal stability of the cured epoxy blends showed a maximum value in the presence of 10 wt.-% ECO content, which was attributed to the excellent network structure in the DGEBA/ECO blends. The storage modulus and glass transition temperature of the blends were lower than those of neat epoxy resins. The mechanical interfacial properties of the cured specimens were significantly increased with increasing the ECO content. This could be interpreted in terms of the addition of larger soft segments of ECO into the epoxy resins and thus reducing the crosslinking density of the epoxy network, which results in increasing toughness in the blends. KIC values of the DGEBA/ECO blends as a function of ECO content. [source] Effects of epoxy content on dynamic mechanical behaviour of PEI-toughened dicyanate,novolac epoxy blendsPOLYMER INTERNATIONAL, Issue 9 2004Dr Baochun Guo Abstract By varying the cyanate/epoxy ratio, three polyetherimide(PEI)-modified bisphenol A dicyanate,novolac epoxy resin blends with different epoxy contents were prepared. The effects of epoxy content on the dynamic mechanical behaviour of those blends were investigated by dynamic mechanical thermal analysis. The results showed that the glass transition temperature of the cyanate,epoxy network (Tg1) in the modified blend decreases with epoxy content. When the epoxy content increases, both the width of the glass transition of the cyanate,epoxy network and its peak density are depressed substantially. Although the tangent delta peak value of PEI is basically independent of epoxy content, the Tg of PEI (Tg2) decreases with epoxy content. Tg1 is independent of the PEI loading. When Tg1 is lower than Tg2, however, the Tg1 in the blend with revised phase structure is substantially lower than other blends. Copyright © 2004 Society of Chemical Industry [source] Thermal and mechanical properties of diglycidylether of bisphenol A/ trimethylolpropane triglycidylether epoxy blends cured with benzylpyrazinium saltsPOLYMER INTERNATIONAL, Issue 5 2002Soo-Jin Park Abstract The effect of blend composition on thermal stability and mechanical properties of diglycidylether of bisphenol A (DGEBA)/trimethylolpropane triglycidylether (TMP) epoxy blends cured with benzylpyrazinium salts (N -benzylpyrazinium hexafluoroantimonate, BPH) as a thermal latent catalyst was investigated. The thermal stability, characterized by the initial decomposition temperature, temperature of maximum rate of weight loss, integral procedural decomposition temperature, and activation energy for decomposition, increase in DGEBA-rich compositions. This could be due to the long repeat unit and stable aromatic ring in the DGEBA. The mechanical properties are also discussed in terms of the fracture toughness (KIC), flexural and impact tests for the blend composition studied. The addition of TMP into DGEBA gives systematic improvements in fracture toughness, which results from the increase in aliphatic and flexible chain segments of TMP. © 2002 Society of Chemical Industry [source] | ||||||||||