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Neat Epoxy (neat + epoxy)

Distribution by Scientific Domains
Polymers and Materials Science83%

Terms modified by Neat Epoxy

  • neat epoxy resin
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    Selected Abstracts

    Asymmmetric Diamino Functionalization of Nanotubes Assisted by BOC Protection and Their Epoxy Nanocomposites

    ADVANCED FUNCTIONAL MATERIALS, Issue 18 2010
    Yao Zhao
    Abstract Homogenous dispersion and strong interfacial bonding are prerequisites for taking full advantage of the mechanical properties of nanotubes in a composite. In order to simultaneously achieve both conditions, a highly efficient and mechanically non-destructive functionalization of nanotubes is developed. With fluoronanotubes as the precursor, asymmetric diamine molecules, N -BOC-1,6-diaminohexane, are used to replace fluorines on the wall of fluoronanotubes and construct covalent bonding to the surface of the nanotubes. A BOC de-protection reaction is conducted and the resulting exposed amino groups create strong covalent bonds with the matrix in the course of epoxy ring-opening etherification and curing chemical reactions. In comparison with the conventional functionalization based on symmetric diamine molecules, the functionalized nanotubes derived from the BOC-protected diamine molecule are more dispersed within the epoxy matrix. Dynamic mechanical analysis shows that the functionalized nanotubes have better crosslinking with the matrix. The composites reinforced by the nanotubes demonstrate improvement in various mechanical properties. The Young's Modulus, ultimate tensile strength, and storage modulus of composites loaded with 0.5 wt% functionalized nanotubes are enhanced by 30%, 25%, and 10%, respectively, compared with the neat epoxy. The increase of the glass transition temperature, as much as 10 °C, makes the composites suited for engineering applications under higher temperatures. The new functionalization method allows for an competitive enhancement in the composite performance in use of relatively low cost raw nanotubes at a small loading level. The reinforcement mechanism of the functionalized nanotubes in the epoxy resin is discussed. [source]

    Study of epoxy toughened by in situ formed rubber nanoparticles

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008
    Jun Ma
    Abstract The effect of rubber nanoparticles on mechanical properties and fracture toughness was investigated. Rubber nanoparticles of 2,3 nm were in situ synthesized in epoxy taking advantage of the reaction of an oligomer diamine with epoxy. The chemical reaction was verified by gel permeation chromatography (GPC) and 1HNMR, and the microstructure was characterized by transmission electron microscope. The rubber nanoparticles caused much less Young's modulus deterioration but toughened epoxy to a similar degree in comparison with their peer liquid rubber that formed microscale particles during curing. Fifteen wt % of rubber nanoparticles increased fracture energy from 140 to 840 J/m2 with Young's modulus loss from 2.85 to 2.49 GPa. The toughening mechanism might be the stress relaxation of the matrix epoxy leading to larger plastic work absorbed at the crack tip; there is no particle cavitation or deformation; neither crack deflection nor particle bridging were observed. The compound containing rubber nanoparticles demonstrates Newtonian liquid behavior with increasing shear rate; it shows lower initial viscosity at low shear rate than neat epoxy; this provides supplementary evidence to NMR and GPC result. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

    Simultaneously improved toughness and dielectric properties of epoxy/core-shell particle blends

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008
    Weitao 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]

    Mechanical and morphological properties of organic,inorganic, hybrid, clay-filled, and cyanate ester/siloxane toughened epoxy nanocomposites

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007
    S. Nagendiran
    Abstract Organic,inorganic hybrids involving cyanate ester and hydroxyl-terminated polydimethylsiloxane (HTPDMS) modified diglycidyl ether of bisphenol A (DGEBA; epoxy resin) filled with organomodified clay [montmorillonite (MMT)] nanocomposites were prepared via in situ polymerization and compared with unfilled-clay macrocomposites. The epoxy-organomodified MMT clay nanocomposites were prepared by the homogeneous dispersion of various percentages (1,5%), and the resulting homogeneous epoxy/clay hybrids were modified with 10% HTPDMS and ,-aminopropyltriethoxysilane as a coupling agent in the presence of a tin catalyst. The siliconized epoxy/clay prepolymer was further modified separately with 10% of three different types of cyanate esters, namely, 4,4,-dicyanato-2,2,-diphenylpropane, 1,1,-bis(3-methyl-4-cyanatophenyl) cyclohexane, and 1,3-dicyanato benzene, and cured with diaminodiphenylmethane as a curing agent. The reactions during the curing process between the epoxy, siloxane, and cyanate were confirmed by Fourier transform infrared analysis. The results of dynamic mechanical analysis showed that the glass-transition temperatures of the clay-filled hybrid epoxy systems were lower than that of neat epoxy. The data obtained from mechanical studies implied that there was a significant improvement in the strength and modulus by the nanoscale reinforcement of organomodified MMT clay with the matrix resin. The morphologies of the siloxane-containing, hybrid epoxy/clay systems showed heterogeneous character due to the partial incompatibility of HTPDMS. The exfoliation of the organoclay was ascertained from X-ray diffraction patterns. The increase in the percentage of organomodified MMT clay up to 5 wt % led to a significant improvement in the mechanical properties and an insignificant decrease in the glass-transition temperature versus the unfilled-clay systems. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source]

    Tribological behaviour of polymeric coatings.

    LUBRICATION SCIENCE, Issue 4 2005
    Part I. Aramid particle-reinforced epoxy nanocomposite systems
    Abstract An epoxy-based nanocomposite containing a low concentration of nanometric TiO2 (4 vol. %), graphite powder (7.21 vol. %), and 2,14 vol. % aramid particles was developed as a coating material. The mechanical and tribological performance of the composites was investigated. The epoxy filled only with TiO2 possessed significantly improved impact strength and flexural properties, whereas the further incorporation of graphite and aramid particles had a deleterious effect on most of the mechanical properties, except the modulus. The tribological behaviour of the composites was tested in sliding and fretting modes. Under sliding conditions, the addition of nanometric TiO2 alone significantly improved the wear resistance and decreased the coefficient of friction compared to the neat epoxy. The sliding wear and friction behaviour was further enhanced with the incorporation of graphite and aramid particles. Contrary to the sliding wear behaviour, the fretting wear and friction behaviour was worse for the epoxy filled only with TiO2, but was significantly enhanced by the incorporation of graphite and aramid particles. The optimum aramid particle content for sliding and fretting wear of the epoxy-based nanocomposite was determined as 10 vol. %. [source]

    Tribological behaviors of aligned carbon nanotube/fullerene-epoxy nanocomposites

    POLYMER ENGINEERING & SCIENCE, Issue 8 2008
    Huan Wang
    The tribological properties of aligned CNT/fullerene-epoxy nanocomposites were studied by nanoscratch, nanowear, and nano-indentation tests. Compared with neat epoxy, aligned CNT/fullerene-epoxy nanocomposites showed lower friction coefficient in scratch tests, a reduction of 38.1 and 26.2%, respectively. In addition, the aligned CNT-epoxy composite showed better wear resistance and its hardness and Young's modulus increased by 29.4 and 16.8%, respectively. In contrast, for a fullerene-epoxy nanocomposite with 10 wt% fullerenes, the hardness decreased by 50% and the Young's modulus decreased by more than 60% when compared with the neat epoxy. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source]