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Showing 1 to 12 of 12 for “"Epoxy Networks"”.

  1. Cresol Novolac/Epoxy Networks: Synthesis, Properties, and Processability

    Void-free phenolic networks have been prepared by the reaction of phenolic novolac resins with various diepoxides. The stoichiometric ratio can be adjusted to achieve networks with good mechanical properties while maintaining excellent flame retardance. A series of linear, controlled molecular …

    vt Repository record for Cresol Novolac/Epoxy Networks: Synthesis, Properties, and Processability (opens in a new tab)

  2. The effects of rubber modification on friction and wear of epoxy networks

    An epoxy resin (Epon 828) was chemically modified with two different elastomers, poly(dimethyl-co-diphenyl) siloxane (PSX) and carboxyl-terminated butadiene-acrylonitrile (CTBN), to enhance its fracture toughness. The friction and wear of specimens modified with different amounts of elastomer were …

    vt Repository record for The effects of rubber modification on friction and wear of epoxy networks (opens in a new tab)

  3. Step-Growth Polymerization Towards the Design of Polymers: Assembly and Disassembly of Macromolecules

    … esters), poly(triazole ether esters), and epoxy networks. Each of these polymeric systems exhibited novel structures, and either photoreactive capabilities, or high performance properties. There is an increasing trend towards the development of photoactive adhesives. In particular these …

    vt Repository record for Step-Growth Polymerization Towards the Design of Polymers: Assembly and Disassembly of Macromolecules (opens in a new tab)

  4. Synthesis and Characterization of Phosphine Oxide Containing Monomers and of the Flame Resistant Polymers Prepared Therefrom

    … In addition, suitable curing schedules for epoxy networks were determined by using dielectric monitoring techniques. The curing rates varied with the structure of the monomers and were slowest for the deactivated control (4,4'aminophenyl sulfone). Epoxy networks containing aryl phosphine …

    vt Repository record for Synthesis and Characterization of Phosphine Oxide Containing Monomers and of the Flame Resistant Polymers Prepared Therefrom (opens in a new tab)

  5. Void-Free Flame Retardant Phenolic Networks: Properties and Processability

    … volatiles during the cure, which produce networks with numerous voids. This results in materials that lack the toughness necessary for structural applications. An alternative to curing with HMTA is to crosslink the pendant phenolic groups in the novolac resin with epoxy reagents. This …

    vt Repository record for Void-Free Flame Retardant Phenolic Networks: Properties and Processability (opens in a new tab)

  6. Synthesis, properties, and modifications of engineering polymers

    … an excellent thermoplastic modifier for brittle epoxy networks. The morphology and properties of these copolymers and copolymer-homopolymer blends were studied as a function of molecular weight and chemical structure. A number of techniques were utilized to elucidate the possible toughening …

    vt Repository record for Synthesis, properties, and modifications of engineering polymers (opens in a new tab)

  7. The Effect of Chemistry and Network Structure on Morphological and Mechanical Properties of Diepoxide Precursors and Poly(Hydroxyethers)

    … between chemistry and network structure in epoxy networks as well as how mechanical properties of the resulting networks are affected by these relationships. The effects of chemistry and network structure on interphase morphology and performance in vinyl ester/carbon fiber composites have …

    vt Repository record for The Effect of Chemistry and Network Structure on Morphological and Mechanical Properties of Diepoxide Precursors and Poly(Hydroxyethers) (opens in a new tab)

  8. Modification, curing and flame retardation of epoxy resin networks

    … flame retardance of di- and higher functionality epoxy resins were investigated. The influence of curing temperature and time on morphological development and fracture behavior was also studied. Arylamine functionalized poly(arylene ether sulfone)s of controlled molecular weight were synthesized …

    vt Repository record for Modification, curing and flame retardation of epoxy resin networks (opens in a new tab)

  9. Synthesis and characterization of novel macromolecules/networks via side chain modifications of amorphous poly(arylene ethers)

    … to induce crosslinking and formed ductile networks which had improved solvent resistance and higher glass transition temperatures. The poly(arylene ethers) containing pendant amines were also reacted with an epoxy resin and 4,4'-diaminodiphenylsulfone to afford epoxy networks which had …

    vt Repository record for Synthesis and characterization of novel macromolecules/networks via side chain modifications of amorphous poly(arylene ethers) (opens in a new tab)

  10. All-atom and Coarse-grained Molecular Dynamics Modeling of Various Polymeric and Composite Materials

    … polyetherimide (PEI)-graphene composites, and epoxy network polymers, by bridging molecular-level behaviors and macroscopic thermomechanical properties. First, all-atom MD simulations are used to improve the design of porous carbon fibers derived from PAN-b-PMMA copolymers for energy storage …

    vt Repository record for All-atom and Coarse-grained Molecular Dynamics Modeling of Various Polymeric and Composite Materials (opens in a new tab)

  11. Part I: Synthesis of Aromatic Polyketones Via Soluble Precursors Derived from Bis(A-Amininitrile)S; Part Ii: Modifications of Epoxy Resins with Functional Hyperbranched Poly(Arylene Ester)s

    … successfully used to modify inherently brittle epoxy resins. The hyperbranched polymers were chemically incorporated into the epoxy networks using triphenylphosphine (TPP) as a catalyst and 4,4'-diaminodiphenyl sulfone (DDS) as a curing agent. The chemistry and the proper formation of …

    vt Repository record for Part I: Synthesis of Aromatic Polyketones Via Soluble Precursors Derived from Bis(A-Amininitrile)S; Part Ii: Modifications of Epoxy Resins with Functional Hyperbranched Poly(Arylene Ester)s (opens in a new tab)