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  • 1
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymerization rate, glass transition temperature, storage modulus, molecular weight between crosslinks and heterogeneity of the final polymer product were studied as a function of the crosslinking agent concentration for several multifunctional methacrylates. The goal of this study was to determine the effect of crosslinking monomer structure and concentration on the rates of polymerization and mechanical properties of the polymer. A series of copolymers with equal concentrations of crosslinking double bonds was prepared using a monomethacrylate plus a di- or trimethacrylate. The trimethacrylate systems had higher glass transition temperatures, larger storage moduli, and smaller molecular weights between crosslinks than the comparable dimethacrylate systems. However, the heterogeneity of the trimethacrylate systems was found to be much more extensive. Additionally, the maximum rate of polymerization was found to increases with increasing crosslinking agent when octyl methacrylate was used as the monomethacrylate, but passed through a maximum when 2-hydroxyethyl methacrylate was used. The relative rates of polymerization between the trimethacrylate and dimethacrylate systems also depended on the monomethacrylate employed and the concentration of the crosslinking agent.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2297-2307 
    ISSN: 0887-6266
    Keywords: crosslinked polymers ; photopolymerizations ; living radical polymerizations ; mechanical properties ; dynamic mechanical analysis ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crosslinked polymer networks are used in a wide variety of applications. To use these materials effectively, a fundamental understanding of their structural evolution and the relationship between material properties and structure is essential. In this article, a novel technique employing “iniferters,” i.e., living radical polymerizations, to photopolymerize these networks is utilized to study the property and structural evolution of these highly desirable materials. Living radical polymerizations are used in this work since this technique avoids the problem of carbon radical trapping encountered while using conventional initiators. Dynamic mechanical measurements are performed on highly crosslinked methacrylate networks to glean information regarding their structural heterogeneity. By performing these measurements on homopolymerized samples at various stages of the reaction and on copolymerized samples of multifunctional methacrylates, the mechanical properties are characterized as a function of double bond conversion and comonomer composition. From such analyses, with respect to both temperature and frequency, quantitative conclusions regarding the structure of the networks are drawn. This effort is aimed at exploiting the living radical polymerizations initiated by p-xylylene bis(N,N-diethyl dithiocarbamate) (XDT), to study the mechanical property evolution and structural heterogeneity of crosslinked polymers which is nearly impossible otherwise. Polymers examined in this study include networks formed by homopolymerization of diethylene glycol dimethacrylate (DEGDMA) and polyethylene glycol 600 dimethacrylate (PEG600DMA) as well as copolymers of DEGDMA and PEG600DMA. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2297-2307, 1997
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 3759-3772 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel method for the synthesis of second harmonic generating (SHG) materials is proposed and tested in which liquid, multifunctional monomers with dissolved dopants are poled and polymerized simultaneously. Instead of requiring multiple steps and hours or days to synthesize SHG materials, this technique is able to produce doped guest/host systems in a single step process which takes two minutes or less. In addition, the polymer that is produced is highly crosslinked and provides good thermal and temporal stability of the SHG. To increase the stability of the SHG signal the dopant can be attached to the crosslinked network further decreasing the mobility. Advantages of this process include its simplicity, speed, stability, and the ability to make SHG materials of any thickness by successively polymerizing layers. This work presents a detailed description of the new procedure as well as results for the effect of dopant concentration, the magnitude of the SHG, and the structure of the crosslinked polymer that serves as the dopant host. Also, a method of synthesizing functionalized Disperse Red 1 that can be incorporated as a side chain is presented. Results are presented for the order parameter and SHG stability at room temperature and 100°C.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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