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  • Polymer and Materials Science  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 753-762 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The α-relaxation process of seven commercial diglycidyl ether of bisphenol-A (DGEBA) epoxy resins of varying molecular weights, without hardener, was characterized by measuring the frequency and temperature dependence of the complex permittivity, (∊ast;). The temperature dependences of the frequency of maximum dipole loss ƒmax and the ionic conductivity σ are non-Arrhenius and can be described by the Williams-Landel-Ferry (WLF) equation. The frequency dependence of the molecular relaxation process is described by the Kohlrausch-Williams-Watts (KWW) relaxation function. The WLF C1 parameter and the KWW β parameter, describing the temperature and frequency dependences, respectively, vary systematically with the molecular weight of the resin. These results are discussed in the context of recent theories of the glass transition.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A new method is presented for controlling the rate of antibody (Ab) release from an inert matrix composed of poly(ethylene-co-vinyl acetate) (EVAc), a biocompatible polymer that is frequently used to achieve controlled release. Using supercritical propane, a parent EVAc sample (Mn = 70 kDa, Mw/Mn = 2.4) was separated into narrow fractions with a range of molecular weights (8.7 〈 Mn 〈 165 kDa, 1.4 〈 Mw/Mn 〈 1.7). Solid particles of Ab were dispersed in matrices composed of different polymer fractions and the rate of Ab release into buffered saline was measured. The rate of Ab release from the EVAc matrix depended on molecular weight: 〉 90% of the incorporated Ab was released from low molecular weight fractions (Mn 〈 40 kDa) during the first 5 days of release, while 〈 10% was released from the high molecular weight fraction (Mn 〉 160 kDa) during 14 days of release. No significant differences in polymer composition, glass-transition temperature, or crystallinity were identified in the different molecular weight fractions of EVAc. Mechanical properties of the polymer did depend on the molecular weight distribution, and correlated directly with Ab release rates. Because it permits rapid and reproducible fractionation of polymers, supercritical fluid extraction can be used to modify the performance of polymeric biomaterials. © 1993 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 19-26 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The release of bovine serum albumin (BSA) from two types of ethylene-co-vinyl acetate (EVAc) polymer matrices was studied over the temperature range 4-50°C. Protein release and weight change of the matrices were evaluated in uitro. The copolymers were characterized using differential scanning calorimetry (DSC) and thermomechanical analysis (TMA). During release, the devices initially exhibit a rapid increase in weight to a maximum, followed by a more gradual decrease for the duration of the release. The time to the maximum weight and the magnitude of the maximum weight gain are temperature dependent. These effects are related to the temperature-dependent diffusivity of the BSA and elastic modulus of the EVAc. The DSC and TMA reveal melting of the crystalline phase of the polymer. The corresponding loss of mechanical integrity of the polymer leads to anomalous weight gains at these temperatures. The observed swelling and release is explained by a model in which the osmotic pressure of the protein within the pore network causes elastic deformation of the polymer matrix.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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