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  • polycarbonate (PC)  (2)
  • Enthalpy relaxation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 4 (1997), S. 213-219 
    ISSN: 1572-8935
    Keywords: Physical aging ; PEI ; Enthalpy relaxation ; Sub-Tg molecular relaxation ; Dynamic mechanical analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Physical aging behavior of glassy, amorphous poly(ether imide) (PEI) at a high aging temperature range (15 ∼ 25 °C below the polymer Tg of 215 °C) was investigated. A quantitative modeling approach was utilized to describe the aging process of PEI. The experimental data of enthalpy of relaxation for constructing the models were obtained using differential scanning calorimetry (DSC). At relatively low aging temperatures, the enthalpy of relaxation simply increases linearly with the logarithm of time. At high temperatures another parameter accounting for distribution is needed for better description. Furthermore, the sub-Tg molecular chain relaxation of aged PEI was characterized using dynamic mechanical analysis (DMA). Physical aging significantly suppressed the β chain relaxation but not the γ-relaxation, suggesting that the chain segmental motion for the β-relaxation is the one responsible for chain conformation changes reaching an equilibrium glassy state.
    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 A: Polymer Chemistry 34 (1996), S. 781-788 
    ISSN: 0887-624X
    Keywords: DGEBA epoxy ; polycarbonate (PC) ; PMMA ; reactions ; IPN ; ternary polymer blends ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Morphology and reaction mechanisms were probed on a model reactive ternary blend system of polycarbonate (PC), poly(methyl methacrylate) (PMMA), and diglycidylether of bisphenol-A (DGEBA) epoxy by using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). Molecular interactions/reactions between the components in the blends after heating treatments are discussed. It was found that reactions took place among the components and that an interpenetrating network was built. The possible reaction mechanisms and the resulting structures after the heating treatments were probed. In the blends, PC and DGEBA reacted to form a network, while PMMA remained free. The semiinterpenetration, however, did not result in a network interlocked into a homogeneous state. The single Tg of the heated ternary DGEBA/PC/PMMA blends actually did not reflect a homogeneous interpenetrating network. Due to relatively small PMMA domains, the ternary blend network exhibited a single Tg. Upon etching the PMMA domains from the blend by acetone, a clearly interpenetrating network of reacted PC and epoxy was exposed and confirmed. The reactions leading to such a morphology are discussed with experimental evidence. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 97-103 
    ISSN: 0887-624X
    Keywords: phenoxy ; polycarbonate (PC) ; exchange reactions ; morphology ; polymer blends ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Effects of trans reactions on the morphology, glass transition, and phase behavior in a classical blend system of a poly(hydroxyl ether bisphenol-A) (phenoxy) with bisphenol-A polycarbonate (PC) were investigated by differential scanning calorimetry (DSC) and optical microscopy. Although two Tgs were observed in the as-prepared PC/phenoxy blends, an apparently single, but broadened, Tg was found in the blends after heating at high temperatures, typically 200-250°C for short times. The optical microscopy results indicated that same scales of heterogeneity did exist in post-heated PC/phenoxy blends as well as unheated blends. Explanations were provided. After heating-induced interchange reactions (—OH and carbonate), randomly linked polymer chains might form at the numerous interfaces of the mutually occluded/included micro-domains. The majority of the chains in the micro-domains are forced to relax in coordinated motion modes after heating, thus showing a single Tg. A mechanism of trans reactions in interfacial regions was briefly discussed in supplement to earlier reports in the literature. © 1997 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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