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  • PVC  (1)
  • blends of poly(ε-caprolactone) and poly(styrene-co-acrylonitrile) phase separation of  (1)
  • crystal orientation of UHMW polyethylene in drawn films  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 94 (1988), S. 283-286 
    ISSN: 1436-5073
    Keywords: orientation ; FTIR ; polymer blends ; PVC ; PMPPL
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effect of the macromolecular plasticizer poly(α-methyl-α-n-propyl-β-propiolactone), PMPPL, on the orientation of poly(vinyl chloride), PVC, has been studied by FTIR spectroscopy. The addition of PMPPL to PVC does not change significantly the degree of orientation of PVC segments. In blends, PMPPL chains are more oriented when the matrix is richer in PVC but the PMPPL orientation function always remains smaller than that of PVC segments.
    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 31 (1993), S. 719-727 
    ISSN: 0887-6266
    Keywords: phase separation of crystalline and miscible polymer blends ; blends of poly(ε-caprolactone) and poly(styrene-co-acrylonitrile) phase separation of ; differential scanning calorimetry (DSC) of blends of poly(ε-caprolactone) and poly(styrene-co-acrylonitrile) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase separation of a crystalline and miscible polymer blend, poly(ε-caprolactone) /poly(styrene-co-acrylonitrile) (PCL/SAN), has been studied by differential scanning calorimetry (DSC), using a SAN containing 28.3% of acrylonitrile units. Several phenomena can be associated with the occurrence of phase separation depending upon the composition of the mixture. Following annealing at high temperatures, below and above the phase separation temperature Tc, three cases can be distinguished. In Case I, there is no sign of crystallization during quenching and DSC scanning, but a melting peak is observed at Tc, and above. In Case II, there is no crystallization on quenching but it does occur during the DSC run; the shift of the crystallization peak can then be related to Tc. In Case III, there is crystallization on quenching, and additional crystallization during the DSC run; the change of area of the crystallization peak is indicative of Tc. From these observations, the phase diagram of the system was determined. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 255-264 
    ISSN: 0887-6266
    Keywords: polyethylene, UHMW, crystal orientation in drawn films of ; x-ray diffraction study of crystal orientation in drawn films of UHMW polyethylene ; crystal orientation of UHMW polyethylene in drawn films ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A wide-angle x-ray diffraction (WAXD) study of the development of molecular orientation in the crystalline phase of ultra-high-molecular weight polyethylene films prepared by the gelation-crystallization method is presented. WAXD scans of the undrawn films show that the lamellae are oriented in the plane of the films. Upon drawing at 130°C, the orientation of the molecular chains changes from the direction normal to the film surface (ND) to the elongation direction. The decrease of the 200/020 intensity ratio at low draw ration (λ 〈10) indicates that double orientation develops during the transformation from the lamellar to the fibrillar morphology, with the a-axis oriented parallel to ND. The orientation distributions of the 110, 200, 020, and 002 planes of the orthorhombic unit cell of polyethylene were studied and characterized by the coefficients of a Legendre polynomial series. At a draw ratio of 4.5, the second-order coefficient, 〈P2(cos χ〉, already gets close to its limiting value, but it is shown that higher order coefficients of the polynomial series can be used to describe the evolution of the orentation, even up to λ = 50. The coefficients relative to the molecular chain orientation, 〈Pn(cos χ)〉c, can be calculated from different crystalline reflections. Curve-fitting calculations were made in order to improve the correlation between the results obtained from the orientation distribution of the 110, 020, and 002 planes. A Person VII function was found to give a better fit of the experimental curves than Gaussian or Lorentzian equations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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