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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 259 (1981), S. 1081-1083 
    ISSN: 1435-1536
    Keywords: Unperturbed chain dimensions ; Thermal degradation ; Polystyrene ; High impact polystyrene ; SAN ; ABS ; Steric factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary Intrinsic viscosity and viscosity average molecular weight data of thermally degraded polystyrene and its co-polymers have been used to determine the unperturbed chain dimensions. Analysis of these data according to Stockmayer and Fixman equation suggests that probably during thermal degradation in air no branched polymers are formed and the chain dimensions $$[〈 r_0^2 〉 /\bar M_v ]^{{\raise0.5ex\hbox{$\scriptstyle 1$}\kern-0.1em/\kern-0.15em\lower0.25ex\hbox{$\scriptstyle 2$}}} $$ remain as for the linear polymers.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 261 (1983), S. 709-716 
    ISSN: 1435-1536
    Keywords: thermal degradation ; HIPS ; SAN ; ABS ; activation energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Molecular weight change studies have shown that the thermal degradation of random copolymers of styrene — namely HIPS, SAN, and ABS-at low temperatures and in air involves random chain scission. The dominant process in the degradation of HIPS is random chain scission due to weak links, whereas in SAN it is intermolecular chain transfer. In ABS, the degradation is initially random scission due to weak links and then mainly intermolecular chain transfer. The infrared spectra show that during degradation the labile weak links are attacked by oxygen and peroxidic free radicals are produced. Via hydrogen abstraction or autoxidation of olefinic links, these free radicals are responsible for the formation of aliphatic ketonic or peroxyester structures, and for isomerization and cyclization. The activation energies of overall degradation of HIPS, SAN, and ABS are 134, 142, and 92 kJ.mol−1 respectively.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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