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  • Polymer and Materials Science  (3)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 187-197 
    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: This article studies the influence of the heating rate and sample weight on the thermal decomposition of polystyrene (first-order kinetics). For this purpose, the kinetic parameters (i.e., frequency factor and activation energy), variables at the maximum decomposition rate (such as conversion, reaction rate, and temperature), as well as some characteristic temperatures have been determined for a series of experiments where the heating rate varies (0.5-11.5 K/min) and also, the sample weight (6.0-25.1 mg). Some mathematical equations have been developed that allow: (1) evaluation of the activation energy of thermal decomposition by different ways and comparing the results obtained; (2) relating different parameters between themselves, such as the heating rate with the temperature at the maximum decomposition rate or the frequency factor with the heating rate and sample weight. Finally, some theoretical explanations of the variation of thermal and kinetic parameters have been proposed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 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: The cure kinetics of a diglycidyl ether of bisphenol A (DGEBA)-based epoxy resin with methyltetrahydrophthalic anhydride and an accelerator was studied by nonisothermal DSC data. The systems were uncured resin and partially cured with the following extents of cure measured by the residual heat method (αDSC): 0.37, 0.63, 0.81, and 0.90. The activation energy calculated by the Kissinger method increases from 63 kJ/mol for the uncured epoxy to 77 kJ/mol for the partially cured with αDSC = 0.90. Additionally, the activation energy calculated by the isoconversional method shows a dependence on the conversion degree α. The activation energy tends to decreases initially with the conversion degree, possibly due to the autocatalytic effect; then, it passes through a minimum about α = 0.4 and, finally, increases slightly due to the increase of crosslinks which reduce the mobility of the unreacted groups. A simple, consistent method of kinetic analysis was applied. This method enables one to select the most convenient model and the calculation of kinetic parameters. A two-parameter (m, n) autocatalytic model (S̆esták-Berggren equation) was found to be the most convenient model to study the curing of epoxy systems. The results show a dependence of the kinetic parameters on the initial degree of crosslinking of the partially cured epoxy. The exponent m tends to decrease with the extent of cure, while the exponent n remains practically invariable. These results show a change of the kinetic when the initial extent of cure of the epoxy system increases. The In A data, A being the preexponenetial factor in the Arrhenius dependence of the temperature on the rate of conversion, increase with the extent of cure, showing a correlation with the calculated activation energy values. The nonisothermal DSC curves theoretically calculated show a very good agreement with the experimental data. The two-parameter (m, n) autocatalytic model gives a good description of the curing kinetics of epoxy resins with different extents of cure. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 153-159 
    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 aging of high-density polyethylene (HDPE) when exposed to drastic climatic conditions (Canadian winter, characterized by low temperature and abrupt temperature variations between the night and the day) was studied. The importance of degradation was determined by evaluating the microstructural changes in HDPE (i.e., oxidations, ramifications, and polymeric chain breaking) by means of FTIR spectrophotometry. The crystallinity variation in HDPE by FTIR and DSC was also studied. Both techniques led to coherent results: there was a loss of crystallinity due to weathering degradation. This crystallinity reduction produced a drastic decrease in impact energy. However, the other properties evaluated were not significantly affected. © 1996 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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