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  • 1995-1999  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 55 (1995), S. 225-232 
    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 chemical structure of an aliphatic epoxy resin was studied by using gel permeation chromatography (GPC), Fourier transform infrared (FTIR), FTIR-TGA (thermogravimetric analysis), mass spectrometry in fast atom bombardment (FAB) mode, and wet analysis. We found that when trimethylolpropane is used as starting monomer, only two OH groups are epoxidized. The resin and its different fractions have a functionality of two. Under the conditions of synthesis used by the supplier, three main products were found with masses of 246,339, and 430. No trifunctional product was detected. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 55 (1995), S. 1507-1516 
    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 study of cure of an epoxy resin based on trimethilolpropane (TMP) used as supplied and in purified form and m-xylylenediamine (m-XDA), as curing agent has been carried out. Thermodynamic functions such as activation energy, activation entropy, activation enthalpy, and free energy of activation were determinated. From kinetic study we have observed that there are two competitive mechanisms; autocatalyzed and n order, with the values of activation energy ranging between 52.9 and 64.6 kJ/mol. The overall order of reaction is found to be 2.5, and the order of reaction with respect to the hydroxyl group is clearly determined and equal to 1. Gelation study was carried out under two conditions: isothermal and adiabatic. From isothermal study we obtained the values of functionality of the resins (approximately two) and the apparent activation energy of the process. The adiabatic study allowed us the determination of the pot-life taking into account the theoretical model used, with reasonable theoretical/experimental agreements. The importance of n-order path for this kind of resins (with high OH contents) is well demonstrated through kinetic and thermodynamic parameters. The thermodynamic functions showed themselves as very sensitive parameters for the following and evolution of the reaction. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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