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  • 1
    Electronic Resource
    Electronic Resource
    The influence of applied heat flux on the combustion of epoxies (1983)
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 7 (1983), S. 216-218 
    Details
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/fam.810070410
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  • 2
    Electronic Resource
    Electronic Resource
    Temperature-sensitive luminescence of tris (β-diketone) europium chelates for monitoring high-speed cationic photopolymerizations (1995)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1735-1744 
    Details
    ISSN: 0887-624X
    Keywords: luminescence ; temperature ; tris(β-diketone) chelates ; europium ; vinyl ether ; cationic photopolymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The temperature-dependent luminescence of tris (β-diketone) chelates of europium was used for in situ temperature measurements during cationic photopolymerizations of vinyl ethers. These molecular-level luminescent probes provided a real-time, noninvasive method for monitoring temperature during these high-speed polymerizations. Two specific probes, tris (benzoyl-1, 1, 1-trifluoroacetone) europium and tris (1,1,1,5,5,5,-hexafluoroacetylacetone) europium, met several stringent spectral and performance requirements for application in our system. The luminescence from these probes exhibits a reproducible temperature dependence over a wide temperature range and is not sensitive to changes in viscosity. In situ temperature profiles obtained using this novel technique verified the importance of thermal effects during these highly exothermic photopolymerizations. These studies have demonstrated the utility of the tris(β-diketone) europium chelates for characterizing the temperature during high-speed photopolymerizations that cannot be monitored using conventional techniques. © 1995 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1995.080331021
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  • 3
    Electronic Resource
    Electronic Resource
    The role of the triplet state in the photosensitization of cationic polymerizations by anthracene (1995)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 247-256 
    Details
    ISSN: 0887-624X
    Keywords: cationic photopolymerization ; photosensitization ; anthracene ; fluorescence ; mechanism ; divinyl ether ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photosensitization mechanism for cationic polymerizations initiated by diaryliodonium salts photosensitized by anthracene was investigated using fluorescence and phosphorescence spectroscopy. In situ photosensitizer fluorescence measurements confirmed that the photosensitization reaction proceeds by an electron transfer process. Transient phosphorescence studies demonstrated that electron transfer occurred from the triplet excited state of anthracene to the initiator, with an intrinsic kinetic rate constant of 2 × 108 L/mol s. Further evidence for the role of the triplet state was provided by an observed seven-fold decrease in the polymerization rate upon addition of a triplet state quencher. Finally, numerical solution of the photophysical kinetic equations indicated that the triplet state concentration was approximately three orders of magnitude higher than that of the singlet state, and that 94-96% of the active cationic centers are produced by reaction of the initiator with the triplet state. These results indicate that the electron transfer occurs primarily from the triplet state of anthracene, with the singlet state providing only a minor contribution to the photosensitization reaction. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1995.080330207
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  • 4
    Electronic Resource
    Electronic Resource
    Kinetics of cationic photopolymerizations of divinyl ethers characterized using in situ Raman spectroscopy (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 403-411 
    Details
    ISSN: 0887-624X
    Keywords: Raman spectroscopy ; cationic ; photopolymerization ; divinyl ether ; kinetic ; monitoring ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In situ Raman spectroscopy experiments were used to determine effective kinetic propagation constants for a series of unsteady-state divinyl ether polymerizations at different isothermal temperatures and light intensities. Raman spectroscopy was found to be ideally suited for monitoring cationic photopolymerizations because the technique allows isothermal experiments to be performed with excellent time resolution and allows several spectral features to be observed simultaneously. In addition, the Raman experiments provided direct information about the vinyl bond concentration in situ as the reaction takes place. For these cationic photopolymerizations, the reaction rate and limiting conversion were both found to increase as the reaction temperature was increased. At all temperatures, the profile for the propagation rate constant, kp, exhibited a dramatic increase at the start of the reaction, plateaued at a value between 10 and 40 l/mol s (depending upon temperature), and then decreased as the reaction reached a limiting conversion due to trapping of the active centers. Finally, the overall activation energy for polymerization was found to be 25.1 ± 6.1 kJ/mol. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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