Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles: DFG German National Licenses  (3)
  • 1995-1999  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Chaos 9 (1999), S. 298-307 
    ISSN: 1089-7682
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Phase separation kinetics and morphology of binary polymer mixtures (A/B) in the presence of photochemical reactions were investigated by using phase-contrast optical microscopy combined with digital image analysis. The polymers were chemically designed in such a way that two types of chemical reactions, intermolecular photodimerization and intramolecular photoisomerization, of polymer segments can be induced and controled by irradiation with ultraviolet light. Unlike the conventional case, the phase separation in the presence of these reactions is spontaneously frozen due to the suppression of the long-wavelength instabilities, resulting in stationary spatial structures with intrinsic periodicities. These characteristic length scales are determined by the competition between the two antagonistic interactions: phase separation as a relatively short-range activation and the photochemical reaction as a long-range inhibition. Furthermore, it was found that the spatial symmetry breaking of concentration fluctuations can emerge from the elastic stress associated with the nonhomogeneous kinetics of the reactions. Experimental data obtained with three types of reactions: A-A only cross-link, A-A and B-B simultaneous cross-links and the reversible A(if and only if)B photoisomerization are described. These results do not only indicate that combination of chemical reactions and phase separation could provide a novel method to control the morphology of multiphase polymer materials, but also suggest that photoreactive polymers can be used as a chemical system to study the mode-selection process in polymers far from thermodynamic equilibrium. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 8388-8394 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 455-462 
    ISSN: 0887-6266
    Keywords: photoreactive polymer blends ; photocrosslinking kinetics ; photodimerization of anthracene ; Kohlrausch-Williams-Watts relaxation ; poly(vinyl methyl ether) ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mixtures of polystyrene derivatives (PSCS) and poly(vinyl methyl ether) (PVME) were made photocrosslinkable by chemically labeling PSCS chains with photoreactive anthracene. Miscibility of these anthracene-labeled PSCS/PVME blends was examined by light scattering under several crosslinking conditions in the one-phase region via photodimerization of anthracenes. As the reaction proceeds, the coexistence curve of PSCS/PVME blends shifts toward the low temperature side. By following the changes in concentration of anthracenes with irradiation time, it was found that the crosslinking reaction of PSCS chains in the blends does not follow the mean-field kinetics. However, it can be well expressed by the Kohlrausch-Williams-Watts (KWW) relaxation mechanism, indicating that the crosslinking reaction proceeds inhomogeneously in the blends. By scaling the reaction time with the average reaction rate obtained from the KWW equation modified for the reaction kinetics, all the crosslinking data obtained in the miscible region of the reacted blends fall on a single master curve. These experimental results suggest the universal behavior of the photocrosslinking kinetics obtained under the “shallow quench” conditions in the region far away from the coexistence curve of the reacting blends. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 455-462, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...