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
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 3 (1992), S. 81-85 
    ISSN: 1042-7147
    Keywords: p-Benzenedithiol ; p-Diethynylbenzene ; Layer structure ; Amorphous state ; Phase transition ; 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
    Notes: Phase transition of the layer structure of poly(p-benzenedithiol-co-p-diethylbenzene) obtained in solid state polymerization was studied by a thermal treatment or UV irradiation under a nitrogen atmosphere. The peak intensities in the X-ray diffraction diagram of polymers gradually decreased with the thermal treatment time above 55°C. Below 50°C the layer structure of polymers hardly changed. The apparent activation energy for the phase transition was about 15 Kcal/mol [63 KJ/mol] at the initial stage and gradually decreased to a few Kcal/mol [ca. 2 KJ/mol]. UV light from a high-pressure mercury lamp also gradually induced the phase transition from the layer structure to an amorphous one. The pristine polymer possesses phase transition points at 75, 95 and 130°C. The exothermic transition at 75°C can be understood as the thermal destruction of the semistable layer structure. The exothermic transition at 95°C may be correspond to the cis → trans thermal isomerization of the C=°C bond in the polymer main chain.The diffuse reflectance spectrum of the pristine polymer differed from that of the amorphous polymer obtained by the thermal treatment of the pristine polymer. SEM photographs of the pristine polymer showed a particular surface structure, i.e. entangled fibrous material. TEM photographs of the pristine polymer exhibited a bright valley-and-hill structure, whereas that of the amorphous polymer obtained by thermal treatment exhibited a plain surface.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 2 (1991), S. 301-305 
    ISSN: 1042-7147
    Keywords: 1,4-Benzenedithiol ; 1,4-Diethynyl-benzene ; Layer structure ; Phase transition ; Microstructure ; 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
    Notes: The effect of light wavelength on the phase transition of the layer structure of poly(1,4-benzenedithiol-co-1,4-diethynylbenzene) was studied under an air atmosphere at 18-22°C. The thin layer polymer crystals were prepared by solid state polymerization, and the amount of the layer structure was evaluated by an X-ray diagram. A monochromatic light with a wavelength in the region of ca. 500-600 nm was used as a light source. The amount of the layer structure was found to be altered by light. There were three characteristic wavelengths at 545.6, 567.8 and 590.1 nm, inducing pronounced peak intensities in the X-ray diagram. On the other hand, at 501.1, 539.6, 571.8 and 588.1 nm the light made the peak intensity decrease steeply. The phase transition was induced by a photon mode, but not by a heat mode. The amount of the layer structure was altered linearly with increasing irradiation time up to 60 min. However, over 60 min the change became dull. The total energy given to the polymers during the irradiation was about 24 X 10-3 J/cm2. Accordingly, the phase transition occurs with a high sensitivity to the light. The polymers were irradiated alternately by the light of 545.6 nm and 571.8 nm at intervals of 60 min, respectively. The amount of the layer structure was controlled reversibly by the light.
    Additional Material: 5 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...