Author:
H. A. Schneider Freiburger Materialforschungszentrum FMF, der Universität Stefan-Meier-Stra\e 31 D-79104 Freiburg Germany

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It is evidenced that due to the kinetic character of the glass transition as a ‘freeze in’ process, PVT measurements extended over the glass transition range depend not only on the thermal history but also on the pressure acting during the formation of the polymeric glasses. As a consequence metastable glasses are formed which show during heating of the glassy polymer through the glass transition range ‘volume relaxation zones’, characterized by a retarded increase or even decrease of the volume. The width of the ‘relaxation zone’ increases with increasing pressure and depends additional on the mode of operation used during the PVT measurements. In the same time a pressure induced shift of the glass temperature to higher temperatures is observed, the shift being the greater the stiffer the polymer, i.e. the higher the glass temperature of the polymer at atmospheric pressure. Due to the metastable character of polymeric glasses the evaluation of universal equations of states is thus not ingenious for polymeric glasses, because the deduced EOS will be valid only for that given glass characterized by a well defined thermal and pressure history. Additionally the EOS is influenced by the unknown time dependent aging and relaxation processes within polymeric glasses.

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Journal of Thermal Analysis and Calorimetry
Language English
Size A4
Year of
Foundation
1969
Volumes
per Year
1
Issues
per Year
24
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Publisher Akadémiai Kiadó
Springer Nature Switzerland AG
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
CH-6330 Cham, Switzerland Gewerbestrasse 11.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 1388-6150 (Print)
ISSN 1588-2926 (Online)

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