z-logo
Premium
Thermostimulated current characterization of poly(ethersulfone)
Author(s) -
Duret N.,
Cotten H.,
Lacabanne C.
Publication year - 2000
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/(sici)1097-4628(20000418)76:3<320::aid-app7>3.0.co;2-2
Subject(s) - glass transition , differential scanning calorimetry , relaxation (psychology) , materials science , characterization (materials science) , thermodynamics , opacity , thermal , thermal analysis , phase transition , transition temperature , polymer , polymer chemistry , composite material , condensed matter physics , physics , optics , nanotechnology , social psychology , superconductivity , psychology
Two thermal analysis techniques, differential scanning calorimetry (DSC) and thermostimulated currents, are used to characterize two Poly(ethersulfones) (PESs) obtained with the same process by two different manufacturers. The glass transition temperature observed by DSC is the same for both PESs and equal to 235°C. When PES samples are heated above the glass transition temperature (250–260°C), one initially white and opaque PES (B) looks transparent while the other one (A) stays in the initial stage. The PES B is visibly degraded upon increasing at a lower temperature than PES A. Below the glass transition temperature, two complex relaxation modes α and β situated at +170–175 and −120°C, respectively, are observed. The analysis of the fine structure shows that they are constituted of elementary processes characterized by relaxation times following compensation laws. For PES A at high temperatures the cooperative movements are precursors of the glass transition. For PES B a double compensation phenomena reveals the biphasic character of the vitreous phase. The comparison between the two PESs reveals different microstructures that could be due to different processing conditions. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 320–325, 2000

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here