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Influence of sorbed carbon dioxide on transition temperatures of poly( p ‐phenylene sulphide)
Author(s) -
Schultze J. D.,
Engelmann I. A. D.,
Boehning M.,
Springer J.
Publication year - 1991
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.1991.220020303
Subject(s) - glass transition , differential scanning calorimetry , materials science , phenylene , poly(p phenylene) , polymer , crystallization , plasticizer , relaxation (psychology) , volume (thermodynamics) , carbon dioxide , molecule , transition temperature , melting point , crystallite , polymer chemistry , chemical engineering , thermodynamics , organic chemistry , composite material , chemistry , psychology , social psychology , physics , superconductivity , quantum mechanics , engineering , metallurgy
Static pressure usually increases the transition temperatures of polymers by decreasing their free volume. If the pressurizing medium is soluble in the polymer matrix, the opposing effect of increasing the free volume is possible. Those shifts of transition temperatures were monitored with a medium‐pressure Differential Scanning Calorimetry (DSC) device. The influences of sorbed and surrounding gas molecules are demonstrated by changes occurring in the transition temperature regions. The results show the severe plasticizing effect of CO 2 on poly(p‐phenylene sulphide) (PPS). The glass transition temperature T G and the temperature of crystallization T C are influenced by sorbed gas molecules. They decrease due to sorbed CO 2 molecules. Glass transition is lowered, but is difficult to interpret, as relaxation phenomena which diminish with increasing pressure occur during DSC runs. In crystallites no gas solution is usually possible, so that the melting point of PPS is mainly affected by influences other than plasticization.