Publication | Closed Access
Molecular weight‐dependence of free volume in polystyrene studied by positron annihilation measurements
106
Citations
23
References
1994
Year
EngineeringFree VolumeGlass-forming LiquidChemistrySoft MatterPositron Annihilation MeasurementsPolymersGlass TransitionMonodisperse PolystyrenesPolymer ProcessingPolymer PhysicRheologyPolymer ChemistryMaterials ScienceOrtho PositroniumPhysical Chemistryτ 3Polymer AnalysisMolecular Weight‐dependencePolymer ScienceApplied PhysicsPolymer CharacterizationPolymer PropertyPolymer Modeling
Abstract Positron annihilation lifetime measurements are reported for four monodisperse polystyrenes with molar mass M = 4,000, 9,200, 25,000, and 400,000. The temperature dependences of ortho positronium ( o ‐Ps) lifetime (τ 3 ) and intensity ( I 3 ) were measured from 5°C to T g + 30°C for each sample. From these data, the free volume hole size, 〈 v f (τ 3 )〉, and fractional free volume h ps = CI 3 〈 v f (τ 3 )〉 were calculated. The temperature dependences of τ 3 , 〈 v f (τ 3 )〉 and h ps show a discrete change in slope at an effective glass transition temperature, T g,ps, which is measurably below the conventional bulk T g . This suggests that τ 3 is sensitive to large holes which retain their liquid‐like mobility in the glassy state. Good agreement was found for T > h g,ps between h ps and the theoretical free volume fraction h th deduced from experimental P‐V‐T data for polystyrene using the statistical mechanical theory of Simha and Somcynsky. Below T g,ps, deviations between h ps and h th are observed, h ps falling increasingly below h th as temperature decreases. Whereas h ps and h th depend strongly on M in the melt, each essentially independent of M in the glass. A free volume quantity, computed from the bulk volume, which is in good numerical agreement with the Simha‐Somcynsky h ‐function in the melt, gives improved agreement with h ps in the glassy state. © 1994 John Wiley & Sons, Inc.
| Year | Citations | |
|---|---|---|
Page 1
Page 1