作者: Valery P Privalko , None
DOI: 10.1016/S0022-3093(99)00371-3
关键词: Polymer 、 Volume fraction 、 Kinetic energy 、 Exponent 、 Range (particle radiation) 、 Thermodynamics 、 Molecule 、 Relaxation (physics) 、 Glass transition 、 Chemistry
摘要: Abstract Detailed analysis of current theoretical approaches and empirical correlations between the KWW stretching exponent β molecular structure single-component polymer systems suggests that values for structural relaxation in glass transition range change continuously with kinetic free volume fraction f g k , rather than are fixed at `universal' value =3/7.