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Journal ArticleDOI

The Microscopic Basis of the Glass Transition in Polymers from Neutron Scattering Studies

Bernhard Frick, +1 more
- 31 Mar 1995 - 
- Vol. 267, Iss: 5206, pp 1939-1945
TLDR
The connection between this boson peak and the fast dynamic process appearing near Tg is discussed, and the time-temperature superposition principle, which is valid for polymers on a macroscopic scale, is not applicable for temperatures approaching Tg.
Abstract
Recent neutron scattering experiments on the microscopic dynamics of polymers below and above the glass transition temperature T g are reviewed. The results presented cover different dynamic processes appearing in glasses: local motions, vibrations, and different relaxation processes such as α- and β-relaxation. For the α-relaxation, which occurs above T g , it is possible to extend the time-temperature superposition principle, which is valid for polymers on a macroscopic scale, to the microscopic time scale. However, this principle is not applicable for temperatures approaching T g . Below T g , an inelastic excitation at a frequency of some hundred gigahertz (on the order of several wave numbers), the "boson peak," survives from a quasi-elastic overdamped scattering law at high temperatures. The connection between this boson peak and the fast dynamic process appearing near T g is discussed.

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Journal ArticleDOI

Formation of glasses from liquids and biopolymers.

TL;DR: The onset of a sharp change in ddT( is the Debye-Waller factor and T is temperature) in proteins, which is controversially indentified with the glass transition in liquids, is shown to be general for glass formers and observable in computer simulations of strong and fragile ionic liquids, where it proves to be close to the experimental glass transition temperature.
Journal ArticleDOI

Characteristics and Significance of the Amorphous State in Pharmaceutical Systems

TL;DR: The amorphous state is critical in determining the solid-state physical and chemical properties of many pharmaceutical dosage forms and some of the most common methods that can be used to measure them are described.
Journal ArticleDOI

Supercooled Liquids and Glasses

TL;DR: A review of recent progress in the study of supercooled liquids and glasses can be found in this article, where several basic features of the dynamics and thermodynamics of super cooled liquid and glasses are described.
Journal ArticleDOI

A topographic view of supercooled liquids and glass formation.

TL;DR: Various static and dynamic phenomena displayed by glass-forming liquids, particularly those near the so-called "fragile" limit, emerge as manifestations of the multidimensional complex topography of the collective potential energy function.
Journal ArticleDOI

Heterogeneity at the glass transition: a review

TL;DR: Theoretical concepts and experimental evidence of heterogeneity in glass-forming liquids and polymers are reviewed in this paper, where the main purpose is to provide an introduction to theoretical developments and recent experiments which have led to rapidly increasing knowledge.
References
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Book

Viscoelastic properties of polymers

John D. Ferry
TL;DR: In this article, the authors describe the nature of Viscoelastic behavior of polymeric systems and approximate relations among the linear Viscoels and approximate interrelations among the Viscelastic Functions.
Journal ArticleDOI

Viscous Liquids and the Glass Transition. II. Secondary Relaxations in Glasses of Rigid Molecules

TL;DR: The dielectric loss factor and permittivity of 8-16 mol% solutions of chlorobenzene, o−dichlorobenzenes, and 1-chloronaphthalene in cis-decalin were measured by DTA as mentioned in this paper.