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2012 | OriginalPaper | Buchkapitel

2. Background to Polymers and Composites

verfasst von : Y. Jack Weitsman

Erschienen in: Fluid Effects in Polymers and Polymeric Composites

Verlag: Springer US

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Abstract

In view of their manufacturing process, such as drawing and extrusion for glass fibers and the sheet-like atomic structure of carbon and graphite fibers, these reinforcements are essentially transversely anisotropic about their longitudinal orientation (Hull 1981), in which direction they possess high stiffness and strength. In view of their small diameter, typically 8 μm, it has been possible to determine their longitudinal modulus only, while no direct data are available about their in-plane stiffnesses.

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Fußnoten
1
It should be noted that a T(T) is obtained from isothermal creep data, plotted against log t and collected over a wide temperature range. These isothermal plots are then coalesced to form a “master curve” by shifting parallel to the horizontal log t axis. This procedure is not error free. To verify its validity, it is necessary to conduct transient temperature tests and compare the resulting data with computational predictions. For temperatures sufficiently below T g the shift factor function a T(T) is given by the Arrhenius expression of the form a T(T) = A exp (−B/T).
 
2
The chemical potential μ, which is conjugate to the fluid concentration m, is a measure of the energy required the increase the concentration while holding other thermodynamic variables constant. Originally introduced by Gibbs, it was defined by means of the Gibbs free energy function G, i.e., \( \mu = \partial G/\partial m \). But other forms of energy can be used.
 
Literatur
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Metadaten
Titel
Background to Polymers and Composites
verfasst von
Y. Jack Weitsman
Copyright-Jahr
2012
Verlag
Springer US
DOI
https://doi.org/10.1007/978-1-4614-1059-1_2

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