| Type of Document |
Dissertation |
| Author |
Arnold, Lisa
|
| URN |
etd-06062008-164002 |
| Title |
Crystallization and melting behavior of (e-caprolactone)-based homopolymer and triblock copolymer |
| Degree |
PhD |
| Department |
Chemistry |
| Advisory Committee |
| Advisor Name |
Title |
| Marand, Hervé L. |
Committee Chair |
| Gibson, Harry W. |
Committee Member |
| Ward, Thomas C. |
Committee Member |
| Wightman, James P. |
Committee Member |
| Wilkes, Garth L. |
Committee Member |
|
| Keywords |
- poly(propylene oxide)
- block copolymer
- poly(e-caprolactone)
|
| Date of Defense |
1995-08-04 |
| Availability |
restricted |
Abstract
The goal of this work is to examine the applicability of the Lauritzen-Hoflinan
(LH) surface nucleation theory to the crystallization kinetics of poly(ε-caprolactone),
PCL. This theory has successfully predicted a number of experimental observations such
as the temperature dependence of spherulitic growth rates and the inverse relation
between undercooling and the lamellar thickness. Claims have appeared in the literature
that analysis of growth rate data using the LH theory does not yield physically meaningful
parameters. This work will show that the lateral and fold interfacial free energy
parameters, σ and σe, found by analysis with the LH theory are related to the chemical
structure of the polymer chain in the case ofPCL. The fold interfacial free energy is
related to the chain stiffness, and a recent proposal relates σ to the characteristic ratio,
C∞. This work will examine the validity of the proposed relationship for the case of PCL.
The effect of polymer chain architecture on the crystallization behavior was also investigated. The crystallization behavior of poly(ε-caprolactone) was compared and
contrasted to that of a triblock copolymer containing (ε-caprolactone) blocks.
|
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| Filename |
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56K Modem |
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ISDN (128 Kb) |
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LD5655.V856_1995.A766.pdf |
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