Thermally induced reorganization in LCP fibers: Molecular origin of mechanical strength
Document Type
Conference Proceeding
Publication Date
7-1-2008
Abstract
The molecular reorganization occurring in liquid crystalline polymer fiber during heat treatment is of great interest for many commercial reasons. Using thermal analysis techniques, WAXS and real time temperature dependent synchrotron SAXS, the structure and morphology of commercial LCP (liquid crystalline polymer), Vectran®, HBA/HNA (p-hydroxybenzoic acid/6-hydroxy-2-naphthoic acid), and its variant polymer fiber COTBP, HBA/HNA/BP/TA (BP-benzophenone, TA-terephthalic acid), have been examined. Both fibers have the typical liquid crystalline polymer structure, i.e., highly aligned with aperiodic sequencing along the fiber axis. There is a three-fold increase in strength in both fibers with heat treatment; however, the modulus is observed to increase significantly in COTBP but not in Vectran®. This paper reports on the changes and the differences on the structural and morphological behavior for both the as-spun and heat-treated LCP fibers. We propose an 'oriented entanglement' model to describe the differences between the two polymer fibers. © 2008 Springer Science+Business Media, LLC.
Identifier
46449128561 (Scopus)
Publication Title
Journal of Thermal Analysis and Calorimetry
External Full Text Location
https://doi.org/10.1007/s10973-007-8867-0
ISSN
13886150
First Page
175
Last Page
182
Issue
1
Volume
93
Grant
W-7405-Eng-48
Fund Ref
U.S. Department of Energy
Recommended Citation
Saw, C. K.; Collins, G.; Menczel, J.; and Jaffe, M., "Thermally induced reorganization in LCP fibers: Molecular origin of mechanical strength" (2008). Faculty Publications. 12756.
https://digitalcommons.njit.edu/fac_pubs/12756
