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Thermoreversible Gelation of Poly(Vinylidene Fluoride) in Propylene Carbonate#.

Authors :
Kim, B.S.
Baek, S.T.
Song, K.W.
Park, I.H.
Lee, J.O.
Nemoto, N.
Source :
Journal of Macromolecular Science: Physics; Jul2004, Vol. 43 Issue 4, p741-754, 14p, 1 Black and White Photograph, 1 Chart, 8 Graphs, 1 Map
Publication Year :
2004

Abstract

Thermoreversible gelation of poly(vinylidene fluoride) (PVDF) in propylene carbonate (PC) solutions at relatively low concentrations (0.5–3.5 wt.%) has been studied in terms of the gelation time (or rate) as a function of temperature and polymer concentration. A master curve could be made for the gelation time–temperature curves using the temperature shift based on the difference in the gel melting temperature (T<subscript>m</subscript><superscript>g</superscript>) at different PVDF concentrations. The apparent activation energy of gelation was estimated to be proportional to (T<subscript>m</subscript><superscript>g</superscript> − T)<superscript>−1.8</superscript>. The gel melting enthalpy (ΔH<subscript>m</subscript><superscript>g</superscript>) determined from the modified Eldrige–Ferry equation was 18.67 kJ/mol. In dried gel films many spherulites connected by tie molecules were observed by scanning electron microscopy (SEM). From the wide angle x‐ray diffraction (WAXD) measurement, crystallites from PVDF gels were found to consist only of the γ‐type crystal with the TTTGTTTG¯ conformation, irrespective of the polymer concentration. As judged from the results obtained, the gelation of PVDF in PC seems to proceed mainly via liquid–liquid phase separation (even if followed by crystallization in the final stage) within the concentration range covered. <superscript>#</superscript>Dedicated to Prof. Won‐Jei Cho on the occasion of his retirement. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222348
Volume :
43
Issue :
4
Database :
Complementary Index
Journal :
Journal of Macromolecular Science: Physics
Publication Type :
Academic Journal
Accession number :
13256475
Full Text :
https://doi.org/10.1081/MB-120030018