Thermal Stability of Fluorinated Polydienes Synthesized by Addition of Difluorocarbene
TENNESSEE UNIV KNOXVILLE DEPT OF CHEMISTRY
Pagination or Media Count:
Linear PCHD and polyisoprenes with different microstructures and molecular weights are synthesized and chemically modified to improve their thermal and chemical stability by forming a three-membered ring structure containing two C-F bonds. Pyrolysis of these fluorinated polydienes proceeds through a two-stage decomposition involving chain scission, crosslinking, dehydrogenation, and dehalogenation. The pyrolysis leads to graphite-like residues, whereas their polydiene precursors decompose completely under the same conditions. The fluorination of PCHD enhances its thermal stability. The stronger C-F bond along with high strain of the three-membered ring structure and formation of relatively stable free radicals play an important role in the thermal stability of fluorinated polydienes.
- Organic Chemistry
- Physical Chemistry
- Polymer Chemistry