Through differential scanning calorimetry, isothermal crystallization from the melt of polytetrafluoroethylene (PTFE) has been investigated. PTFE was regarded as one of the polymers for which crystallization is so rapid that the samples crystallize during the cooling from the melt to the selected cr
Extreme thermal behaviors of polytetrafluoroethylene and random tetrafluoroethylene fluorinated copolymers
โ Scribed by Rachele Pucciariello; Claudia Mancusi
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 174 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
By differential scanning calorimetry (DSC), the thermal behavior of polytetrafluoroethylene (PTFE) and random fluorinated copolymers of tetrafluoroethylenecontaining hexafluoropropylene (FEP copolymers) or perfluoroalkylvinylether (PFA copolymers) as comonomers was investigated. Rapid-melt crystallization was employed to provide new data about the problem of inclusion/exclusion of co-units from the homopolymer crystal lattice. Equilibrium melting points were determined and tested in light of random copolymer predictions. Both nonequilibrium and equilibrium behaviors seem to point to the inclusion of OCF 3 side groups and the exclusion of larger ones. Finally, a new value of the equilibrium melting point of PTFE is given, in good agreement with those present in the literature.
๐ SIMILAR VOLUMES
In the present article, we investigate by differential scanning calorimetry (DSC) the thermal behavior (melting, crystallization, and crystal-crystal transitions) far from equilibrium of blends constituted of two crystalline polymers. In particular, the following blends are examined: PTFE-PFMVE, PTF