Abstract
AbstractThe influence of intramolecular dipole–dipole interaction changes on structure formation peculiarities and some electrophysical properties were investigated with example of copolymers of vinylidene fluoride with tetrafluoroethylene and hexafluoropropylene with different compositions. The decrease of such dipole–dipole interactions in vinylidene fluoride/tetrafluoroethylene copolymers leads to an increase of the a and b parameters of the ferroelectric phase lattice and were accompanied by a shift of the Curie point to lower temperatures. The presence of peak‐halo at angles near 2θ = 18° were attributed to a paraelectric phase localized in the interfacial domains at the crystal–amorphous phase boundaries. Similar peak‐halos for vinylidene fluoride/hexafluoropropylene copolymers crystallizing into the nonpolar α phase were associated with the presence of an antiferroelectric phase formed by the chains in the planar zigzag conformation. The temperature range where dielectric anomalies were detected was characterized by conformational changes at which the decrease in planar zigzag conformation isomers took place. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.