TY - JOUR
T1 - Fluoropolymer microstructure and dynamics
T2 - Influence of molecular orientation induced by uniaxial drawing
AU - Miranda, Daniel F.
AU - Yin, Chaoqing
AU - Zhang, Shihai
AU - Runt, James
N1 - Publisher Copyright:
© 2016 Elsevier Ltd. All rights reserved.
PY - 2016/5/17
Y1 - 2016/5/17
N2 - Fluorinated semi-crystalline polymers are attractive for dielectric film applications due to their chemical inertness and high thermal stability. In the present investigation we explore the influence of orientation induced by uniaxial drawing on the crystalline microstructure and relaxation processes of poly(ethylene-tetrafluoroethylene) (ETFE), in order to ascertain how morphological control can benefit polymer dielectric design. When drawn below or near the Tg, the crystallinity of the drawn films is unchanged, and oriented amorphous structures and crystalline microfibrils form at high draw ratios. This orientation slows segmental relaxation, reflected by an increase in the dynamic Tg. When drawing above Tg, the films undergo strain-induced crystallization at high draw ratios. For these films, an increase in dynamic Tg is also observed, in addition to a second segmental relaxation process, appearing as a shoulder on the primary process. We propose that this represents a contribution from a rigid amorphous fraction, having slowed chain dynamics.
AB - Fluorinated semi-crystalline polymers are attractive for dielectric film applications due to their chemical inertness and high thermal stability. In the present investigation we explore the influence of orientation induced by uniaxial drawing on the crystalline microstructure and relaxation processes of poly(ethylene-tetrafluoroethylene) (ETFE), in order to ascertain how morphological control can benefit polymer dielectric design. When drawn below or near the Tg, the crystallinity of the drawn films is unchanged, and oriented amorphous structures and crystalline microfibrils form at high draw ratios. This orientation slows segmental relaxation, reflected by an increase in the dynamic Tg. When drawing above Tg, the films undergo strain-induced crystallization at high draw ratios. For these films, an increase in dynamic Tg is also observed, in addition to a second segmental relaxation process, appearing as a shoulder on the primary process. We propose that this represents a contribution from a rigid amorphous fraction, having slowed chain dynamics.
UR - http://www.scopus.com/inward/record.url?scp=84962793790&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84962793790&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2016.03.057
DO - 10.1016/j.polymer.2016.03.057
M3 - Article
AN - SCOPUS:84962793790
SN - 0032-3861
VL - 91
SP - 211
EP - 221
JO - Polymer
JF - Polymer
ER -