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Download fileFormation of Asymmetric Leaf-Shaped Crystals in Ultrathin Films of Oriented Polyethylene Molecules Resulting from High-Temperature Relaxation and Recrystallization
journal contribution
posted on 2019-12-26, 14:34 authored by Huihui Li, Duanzijing Liu, Xinyun Bu, Zhenzhen Zhou, Zhongjie Ren, Xiaoli Sun, Renate Reiter, Shouke Yan, Günter ReiterWe melted, annealed, and recrystallized ultrathin films
of oriented
polyethylene (PE) molecules prepared by melt-drawing. A large number
of randomly oriented asymmetric leaf-shaped crystalline structures
consisting of preferentially oriented lamellae were formed simultaneously,
as observed by optical and atomic force microscopies. The structural
arrangement within these leaf-shaped crystalline structures was identified
by grazing incidence X-ray diffraction. These structures consisted
of two distinct sections, both differing strongly from circular spherulites
obtained by crystalizing an isotropic melt. Besides, regions containing
groups of stacks of slightly inclined but well-aligned flat-on lamellae
and regions of less orderly arranged edge-on lamellae were found.
When increasing the annealing temperature and/or annealing time, a
change in morphology from the leaf-shaped crystalline structures to
spherulites with two symmetric “eyes” was observed.
Intriguingly, the annealing times required for such a change in crystalline
morphology were about four orders of magnitude longer than the longest
bulk relaxation time (reptation time). Because the appearance of spherulites
indicates that films became equilibrated and reached a state of an
isotropic melt before recrystallization, we may conclude that oriented
PE chains in ultrathin films possessed a long-term memory of the preparation-induced
chain stretching. Considering that the morphology and relaxation kinetics
of PE films depended appreciably on the substrate properties and film
thickness, we conclude that the formation of asymmetric leaf-shaped
crystalline structures was also affected by the interaction of PE
chains with the substrate and spatial confinement. The present results
may shed new light on slow relaxation and reorganization processes
encountered when long-chain polymers became oriented during sample
processing.