Formation of shish-like fibril crystals from the melt of blends of cyclic and linear polyethylene under shear flow
The role of chain entanglements in shear-induced crystallization is one of the most important unsolved problems. The entanglements formed by topologically distinct cyclic and linear polymers are particularly notable. The shear-induced crystallization behavior of a blend of cyclic polyethylene (C-PE)...
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Published in | Polymer journal Vol. 54; no. 7; pp. 913 - 920 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.07.2022
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | The role of chain entanglements in shear-induced crystallization is one of the most important unsolved problems. The entanglements formed by topologically distinct cyclic and linear polymers are particularly notable. The shear-induced crystallization behavior of a blend of cyclic polyethylene (C-PE) and linear polyethylene (L-PE) was investigated. Using C-PE as a matrix and L-PE as an additive, we changed the molecular weight and blend ratio of C-PE and L-PE and measured the formation rate of shish-like fibril crystals,
I
. In both blend systems of C-PE(230k)/L-PE(42k) and C-PE(230k)/L-PE(104k), where the values in parentheses represent the molecular weight,
I
reached a maximum at a certain weight fraction of L-PE,
Φ
L-PE
. As the
Φ
L-PE
was increased, that is, the entanglement density was increased, the formation of the oriented melt was promoted while crystallization was simultaneously suppressed by entanglements. The maximum value of
I
was observed owing to these two competing factors. Similar behavior was observed in the blend systems of C-PE(230k)/L-PE(42k), C-PE(130k)/L-PE(42k), and C-PE(86k)/L-PE(42k).
The shear-induced crystallization behavior of the blends of cyclic polyethylene (C-PE) and linear polyethylene (L-PE) was investigated. This figure shows the formation rate of shish-like fibril crystals (
I
) in the blend systems of C-PE(230k)/L-PE(42k) and C-PE(230k)/L-PE(104k) against the weight fraction of L-PE,
Φ
L-PE
.
I
reached a maximum at a certain
Φ
L-PE
. As
Φ
L-PE
increased, that is, as the entanglement density increased, the formation of the oriented melt was promoted. Crystallization was also suppressed by the entanglements. The maximum value of
I
was observed owing to these two competing factors. |
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ISSN: | 0032-3896 1349-0540 |
DOI: | 10.1038/s41428-022-00643-x |