Power law of molecular weight of the nucleation rate of folded chain crystals of polyethylene

Swapan K. Ghosh, Masamichi Hikosaka, Akihiko Toda, Shinichi Yamazaki, Koji Yamada

研究成果査読

20 被引用数 (Scopus)

抄録

The molecular weight (Mn) dependence of the primary nucleation rate (I) of folded chain single crystals (FCSCs) of polyethylene (PE) was studied. A power law for the nucleation rate, I ∝ Mn-2.4, was found. The FCSCs were formed by isothermal crystallization from the melt into an ordered phase (=orthorhombic phase). A new experimental method was established to obtain reliable I, which has been difficult in the case of heterogeneous nucleation for long years. The degree of supercooling (ΔT) dependence of I fits well with the theoretical I given by classical nucleation theory, I = I0 exp(-ΔG*/kT) ∝ D exp(-C/ΔT2), where I0 is proportional to the topological diffusion coefficient of polymer chains (D), ΔG* is the free energy for forming a critical nucleus, k is the Boltzmann constant, T is temperature, and C is a constant. It is found that ΔG* (∝C) does not depend on Mn, while I0 decreases with increase of Mn, from which it is concluded that formation of a critical nucleus is not controlled by Mn, while only topologic diffusion of polymers is controlled by Mn, i.e., I ∝ D(Mn). Similar power laws of PE were already found by the present authors on I of extended chain single crystals (ECSCs), i.e., I ∝ Mn-1.0, and on the lateral growth rates (V) of ECSCs and FCSCs, V ∝ Mn-0.7 and V ∝ Mn-1.7, respectively. ECSCs were formed by isothermal crystallization from the melt into a disordered phase (=hexagonal phase). Therefore, it is concluded that a common power law, I, V ∝ D(Mn) ∝ Mn-H of PE is confirmed, irrespective of nucleation or growth and irrespective of crystalline phases, ordered or disordered phases. It is to be noted that the power H depends on the degree of order of the crystalline phase, from which it is concluded that both nucleation and growth are controlled by the "topological" diffusion of polymer chains within interface between a nucleus (or crystal) and the melt and/or within the nucleus. The "topological" diffusion is related to chain sliding diffusion and disentanglements.

本文言語English
ページ(範囲)6985-6991
ページ数7
ジャーナルMacromolecules
35
18
DOI
出版ステータスPublished - 8月 27 2002
外部発表はい

ASJC Scopus subject areas

  • 有機化学
  • ポリマーおよびプラスチック
  • 無機化学
  • 材料化学

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