4.2 Article

Re-examination of terminal relaxation behavior of high-molecular-weight ring polystyrene melts

期刊

RHEOLOGICA ACTA
卷 56, 期 6, 页码 567-581

出版社

SPRINGER
DOI: 10.1007/s00397-017-1014-3

关键词

Ring polymer; Linear contaminant; Linear viscoelasticity; Birefringence; Fractal loopy globule model

资金

  1. Japan Society for the Promotion of Science [15H03865]
  2. Collaborative Research Program of Institute for Chemical Research, Kyoto University [2015-58]
  3. ACCEL program of the Japan Science and Technology Agency (JST)
  4. Grants-in-Aid for Scientific Research [16H04204, 15H03865] Funding Source: KAKEN

向作者/读者索取更多资源

For high-molecular-weight (M) ring polymers with low contamination of linear chains, recent viscoelastic tests revealed broad terminal relaxation associated with no clear entanglement plateau. This relaxation behavior is qualitatively similar to that deduced from molecular models (double-folded lattice-animal model and the fractal loopy globule model) for entangled ring polymers, but quantitatively important differences are also noted: For example, the full terminal relaxation of those polymers is slower than the model prediction. This study re-examined the viscoelastic data of entangled high-M ring polystyrene (PS) samples (coded as R-240; M = 244x10(3)) specifically for two points: the purity of the ring samples after the viscoelastic tests and the molecular origin of the stress. For the first point, the R-240 samples contaminated with linear chains at low but different levels were prepared by tuning either the purification efficiency or the retention time of the sample at high temperature (T) before/during the viscoelastic test. The fraction w (L) of the linear contaminant, determined after the viscoelastic measurement, was ranging from 0.7 to 4.9%, and the extrapolation of the modulus data to w (L) = 0 gave the data for the ideally pure ring melt. This pure ring melt exhibited broad terminal relaxation that started faster but completed slower compared to the model prediction, indicating that the ring relaxation is not well described by the current model(s) even in the absence of linear contaminant. For the second point, dynamic birefringence measurements were conducted for the R-240 samples with w (L) = 4.6 and 1.0%. These samples obeyed the stress-optical rule, and their stress-optical coefficient was indistinguishable from that for linear PS samples, revealing that the stress of the ring PS chains reflects the orientational anisotropy of the chains (as is the case also for linear chains). The relaxation behavior of pure ring PS melt is discussed on the basis of these findings, with the focus being placed on the ring-ring threading not considered in the models.

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