Conformations of Ring Polystyrenes in Semidilute Solutions and in Linear Polymer Matrices Studied by SANS

Takuro Iwamoto, Yuya Doi, Keita Kinoshita, Atsushi Takano, Yoshiaki Takahashi, Eunhye Kim, Tae Hwan Kim, Shin Ichi Takata, Michihiro Nagao, Yushu Matsushita

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Conformations of highly purified ring polystyrene, R-70, with the molar mass of 70 kg/mol, in a good solvent and in linear polymer homologue matrices were examined by small-angle neutron scattering (SANS) measurements. The radii of gyration Rg of R-70 were estimated by the Guinier's approximation from the SANS profiles obtained, and the polymer volume fraction φ dependence of Rg 2 was discussed. In deuterated toluene as a good solvent, R-70 exhibits the Rg 2 ∼ φ-0.29±0.01 dependence at high φ above the overlap volume fraction, φ0∗ (i.e., 1 < φ/ φ0∗ < 20). This exponent -0.29 shows stronger φ dependence than that for semidilute solutions of linear polymers, -0.25, predicted from the scaling theory, suggesting that the ring expands more sensitively than linear chains when φ decreases in semidilute regime. In contrast, the φ dependence of Rg 2 of R-70 is evidently weaker than that of the recent simulation for ring polymer solutions (Rg 2 ∼ φ-0.59) by Reigh et al. This difference is thought to originate from the difference in the ring chain length; i.e., the simulation treated much longer rings than the ring adopted in this study. Therefore, it is expected that the exponent -0.29 for the ring polymer solutions obtained in this study is not a limiting value but is a transit one toward higher φ/ φ0∗ region. The size of R-70 is also increased when the ring was diluted with linear polystyrenes. However, the degree of expansion of the rings in linear polymer matrices is considerably lower than that in toluene solutions. Moreover, the molar masses of the linear chains added hardly effect the expansion behavior of the rings. In fact, the dimension of rings gets closer to that of the Gaussian rings as a larger amount of linear chains is added.

Original languageEnglish
Pages (from-to)6836-6847
Number of pages12
JournalMacromolecules
Volume51
Issue number17
DOIs
Publication statusPublished - Sep 11 2018

Fingerprint

Molar mass
Polystyrenes
Toluene
Polymer solutions
Neutron scattering
Polymer matrix
Conformations
Volume fraction
Polymers
Chain length

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

Cite this

Conformations of Ring Polystyrenes in Semidilute Solutions and in Linear Polymer Matrices Studied by SANS. / Iwamoto, Takuro; Doi, Yuya; Kinoshita, Keita; Takano, Atsushi; Takahashi, Yoshiaki; Kim, Eunhye; Kim, Tae Hwan; Takata, Shin Ichi; Nagao, Michihiro; Matsushita, Yushu.

In: Macromolecules, Vol. 51, No. 17, 11.09.2018, p. 6836-6847.

Research output: Contribution to journalArticle

Iwamoto, T, Doi, Y, Kinoshita, K, Takano, A, Takahashi, Y, Kim, E, Kim, TH, Takata, SI, Nagao, M & Matsushita, Y 2018, 'Conformations of Ring Polystyrenes in Semidilute Solutions and in Linear Polymer Matrices Studied by SANS', Macromolecules, vol. 51, no. 17, pp. 6836-6847. https://doi.org/10.1021/acs.macromol.8b00934
Iwamoto, Takuro ; Doi, Yuya ; Kinoshita, Keita ; Takano, Atsushi ; Takahashi, Yoshiaki ; Kim, Eunhye ; Kim, Tae Hwan ; Takata, Shin Ichi ; Nagao, Michihiro ; Matsushita, Yushu. / Conformations of Ring Polystyrenes in Semidilute Solutions and in Linear Polymer Matrices Studied by SANS. In: Macromolecules. 2018 ; Vol. 51, No. 17. pp. 6836-6847.
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abstract = "Conformations of highly purified ring polystyrene, R-70, with the molar mass of 70 kg/mol, in a good solvent and in linear polymer homologue matrices were examined by small-angle neutron scattering (SANS) measurements. The radii of gyration Rg of R-70 were estimated by the Guinier's approximation from the SANS profiles obtained, and the polymer volume fraction φ dependence of Rg 2 was discussed. In deuterated toluene as a good solvent, R-70 exhibits the Rg 2 ∼ φ-0.29±0.01 dependence at high φ above the overlap volume fraction, φ0∗ (i.e., 1 < φ/ φ0∗ < 20). This exponent -0.29 shows stronger φ dependence than that for semidilute solutions of linear polymers, -0.25, predicted from the scaling theory, suggesting that the ring expands more sensitively than linear chains when φ decreases in semidilute regime. In contrast, the φ dependence of Rg 2 of R-70 is evidently weaker than that of the recent simulation for ring polymer solutions (Rg 2 ∼ φ-0.59) by Reigh et al. This difference is thought to originate from the difference in the ring chain length; i.e., the simulation treated much longer rings than the ring adopted in this study. Therefore, it is expected that the exponent -0.29 for the ring polymer solutions obtained in this study is not a limiting value but is a transit one toward higher φ/ φ0∗ region. The size of R-70 is also increased when the ring was diluted with linear polystyrenes. However, the degree of expansion of the rings in linear polymer matrices is considerably lower than that in toluene solutions. Moreover, the molar masses of the linear chains added hardly effect the expansion behavior of the rings. In fact, the dimension of rings gets closer to that of the Gaussian rings as a larger amount of linear chains is added.",
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AU - Takahashi, Yoshiaki

AU - Kim, Eunhye

AU - Kim, Tae Hwan

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