TY - JOUR
T1 - In situ synchrotron radiation x-ray scattering investigation of a microphase-separated structure of thermoplastic elastomers under uniaxial and equi-biaxial deformation modes
AU - Dechnarong, Nattanee
AU - Kamitani, Kazutaka
AU - Cheng, Chao Hung
AU - Masuda, Shiori
AU - Nozaki, Shuhei
AU - Nagano, Chigusa
AU - Amamoto, Yoshifumi
AU - Kojio, Ken
AU - Takahara, Atsushi
N1 - Funding Information:
This work was supported by the Impulsing Paradigm Change through Disruptive Technology (ImPACT) Program, JST CREST Grant Number JPMJCR17J4, and JST-Mirai Program Grant Number JPMJMI18A2, Japan. Synchrotron radiation X-ray scattering measurements were performed at BL05XU and BL40XU in the SPring-8 facility with the approval of the Japan Synchrotron Radiation Research Institute (JASRI; Proposal Nos. 2018B1035, 2019A1015, 2019B1011, 2020A1007). The supercomputer system ITO at Kyushu University is acknowledged for the model calculation procedure. N.D. gratefully thanks Natsuda Klongvessa (Ph.D. student at Institut Lumiere Matiere, Universite Claude Bernard Lyon 1) for her kind suggestions for the physics calculations. Financial support for N.D. was provided by the International Graduate Course on Chemistry for Molecular Systems, Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.
Funding Information:
This work was supported by the Impulsing Paradigm Change through Disruptive Technology (ImPACT) Program, JST CREST Grant Number JPMJCR17J4, and JST-Mirai Program Grant Number JPMJMI18A2, Japan. Synchrotron radiation X-ray scattering measurements were performed at BL05XU and BL40XU in the SPring-8 facility with the approval of the Japan Synchrotron Radiation Research Institute (JASRI; Proposal Nos. 2018B1035, 2019A1015, 2019B1011, 2020A1007). The supercomputer system ITO at Kyushu University is acknowledged for the model calculation procedure. N.D. gratefully thanks Natsuda Klongvessa (Ph.D. student at Institut Lumière Matière, Université Claude Bernard Lyon 1) for her kind suggestions for the physics calculations. Financial support for N.D. was provided by the International Graduate Course on Chemistry for Molecular Systems, Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/10/27
Y1 - 2020/10/27
N2 - Changes in the microphase-separated structure of the poly(styrene-b-ethylene-co-butylene-b-styrene) (SEBS) triblock copolymer (13 wt % polystyrene (PS) block) were investigated during mechanical deformation. In situ synchrotron radiation small-angle X-ray scattering (SAXS)/wide-angle X-ray scattering (WAXS) measurements were successfully performed for SEBS under equi-biaxial deformation as well as under uniaxial deformation. In situ SAXS/WAXS measurements revealed changes in (1) the shape of spherical PS domains, (2) the spacing of PS domains packed in the body-centered cubic structure in the initial state, (3) their ordering, and (4) the orientation of PEB chains during deformations. In terms of the microdomain structure, affine deformation was kept below a certain strain (εd-A), which are 4 and 1.2 for uniaxial and equi-biaxial deformation, respectively. In contrast, the ordering of the arranged PS domains decreased from the initial strain region. Above the εd-A value, deviation from affine deformation started to occur. This deviation is related to contact of PS domains under mechanical deformation. Uniaxial stretching still showed the plane-independent behavior, while equi-biaxial stretching did not. Moreover, the εd-A value for equi-biaxial deformation was smaller than that for uniaxial deformation and further smaller than expected. This might be because the entanglement effect was enhanced for equi-biaxial deformation. Furthermore, after contact of PS domains at around strains of 6 and 2, during uniaxial and equi-biaxial deformation, respectively, the ordering of PS domains suddenly increased with an increase in strain. It is inferred that the locked state between the PS domains and the extended PEB chains formed during deformation may have been released and repacked at a certain strain.
AB - Changes in the microphase-separated structure of the poly(styrene-b-ethylene-co-butylene-b-styrene) (SEBS) triblock copolymer (13 wt % polystyrene (PS) block) were investigated during mechanical deformation. In situ synchrotron radiation small-angle X-ray scattering (SAXS)/wide-angle X-ray scattering (WAXS) measurements were successfully performed for SEBS under equi-biaxial deformation as well as under uniaxial deformation. In situ SAXS/WAXS measurements revealed changes in (1) the shape of spherical PS domains, (2) the spacing of PS domains packed in the body-centered cubic structure in the initial state, (3) their ordering, and (4) the orientation of PEB chains during deformations. In terms of the microdomain structure, affine deformation was kept below a certain strain (εd-A), which are 4 and 1.2 for uniaxial and equi-biaxial deformation, respectively. In contrast, the ordering of the arranged PS domains decreased from the initial strain region. Above the εd-A value, deviation from affine deformation started to occur. This deviation is related to contact of PS domains under mechanical deformation. Uniaxial stretching still showed the plane-independent behavior, while equi-biaxial stretching did not. Moreover, the εd-A value for equi-biaxial deformation was smaller than that for uniaxial deformation and further smaller than expected. This might be because the entanglement effect was enhanced for equi-biaxial deformation. Furthermore, after contact of PS domains at around strains of 6 and 2, during uniaxial and equi-biaxial deformation, respectively, the ordering of PS domains suddenly increased with an increase in strain. It is inferred that the locked state between the PS domains and the extended PEB chains formed during deformation may have been released and repacked at a certain strain.
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U2 - 10.1021/acs.macromol.0c00962
DO - 10.1021/acs.macromol.0c00962
M3 - Article
AN - SCOPUS:85094668588
SN - 0024-9297
VL - 53
SP - 8901
EP - 8909
JO - Macromolecules
JF - Macromolecules
IS - 20
ER -