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The structure and dynamic properties of thermoplastic polyurethane elastomer/hindered phenol hybrids
Author(s) -
Xiao Daling,
Zhao Xiuying,
Feng Yiping,
Xiang Ping,
Zhang Liqun,
Wang Weimin
Publication year - 2010
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.31828
Subject(s) - glass transition , thermoplastic polyurethane , materials science , elastomer , ultimate tensile strength , polyurethane , composite material , dynamic mechanical analysis , thermoplastic elastomer , microstructure , polymer , copolymer
The organic hybrids of thermoplastic polyurethane (TPU)/hindered phenol (AO‐80) were prepared through melt blending, which was followed by hot and cold pressing procedure. The microstructure and dynamic mechanical properties of the hybrids were systematically investigated through SEM, DSC, XRD, FTIR, DMA and a tensile tester. The experimental results indicated that AO‐80 was completely dissolved in the matrix. The glass transition of the soft segments of TPU was found to shift to higher temperature with the amount of AO‐80 increasing, whereas the glass transition of the hard segments exhibited nearly no evident change, indicating that AO‐80 was selectively located in the soft region of TPU and the formation of the strong intermolecular interactions (hydrogen bonding) between AO‐80 and the soft region of TPU. With the increase of AO‐80 in the hybrids, the tanδ peak gradually shifted to higher temperatures and the maximal tanδ value increased from 0.4 to 1.6. Meanwhile, the glass transition temperature ranges broadened and the TA value increased greatly with the more content of AO‐80. Because of the decrease of the hard segments amount in the hybrids, the tensile stress of these hybrids decreased, but still maintained at a high level. The hybrids were expected to have potential applications as high performance damping materials combined with good mechanical properties. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010