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Effect of chemical interaction on morphology and mechanical properties of CPI‐OH/SiO 2 hybrid films with coupling agent
Author(s) -
Qin Jiaqiang,
Zhao Hui,
Zhu Rongqi,
Zhang Xinyuan,
Gu Yi
Publication year - 2007
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.25668
Subject(s) - ultimate tensile strength , materials science , elongation , morphology (biology) , fourier transform infrared spectroscopy , tensile strain , composite number , polymer chemistry , hydrolysis , coupling (piping) , composite material , dynamic mechanical analysis , particle size , chemical engineering , polymer , chemistry , organic chemistry , genetics , engineering , biology
A novel hybrid film composed of copolyimide with hydroxyl group, silica and γ‐glycidyloxypropyltrimethoxysilane (CPI‐OH/SiO 2 /GOTMS) was prepared by the sol–gel process based on hydrolyzed tetraethoxysilane (TEOS) under acidic condition. GOTMS, as the coupling agent, and hydroxyl group in PI chain were used to improve the compatibility between the PI and SiO 2 . The components, morphologies, and mechanical properties of the hybrids were investigated by FTIR, UV–vis, SEM, stress–strain tests, and DMA. The results showed that SiO 2 particle size significantly decreased, fractured cross sections of hybrid were rougher, and the surfaces of spherical SiO 2 particles were more widely covered by PI component. The tensile mechanical properties of hybrids increased when adding GOTMS. The critical points of maximum tensile strength and elongation at break move from 11 to 16 wt % SiO 2 content. DMA results showed that the storage moduli of hybrids with GOTMS, when above 260°C, were obviously higher than those without GOTMS; the tan δ transition temperature of hybrid films went up from 317 to 337°C. It suggests that chemical interaction between CPI‐OH and SiO 2 is formed and the PI molecular mobility is restricted by the chemical interaction. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3530–3538, 2007