Abstract

Polyimides (PIs) as high-performance organic matrices are used in the preparation of PI composites because of their excellent mechanical, thermal and dielectric properties. The sol–gel method is a promising technique for preparing these PI composites due to the mild reaction conditions and the process being controllable. Although sulfonated polyimide (SPI) proton-exchange membranes have attracted much attention recently, studies on preparing SPI-based hybrid proton-exchange membranes for fuel cells have been rare. A series of SPISiO2 hybrid proton-exchange membranes were prepared from amino-terminated SPI pre-polymers, 3-glycidoxypropyltrimethoxysilane (KH-560) and tetraethylorthosilicate through a co-hydrolysis and condensation process using an in situ sol–gel method. The reactive silane KH-560 was used to react with amino-terminated SPI to form silane-capped SPI in order to improve the compatibility between the polymer matrix and the inorganic SiO2 phase. The microstructure and mechanical, thermal and proton conduction properties were studied in detail. The hybrid membranes were highly uniform without phase separation up to 30 wt% SiO2. The storage modulus and tensile strength of the hybrid membranes increased with increasing SiO2 content. The introduction of SiO2 improved the methanol resistance while retaining good proton conductivity. The hybrid membrane with 30 wt% SiO2 exhibited a proton conductivity of 10.57 mS cm−1 at 80 °C and methanol permeability of 2.3 × 10−6 cm2 s−1 possibly because the crosslinking structure and SiO2 phases formed in the hybrids could retain water and were helpful to proton transport. Copyright © 2010 Society of Chemical Industry

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.