Abstract

5-Vinyltetrazole (VT)-based polymer is mainly produced by ‘click chemistry’ from polyacrylonitrile due to the unavailability of 5-vinyltetrazole monomer, which usually produces copolymers of VT and acrylonitrile rather than pure poly(5-vinyltetrazole) (PVT). In present work, VT was synthesized from 5-(2-chloroethyl)tetrazole via dehydrochlorination. A series of PVT with different molecular weight were synthesized by normal free radical polymerization. The chemical structures of VT and PVT were characterized by 1H NMR and FTIR. PVT without any doped acid exhibits certain proton conductivity at higher temperature and anhydrous state. The proton conductivity of PVT decreases at least 2 orders of magnitude after methylation of tetrazole. PVT and PVT/H 3PO 4 composite membranes are thermally stable up to 200 °C. The glass transition temperature ( T g) of PVT/ xH 3PO 4 composite membranes is shifted from 90 °C for x = 0.5 to 55 °C for x = 1. The temperature dependence of DC conductivity for pure PVT exhibits a simple Arrhenius behavior in the temperature range of 90–160 °C, while PVT/ xH 3PO 4 composite membranes with higher H 3PO 4 concentration can be fitted by Vogel–Tamman–Fulcher (VTF) equation. PVT/1.0H 3PO 4 exhibits an anhydrous proton conductivity of 3.05 × 10 −3 at 110 °C. The transmission of the PVT/ xH 3PO 4 composite membrane is above 85% in the wavelength of visible light and changes little with acid contents. Thus, PVT/ xH 3PO 4 composite membranes have potential applications not only in intermediate temperature fuel cells but also in solid electrochromic device.

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.