Investigation of perfluorinated proton exchange membranes prepared via a facile strategy of chemically combining poly(vinylphosphonic acid) with PVDF by means of poly(glycidyl methacrylate) grafts

13Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A versatile and diverse grafting method was employed in the preparation of perfluorinated PEMs, in which poly(vinyl phosphonic acid) (PVPA) and poly(vinylidene fluoride) (PVDF) were chemically combined by means of poly(glycidyl methacrylate) (PGMA) grafts. Alkaline treated PVDF was used as a macromolecule in conjunction with GMA in the graft copolymerization. Various PVDF-g-PGMA-g-PVPA membranes were obtained upon simply mixing PVDF-g-PGMA and PVPA at several ratios by mass. The composition and the structure of the membranes were characterized by Energy Dispersive X-ray spectroscopy (EDS), 1 H-NMR, 19 F-NMR, and FTIR. Thermogravimetric analysis (TGA) demonstrated that the PVDF-g-PGMA and PVDF-g-PGMA-g-PVPA membranes were thermally stable up to 275 and 210 °C, respectively. The surface roughness and morphology of the membranes were studied using Atomic Force Microscopy (AFM), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). The proton conductivity increased with increasing temperature and PVPA ratio in the absence of humidity. The maximum proton conductivity in anhydrous conditions at 150 °C was 0.0023 Scm −1 while in humidified conditions (under 50 % of RH) at 100 °C a value of 0.034 Scm −1 was found.

Cite

CITATION STYLE

APA

Sinirlioglu, D., Muftuoglu, A. E., & Bozkurt, A. (2015). Investigation of perfluorinated proton exchange membranes prepared via a facile strategy of chemically combining poly(vinylphosphonic acid) with PVDF by means of poly(glycidyl methacrylate) grafts. Journal of Polymer Research, 22(8). https://doi.org/10.1007/s10965-015-0796-1

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free