Volume 52, Issue 13 pp. 1885-1897
Article

Investigation of proton conductivity of anhydrous proton exchange membranes prepared via grafting vinyltriazole onto alkaline-treated PVDF

Deniz Sinirlioglu

Deniz Sinirlioglu

Department of Chemistry, Faculty of Arts and Sciences, Fatih University, 34500 Buyukcekmece, Istanbul, Turkey

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Ali Ekrem Muftuoglu

Corresponding Author

Ali Ekrem Muftuoglu

Department of Chemical Engineering, Faculty of Chemical and Metallurgical Engineering, Yildiz Technical University, Davutpasa Campus, 34220 Esenler, Istanbul, Turkey

Correspondence to: A. Muftuoglu (E-mail: [email protected])Search for more papers by this author
Kurtulus Golcuk

Kurtulus Golcuk

Department of Physics, Faculty of Arts and Sciences, Fatih University, 34500 Buyukcekmece, Istanbul, Turkey

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Ayhan Bozkurt

Ayhan Bozkurt

Department of Chemistry, Faculty of Arts and Sciences, Fatih University, 34500 Buyukcekmece, Istanbul, Turkey

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First published: 22 April 2014
Citations: 23

ABSTRACT

This work uses a simple “grafting through” approach in the preparation of anhydrous poly(vinylidene fluoride) (PVDF)-g-PVTri polymer electrolyte membranes (PEMs). Alkaline-treated PVDF was used as a macromolecule in conjunction with vinyltriazole in the graft copolymerization. The obtained polymer was subsequently doped with triflic acid (TA) at different stoichiometric ratios with respect to triazole units and the anhydrous PEMs (PVDF-g-PVTri-(TA)x) were prepared. All samples were characterized by FTIR and 1H NMR. The composition of PVDF-g-PVTri was determined by energy dispersive spectroscopy. Thermal properties of the membranes were examined by thermogravimetric analysis and differential scanning calorimetry. The surface roughness and morphology of the membranes were studied using atomic force microscopy, X-ray diffraction, and scanning electron microscopy. PVDF-g-PVTri-(TA)3 (C3-TA3) with a degree of grafting of 47.22% showed a maximum proton conductivity of 0.09 S cm−1 at 150 °C and anhydrous conditions. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 1885–1897

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