Ionic liquid polymeric gel membranes containing from 20 wt % to 80 wt % of the ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIM][TFSI]) in poly(vinylidene fluorideco-hexafluoropropylene) (p(VDF-HFP)) were prepared by solvent casting from a solution in acetone. The effect of the ionic liquid on the performance and properties of the membranes was discussed and compared with the neat polymer. In the presence of an excess of ionic liquid, p(VDF-HFP) membranes swell in a significant way, especially above 70°C, becoming completely soluble above 90°C. DSC analysis shows a gradual decrease of the melting point of the gel and a decrease in the overall melting enthalpy with increasing IL content, whereas the melting enthalpy normalized for the polymer fraction shows an initial drop and then a gradual increase. In the presence of the ionic liquid, the elastic modulus and break strength decrease dramatically, while the maximum deformation first increases due to higher flexibility of the plasticized polymer and then rapidly decreases above 40 wt % of IL as a consequence of the progressive decrease of the number of entanglements. X-ray studies demonstrate a reduction in the overall crystal content. The position of the strongest diffraction peak remains unaltered in all samples, suggesting that only the polymer chains crystallize and that no cocrystallization of ionic liquid and polymer takes place. Preliminary gas permeation measurements show a significant increase of the permeability in the presence of [EMIM][TFSI], especially for carbon dioxide. This suggests a potential application in gas separation membranes, for instance for natural gas treatment or for CO 2 sequestration from flue gas.

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New ion-exchange acid/base-blend (SPPO/PBI) membranes were prepared by mixing N,N-dimethylacetamide (DMA) solutions of sulfonated poly(2,6-dimethyl-1,4-phenylene oxide) (SPPO) in the ammonium form and of polybenzimidazole (PBI), casting the solution as a thin film, evaporating the solvent, and treating the membrane with aqueous hydrochloric acid. The resulting membranes were found insoluble in DMA. The preliminary tests of the membranes were carried out in an H 2 /O 2 fuel cell at room temperature. Their performance in the fuel cell increased with the increase in the concentration of SPPO sulfonic acid groups in the blend, but the membranes formed with the highly sulfonated SPPO alone or predominanting, which swelled excessively in water, did not give reproducible results, and their performance was usually inferior to that of the membranes having an optimum ratio of both components.

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