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- W2804577029 abstract "Abstract Within this study various partially fluorinated polyaromatic and PBI blend components were covalent-ionically cross-linked to obtain acid and base-excess proton exchange membranes that can be applied in high temperature fuel cells and SO2 electrolysis. A stability assessment of the blend membranes included an extraction experiment in the organic solvent N,N-dimethylacetamide (DMAc), Fenton’s Test (FT) and an 80 wt% H2SO4 treatment for 120 hours at 100 °C. Furthermore the thermal stability of the materials were evaluated by TGA-FTIR coupling, and the H+-conductivity determined for the phosphoric acid-doped (PA) membranes in temperature ranges 60-140 °C. It was found that all blend membranes showed good chemical stability during the H2SO4 treatment; though the base-excess blend membranes reported better chemical stabilities in the FT and DMAc extraction experiments in comparison to the acid-excess blends. The earliest thermal degradation for a blend membrane was found to start at 277 °C, only after the H2SO4 treatment, supporting the thermal stability. For the PA-doped blend membranes conductivities of 39,6 mS/cm reported at 140 °C was comparable to earlier work on similar membrane blends, but now achieved at a lower PA-doping level. Furthermore the base-excess membrane selected for fuel cell (FC) testing reported comparable in the polarization curves recorded at 140 ⁰C, however a maximum power density of 88.2 mW/cm2 was reached in comparison to the 72.8 mW/cm2 of Celtec®-P under the same operation conditions for similarly prepared MEAs. This all proves promising for further testing and optimization of the blend membranes for HTFC and SO2 electrolysis applications." @default.
- W2804577029 created "2018-06-01" @default.
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- W2804577029 date "2018-01-01" @default.
- W2804577029 modified "2023-10-18" @default.
- W2804577029 title "Novel cross-linked PBI-blended membranes evaluated for high temperature fuel cell application and SO 2 electrolysis" @default.
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- W2804577029 doi "https://doi.org/10.1016/j.matpr.2017.12.384" @default.
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