Multilayer composite proton exchange film containing perfluorosulfonic acid resin and preparation method thereof
A perfluorosulfonic acid resin and proton exchange membrane technology, applied in the field of ion exchange membranes, can solve the problems of poor diaphragm performance and high cost, and achieve the effects of high compatibility, large-scale production, and high ion selectivity
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Embodiment 1
[0036] In this example, 100 g of recovered perfluorosulfonic acid resin was dissolved in N,N-dimethylformamide, and centrifuged at 5000 rpm for 20 min to obtain a film-forming solution with a mass concentration of 15%. A wet film with a thickness of 150 μm was scratched on the surface of a glass plate, and cured at 140° C. for 3 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 65 μm.
[0037] In terms of weight ratio, a functional material precursor solution of ethyl orthosilicate: tetrapropylammonium hydroxide: sodium hydroxide: water = 1:0.5:0.5:300 was prepared, the synthesis temperature was 100° C., and the synthesis time was 3 hours. Add a 4×4cm perfluorosulfonic acid resin base film and 200ml functional material precursor solution into a stainless steel reaction kettle, and conduct a hydrothermal reaction at 80°C for 1.5h. The perfluorosulfonic acid resin base film was taken out, soaked in excess deionized water, and then dried at 120°C. The ...
Embodiment 2
[0040] In this example, 50 g of recovered perfluorosulfonic acid resin was dissolved in N,N-dimethylformamide, and centrifuged at 3000 rpm for 30 min to obtain a film-forming solution with a mass concentration of 10%. A wet film with a thickness of 100 μm was scratched on the surface of a glass plate, and cured at 130° C. for 5 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 32 μm.
[0041] In terms of weight ratio, a functional material precursor solution of ethyl orthosilicate: tetrapropylammonium hydroxide: sodium hydroxide: water = 1:0.3:0.3:150 was prepared, the synthesis temperature was 80° C., and the synthesis time was 5 hours. Add a 4×4cm perfluorosulfonic acid resin base film and 200ml functional material precursor solution into a stainless steel reaction kettle, and conduct a hydrothermal reaction at 120°C for 0.5h. The perfluorosulfonic acid resin base film was taken out, soaked in excess deionized water, and then dried at 120°C. The p...
Embodiment 3
[0044] In this example, 200 g of recovered perfluorosulfonic acid resin was dissolved in N,N-dimethylacetamide, and centrifuged at 3000 rpm for 20 min to obtain a film-forming solution with a mass concentration of 20%. A wet film with a thickness of 40 μm was scratched on the surface of a glass plate, and further cured and molded at 110° C. for 3 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 23 μm.
[0045]In terms of weight ratio, a functional material precursor solution of ethyl orthosilicate: tetrapropylammonium hydroxide: sodium hydroxide: water = 1:0.15:0.25:200 was prepared, the synthesis temperature was 120° C., and the synthesis time was 1 h. Add a 4×4cm perfluorosulfonic acid resin base film and 200ml functional material precursor solution into a stainless steel reaction kettle, and conduct a hydrothermal reaction at 140°C for 6h. The perfluorosulfonic acid resin base film was taken out, soaked in excess deionized water, and then dried a...
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