Multilayer composite proton exchange membrane containing perfluorosulfonic acid resin and preparation method thereof
A technology of perfluorosulfonic acid resin and proton exchange membrane, applied in the field of ion exchange membrane, can solve the problems of poor membrane performance and high cost, and achieve the effects of high compatibility, large-scale production, and easy large-scale production.
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Embodiment 1
[0036] In this example, 100 g of the 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 scraped on the surface of the glass plate, and further cured at 140° C. for 3 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 65 μm.
[0037] According to the weight ratio, the functional material precursor solution of ethyl orthosilicate: tetrapropyl ammonium hydroxide: sodium hydroxide: water = 1:0.5:0.5:300 was prepared, the synthesis temperature was 100°C, and the synthesis time was 3h. A 4 × 4 cm perfluorosulfonic acid resin-based membrane and 200 ml of functional material precursor solution were added to a stainless steel reactor, and the hydrothermal reaction was carried out at 80 °C for 1.5 h. The perfluorosulfonic acid resin-based membrane was taken out, soaked in excess deionize...
Embodiment 2
[0040] In this example, 50 g of the 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 scraped on the surface of the glass plate, and further cured at 130° C. for 5 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 32 μm.
[0041] According to the weight ratio, the 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 5h. A 4 × 4 cm perfluorosulfonic acid resin-based membrane and 200 ml of functional material precursor solution were added to a stainless steel reactor, and the hydrothermal reaction was carried out at 120 °C for 0.5 h. The perfluorosulfonic acid resin-based membrane was taken out, soaked in excess deionized ...
Embodiment 3
[0044] In this example, 200 g of the 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 scraped on the surface of the glass plate, and further cured at 110° C. for 3 hours to obtain a perfluorosulfonic acid resin-based film with a dry film of 23 μm.
[0045]According to the weight ratio, the functional material precursor solution of ethyl orthosilicate: tetrapropyl ammonium 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. A 4 × 4 cm perfluorosulfonic acid resin-based membrane and 200 ml of functional material precursor solution were added to a stainless steel reactor, and the hydrothermal reaction was carried out at 140 °C for 6 h. The perfluorosulfonic acid resin-based membrane was taken out, soaked in excess deioniz...
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