Composite organic phosphonic acid high-temperature proton exchange membrane for fuel cell and preparation method of composite organic phosphonic acid high-temperature proton exchange membrane
A technology of proton exchange membrane and organic phosphonic acid, which is applied in the direction of fuel cells, circuits, electrical components, etc., can solve the problems of complex membrane production process, affecting membrane dimensional stability, service life, and complex process
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Embodiment 1
[0065] m-PBI and [2-[(4-vinylbenzyloxy)methyl]oxirane-vinylphosphonic acid bis(trimethylsilyl)ester] copolymer B 1 Preparation of composite membrane:
[0066]
[0067] (1) 2-[(4-vinylbenzyloxy)methyl]oxirane-vinylphosphonic acid bis(trimethylsilyl)ester copolymer B 1 (molar ratio 1:4) preparation:
[0068] Under nitrogen protection, 2-[(4-vinylbenzyloxy)methyl]oxirane (190.1mg, 1mmol) and vinylphosphonic acid bis(trimethylsilyl) were successively added to the three-necked reaction flask (757.2mg, 4mmol), deionized water (200mL) was used as solvent, and then a free radical chain initiator azobisisobutyronitrile (AIBN, 8.20mg, 0.05mmol) was added. Stir (mechanical stirring) and heat to 80°C for reaction. After reacting for 24h, the solution became viscous, the reaction was stopped, and it was cooled to room temperature. Pour the reaction solution into ethyl acetate, and keep stirring, there is solid precipitation, filter, and vacuum dry to obtain organic phosphonic acid c...
Embodiment 2
[0072] B 2 Preparation of composite membrane:
[0073]
[0074] (1) [2-[(4-vinylphenoxy)methyl]oxirane-allylphosphonic acid bis(triethylsilyl)ester]copolymer B 2 (Molar ratio 1:5) preparation:
[0075] Under the protection of nitrogen, 2-[(4-vinylphenoxy)methyl]oxirane (176.2mg, 1mmol) and allylphosphonic acid bis(triethylsilane) were successively added to the three-necked reaction flask. Ester (1752.9mg, 5mmol), deionized water (250mL) was used as solvent, and then a free radical chain initiator azobisisobutyronitrile (AIBN, 19.71mg, 0.12mmol) was added. Stir (mechanical stirring) and heat to 80°C for reaction. After reacting for 24h, the solution became viscous, the reaction was stopped, and it was cooled to room temperature. Pour the reaction solution into ethyl acetate, and keep stirring, there is solid precipitation, filter, and vacuum dry to obtain organic phosphonic acid copolymer B 2 .
[0076] (2) Py-PBI and Copolymer B 2 (Molar ratio 1:1) Preparation of com...
Embodiment 3
[0079] O-PBI and [2-[(2-vinylphenoxy)methyl]oxirane-1,1-vinyl diphosphonic acid tetramethyl ester] copolymer B 3 Preparation of composite membrane:
[0080]
[0081] (1) [2-[(2-vinylphenoxy)methyl]oxirane-1,1-vinyl diphosphonic acid tetramethyl ester] copolymer B 3 (Molar ratio 1:3) preparation:
[0082] Under the protection of nitrogen, 2-[(2-vinylphenoxy)methyl]oxirane (176.2mg, 1mmol) and tetramethyl 1,1-vinyldiphosphonate were successively added to the three-necked reaction flask (732.4mg, 3mmol), deionized water (200mL) was used as solvent, and then a free radical chain initiator azobisisobutyronitrile (AIBN, 13.1mg, 0.08mmol) was added. Stir (mechanical stirring) and heat to 80°C for reaction. After reacting for 24h, the solution became viscous, the reaction was stopped, and it was cooled to room temperature. Pour the reaction solution into ethyl acetate, and keep stirring, solids are precipitated, filtered, and vacuum-dried to obtain copolymer B 3
[0083] (2) ...
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