COMPOSITE POLYMER ELECTROLYTIC MEMBRANE, AND MEMBRANE ELECTRODE COMPOSITE AND SOLID POLYMER FUEL CELL USING the SAME
A polymer electrolyte and composite polymer technology, applied in fuel cells, fuel cell parts, conductive materials, etc., can solve the problem of large dimensional changes and achieve small dimensional change rates, high output, mechanical strength and chemical stability excellent effect
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[0137] Hereinafter, the present invention will be described in more detail through examples, but the present invention is not limited thereto. In addition, various measurement conditions are as follows.
[0138] (1) Molecular weight of the polymer
[0139] The number average molecular weight and weight average molecular weight of the polymer solution were measured by GPC. HLC-8022GPC manufactured by TOSOH was used as an integrated device for ultraviolet detector and differential refractometer, and two TSK gelSuperHM-H (inner diameter 6.0 mm, length 15 cm) manufactured by TOSOH were used as GPC columns. The 2-pyrrolidone solvent (N-methyl-2-pyrrolidone solvent containing 10 mmol / L lithium bromide) was measured at a flow rate of 0.2 mL / min, and the number average molecular weight and weight average molecular weight were determined in terms of standard polystyrene.
[0140] (2) Ion exchange capacity (IEC)
[0141] Determined by neutralization titration. The measurement was ca...
Synthetic example 1
[0228] (Synthesis of 2,2-bis(4-hydroxyphenyl)-1,3-dioxolane (K-DHBP) represented by the following general formula (G1))
[0229] Put 49.5g of 4,4'-dihydroxybenzophenone, 134g of ethylene glycol, 96.9g of trimethyl orthoformate, and p-toluenesulfonic acid monohydrate into a 500ml flask equipped with a stirrer, a thermometer, and a distillation tube 0.50 g was dissolved. Then keep stirring at 78-82°C for 2 hours. Further, the internal temperature was gradually raised to 120° C., and heating was performed until the distillation of methyl formate, methanol, and trimethyl orthoformate completely stopped. After cooling the reaction solution to room temperature, the reaction solution was diluted with ethyl acetate, and the organic layer was washed and separated with 100 ml of a 5% potassium carbonate aqueous solution, and then the solvent was distilled off. 80 ml of dichloromethane was added to the residue to precipitate crystals, which were filtered and dried to obtain 52.0 g of 2...
Synthetic example 2
[0232] (Synthesis of 3,3'-disodium disulfonate-4,4'-difluorobenzophenone represented by the following general formula (G2))
[0233] Make 4,4'-difluorobenzophenone 109.1g (Aldrich reagent) in fuming sulfuric acid (50%SO 3 ) in 150mL (Wako Pure Chemical Chemicals) at 100°C for 10 hours. Thereafter, a small amount was poured into a large amount of water one by one, and after neutralizing with NaOH, 200 g of common salt (NaCl) was added to precipitate the composite. The obtained precipitate was separated by filtration and recrystallized from an aqueous ethanol solution to obtain 3,3'-disodium disulfonate-4,4'-difluorobenzophenone represented by the above general formula (G2). The purity is 99.3%.
[0234]
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