Electrolyte film and solid polymer fuel cell using the same
A solid polymer and electrolyte membrane technology, applied in solid electrolyte fuel cells, fuel cells, fuel cell components, etc., can solve the problem of reducing the importance of durability
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[0065] The present invention is further described in detail using the examples of the present invention, but the present invention is not limited to the present examples.
[0066] Base material preparation example 1
[0067] 20 parts by weight of polymer composition (by norbornene ring-opening polymer powder (manufactured by Nippon Zeon Co., Ltd., trade name: ノ-solex NB, weight average molecular weight (hereinafter referred to as Mw): more than 2 million) 12wt % and ultra-high molecular weight polyethylene (Mw: 3,000,000) 88wt% composition) and 80 parts by weight of liquid paraffin are uniformly mixed into a slurry, dissolved and mixed with a small kneader at a temperature of 160 ° C for about 60 minutes. The resulting mixture was sandwiched between rolls or metal plates cooled to 0°C, and quenched into a sheet to obtain a sheet-like resin.
[0068] The sheet-like resin is hot-pressed at a temperature of 115°C until the thickness of the sheet is 0.4-0.6mm, and the vertical an...
Embodiment 2
[0085] Film B-2 was obtained by substituting the AAVS system described below for AA in Example 1.
[0086] AAVS department:
[0087] Prepare a 70wt% aqueous solution with 79mol% of acrylic acid, 20mol% of sodium vinylsulfonate, and 1mol% of divinylbenzene as a cross-linking agent, and add 1mol% to 100mol% of the combined acrylic acid and vinylsulfonic acid The water-soluble azo-based initiator V-50, thus obtaining a solution. Substrate A-1 was immersed in this solution, and after irradiating with visible light for 6 minutes, it heated in the oven of 50 degreeC for 18 hours.
[0088] Afterwards, excess polymer on the surface of the membrane was removed, ion-exchanged with a large excess of 1N hydrochloric acid, thoroughly washed with distilled water, and dried in an oven at 50°C to obtain membrane B-2. Membrane B-2 was also performed in the same manner as in Example 1: 1) measurement of membrane area change rate; 2) evaluation of methanol permeation performance; 3) measuremen...
Embodiment 3
[0090] Using the ATBS system described below in place of AA in Example 1, film B-3 was obtained.
[0091] Department of ATBS:
[0092] Dilute a mixed monomer of 2-acrylamide-2-methylpropanesulfonic acid (hereinafter referred to as "ATBS") 99mol% and crosslinking agent: methylenebisacrylamide 1mol% to 50wt% with water, and prepare an aqueous solution. The total of ATBS and methylenebisacrylamide was 100 mol%, and 1 mol% of water-soluble azo-based initiator V-50 was added to obtain a solution. Substrate A-1 was immersed in this solution, and after irradiating with visible light for 6 minutes, it heated in the oven of 50 degreeC for 18 hours.
[0093] Thereafter, excess polymer on the surface of the membrane was removed, ion-exchanged with a large excess of 1N hydrochloric acid, thoroughly washed with distilled water, and dried in an oven at 50°C to obtain membrane B-3. Membrane B-3 was also performed in the same manner as in Example 1: 1) measurement of membrane area change ra...
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