Iron negative electrode binder of iron-nickel secondary battery
A secondary battery and iron negative electrode technology, which is applied in the field of alkaline secondary batteries, can solve the problems of increased battery manufacturing cost, small adhesive force, complicated manufacturing process, etc., achieve good weather resistance and widen the use temperature range.
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[0023] The preparation method of the binder iron negative electrode of the present invention is to mix the iron negative electrode material (containing 10-25% conductive agent) and the resin solution according to the content of 30%-60% and 40%-70% respectively. The slurry is coated on the conductive current collector substrate by spraying, brushing or scraping, and then dried and pressurized to form the iron negative electrode.
[0024] Preferably, the contents of the iron negative electrode material and the resin solution are 40%-50% and 50%-70%, respectively.
[0025] The above-mentioned iron negative electrode material can be a mixture of one or more of Fe2O3, Fe3O4 or iron powder; the above-mentioned conductive agent can be one or more of carbon materials such as graphite, acetylene black, carbon nanotubes, graphene, etc. The above-mentioned conductive current collector substrate material can be nickel foam, perforated nickel strip, perforated nickel-plated stainless steel...
Embodiment 1
[0028] Mix 3 g of high-molecular-weight high-chlorinated polyethylene, 1.5 g of hydroxypropyl cellulose and 95.5 g of xylene in a conical flask container, seal it, place it in a full-temperature oscillator, heat it to 50 ° C, and shake it for 5 hours to obtain Clear solution, save for future use. After mixing 1 gram of Fe2O3 and 0.10 gram of graphite powder evenly, take 1 gram of the above-mentioned solution prepared in this example and mix it with it, fully stir, defoam, and then apply 2cm×5cm, the thickness is 2.2mm, and the number of openings is On top of 100PPI foamed nickel, dry it and roll it to a thickness of 0.4mm. Test method: Take an industrialized sintered nickel electrode of the same size and a thickness of 1mm as the working electrode, and a 0.2mm hydrophilic polypropylene felt as the diaphragm to form a single cell for evaluation. The electrolytes are 6M KOH and 0.1M Li(OH) aqueous solutions, and the test temperatures are 20°C and 70°C. The charging and dischar...
Embodiment 2
[0031] Mix 3g of high-chlorinated polyethylene with medium molecular weight, 2g of hydroxypropyl cellulose and 95g of xylene in a conical flask container, seal it, place it in a full-temperature shaker, heat it to 50°C, shake it for 5h, and obtain a transparent solution, save for later use. After mixing 1 gram of Fe3O4 and 0.15 gram of graphite powder evenly, take 1 gram of the above-mentioned solution prepared in this example and mix it with it, stir thoroughly, defoam, and then coat 2cm×7.5cm with a thickness of 1.8mm and the number of openings On top of 120PPI foamed nickel, dry it and roll it to a thickness of 0.3mm. Test method and charging and discharging system are identical with embodiment 1, and the test result of the capacity of first 6 six cycles is as follows:
[0032] Cycles
[0033] Effects of the invention: From the implementations 1 and 2, it can be seen that the iron negative electrode prepared by using the binder of the present invention has a rela...
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