• 专利标题:   Preparing catalyst for hydrogen purification of energy fuel cell, involves adding 25ml of concentrated sulfuric acid into flask, cooling, adding natural flake graphite, sodium nitrate, and potassium permanganate particles, and stirring.
  • 专利号:   CN112973731-A
  • 发明人:   BAI Y
  • 专利权人:   JIANGSU MEIMA TECHNOLOGY CO LTD
  • 国际专利分类:   B01D053/62, B01D053/86, B01J023/89, B01J035/10, H01M008/0612
  • 专利详细信息:   CN112973731-A 18 Jun 2021 B01J-023/89 202167 Pages: 14 Chinese
  • 申请详细信息:   CN112973731-A CN10247436 05 Mar 2021
  • 优先权号:   CN10247436

▎ 摘  要

NOVELTY - Preparing catalyst involves adding 25ml of concentrated sulfuric acid into flask, cooling to 0-2 degrees C, adding 0.5g natural flake graphite, 0.5g sodium nitrate, and 3g potassium permanganate particles, and stirring, placing the flask in a constant temperature water bath at 35 divide by 2 degrees C, and continue stirring when the temperature of the reaction solution rises to 35 divide by 2 degrees C, adding 46ml deionized water to the solution, stirring for 15 minutes at 98 divide by 2 degrees C, adding 140ml deionized water and 3ml 30 wt.% hydrogen peroxide to react for 40 minutes after high temperature reaction, washing with 1-3 wt.% hydrochloric acid solution, and then washing with deionized water to neutrality multiple times to obtain 5-15 wt.% graphene oxide suspension, adding certain amount of citric acid, concentrated nitric acid, and tetrabutyl zirconate to the above graphene oxide solution, and magnetically stirring to obtain a sol. USE - Method for preparing catalyst used for hydrogen purification of energy fuel cell. ADVANTAGE - The method has high surface area and high hydrogen purification efficiency. DETAILED DESCRIPTION - Preparing catalyst involves adding 25ml of concentrated sulfuric acid into flask, cooling to 0-2 degrees C, adding 0.5g natural flake graphite, 0.5g sodium nitrate, and 3g potassium permanganate particles, and stirring, placing the flask in a constant temperature water bath at 35 divide by 2 degrees C, and continue stirring when the temperature of the reaction solution rises to 35 divide by 2 degrees C, adding 46ml deionized water to the solution, stirring for 15 minutes at 98 divide by 2 degrees C, adding 140ml deionized water and 3ml 30 wt.% hydrogen peroxide to react for 40 minutes after high temperature reaction, washing with 1-3 wt.% hydrochloric acid solution, and then washing with deionized water to neutrality multiple times to obtain 5-15 wt.% graphene oxide suspension, adding certain amount of citric acid, concentrated nitric acid, and tetrabutyl zirconate to the above graphene oxide solution, and magnetically stirring to obtain a sol. The molar ratio of the citric acid, nitric acid, and tetrabutyl zirconate is (2-3):(0.2-0.3):1, introducing the above-mentioned sol into a test tube, sealing, and placing in a vacuum drying oven at 80-90 degrees C, and reacting for 24-36 hours to obtain a shaped gel. The gel is introduced in multiple test tubes into a hydrothermal reaction kettle containing an aqueous solution of chloroplatinic acid and nickel nitrate, the nitrogen is used to remove the air, and performed a hydrothermal reaction to obtain a catalyst precursor, filtered and washed the catalyst precursor, freeze-dried, and performed reduction treatment in a reducing atmosphere to obtain product.