• 专利标题:   Preparation of bismuth oxyfluoride/graphene composite visible light catalyst used for degrading difficult to degrade organic pollutant includes mixing bismuth nitrate pentahydrate in ethylene glycol, adding graphene oxide and drying.
  • 专利号:   CN104148094-A, CN104148094-B
  • 发明人:   DONG S, HU L
  • 专利权人:   UNIV HENAN NORMAL
  • 国际专利分类:   B01J027/06, C02F001/30
  • 专利详细信息:   CN104148094-A 19 Nov 2014 B01J-027/06 201505 Pages: 7 Chinese
  • 申请详细信息:   CN104148094-A CN10330510 14 Jul 2014
  • 优先权号:   Y, SUN J, ZHANG C, LI Y, FENG J, LI QCN10330510

▎ 摘  要

NOVELTY - Preparation of bismuth oxyfluoride/graphene composite visible light catalyst comprises dissolving bismuth nitrate pentahydrate in ethylene glycol; dissolving sodium fluoride in ethylene glycol; mixing prepared solutions, gradually adding deionized water, filtering, washing with deionized water and ethanol, filtering, drying, and insulating; adding graphene oxide to deionized water, ultrasonic dispersing, adding third step product, and stirring; adding hydrazine hydrate and heating; and cooling to room temperature, filtering, washing with deionized water and ethanol, and drying. USE - Method for preparing bismuth oxyfluoride/graphene composite visible light catalyst (claimed) used for degrading difficult to degrade organic pollutant. ADVANTAGE - The catalyst has wide absorption spectrum range, steady property, no toxicity, and high efficiency and is cheap. DETAILED DESCRIPTION - Preparation of bismuth oxyfluoride/graphene composite visible light catalyst comprises: (A) dissolving 2.5 mmol bismuth nitrate pentahydrate in 20 mL ethylene glycol to obtain first solution; (B) dissolving 2.5 mmol sodium fluoride in 20 mL ethylene glycol to obtain second solution; (C) mixing first and second solution, gradually adding 10 mL deionized water to obtain white precipitate, filtering, washing with deionized water and ethanol for 3 times, filtering, drying for 5 hours at 80 degrees C, and insulating at 300 degrees C for 2 hours; (D) adding 1.52-18.30 mg graphene oxide to 50 mL deionized water, ultrasonic dispersing for 60 minutes, adding 2.5 mmol product in third step, and stirring at normal temperature for 2 hours; (E) adding hydrazine hydrate, and water bath heating at 80 degrees C to restore precipitation polymerization; and (F) cooling to room temperature, filtering, washing with deionized water and ethanol for 3 times, and drying at 80 degrees C for 5 hours.