• 专利标题:   Preparation of graphene photothermal conversion material involves placing sodium nitrate, flake graphite and concentrated sulfuric acid in the reactor, stirring, adding potassium permanganate, reacting and stirring.
  • 专利号:   CN107964396-A
  • 发明人:   FANG J, ZHANG P, CHEN Z
  • 专利权人:   UNIV SHAANXI TECHNOLOGY
  • 国际专利分类:   B82Y030/00, B82Y040/00, C09K005/14
  • 专利详细信息:   CN107964396-A 27 Apr 2018 C09K-005/14 201835 Pages: 4 Chinese
  • 申请详细信息:   CN107964396-A CN11244876 30 Nov 2017
  • 优先权号:   CN11244876

▎ 摘  要

NOVELTY - Preparation of graphene photothermal conversion material involves placing 3-5 pts. wt. sodium nitrate, 4-6 pts. wt. flake graphite and 180-220 pts. wt. concentrated sulfuric acid in the reactor, stirring for 50-70 minutes, adding 40-45 g potassium permanganate, reacting at 15-20 degrees C for 3-4 hours, adding dilute sulfuric acid and sodium hydroxide solution and continuously stirring until free of bubbles. USE - Method for preparing graphene photothermal conversion material. ADVANTAGE - The method is energy-saving, environment-friendly, safe, simple and fast; and does not produce harmful substances. DETAILED DESCRIPTION - Preparation of graphene photothermal conversion material comprises: (A) placing 3-5 pts. wt. sodium nitrate, 4-6 pts. wt. flake graphite and 180-220 pts. wt. concentrated sulfuric acid in the reactor, stirring for 50-70 minutes, adding 40-45 g potassium permanganate, reacting at 15-20 degrees C for 3-4 hours, adding dilute sulfuric acid and sodium hydroxide solution and continuously stirring until free of bubbles; (B) taking khaki-colored solution and washing with dilute sulfuric acid and deionized water to neutrality; (C) ultrasonically crushing for greater than or equal to 2.5 hours to ensure complete stripping of graphene; (D) centrifuging to remove the graphene that has not been completely stripped with rotation speed of not lower than 12000 revolutions/minute and taking graphene oxide left in the supernatant; (E) mixing upper layer containing graphene oxide with ferrous sulfate and iron chloride where graphene oxide is used as carrier which forms iron oxide nanoparticle layer on its surface; (F) adding poly(N-isopropylacrylamide) hydrogel and stirring to obtain graphene hydrogel composite material containing iron oxide; and (G) inspecting by scanning electron microscopy and transmission electron microscopy and performing line characterization to obtain composite nanoparticles with particle size of 110-120 nm.