• 专利标题:   Preparation of phenyl-modified magnetic graphene/mesoporous silica composite material used as solid phase extracting agent, comprises dispersing magnetic graphite and hexadecyl trimethyl ammonium bromide in deionized water, and dispersing.
  • 专利号:   CN105597714-A, CN105597714-B
  • 发明人:   HUANG P, MA X, WANG H, WANG X, LU M
  • 专利权人:   UNIV NORTHWEST NORMAL, UNIV NORTHWEST NORMAL
  • 国际专利分类:   B01J020/28, B01J020/281, B01J020/30, C02F001/28
  • 专利详细信息:   CN105597714-A 25 May 2016 B01J-020/281 201669 Pages: 16 Chinese
  • 申请详细信息:   CN105597714-A CN10156374 18 Mar 2016
  • 优先权号:   CN10156374

▎ 摘  要

NOVELTY - Preparation of phenyl-modified magnetic graphene/mesoporous silica composite material comprises dispersing magnetic graphite and hexadecyl trimethyl ammonium bromide in deionized water, adding sodium hydroxide, ultrasonically dispersing, heating at 50-60 degrees C, stirring 30-60 minutes, adding with ethanol, mixture of tetraethyl orthosilicate and phenyl triethoxysilane, continuously stirring for 10-12 hours, magnetically separating, washing with deionized water, refluxing, removing template agent, vacuum freezing at - 55 to - 50 degrees C, and drying to obtain the product. USE - Method of preparation of phenyl-modified magnetic graphene/mesoporous silica composite material used as solid phase extracting agent in treatment of wastewater of pesticide (claimed). ADVANTAGE - The material has quick absorption speed, and good adsorption efficiency. DETAILED DESCRIPTION - Preparation of phenyl-modified magnetic graphene/mesoporous silica composite material comprises dispersing graphene oxide in ethanediol, ultrasonically peeling for 0.5-1 hours, adding iron chloride hexahydrate, ultrasonically dispersing, stirring at 30-40 degrees C for 2-3 hours, adding with sodium acetate and polyethylene glycol, continuously stirring for 0.5-1 hours, reacting at 180-200 degrees C for 20-24 hours in reaction kettle, washing with alcohol, vacuum drying, and obtaining magnetic graphite; and dispersing magnetic graphite and hexadecyl trimethyl ammonium bromide in deionized water, adding sodium hydroxide, ultrasonically dispersing, heating at 50-60 degrees C, stirring 30-60 minutes, adding with ethanol, mixture of tetraethyl orthosilicate and phenyl triethoxysilane, continuously stirring for 10-12 hours, magnetically separating, washing with deionized water, refluxing, removing template agent, vacuum freezing at - 55 to - 50 degrees C, and drying to obtain the product.