• 专利标题:   Preparing surface molecularly imprinted polymer of reduced graphene oxide from composite monomer comprises e.g. adding graphene oxide into water, ultrasonicating, adding 4-nitrophenol and methanol, and removing solvent p-nitrophenyl acetate.
  • 专利号:   CN108384044-A
  • 发明人:   HUANG L, WANG X, ZHAO J
  • 专利权人:   FOSHAN YINNUOWEI TECHNOLOGY CO LTD
  • 国际专利分类:   C08J009/26, C08F220/06, C08F220/56, C08F222/14, C08K003/04
  • 专利详细信息:   CN108384044-A 10 Aug 2018 C08J-009/26 201862 Pages: 5 Chinese
  • 申请详细信息:   CN108384044-A CN11490495 30 Dec 2017
  • 优先权号:   CN11490495

▎ 摘  要

NOVELTY - Preparing surface molecularly imprinted polymer of reduced graphene oxide from composite monomer comprises e.g. (i) adding graphene oxide into water, ultrasonicating for 2 hours, then adding hydrazine hydrate solution, concentrated aqueous ammonia and fumed silica, and ultrasonicating for 1-2 hours to obtain dispersion, then heating dispersion at 95-105 degrees C for 0.5-2 hours, washing with water for 2-3 times, filtering, and drying at 60 degrees C under vacuum to obtain reduced graphene oxide, and (ii) adding 4-nitrophenol, methanol, reduced graphene oxide obtained in step (i) and functional monomer into reaction vessel, magnetically stirring for 2 hours, then adding trimethylolpropane trimethacrylate and azobisisobutyronitrile into reaction vessel filled with nitrogen, reacting under water bath at 60-65 degrees C for 28-36 hours, removing solvent p-nitrophenyl acetate by Soxhlet extraction method, and drying to obtain surface molecularly imprinted polymer material of reduced graphene oxide. USE - The method is useful for preparing surface molecularly imprinted polymer of reduced graphene oxide from composite monomer. ADVANTAGE - The method: increases the specific surface area; reduces adsorption and desorption mass transfer resistance; shortens the response time; and improves detection sensitivity. DETAILED DESCRIPTION - Preparing surface molecularly imprinted polymer of reduced graphene oxide from composite monomer comprises (i) adding 10-20 pts. wt. graphene oxide into 200-400 pts. wt. water, ultrasonicating for 2 hours, then adding 0.1-0.5 pts. wt. hydrazine hydrate solution, 1.5-5 pts. wt. concentrated aqueous ammonia and 0.5-1.2 pts. wt. fumed silica, and ultrasonicating for 1-2 hours to obtain dispersion, then heating dispersion while stirring at 95-105 degrees C for 0.5-2 hours, washing with water for 2-3 times, filtering, and drying at 60 degrees C under vacuum to obtain reduced graphene oxide, and (ii) adding 0.3-0.7 pts. wt. 4-nitrophenol, 35-60 pts. wt. methanol, 90-110 pts. wt. reduced graphene oxide obtained in step (i) and 1-4 pts. wt. functional monomer into reaction vessel, magnetically stirring for 2 hours, then adding 2-5 pts. wt. trimethylolpropane trimethacrylate and 25-55 pts. wt. azobisisobutyronitrile into reaction vessel filled with nitrogen, reacting for 15-25 minutes, sealing the vessel, reacting under water bath at 60-65 degrees C for 28-36 hours, removing solvent p-nitrophenyl acetate by Soxhlet extraction method, and drying to obtain surface molecularly imprinted polymer material of reduced graphene oxide, where functional monomer is methacrylic acid, triethanolamine or acrylamide.