• 专利标题:   Nanoflame retardant preparation used as additive for preparing base material involves preparing acid functionalized graphene, ultrasonic dispersing in tetrahydrofuran, cooling, adding hexachloro cyclotriphosphazene and reacting.
  • 专利号:   CN105348578-A, CN105348578-B
  • 发明人:   LIU C, WANG F, WANG J
  • 专利权人:   SHENYANG SHUNFENG XINCHENG BUILDING, SHENYANG SHUNFENG NEW MATERIAL CO LTD
  • 国际专利分类:   C08K013/06, C08K003/04, C08K003/06, C08K003/22, C08K005/09, C08K005/47, C08K009/04, C08L023/12, C08L007/00
  • 专利详细信息:   CN105348578-A 24 Feb 2016 C08L-007/00 201645 Pages: 7 English
  • 申请详细信息:   CN105348578-A CN10887060 27 Nov 2015
  • 优先权号:   CN10887060

▎ 摘  要

NOVELTY - A nanoflame retardant preparation involves preparing acid functionalized graphene; and ultrasonic dispersing 1-3 g acid functionalized graphene in 100 ml tetrahydrofuran, pouring into 500 ml three-necked flask, filling with nitrogen, cooling in ice bath, adding 5-12 g triethylamine, stirring for 1-2 hours, adding 3-5 g hexachloro cyclotriphosphazene, stirring for 2 hours and reacting under nitrogen atmosphere for 5-8 hours with stirring to get acid/hexachloro cyclotriphosphazene functionalized graphene as nanoflame retardant. USE - Method for preparing nanoflame retardant used as additive for preparing base material such as natural rubber, ethylene propylene diene monomer, styrene-butadiene rubber and polypropylene plastic (claimed). ADVANTAGE - The flame retardant has improved dispersion, performance and compatibility, strong anti-surface migration, ideal retardant effect and high carbon capacity. DETAILED DESCRIPTION - A nanoflame retardant preparation comprises adding 1-2 g p-aminobenzoic acid and 0.2-0.4 g sodium hydroxide to reaction vessel, pouring 50-100 ml distilled water, reacting at 0-5 degrees C, adding slowly 0.5-1 g sodium nitrite and 5-10 ml 20% hydrochloric acid, stirring for 45-60 minutes, adding 0.2-0.5 g reduction graphene, stirring at 0-5 degrees C for 3-4 hours, adjusting pH value to 2-3, dialyzing 2-3 times with dialysis membrane and washing using organic solvent to neutralized to get acid functionalized graphene; and ultrasonic dispersing 1-3 g acid functionalized graphene in 100 ml tetrahydrofuran, pouring into 500 ml three-necked flask, filling with nitrogen, cooling in ice bath, adding 5-12 g triethylamine, stirring for 1-2 hours, adding 3-5 g hexachloro cyclotriphosphazene, stirring for 2 hours and reacting under nitrogen atmosphere for 5-8 hours with stirring to get acid/hexachloro cyclotriphosphazene functionalized graphene as nanoflame retardant.