• 专利标题:   Preparing of graft-modified polybenzoxazole fibers, the present the thionyl chloride and , adding a graphene oxide powder, ultrasonicating for heating and refluxing under nitrogen atmosphere.
  • 专利号:   CN103820996-A, CN103820996-B
  • 发明人:   HUANG Y, WANG F, WEI F, LIU L, CHEN L, CHENG W, HU Z
  • 专利权人:   HARBIN INST TECHNOLOGY
  • 国际专利分类:   C08J005/06, C08L063/00, D06M011/01, D06M011/55, D06M011/74, D06M013/513, D06M101/30
  • 专利详细信息:   CN103820996-A 28 May 2014 D06M-013/513 201449 Pages: 10 Chinese
  • 申请详细信息:   CN103820996-A CN10076725 04 Mar 2014
  • 优先权号:   CN10076725

▎ 摘  要

NOVELTY - Binary graft-modified polybenzoxazole fiber is prepared by combining 10-100 ml thionyl chloride and 1-5 ml N,N-dimethylformamide, adding 0.1-0.4 g graphene oxide powder, ultrasonicating for 0.5-2 hours, heating and refluxing under nitrogen atmosphere for 12-72 hours, distilling under reduced pressure to remove solvent and obtain functionalized graphene oxide, winding polybenzoxazole fiber around square glass frame, immersing in sulfuric acid solution, stirring at room temperature for 1-4 hours, taking out, washing with deionized water 1-7 times, and drying at 80-150 degrees C for 10-60 minutes. USE - Preparation of binary graft-modified PBO fiber (claimed). ADVANTAGE - Binary graft-modified PBO fiber has improved wettability, tensile strength retention rate, interfacial shear strength, and contact area between fiber surface and resin matrix. DETAILED DESCRIPTION - Binary graft-modified polybenzoxazole (PBO) fiber is prepared by combining 10-100 ml thionyl chloride and 1-5 ml N,N-dimethylformamide, adding 0.1-0.4 g graphene oxide powder, ultrasonicating for 0.5-2 hours, heating and refluxing under nitrogen atmosphere for 12-72 hours, distilling under reduced pressure to remove solvent and obtain functionalized graphene oxide, winding PBO fiber around square glass frame, immersing in sulfuric acid solution, stirring at room temperature for 1-4 hours, taking out, washing with deionized water 1-7 times, 1st drying at 80-150 degrees C for 10-60 minutes to obtain activated PBO fiber, adding 0.02-0.08 g activated PBO fiber to 25-100 ml lithium aluminum hydride-diethyl ether saturated solution, heating and refluxing under nitrogen atmosphere for 0.5-2 hours, washing with deionized water 1-7 times, 2nd drying at 80-150 degrees C for 10-60 minutes to obtain hydroxyl-functionalized PBO fiber, adding 0.5-2 ml 3-aminopropyl trimethoxysilane (APTMS) to 50-150 ml anhydrous ethanol, mixing, adding 0.02-0.08 g hydroxyl-functionalized PBO fiber, stirring at 30-60 degrees C for 6-24 hours, washing with anhydrous ethanol 1-7 times, 3rd drying to obtain APTMS-grafted PBO fiber, dissolving 0.05-0.15 g functionalized graphene oxide in 40-100 ml N,N-dimethylformamide, ultrasonicating for 1-3 hours, adding 0.02-0.08 g APTMS-grafted PBO fiber, heating and refluxing under nitrogen atmosphere for 24-72 hours, washing with N,N-dimethylformamide 1-7 times, and 4th drying. DESCRIPTION OF DRAWING(S) - The drawing shows a scanning electron microscope (SEM) image of binary graft-modified PBO fiber.