• 专利标题:   Preparation of graphene-carbon nanotube three-dimensional structural composite material involves performing ultrasonic-assisted dispersion of graphene microsheet in liquid carbon source, spraying to furnace chamber, reacting and cooling.
  • 专利号:   CN105000542-A, CN105000542-B
  • 发明人:   CHU J, LI C, SHI H, ZHANG H
  • 专利权人:   CHINESE ACAD SCI CHONGQING GREEN INTEL
  • 国际专利分类:   C01B031/00, C01B032/158, C01B032/182
  • 专利详细信息:   CN105000542-A 28 Oct 2015 C01B-031/00 201610 Pages: 14 Chinese
  • 申请详细信息:   CN105000542-A CN10204558 27 Apr 2015
  • 优先权号:   CN10204558

▎ 摘  要

NOVELTY - Preparation of graphene-carbon nanotube three-dimensional structural composite material involves taking graphene microsheet, performing ultrasonic-assisted dispersion in liquid carbon source to obtain precursor solution, heating pre-heating zone at 300-600 degrees C and main reaction zone at 1000-1300 degrees C of dual-zone vertical chemical vapor deposition device, purging furnace chamber at 400-25000 mL/minute argon for 20 minutes, introducing 400-25000 mL/minute argon and 400-2500 mL/minute hydrogen, spraying with 0.08-0.25 mL/minute precursor solution after 5 minutes and reacting for 30-1000 minutes. USE - Method for preparing graphene-carbon nanotube three-dimensional structural composite material. ADVANTAGE - The method is not limited by shape of substrate surface, has good controllability and reproducibility, and is suitable for mass production. DETAILED DESCRIPTION - Preparation of graphene-carbon nanotube three-dimensional structural composite material comprises taking graphene microsheet, performing ultrasonic-assisted dispersion in liquid carbon source to obtain precursor solution with 0.05-1.0 wt.%% graphene content, heating pre-heating zone at 300-600 degrees C and main reaction zone at 1000-1300 degrees C of dual-zone vertical chemical vapor deposition device, purging furnace chamber at 400-25000 mL/minute argon for 20 minutes, introducing 400-25000 mL/minute argon and 400-2500 mL/minute hydrogen continuously, spraying with 0.08-0.25 mL/minute precursor solution after 5 minutes, reacting for 30-1000 minutes, cooling pre-heating zone and main reaction zone to 200 degrees C, stopping filling of hydrogen and cooling to room temperature.