Abstract
ABSTRACTA nanocomposite carbon composed with single wall carbon nanotube (SWNT) and nanoporous carbon (NPC) was prepared by grafting a carbonizable polymer, poly(furfuryl alcohol) (PFA) to a SWNT. The SWNT was first functionalized with arylsulfonic acid groups on sidewall (SA-SWNT) and then converted to PFA-functionalized SWNT (PFA-SWNT) by in situ polymerization of furfuryl alcohol (FA). SWNT/NPC nanocomposite carbon was generated by heating PFA-SWNT in argon at 600°C. A continuous phase was formed between SWNT and NPC. The deformation of the nanocomposite carbon at high temperature was studied by heating it at temperatures from 1200 to 2000 °C and characterized with HRTEM and Raman spectra. It was found that NPC tended to graphitize along the axis of neighboring nanotubes at temperature higher than 1400°C. Complete graphitization of NPC and SWNTs was obtained at 2000 °C, when the NPC transformed to graphitic nanoribbon (GNR) and SWNT or DWNT collapsed within the confines of the GNR. Nanocomposite polymer and carbon fibers were prepared by dispersing small amount of SA-SWNT in FA, followed with polymerization, thermosetting and pyrolysis. The composite polymer fibers' Young's modulus was lower than the pure PFA fibers prepared at the same conditions. However, after heated in argon at 300 °C, 400 °C, 500 °C and 600 °C respectively, the Young's modulus of the nanocomposite carbon fibers turned to be higher than the fibers derived from pure PFA and the enhancement by SWNT increase with increasing temperature. For the nanocomposite carbon fibers treated at 600 °C, the fibers had ∼20% increase of Young's modulus over the fibers from pure PFA with only 0.1wt% of SA-SWNT in FA.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.