Abstract

Reaction of herring-bone graphitic carbon nanofibers (GCNFs) containing surface-bound acid chloride functional groups with 3-aminopropyl triethoxysilane (APTES) leads to amide condensation and formation of carbon nanofibers surface-derivatized with pendant Si—OEt and Si—OH functional groups, GCNF-[C(O)NH(CH2)3Si(OEt)(OH)2] x . Addition of these GCNFs containing covalently bound 3-amidopropylsilyl linker molecules to silica sol-gel formulations gives GCNF/silica xerogels as dry black powders. Covalent binding of the linker molecule across the GCNF/ceramic interface is indicated by intermediate formation of especially stable GCNF/silica sol dispersions and the isolation of uniformly black GCNF/silica xerogel powders. SEM micrographs reveal excellent wetting of the carbon nanofiber surface by the silica xerogel matrix, and the presence of amido-carbonyl groups is confirmed from infrared spectral data. TGA plots show mass losses consistent with dehydration of the gel matrix and thermal decomposition of linker molecules at elevated temperature.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call