Titanium nitride (TiN) coatings were applied to graphite-fiber tows by
dip coating desized (900 degrees C in nitrogen) fibers in hexane solu
tions containing 0.5, 1, or 2 equivalent wt% TiN as the precursor, -[T
i(NMe(2))(x)(mu-NCHMe(2))(4-2x)](n)-. The precursor was characterized
by thermogravimetric analysis (TGA), chemical analysis, and nuclear ma
gnetic resonance, Bulk samples of precursor were heated to selected te
mperatures in argon, Based on microstructural and chemical analyses, t
wo pyrolysis temperatures-900 degrees and 1200 degrees C-were selected
for more-detailed studies predicated on fiber oxidation-resistance be
havior. At 900 degrees C, the bulk material exhibited a powder X-ray d
iffractometry (XRD) pattern consistent with microcrystalline TIN, alth
ough some free carbon remained, XRD analysis of the samples pyrolyzed
to 1200 degrees C indicated a higher degree of crystallinity and some
carbon incorporation in the TiN lattice; e.g., a TiCN solid solution f
orms, as supported by chemical and TGA analyses, Fibers coated with pr
ecursor were heated at a rate of 10 degrees C/min in argon to selected
temperatures, followed by a hold for 1 h, and the resulting coatings
were characterized by scanning electron microscopy, X-ray photoemissio
n spectroscopy, and oxidation resistance at 700 degrees C for 2 h in a
ir, Coated fibers pyrolyzed to 900 degrees and 1200 degrees C mere stu
died in detail, Fibers heat treated at 900 degrees C exhibited better
oxidation resistance than fibers pretreated at 1200 degrees C, as dete
rmined by mass loss, Uncoated fiber tows fully oxidized after 80 min,
The oxidation-resistance studies on fiber tows pretreated at 900 degre
es C and coated with 0.5, 1, and 2 equivalent wt% TiN indicated that t
he sample with a coating of 1 wt%, with thicknesses of 0.1-0.2 mu m, w
as the most stable. The coatings of 0.5 equivalent wt% TiN were irregu
lar, whereas the coatings of 2 equivalent wt% TiN exhibited process-re
lated cracking, leading to poor oxidation resistance.