X-ray photoelectron spectroscopic study of carbon fiber surfaces. 23. Interfacial interactions between polyvinyl alcohol and carbon fibers electrochemically oxidized in nitric acid solution
Yq. Wang et al., X-ray photoelectron spectroscopic study of carbon fiber surfaces. 23. Interfacial interactions between polyvinyl alcohol and carbon fibers electrochemically oxidized in nitric acid solution, CHEM MATER, 11(9), 1999, pp. 2573-2583
The paper examines the interaction of a carbon fiber surface, surface-treat
ed by galvanostatic electrochemical oxidation in nitric acid solution, with
poly(vinyl alcohol) (PVA). The surface chemistry of the fiber before and a
fter interaction was examined by core and valence band X-ray photoelectron
spectroscopy (XPS), X-ray diffraction (XRD), and atomic force microscopy (A
FM). Various surface treatment conditions were applied, with the previously
reported hydrogen-bridge oxide structure (HBS) being the predominant speci
es under most conditions, with much smaller amounts of surface hydroxide, c
arbonyl, and carboxyl groups. The amount of surface roughening increased wi
th the level of surface oxidation. The surface of the fibers became serious
ly damaged when the oxidation was conducted for prolonged periods of galvan
ostatic treatment (more than 60 s at 0.5 A). Interfacial chemical interacti
on was observed between the oxidized carbon fiber surface and the PVA, by e
xamination of a film of PVA on the fiber surface that was sufficiently thin
to allow the interface region to be examined. The valence band XPS spectru
m of PVA is predicted by a band structure calculation, complemented by mole
cular orbital calculations based upon the polymer repeat unit. The valence
band spectrum is seen to be an effective fingerprint of the PVA structure.
An interfacial reaction was found to occur between the oxidized fiber and P
VA involving reaction between the hydroxide group in PVA and the HBS oxide
on the fiber surface. The results have a wider relevance to size molecules
containing -OH functionality and adjust the interfacial bonding in composit
es.