In this paper, the chemical functionalization of multi-walled carbon nanotubes by a fluorinated trichlorosilane ((tridecafluoro-1,1,2,2-tetrahydrooctyl)trichlorosilane) is investigated. The chlorosilane has been shown to react with carboxylic acid moieties, created by an oxidative process on the nanotube walls, as well as with alcohol groups obtained by a reductive reaction of these previous oxidized nanotubes. The derivatizations were directly confirmed by x-ray photoelectron spectroscopy and thermogravimetry analyses. Little difference in the functionalization was observed for the oxidized or reduced nanotubes. However, the amount of grafted silane seems to be slightly more important when the silanization is carried out with reduced nanotubes.

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An adherent polymer film based on a composite of polyacrylonitrile/multiwall carbon nanotubes (PAN/MWNTs) have been elaborated on a copper substrate. The first layer is an electrografted PAN brush on which of a subsequent layer of PAN/carbon nanotubes composite has been deposited by simple dipping from solution in dimethylformamide (DMF). MWNTs have been previously chemically functionalized with 3-cyanopropyltrichlorosilane to promote de-bundling and homogeneous dispersion of the carbon nanotubes in the composite.

Multi-walled carbon nanotubes functionalized with F3C-(CF2)5-(CH2)2-SiCl3, a molecule bearing a fluorinated terminal group is found to favor the carbon nanotubes dispersion in three perfluoropolyether fluids (Galden SV70, Fomblin Y25 and Fomblin YR1800). The stability of the suspension appears to be related to the perfluoropolyether viscosity. With respect to time, Fomblin YR1800, the more viscous fluid, leads to the most stable solutions, followed in order by Fomblin Y25 and Galden SV70. In general the smallest particles stay in suspensions. Stability extending over more than one year is observed in the case of Fomblin YR1800.