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a fluorocarbon surface layer, which is absent in the case of CF 4 -treated alumina, increases
from C 3 F 8 to c-C 4 F 8 treatments.
In the case of C 3 F 8 fluorinated sample, an inhomogeneity of the layer composition is
noticeable on both F1s and C1s spectra. New components at a high BE are indeed present
(at 688.6 and 293.7 eV), which account for the presence of overfluorinated -CF 3 groups
with respect to CF 2 and CF groups, which constitute most species of the c-C 4 F 8 fluorinated
sample. Moreover, for similar deposition conditions, it is necessary to etch the c-C 4 F 8
fluorinated layer upon 10 nm before observing the presence of aluminium, whereas this
element is observed during the surface analysis of the C 3 F 8 fluorinated sample. It is clear
that the polymerized layer is thicker using the c-C 4 F 8 than the C 3 F 8 medium and leads to
more homogeneous and less crosslinked layers.
19.6 Conclusion
In conclusion, by rf-plasma fluorination the outmost surface of the hydrophilic anodized
aluminium support is hydrophobized, or in other words, the hydrophilic support is con-
verted into a support with hydrophobic properties, as shown in Figure 19.5. This conver-
sion from a hydrophilic to a hydrophobic state is characterized by an increase of the contact
angle measured on the surface, indicating an increase in the hydrophobic-to-hydrophilic
ratio. The most adapted route to drastically switch from a pristine hydrophilic surface of
porous alumina into a hydrophobic layer is clearly the c-C 4 F 8 treatment. It has been shown
θ
γ
SV =
γ
+
γ
L cos
SL
γ
SV : surface energy solid/liquid vapour
γ
L
γ
SL : interfacial energy solid/liquid
γ SV
θ
γ
L : superficial tension of the liquid
γ SL
θ
: contact angle of the liquid on the solid
substrate
Untreated substrate
CF 4 rf plasma
C 4 F 8 rf plasma
Contact angle
θ
20
°
60 °
130 °
hydrophilic
hydrophobic
Figure 19.5 Contact angles of pristine and plasma-treated porous alumina. Reproduced by
permission of Science China, Ser. E-Technolog. Sciences 52, pp. 104-110, Springer (2009)
Copyright Science in China Press
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