The adsorption of asphal
tenes and other natural surfactants at the water/toluene interfacehas been studied here, using both the ring and pendant drop method to measure the interfacial
tension (
). The dependence of
on the logarithm of the sample concentration (ln
C) (representedas the
(ln
C) isotherm) leads to a stepwise isotherm similar to that corresponding to theadsorption of asphal
tenes at the toluene/silica interface. As is the case for the toluene/silicainterface, the stepwise
(ln
C) isotherm seems to be the result of adsorption at the toluene/waterinterface of molecules, as well as aggregates formed in solution. Once adsorbed, these aggregatesflocculate at the interface, leading to the well-known three-dimensional asphal
tene films. Inagreement with previous evidence from thermal lens experiments, the onset of asphal
teneaggregation was observed near a sample concentration of
C = 60 mg/L. Although the presence ofaliphatic (acid fraction soluble in heptane, AFSH) and other types of acidic components in theasphal
tene mixture increases the interfacial activity of asphal
tenes, the removal of thesecomponents does not prevent the adsorption and leads to a film with an interfacial
tension of
= 26 mJ/m
2. This shows that such asphal
tene films are less hydrophobic than what might beexpected. As suggested by the detailed description of the results given in this paper, the asphal
teneinterfacial film is a mixed film formed by both AFSH and asphal
tenes, where the role of AFSHis to reduce the value of
and the role of asphal
tenes is to reduce hydrophobic effects by forminga film that effectively separates oil from water.