A spectrum of low-frequency (20‒30 Hz) amplitude fluctuations of the ultrasonic (10 MHz) signal specularly scattered from water surfaces covered with monomolecular and thicker crude oil origin films of well-defined, oceanographically relevant viscoelastic properties was examined in laboratory and at-sea conditions. The relationship between the Surface water wave (30 Hz) damping coefficient and the oil layer thickness was established, and compared to the one predicted by the classical Stokes theory. The depression of the spectral energy density of wind-driven waves by surface films was inferred from the ratio of acoustic signal fluctuations spectra with/without films, and compared to that resulting from the Marangoni damping theory applicable to monolayers of particular surface viscoelasticity. The agreement between the theory and experimental data was satisfactory. As shown in at-sea experiments performed with a free-floating, buoy-like acoustic system, and an artificial oil slick spread over the Baltic Sea surface, the film’s rheological Surface properties can be recovered from acoustic surface probing, as well as oil spill edge detection. Simultaneous statistical analyses of the scattered signal amplitude distribution parameters turned out to be unequivocally related to the oil substance fraction weight, oil layer thickness, and the form of oil contamination.
It has been shown in the present paper that exploitation of the experimental potential of a photoacoustic technique can provide information on a type of intermolecular interactions in aqueous mixtures containing organic liquids, when the basic parameters of these mixtures, such as density, ρ, specific heat, cp, or thermal conductivity, λ, are unknown. Earlier investigations of concentration dependence of effusivity in different aqueous solutions of organic liquids demonstrated that the photoacoustics method is a sensitive tool to identify hydrophobic properties of such liquids. In our experiment this suggestion was exploited for a solution of methanol which is known to display much weaker hydrophobicity than other alcohols. It was confirmed that the location of extreme deviations from linearity for the thermal effusivity, Δe, agrees well with that of characteristic points for the isentropic compressibility coefficient, κS, and the excess molar volume, VEm , as a function of the concentration.
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