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A technique that is an extension of an earlier approach for marine sediments is presented for determining the acoustic attenuation and backscattering coefficients of suspensions of particles of arbitrary materials of general engineering interest. It is necessary to know these coefficients (published values of which exist for quartz sand only) in order to implement an ultrasonic dual-frequency inversion method, in which the backscattered signals received by transducers operating at two frequencies in the megahertz range are used to determine the concentration profile in suspensions of solid particles in a carrier fluid. To demonstrate the application of this dual-frequency method to engineering flows, particle concentration profiles are calculated in turbulent, horizontal pipe flow. The observed trends in the measured attenuation and backscatter coefficients, which are compared to estimates based on the available quartz sand data, and the resulting concentration profiles, demonstrate that this method has potential for measuring the settling and segregation behavior of real suspensions and slurries in a range of applications, such as the nuclear and minerals processing industries, and is able to distinguish between homogeneous, heterogeneous, and bed-forming flow regimes.

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The influence of particle adsorption on liquid/liquid interfacial tension is not well understood, and much previous research has suggested conflicting behaviors. In this paper we investigate the surface activity and adsorption kinetics of charge stabilized and pH-responsive polymer stabilized colloids at oil/water interfaces using two tensiometry techniques: (i) pendant drop and (ii) microtensiometer. We found, using both techniques, that charge stabilized particles had little or no influence on the (dynamic) interfacial tension, although dense silica particles affected the "apparent" measured tension in the pendent drop, due to gravity driven elongation of the droplet profile. Nevertheless, this apparent change additionally allowed the study of adsorption kinetics, which was related qualitatively between particle systems by estimated diffusion coefficients. Significant and real interfacial tension responses were measured using ∼53 nm core-shell latex particles with a pH-responsive polymer stabilizer of poly(methyl methacrylate)-b-poly(2-(dimethylamino)ethyl methacrylate) (pMMA-b-pDMAEMA) diblock copolymer. At pH 2, where the polymer is strongly charged, behavior was similar to that of the bare charge-stabilized particles, showing little change in the interfacial tension. At pH 10, where the polymer is discharged and poorly soluble in water, a significant decrease in the measured interfacial tension commensurate with strong adsorption at the oil-water interface was seen, which was similar in magnitude to the surface activity of the free polymer. These results were both confirmed through droplet profile and microtensiometry experiments. Dilational elasticity measurements were also performed by oscillation of the droplet; again, changes in interfacial tension with droplet oscillation were only seen with the responsive particles at pH 10. Frequency sweeps were performed to ascertain the dilational elasticity modulus, with measured values being significantly higher than previously reported for nanoparticle and surfactant systems, and similar in magnitude to protein stabilized droplets.