A rheological phase diagram of aqueous solutions based on Pluronic L64 was experimentally evaluated and validated via DPD simulations.
The rising of spherical bodies in structured fluids with yield stress is studied. The system is a suspension of hydrogenated castor oil colloidal fibers in a surfactant micellar solution. The fiber network confers to the fluid a viscoelastic behavior, with a well-defined yield stress, which increases with increasing fiber concentration. Various fluids with different fiber contents are prepared and rheologically characterized. A home-made time-lapse photography setup is used to monitor the time evolution position of the spherical particles, and the rising motion of both hollow spheres and air bubbles, in the diameter range 65–550 μm, is measured. The experiments last as long as several weeks, corresponding to significantly low measured velocities. Finite element simulations are performed to support the experimental data, assuming both interfacial slip and no slip conditions. The fluid dynamic phenomenon is studied and discussed in terms of dimensionless numbers, such as yield ratio, Bingham number, and Stokes drag coefficient. The results are novel for the system (suspending medium and hollow spheres) and for the covered Bingham number range, which is extended over three orders of magnitude in comparison with already available literature results. Our values provide quantitative data of the mechanical properties (i.e., yield stress value) at very low shear rates, in a prohibitive range for a traditional rheometer, and agree with the macroscopic rheological response. Moreover, the important role of the power law index n of the Herschel-Bulkley model, used to fit the data, has been highlighted. Our results, based on a Bingham-like fluid, are compared with the experimental data already available with Carbopol, treated as a Herschel Bulkley fluid with n = 0.5. The results could have important implications in the fabric and personal care detergency, a technological area where many fluids have composition and show rheological properties similar to those considered in the current work.
We investigate the rheological properties of a simplified version of a liquid detergent composed of an aqueous solution of the Linear Alkylbenzene Sulphonate (LAS) surfactant, in which a small amount of fibers made of Hydrogenated Castor Oil (HCO) is dispersed. At the concentration typically used in detergents, LAS is in a worm-like micellar phase exhibiting a Maxwellian behavior. The presence of HCO fibers provides elastic properties, such that the system behaves as a simple Zener body, mechanically characterized by a parallel connection of a spring and a Maxwell element. Despite this apparent independence of the contributions of the fibers and the surfactant medium to the mechanical characteristics of the system, we find that the low frequency modulus increases with increasing LAS concentration. This indicates that LAS induces attractive interactions among the HCO fibers, resulting in the formation of a stress-bearing structure that withstands shear at HCO concentrations, where the HCO fibers in the absence of attractive interactions would not sufficiently overlap to provide stress-bearing properties to the system.
We analyzed bubble rupture and hole opening dynamics in a non-Newtonian fluid by investigating the retraction process of thin films after inflation at different blowing rates. The experiments were modeled through a dimensional analysis, with the aim of establishing a general approach on the bubble rupture dynamics and discerning the role of viscous, elastic, surface, and inertial forces on the opening velocity, according to the nature of the specific fluid. A new mathematical model, which includes all possible contributions to the hole opening dynamics, was proposed, to the best of our knowledge for the first time. The experimental evidence on the opening velocity as a function of the inflation rate was found to be in good agreement with the prediction of the model. The sensitivity of our modeling was tested by comparing our results with the existing models of retracting velocity.
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