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Register a new userFoaming and antifoaming in non-aqueous liquids
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Added by
Vineeth Chandran Suja
Publication date
2021
fields
Physics
and research's language is
English
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Investigation into the physics of foaming has traditionally been focused on aqueous systems. Non-aqueous foams, by contrast, are not well understood, but have been the subject of a recent surge in interest motivated by the need to manage foaming across industrial applications. In this review, we provide a comprehensive discussion of the current state-of-the-art methods for characterizing non-aqueous foams, with a critical evaluation of the advantages and limitations of each. Subsequently we present a concise overview of the current understanding of the mechanisms and methods used for stabilizing and destabilizing non-aqueous foams. We conclude the review by discussing open questions to guide future investigations.
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The growth of surface plasmonic microbubbles in binary water/ethanol solutions is experimentally studied. The microbubbles are generated by illuminating a gold nanoparticle array with a continuous wave laser. Plasmonic bubbles exhibit ethanol concentration-dependent behaviors. For low ethanol concentrations (f_e) of < 67.5%, bubbles do not exist at the solid-liquid interface. For high f_e values of >80%, the bubbles behave as in pure ethanol. Only in an intermediate window of 67.5% < f_e < 80% do we find sessile plasmonic bubbles with a highly nontrivial temporal evolution, in which as a function of time three phases can be discerned. (1) In the first phase, the microbubbles grow, while wiggling. (2) As soon as the wiggling stops, the microbubbles enter the second phase in which they suddenly shrink, followed by (3) a steady reentrant growth phase. Our experiments reveal that the sudden shrinkage of the microbubbles in the second regime is caused by a depinning event of the three phase contact line. We systematically vary the ethanol concentration, laser power, and laser spot size to unravel water recondensation as the underlying mechanism of the sudden bubble shrinkage in phase 2.
Thin elastic films can spontaneously attach to liquid interfaces, offering a platform for tailoring their physical, chemical, and optical properties. Current understanding of the elastocapillarity of thin films is based primarily on studies of planar sheets. We show that curved shells can be used to manipulate interfaces in qualitatively different ways. We elucidate a regime where an ultrathin shell with vanishing bending rigidity imposes its own rest shape on a liquid surface, using experiment and theory. Conceptually, the pressure across the interface inflates the shell into its original shape. The setup is amenable to optical applications as the shell is transparent, free of wrinkles, and may be manufactured over a range of curvatures.
In this paper general dynamic equations describing the time evolution of isothermal quasi-incompressible multicomponent liquids are derived in the framework of the classical Ginzburg-Landau theory of first order phase transformations. Based on the fundamental {equations of continuum mechanics}, a general convection-diffusion dynamics is set up first for compressible liquids. The constitutive relations for the diffusion fluxes and the capillary stress are determined in the framework of gradient theories. {Next the general definition of incompressibility is given}, which is taken into account {in the derivation} by using the Lagrange multiplier method. To validate the theory, the dynamic equations are solved numerically for the quaternary quasi-incompressible Cahn-Hilliard system. It is demonstrated that variable density (i) has no effect on equilibrium (in case of a suitably constructed free energy functional), {and (ii) can} influence non-equilibrium pattern formation significantly.
Particles suspended in a Newtonian fluid raise the viscosity and also generally give rise to a shear-rate dependent rheology. In particular, pronounced shear thickening may be observed at large solid volume fractions. In a recent article (R. Seto, R. Mari, J. F. Morris, and M. M. Denn., Phys. Rev. Lett., 111:218301, 2013) we have considered the minimum set of components to reproduce the experimentally observed shear thickening behavior, including Discontinuous Shear Thickening (DST). We have found frictional contact forces to be essential, and were able to reproduce the experimental behavior by a simulation including this physical ingredient along with viscous lubrication. In the present article, we thoroughly investigate the effect of friction and express it in the framework of the jamming transition. The viscosity divergence at the jamming transition has been a well known phenomenon in suspension rheology, as reflected in many empirical laws for the viscosity. Friction can affect this divergence, and in particular the jamming packing fraction is reduced if particles are frictional. Within the physical description proposed here, shear thickening is a direct consequence of this effect: as the shear rate increases, friction is increasingly incorporated as more contacts form, leading to a transition from a mostly frictionless to a mostly frictional rheology. This result is significant because it shifts the emphasis from lubrication hydrodynamics and detailed microscopic interactions to geometry and steric constraints close to the jamming transition.
We analyze the consolidation of freshly deposited cohesive and non-cohesive sediment by means of particle-resolved direct Navier-Stokes simulations based on the Immersed Boundary Method. The computational model is parameterized by material properties and does not involve any arbitrary calibrations. We obtain the stress balance of the fluid-particle mixture from first principles and link it to the classical effective stress concept. The detailed datasets obtained from our simulations allow us to evaluate all terms of the derived stress balance. We compare the settling of cohesive sediment to its non-cohesive counterpart, which corresponds to the settling of the individual primary particles. The simulation results yield a complete parameterization of the Gibson equation, which has been the method of choice to analyze self-weight consolidation.
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