scispace - formally typeset
Journal ArticleDOI

Interfacial turbulence: Hydrodynamic instability and the marangoni effect

C.V. Sternling, +1 more
- 01 Dec 1959 - 
- Vol. 5, Iss: 4, pp 514-523
TLDR
In this article, a simplified mathematical model has been analyzed in order to detail the mechanism of the "interfacial engine" which supplies the mechanical energy of interfacial turbulence, which is a manifestation of hydrodynamic instability, touched off by ever present, small, random fluctuations about the interface.
Abstract
The origin of interfacial turbulence, spontaneous agitation of the interface between two unequilibrated liquids, has been explained in terms of classical flow, diffusion, and surface processes. The essence of the explanation is the long-known though much neglected Marangoni effect, wherein movement in an interface is caused by longitudinal variations of interfacial tension. It is proposed that interfacial turbulence is a manifestation of hydrodynamic instability, which is touched off by ever present, small, random fluctuations about the interface. A simplified mathematical model has been analyzed in order to detail the mechanism of the “interfacial engine” which supplies the mechanical energy of interfacial turbulence. In its present form the analysis incorporates several drastic simplifications, though ways of removing some of these have been suggested. The groundwork has been laid for the more elaborate analyses that are needed for a decisive test of the theory. The analysis shows how some systems may be stable with solute transfer in one direction yet unstable with transfer in the opposite direction, a striking result. It also suggests that interfacial turbulence is usually promoted by (1) solute transfer out of the phase of higher viscosity, (2) solute transfer out of the phase in which its diffusivity is lower, (3) large differences in kinematic viscosity and solute diffusivity between the two phases, (4) steep concentration gradients near the interface, (5) interfacial tension highly sensitive to solute concentration, (6) low viscosities and diffusivities in both phases, (7) absence of surface-active agents, and (8) interfaces of large extent. That some of these effects have been observed in the laboratory lends credence to the theory.

read more

Citations
More filters
Journal ArticleDOI

Three-dimensional numerical simulation of gas-liquid interfacial mass transfer with Rayleigh convection using hybrid LBM-FDM and its mass transfer coefficient model

TL;DR: In this article, a three-dimensional hybrid Lattice Boltzmann Method-Finite Difference Method (LBM-FDM) was employed to simulate the Rayleigh convection emerging in the CO2-ethanol absorption process.
Journal ArticleDOI

On the Earnshaw and the Van den Tempel–Lucassen Compositional Viscoelastic Theories

TL;DR: A diffusion-controlled solute transfer is considered and the reasons to study the complete convective-diffusive equation to determine the coupling resonant domain between capillary and longitudinal waves in terms of viscoelastic compositional behavior are discussed.
Journal ArticleDOI

Surfactant- and gravity-dependent instability of two-layer channel flows: linear theory covering all wavelengths. Part 1. ‘Long-wave’ regimes

TL;DR: In this article, a linear stability analysis of a two-layer plane Couette flow of two immiscible fluid layers with different densities, viscosities and thicknesses, bounded by two infinite parallel plates moving at a constant relative velocity to each other, with an insoluble surfactant monolayer along the interface and in the presence of gravity is carried out.
Book ChapterDOI

The Development of Fluid Mechanics in Chemical Engineering

TL;DR: A survey of the development of fluid mechanics in chemical engineering from 1888 to the centennial year of 1988 can be found in this paper, however, the events that occurred in 1960 prevent any survey written at this time to go beyond the year of 1960.
Journal ArticleDOI

Solvent molecular descriptors on poly(d, l-lactide-co-glycolide) particle size in emulsification–diffusion process

TL;DR: Choi et al. as discussed by the authors introduced the concept of solvent molecular descriptors for elucidating the effect of solvent on the poly(d, l-lactide-co-glycolide) (PLGA) nanoparticle size in the emulsification-diffusion method.
Related Papers (5)