Theoretical investigation of the interfacial stability of inviscid fluids in motion, considering surface tension

1972 ◽  
Vol 54 (1) ◽  
pp. 129-141 ◽  
Author(s):  
Jan Berghmans

The present work is an analytical study of the stability of interfaces between fluids in motion, special attention being given to the role of surface tension without consideration of viscous effects. A variational approach based upon the principle of minimum free energy, which was first formulated for stagnant fluids, is applied to fluids in motion. This generalization is possible if viscous and inertia effects are unimportant as far as stability is concerned. One stability problem is studied in detail: a gas jet impinging on a free liquid. The analytical results obtained by this variational technique lie within the range of accuracy (15%) of the experimental results for this gas-jet problem. The method is very general and therefore can be applied to quite a number of interface stability problems.

1983 ◽  
Vol 126 ◽  
pp. 491-506 ◽  
Author(s):  
Arijit Bose ◽  
Harvey J. Palmer

When a liquid evaporates under vacuum, its free surface is potentially unstable to local variations in evaporative flux, surface depressions being produced by the recoil force of the departing vapour and sustained convection in the liquid being driven by the shearing action of the vapour on the distorted liquid surface. For a binary mixture, local variations in evaporative flux may be produced by fluctuations in both surface concentration and temperature. With the aid of linear hydrodynamic-stability theory, this paper examines the extents to which key mass-transfer properties affect the interfacial stability of the system. The mass-transfer aspects that distinguish this problem from its heat-transfer analogue centre on the dependence of relative volatility on temperature and composition as well as the importance of the bulk-flow term in Fick's law. Results indicate that the stability criteria for interfacial convection are extremely sensitive to the difference in volatility between the two components, that the destabilizing effects of surface concentration and temperature on evaporative flux are additive in determining stability limits, and that for certain operating pressures spontaneous convection can only be induced by adverse concentration gradients. Attention is limited to low-surface-tension mixtures for which there are no concentration effects on surface tension (Marangoni instability).


1999 ◽  
Vol 382 ◽  
pp. 331-349 ◽  
Author(s):  
S. HANSEN ◽  
G. W. M. PETERS ◽  
H. E. H. MEIJER

The effect of surfactant on the breakup of a viscous filament, initially at rest, surrounded by another viscous fluid is studied using linear stability analysis. The role of the surfactant is characterized by the elasticity number – a high elasticity number implies that surfactant is important. As expected, the surfactant slows the growth rate of disturbances. The influence of surfactant on the dominant wavenumber is less trivial. In the Stokes regime, the dominant wavenumber for most viscosity ratios increases with the elasticity number; for filament to matrix viscosity ratios ranging from about 0.03 to 0.4, the dominant wavenumber decreases when the elasticity number increases. Interestingly, a surfactant does not affect the stability of a filament when the surface tension (or Reynolds) number is very large.


2017 ◽  
Vol 38 (1) ◽  
pp. 5-18 ◽  
Author(s):  
Lusi Ernawati ◽  
Ratna Balgis ◽  
Takashi Ogi ◽  
Kikuo Okuyama ◽  
Tomonori Takada

Abstract A modified emulsion polymerisation synthesis route for preparing highly dispersed cationic polystyrene (PS) nanoparticles is reported. The combined use of 2,2′-azobis[2-(2-imidazolin- 2-yl)propane] di-hydrochloride (VA-044) as the initiator and acetone/water as the solvent medium afforded successful synthesis of cationic PS particles as small as 31 nm in diameter. A formation mechanism for the preparation of PS nanoparticles was proposed, whereby the occurrence of rapid acetone diffusion caused spontaneous rupture of emulsion droplets into smaller droplets. Additionally, acetone helped to reduce the surface tension and increase the solubility of styrene, thus inhibiting aggregation and coagulation among the particles. In contrast, VA-044 initiator could effectively regulate the stability of the PS nanoparticles including both the surface charge and size. Other reaction parameters i.e. VA-044 concentration and reaction time were examined to establish the optimum polymerisation conditions.


2015 ◽  
Vol 777 ◽  
pp. 1-26 ◽  
Author(s):  
Vivek Narsimhan ◽  
Andrew P. Spann ◽  
Eric S. G. Shaqfeh

Tubular vesicles in extensional flow can undergo ‘pearling’, i.e. the formation of beads in their central neck reminiscent of the Rayleigh–Plateau instability for droplets. In this paper, we perform boundary integral simulations to determine the conditions for the onset of this instability. Our simulations agree well with experiments, and we explore additional topics such as the role of the vesicle’s initial shape on the number of pearls formed. We also compare our simulations to simple physical models of pearling that have been presented in the literature, where the vesicle is approximated as an infinitely long cylinder with a constant surface tension and bending modulus. We present a complete linear stability analysis of this idealized problem, including the effects of non-axisymmetric deformations as well as surface viscosity. We demonstrate that, while such models capture the essential physics of pearling, they cannot capture the stability of these transitions accurately, since finite length effects and non-uniform surface tension effects are important. We close our paper with a brief discussion of vesicles in compressional flows. Unlike quasi-spherical vesicles, we find that tubular vesicles can transition to a wide variety of permanent, buckled states under compression. The idealized problem mentioned above gives the essential physics behind these instabilities, which to our knowledge has not been examined heretofore.


1952 ◽  
Vol 5 (4) ◽  
pp. 697 ◽  
Author(s):  
WE Ewers ◽  
KL Sutherland

A new theory of foam stability is proposed which demonstrates that the transport of substrate. accompanying a movement of the surface of the bubble film, is a dominant factor in the stability of foams and in the action of foam breakers. The surface moves from a region of low surface tension (high surface pressure) to a region of high surface tension. The surface tension gradients arise from disturbances which may be caused by mechanical or thermal shocks, or by the addition to the surface of particles, droplets, or vapour of a surface-active material. When the surface tension is highest at the centre of disturbance the film mill be stable ; when the surface tension is lowest at this point the surface film and hence the substrate will be moved away from this point and the film will rupture.


TAPPI Journal ◽  
2009 ◽  
Vol 8 (1) ◽  
pp. 20-26 ◽  
Author(s):  
PEEYUSH TRIPATHI ◽  
MARGARET JOYCE ◽  
PAUL D. FLEMING ◽  
MASAHIRO SUGIHARA

Using an experimental design approach, researchers altered process parameters and material prop-erties to stabilize the curtain of a pilot curtain coater at high speeds. Part I of this paper identifies the four significant variables that influence curtain stability. The boundary layer air removal system was critical to the stability of the curtain and base sheet roughness was found to be very important. A shear thinning coating rheology and higher curtain heights improved the curtain stability at high speeds. The sizing of the base sheet affected coverage and cur-tain stability because of its effect on base sheet wettability. The role of surfactant was inconclusive. Part II of this paper will report on further optimization of curtain stability with these four variables using a D-optimal partial-facto-rial design.


2020 ◽  
Author(s):  
Ryan Weber ◽  
Martin McCullagh

<p>pH-switchable, self-assembling materials are of interest in biological imaging and sensing applications. Here we propose that combining the pH-switchability of RXDX (X=Ala, Val, Leu, Ile, Phe) peptides and the optical properties of coumarin creates an ideal candidate for these materials. This suggestion is tested with a thorough set of all-atom molecular dynamics simulations. We first investigate the dependence of pH-switchabiliy on the identity of the hydrophobic residue, X, in the bare (RXDX)<sub>4</sub> systems. Increasing the hydrophobicity stabilizes the fiber which, in turn, reduces the pH-switchabilty of the system. This behavior is found to be somewhat transferable to systems in which a single hydrophobic residue is replaced with a coumarin containing amino acid. In this case, conjugates with X=Ala are found to be unstable and both pHs while conjugates with X=Val, Leu, Ile and Phe are found to form stable β-sheets at least at neutral pH. The (RFDF)<sub>4</sub>-coumarin conjugate is found to have the largest relative entropy value of 0.884 +/- 0.001 between neutral and acidic coumarin ordering distributions. Thus, we posit that coumarin-(RFDF)<sub>4</sub> containing peptide sequences are ideal candidates for pH-sensing bioelectronic materials.</p>


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