The retraction of a deformed drop back to the spherical, equilibrium shape at rest has been the subject of several studies in the literature with the aim of measuring the interfacial tension between the drop and the continuous phase. In this work, the retraction of a drop deformed under the action o
Interfacial tension coefficient from the retraction of ellipsoidal drops
β Scribed by A. Luciani; M. F. Champagne; L. A. Utracki
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 263 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
A new method for the determination of the interfacial tension coefficient between two immiscible fluids is proposed. The method is particularly useful for the binary polymer blends. The deformed drop retraction method, DDRM, makes it possible to determine the dynamic interfacial tension coefficient, n, from the time evolution of a distorted fluid drop toward its equilibrium form. Analysis of this interfacial tensiondriven process led to a theoretical relation between the shape retraction rate and the system's geometrical and rheological characteristics. Measurements of either low viscosity model systems or high viscosity industrial polymer mixtures led to a good agreement with values obtained from the widely used breaking thread method. DDRM enables to measure n in polymeric blends of commercial interest-the high viscosity systems that would be very difficult to characterize by other techniques. Furthermore, for the first time it is possible to follow the time dependence of the interfacial tension coefficient, thus unambiguously determine the dynamic and equilibrium values of n 12 . For example, in low density polyethylene blends with polystyrene, LDPE/PS, n decreased with the polymer-polymer contact time, t c , from n Γ 6.9 mN/m at t c Γ 12 min, to n Γ 5.2 mN/m at t c Β’ 75 min-the latter may represent the true thermodynamic equilibrium value, n 12 . However, it is not clear whether such a reduction is exclusively due to the thermodynamically driven migration of chain-ends, low molecular weight fractions and additives, or by the thermal degradation as well. The contact time dependence of n explained some of the differences reported for the data obtained using different measurement techniques, viz. pendant drop, capillary breakup, or ellipsoid retraction techniques.
π SIMILAR VOLUMES
Described herein is a two-phase nonempirical method for the determination of surface or interfacial tension of stationary systems that also allows the determination of drop correction factor. The method is based on the theoretical calculation of the drop profile associated with the maximum volume of
methods for the determination of both surface and interfacial A method of profile optimization for determining the surface tension of liquid-fluid systems and may be the only choice and interfacial tension (IFT) of liquid-fluid systems from the for the IFT measurement of viscous liquids such as poly
The reliability of the method described in the preceding paper interfaces, especially for systems containing components of (B. Song and J. Springer, J. Colloid Interface Sci. 183, in press, polymer melts or liquid crystals, in which we are particularly 1996) for the determination of surface and inte