Measurement of interfacial tension in simple two-phase ternary systems along an isothermal linear path to the critical point

1984 ◽  
Vol 88 (19) ◽  
pp. 4397-4401 ◽  
Author(s):  
Dorothy Wielebinski ◽  
Gerhard H. Findenegg
Keyword(s):  
Interfacial Tension ◽  
Critical Point ◽  
Ternary Systems ◽  
Two Phase ◽  
Linear Path

Phase Inversion in Two-Phase Liquid Systems

1992 ◽  
Vol 57 (7) ◽  
pp. 1419-1423
Author(s):  
Jindřich Weiss
Keyword(s):  
Interfacial Tension ◽  
Phase Inversion ◽  
Continuous Phase ◽  
Considerable Effect ◽  
Weak Dependence ◽  
Dispersed Phase ◽  
Two Phase ◽  
Liquid Systems ◽  
Phase Liquid

New data on critical holdups of dispersed phase were measured at which the phase inversion took place. The systems studied differed in the ratio of phase viscosities and interfacial tension. A weak dependence was found of critical holdups on the impeller revolutions and on the material contactor; on the contrary, a considerable effect of viscosity was found out as far as the viscosity of continuous phase exceeded that of dispersed phase.

scholarly journals Effects of Polydispersity on the Phase Behavior of Additive Hard Spheres in Solution

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1543
Author(s):  
Luka Sturtewagen ◽  
Erik van der Linden
Keyword(s):  
Phase Behavior ◽  
Critical Point ◽  
Volume Fraction ◽  
Hard Spheres ◽  
Second Virial Coefficient ◽  
Two Phase ◽  
Different Types ◽  
Asymmetric Partitioning ◽  
Average Size ◽  
Liquid Liquid Phase Separation

The ability to separate enzymes, nucleic acids, cells, and viruses is an important asset in life sciences. This can be realised by using their spontaneous asymmetric partitioning over two macromolecular aqueous phases in equilibrium with one another. Such phases can already form while mixing two different types of macromolecules in water. We investigate the effect of polydispersity of the macromolecules on the two-phase formation. We study theoretically the phase behavior of a model polydisperse system: an asymmetric binary mixture of hard spheres, of which the smaller component is monodisperse and the larger component is polydisperse. The interactions are modelled in terms of the second virial coefficient and are assumed to be additive hard sphere interactions. The polydisperse component is subdivided into sub-components and has an average size ten times the size of the monodisperse component. We calculate the theoretical liquid–liquid phase separation boundary (the binodal), the critical point, and the spinodal. We vary the distribution of the polydisperse component in terms of skewness, modality, polydispersity, and number of sub-components. We compare the phase behavior of the polydisperse mixtures with their concomittant monodisperse mixtures. We find that the largest species in the larger (polydisperse) component causes the largest shift in the position of the phase boundary, critical point, and spinodal compared to the binary monodisperse binary mixtures. The polydisperse component also shows fractionation. The smaller species of the polydisperse component favor the phase enriched in the smaller component. This phase also has a higher-volume fraction compared to the monodisperse mixture.

Behaviour of biomolecules in water-organic solvent-inorganic salt two-phase ternary systems

1981 ◽  
Vol 216 ◽  
pp. 346-349 ◽  
Author(s):  
Vladimir Yur'evich Ryashentsev ◽  
Mikhail Arkad'evich Voskoboinikov ◽  
Efim Semenovich Vainerman ◽  
Sergei Vasil'evich Rogozhin
Keyword(s):  
Organic Solvent ◽  
Inorganic Salt ◽  
Ternary Systems ◽  
Two Phase

scholarly journals Two-phase equilibrium in binary and ternary systems II. The system methane-ethylene III. The system methane-ethane-ethylene

1940 ◽  
Vol 176 (964) ◽  
pp. 140-152 ◽  
Keyword(s):  
Phase Equilibrium ◽  
Ternary System ◽  
Binary Systems ◽  
Ternary Systems ◽  
Two Phase ◽  
Composition Diagram ◽  
Wide Range ◽  
Binary And Ternary Systems

The liquid-vapour equilibrium of the system methane-ethylene has been determined at 0, -42 , -78, -88 and -104° C over a wide range of pressures and the results are shown on a pressure-composition-temperature diagram and by a series of pressure-composition curves. The liquid-vapour equilibrium of the ternary system methane-ethane-ethylene has been determined at -104, -78 and 0° C. Values for the two binary systems methane-ethane and methane-ethylene and for the ternary system methane-ethane-ethylene are shown on a composite pressure-composition diagram.

scholarly journals The multivariate calculation of material balances of flowsheets for separating ternary mixtures of different physical-chemical nature

2016 ◽  
Vol 11 (3) ◽  
pp. 47-57 ◽  
Author(s):  
A. V. Frolkova ◽  
M. A. Ablizin ◽  
M. A. Mayevskiy ◽  
A. K. Frolkova
Keyword(s):  
Phase Diagrams ◽  
Chemical Nature ◽  
Material Balance ◽  
Ternary Systems ◽  
Butyl Alcohol ◽  
Ternary Mixtures ◽  
Two Phase ◽  
Physical Chemical ◽  
Alcohol Water

An approach to the determination of free variables required for calculating the material balance of the flowsheet of ternary mixtures separation is presented. Phase diagrams of the considered ternary systems are characterized by the presence of a two-phase splitting area and by the presence of different amounts of azeotropes (classes 3.1.0, 3.1.1, 3.2.1 and 3.3.1). For all the systems flowsheets containing three rectification columns and a florentine vessel for separation were suggested. The multivariance of the solution of the balance problem was shown. The approach was illustrated by the example of real ternary systems characterized by different phase diagrams (methanol - chloroform - water, butyl alcohol - water - toluene, nitromethane - hexane - water). The parameters of the rectification columns were presented.

Interfacial Tension Effect on Cell Partition in Aqueous Two-Phase Systems

2015 ◽  
Vol 7 (38) ◽  
pp. 21305-21314 ◽  
Author(s):  
Ehsan Atefi ◽  
Ramila Joshi ◽  
Jay Adin Mann ◽  
Hossein Tavana
Keyword(s):  
Interfacial Tension ◽  
Two Phase ◽  
Aqueous Two Phase Systems ◽  
Phase Systems ◽  
Cell Partition
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