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Corresponding states, physical properties

Schemes for classifying surfactants are based upon physical properties or upon functionality. Charge is tire most prevalent physical property used in classifying surfactants. Surfactants are charged or uncharged, ionic or nonionic. Charged surfactants are furtlier classified as to whetlier tire amphipatliic portion is anionic, cationic or zwitterionic. Anotlier physical classification scheme is based upon overall size and molecular weight. Copolymeric nonionic surfactants may reach sizes corresponding to 10 000-20 000 Daltons. Physical state is anotlier important physical property, as surfactants may be obtained as crystalline solids, amoriDhous pastes or liquids under standard conditions. The number of tailgroups in a surfactant has recently become an important parameter. Many surfactants have eitlier one or two hydrocarbon tailgroups, and recent advances in surfactant science include even more complex assemblies [7, 8 and 9]. Schemes for classifying surfactants are based upon physical properties or upon functionality. Charge is tire most prevalent physical property used in classifying surfactants. Surfactants are charged or uncharged, ionic or nonionic. Charged surfactants are furtlier classified as to whetlier tire amphipatliic portion is anionic, cationic or zwitterionic. Anotlier physical classification scheme is based upon overall size and molecular weight. Copolymeric nonionic surfactants may reach sizes corresponding to 10 000-20 000 Daltons. Physical state is anotlier important physical property, as surfactants may be obtained as crystalline solids, amoriDhous pastes or liquids under standard conditions. The number of tailgroups in a surfactant has recently become an important parameter. Many surfactants have eitlier one or two hydrocarbon tailgroups, and recent advances in surfactant science include even more complex assemblies [7, 8 and 9].
The physical properties of argon, krypton, and xenon are frequendy selected as standard substances to which the properties of other substances are compared. Examples are the dipole moments, nonspherical shapes, quantum mechanical effects, etc. The principle of corresponding states asserts that the reduced properties of all substances are similar. The reduced properties are dimensionless ratios such as the ratio of a material s temperature to its critical... [Pg.6]

Generalized Correla.tions. A simple and rehable method for the prediction of vapor—Hquid behavior has been sought for many years to avoid experimentally measuring the thermodynamic and physical properties of every substance involved in a process. Whereas the complexity of fluids makes universal behavior prediction an elusive task, methods based on the theory of corresponding states have proven extremely useful and accurate while still retaining computational simplicity. Methods derived from corresponding states theory are commonly used in process and equipment design. [Pg.239]

Obtain the Taylor-Prandtl modification of the Reynolds Analogy between momentum transfer and mass transfer (equimolecular counterdiffusion) for the turbulent flow of a fluid over a surface. Write down the corresponding analogy for heat transfer. State clearly the assumptions which are made. For turbulent flow over a surface, the film heat transfer coefficient for the fluid is found to be 4 kW/m2 K. What would the corresponding value of the mass transfer coefficient be. given the following physical properties ... [Pg.865]

Abstract In corresponding states (CS) theory the PVT properties of fluids are expressed in terms of the critical constants and one or more additional parameters. In this chapter the use of CS theory to correlate isotope effects on the physical properties of fluids is explored. [Pg.413]

Commonly encountered cubic equations of state are classical, and, of themselves, cannot rationalize IE s on PVT properties. Even so, the physical properties of iso-topomers are nearly the same, and it is likely in some sense they are in corresponding state when their reduced thermodynamic variables are the same that is the point explored in this chapter. By assuming that isotopomers are described by EOS s of identical form, the calculation of PVT isotope effects (i.e. the contribution of quantization) is reduced to a knowledge of critical property IE s (or for an extended EOS, to critical property IE s plus the acentric factor IE). One finds molar density IE s to be well described in terms of the critical property IE s alone (even though proper description of the parent molar densities themselves is impossible without the use of the acentric factor or equivalent), but rationalization of VPIE s requires the introduction of an IE on the acentric factor. [Pg.414]

Also, micelles are equilibrium systems. What does this mean It means that the final state, for example the average micellar size and all corresponding physical properties, are reached regardless of the pathway used to form them. The final state is thus independent of the mixing order of the components, and does not depend on the previous history of the sample. It is possible to make larger or smaller micelles by changing the environmental parameters (e.g., salt concentration) - and if two... [Pg.190]

Problem 16.3 Account for the following physical properties of carboxylic acids, (a) Only RCOOH s with five or fewer C s are soluble in water, but many with six or more C s dissolve in alcohols. (f>) Acetic acid in the vapor state has a molecular weight of 120 not 60. (c) Their boiling and melting points are higher than those of corresponding alcohols. M... [Pg.345]


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See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.313 ]

See also in sourсe #XX -- [ Pg.433 ]




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Corresponding states

Physical state

State property

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