Dynamic viscosities

It was made clear in Chapter II that the surface tension is a definite and accurately measurable property of the interface between two liquid phases. Moreover, its value is very rapidly established in pure substances of ordinary viscosity dynamic methods indicate that a normal surface tension is established within a millisecond and probably sooner [1], In this chapter it is thus appropriate to discuss the thermodynamic basis for surface tension and to develop equations for the surface tension of single- and multiple-component systems. We begin with thermodynamics and structure of single-component interfaces and expand our discussion to solutions in Sections III-4 and III-5. 

Viscosity, dynamic Sometimes called absolute viscosity, the shear stress in a fluid divided by the velocity gradient. 

A study on a commonly used demulsifier, namely, a phenol-formaldehyde resin, elucidated how various parameters such as interfacial tension, interfacial shear viscosity, dynamic interfacial-tension gradient, dilatational elasticity, and demulsifier clustering affect the demulsification effectiveness [1275]. 

Moment of inertia Momentum Angular momentum Viscosity, dynamic... 

Our goal is to develop a property-performance relationship for different types of demulsifiers. The important interfacial properties governing water-in-oil emulsion stability are shear viscosity, dynamic tension and dilational elasticity. We have studied the relative importance of these parameters in demulsification. In this paper, some of the results of our study are presented. In particular, we have found that to be effective, a demulsifier must lower the dynamic interfacial tension gradient and its ability to do so depends on the rate of unclustering of the ethylene oxide groups at the oil-water interface. 

The viscosity (dynamic, 17, or kinematic, v) and density, p (Eq. 47), influence the dissolution rate if the dissolution is transport-controlled, but not if the dissolution is reaction-controlled. In transport-controlled dissolution, increasing 17 or v will decrease D (Eq. 53), will increase h (Eqs. 46 and 49) and will reduce J (Eqs. 51 and 52). These effects are complex. For example, if an additional solute (such as a macromolecule) is added to the dissolution medium to increase 17, it may also change p and D. The ratio of 17/p = v (Eq. 47) and D directly influence h and J in the rotating disc technique, while v directly influences the Reynolds number (and hence J) for transport-controlled dissolution in general [104]. 

Viscosity, dynamic Newton-second per square meter — N-s/m2... 

Rabin Y, Ottinger HCh (1990) Dilute polymer solutions internal viscosity, dynamic scaling, shear thinning, and frequency-dependent viscosity. Europhys Lett 13(5) 423—428 Rallison JM, Hinch EJ (1988) Do we understand the physics in the constitutive equation J Non-Newton Fluid Mech 29(l) 37-55... 

An effect closely related to magnetic viscosity is the dependence of the coercivity on the sweep rate rj = dH/dt Hc is largest for high sweep rates, that is, for fast hysteresis-loop measurements (Fig. 15). Sweep-rate and magnetic-viscosity dynamics have the same origin, but there is a very simple way of deriving a relation for the sweep-rate dependence. Let us assume that the energy barriers exhibit a power-law dependence... 

Poiseuille (pascal- second) PI absolute viscosity, dynamic viscosity 1 PI = lkgm-1 s 1... 

For viscoelastic fluids, the formalism of a viscous fluid and an elastic solid are mixed [31]. The equations for the effective viscosity, dynamic viscosity, and the creep compliance are given in Table 12.4 for a viscous fluid, an elastic solid, and a visco-elastic solid and fluid. For the viscoelastic fluid model the dynamic viscosity, >j (tu), and the elastic contribution, G (ti)), are plotted as a function of (w) in Figure 12.31. With one relaxation time, X, the breaks in the two curves occur at co. 

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