Factor friction

With turbulent flows we normally have to resort to the correlation of experimental data. Friction between fluids and surfaces are normally characterised by friction factors. Different flow situations give rise to different friction factors. 

1 Fanning Friction Factor. The Fanning friction factor for pipe flow, Cf, is defined by  

Recall that, using dimensional analysis for pipe flow, we saw (see Section 3.2)  

2 Other Friction Factors. Beware, there are other definitions of friction factor. 

The form of the Cf Re relationship depends upon the flow regime. 

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Reference 115 gives the diffusion coefficient of DTAB (dodecyltrimethylammo-nium bromide) as 1.07 x 10" cm /sec. Estimate the micelle radius (use the Einstein equation relating diffusion coefficient and friction factor and the Stokes equation for the friction factor of a sphere) and compare with the value given in the reference. Estimate also the number of monomer units in the micelle. Assume 25°C. 

There are a number of important concepts which emerge in our discussion of viscosity. Most of these will come up again in subsequent chapters as we discuss other mechanical states of polymers. The important concepts include free volume, relaxation time, spectrum of relaxation times, entanglement, the friction factor, and reptation. Special attention should be paid to these terms as they are introduced. 

In Chap. 9 we shall discuss in considerable detail a parameter called the molecular friction factor f. For velocities that are not too great, the friction factor expresses the proportionality between the frictional force a particle experiences and its velocity ... 

This is precisely the kind of thing we are looking for. Before proceeding, let us summarize some important properties of the friction factor ... 

For spherical particles of radius R moving through a medium of viscosity 17, Stokes showed that the friction factor is given by... 

The segmental friction factor introduced in the derivation of the Debye viscosity equation is an important quantity. It will continue to play a role in the discussion of entanglement effects in the theory of viscoelasticity in the next chapter, and again in Chap. 9 in connection with solution viscosity. Now that we have an idea of the magnitude of this parameter, let us examine the range of values it takes on. 

To the extent that the segmental friction factor f is independent of M, then Eq. (2.56) predicts a first-power dependence of viscosity on the molecular weight of the polymer in agreement with experiment. A more detailed analysis of f shows that segmental motion is easier in the neighborhood of a chain end because the wagging chain end tends to open up the structure of the melt and... 

Equation (2.56) not only enables us to understand the basis for the first-power dependence of rj on M, but also presents us with a new and important theoretical parameter, the segmental friction factor. We shall see in the next chapter that it is a quantity which can also be extracted from measurements of the viscoelasticity of polymers. 

Table 2.3 Segmental Friction Factors Ranked in Order of Decreasing Values for Polymers Compared 100°C Above Their Respective Glass Transition Temperatures...

Since the tube friction factor measures the force needed to impart a unit velocity to the chain along the tube direction, we can think of applying this force, one segment at a time, to the diffusing chain. Since the friction factor per segment is f, Eq. (2.65) becomes... 

Whether the beads representing subchains are imbedded in an array of small molecules or one of other polymer chains changes the friction factor in Eq. (2.47), but otherwise makes no difference in the model. This excludes chain entanglement effects and limits applicability to M < M., the threshold molecular weight for entanglements. 

Although we still need to explain the use of this theory, Eq. (3.98) shows that segmental friction factors are accessible through viscoelastic studies. This fact was anticipated in the list of f values given in Table 2.3. 

Another parameter that plays an important role in unifying viscosity, diffusion, and sedimentation is the friction factor. This proportionality factor between velocity and the force of frictional resistance was introduced in Chap. 2, and its role in interrelating the topics of this chapter is reflected in the title of the chapter. 

The spherical geometry assumed in the Stokes and Einstein derivations gives the highly symmetrical boundary conditions favored by theoreticians. For ellipsoids of revolution having an axial ratio a/b, friction factors have been derived by F. Perrin, and the coefficient of the first-order term in Eq. (9.9) has been derived by Simha. In both cases the calculated quantities increase as the axial ratio increases above unity. For spheres, a/b = 1. 

We shall see in Sec. 9.10 that sedimentation and diffusion data yield experimental friction factors which may also be described-by the ratio of the experimental f to fQ, the friction factor of a sphere of the same mass-as contours in solvation-ellipticity plots. The two different kinds of contours differ in detailed shape, as illustrated in Fig. 9.4b, so the location at which they cross provides the desired characterization. For the hypothetical system shown in Fig. 9.4b, the axial ratio is about 2.5 and the protein is hydrated to the extent of about 1.0 g water (g polymer)". ... 

An alternative point of view assumes that each repeat unit of the polymer chain offers hydrodynamic resistance to the flow such that f-the friction factor per repeat unit-is applicable to each of the n units. This situation is called the free-draining coil. The free-draining coil is the model upon which the Debye viscosity equation is based in Chap. 2. Accordingly, we use Eq. (2.53) to give the contribution of a single polymer chain to the rate of energy dissipation ... 

Rather than discuss the penetration of the flow streamlines into the molecular domain of a polymer in terms of viscosity, we shall do this for the overall friction factor of the molecule instead. The latter is a similar but somewhat simpler situation to examine. For a free-draining polymer molecule, the net friction factor f is related to the segmental friction factor by... 

This result shows that the friction factor of the coil equals nf when KX < 1, and equals a numerical factor times i o(rg when KX > 1. The first of... 

This concludes our discussion of the viscosity of polymer solutions per se, although various aspects of the viscous resistance to particle motion continue to appear in the remainder of the chapter. We began this chapter by discussing the intrinsic viscosity and the friction factor for rigid spheres. Now that we have developed the intrinsic viscosity well beyond that first introduction, we shall do the same (more or less) for the friction factor. We turn to this in the next section, considering the relationship between the friction factor and diffusion. 

Before pursuing the diffusion process any further, let us examine the diffusion coefficient itself in greater detail. Specifically, we seek a relationship between D and the friction factor of the solute. In general, an increment of energy is associated with a force and an increment of distance. In the present context the driving force behind diffusion (subscript diff) is associated with an increment in the chemical potential of the solute and an increment in distance dx ... 

We shall see in Sec. 9.9 that D is a measurable quantity hence Eq. (9.79) provides a method for the determination of an experimental friction factor as well. Note that no assumptions are made regarding the shape of the solute particles in deriving Eq. (9.79), and the assumption of ideality can be satisfied by extrapolating experimental results to c = 0, where 7=1. 

In contrast with Eq. (9.79), prior theoretical discussions of the friction factor for various particles were based on some assumed structure or geometry for the molecule ... 

Random coils. Equation (9.53) gives the Kirkwood-Riseman expression for the friction factor of a random coil. In the free-draining limit, the segmental friction factor can, in turn, be evaluated from f. In the nondraining limit the radius of gyration can be determined. We have already discussed f in Chap. 2 and (rg ) in this chapter and again in Chapter 10, so we shall not examine the information provided by D for the random coil any further. 

Rigid particles other than unsolvated spheres. It is easy to conclude qualitatively that either solvation or ellipticity (or both) produces a friction factor which is larger than that obtained for a nonsolvated sphere of the same mass. This conclusion is illustrated in Fig. 9.10, which shows the swelling of a sphere due to solvation and also the spherical excluded volume that an ellipsoidal particle requires to rotate through all possible orientations. 

Since f is a measurable quantity for, say, a protein, and since the latter can be considered to fail into category (3) in general, the friction factor provides some information regarding the eilipticity and/or solvation of the molecule. In the following discussion we attach the subscript 0 to both the friction factor and the associated radius of a nonsolvated spherical particle and use f and R without subscripts to signify these quantities in the general case. Because of Stokes law, we write... 

The particle can be assumed to be spherical, in which case M/N can be replaced by (4/3)ttR P2, and f by 671770R- In this case the radius can be evaluated from the sedimentation coefficient s = 2R (p2 - p)/9t7o. Then, working in reverse, we can evaluate M and f from R. These quantities are called, respectively, the mass, friction factor, and radius of an equivalent sphere, a hypothetical spherical particle which settles at the same rate as the actual molecule. 

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