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Non-Newtonian turbulence: viscoelastic fluids and binary mixtures.

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2.1. Polymer dynamics in <strong>fluids</strong> 35<br />

Figure 2.3: Single DNA molecule (40µm) relaxing to the coiled state. In this<br />

experiment a latex bead (1µm) is tethered to an end of the molecule. The DNA,<br />

coloured with a fluorescent dye, is stretched by a uniform flow <strong>and</strong> successively<br />

let free to relax. Images are taken at 5s time intervals, from left to right [34].<br />

where µ is the dynamic viscosity of the solvent. Experiments with DNA molecules<br />

[34] confirm that relaxation can be safely considered linear, provided the elongation<br />

is small compared to the maximum extension R ≪ Rmax (see fig. 2.3).<br />

Actually, the relaxation process can be much more complex than the simple<br />

description of Zimm model. Several microscopic models of polymeric dynamics<br />

have been developed to characterize this process. An introduction to this subject<br />

can be found in the book by Doi <strong>and</strong> Edwards [35]. Nevertheless, the simple linear<br />

relaxation is able to catch, at least qualitatively, the basic features of polymer<br />

dynamics in <strong>fluids</strong>.<br />

Finally, let us mention that the description of a polymer as a freely jointed<br />

chain does not consider excluded-volume effects, which are experimentally known<br />

to alter the scaling R0 ∼ M 1/2 of the gyration radius with the degree of polymerization.<br />

The scaling exponent is, indeed, found to be ν = (0.55 ÷0.6). The origin<br />

of these effects is the possibility that segments of the chain have, in the model, to<br />

intersect or superpose to each other, which is not realistic. A better approximation<br />

of the chain dynamics is based on a self-avoiding r<strong>and</strong>om walk. While the theory<br />

of the st<strong>and</strong>ard r<strong>and</strong>om walk is quite simple, the treatment of the self-avoiding<br />

problem is more difficult. A theoretical estimation of ν has been given by Flory<br />

[36] for spatial dimensionality d < 4:<br />

ν = 3<br />

d + 2<br />

(2.11)<br />

which, for d = 3, gives the value ν = 3/5 = 0.6, not far from the experimental<br />

measures; in two dimensions, Flory’s result is exact. When d ≥ 4 the value<br />

ν = 1/2 of the ideal chain is recovered, meaning that the segments have "enough<br />

room" to avoid each other.<br />

35

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