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P. 30

A4
                                      LIQUIDS



        Key Notes
                                Liquids have a limited degree of short-range order, but virtually
                                no long-range order, and are most adequately described in terms
                                of a radial distribution function—the probability of finding a
                                neighbor at a given radial distance. The radial distribution
                                function displays a temperature dependence which correlates with
                                the effects of temperature on the structure. Generally, increasing
                                temperature increases the radial distance of the peaks in the radial
                                distribution function, corresponding to the thermal expansion of
                                the liquid. The peak intensities also become reduced, as
                                increasing temperature leads to a more chaotic and dynamic
                                liquid structure.
                                Viscosity characterizes the motion of fluids in the presence of a
                                mechanical shear force. A fluid passing through a capilliary
                                experiences a retarding force from the walls of the tube, resulting
                                in a higher velocity along the central axis than at the walls. For
                                any given small bore capilliary, it is found that a specified
                                volume of fluid, of density, ρ, flows through the capilliary in a


                                time, t, given by the         .
                                It is convenient to define a quantity known as the frictional
                                coefficient, f, which is directly related to molecular shapes
                                through Stoke’s law. In the ideal case of spherical particles this
                                may be expressed simply as f=6πηr.
                                The tendency of a solute to spread evenly throughout the solvent
                                in a series of small, random jumps is known as diffusion. The
                                fundamental law of diffusion is Fick’s first law. In the ideal case
                                of diffusion in one dimension, the rate of diffusion of dn moles of
                                solute, dn/dt, across a plane of area A, is proportional to the
                                diffusion coefficient, D, and the negative of the concentration
                                gradient, −dc/dx:

                                                 dn/dt=−DA dc/dx
                                The diffusion coefficient for a spherical molecule, of radius r, is
                                related to the viscosity of the solvent through D=kT/(6πηr). If it is
                                assumed that the molecule makes random steps, then D also
                                                                   2
                                allows calculation of the mean square distance, x , over which a
                                molecule diffuses in a time, t, by the relation   .
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