Abstract

Low frequency dielectric (10–2 to 105 Hz) and Kerr-effect (10–5 to 102 s) relaxation behaviour of pure liquid tritolylphosphate, super-cooled o-terphenyl and three tritolylphosphate +o-terphenyl mixtures have been examined. The Kerr-effect rise and decay transients for each of these systems at a given temperature, are characterized by the same relaxation time τK,r and τK,d respectively. For both pure liquids τK,r and τK,d are essentially the same as the dielectric relaxation time τD, and the dielectric loss curves and Kerr-effect transients are adequately described by the William–Watts empirical relaxation function. These results suggest that reorientational motions in highly viscous liquids do not occur by rotational diffusion, but that they are entirely consistent with a “fluctuation relaxation” mechanism, and they are discussed in terms of the Ivanov and Anderson models of rotational Brownian motion. For some o-terphenyl + tritolylphosphate mixtures τK,r=τK,d > τD and possible explanations of this result are considered.

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