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Title: Critical point behaviour in binary and ternary liquid mixtures with particular reference to rheological and interfacial properties in model mixtures for microemulsions
Author: Clements, Patricia J.
ISNI:       0000 0001 3558 9415
Awarding Body: University of Sheffield
Current Institution: University of Sheffield
Date of Award: 1997
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The phase behaviour, rheological effects and interfacial properties of binary and ternary liquid mixtures have been studied near critical points. In particular, measurements have been made of the viscosity-at the bulk macroscopic level by capillary viscometry and at the microscopic level by fluorescence depolarisatiorr-and of critical-point wetting and adsorptiorr-at the solid-liquid interface using evanescent-wave-generated fluorescence spectroscopy and at the liquid-vapour interface using specular neutron reflection. The systems investigated have been mostly alkane + perfluoroalkane mixtures or 2-butoxyethanol + H20 or D20 mixtures, although in some cases hexamethyldisiloxane, propanenitrile and perfluorooctyloctane have also been the components of mixtures. The main outcomes of this study are: • Macroscopic viscosity: The divergence to infinity in the shear viscosity of hexane + perfluorohexane at the critical endpoint for approach along the path of constant critical composition both from the single phase and along both limbs of the coexistence curve is described well using the Renormalisation Group Theory critical exponent y = 0.04. The correlation length amplitude obtained by fitting the sheargradient dependence of the viscosity is ~o = (S.S±l.S) A. • Microscopic viscosity: The product of the rotational correlation time and the temperature 'tR"T, often taken as a measure of the microscopic viscosity, exhibits an anomaly as the critical point is approached as a function of temperature. This anomaly mirrors that in the macroscopic viscosity for some fluorescent dye probes, but for others the anomaly is in the opposite sense indicating that other effects such as solvent structure must playa part in the near-critical behaviour of'tR·T. • Critical-point wetting at the solid-liquid interface: The wetting transition temperature has been identified for heptane + perfluorohexane at the quartz-liquid interface from fluorescence lifetime measurements of a probe. The wetting layer is of the same composition as the bulk heptane-rich phase and the transition is tentatively identified as first-order. • Adsorption and wetting at the liquid-vapour interface: The surface structure of several mixtures has been determined by neutron reflection. The results are in general agreement with the expectations of critical-point wetting and adsorption. The surface is complex and in some mixtures an oscillatory scattering length density profile through the interface is required to model the reflectivity data. • Ternary mixtures: The phase behaviour of three mixtures exhibiting tunnel phase behaviour has been studied experimentally and various characteristics of the shape of the twmel identified. A theoretical study on one of the mixtures predicts the drop in temperature for the locus of maximum phase separation temperatures which is observed experimentally.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Microscopic viscosity; Solid-liquid interface