Surface tension experiments were performed using the drop profile analysis tensiometry method. The hexane was injected into the measuring cell at certain times before the formation of the solution drop. The influence of the capillary diameter and solution drop size on the measured apparent dynamic surface tension was studied. The amount of hexane transferred from the vapor phase to the drop was estimated. For large pure water drops, it was shown that the ageing of the drop in the hexane vapor during a long time resulted in the formation of a liquid hexane phase covering the drop, but the volume of this phase did not exceed 0.5 mm(3). On the contrary, for surfactant solution drops the volume of the hexane phase covering the drop was essentially larger. Experiments with solution drops were performed to measure the surface tension within a wide range of surfactant concentration. It was found that the dependencies of dynamic surface tension on the C13DMPO and C(14)EO(8)solutions concentration exhibit maxima at concentrations of about 1-2 mu mol/L for C(14)EO(8)and 2-5 mu mol/L for C13DMPO at ageing times of 100 to 1000 s; these maxima were shown to exist also at equilibrium. This phenomenon is presumably ascribed to the competitive character of simultaneous adsorption of hexane and surfactant.

Drop Size Dependence of the Apparent Surface Tension of Aqueous Solutions in Hexane Vapor as Studied by Drop Profile Analysis Tensiometry

Liggieri L;
2020

Abstract

Surface tension experiments were performed using the drop profile analysis tensiometry method. The hexane was injected into the measuring cell at certain times before the formation of the solution drop. The influence of the capillary diameter and solution drop size on the measured apparent dynamic surface tension was studied. The amount of hexane transferred from the vapor phase to the drop was estimated. For large pure water drops, it was shown that the ageing of the drop in the hexane vapor during a long time resulted in the formation of a liquid hexane phase covering the drop, but the volume of this phase did not exceed 0.5 mm(3). On the contrary, for surfactant solution drops the volume of the hexane phase covering the drop was essentially larger. Experiments with solution drops were performed to measure the surface tension within a wide range of surfactant concentration. It was found that the dependencies of dynamic surface tension on the C13DMPO and C(14)EO(8)solutions concentration exhibit maxima at concentrations of about 1-2 mu mol/L for C(14)EO(8)and 2-5 mu mol/L for C13DMPO at ageing times of 100 to 1000 s; these maxima were shown to exist also at equilibrium. This phenomenon is presumably ascribed to the competitive character of simultaneous adsorption of hexane and surfactant.
2020
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
drop profile analysis tensiometry
solution-alkane vapor interface
dynamic apparent surface tension
non-ionic surfactant
thermodynamic model
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Descrizione: Drop Size Dependence of the Apparent Surface Tension of Aqueous Solutions in Hexane Vapor as Studied by Drop Profile Analysis Tensiometry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/418007
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