AN ELECTRICAL SUSPENSION METHOD FOR MEASURING THE ELECTRIC CHARGE ON SMALL SILICONE OIL DROPLETS DISPERSED IN AQUEOUS-SOLUTIONS

Authors
Citation
Yg. Gu et Dq. Li, AN ELECTRICAL SUSPENSION METHOD FOR MEASURING THE ELECTRIC CHARGE ON SMALL SILICONE OIL DROPLETS DISPERSED IN AQUEOUS-SOLUTIONS, Journal of colloid and interface science, 195(2), 1997, pp. 343-352
Citations number
40
ISSN journal
00219797
Volume
195
Issue
2
Year of publication
1997
Pages
343 - 352
Database
ISI
SICI code
0021-9797(1997)195:2<343:AESMFM>2.0.ZU;2-7
Abstract
The electric charge on small liquid droplets dispersed in another immi scible liquid is of fundamental interest in various colloidal and inte rfacial phenomena and industrial processes. In this paper, the authors present a new experimental method to measure the charge on small sili cone oil droplets in aqueous solutions. Basically, an oil droplet was kept stationary inside a test cell between two electrode plates by app lication of an electric field of an appropriate polarity and strength. Thus, the electric charge on the oil droplet was determined from the force balance among the electrical force, the gravitational force, and the buoyancy force exerted on it. By using the electrical suspension method, the effects of two different silicone oils, pH values, valence s, and concentrations of three different electrolytes on the measured electric charge were investigated. One of the two silicone oils is hea vier (rho(1) = 1050 kg m(-3)) and the other is lighter (rho(2) = 963 k g m(-3)) than the aqueous solutions. There was an appreciable differen ce between the measured electric charges for the two silicone oils. Th e point of zero charge (pzc) for the heavier oil droplets was found to be pH approximate to 5.0, which is essentially the same as the value for the mineral oil droplets in the oil-in-water (O/W) emulsions repor ted by other researchers. It was also observed that the electric charg e depends strongly on not only the concentrations but also the ionic v alences of electrolytes added to the solutions. More specifically, div alent and trivalent cations, such as Ca2+ and Al3+, were more readily adsorbed on the oil-water interface. Therefore, their effects were mor e pronounced than that of monovalent cations, Na+, on reducing the neg ative charge or even reversing the charge polarity as their ionic conc entrations increase, in accordance with the valence difference. (C) 19 97 Academic Press.