The effect of Gibbs adsorption on Marangoni Instability
Name
52101991-MIT.pdf
Description
Full printable version
Size
13.33 MB
Format
Adobe PDF
Checksum (MD5)
ef8dc5ad016629d514d37972aaf79344
Author(s)
Ross, John Richard, 1945-
Advisor(s)
J.E. Vivian.
Date Issued
1974
Publisher
Massachusetts Institute of Technology
Abstract
An investigation has been performed to determine the conditions at the onset of surface tension-driven instability, in gas-liquid systems, as characterized by the critical value of a dimensionless Marangoni number. A theoretical analysis, for the case in which a surface tension-lowering solute transfers from a liquid according to penetration theory, shows that adsorption of the solute in the Gibbs layer, at the gas-liquid interface, has a strong ability to retard convective instability. Theories which ignore Gibbs adsorption predict the onset of convection at Marangoni numbers as much as ten thousand times higher than the values found experimentally. With Gibbs adsorption included in the new theory, the discrepancy is very substantially reduced, to a factor of ten or less. Frequently, the residual disagreement has been blamed on the presence of minute amounts of impurities, adsorbed in the Gibbs layer, in the experimental liquids. The revised theory confirms that this influence can be strong under some circumstances. However, new experimental determinations of the critical Marangoni number, during triethylamine desorption from water, show that in typical systems the presence of trace contaminants is inconsequential. It is suggested that further efforts, to resolve the data-theory discrepancy, should focus on the relation between predictions of the critical Marangoni number and assumptions made in the stability theory concerning the size of the convective disturbance cells.
Description
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1974.
Vita.
Includes bibliographical references (leaves 262-267).
Subjects
Chemical Engineering.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Terms of Use
M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
Persistent DSpace Link