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Further Studies on the Effect of Degassing on the Dispersion and Stability of Surfactant-Free Emulsions

dc.contributor.authorMaeda, Nobuo
dc.contributor.authorRosenberg, Kenneth
dc.contributor.authorIsraelachvili, Jacob N
dc.contributor.authorPashley, Richard
dc.date.accessioned2015-12-13T22:43:42Z
dc.date.available2015-12-13T22:43:42Z
dc.date.issued2004
dc.date.updated2015-12-11T10:13:47Z
dc.description.abstractRecently reported results indicate that the formation of surfactant-free, oil-in-water emulsions can be significantly enhanced by the almost complete removal of dissolved gases and that the reintroduction of dissolved gases does not immediately destabilize the already-formed emulsions. These initial experiments have been repeated and extended to include a wider range of organic liquids and the application of light scattering to determine droplet size and distribution. The earlier observations have been confirmed. In addition, a systematic trend was found between the solubility of the oil in water and the stability (lifetime) of the degassed oil droplets in water. The lower the solubility, the more stable the emulsion, and for oils that are sparingly soluble in water such as squalane, the small droplets remain stable for several weeks, with buoyancy separation being the main cause of instability of the large droplets with time. The addition of electrolytes, up to molar concentrations, substantially reduces the enhancement of the dispersions on degassing but appears to have little effect on the stability of the already-formed emulsions. The reduction of pH to about 2 significantly reduces both the enhancement of the dispersions on degassing and the stability of the already-formed emulsions. In contrast, the increase of pH to about 11 hardly affects the enhancement of the dispersions on degassing or the stability of the already-formed emulsions. We have confirmed the importance of dissolved gas and its association with the electrostatic effects, but we still cannot provide a complete explanation for the effect of degassing on the hydrophobic dispersions.
dc.identifier.issn0743-7463
dc.identifier.urihttp://hdl.handle.net/1885/79321
dc.publisherAmerican Chemical Society
dc.sourceLangmuir
dc.subjectKeywords: Droplet size; Electrostatic effects; Electrostatic potential; Molar concentrations; Buoyancy; Chemical engineering; Degassing; Dispersions; Electrolytes; Hydrophobicity; Light scattering; pH effects; Solubility; Surface active agents; Emulsions; Chemical
dc.titleFurther Studies on the Effect of Degassing on the Dispersion and Stability of Surfactant-Free Emulsions
dc.typeJournal article
local.bibliographicCitation.issue8
local.bibliographicCitation.lastpage3137
local.bibliographicCitation.startpage3129
local.contributor.affiliationMaeda, Nobuo, University of California
local.contributor.affiliationRosenberg, Kenneth, University of California
local.contributor.affiliationIsraelachvili, Jacob N, University of California
local.contributor.affiliationPashley, Richard, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidPashley, Richard, u8002457
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030603 - Colloid and Surface Chemistry
local.identifier.ariespublicationMigratedxPub7788
local.identifier.citationvolume20
local.identifier.scopusID2-s2.0-2342444064
local.type.statusPublished Version

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