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Persistent URL
http://purl.org/net/epubs/work/65416
Record Status
Checked
Record Id
65416
Title
The impact of alkyl sulfate surfactant geometry and electrolyte on the co-adsorption of anionic surfactants with model perfumes at the air-solution interface
Contributors
R Bradbury (Physical and Theoretical Chemistry Laboratory)
,
J Penfold (STFC Rutherford Appleton Lab.)
,
RK Thomas (STFC Rutherford Appleton Lab.)
,
IM Tucker (Unilever Research and Development Laboratory)
,
JT Petkov (Unilever Research and Development Laboratory)
,
C Jones (Unilever Research and Development Laboratory)
Abstract
The impact of surfactant geometry and electrolyte on the co-adsorption of anionic surfactants and model perfumes at the air-solution interface has been studied by neutron reflectivity. The more hydrophobic perfume linalool, competes more favourably for the surface with sodium dodecylsulfate than was previously reported for the anionic surfactant, sodium dodecyl 6-benzenesulfonate. Due to an increase in surface activity of the sodium dodecylsulfate, the addition of electrolyte results in a reduction in the linalool adsorption. Changing the alkyl chain length affects the relative adsorption of linalool and surfactant at the interface. Similar measurements for the different alkyl sulfates and with electrolyte with the more hydrophilic perfume phenyl ethanol, reveal broadly similar trends. Although the relative adsorption of phenyl ethanol with sodium dodecylsulfate is substantially enhanced compared to sodium dodecyl-6-benzenesulfonate the effects are not as significant as was observed with linalool. The variations with alkyl chain geometry show the importance of the hydrophobic interaction between the perfume and surfactant and changes in the packing constraints on the relative adsorption. The results highlight the importance of the specific interaction between the surfactant and perfume, and the surfactant and perfume geometries on the relative adsorption at the interface.
Organisation
ISIS
,
ISIS-SURF
,
STFC
Keywords
Funding Information
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Language
English (EN)
Type
Details
URI(s)
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Year
Journal Article
J Coll Int Sci
(2013).
doi:10.1016/j.jcis.2013.04.040
2013
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