Interaction between gelatin and sodium dodecyl sulfate at the air/water interface: A neutron reflection study

Citation
Dj. Cooke et al., Interaction between gelatin and sodium dodecyl sulfate at the air/water interface: A neutron reflection study, LANGMUIR, 16(16), 2000, pp. 6546-6554
Citations number
46
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
16
Issue
16
Year of publication
2000
Pages
6546 - 6554
Database
ISI
SICI code
0743-7463(20000808)16:16<6546:IBGASD>2.0.ZU;2-X
Abstract
Neutron reflection has been used to study the composition and structure of layers adsorbed at the air/water surface of solutions of gelatin and sodium dodecyl sulfate (SDS) and these results have been compared with the surfac e tension of the same solutions. Above a concentration where free micelles of SDS can be expected to form in the bulk solution the layer is exactly as would be expected for solutions of SDS on its own. However, at low SDS con centrations the presence of gelatin greatly enhances the adsorption of SDS in comparison with solutions just containing surfactant, and in the interme diate range of SDS concentration, where the surface tension is relatively c onstant, the surface excess of SDS is also constant at gelatin concentratio ns of 0.1 wt %. The thickness of the surfactant layer in the two lower rang es of SDS concentration is much larger than a simple surfactant layer, rang ing from 35 down to 22 Angstrom (in comparison with 19 Angstrom for the pur e surfactant layer), suggesting that the layer is not only roughened by bin ding of gelatin at the surface but that a proportion of the bound SDS molec ules are completely immersed just below the surface. This is confirmed by m easurements of the layer structure at different isotopic compositions. The presence of gelatin at the surface and the enhancement of the adsorption of SDS indicate that complexes of gelatin and SDS are strongly surface active . Furthermore, the measured thickness of the SDS layer at the surface shows that these complexes probably do not contain surfactant in the form of mic elles. This further suggests that it may not be reliable to interpret the f irst discontinuity in the surface tension-log(concentration) plot in such s trongly interacting systems as the point at which there is an onset in aggr egation of the surfactant on the polyelectrolyte (critical aggregation conc entration, or CAC).