Effect of interfacial alcohol concentrations on oil solubilization by sodium dodecyl sulfate micelles

Authors
Citation
Mf. Zhou et Rd. Rhue, Effect of interfacial alcohol concentrations on oil solubilization by sodium dodecyl sulfate micelles, J COLL I SC, 228(1), 2000, pp. 18-23
Citations number
29
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF COLLOID AND INTERFACE SCIENCE
ISSN journal
00219797 → ACNP
Volume
228
Issue
1
Year of publication
2000
Pages
18 - 23
Database
ISI
SICI code
0021-9797(20000801)228:1<18:EOIACO>2.0.ZU;2-S
Abstract
Alcohol partitioning and its effect on oil solubilization in Winsor Type I microemulsion systems was investigated. The microemulsion systems consisted of sodium dodecyl sulfate (SDS), pentanol, isopropanol (IPA), and dodecane , with either deionized water or an aqueous solution of 50 mM CaCl2. Alcoho l partitioning between aqueous, oil, and interfacial phases of the microemu lsion was described using a pseudophase model in which the alcohol was assu med to self-associate in the oil phase. Partitioning in these miroemulsions was consistent with pentanol self-association in the oil phase. IPA did no t self-associate but co-associated with pentanol in the oil phase. IPA conc entrations as high as 20 g/kg of water had no effect on pentanol partitioni ng. The partition coefficient for pentanol between aqueous and interfacial phases was about 220 on a mole fraction basis. However, pentanol saturated the interfacial phase at a mole ratio of 3 : 1 pentanol to SDS. Addition of pentanol beyond that sufficient to saturate the interface resulted in larg e amounts of pentanol partitioning into the oil, reaching concentrations in excess of 25 g dL(-1) of oil phase. Dodecane solubilization increased line arly with pentanol mole fraction in the interface up to the 3:1 pentanol-to -SDS saturation level. The fact that dodecane solubilization was unaffected by pentanol at concentrations beyond those necessary for interfacial satur ation suggests that pentanol behaves as a cosurfactant and not a cosolvent in these microemulsion systems, (C) 2000 Academic Press.