USING THE OPTICAL PROBE METHYL-ORANGE TO DETERMINE THE ROLE OF SURFACTANT AND ALCOHOL CHAIN-LENGTH IN THE ASSOCIATION OF 1-ALKANOLS WITH ALKYLTRIMETHYLAMMONIUM BROMIDE MICELLES

Citation
Kk. Karukstis et al., USING THE OPTICAL PROBE METHYL-ORANGE TO DETERMINE THE ROLE OF SURFACTANT AND ALCOHOL CHAIN-LENGTH IN THE ASSOCIATION OF 1-ALKANOLS WITH ALKYLTRIMETHYLAMMONIUM BROMIDE MICELLES, JOURNAL OF PHYSICAL CHEMISTRY B, 101(11), 1997, pp. 1968-1973
Citations number
27
Categorie Soggetti
Chemistry Physical
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
11
Year of publication
1997
Pages
1968 - 1973
Database
ISI
SICI code
1089-5647(1997)101:11<1968:UTOPMT>2.0.ZU;2-A
Abstract
We have used the optical probe methyl orange to characterize the inter action of primary alcohol additives with micelles assembled from a ser ies of alkyltrimethylammonium bromide (C(n)TAB) surfactants in aqueous solution. The anionic methyl orange (MO) interacts electrostatically with the cationic C(n)TAB headgroups to reveal micellar properties thr ough variations in the probe's absorption wavelength maximum. The sens itivity of the absorbance of methyl orange to its microenvironment is interpreted to reflect the nature of the association of 1-alkanols wit h C(n)TAB micelles, an association dependent on both the surfactant an d alcohol chain lengths. From the observed effect of alcohol addition on the methyl orange absorption lambda(max), we propose three distinct roles for 1-alkanols: cosolvent at the micellar surface, coaggregate within the micellar palisade layer, and cosurfactant via extension of the alcohol into the micellar core. Our suggestions for the surfactant and 1-alkanol chain length criteria that determine the role of alcoho l additives within C(n)TAB micelles are presented.