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
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
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.