Me. Montgomery et Mj. Wirth, SPECTROSCOPIC INVESTIGATION OF SODIUM DODECYL-SULFATE ADSORPTION ON AHYDROCARBON MONOLAYER, Langmuir, 10(3), 1994, pp. 861-869
Sodium dodecyl sulfate (SDS), adsorbed from aqueous solution onto a mo
nolayer of dimethyloctadecylsiloxane (C18) bonded to silica, was chara
cterized spectroscopically. The structural and dynamical properties of
the adsorbed SDS were probed by the fluorescence anisotropy of a dilu
te hydrophobic fluorophor, 1,4-bis(o-methylstyryl)benzene. Just below
the critical micelle concentration (cmc) of 8.3 mM, the orientational
distribution of the probe is narrowed and tilted more toward the surfa
ce normal, and its rotational diffusion slows, as compared to its beha
vior above the cmc. These properties below the cmc were most extreme a
t 7 mM in SDS concentration. FTIR spectroscopy was used to measure the
amount of adsorbed SDS, and it revealed that there is about 3 times a
s much SDS adsorbed below the cmc as there is above it. A distinct max
imum in the adsorption isotherm occurs at 7 mM, the same concentration
at which the rotational diffusion behavior is most extreme. The FTIR
spectral bands are narrowed and shifted below the cmc, showing that th
e adsorbed SDS in the premicellar region is organized densely.