Single- and bisolute competitive adsorptions were carried out to investigat
e the adsorption behavior of an anionic dye, Orange II, and an anionic surf
actant, dodecylbenzenesulfonate (DBS), from water at 25 degrees C onto mont
morillonite treated with hexadecyltrimethylammonium (HDTMA) cation. The mon
ovalent HDTMA cation was exchanged for the metal cations on the montmorillo
nite to prepare HDTMA-montmorillonite, changing its surface property from h
ydrophilic to organophilic. Adsorption affinity of DBS on HDTMA-montmorillo
nite was found to be slightly higher than that of Orange II, probably due t
o hydrophobic or nonpolar interactions between the long hydrocarbon chains
of the HDTMA with an anion. The single-solute adsorption data were fitted t
o the Langmuir and the Redlich-Peterson (RP) adsorption models. The competi
tive Langmuir model and the ideal adsorbed solution theory (IAST) coupled w
ith the single-solute adsorption models were used to predict the bisolute c
ompetitive adsorption equilibria. Among the models, the IAST coupled with t
he Langmuir and the RP models for DBS and Orange II, respectively, yielded
the most favorable representation of the bisolute competitive adsorption be
havior.