A “sorbent
mass variation” (SMV) method has been
suggested to investigate the adsorption at solid–liquid interfaces,
which can provide information on the adsorbed layer structure including
its thickness and composition. However, there has been little research
focused on the method, and therefore, it is essential to examine its
general applicability. Herein, the adsorption of benzyldimethyldodecylammonium
bromide (BDDABr), a cationic surfactant, on silica (SiO2) nanoparticles (with ∼12 and 24 nm in size, denoted as S-SiO2 and L-SiO2, respectively) in water was investigated
using the SMV method. The adsorption isotherms all show a linearly
declining tendency in the saturated adsorption regime, consistent
with the prediction of the SMV model. The adsorption is interpreted
to form noncomplete bilayers (or isolated admicelles). The thicknesses
of the adsorbed bilayers on S-SiO2 and L-SiO2 are estimated to be ∼2.9 and 2.7 nm, respectively, and the
volume fractions of BDDABr in the saturated adsorbed layers are 0.63
and 0.68, respectively. In addition, the change in the Gibbs free
energy of the adsorption process is also analyzed, showing its spontaneous
nature. This work demonstrates that the SMV method is available for
investigation on the adsorption of surfactants at solid–liquid
interfaces, which can provide information on the structure and formation
thermodynamics of adsorbed layers.