The presence of molecular oxygen in the test environment promotes oxid
ative coupling (polymer formation) of phenolic compounds on the surfac
e of granular activated carbon (GAC). Both adsorption equilibria and a
dsorption kinetics are affected by these chemical reactions. Lack of m
olecular oxygen interference with adsorption kinetics during the initi
al phase (first 12 h) of adsorbent-adsorbate contact, observed for the
experimental conditions tested, can be explained by the lower rate of
adsorbate polymerization when compared to the rate of pure adsorption
. The homogeneous surface diffusion model (HSDM) adequately describes
adsorption kinetics under anoxic conditions, but it fails to accuratel
y predict experimental data collected in the presence of molecular oxy
gen. For the experimental conditions tested in this study, GAC particl
e size did not influence the magnitude of the surface diffusion coeffi
cient. However, the increase in the initial adsorbate concentration yi
elded an increase in the surface diffusion coefficient. This may be at
tributed to a decrease in the adsorption forces for higher surface cov
erage.