The adsorption of Cd(II) and Co(TI) onto goethite was measured at five temp
eratures between 10 and 70 degrees C. For both cations the amount adsorbed
at any given pH increased as the temperature was increased. Cd(II) adsorbed
at a slightly lower pH at each temperature than Co(II). Adsorption isother
ms at pH 7.00 for Cd(II) could be fitted closely by a simple Langmuir model
, but a two-site Langmuir model was needed for Co(II). Potentiometric titra
tions of goethite suspensions in the presence and absence of added cation c
ould be modeled closely by a constant-capacitance surface complexation mode
l that assumed the adsorption reactions M2+ + SOH reversible arrow SOM+ + H
+ and M2+ + SOH + H2O reversible arrow SOMOH + 2H(+), where M represents Cd
or Co. This model also fitted the experimental data from the adsorption ed
ge and adsorption isotherm experiments. Thermodynamic parameters estimated
from both Langmuir and surface complexation models showed that the adsorpti
on of both metals was endothermic. Values obtained for the adsorption entha
lpies from both modeling schemes were similar for both cations. Estimates o
f the adsorption entropies were model-dependent: Langmuir parameters yielde
d positive entropies, while some of the surface complexation parameters gen
erated negative adsorption entropies. (C) 1999 Academic Press.