The role of granular activated carbon (GAC) surface
chemistry on the adsorption of four model dissolved organic
material (DOM) isolates and four surface water natural
organic material (NOM) samples was investigated by using
() ten carbons prepared by modifying the surfaces of a coal-based and a wood-based carbon and () seven different
as-received GACs. Because changes in the pore structure
resulting from surface treatment were small, while
changes in the surface chemistry were significant, the
impact on the DOM and NOM uptake by surface-treated
carbons was systematically linked to the changes in the
carbon surface chemistry alone. For the surface-treated
coal-based carbons, there was () no significant capacity
difference between acid-washed and heat-treated
carbon samples, () oxidation of the carbon surface
significantly decreased the uptake, and () the capacity
was partially restored by subsequent heat treatment of the
oxidized surfaces. A decreasing uptake with increasing
surface acidity was evident, and the effects of surface
acidity on uptake were qualitatively similar to the two SOCs
studied in Part 1 of this series. The experiments with as-received coal-based carbons exhibited the same behavior;
however, the reactivity of modified and as-received
carbons for DOM and NOM uptake was significantly
different. For the wood-based carbon, the impact of surface
treatment on adsorption of DOMs and NOM was
surprisingly minimal or absent. This finding was in contrast
to the effects of surface acidity on uptake of the two
SOCs studied in Part 1 in this series. Overall, the reactivity
of carbon surfaces to DOM and NOM uptake depended
on the raw material type, activation conditions and surface
treatment.