We use a selection of wood-based and coconut-based activated carbons to inv
estigate the factors controlling the removal of the hepatotoxin microcystin
-LR (m-LR) from aqueous solutions. The wood carbons contain both micropores
and mesopores. The coconut carbons contain micropores only, Confirming pre
viously published observations, we also find that the wood-based carbons ad
sorb more microcystin than the coconut-based carbons. From a combination of
a judicious modification of a wood-based carbon's surface chemistry and of
the solution chemistry, we demonstrate that both surface and solution chem
istry play minor roles in the adsorption process, with the adsorbent surfac
e chemistry exhibiting less influence than the solution chemistry. Conforma
tional changes at low solution pH probably contribute to the observed incre
ase in adsorption by both classes of adsorbent. At the solution pH of 2.5,
the coconut-based carbons exhibit a 400% increased affinity for m-LR compar
ed with 100% increases for the wood-based carbons. In an analysis of the th
ermodynamics of adsorption, using multiple temperature adsorption chromatog
raphy methods, we indicate that m-LR adsorption is an entropy-driven proces
s for each of the carbons, except the most hydrophilic and mesoporous carbo
n, Bl. In this case, exothermic enthalpy contributions to adsorption also e
xist. From our overall observations, since m-LR contains molecular dimensio
ns in the secondary micropore width range, we demonstrate that it is import
ant to consider both the secondary micropore and the mesopore volumes for t
he adsorption of m-LR from aqueous solutions. (C) 2001 Academic Press.