In this work, the
influence of phosphoric groups on the surface
of activated carbon on the adsorption of elemental mercury (Hg0) is systematically investigated for the first time. The influence
of functional oxygen groups–controversially discussed in the
literature–on the single-component adsorption of Hg0 as well as the co-adsorption of water and Hg0 are thoroughly
analyzed, leading to a new mechanistic proposal. Single-component
adsorption of Hg0 and co-adsorption of mercury and water
on modified activated carbons are investigated by breakthrough curves
as well as by coupled adsorption and temperature-programmed desorption
(TPD) experiments. The modification of a basic activated carbon with
phosphoric acid evolves phosphoric acid esters on the surface, which
significantly increase the chemisorptive capacity for Hg0. TPD experiments reveal that only a single chemisorptive mechanism
is involved. Based on these findings, a schematic mechanism for the
chemisorptive attachment of Hg0 is proposed. In contrast
to this, physisorptive interactions between Hg0 and surface
groups dominate at the basic activated carbon and at the activated
carbon modified with nitric acid. Oxygen-containing functional groups
formed by nitric acid do not significantly enhance the one-component
adsorption of elemental mercury. The experiments on the co-adsorption
of mercury and water prove that the surface complexes of oxygen functional
groups and Hg0 are strongly stabilized by water from the
gas phase. A schematic chemisorptive mechanism is also proposed here.
The chemical reaction of Hg0 with phosphoric acid esters,
on the other hand, is not influenced by water from the gas phase in
the concentration range investigated.