Supercritically
dried, mesoporous silica–gelatin hybrid
aerogels of 4–24 wt % gelatin content show high selectivity
for the adsorption of aqueous Hg(II) in the simultaneous presence
of Cu(II), Cd(II), Co(II), Pb(II), Ni(II), Ag(I), and Zn(II), as demonstrated
by batch adsorption experiments with multiple competing ions. The
aerogels are characterized by SEM and N2 porosimetry, and
their aqueous particle size distributions and zeta potentials are
reported. The adsorption properties of the hybrid aerogels are studied
as a function of their composition, initial aqueous Hg(II) concentration,
contact time, and pH. The optimum pH for adsorption is 6.0, where
the surface of the aerogel is already negatively charged, but Hg(II)
does not completely hydrolyze. The Hg(II) uptake of the hybrid aerogels
increases with increasing gelatin content and levels off at 24 wt
% gelatin. The adsorption capacity of the 24 wt % gelatin hybrid is
estimated to be S = 209 mg g–1 by
fitting the isotherm with the Langmuir model (K
L = 0.032 L mg–1). This translates to 91%
Hg(II) removal at c
0(Hg) = 1.0 mg L–1 and c
0(aerogel) = 0.32
g L–1. Gelatin provides the active sites for Hg(II)
binding; thus, higher gelatin content results in higher adsorption
capacity. However, high gelatin content also induces the extensive
swelling of backbone and the partial collapse of the open porous structure,
which decreases the specific surface area. Time-resolved experiments
show that the adsorption equilibrium is established within 15 min
contact time with aqueous Hg(II). Washing the equilibrated aerogels
with a 2.5 mM solution of EDTA complexing agent quantitatively liberates
bound Hg(II). The regenerated aerogels demonstrate practically intact
adsorption capacities in five cycles of reuse. Coordination chemistry
based considerations reveal that Hg(II) is selectively complexed by
the soft Lewis-base side chains of collagen.