Atomistic molecular dynamics (MD)
simulations are performed in
order to understand the adsorption behavior of UO2
2+ ions from an aqueous medium. The dibenzo crown ether (DBCE)
and dicyclo hexano crown ether (DCHCE) grafted on the polystyrene
surface is used as the adsorbent. We investigated the role of grafting
density ρs (mol/nm2) of DBCE and DCHCE
on the adsorption behavior with increasing UO2
2+ ion concentration C
s (M). The amount
of adsorption (q
e) (mg/g) increases with
an increase in UO2
2+ salt concentration and
follows the Langmuir adsorption isotherm model. The maximum amount
of adsorption (q
max) (mg/g) increases
with increasing grafting density for both DBCE and DCHCE. The DCHCE
shows higher q
max values compared to DBCE
over the entire range of ρs: 0.25 mol/nm2 < ρs < 2.07 mol/nm2. Overall, q
max show a 5-fold increase for DBCE and DCHCE
with an increase in ρs from 0.25 mol/nm2 to 2.07 mol/nm2. The optimum ρs for
the maximum adsorption is found to be 1.25 mol/nm2 for
both DBCE and DCHCE. The dynamical behavior of the adsorbed UO2
2+ is also investigated by calculating the self-diffusion
coefficient (D) and mean residence time (τ).
The D value decreases by ∼47% for DBCE and
∼61% for DCHCE, for the entire range of ρs, with an increase in C
s. Similarly,
the τ value shows more than a 5-fold increase irrespective of
grafting densities for both DBCE and DCHCE with increasing C
s. In the end, we investigate the UO2
2+ binding structure with DBCE and DCHCE. The potential
of mean force (PMF) analysis shows a favorable free-energy for the
binding of UO2
2+ to DCHCE compared to DBCE.