Per- and polyfluoroalkyl substances (PFAS) are persistent,
bioaccumulative,
and ubiquitous contaminants that are harmful to both humans and ecosystem
health. To remove PFAS effectively and efficiently from the aqueous
environment, a clay-based adsorbent was synthesized via the modification
of montmorillonite by a cationic surfactant cetyltrimethylammonium
chloride (CTAC). Through the coexposure adsorption tests with organic
dyes and PFAS mixtures, the optimal ratio of CTAC to cation exchange
capacity (CEC) was identified. The optimal modified clay exhibited
drastically improved adsorption performance, achieving 100% removal
efficiency of the PFAS mixture consisting of nine short- and long-chain
PFAAs, GenX, and three precursors at initial concentrations of the
parts per billion (ppb) level. Additionally, the modified clay outperformed
other commercial adsorbents with respect to adsorption performance.
The adsorption kinetic data of all PFAS, which were well described
by the pseudo-second-order model, suggested an expeditious adsorption
process and an adsorption behavior dependent on the initial concentration
and carbon chain length. Among the three examined adsorption isotherms,
the Sips model combining Langmuir and Freundlich models showed the
best fitting correlation, indicating that multiple interactions might
be involved in the adsorption process. This hypothesis was supported
by characterizations showing that the modified clay possessed physicochemical
properties favorable for electrostatic interactions and hydrophobic
interactions.