Universal pathway towards metal sulfides decorated 3D porous Ti3C2Tx MXene aerogel for vapor-phase mercury removal
Utilization of monolithic mineral sulfide-based sorbent for the fix-bed elemental mercury (Hg 0 ) removal is regarded as a predominant predicament in the field of Hg 0 abatement. In this work, a general and facile route was exploited to establish CuS particles decorated 3D porous Ti 3 C 2 T x MXene aerogel via divalent Cu 2+ cations induced assembly combined with subsequent high-temperature sulfurization treatment, during which, uniform CuS particles were homogeneously anchored throughout the Ti 3 C 2 T x substrate. The obtained 3D CuS/Ti 3 C 2 T x MXene aerogel exhibited satisfactory textural property, hierarchical pore structure and strong interaction between Ti 3 C 2 T x MXene and CuS. Meanwhile, the inherent restacking of Ti 3 C 2 T x MXene nanosheet and serious agglomeration of CuS can also be effectively avoided in the formation of aerogel. Those structural advantages originating from this novel gelation process favorably contributes to satisfactory Hg 0 mass transfer and sufficient utilization of CuS active ligands, which largely strengthens Hg 0 removal performance and broadens the fix-bed application of mineral sulfides. Consequently, the Hg 0 capture capacity and adsorption rate of CuS/Ti 3 C 2 T x MXene aerogel reached 90596.4 g m −3 and 120.64 g m −3 min −1 , respectively, far outbalancing those of the reported in-situ selenized copper foam with excellent Hg 0 removal activity. The impressive Hg 0 sequestration performance is attributed to its relatively large specific surface area, layered pore channel, and highly dispersed CuS particles, largely boosting Hg 0 mass transfer and following sequestration. Moreover, other mineral sulfides/Ti 3 C 2 T x MXene aerogels can also be constructed by just replacing divalent metal cations, which makes the initial effort towards the fix-bed utilization of mineral sulfides-based aerogel for vapor-phase Hg 0 immobilization.
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