Adsorptive removal of heavy metal ions from water is an energy- and cost-effective water decontamination technology. Schiff base functionalities can be incorporated into the pore cages of metal-organic frameworks (MOFs) via direct synthesis, post-synthetic modification, and composite formation. Such incorporation can efficiently enhance the interactions between the MOF adsorbent and target heavy metal ions to promote the selective adsorption of the latter. Accordingly, Schiff base-functionalized MOFs have great potential to selectively remove a particular metal ion from the aqueous solutions in the presence of coexisting (interfering) metal ions through the binding sites within their pore cages. Schiff base-functionalized MOFs can bind divalent metal ions (e.g., Pb(II), Co(II), Cu(II), Cd (II), and Hg (II)) more strongly than trivalent metal ions (e.g., Cr(III)). The adsorption capacity range of Schiff base-functionalized MOFs for divalent ions is thus much more broad (22.4-713 mg g-1) than that of trivalent metal ions (118-127 mg g-1). To evaluate the adsorption performance between different adsorbents, the two parameters (i.e., adsorption capacity and partition coefficient (PC)) are derived and used for comparison. Further, the possible interactions between the Schiff base sites and the target heavy metal ions are discussed to help understand the associated removal mechanisms. This review delivers actionable knowledge for developing Schiff-base functionalized MOFs toward the adsorptive removal of heavy metal ions in water in line with their performance evaluation and associated removal mechanisms. Finally, this review highlights the challenges and forthcoming research and development needs of Schiff base-functionalized MOFs for diverse fields of operations.
Keywords: Adsorption; Functionalization; Heavy metal ions; Metal-organic frameworks; Post-synthetic modification; Schiff base ligand; Water decontamination.
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