Abstract
In this study, we report the synthesis and characterization of a novel NH(2)-MIL-101(Fe) magnetic composite, developed via in situ formation of NH(2)-MIL-101(Fe) in the presence of Fe(3)O(4) nanoparticles embedded within a chloropropyl-modified mesoporous silica layer. This hybrid composite retains the high adsorption capacity of NH(2)-MIL-101(Fe) while benefiting from the easy magnetic separation enabled by Fe(3)O(4) nanoparticles. The mesoporous silica forms a protective porous coating around the magnetic nanoparticles, significantly enhancing its chemical stability and preventing clumping. Beyond protection, the mesoporous silica layer provides a high-surface-area scaffold that promotes the uniform in situ growth of NH(2)-MIL-101(Fe). Functionalization of the silica surface with chloride groups enables strong electrostatic interactions between the magnetic component and metal organic framework (MOF), ensuring a homogeneous and stable hybrid structure. The new composite's capacity to remove Pb(II) and Cd(II) ions from aqueous solutions was systematically investigated. The adsorption data showed a good fit with the Langmuir isotherm model for both ions, the maximum adsorption capacities calculated being 214.6 mg g(-1) for Pb(II) and 181.6 mg g(-1) Cd(II). Furthermore, the kinetic behavior of the adsorption process was accurately described by the pseudo-second-order model. These findings confirm the effectiveness of this composite for the removal of Pb(II) and Cd(II) ions from aqueous solutions, demonstrating its potential as an efficient material for environmental remediation. The combination of magnetic recovery, high adsorption capacity, and stability makes this novel composite a promising candidate for heavy metal removal applications in water treatment processes.