Hierarchical zeolites, which exhibit a distinctive structure characterized by interconnected micropores and mesopores, are versatile materials that can overcome the typical issues related to microporous materials, including poor mass transfer, hindered diffusion, and strict selectivity of resulting products. One possible route to obtain hierarchical porous materials is through top-down approaches, in which secondary porosity is introduced via post-synthetic modification of a pre-existing microporous matrix.[1,2] In this contribution, a top-down method was employed to obtain hierarchical porous materials with different properties. In detail: two commercial zeolites, HZSM5 and HUSY (both with SiO2/Al2O3 = 80) with a MFI and FAU structure respectively, and a natural clinoptilolite (HCLI, Si/Al = 5) with HEU structure were desilicated using NaOH solutions at varying concentrations, to evaluate the treatment efficiency. The synthesized hierarchical architectures were characterized by multi-technique approach using XRD, N2 physisorption at 77K, TGA and FTIR spectroscopy of adsorbed probe molecules, to assess the nature, strength and accessibility of the acid sites (Figure 1A,A’). The obtained hierarchical zeolites were evaluated for their ability to recover Cu2+ and Co2+ ions from aqueous solutions by using UV-Vis spectroscopy. Selectivity tests were also carried out to determine the materials' affinity for the target ions. The three investigated zeolites exhibited distinct behaviors, based on their different physicochemical properties (Figure 1B). HZSM5 demonstrated the highest adsorption capacity but showed no specific affinity for either metal ion, in contrast to HUSY and HCLI, which displayed a clear preference for Co2+ (Figure 1B). Notably, the desilication treatment significantly enhanced the adsorption efficiency of the studied materials. Dr. Gioele Ancora holds a PhD career grant supported by Next Generation EU – MUR.

HIERARCHICAL ZEOLITES FROM TOP-DOWN APPROACH: A SYSTEMATIC INVESTIGATION OF THEIR STRUCTURAL AND ADSORPTION PROPERTIES

Gioele Ancora;Federico Morari;Leonardo Marchese;Chiara Bisio;Enrica Gianotti
2025-07-01

Abstract

Hierarchical zeolites, which exhibit a distinctive structure characterized by interconnected micropores and mesopores, are versatile materials that can overcome the typical issues related to microporous materials, including poor mass transfer, hindered diffusion, and strict selectivity of resulting products. One possible route to obtain hierarchical porous materials is through top-down approaches, in which secondary porosity is introduced via post-synthetic modification of a pre-existing microporous matrix.[1,2] In this contribution, a top-down method was employed to obtain hierarchical porous materials with different properties. In detail: two commercial zeolites, HZSM5 and HUSY (both with SiO2/Al2O3 = 80) with a MFI and FAU structure respectively, and a natural clinoptilolite (HCLI, Si/Al = 5) with HEU structure were desilicated using NaOH solutions at varying concentrations, to evaluate the treatment efficiency. The synthesized hierarchical architectures were characterized by multi-technique approach using XRD, N2 physisorption at 77K, TGA and FTIR spectroscopy of adsorbed probe molecules, to assess the nature, strength and accessibility of the acid sites (Figure 1A,A’). The obtained hierarchical zeolites were evaluated for their ability to recover Cu2+ and Co2+ ions from aqueous solutions by using UV-Vis spectroscopy. Selectivity tests were also carried out to determine the materials' affinity for the target ions. The three investigated zeolites exhibited distinct behaviors, based on their different physicochemical properties (Figure 1B). HZSM5 demonstrated the highest adsorption capacity but showed no specific affinity for either metal ion, in contrast to HUSY and HCLI, which displayed a clear preference for Co2+ (Figure 1B). Notably, the desilication treatment significantly enhanced the adsorption efficiency of the studied materials. Dr. Gioele Ancora holds a PhD career grant supported by Next Generation EU – MUR.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11579/237747
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