Issue 9, 2024

UiO(Zr)-based MOF catalysts for light-driven aqueous pollutant degradation

Abstract

Zirconium-carboxylate metal–organic frameworks (MOFs) of isoreticular crystal morphologies and contrasting pore sizes are examined to understand the relative influence of linker size (UiO-67 vs. UiO-68) and secondary metal incorporation in photocatalytic aqueous pollutant degradation. Here, iron (Fe) is chosen given its prevalence in wastewater treatment literature and applications, resulting from its low toxicity and ability to activate benign oxidants. UiO-67 with Fe incorporated (Fe-UiO-67) via incipient wetness impregnation demonstrates reduced band gap energy relative to the UiO-67 parent and higher apparent photocatalytic degradation under UV light toward methylene blue dye using hydrogen peroxide (H2O2), with catalyst mass-normalized pseudo-first order rate constants of 6.8 ± 0.5 g−1 ks−1 and 2.0 ± 0.3 g−1 ks−1, respectively. While structural characterization via X-ray diffraction remains unperturbed for Fe-UiO-67 before and after reaction, some Fe leaching is evident, as indicated by recharge experiments in the filtrate. Synthesized UiO-68, which possesses increased pore size, also has reduced band gap energy resulting in higher UV-light activation than UiO-67 (pseudo-first order rate constant of 3.5 ± 0.4 g−1 ks−1). Further, UiO-68 demonstrates high stability and exhibits a higher productive H2O2 utilization fraction than either of the UiO-67 catalysts. Together, this work clarifies the relative influence of linker modulation and active metal incorporation in UiO-MOFs for pollutant degradation and aqueous applications broadly.

Graphical abstract: UiO(Zr)-based MOF catalysts for light-driven aqueous pollutant degradation

Supplementary files

Article information

Article type
Paper
Submitted
31 mar 2024
Accepted
04 jun 2024
First published
12 jun 2024
This article is Open Access
Creative Commons BY-NC license

React. Chem. Eng., 2024,9, 2333-2344

UiO(Zr)-based MOF catalysts for light-driven aqueous pollutant degradation

S. C. Moore, I. L. Hubble, A. L. Ritchie, J. E. Barzach and M. L. Sarazen, React. Chem. Eng., 2024, 9, 2333 DOI: 10.1039/D4RE00172A

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