Engineered MnO <sub>2</sub> /UiO-66- <i>x</i> Heterostructure with Tailored Interfaces for Efficient Capture of NSAIDs: Performance and Mechanistic Insights

The widespread misuse of nonsteroidal anti-inflammatory drugs (NSAIDs) has become a growing concern due to their severe threats to aquatic ecosystems and human health. Current adsorption technologies face limitations including low capacity, poor efficiency for trace-level contaminants, and unclear removal mechanisms. These limitations stem from poorly optimized pore architectures and surface chemistries in existing materials, necessitating the development of multifunctional adsorbents with tailored active sites. Herein, a series of MnO<sub>2</sub>/UiO-66-<i>x</i> composites were rationally designed via a solvothermal approach and comprehensively characterized using powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) spectroscopy, N<sub>2</sub> physisorption, scanning electron microscopy (SEM), and zeta potential analysis. Systematic optimization demonstrated that MnO<sub>2</sub>/UiO-66-1 (5 mg) achieved exceptional adsorption capacity (<i>q</i><sub>max</sub> = 659.49 mg·g<sup>-1</sup>) for diclofenac sodium (DCF, 20 mg·L<sup>-1</sup>, 30 mL), with >90% removal within 10 min (<i>k</i><sub>2</sub> = 0.0081 g·mg<sup>-1</sup>·min<sup>-1</sup>). Mechanistic studies revealed that this performance was attributed to hierarchical porosity (micro-/mesopores), which enables size-selective uptake, synergistic binding, and pH-dependent electrostatic enhancement. Structure-activity relationships indicated that NSAIDs adsorption efficiency (naproxen ≈ ibuprofen ≈ ketoprofen > indomethacin > paracetamol) was governed by molecular structure, size, and p<i>K</i><sub>a</sub> values. Thermodynamic and kinetic studies confirmed a spontaneous (Δ<i>G</i><sup>0</sup> < 0), endothermic (Δ<i>H</i><sup>0</sup> > 0), and entropy-driven (Δ<i>S</i><sup>0</sup> > 0) process dominated by chemisorption through synergistic interactions (including coordination bonding, hydrogen bonding, Lewis acid-base effects, electrostatic attraction, and π-π stacking). This study establishes a new paradigm for metal-organic-framework-based adsorbent design through precise control of metal-organic interfaces and defect engineering. With 87% capacity retention after 5 regeneration cycles, MnO<sub>2</sub>/UiO-66-<i>x</i> shows strong potential for practical water remediation applications.

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Publication Details

Journal
Langmuir
Published
2026-03-23
DOI
https://doi.org/10.1021/acs.langmuir.6c00335
Primary Topic
Adsorption and biosorption for pollutant removal
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article
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article

Engineered MnO 2 /UiO-66- x Heterostructure with Tailored Interfaces for Efficient Capture of NSAIDs: Performance and Mechanistic Insights

Yunyun Li, Ge Wang, Xiaohui Zeng, Dingyi Zhang
Langmuir
Adsorption and biosorption for pollutant removal
article

Engineered MnO 2 /UiO-66- x Heterostructure with Tailored Interfaces for Efficient Capture of NSAIDs: Performance and Mechanistic Insights

Yunyun Li, Ge Wang, Xiaohui Zeng, Dingyi Zhang
article en

Abstract

The widespread misuse of nonsteroidal anti-inflammatory drugs (NSAIDs) has become a growing concern due to their severe threats to aquatic ecosystems and human health. Current adsorption technologies face limitations including low capacity, poor efficiency for trace-level contaminants, and unclear removal mechanisms. These limitations stem from poorly optimized pore architectures and surface chemistries in existing materials, necessitating the development of multifunctional adsorbents with tailored active sites. Herein, a series of MnO<sub>2</sub>/UiO-66-<i>x</i> composites were rationally designed via a solvothermal approach and comprehensively characterized using powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) spectroscopy, N<sub>2</sub> physisorption, scanning electron microscopy (SEM), and zeta potential analysis. Systematic optimization demonstrated that MnO<sub>2</sub>/UiO-66-1 (5 mg) achieved exceptional adsorption capacity (<i>q</i><sub>max</sub> = 659.49 mg·g<sup>-1</sup>) for diclofenac sodium (DCF, 20 mg·L<sup>-1</sup>, 30 mL), with >90% removal within 10 min (<i>k</i><sub>2</sub> = 0.0081 g·mg<sup>-1</sup>·min<sup>-1</sup>). Mechanistic studies revealed that this performance was attributed to hierarchical porosity (micro-/mesopores), which enables size-selective uptake, synergistic binding, and pH-dependent electrostatic enhancement. Structure-activity relationships indicated that NSAIDs adsorption efficiency (naproxen ≈ ibuprofen ≈ ketoprofen > indomethacin > paracetamol) was governed by molecular structure, size, and p<i>K</i><sub>a</sub> values. Thermodynamic and kinetic studies confirmed a spontaneous (Δ<i>G</i><sup>0</sup> < 0), endothermic (Δ<i>H</i><sup>0</sup> > 0), and entropy-driven (Δ<i>S</i><sup>0</sup> > 0) process dominated by chemisorption through synergistic interactions (including coordination bonding, hydrogen bonding, Lewis acid-base effects, electrostatic attraction, and π-π stacking). This study establishes a new paradigm for metal-organic-framework-based adsorbent design through precise control of metal-organic interfaces and defect engineering. With 87% capacity retention after 5 regeneration cycles, MnO<sub>2</sub>/UiO-66-<i>x</i> shows strong potential for practical water remediation applications.

Langmuir
Yan'an University (CN)
Openalex Percentile: Top 12%
Adsorption and biosorption for pollutant removal
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