Adsorption and modeling of humic acid by Cu-doped metal-organic framework meta-ZIF-8

This work explores humic acid (HA) removal using ZIF-8, along with Cu doping introduced to boost its adsorption efficiency. The structural properties and morphology of the synthesized ZIF-8 and Cu-ZIF-8 were characterized by FE-SEM, XRD, FTIR spectroscopy, pHpzc, and N 2 adsorption-desorption techniques. The comparative adsorption efficiency by ZIF-8 and Cu-ZIF-8 indicated an ∼8% improvement in HA removal. Based on the model development and optimization, HA adsorption was highest at Cu-ZIF-8 dosage = 0.75 g L -1 , HA concentration: 25 mg L -1 , and pH= 4. Kinetics of adsorption for HA removal obeys the intraparticle diffusion (IPD) model and the Sips isotherm model at equilibrium. The maximum adsorption capacity for Cu-ZIF-8 was 115.4 mg g -1 , which compared favorably to many other adsorbents in the literature. Thermodynamic analysis revealed that HA adsorption onto Cu-ZIF-8 is spontaneous, exothermic, and governed by physisorption. Coexisting ions in real water samples influenced HA adsorption by Cu-ZIF-8, with moderate ionic strength enhancing removal and excessive ionic strength reducing efficiency. The level of metal ions (Zn and Cu) leached from the Cu-ZIF-8 structure was well below drinking water standards. A dramatic decline in adsorption efficiency highlighted the limited adsorbent regenerability, indicating the need for further investigation. Cost analysis showed that Cu-ZIF-8 entails higher synthesis costs than pristine ZIF-8, while both remain economically viable for scale-up. Electrostatic attraction, hydrogen bonding, π–π interactions, and pore entrapment contribute to HA uptake by Cu-ZIF-8, as supported by FTIR spectral and literature results. XRD confirms that Cu-ZIF-8 retains its crystal structure after HA adsorption, indicative of strong stability. • Cu-doped ZIF-8 revealed enhanced humic acid adsorption by versus undoped ZIF-8 • The maximum equilibrium adsorption capacity was 115.4 mg/g based on the Sips model • HA uptake followed IPD kinetics at 0.75 g/L Cu-ZIF-8, 25 mg/L HA, & pH 4 • Adsorption includes pore entrapment, hydrogen, bonding, electrostatic & π–π interactions

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Publication Details

Journal
Materials Chemistry and Physics
Published
2026-01-08
DOI
https://doi.org/10.1016/j.matchemphys.2026.132038
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
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article

Adsorption and modeling of humic acid by Cu-doped metal-organic framework meta-ZIF-8

Elmina Gadirova, Lee D. Wilson, Zohreh Niazi, Mahmoud Y. Shams et al.
Materials Chemistry and Physics
Metal-Organic Frameworks: Synthesis and Applications
article

Adsorption and modeling of humic acid by Cu-doped metal-organic framework meta-ZIF-8

Elmina Gadirova, Lee D. Wilson, Zohreh Niazi, Mahmoud Y. Shams, Osmanova Sabiya Farkhad, Musayeva Sima Arif
article en

Abstract

This work explores humic acid (HA) removal using ZIF-8, along with Cu doping introduced to boost its adsorption efficiency. The structural properties and morphology of the synthesized ZIF-8 and Cu-ZIF-8 were characterized by FE-SEM, XRD, FTIR spectroscopy, pHpzc, and N 2 adsorption-desorption techniques. The comparative adsorption efficiency by ZIF-8 and Cu-ZIF-8 indicated an ∼8% improvement in HA removal. Based on the model development and optimization, HA adsorption was highest at Cu-ZIF-8 dosage = 0.75 g L -1 , HA concentration: 25 mg L -1 , and pH= 4. Kinetics of adsorption for HA removal obeys the intraparticle diffusion (IPD) model and the Sips isotherm model at equilibrium. The maximum adsorption capacity for Cu-ZIF-8 was 115.4 mg g -1 , which compared favorably to many other adsorbents in the literature. Thermodynamic analysis revealed that HA adsorption onto Cu-ZIF-8 is spontaneous, exothermic, and governed by physisorption. Coexisting ions in real water samples influenced HA adsorption by Cu-ZIF-8, with moderate ionic strength enhancing removal and excessive ionic strength reducing efficiency. The level of metal ions (Zn and Cu) leached from the Cu-ZIF-8 structure was well below drinking water standards. A dramatic decline in adsorption efficiency highlighted the limited adsorbent regenerability, indicating the need for further investigation. Cost analysis showed that Cu-ZIF-8 entails higher synthesis costs than pristine ZIF-8, while both remain economically viable for scale-up. Electrostatic attraction, hydrogen bonding, π–π interactions, and pore entrapment contribute to HA uptake by Cu-ZIF-8, as supported by FTIR spectral and literature results. XRD confirms that Cu-ZIF-8 retains its crystal structure after HA adsorption, indicative of strong stability. • Cu-doped ZIF-8 revealed enhanced humic acid adsorption by versus undoped ZIF-8 • The maximum equilibrium adsorption capacity was 115.4 mg/g based on the Sips model • HA uptake followed IPD kinetics at 0.75 g/L Cu-ZIF-8, 25 mg/L HA, & pH 4 • Adsorption includes pore entrapment, hydrogen, bonding, electrostatic & π–π interactions

Materials Chemistry and PhysicsVol. 352
Azerbaijan National Academy of Sciences (AZ), Mashhad University of Medical Sciences (IR), Baku State University (AZ), Azerbaijan Technical University (AZ), University of Saskatchewan (CA), Ferdowsi University of Mashhad (IR)
Clean water and sanitation
Openalex Percentile: Top 94%
Metal-Organic Frameworks: Synthesis and Applications
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