AI Article Synopsis

  • A novel calcium-based metal-organic framework (CaMOF@LSB) was created to selectively detect and remove Cu ions from water, showing stability across different solvents and pH levels.
  • It achieved impressive colorimetric detection and an adsorption capacity of 484.2 mg/g, along with effective endothermic and spontaneous Cu ion adsorption behavior.
  • The framework can be regenerated easily for repeated use, maintaining a good adsorption capacity over multiple cycles, highlighting its potential for addressing heavy metal pollution and applications in water purification.

Article Abstract

A novel calcium-based metal-organic framework (CaMOF@LSB) was designed and synthesized, exhibiting dual functionality for both selective detection and removal of Cu ions from aqueous solutions. The framework's stability, including solvent and pH variations, was established with notable thermal resilience. Colorimetric Cu detection (≥5 ppm) with a high capture capacity of 484.2 mg g by CaMOF@LSB places this material among the few that ensure efficient colorimetric detection and high removal capabilities of Cu ions. Batch adsorption experiments revealed pH-dependent behavior and competitive interactions. Langmuir and pseudo-second-order kinetics models aptly described adsorption isotherms and kinetics, respectively. Thermodynamic assessments confirmed spontaneous and endothermic adsorption. Mechanistically, nanoparticle deposition contributes to the Cu uptake. CaMOF@LSB also exhibited one of the best removal behaviour of Cu by means of oxide formation on the surface. Regeneration of CaMOF@LSB was achieved by simple sonication in 0.1 M aqueous NaOH solution. The recyclability was also tested up to 5 cycles, and it exhibited a small decrease in adsorption capacity observed across the cycles. This research presents a promising avenue for addressing heavy metal pollution using metal-organic frameworks, thereby offering potential applications in water purification and environmental pollution monitoring and remediation.

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Source
http://dx.doi.org/10.1002/chem.202400587DOI Listing

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