4.7 Article

Development of ion-imprinted polymers for the selective extraction of Cu(II) ions in environmental waters

Journal

TALANTA
Volume 256, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2023.124295

Keywords

Ion-imprinted polymer; Copper; Solid-phase extraction; Environmental water; ICP-MS

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Several ion-imprinted polymers (IIPs) were synthesized for selective extraction of Cu(II) ions. The best IIP exhibited high specificity and good selectivity, with an adsorption capacity of 63 μg g(-1) and an enrichment factor of 24. The method was successfully applied to real samples and Brunauer-Emmett-Teller analysis showed the impact of post-treatment on the porous structure.
Several ion-imprinted polymers (IIPs) were synthesized via bulk polymerization with Cu(II) as template ion, methacrylic acid as functional monomer, ethylene glycol dimethacrylate as crosslinking agent, and azobisisobutyronitrile as initiator in acetonitrile or methanol as porogen solvent. Non-imprinted polymers (NIPs) were similarly synthesized but without Cu(II). After grounding and sieving, the template ions were removed from IIPs particles through several cycles of elimination in 3 M HCl. All NIPs were equally subjected to this acid treatment with the exception of one NIP, called unwashed NIP. The resulting IIP/NIP particles were packed in solid phase extraction (SPE) cartridges for characterization. The SPE protocol was designed by optimizing a washing step following the sample percolation to eliminate potential interfering ions prior to the elution of Cu(II), all fractions analyzed by inductively coupled plasma mass spectrometry. The best IIP showed a high specificity (recovery of Cu(II) vs. interfering ions) and a good selectivity (retention on IIP vs. NIP). Its adsorption capacity was determined to be 63 mu g g(-1). Then, a volume of 50 mL was percolated with 30 mg of IIP, thus giving rise to an enrichment factor of 24. Finally, applications to real samples (mineral and sea waters) were successfully performed. In addition, Brunauer-Emmett-Teller analyses showed that the surface area of the washed NIP was almost double that of the unwashed one (140.70 vs. 74.49 m(2) g(-1)), demonstrating for the first time that the post-treatment of a NIP after its synthesis may have a significant impact on its porous structure, and thus need to be more precisely detailed by authors in the future papers.

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