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

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-imprin...

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Published inTalanta (Oxford) Vol. 256; p. 124295
Main Authors Cao, Pengchao, Pichon, Valérie, Dreanno, Catherine, Boukerma, Kada, Delaunay, Nathalie
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.05.2023
Elsevier
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Summary: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 μg 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 m2 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. [Display omitted] •Benefit of extending the complexation time between template ion and ligands.•First study to date on the effect of acid treatment on NIP.•Fine optimization of the washing step of the SPE protocol.•Remarkable specificity towards Cu(II) with respect to interfering ions.•Determination of Cu(II) at trace levels in environmental waters.
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ISSN:0039-9140
1873-3573
DOI:10.1016/j.talanta.2023.124295