Nanopowder synthesis of novel Sn(II)-imprinted poly(dimethyl vinylphosphonate) by ultrasound-assisted technique: Adsorption and pre-concentration of Sn(II) from aqueous media and real samples
•A novel Sn(II)-imprinted poly(dimethyl vinylphosphonate) nanopowder was prepared.•The formation of Sn(II)-IPDMVPN was confirmed by FT-IR, 1H NMR and 31P NMR.•Favorable results were obtained for adsorption of Sn(II) from aqueous media.•The maximum recovery was obtained by 1 M HNO3. In this research,...
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Veröffentlicht in: | Ultrasonics sonochemistry 2018-06, Vol.44, p.129-136 |
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Sprache: | eng |
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Zusammenfassung: | •A novel Sn(II)-imprinted poly(dimethyl vinylphosphonate) nanopowder was prepared.•The formation of Sn(II)-IPDMVPN was confirmed by FT-IR, 1H NMR and 31P NMR.•Favorable results were obtained for adsorption of Sn(II) from aqueous media.•The maximum recovery was obtained by 1 M HNO3.
In this research, a novel Sn(II)-imprinted poly(dimethyl vinylphosphonate) nanopowder (Sn(II)-IPDMVPN) was prepared using Sn2+, dimethyl vinylphosphonate, azobis isobutyronitril and ethylene glycol dimethacrylate as the template, ligand, initiator and cross linker, respectively. The non-imprinted poly(dimethyl vinylphosphonate) nanopowder (NIPDMVPN) was also synthesized utilizing the same procedure without using SnCl2·2H2O in order to compare the results with the Sn(II)-IPDMVPN. The structure, morphology and composition of the products were characterized by XRD, SEM, EDX, XRF, BET, FT-IR and NMR techniques. Some experimental conditions including pH, eluent concentration and sample volume were optimized to maximize Sn(II) adsorption by the Sn(II)-IPDMVPN. It was found that the optimum conditions are pH = 5, 1.00 M of HNO3 as eluent and sample volume up to 50 mL. The results obtained by ICP-MS indicated that the Sn(II)-IPDMVPN had much higher adsorption capacity for Sn(II) ions (about threefold) than the NIPDMVPN. The applicability of the Sn(II)-IPDMVPN was also investigated in three different real samples. Under the best experimental conditions, the calibration graphs were linear in the range of 0.19–90 μg L−1 with a coefficient of determination (R2) of 0.990. The detection limit was calculated to be 0.06 μg L−1. The relative standard deviation (RSD) for six replicate measurements of Sn(II) at 1.00 ng mL−1 was determined to be 1.8%. The results showed that the Sn(II)-IPDMVPN-ICP-MS is a very simple, rapid, sensitive and efficient method for the determination of Sn(II) ions in water samples. |
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ISSN: | 1350-4177 1873-2828 |
DOI: | 10.1016/j.ultsonch.2018.02.019 |