Loading…
Synthesis and application of ion-imprinted polymer for the determination of mercury II in water samples
In this study, an innovative analytical methodology capable of selectively identifying and quantifying mercury contamination by the association of solid-phase extraction using ion-imprinted polymers as a sorbent phase and differential pulse anodic stripping voltammetry is proposed. To this end, the...
Saved in:
Published in: | Environmental science and pollution research international 2019-07, Vol.26 (19), p.19588-19597 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | In this study, an innovative analytical methodology capable of selectively identifying and quantifying mercury contamination by the association of solid-phase extraction using ion-imprinted polymers as a sorbent phase and differential pulse anodic stripping voltammetry is proposed. To this end, the ion-imprinted polymers were synthesized and characterized by infrared spectroscopy and atomic force microscopy. The sorption capacities and the selectivity of the ion-imprinted polymers were compared to the ones related to the non-imprinted ones. Next, the experimental parameters of this solid-phase extraction method (IIP-SPE) were evaluated univariately. The selectivity of this polymeric matrix against other cations (Cd II, Pb II, and Cu II) was also evaluated. Limits of detection (LOD) and quantification (LOQ) obtained for the here proposed methodology were 0.322 μg L
−1
and 1.08 μg L
−1
, respectively. Also, the precision of 4.0% was achieved. The method was finally applied to three water samples from different sources: for the
Piratininga
and
Itaipu
Lagoon waters, Hg II concentrations were below the LOQ and for
Vargem
River waters a concentration equal to 1.35 ± 0.07 mg L
−1
was determined. These results were confirmed by recovery tests, resulting in a recovery of 96.2 ± 4.0%, and by comparison with flame atomic absorption spectrometry, resulting in statistical conformity between the two methods at 95% confidence level. |
---|---|
ISSN: | 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-019-05178-y |