A new strategy for RRS-based determination of phosphate with a bifunctional FeO magnetic nanoparticle surface molecularly imprinted polydopamine probe
In this paper, a magnetic nanoparticle surface molecularly imprinted polydopamine RRS probe Fe 3 O 4 @MIP was prepared using phosphomolybdic acid (PMo) as the template, Fe 3 O 4 magnetic nanoparticles as the substrate and dopamine hydrochloride (PD) as the monomer and crosslinking agent for the dete...
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Published in | Analytical methods Vol. 16; no. 22; pp. 354 - 3514 |
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Main Authors | , , , , |
Format | Journal Article |
Published |
06.06.2024
|
Online Access | Get full text |
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Summary: | In this paper, a magnetic nanoparticle surface molecularly imprinted polydopamine RRS probe Fe
3
O
4
@MIP was prepared using phosphomolybdic acid (PMo) as the template, Fe
3
O
4
magnetic nanoparticles as the substrate and dopamine hydrochloride (PD) as the monomer and crosslinking agent for the determination of PO
4
3−
. Under acidic conditions, phosphomolybdic acid is formed by the reaction of PO
4
3−
with ammonium molybdate (MSA), which can be imprinted with the Fe
3
O
4
@MIP probe surface and reduced to phosphomolybdic blue (PMoB) by ascorbic acid (Aa). Strong resonance Rayleigh scattering energy transfer (RRS-ET) occurs between the probe and PMoB, resulting in a decrease in the RRS signal value. A new, simple and selective RRS method for the determination of PO
4
3−
in water samples was developed. The linear range of this method is 1-22.5 μmol L
−1
, and the detection limit (DL) is 0.49 μmol L
−1
. Furthermore, the magnetic enrichment ability of Fe
3
O
4
@MIP is discussed. Experimental data show that even 0.2 μmol L
−1
of phosphate can be detected within a 20% error range.
In this paper, a magnetic nanoparticle surface molecularly imprinted polydopamine RRS probe Fe
3
O
4
@MIP was prepared using phosphomolybdic acid (PMo) as the template, Fe
3
O
4
magnetic nanoparticles as the substrate and dopamine hydrochloride (PD) as the monomer and crosslinking agent for the determination of PO
4
3−
. |
---|---|
Bibliography: | https://doi.org/10.1039/d4ay00035h Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1759-9660 1759-9679 |
DOI: | 10.1039/d4ay00035h |