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Colorimetric determination of trace orthophosphate in water by using C-18-functionalized silica coated magnetite
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Metadata
Document Title
Colorimetric determination of trace orthophosphate in water by using C-18-functionalized silica coated magnetite
Author
Phouthavong V, Manakasettharn S, Viboonratanasri D, Buajarern S, Prompinit P, Sereenonchai K
Name from Authors Collection
Affiliations
Thammasat University; National Science & Technology Development Agency - Thailand; National Nanotechnology Center (NANOTEC)
Type
Article
Source Title
SCIENTIFIC REPORTS
ISSN
2045-2322
Year
2021
Volume
11
Issue
1
Page
-
Open Access
gold, Green Published
Publisher
NATURE PORTFOLIO
DOI
10.1038/s41598-021-02516-4
Format
Abstract
In this study, we customized magnetic sorbents by functionalizing silica coated magnetite with octadecyl(C-18)silane (Fe3O4@SiO2@C-18). This sorbent was intended for the determination of trace orthophosphate (o-PO43-) in unpolluted freshwater samples. The o-PO43- was transformed to phosphomolybdenum blue (PMB), a known polyoxometalate ion. Then the PMB were coupled with cetyl trimethyl ammonium bromide (CTAB), cationic surfactant, in order to hydrophobically bound with the Fe3O4@SiO2@C-18 particles through dispersive magnetic solid-phase extraction (d-MSPE) as part of sample preconcentration. The PMB-CTAB-magnetic particles are simply separated from the aqueous solution by the external magnet. The acidified ethanol 0.5 mL was used as PMB-CTAB eluent to produce an intense blue solution, which the absorbance was measured using a UV-Vis spectrophotometer at 800 nm. The proposed method (employing 2 mg of Fe3O4@SiO2@C-18) yielded an enhancement factor of 32 with a linear range of 1.0-30.0 mu g P L-1. Precision at 6.0 mu g P L-1 and 25.0 mu g P L-1 were 3.70 and 2.49% (RSD, n = 6) respectively. The lower detection limit of 0.3 mu g P L-1 and quantification limit of 1.0 mu g P L-1 allowed trace levels analysis of o-PO43- in samples. The reliability and accuracy of the proposed method were confirmed by using a certified reference material. Our method offers highly sensitive detection of o-PO43- with simple procedures that can be operated at room temperature and short analysis time.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Funding Sponsor
Thailand National Nanotechnology center (NANOTEC), NSTDA [P 1450172 ., P 1750205]; Thammasat University Research Fund [SciGR18/2563]
Publication Source
WOS