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Colorimetric determination of trace orthophosphate in water by using C18-functionalized silica coated magnetite
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by นพพร ม่วงระย้า  
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Colorimetric determination of trace orthophosphate in water by using C18-functionalized silica coated magnetite
Metadata
Document Title
Colorimetric determination of trace orthophosphate in water by using C18-functionalized silica coated magnetite
Author
Phouthavong V., Manakasettharn S., Viboonratanasri D., Buajarern S., Prompinit P., Sereenonchai K.
Name from Authors Collection
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Affiliations
Department of Chemistry, Faculty of Science and Technology, Thammasat University, Pathumthani, 12120, Thailand; Department of Chemistry, Faculty of Natural Sciences, National University of Laos, P. O. Box 7322, Vientiane, Laos; National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency (NSTDA), Thailand Science Park, Pathumthani, 12120, Thailand; Flow Innovation-Research for Science and Technology Laboratories (FIRST Labs), Bangkok, Thailand
Type
Article
Source Title
Scientific Reports
ISSN
20452322
Year
2021
Volume
11
Issue
1
Open Access
Gold, Green
Publisher
Nature Research
DOI
10.1038/s41598-021-02516-4
Abstract
In this study, we customized magnetic sorbents by functionalizing silica coated magnetite with octadecyl(C18)silane (Fe3O4@SiO2@C18). 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@C18 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@C18) yielded an enhancement factor of 32 with a linear range of 1.0–30.0 µg P L−1. Precision at 6.0 µg P L−1 and 25.0 µg P L−1 were 3.70 and 2.49% (RSD, n = 6) respectively. The lower detection limit of 0.3 µg P L−1 and quantification limit of 1.0 µg 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. © 2021, The Author(s).
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
National Science and Technology Development Agency; Thammasat University; National Nanotechnology Center
License
CC BY
Rights
Author
Publication Source
Scopus