Poly(methyl methacrylate)-modified cellulose fibers patterned with highly selective chromogenic reagent for rapid and trace determination of Co 2+ in water
A simple one-step assay for the trace determination of Co 2+ was developed on filter paper modified with solubilized polymethyl methacrylate (PMMA) and arrays of 3-[(2-mercapto-vinyl)-hydrazono]-1,3-dihydro-indol-2-one (MHDI) reagent. The paper modified with a thin film of PMMA transformed its surfa...
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Veröffentlicht in: | Analytical methods 2018, Vol.10 (36), p.4454-4462 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A simple one-step assay for the trace determination of Co
2+
was developed on filter paper modified with solubilized polymethyl methacrylate (PMMA) and arrays of 3-[(2-mercapto-vinyl)-hydrazono]-1,3-dihydro-indol-2-one (MHDI) reagent. The paper modified with a thin film of PMMA transformed its surface wettability from hydrophilic (
θ
∼ 0°) to hydrophobic (
θ
∼ 92°). Goniometry and scanning electron microscopy confirmed modification of cellulose fibers. On a low-wetting surface, analyte droplet could be confined onto the MHDI spot, allowing visual detection of 1 μM concentration of Co
2+
within 10 min. The limit of detection (LOD) was three orders of magnitude superior to that of a similar assay executed on unmodified paper. The established method is the first of its kind for Co
2+
determination with a wide linear dynamic range (10
1
to 10
4
μM) coupled with good reproducibility, ruggedness and point-of-use testing. Due to high selectivity towards Co
2+
and minimum interference from diverse ions, the developed probe was successfully applied for the trace analysis of Co
2+
in tap and industrial wastewater samples. The established method was successfully validated using ICP-OES analysis. The proposed assay could be compared favorably to most of the reported methods for Co
2+
determination in terms of ease, cost-effectiveness and analysis time. The recoveries from the recognized method were >90%, confirming its potential use for sensing Co
2+
. |
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ISSN: | 1759-9660 1759-9679 |
DOI: | 10.1039/C8AY01746H |