Determination of trace silver by solid substrate-room temperature phosphorescence quenching method based on double catalytic system of meta-nitrophenyfluorone-polyoxyethylene-chromium-potassium bromate-β-cyclodextrin
A new solid substrate-room temperature phosphorescence (SS-RTP) quenching method for the determination of trace silver has been established. It is based on the fact that when using Mg 2+ as ion perturber and β-CD as surfactant, the system of meta-nitrophenyfluorone (R)-polyoxyethylene-Cr(III) can em...
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Veröffentlicht in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2006-09, Vol.65 (1), p.106-112 |
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Sprache: | eng |
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Zusammenfassung: | A new solid substrate-room temperature phosphorescence (SS-RTP) quenching method for the determination of trace silver has been established. It is based on the fact that when using Mg
2+ as ion perturber and β-CD as surfactant, the system of
meta-nitrophenyfluorone (R)-polyoxyethylene-Cr(III) can emit strong and stable room temperature phosphorescence signal on filter paper whose surface is modified by polyvinyl alcohol (PVA)-H
3BO
3-NaOH. Ag(I) can catalyze KBrO
3 oxidizing R-PEO-Cr(III) system which causes the quenching of SS-RTP. The reducing value of phosphorescence intensity (Δ
I
p) is directly proportional to the concentration of Ag(I) in the range of 3.2–160
ag
spot
−1 (corresponding concentration: 2.43
fg
ml
−1, the sample volume: 0.40
μl
spot
−1) with a detection limit (LD) of 0.97
ag
spot
−1. The regression equation of working curve can be expressed as Δ
I
p
=
13.92
+
0.3089
m
A
g
+
(ag
spot
−1) (
r
=
0.9983,
n
=
6). This method has many advantages, such as a wide linear dynamic range, high sensitivity, good repeatability and selectivity. It has been applied to the determination of trace silver in real samples with satisfactory results. What is more, the mechanism of SS-RTP quenching method based on Ag(I) catalyzing KBrO
3 oxidizing
meta-nitrophenyfluorone has also been discussed. |
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ISSN: | 1386-1425 |
DOI: | 10.1016/j.saa.2005.09.041 |