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Simultaneous application of cloud point and solid-phase extraction for determination of Fe(III) and Cu(II) ions by using SnO2 nanopowder in micellar medium
被引:17
作者:
Nekouei, Shahram
[1
]
Nekouei, Farzin
[1
]
Ulusoy, Halil Ibrahim
[2
]
Noorizadeh, Hossein
[3
]
机构:
[1] Islamic Azad Univ, Sci & Res Branch, Young Researchers & Elite Club, Tehran, Iran
[2] Cumhuriyet Univ, Fac Pharm, Dept Analyt Chem, Sivas, Turkey
[3] Islamic Azad Univ, Dept Chem, Shiraz Branch, Shiraz, Iran
关键词:
Solid-phase extraction;
Cloud point extraction;
Fe(III);
Cu(II);
SnO2;
nanopowder;
Water samples;
Flame atomic absorption spectrometry;
WALLED CARBON NANOTUBES;
POLYCYCLIC AROMATIC-HYDROCARBONS;
ATOMIC-ABSORPTION-SPECTROMETRY;
TIO2;
NANOTUBES;
MICROEXTRACTION;
PRECONCENTRATION;
WATER;
SAMPLES;
NANOPARTICLES;
PERFORMANCE;
D O I:
10.1080/19443994.2015.1054888
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
A new approach was developed for sensitive determination of Fe(III) and Cu(II) ions using SnO2 nanopowder in the micellar medium on the contrary conventional cloud point extraction studies. The presented method contains a combination of solid-phase extraction and cloud point extraction. According to this procedure, the metal ions were firstly retained on modified SnO2 nanopowder and then passed to the surfactant-rich phase. The effect of experimental variables including pH, concentration of reagents, eluting solution, incubation time, equilibration temperature, sample volume, and effects of interfering ions have been investigated and optimized systematically. The calibration graphs were linear in the range of 0.23-100.00g L-1 and 0.30-110.00g L-1 for Fe(III) and Cu(II), respectively. Under optimized conditions, the limits of detections were 0.07 and 0.09g L-1 for Fe(III) and 0.09g L-1 for Cu(II). The proposed method offers satisfactory analytical features by means of combining two different and efficient preconcentration techniques. In addition, the method can be evaluated as an alternative and fast method according to only-surfactant-mediated extractions. The validation of method was carried out by recovery tests and certified reference material (CRM) analysis. The acceptable and compatible results were obtained in the analysis of CRM and real samples.
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页码:12653 / 12662
页数:10
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