Selective Solid-Phase Extraction of Zinc(II) from Environmental Water Samples Using Ion Imprinted Activated Carbon

被引:5
|
作者
Moniri, Elham [1 ]
Panahi, Homayon Ahmad [2 ]
Aghdam, Khaledeh [3 ]
Sharif, Amir Abdollah Mehrdad [4 ]
机构
[1] Islamic Azad Univ, Dept Chem, Varamin Pishva Branch, Tehran, Iran
[2] Islamic Azad Univ, Dept Chem, Cent Tehran Branch, Tehran, Iran
[3] Islamic Azad Univ, Fac Marine Sci & Technol, Dept Sea Chem, North Tehran Branch, Tehran, Iran
[4] Islamic Azad Univ, Dept Chem, North Tehran Branch, Tehran, Iran
关键词
AMBERLITE XAD-2; SILICA-GEL; TRACE-ELEMENTS; METAL SORPTION; PRECONCENTRATION; ENRICHMENT; SPECTROMETRY;
D O I
10.5740/jaoacint.11-293
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple ion imprinted amino-functionalized sorbent was synthesized by coupling activated carbon with iminodiacetic acid, a functional compound for metal chelating, through cyanoric chloride spacer. The resulting sorbent has been characterized using FTIR spectroscopy, elemental analysis, and thermogravimetric analysis and evaluated for the preconcentration and determination of trace Zn(II) in environmental water samples. The optimum pH value for sorption of the metal ion was 6-7.5. The sorption capacity of the functionalized sorbent was 66.6 mg/g. The chelating sorbent can be reused for 10 cycles of sorption-desorption without any significant change in sorption capacity. A recovery of 100% was obtained for the metal ion with 0.5 M nitric acid as the eluent. Compared with nonimprinted polymer particles, the prepared Zn-imprinted sorbent showed high adsorption capacity, significant selectivity, and good site accessibility for Zn(II). Scatchard analysis revealed that the homogeneous binding sites were formed in the polymer. The equilibrium sorption data of Zn(II) by modified resin were analyzed by Langmuir, Freundlich, Temkin, and Redlich-Peterson models. Based on equilibrium adsorption data, the Langmuir, Freundlich, and Temkin constants were determined as 0.139, 12.82, and 2.34, respectively, at 25 degrees C.
引用
收藏
页码:206 / 212
页数:7
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