Voltammetric determination of ultratrace levels of cerium(III) using a carbon paste electrode modified with nano-sized cerium-imprinted polymer and multiwalled carbon nanotubes
被引:103
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Alizadeh, Taher
[1
]
Ganjali, Mohammad Reza
论文数: 0引用数: 0
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机构:
Univ Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, IranUniv Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, Iran
Ganjali, Mohammad Reza
[1
]
Akhoundian, Maede
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Univ Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, IranUniv Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, Iran
Akhoundian, Maede
[1
]
Norouzi, Parviz
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Univ Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, IranUniv Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, Iran
Norouzi, Parviz
[1
]
机构:
[1] Univ Tehran, Univ Coll Sci, Fac Chem, Dept Analyt Chem, POB 14155-6455, Tehran, Iran
Square wave voltammetry;
Ion imprinted polymer;
Nanomaterial;
Precipitation polymerization;
Scanning electron microscopy;
Zeta potential;
ELECTROCHEMICAL SENSOR;
TRACE DETERMINATION;
D O I:
10.1007/s00604-015-1702-6
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A carbon paste electrode was modified with a Ce(III)-imprinted polymer (Ce-IP) and used for voltammetric determination of Ce(III) ions in real water samples. Precipitation polymerization was used for synthesis of the nano-sized Ce-IP from vinylpyridine and methacrylic acid (acting as the complexing ligands and functional monomers), divinylbenzene (cross-linker) and AIBN as the radical starter. The Ce-IP was characterized by scanning electron microscopy and zeta potentials. A carbon paste electrode (CPE) was then impregnated with the Ce-IP and used for the extraction and subsequent determination of Ce(III). Oxidative square wave voltammetry showed the electrode to give a significantly better response than an electrode modified with the non-imprinted polymer. The addition of multiwalled carbon nanotubes to the Ce-IP-modified electrode further improves the signal, thereby increasing the sensitivity of the method. The effects of electrode composition, extraction pH value, volume and time were optimized. The electrode, if operated at a voltage of 1.05 V (vs. Ag/AgCl), displays a linear response to Ce(III) in the 1.0 mu M to 25 pM concentration range, and the detection limit is 10 pM (at an S/N ratio of 3). The relative standard deviation of 5 separate determinations is 3.1 %. The method was successfully applied to the determination of Ce(III) in the spiked samples of drinking water and sea water.