Molecularly imprinted polymers for on-line preconcentration by solid phase extraction of pirimicarb in water samples

被引:99
|
作者
Mena, ML
Martínez-Ruiz, P
Reviejo, AJ
Pingarrón, JM [1 ]
机构
[1] Univ Complutense Madrid, Fac Chem, Dept Analyt Chem, E-28040 Madrid, Spain
[2] Univ Complutense Madrid, Fac Chem, Dept Organ Chem, E-28040 Madrid, Spain
关键词
molecularly imprinted polymers (MIPs); preconcentration; solid phase extraction; pirimicarb;
D O I
10.1016/S0003-2670(01)01421-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The synthesis and performance of a molecularly imprinted polymers (MIPs) as a selective solid phase extraction sorbent for the preconcentration of the carbamate pirimicarb from water samples is described. The MIP was prepared using pirimicarb as the template, methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linking monomer, and using chloroform as the solvent. The detection of pirimicarb was carried out by differential pulse voltammetry (DPV) at a hanging mercury drop electrode (HMDE) in 0.1 mol l(-1) HCl. Solvents of different polarities were checked for the polymer synthesis, and different experimental variables (sample pH, selection of the eluent used, eluent volume, analyte and eluent flow rates and sample volume) associated with the rebinding/extraction process were optimised. For a 25 ml sample, the process took about 13 min and resulted in a nominal enrichment factor of 50 (eluent MeOH:H2O:HAc, 7:2:1; 0.5 ml) for pirimicarb. A limit of detection of 4.1 mug l(-1) was obtained, and a good reproducibility of the measurements using different MIP microcolumns was found. Furthermore, the MIP selectivity was evaluated by checking several substances with similar and different molecular structures to that of pirimicarb. As an application, pirimicarb was determined in water samples of diverse origin which were spiked at a concentration level of 71.5 mug l(-1). (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:297 / 304
页数:8
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