Copyright © 2006 Elsevier B.V. All rights reserved.
Determination of phthalates in water samples using polyaniline-based solid-phase microextraction coupled with gas chromatography
Received 19 March 2006;
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Abstract
A simple solid-phase microextraction (SPME) device, coupled with gas chromatography-flame ionization detection (GC-FID), was developed to detect trace levels of phthalates in environmental water samples. Polyaniline (PANI) was chosen as the sorbent for the SPME device and was electrochemically deposited on a stainless steel wire to achieve high thermal and mechanical stability. The porous structure of the PANI film, characterized by scanning electron microscopy (SEM), suggested large extraction capability. Key parameters were optimized and five phthalates were selected to evaluate the SPME-GC procedures. The method was also applied to the analysis of lake and river water samples. Control experiments were carried out using commercial polyacrylate (PA) fiber. The new PANI-SPME-GC method offers high accuracy, precision and sensitivity and low detection limits. Thus, the method developed could be used as a new way to monitor the trace levels of phthalates in water medium. A possible extraction mechanism was investigated using electrochemical impedance spectroscopy (EIS).
Keywords: Solid-phase microextraction; Polyaniline; Phthalates; Gas chromatography; Electrochemical technology
Article Outline
- 1. Introduction
- 2. Experimental
- 2.1. Reagents and standards
- 2.2. Collection of water samples
- 2.3. Instrumentation
- 2.4. Preparation of polyaniline SPME fiber
- 2.5. The SPME-GC analysis
- 3. Results and discussion
- 3.1. Electropolymerization and surface structure of PANI fiber
- 3.2. Stability of PANI-SPME fiber
- 3.3. Possible microextraction mechanism of PANI film
- 3.4. Optimization of SPME procedures
- 3.4.1. Effect of desorption parameters on the GC analysis
- 3.4.2. Effect of extraction time and temperature on the extraction capability
- 3.4.3. Effect of pH values of the water sample on the extraction capability
- 3.4.4. Effect of NaCl addition on the extraction capability
- 3.5. Validation of the method
- 3.6. Analysis of environmental water samples
- 4. Conclusions
- Acknowledgements
- References






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