## Abstract The analysis of samples contaminated by organic compounds is an important aspect of environmental monitoring. Because of the complex nature of these samples, isolating target organic compounds from their matrices is a major challenge. A new isolation technique, solid phase microextracti
Environmental analysis of organic compounds in water using solid phase micro extraction
β Scribed by Arthur, Catherine L. ;Pratt, Katherine ;Motlagh, Safa ;Pawliszyn, Janusz ;Belardi, Robert P.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 419 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0935-6304
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β¦ Synopsis
Abstract
Solid Phase Micro Extraction (SPME) involves exposing a fused silica fiber coated with stationary phase to a contaminated water sample. The organic analytes become partitioned between the stationary phase and the water and when equilibrium is reached the fiber is removed from the solution and the analytes are thermally desorbed in the injector of a gas chromatograph. The fiber is contained in a syringe to facilitate handling.
Factors which affect linear range, limit of detection, and total analysis time are discussed with regard to the development of a method for analysis of volatile compounds in environmental water samples. The sensitivity of the method was determined by the thickness of the film of stationary phase; the equilibration time, however, increased with the film thickness, although it can be minimized by use of a crossβshaped stirrer bar.
Increasing the thickness of stationary phase in the analytical column enables the cryofocusing temperature to be increased from β40 to β15Β°C. With an ion trap mass spectrometer, detection limits required by the US Environmental Protection Agency are met for all compounds except chloromethane and chloroethane. The method has been applied to environmental water samples.
π SIMILAR VOLUMES
In this work, a solid-phase microextraction (SPME) method for the extraction of volatile organic compounds (VOCs) from water samples has been developed. Fifty-five volatile compounds (from the sixty listed in EPA method no. 524.2) were extracted from aqueous solutions using an SPME fiber coated with
A method for simultaneous analysis of fenoxaprop-ethyl and its main metabolite fenoxaprop in drinking water is described. C-18 solid-phase extraction was used for pre-concentration of the analytes. Two different approaches for increasing the retention of the acidic metabolite by reversed-phase solid