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Analysis of aqueous pyrethroid residuals by one-step microwave-assisted headspace solid-phase microextraction and gas
Hong-Ping Li1, Chiu-Hua Lin, Jen-Fon Jen
1Residue Control Division, Taiwan Agricultural Chemicals and Toxic Substances Research Institute, Council of Agriculture, Wu-Fong, Taichung County 413, Taiwan. hplee@tactri.gov.tw
Abstract:
A one-step microwave-assisted headspace solid-phase microextraction (MA-HS-SPME) has been applied to be a pretreatment step in the analysis of aqueous pyrethroid residuals by gas chromatography (GC) with electron capture detection (ECD). Microwave heating was applied to accelerate the vaporization of pyrethroids (bioallenthrin, bifenthrin, fenpropathrin, cyhalothrin, permethrin, cyfluthrin, cypermethrin, fluvalinate, fenvalerate and deltamethrin) into the headspace, and then being absorbed directly on a SPME fiber under the controlled conditions. Optimal conditions for the SPME sampling, such as the selection of sampling fiber, sample pH, sampling temperature and time, microwave irradiation power, desorption temperature and time were investigated and then applied to real sample analysis. Experimental results indicated that the extraction of pyrethroids from a 20-mL aquatic sample (pH 4.0) was achieved with the best efficiency through the use of a 100-microm PDMS fiber, microwave irradiation of 157 W and sampling at 30 degrees C for 10 min. Under optimum conditions, the detections were linear in the range of 0.05-0.5 microg/L with the square of correlation coefficients (R(2)) of >0.9913 for pyrethroids except bifenthrin being 0.9812. Method detection limits (MDL) were found to be varied from 0.2 to 2.6 ng/L for different pyrethroids based on S/N (signal to noise)=3. The coefficients of variation (CVs) for repeatability were 7-21%. A field underground water sample was analyzed with recovery between 88.5% to 115.5%. This method was proven to be a very simple, rapid, and solvent-free process to achieve the sample pretreatment before the analysis of trace pyrethroids in aqueous samples by gas chromatography.
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