Development of liquid phase microextraction method based on solidification of floated organic drop for extraction and preconcentration of organochlorine pesticides in water samples
Creators
- 1. Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)
- 2. Department of Chemistry, Faculty of Sciences, Islamic Azad University, Rasht Branch, Rasht (Iran, Islamic Republic of)
- 3. Department of Water Quality Control and Laboratories, Tehran Water and Sewerage Company, Tehran (Iran, Islamic Republic of)
Description
A simple and efficient liquid-phase microextraction (LPME) in conjunction with gas chromatography-electron capture detector (GC-ECD) has been developed for extraction and determination of 11 organochlorine pesticides (OCPs) from water samples. In this technique a microdrop of 1-dodecanol containing pentachloronitrobenzene (internal standard) is delivered to the surface of an aqueous sample while being agitated by a stirring bar in the bulk of solution. Following completion of extraction, the sample vial was cooled by putting it into an ice bath for 5 min. Finally 2 μL of the drop was injected into the GC for analysis. Factors relevant to the extraction efficiency were studied and optimized. Under the optimized extraction conditions (extraction solvent: 1-dodecanol; extraction temperature: 65 deg. C; sodium chloride concentration: 0.25 M; microdrop and sample volumes: 8 μL and 20 mL respectively; the stirring rate: 750 rpm and the extraction time: 30 min), figures of merit of the proposed method were evaluated. The detection limits of the method were in the range of 7-19 ng L-1 and the RSD% for analysis of 2 μg L-1 of OCPs was below 7.2% (n = 5). A good linearity (r2 ≥ 0.993) and a relatively broad dynamic linear range (25-2000 ng L-1) were obtained. After 30 min of extraction, preconcentration factors were in the range of 708-1337 for different organochlorine pesticides and the relative errors ranged from -10.1 to 10.9%. Finally the proposed method was successfully utilized for preconcentration and determination of OCPs in different real samples
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aca.2008.08.001Additional details
Identifiers
- DOI
- 10.1016/j.aca.2008.08.001;
- PII
- S0003-2670(08)01420-7;
Publishing Information
- Journal Title
- Analytica Chimica Acta
- Journal Volume
- 626
- Journal Issue
- 2
- Journal Page Range
- p. 166-173
- ISSN
- 0003-2670
- CODEN
- ACACAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40011561
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ELECTRON-CAPTURE DETECTORS; GAS CHROMATOGRAPHY; ORGANIC CHLORINE COMPOUNDS; PESTICIDES; SENSITIVITY; SOLIDIFICATION; SOLVENT EXTRACTION; STANDARDS
- Descriptors DEC
- CHROMATOGRAPHY; EXTRACTION; MEASURING INSTRUMENTS; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; PHASE TRANSFORMATIONS; RADIOMETRIC GAGES; SEPARATION PROCESSES
Optional Information
- Copyright
- Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.