Trace Analysis of Xylene in Occupational Exposures Monitoring

Background: Determination of organic pollutants usually requires extraction of the pollutants from samples, using hazard­ous solvent. Solid phase micro-extraction (SPME) is a solvent-free equilibrium extraction method, in which, proper calibra­tion can allow quantitative measurements of organic poll...

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Main Authors: HR Heidari, SJ Shahtaheri, M Alimohammadi, A Rahimi-Froshani
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2009-03-01
Series:Iranian Journal of Public Health
Subjects:
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/3216
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spelling doaj-b2e6f3facaa749ad8e698c88c639690f2020-12-02T18:55:52ZengTehran University of Medical SciencesIranian Journal of Public Health2251-60852251-60932009-03-01381Trace Analysis of Xylene in Occupational Exposures Monitoring HR Heidari0SJ Shahtaheri 1M Alimohammadi 2A Rahimi-Froshani 3Dept. of Occupational HealthDept. of Occupational Health, Center for Environmental ResearchDept .of Environmental HealthDept. of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical ScienBackground: Determination of organic pollutants usually requires extraction of the pollutants from samples, using hazard­ous solvent. Solid phase micro-extraction (SPME) is a solvent-free equilibrium extraction method, in which, proper calibra­tion can allow quantitative measurements of organic pollutants at a very good sensitivity without the use of any organic sol­vent. Because individual VOCs are generally present in urine only at trace levels, a sensitive and accurate determination technique is essential. Methods: This study describes the optimization of headspace solid phase micro-extraction (HS-SPME) followed by gas chromatography equipped with flame ionization detector (GC-FID) for xylene in spiked urine. Through this investigation, the parameters affecting the extraction and GC determination of xylene, including extraction time, temperature, desorption temperature, desorption time, salt addition, sample pH, sample volume and sample agitation were studied. Results: An op­timized headspace extraction was carried out at 30°C for 6 min in presence of 0.2 gml-1 of NaCl in the sample solution. De­sorption of the xylene was carried out for 60 sec. at 250°C. The optimized procedure was also validated with three different pools of spiked urine samples and showed a good reproducibility over six consecutive days as well as six within-day ex­periments. In this study, the accuracy, linearity, and detection limits were also determined. Conclusion: The HS-SPME-GC-FID technique provided a relatively simple, convenient, practical procedure, which can be successfully applied for determination of xylene in spiked urine when an occupational exposure monitoring is required. https://ijph.tums.ac.ir/index.php/ijph/article/view/3216HeadspaceSolid phase microextractionGas chromatographyXylene
collection DOAJ
language English
format Article
sources DOAJ
author HR Heidari
SJ Shahtaheri
M Alimohammadi
A Rahimi-Froshani
spellingShingle HR Heidari
SJ Shahtaheri
M Alimohammadi
A Rahimi-Froshani
Trace Analysis of Xylene in Occupational Exposures Monitoring
Iranian Journal of Public Health
Headspace
Solid phase microextraction
Gas chromatography
Xylene
author_facet HR Heidari
SJ Shahtaheri
M Alimohammadi
A Rahimi-Froshani
author_sort HR Heidari
title Trace Analysis of Xylene in Occupational Exposures Monitoring
title_short Trace Analysis of Xylene in Occupational Exposures Monitoring
title_full Trace Analysis of Xylene in Occupational Exposures Monitoring
title_fullStr Trace Analysis of Xylene in Occupational Exposures Monitoring
title_full_unstemmed Trace Analysis of Xylene in Occupational Exposures Monitoring
title_sort trace analysis of xylene in occupational exposures monitoring
publisher Tehran University of Medical Sciences
series Iranian Journal of Public Health
issn 2251-6085
2251-6093
publishDate 2009-03-01
description Background: Determination of organic pollutants usually requires extraction of the pollutants from samples, using hazard­ous solvent. Solid phase micro-extraction (SPME) is a solvent-free equilibrium extraction method, in which, proper calibra­tion can allow quantitative measurements of organic pollutants at a very good sensitivity without the use of any organic sol­vent. Because individual VOCs are generally present in urine only at trace levels, a sensitive and accurate determination technique is essential. Methods: This study describes the optimization of headspace solid phase micro-extraction (HS-SPME) followed by gas chromatography equipped with flame ionization detector (GC-FID) for xylene in spiked urine. Through this investigation, the parameters affecting the extraction and GC determination of xylene, including extraction time, temperature, desorption temperature, desorption time, salt addition, sample pH, sample volume and sample agitation were studied. Results: An op­timized headspace extraction was carried out at 30°C for 6 min in presence of 0.2 gml-1 of NaCl in the sample solution. De­sorption of the xylene was carried out for 60 sec. at 250°C. The optimized procedure was also validated with three different pools of spiked urine samples and showed a good reproducibility over six consecutive days as well as six within-day ex­periments. In this study, the accuracy, linearity, and detection limits were also determined. Conclusion: The HS-SPME-GC-FID technique provided a relatively simple, convenient, practical procedure, which can be successfully applied for determination of xylene in spiked urine when an occupational exposure monitoring is required.
topic Headspace
Solid phase microextraction
Gas chromatography
Xylene
url https://ijph.tums.ac.ir/index.php/ijph/article/view/3216
work_keys_str_mv AT hrheidari traceanalysisofxyleneinoccupationalexposuresmonitoring
AT sjshahtaheri traceanalysisofxyleneinoccupationalexposuresmonitoring
AT malimohammadi traceanalysisofxyleneinoccupationalexposuresmonitoring
AT arahimifroshani traceanalysisofxyleneinoccupationalexposuresmonitoring
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