Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28195
Title: Context sensitive links 1 of 1 fast determination of octinoxate and oxybenzone uv filters in swimming pool waters by gas chromatography/mass spectrometry after solid-phase microextraction
Authors: Kanakaki, C.
Rosenberg, Erwin
Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.
0000-0002-1074-3612
Yılmazcan, Özlem
İzgi, Belgin
AAE-8564-2020
57494368900
8130734000
Keywords: Low-pressure gas chromatography
Mass spectrometry
Octinoxate
Oxybenzone
Solid-phase microextraction
Swimming pool water
Bar sorptive extraction
Ultraviolet filters
Bathing waters
Recent trends
Samples
Benzophenone
Optimization
Configurations
Sunscreens
Chemistry
Endocrine disrupters
Gas chromatography
Lakes
Swimming pools
Uncertainty analysis
Low-pressure gas chromatography
Extraction
Issue Date: Jul-2015
Publisher: Wiley
Citation: Yılmazcan, Ö. vd. (2015). "Context sensitive links 1 of 1 fast determination of octinoxate and oxybenzone uv filters in swimming pool waters by gas chromatography/mass spectrometry after solid-phase microextraction". Journal of Separation Science, 38(13), 2286-2297.
Abstract: A fast gas chromatography/mass spectrometry method was developed and validated for the analysis of the potential endocrine disrupters octinoxate and oxybenzone in swimming pool water samples based on the solvent-free solid-phase microextraction technique. The low-pressure gas chromatography/mass spectrometry method used for the fast identification of UV filter substances was compared to a conventional method in terms of sensitivity and speed. The fast method proposed resulted in 2 min runs, leading to an eightfold decrease in the total analysis time and a sevenfold improvement in detection limits. The main parameters affecting the solid-phase microextraction process were also studied in detail and the optimized conditions were as follows: fiber coating, polyacrylate; extraction mode, direct immersion; extraction temperature, 25 degrees C; sample volume, 5 mL; extraction time 45 min; pH 6.5. Under the optimized conditions, a linear response was obtained in the concentration range of 0.5-25 mu g/L with correlation coefficients in the range 0.990-0.999. The limits of detection were 0.17-0.29 mu g/L, and the recoveries were 80-83%. Combined method uncertainty was assessed and found to be less than 7% for both analytes for concentrations equal to or higher than 5 mu g/L. Pool water samples were analyzed to demonstrate the applicability of the proposed method. Neither octinoxate nor oxybenzone were detected in the swimming pool water samples at concentrations above the respective limits of detection.
URI: https://doi.org/10.1002/jssc.201401250
https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/jssc.201401250
http://hdl.handle.net/11452/28195
ISSN: 1615-9306
1615-9314
Appears in Collections:Web of Science

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