Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry

In this study a determination method has been developed for seven different micropollutants, that were selected to represent different compound groups. The selected compounds were: 4-nonylphenol (4-NP), 4-octylphenol (4-OP), anthracene (Ant), alachlor (Ac), heptachlor (Hc), heptachlor epoxide (Hce),...

Full description

Bibliographic Details
Main Authors: Marek Król, Mariusz Dudziak
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Proceedings
Subjects:
Online Access:https://www.mdpi.com/2504-3900/16/1/57
id doaj-ffd19ead3d8c4c009e832d7df16b19a2
record_format Article
spelling doaj-ffd19ead3d8c4c009e832d7df16b19a22020-11-24T20:48:10ZengMDPI AGProceedings2504-39002019-08-011615710.3390/proceedings2019016057proceedings2019016057Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass SpectrometryMarek Król0Mariusz Dudziak1Dempol-Eco, ul. Składowa 9, 45-125 Opole, PolandSilesian University of Technology, Faculty of Energy and Environmental Engineering, Institute of Water and Wastewater Engineering, ul. Konarskiego 18, 44-100 Gliwice, PolandIn this study a determination method has been developed for seven different micropollutants, that were selected to represent different compound groups. The selected compounds were: 4-nonylphenol (4-NP), 4-octylphenol (4-OP), anthracene (Ant), alachlor (Ac), heptachlor (Hc), heptachlor epoxide (Hce), and bis(2-ethylhexyl)phthalate (DEHP). Chromatographic separation and mass spectrometer detection conditions were optimized to achieve the best micropollutants separation and the best detection sensitivity. A calibration curves were created at different calibration levels suited of each type of detection mode (Full Scan and Selected Ion Monitoring) and limits of detection (LOD) and limits of quantification (LOQ) were calculated. Furthermore, recovery values were determined for each compound in spiked water samples at levels equal to 10%, 50%, and 90% of the calibration curve range and compared to other studies in which similar methods of determination were used.https://www.mdpi.com/2504-3900/16/1/57micropollutantsgas chromatographymass spectrometrylimits of detectionlimits of quantificationdetermination method
collection DOAJ
language English
format Article
sources DOAJ
author Marek Król
Mariusz Dudziak
spellingShingle Marek Król
Mariusz Dudziak
Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
Proceedings
micropollutants
gas chromatography
mass spectrometry
limits of detection
limits of quantification
determination method
author_facet Marek Król
Mariusz Dudziak
author_sort Marek Król
title Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
title_short Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
title_full Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
title_fullStr Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
title_full_unstemmed Determination of Organic Micropollutants in Water Using Gas Chromatography-Mass Spectrometry
title_sort determination of organic micropollutants in water using gas chromatography-mass spectrometry
publisher MDPI AG
series Proceedings
issn 2504-3900
publishDate 2019-08-01
description In this study a determination method has been developed for seven different micropollutants, that were selected to represent different compound groups. The selected compounds were: 4-nonylphenol (4-NP), 4-octylphenol (4-OP), anthracene (Ant), alachlor (Ac), heptachlor (Hc), heptachlor epoxide (Hce), and bis(2-ethylhexyl)phthalate (DEHP). Chromatographic separation and mass spectrometer detection conditions were optimized to achieve the best micropollutants separation and the best detection sensitivity. A calibration curves were created at different calibration levels suited of each type of detection mode (Full Scan and Selected Ion Monitoring) and limits of detection (LOD) and limits of quantification (LOQ) were calculated. Furthermore, recovery values were determined for each compound in spiked water samples at levels equal to 10%, 50%, and 90% of the calibration curve range and compared to other studies in which similar methods of determination were used.
topic micropollutants
gas chromatography
mass spectrometry
limits of detection
limits of quantification
determination method
url https://www.mdpi.com/2504-3900/16/1/57
work_keys_str_mv AT marekkrol determinationoforganicmicropollutantsinwaterusinggaschromatographymassspectrometry
AT mariuszdudziak determinationoforganicmicropollutantsinwaterusinggaschromatographymassspectrometry
_version_ 1716808690963578880