Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry

BackgroundPrevious research on chlorinated paraffins (CPs) in fine particulate matter (PM2.5) has predominantly focused on short- and medium-chain chlorinated paraffins (SCCPs and MCCPs), and few studies could simultaneously determine short-, medium-, and long-chain chlorinated paraffins (LCCPs). Si...

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Main Authors: Wenyan YAN, Chao WANG, Juan LIU, Yibin SUN, Wen GU, Yifu LU, Ke FANG, Yi WAN, Song TANG
Format: Article
Language:English
Published: Editorial Committee of Journal of Environmental and Occupational Medicine 2024-10-01
Series:环境与职业医学
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Online Access:http://www.jeom.org/article/cn/10.11836/JEOM24156
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author Wenyan YAN
Chao WANG
Juan LIU
Yibin SUN
Wen GU
Yifu LU
Ke FANG
Yi WAN
Song TANG
author_facet Wenyan YAN
Chao WANG
Juan LIU
Yibin SUN
Wen GU
Yifu LU
Ke FANG
Yi WAN
Song TANG
author_sort Wenyan YAN
collection DOAJ
description BackgroundPrevious research on chlorinated paraffins (CPs) in fine particulate matter (PM2.5) has predominantly focused on short- and medium-chain chlorinated paraffins (SCCPs and MCCPs), and few studies could simultaneously determine short-, medium-, and long-chain chlorinated paraffins (LCCPs). Simultaneous extraction and determination of SCCPs, MCCPs, and LCCPs in PM2.5 could provide technical support for their environmental monitoring and human health risk assessment.ObjectiveTo establish a method based on QUEChERS pretreatment method in conjunction with ultra-performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry for simultaneously determining the levels of SCCPs, MCCPs, and LCCPs in PM2.5. MethodsThe extraction solvents, extraction salts, and extraction steps of a QuEChERS method were optimized. The extraction efficiencies of the target substances were compared under 4 extraction solvents [acetonitrile, dichloromethane, and n-hexane solvents in sequence; acetonitrile: dichloromethane: n-hexane = 1: 1: 2 (v/v/v) mixed solvent; 1% acetic acid-acetonitrile: dichloromethane: n-hexane = 1: 1: 1 (v/v/v) mixed solvent; acetonitrile: dichloromethane: n-hexane = 1: 1: 1 (v/v/v) mixed solvent], 2 dehydrated salts (anhydrous MgSO4+NaCl and anhydrous Na2SO4+NaCl), 2 purification salts (C18 and PSA), and 4 vortex time (5, 7.5, 10, and 12.5 min) conditions. Then internal standard was utilized to estimate linear range and detection limit of the refined QuEChERS approach. ResultsThe linearities of SCCPs, MCCPs, and LCCPs were good in the range of 10~1000 ng·mL−1 with the correlation coefficients all greater than 0.96. The method detection limits (MDLs) ranged from 0.01 to 0.29 ng·m−3. The spiked recoveries of SCCPs, MCCPs, and LCCPs at the low, medium, and high concentrations were 77.38%-81.64%, 93.11%-99.78%, and 87.41%-101.39%, respectively, and the relative standard deviations (RSDs) were 2.90%-12.84%. This method was used to determine the CPs levels in 11 PM2.5 samples from Shijiazhuang. The positive rates of ∑SCCPs, ∑MCCPs, and ∑LCCPs were all 100%, the concentration ranges were 0.24-2.18 ng·m−3 (mean 0.84 ng·m−3), 0.17-1.67 ng·m−3 (mean 0.70 ng·m−3), and 0.01-0.16 ng·m−3 (mean 0.04 ng·m−3), respectively, and the percentages to ΣCPs were 52.95%, 44.39%, and 2.66%, respectively. ConclusionThe method established in this study is simple, time-saving, solvent saving, and can simultaneously detect SCCPs, MCCPs, and LCCPs in PM2.5, which is suitable for the determination of PM2.5 samples in large quantities, and can also provide a reference for the detection methods of other halogenated organic compounds in PM2.5.
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spelling doaj-art-5712d7ea7214412aa7e7a91d0f53e7c02025-08-20T02:14:19ZengEditorial Committee of Journal of Environmental and Occupational Medicine环境与职业医学2095-99822024-10-0141101087109410.11836/JEOM2415624156Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometryWenyan YAN0Chao WANG1Juan LIU2Yibin SUN3Wen GU4Yifu LU5Ke FANG6Yi WAN7Song TANG8Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 211166, ChinaChina CDC Key Laboratory of Environment and Population Health/ National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing 100021, ChinaChina CDC Key Laboratory of Environment and Population Health/ National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing 100021, ChinaCollege of Urban and Environmental Sciences, Peking University, Beijing 100871, ChinaChina CDC Key Laboratory of Environment and Population Health/ National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing 100021, ChinaChina CDC Key Laboratory of Environment and Population Health/ National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing 100021, ChinaChina CDC Key Laboratory of Environment and Population Health/ National Institute of Environmental Health, Chinese Center for Disease Control and Prevention, Beijing 100021, ChinaCollege of Urban and Environmental Sciences, Peking University, Beijing 100871, ChinaCenter for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 211166, ChinaBackgroundPrevious research on chlorinated paraffins (CPs) in fine particulate matter (PM2.5) has predominantly focused on short- and medium-chain chlorinated paraffins (SCCPs and MCCPs), and few studies could simultaneously determine short-, medium-, and long-chain chlorinated paraffins (LCCPs). Simultaneous extraction and determination of SCCPs, MCCPs, and LCCPs in PM2.5 could provide technical support for their environmental monitoring and human health risk assessment.ObjectiveTo establish a method based on QUEChERS pretreatment method in conjunction with ultra-performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry for simultaneously determining the levels of SCCPs, MCCPs, and LCCPs in PM2.5. MethodsThe extraction solvents, extraction salts, and extraction steps of a QuEChERS method were optimized. The extraction efficiencies of the target substances were compared under 4 extraction solvents [acetonitrile, dichloromethane, and n-hexane solvents in sequence; acetonitrile: dichloromethane: n-hexane = 1: 1: 2 (v/v/v) mixed solvent; 1% acetic acid-acetonitrile: dichloromethane: n-hexane = 1: 1: 1 (v/v/v) mixed solvent; acetonitrile: dichloromethane: n-hexane = 1: 1: 1 (v/v/v) mixed solvent], 2 dehydrated salts (anhydrous MgSO4+NaCl and anhydrous Na2SO4+NaCl), 2 purification salts (C18 and PSA), and 4 vortex time (5, 7.5, 10, and 12.5 min) conditions. Then internal standard was utilized to estimate linear range and detection limit of the refined QuEChERS approach. ResultsThe linearities of SCCPs, MCCPs, and LCCPs were good in the range of 10~1000 ng·mL−1 with the correlation coefficients all greater than 0.96. The method detection limits (MDLs) ranged from 0.01 to 0.29 ng·m−3. The spiked recoveries of SCCPs, MCCPs, and LCCPs at the low, medium, and high concentrations were 77.38%-81.64%, 93.11%-99.78%, and 87.41%-101.39%, respectively, and the relative standard deviations (RSDs) were 2.90%-12.84%. This method was used to determine the CPs levels in 11 PM2.5 samples from Shijiazhuang. The positive rates of ∑SCCPs, ∑MCCPs, and ∑LCCPs were all 100%, the concentration ranges were 0.24-2.18 ng·m−3 (mean 0.84 ng·m−3), 0.17-1.67 ng·m−3 (mean 0.70 ng·m−3), and 0.01-0.16 ng·m−3 (mean 0.04 ng·m−3), respectively, and the percentages to ΣCPs were 52.95%, 44.39%, and 2.66%, respectively. ConclusionThe method established in this study is simple, time-saving, solvent saving, and can simultaneously detect SCCPs, MCCPs, and LCCPs in PM2.5, which is suitable for the determination of PM2.5 samples in large quantities, and can also provide a reference for the detection methods of other halogenated organic compounds in PM2.5.http://www.jeom.org/article/cn/10.11836/JEOM24156chlorinated paraffinsfine particulate matterquick, easy, cheap, effective, rugged, and safeultra-high performance liquid chromatographyquadrupole/orbitrap high resolution mass spectrometry
spellingShingle Wenyan YAN
Chao WANG
Juan LIU
Yibin SUN
Wen GU
Yifu LU
Ke FANG
Yi WAN
Song TANG
Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
环境与职业医学
chlorinated paraffins
fine particulate matter
quick, easy, cheap, effective, rugged, and safe
ultra-high performance liquid chromatography
quadrupole/orbitrap high resolution mass spectrometry
title Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
title_full Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
title_fullStr Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
title_full_unstemmed Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
title_short Determination of chlorinated paraffins in PM2.5 by QuEChERS combined with ultra-high performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry
title_sort determination of chlorinated paraffins in pm2 5 by quechers combined with ultra high performance liquid chromatography quadrupole orbitrap high resolution mass spectrometry
topic chlorinated paraffins
fine particulate matter
quick, easy, cheap, effective, rugged, and safe
ultra-high performance liquid chromatography
quadrupole/orbitrap high resolution mass spectrometry
url http://www.jeom.org/article/cn/10.11836/JEOM24156
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