Quantification of oxygenated polycyclic aromatic hydrocarbons in ambient aerosol samples using in-injection port thermal desorption-gas chromatography/mass spectrometry: Method exploration and validation | |
Li, LJ (Li, Lijuan)[ 1,2,3,4 ]; Ho, SSH (Ho, Steven Sai Hang)[ 1,2,3,5 ]; Chow, JC (Chow, Judith C.)[ 2,5 ]; Watson, JG (Watson, John G.)[ 2,5 ]; Qu, LL (Qu, Linli)[ 6 ]; Wang, LQ (Wang, Liqin)[ 1,2 ]; Cao, JJ (Cao, Junji)[ 1,2,3 ] | |
刊名 | International Journal of Mass Spectrometry |
2018-10 | |
卷号 | 433页码:25-30 |
关键词 | O-pahs Thermal Desorption Electronic Ionization Aerosol Filters Method Comparison |
ISSN号 | 1387-3806 |
DOI | 10.1016/j.ijms.2018.08.005 |
通讯作者 | Ho, Steven Sai Hang(stevenho@hkpsrl.org) ; Cao, Junji(cao@loess.llqg.ac.cn) |
文献子类 | 期刊论文 |
英文摘要 | In-injection port thermal desorption (TD) was evaluated for determination of particulate phase oxygenated-polycyclic aromatic hydrocarbons (O-PAHs) collected on filters coupled with a gas chromatography/mass spectrometry (GC/MS). The analytical parameters were optimized with standard testing and ambient samples. Ten of the most abundant O-PAHs in ambient air were included in the demonstration. A desorption temperature of 275 °C for 9 min was sufficient to transfer entire target compounds to the analytical system. Good linearity (R2 >0.99) on the calibrations for each analyte was achieved. The limit of detection (LOD) ranged from 21 to 269 pg per loading. Method precisions, determined by replicate analyses of calibration standards and ambient samples, was less than 10% for target compounds. Comparisons were conducted on batches of 28 ambient aerosol filter samples using our TD and the traditional SE methods. Reasonably good agreement (R2 = 0.98) by the two methods was demonstrated for most of O-PAHs. The in-injection port TD can improve laboratory efficiency and reduce solvent-based costs for the measurement of O-PAHs. |
资助项目 | Ministry of Science of Technology[2013FY112700] ; National Natural Science Foundation of China[41503117] |
WOS关键词 | MASS-SPECTROMETRY ; NITRATED-PAHS ; CENTRAL CHINA ; URBAN ; DERIVATIVES ; RISK ; COLLECTION ; ATMOSPHERE ; EMISSIONS ; MARINE |
WOS研究方向 | Physics ; Spectroscopy |
语种 | 英语 |
出版者 | ELSEVIER SCIENCE BV |
WOS记录号 | WOS:000446396300005 |
资助机构 | Ministry of Science of Technology ; National Natural Science Foundation of China |
内容类型 | 期刊论文 |
源URL | [http://ir.ieecas.cn/handle/361006/9569] |
专题 | 地球环境研究所_粉尘与环境研究室 |
通讯作者 | Ho, SSH (Ho, Steven Sai Hang)[ 1,2,3,5 ]; Cao, JJ (Cao, Junji)[ 1,2,3 ] |
作者单位 | 1.University of Chinese Academy of Sciences, Beijing, China; 2.Key Laboratory of Aerosol Chemistry & Physics (KLACP), Institute of Earth Environment, Chinese Academy of Sciences, Xi’an, 710061, China; 3.State Key Laboratory of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi’an, 710061, China; 4.Shaanxi Key Laboratory of Atmospheric and Haze-fog Pollution Prevention, Institute of Earth Environment, Chinese Academy of Sciences, China; 5.Division of Atmospheric Sciences, Desert Research Institute, Reno, NV, 89512, United States; 6.Hong Kong Premium Services and Research Company, Lai Chi Kok, Kowloon, Hong Kong |
推荐引用方式 GB/T 7714 | Li, LJ ,Ho, SSH ,Chow, JC ,et al. Quantification of oxygenated polycyclic aromatic hydrocarbons in ambient aerosol samples using in-injection port thermal desorption-gas chromatography/mass spectrometry: Method exploration and validation[J]. International Journal of Mass Spectrometry,2018,433:25-30. |
APA | Li, LJ .,Ho, SSH .,Chow, JC .,Watson, JG .,Qu, LL .,...&Cao, JJ .(2018).Quantification of oxygenated polycyclic aromatic hydrocarbons in ambient aerosol samples using in-injection port thermal desorption-gas chromatography/mass spectrometry: Method exploration and validation.International Journal of Mass Spectrometry,433,25-30. |
MLA | Li, LJ ,et al."Quantification of oxygenated polycyclic aromatic hydrocarbons in ambient aerosol samples using in-injection port thermal desorption-gas chromatography/mass spectrometry: Method exploration and validation".International Journal of Mass Spectrometry 433(2018):25-30. |
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