4.6 Article

Offline analysis of secondary formation markers in ambient organic aerosols by liquid chromatography coupled with time-of-flight mass spectrometry

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JOURNAL OF CHROMATOGRAPHY A
卷 1702, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.chroma.2023.464092

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HPLC-ESI-TOF-MS; Atmospheric aerosols; Pinene markers; Nitrophenols; Molecular analysis

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The present study comprehensively analyzes pinene markers, biomass-burning related phenols, and other relevant carboxylic acids in atmospheric aerosol samples using high-performance liquid chromatography coupled with dual orthogonal electrospray ionization time-of-flight mass spectrometry (HPLC-ESI-TOF-MS). The study provides important insights into the optimization of chromatographic separation, ionization source, and mass spectrometer performance for quantitative determination. The developed method demonstrates reliable quantification of targeted compounds in real atmospheric aerosol samples, and molecular mass determination with high accuracy.
The present study provides a comprehensive assessment of the quantitative analysis by high-performance liquid chromatography coupled with dual orthogonal electrospray ionization time-of-flight mass spec-trometry (HPLC-ESI-TOF-MS) of pinene markers, biomass-burning related phenols, and other relevant car-boxylic acids in atmospheric aerosol samples. Significant insights into the quantitative determination are offered on the basis of systematic experiments targeting the optimization of chromatographic separation, ionization source, and mass spectrometer performance. After testing three analytical columns, the best separation of the compounds of interest was achieved on a Poroshell 120 EC -C18 column (4.6 x 50 mm, 2.7 mu m) thermostated at 35 degrees C, operating in gradient elution mode with 0.1% acetic acid in water and acetonitrile at a 0.8 mL min -1 flow rate. Optimal operational conditions for the ESI-TOF-MS instrument were identified as a 350 degrees C drying gas temperature, 13 L min -1 drying gas flow rate, 60 psig nebulizer pressure, 30 0 0 V for the ion transfer capillary, 60 V for the skimmer, and 150 V for the fragmentor. Ad-ditionally, the matrix effect on the ESI efficiency and the spike recovery factors of the compounds were tested. Method quantification limits can go as low as in the 0.88-48.0 mu g L - 1 (3.67-200 pg m - 3 , at 120 m3 of sampled air) range. The developed method was shown to be reliable for the quantification of the targeted compounds in real atmospheric aerosol samples. The accuracy in the molecular mass deter-mination of less than 5 ppm and the acquisition in the full scan mode were shown to bring additional insights into the organic constituents in atmospheric aerosols. (c) 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

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