Response of protonated, adduct, and fragmented ions in Vocus proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS)
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Published:2024-04-23
Issue:8
Volume:17
Page:2415-2427
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ISSN:1867-8548
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Container-title:Atmospheric Measurement Techniques
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language:en
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Short-container-title:Atmos. Meas. Tech.
Author:
Li Fangbing, Huang Dan DanORCID, Tian Linhui, Yuan BinORCID, Tan Wen, Zhu Liang, Ye Penglin, Worsnop Douglas, Hoi Ka In, Mok Kai Meng, Li Yong Jie
Abstract
Abstract. Volatile organic compounds (VOCs) affect secondary pollutant formation via active chemistry. Proton-transfer-reaction mass spectrometry (PTR-MS) is one of the most important techniques to study the highly variable spatial and temporal characteristics of VOCs. The response of protonated, adduct, and fragmented ions in PTR-MS in changing instrument settings and varying relative humidity (RH) requires rigorous characterization. Herein, we present dedicatedly designed laboratory experiments conducted to investigate the response of these ions for 21 VOCs, including 12 oxygenated VOCs and 2 nitriles, using the recently developed Vocus PTR-MS. Our results show that the focusing ion–molecule reactor (FIMR) axial voltage increases sensitivity by 3 to 4 orders of magnitude but does not significantly change the fractions of protonated ions. Reducing the FIMR pressure, however, substantially increases fragmentation. Applying a high radio frequency (RF) amplitude radially to the FIMR can enhance sensitivity by 1 to 2 orders of magnitude without affecting the protonated ion fractions. The change in big segmented quadrupole (BSQ) amplitude mainly affects sensitivity and protonated ion fraction by modifying ion transmission. The relationship between sensitivity and proton-transfer reaction rate constant is complicated by the influences from both ion transmission and protonated ion fraction. The protonated ions of most VOCs studied (19 out of 21) show less than 15 % variations in sensitivity as RH increases from ∼ 5% to ∼ 85 %, except for some long-chain aldehydes which show a positive RH variation of up to 30 %. Our results suggest that the Vocus PTR-MS can reliably quantify the majority of VOCs under ambient conditions with varying RH. However, caution is advised for small oxygenates such as formaldehyde and methanol due to their low sensitivity and for long-chain aldehydes due to their slight RH dependence and fragmentation.
Funder
Fundo para o Desenvolvimento das Ciências e da Tecnologia Universidade de Macau
Publisher
Copernicus GmbH
Reference41 articles.
1. Baasandorj, M., Millet, D. B., Hu, L., Mitroo, D., and Williams, B. J.: Measuring acetic and formic acid by proton-transfer-reaction mass spectrometry: sensitivity, humidity dependence, and quantifying interferences, Atmos. Meas. Tech., 8, 1303–1321, https://doi.org/10.5194/amt-8-1303-2015, 2015. 2. Cappellin, L., Karl, T., Probst, M., Ismailova, O., Winkler, P. M., Soukoulis, C., Aprea, E., Märk, T. D., Gasperi, F., and Biasioli, F.: On Quantitative Determination of Volatile Organic Compound Concentrations Using Proton Transfer Reaction Time-of-Flight Mass Spectrometry, Environ. Sci. Technol., 46, 2283–2290, https://doi.org/10.1021/es203985t, 2012. 3. Claflin, M. S., Pagonis, D., Finewax, Z., Handschy, A. V., Day, D. A., Brown, W. L., Jayne, J. T., Worsnop, D. R., Jimenez, J. L., Ziemann, P. J., de Gouw, J., and Lerner, B. M.: An in situ gas chromatograph with automatic detector switching between PTR- and EI-TOF-MS: isomer-resolved measurements of indoor air, Atmos. Meas. Tech., 14, 133–152, https://doi.org/10.5194/amt-14-133-2021, 2021. 4. Cui, L., Zhang, Z., Huang, Y., Lee, S. C., Blake, D. R., Ho, K. F., Wang, B., Gao, Y., Wang, X. M., and Louie, P. K. K.: Measuring OVOCs and VOCs by PTR-MS in an urban roadside microenvironment of Hong Kong: relative humidity and temperature dependence, and field intercomparisons, Atmos. Meas. Tech., 9, 5763–5779, https://doi.org/10.5194/amt-9-5763-2016, 2016. 5. de Gouw, J. and Warneke, C.: Measurements of volatile organic compounds in the earths atmosphere using proton-transfer-reaction mass spectrometry, Mass Spectrom. Rev., 26, 223–257, https://doi.org/10.1002/mas.20119, 2007.
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