Online Calibration of a Chemical Ionization Mass Spectrometer for Multifunctional Biogenic Organic Nitrates

Michael A. Robinson*, James M. Roberts, J. Andrew Neuman, Christopher M. Jernigan, Lu Xu, Matthew M. Coggon, Chelsea E. Stockwell, Carsten Warneke, Jeff Peischl, Jessica B. Gilman, Aaron Lamplugh, Andrew W. Rollins, Kristen Zuraski, Jean C. Rivera-Rios, Yuchen Wang, Nga L. Ng, Shang Liu, Steven S. Brown and Patrick R. Veres*, 
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Abstract

Multifunctional organic nitrates derived from biogenic volatile organic compounds are important for understanding ozone and secondary organic aerosol production from oxidation reactions in the presence of nitrogen oxides. Their measurement is challenging, in part because the quantification of these compounds is difficult and time consuming due to the techniques required to synthesize and purify authentic standards. We describe a novel online synthesis and separation technique and demonstrate its use for calibration of a chemical ionization mass spectrometer using iodide reagent ions (I CIMS) to measure four isomers of isoprene hydroxy nitrate (IHN; C5H9NO4), two isomers of methyl vinyl ketone hydroxy nitrate (MVKHN; C4H7NO5), and four isomers of monoterpene hydroxy nitrate (MTHN; C10H17NO4). We further apply our separation technique to an isoprene + NO3 + HO2 online reactor to calibrate for six isomers of isoprene hydroperoxide nitrate (C5H9NO5). We find a large range of detection sensitivities and ion molecule reactor (IMR) temperature dependencies among the reported analytes measured as iodide (I) clusters. We report a wide range of normalized sensitivities (normalized Hz pptv–1; nHz pptv–1) normalized by the [I·H2O] reagent ion signal for this class of analytes (0.2–82 nHz pptv–1). The (4,3)-MVKHN isomer is exceptional for its high sensitivity with this ion chemistry (82 ± 5 nHz pptv–1), which can lead to an inaccurate representation of the organic nitrate budget if a moderate sensitivity is assumed. The I CIMS demonstrates a much smaller range of sensitivities to IHNs (10–34 nHz pptv–1), with the two most abundant isomers having similar sensitivities ((1,2): 24 ± 3 nHz pptv–1; (4,3): 30 ± 4 nHz pptv–1). These calibrations reveal a significantly different distribution of organic nitrates than would be determined assuming uniform sensitivity for measurements with an I CIMS at a ground site in Pasadena, CA, during the summer of 2021. A comparison with another calibrated CIMS (using CF3O reagent ions) for select compounds showed good agreement for IHN and MVKHN.

Abstract Image

在线校准化学电离质谱仪以检测多功能生物有机硝酸盐
从生物挥发性有机化合物中提取的多功能有机硝酸盐对于了解氮氧化物存在时氧化反应产生的臭氧和二次有机气溶胶非常重要。对它们的测量具有挑战性,部分原因是由于合成和纯化真实标准物质所需的技术,这些化合物的定量既困难又耗时。我们介绍了一种新颖的在线合成和分离技术,并演示了如何使用碘化试剂离子(I- CIMS)校准化学电离质谱仪,以测量羟基硝酸异戊二烯(IHN;C5H9NO4)的四种异构体、羟基硝酸甲基乙烯酮(MVKHN;C4H7NO5)的两种异构体以及羟基硝酸单萜烯(MTHN;C10H17NO4)的四种异构体。我们进一步将分离技术应用于异戊二烯 + NO3 + HO2 在线反应器,以校准过氧化氢硝酸异戊二烯(C5H9NO5)的六种异构体。我们发现,在报告的以碘化物 (I-) 簇测量的分析物中,检测灵敏度和离子分子反应器 (IMR) 温度依赖性的范围很大。我们报告了该类分析物以[I-H2O]-试剂离子信号(0.2-82 nHz pptv-1)归一化的宽范围归一化灵敏度(归一化 Hz pptv-1;nHz pptv-1)。(4,3)-MVKHN异构体对这种离子化学反应的灵敏度较高(82 ± 5 nHz pptv-1),如果假定灵敏度适中,则可能导致对有机硝酸盐预算的不准确表述。I- CIMS 对 IHNs 的灵敏度范围要小得多(10-34 nHz pptv-1),最丰富的两种异构体具有相似的灵敏度((1,2):24 ± 3 nHz pptv-1;(4,3):30 ± 4 nHz pptv-1)。这些校准结果显示,有机硝酸盐的分布与 2021 年夏季在加利福尼亚州帕萨迪纳的一个地面站点使用 I- CIMS 测量时假定灵敏度相同而确定的有机硝酸盐分布有很大不同。与另一个经过校准的 CIMS(使用 CF3O- 试剂离子)对特定化合物进行的比较显示,IHN 和 MVKHN 的校准结果非常一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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