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Effect of relative humidity on SOA formation from isoprene/NO photooxidation: enhancement of 2-methylglyceric acid and its corresponding oligoesters under dry conditions

机译:相对湿度对异戊二烯/ NO光氧化的SOA形成的影响:在干燥条件下提高2-甲基甘露酸及其相应的寡酯

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The effect of relative humidity (RH) on secondary organic aerosol (SOA) formation from the photooxidation of isoprene under initially high nitric oxide (NO) conditions (i.e., isoprene/NO ~3) was investigated in a dual outdoor smog chamber. Based upon particle volume concentration measurements and the detailed chemical characterization of isoprene SOA using gas chromatography/mass spectrometry (GC/MS) and ultra performance liquid chromatography/electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (UPLC/ESI-HR-Q-TOFMS), enhanced SOA formation was observed under lower RH conditions (15–40 %) compared to higher RH conditions (40–90 %). 2-methylglyceric acid (2-MG) and its corresponding oligoesters, which have been previously shown to form from further oxidation of methacryloylperoxynitrate (MPAN), were enhanced in the particle-phase under lower RH conditions. In addition, an abundant unknown SOA tracer likely derived from the further oxidation of MPAN was detected and enhanced under lower RH conditions. In contrast, the 2-methyltetrols, which are known to mainly form from the reactive uptake of isoprene epoxydiols (IEPOX) under low-NO conditions in the presence of acidified aerosol, did not substantially vary under different RH conditions; however, isoprene-derived organosulfates were found to be enhanced under high-RH conditions, indicating the likely importance of the aqueous aerosol phase in their formation. Based upon the detailed chemical characterization results, particle-phase organic esterification is tentatively proposed to explain the observed enhancements of isoprene SOA mass under lower RH conditions. Alternative mechanisms explaining the enhancement of 2-MG and its corresponding oligoesters cannot be completely ruled out. This is one of only a few chamber studies that have examined the effect of RH on isoprene SOA formation. In comparison to our recent results obtained from aromatic SOA formation, the effect of RH on isoprene SOA formation is reversed. The results of this study highlight the importance of elucidating the key reactive intermediates that lead to SOA formation, especially since RH likely affects their ability in forming SOA. Furthermore, ignoring the effects of RH may significantly affect the accuracy of both regional and global SOA models.
机译:在双户外烟雾室中研究了在初始高一氧化物(NO)条件下的异戊二烯光氧化中相对湿度(RH)对二次有机气溶胶(SOA)形成的影响,在双户外烟雾室中研究了异戊二烯(即,异戊二烯/ NO〜3)。基于颗粒体积浓度测量和异戊二烯SOA的详细化学表征使用气相色谱/质谱/质谱法和超级性能液相色谱/电喷雾电离高分辨率高度飞行时间质谱法(UPLC / ESI-HR -Q-TOFMS),与较高的RH条件(40-90%)相比,在较低的RH条件下(15-40%)观察到增强的SOA形成。在低温条件下,在颗粒相中提高了从进一步氧化的2-甲基甘氨酸(2-Mg)及其预先从进一步氧化形成的寡聚酯。此外,在低温条件下,检测到可能源于MPAN的进一步氧化的丰富未知的SOA示踪剂。相反,在酸化气溶胶存在下,从异戊二烯环氧二醇(IePox)的反应性摄取主要形成的2-甲基四氧化醇在不同RH条件下没有显着变化;然而,发现异戊二烯衍生的有机氢盐在高温条件下增强,表明含水气溶胶期在其形成中的重要性。基于详细的化学表征结果,暂时提出颗粒相机酯化,以解释在低温条件下观察到异戊二烯SOA质量的增强。解释2-Mg和其相应的低收解器的增强的替代机制不能完全排除出来。这是仅研究RH对异戊二烯SOA形成的影响的几个分布研究之一。与我们最近从芳香SOA形成获得的结果相比,RH对异戊二烯SOA形成的影响是逆转的。本研究的结果突出了阐明导致SOA形成的关键反应性中间体的重要性,特别是因为RH可能影响其形成SOA的能力。此外,忽略RH的效果可能会显着影响区域和全球SOA模型的准确性。

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