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Gas phase formation of extremely oxidized pinene reaction products in chamber and ambient air

机译:室内和环境空气中极端氧化的醌反应产物的气相形成

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High molecular weight (300–650 Da) naturally charged negative ions have previously been observed at a boreal forest site in Hyyti?l?, Finland. The long-term measurements conducted in this work showed that these ions are observed practically every night between spring and autumn in Hyyti?l?. The ambient mass spectral patterns could be reproduced in striking detail during additional measurements of α-pinene (C10H16) oxidation at low-OH conditions in the Jülich Plant Atmosphere Chamber (JPAC). The ions were identified as clusters of the nitrate ion (NO3) and α-pinene oxidation products reaching oxygen to carbon ratios of 0.7–1.3, while retaining most of the initial ten carbon atoms. Attributing the ions to clusters instead of single molecules was based on additional observations of the same extremely oxidized organics in clusters with HSO4 (Hyyti?l?) and C3F5O2 (JPAC). The most abundant products in the ion spectra were identified as C10H14O7, C10H14O9, C10H16O9, and C10H14O11. The mechanism responsible for forming these molecules is still not clear, but the initial reaction is most likely ozone attack at the double bond, as the ions are mainly observed under dark conditions. β-pinene also formed highly oxidized products under the same conditions, but less efficiently, and mainly C9 compounds which were not observed in Hyyti?l?, where β-pinene on average is 4–5 times less abundant than α-pinene. Further, to explain the high O/C together with the relatively high H/C, we propose that geminal diols and/or hydroperoxide groups may be important. We estimate that the night-time concentration of the sum of the neutral extremely oxidized products is on the order of 0.1–1 ppt (~106–107 molec cm?3). This is in a similar range as the amount of gaseous H2SO4 in Hyyti?l? during day-time. As these highly oxidized organics are roughly 3 times heavier, likely with extremely low vapor pressures, their role in the initial steps of new aerosol particle formation and growth may be important and needs to be explored in more detail in the future.
机译:高分子量(300-650Da)在Hyyti的北部森林部位之前已经观察到天然带电的负离子?L?,芬兰。在这项工作中进行的长期测量表明,在Hyyti的春季和秋季几乎在每晚观察到这些离子?在Jülich植物大气室(JPAC)的低OH条件下的α-PinENE(C10H16)氧化的额外测量期间,可以在β-折烯(C10H16)氧化的额外测量期间以初步细节再现。将离子鉴定为硝酸根离子(NO3)和α-焦烯氧化产物的簇,达到氧比的碳比为0.7-1.3,同时保留大部分初始十个碳原子。将离子归因于簇代替单个分子,基于与HSO4(HyyTIα)和C3F5O2(JPAC)的相同极其氧化有机物的额外观察。离子光谱中最丰富的产品被鉴定为C10H14O7,C10H14O9,C10H16O9和C10H14O11。负责形成这些分子的机制仍然尚不清楚,但初始反应很可能在双键处臭氧攻击,因为离子主要在暗条件下观察到。 β-Pine烯还在相同条件下形成高度氧化的产物,但较低有效,主要是在HyyTIα-L 1中观察到的C9化合物,其中β-Pine烯平均比α-pine少4-5倍。此外,为了将高O / C与相对高的H / C一起解释,我们提出了牙型二醇和/或氢过氧化物基团可能是重要的。我们估计中性极端氧化产物总和的夜间浓度约为0.1-1 ppt(〜106-107分子cm≤3)。这在类似的范围内作为Hyyti的气态H2SO4的量?在白天。由于这些高度氧化有机物大约是较重的3倍,可能具有极低的蒸气压力,因此它们在新的气溶胶颗粒形成和生长的初始步骤中的作用可能是重要的,并且需要在未来更详细地探索。

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