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Atmospheric organic vapors in two European pine forests measured by a Vocus PTR-TOF: insights into monoterpene and sesquiterpene oxidation processes

机译:由VOCUS PTR-TOF测量的两个欧洲松树林中的大气有机蒸气:洞察单萜和筛标氧化过程

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Atmospheric organic vapors play essential roles in the formation of secondary organic aerosol. Source identification of these vapors is thus fundamental to understanding their emission sources and chemical evolution in the atmosphere and their further impact on air quality and climate change. In this study, a Vocus proton-transfer-reaction time-of-flight mass spectrometer?(PTR-TOF) was deployed in two forested environments, the Landes forest in southern France and the boreal forest in southern Finland, to measure atmospheric organic vapors, including both volatile organic compounds?(VOCs) and their oxidation products. For the first time, we performed binned positive matrix factorization?(binPMF) analysis on the complex mass spectra acquired with the Vocus PTR-TOF and identified various emission sources as well as oxidation processes in the atmosphere. Based on separate analysis of low- and high-mass ranges, 15 PMF factors in the Landes forest and nine PMF factors in the Finnish boreal forest were resolved, showing a high similarity between the two sites. Particularly, terpenes and various terpene reaction products were separated into individual PMF factors with varying oxidation degrees, such as lightly oxidized compounds from both monoterpene and sesquiterpene oxidation, monoterpene-derived organic nitrates, and monoterpene more oxidized compounds. Factors representing monoterpenes dominated the biogenic VOCs in both forests, with lower contributions from the isoprene factors and sesquiterpene factors. Factors of the lightly oxidized products, more oxidized products, and organic nitrates of monoterpenes/sesquiterpenes accounted for 8?%–12?% of the measured gas-phase organic vapors in the two forests. Based on the interpretation of the results relating to oxidation processes, further insights were gained regarding monoterpene and sesquiterpene reactions. For example, a strong relative humidity?(RH) dependence was found for the behavior of sesquiterpene lightly oxidized compounds. High concentrations of these compounds only occur at high?RH; yet similar behavior was not observed for monoterpene oxidation products.
机译:大气有机蒸气在次级有机气溶胶的形成中起重要作用。因此,对这些蒸气的源识别是理解其在大气中的排放来源和化学演变的基础以及它们对空气质量和气候变化的进一步影响。在这项研究中,VOCUS质子转移反应 - 飞行时间 - 飞行时间 - (PTR-TOF)部署在法国南部的两种森林环境中,南部南部的北部北部林林,测量大气有机蒸汽,包括挥发性有机化合物?(VOC)及其氧化产品。我们首次进行了Binned阳性矩阵分解?(binPMF)对随着VOCUS PTR-TOF获得的复杂质谱分析,并确定了大气中的各种发射源以及氧化过程。基于对低质量和大质量范围的单独分析,地区森林的15个PMF因子和芬兰北欧森林中的九个PMF因子进行了解决,在两个地点之间显示出高度相似之处。特别地,将萜烯和各种萜烯反应产物分离成具有不同氧化度的单独PMF因子,例如从单萜和倍霉酮氧化,单萜衍生的有机硝酸盐的轻质氧化化合物,并且单萜类化合物更加氧化化合物。代表单调位的因素主导了两种森林中的生物转霉型,从异戊二烯因素和筛窦因子中贡献较低。轻氧化产物的因素,更氧化的产物和单色素/倍氏菌属的有机硝酸盐占两种森林中测量的气相有机蒸气的8?% - 12?%。基于对氧化过程的结果的解释,对单萜和筛窦反应获得了进一步的见解。例如,发现倍二萜烯轻氧化化合物的行为的强烈相对湿度?(RH)依赖性。高浓度的这些化合物仅在高温λ中发生;单萜氧化产品未观察到类似的行为。

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