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Factor analysis of combined organic and inorganic aerosol mass spectra from high resolution aerosol mass spectrometer measurements

机译:高分辨率气溶胶质谱仪测量有机和无机气溶胶组合质谱的因子分析

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Positive matrix factorization (PMF) was applied to the merged high resolution mass spectra of organic and inorganic aerosols from aerosol mass spectrometer (AMS) measurements to investigate the sources and evolution processes of submicron aerosols in New York City in summer 2009. This new approach is able to study the distribution of organic and inorganic species in different types of aerosols, the acidity of organic aerosol (OA) factors, and the fragment ion patterns related to photochemical processing. In this study, PMF analysis of the unified AMS spectral matrix resolved 8 factors. The hydrocarbon-like OA (HOA) and cooking OA (COA) factors contain negligible amounts of inorganic species. The two factors that are primarily ammonium sulfate (SO_4-OA) and ammonium nitrate (NO_3-OA), respectively, are overall neutralized. Among all OA factors the organic fraction of SO_4-OA shows the highest degree of oxidation (O/C = 0.69). Two semi-volatile oxygenated OA (OOA) factors, i.e., a les oxidized (LO-OOA) and a more oxidized (MO-OOA), were also identified. MO-OOA represents local photochemical products with a diurnal profile exhibiting a pronounced noon peak, consistent with those of formalde-hyde (HCHO) and O_x(= O_3 +NO_2). The NO~+/NO_2~+ ion ratio in MO-OOA is much higher than that in NO3-OA and in pure ammonium nitrate, indicating the formation of organic nitrates. The nitrogen-enriched OA (NOA) factor contains ~25 % of acidic inorganic salts, suggesting the formation of secondary OA via acid-base reactions of amines. The size distributions of OA factors derived from the size-resolved mass spectra show distinct diurnal evolving behaviors but overall a progressing evolution from smaller to larger particle mode as the oxidation degree of OA increases. Our results demonstrate that PMF analysis of the unified aerosol mass spectral matrix which contains both inorganic and organic aerosol signals may enable the deconvolution of more OA factors and gain more insights into the sources, processes, and chemical characteristics of OA in the atmosphere.
机译:将正矩阵分解(PMF)应用于气溶胶质谱仪(AMS)测量的有机和无机气溶胶的高分辨率合并质谱图,以研究2009年夏季纽约市的亚微米气溶胶的来源和演变过程。这种新方法是能够研究不同类型气溶胶中有机物和无机物的分布,有机气溶胶(OA)因子的酸度以及与光化学处理有关的碎片离子图谱。在这项研究中,统一AMS频谱矩阵的PMF分析解决了8个因素。类烃OA(HOA)和蒸煮OA(COA)因子中无机物的含量可以忽略不计。总的来说,这两个因素分别主要是硫酸铵(SO_4-OA)和硝酸铵(NO_3-OA)。在所有OA因子中,SO_4-OA的有机部分显示出最高的氧化度(O / C = 0.69)。还确定了两个半挥发性的氧化OA(OOA)因子,即les氧化(LO-OOA)和更氧化的(MO-OOA)。 MO-OOA代表局部光化学产物,其昼夜曲线表现出明显的正午峰,与甲醛-氢(HCHO)和O_x(= O_3 + NO_2)一致。 MO-OOA中的NO〜+ / NO_2〜+离子比远高于NO3-OA和纯硝酸铵中的NO〜+ / NO_2〜+离子,表明有机硝酸盐的形成。富氮的OA(NOA)因子含有约25%的酸性无机盐,表明通过胺的酸碱反应形成了次要OA。由尺寸分辨质谱得出的OA因子的尺寸分布表现出明显的昼夜演化行为,但总体上随着OA氧化度的增加,从较小的颗粒模式向较大的颗粒模式逐渐发展。我们的结果表明,对包含无机和有机气溶胶信号的统一气溶胶质谱矩阵进行PMF分析,可以使更多OA因子解卷积,并获得对大气中OA的来源,过程和化学特性的更多见解。

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