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Source apportionment of carbonaceous aerosols in Xi'an, China: insights from a full year of measurements of radiocarbon and the stable isotope 13C

机译:西安碳质气溶胶的源分摊:从无线电金的全年测量和稳定同位素13c的洞察

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Sources of organic carbon (OC) and elemental carbon (EC) in Xi'an, China, are investigated based on 1-year radiocarbon and stable carbon isotope measurements. The radiocarbon results demonstrate that EC is dominated by fossil sources throughout the year, with a mean contribution of 83±5% (7±2μg?m?3). The remaining 17±5% (1.5±1μg?m?3) is attributed to biomass burning, with a higher contribution in the winter (~24%) compared to the summer (~14%). Stable carbon isotopes of EC (δ13CEC) are enriched in winter (-23.2±0.4‰) and depleted in summer (-25.9±0.5‰), indicating the influence of coal combustion in winter and liquid fossil fuel combustion in summer. By combining radiocarbon and stable carbon signatures, relative contributions from coal combustion and liquid fossil fuel combustion are estimated to be 45% (median; 29%–58%, interquartile range) and 31% (18%–46%) in winter, respectively, whereas in other seasons more than one half of EC is from liquid fossil combustion. In contrast with EC, the contribution of non-fossil sources to OC is much larger, with an annual average of 54±8% (12±10μg?m?3). Clear seasonal variations are seen in OC concentrations both from fossil and non-fossil sources, with maxima in winter and minima in summer because of unfavorable meteorological conditions coupled with enhanced fossil and non-fossil activities in winter, mainly biomass burning and domestic coal burning. δ13COC exhibited similar values to δ13CEC, and showed strong correlations (r2=0.90) in summer and autumn, indicating similar source mixtures with EC. In spring, δ13COC is depleted (1.1‰–2.4‰) compared to δ13CEC, indicating the importance of secondary formation of OC (e.g., from volatile organic compound precursors) in addition to primary sources. Modeled mass concentrations and source contributions of primary OC are compared to the measured mass and source contributions. There is strong evidence that both secondary formation and photochemical loss processes influence the final OC concentrations.
机译:中国西安有机碳(OC)和元素碳(EC)的来源是基于1年的无线电碳和稳定的碳同位素测量来研究。 RadioCarbon结果表明EC全年由化石源主导,平均贡献为83±5%(7±2μg≤3)。剩下的17±5%(1.5±1μg≤M≤3)归因于生物质燃烧,冬季(〜24%)贡献更高(〜24%)(〜14%)。 EC(δ13CEC)的稳定同位素碳冬季富集(-23.2±0.4‰)和在夏季(-25.9±0.5‰)耗尽,表明煤燃烧的在冬季和液体化石燃料燃烧在夏季的影响。通过结合放射性碳和碳稳定签名,从煤燃烧和液体化石燃料燃烧的相对贡献估计为45%(中值:29%-58%,四分位数间距)和31%(18%-46%)在冬天,分别,而在其他季节中超过一半的EC来自液体化石燃烧。与欧共体相比,非化石源对oC的贡献要大得多,年平均值为54±8%(12±10μg≤3)。在化石和非化石源的OC浓度下,冬季和夏季最小二的冬季和最小值的季节性变化是看不到的,因为冬季增强的化石和非化石活动,主要是生物量燃烧和国内煤炭燃烧的冬季和最小值。 Δ13coc表现出类似的值Δ13cec,并且在夏季和秋季显示出强烈的相关性(R2 = 0.90),表明与EC的类似源混合物。与δ13CEC相比,Δ13CoC耗尽(1.1÷-2.4℃),表明除了主要来源之外,表明oc(例如,从挥发性有机化合物前体)的二次形成的重要性。模拟了主要OC的质量浓度和源贡献与测量的质量和源贡献进行了比较。有强有力的证据表明,二次形成和光化学损失过程都影响了最终的OC浓度。

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