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An approach to monitor the fraction of elemental carbon in the ultrafine aerosol

机译:一种监测超细气溶胶中碳元素含量的方法

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Attempts were made to measure the fraction of elemental carbon (EC) in ultrafine aerosol by modifying an Ambient Carbonaceous Particulate Monitor (ACPM, R&P 5400). The main modification consisted in placing a quartz filter in one of the sampling lines of this dual-channel instrument. With the filter all aerosol and EC contained in it is collected, while in the other line of the instrument the standard impactor samples only particles larger than 0.14 μm. The fraction of EC in particles smaller than 0.14 μm is derived from the difference in concentration as measured via the two sampling lines. Measurements with the modified instrument were made at a suburban site in Amsterdam, The Netherlands. An apparent adsorption artefact, which could not be eliminated by the use of denuders, precluded meaningful evaluation of the data for total carbon. Blanks in the measurements of EC were negligible and the EC data were hence further evaluated. We found that the concentration of EC obtained via the channel with the impactor was systematically lower than that in the filter-line. The average ratio of the concentrations was close to 0.6, which indicates that approximately 40% of the EC was in particles smaller than 0.14 μm. Alternative explanations for the difference in the concentration in the two sampling lines could be excluded, such as a difference in the extent of oxidation. This should be a function of loading, which is not the case. Another reason for the difference could be that less material is collected by the impactor due to rebound, but such bounce of aerosol is very unlikely in The Netherlands due to co-deposition of abundant deliquesced and thus viscous ammonium compounds. The conclusion is that a further modification to assess the true fraction of ultrafine EC, by installing an impactor with cut-off diameter at 0.1 μm, would be worth pursuing.
机译:尝试通过修改环境碳质颗粒监测仪(ACPM,R&P 5400)来测量超细气溶胶中元素碳(EC)的比例。主要修改包括在此双通道仪器的采样线之一中放置一个石英过滤器。使用过滤器可以收集其中包含的所有气溶胶和EC,而在仪器的另一行中,标准冲击器仅采样大于0.14μm的颗粒。小于0.14μm的颗粒中EC的比例由通过两条采样线测得的浓度差得出。使用改良仪器进行的测量是在荷兰阿姆斯特丹的一个郊区进行的。明显的吸附伪影无法通过使用剥蚀仪消除,因此无法对总碳数据进行有意义的评估。 EC测量中的空白可以忽略不计,因此可以进一步评估EC数据。我们发现,通过撞击器通过通道获得的EC浓度总体上低于过滤器管线中的EC浓度。浓度的平均比率接近0.6,这表明大约40%的EC位于小于0.14μm的颗粒中。可以排除两条采样线中浓度差异的替代解释,例如氧化程度的差异。这应该是加载的函数,事实并非如此。造成这种差异的另一个原因可能是冲击器由于反弹而收集到的材料较少,但是由于大量的潮解液和粘性铵化合物的共同沉积,这种气溶胶在荷兰的反弹不太可能。结论是,通过安装截止直径为0.1μm的冲击器,进一步评估超细EC的真实分数将是值得追求的。

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