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Single-particle measurements of bouncing particles and in situ collection efficiency from an airborne aerosol mass spectrometer (AMS) with light-scattering detection

机译:弹性颗粒的单粒子测量和具有光散射检测的空气机气溶胶质谱仪(AMS)的原位收集效率

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A light-scattering module was coupled to an airborne, compact time-of-flight aerosol mass spectrometer (LS-AMS) to investigate collection efficiency (CE) while obtaining nonrefractory aerosol chemical composition measurements during the Southeast Nexus (SENEX) campaign. In this instrument, particles scatter light from an internal laser beam and trigger saving individual particle mass spectra. Nearly all of the single-particle data with mass spectra that were triggered by scattered light signals were from particles larger than similar to 280 nm in vacuum aerodynamic diameter. Over 33 000 particles are characterized as either prompt (27 %), delayed (15 %), or null (58 %), according to the time and intensity of their total mass spectral signals. The particle mass from single-particle spectra is proportional to that derived from the light-scattering diameter (d(va-LS)) but not to that from the particle time-of-flight (PToF) diameter (d(va-MS)) from the time of the maximum mass spectral signal. The total mass spectral signal from delayed particles was about 80% of that from prompt ones for the same d(va-LS). Both field and laboratory data indicate that the relative intensities of various ions in the prompt spectra show more fragmentation compared to the delayed spectra. The particles with a delayed mass spectral signal likely bounced off the vaporizer and vaporized later on another surface within the confines of the ionization source. Because delayed particles are detected by the mass spectrometer later than expected from their d(va-LS) size, they can affect the interpretation of particle size (PToF) mass distributions, especially at larger sizes. The CE, measured by the average number or mass fractions of particles optically detected that had measurable mass spectra, varied significantly (0.2-0.9) in different air masses. The measured CE agreed well with a previous parameterization when CE > 0.5 for acidic particles but was sometimes lower than the minimum parameterized CE of 0.5.
机译:光散射模块耦合到空气中,紧凑的飞行时间气溶胶质谱仪(LS-AMS),以研究收集效率(CE),同时在东南部(SENEX)运动期间获得非致反应气溶胶化学成分测量。在该仪器中,粒子散射来自内部激光束的光并触发各个粒子质谱。几乎所有由散射光信号触发的质谱的所有单粒子数据都来自大于类似于280nm的颗粒,真空空气动力学直径。根据其总质量光谱信号的时间和强度,超过33 000颗粒的特征在于提示(27%),延迟(15%)或零(58%)。来自单粒子光谱的颗粒质量与源自光散射直径(D(Va-LS))成比例,但不是从颗粒飞行时间(Ptof)直径(D(Va-MS)的颗粒)从最大质谱信号的时间。来自延迟粒子的总质谱信号从促进同一D(VA-LS)的提示颗粒的总质谱信号约为80%。该领域和实验室数据表明,与延迟光谱相比,提示光谱中各种离子的相对强度显示出更多的碎片。具有延迟质谱信号的颗粒可能会反弹蒸发器,并在电离源的限制内后来蒸发。由于延迟颗粒由质谱仪检测到于其D(Va-LS)尺寸的预期,因此它们可以影响粒度(PTOF)质量分布的解释,尤其是在较大的尺寸下。通过光学检测的颗粒的平均数量或质量分数测量的CE测量,所述粒子具有可测量的质谱,在不同的空气质量中显着变化(0.2-0.9)。当酸性颗粒的Ce> 0.5时,测量的CE与先前的参数化同意,但有时低于0.5的最小参数化Ce。

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