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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:带有光散射检测的机载气溶胶质谱仪(AMS)对反弹粒子的单粒子测量和原位采集效率

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摘要

A light-scattering module was coupled to an airborne, compacttime-of-flight aerosol mass spectrometer (LS-AMS) to investigate collectionefficiency (CE) while obtaining nonrefractory aerosol chemical compositionmeasurements during the Southeast Nexus (SENEX) campaign. In this instrument,particles scatter light from an internal laser beam and trigger savingindividual particle mass spectra. Nearly all of the single-particle data withmass spectra that were triggered by scattered light signals were fromparticles larger than ∼ 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 theirtotal mass spectral signals. The particle mass from single-particle spectrais proportional to that derived from the light-scattering diameter() but not to that from the particle time-of-flight (PToF)diameter () from the time of the maximum mass spectralsignal. The total mass spectral signal from delayed particles was about80 % of that from prompt ones for the same . Both fieldand laboratory data indicate that the relative intensities of various ions inthe prompt spectra show more fragmentation compared to the delayed spectra.The particles with a delayed mass spectral signal likely bounced off thevaporizer and vaporized later on another surface within the confines of theionization source. Because delayed particles are detected by the massspectrometer later than expected from their size, they canaffect the interpretation of particle size (PToF) mass distributions,especially at larger sizes. The CE, measured by theaverage number or mass fractions of particles optically detected that hadmeasurable mass spectra, varied significantly (0.2–0.9) in different airmasses. The measured CE agreed well with a previous parameterization whenCE  0.5 for acidic particles but was sometimes lower than the minimumparameterized CE of 0.5.
机译:将光散射模块与机载紧凑型飞行时间气溶胶质谱仪(LS-AMS)耦合,以研究收集效率(CE),同时在Southeast Nexus(SENEX)战役中获得非难熔气溶胶化学成分测量值。在这种仪器中,粒子散射来自内部激光束的光并触发保存单个粒子质谱图。几乎所有由散射光信号触发的具有质谱图的单粒子数据均来自真空空气动力学直径大于280 nm的粒子,超过33 000个粒子的特征是迅速(27%),延迟(15%)或根据总质谱信号的时间和强度为零(58%)。单粒子光谱的粒子质量与从光散射直径()得出的质量成正比,但与最大质谱信号开始时的粒子飞行时间(PToF)直径()的质量成正比。延迟粒子的总质谱信号约为相同时间的质谱信号的80 signal%。现场和实验室数据均表明,与延迟光谱相比,即时光谱中各种离子的相对强度显示出更多的碎片化。具有延迟质谱信号的粒子可能会从蒸发器中反弹并随后在电离源范围内的另一个表面上蒸发。由于质谱仪检测到的延迟粒子比预期的要晚,因此它们会影响对粒子尺寸(PToF)质量分布的解释,尤其是在较大尺寸的情况下。通过光学检测的具有可测量质谱的粒子的平均数量或质量分数来衡量的CE,在不同的气团中变化显着(0.2–0.9)。对于酸性颗粒,当CE> 0.5时,测得的CE与先前的参数设置非常吻合,但有时低于最小参数化CE 0.5。

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