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Design of a Real-Time Scanning Electrical Mobility Spectrometer and its Application in Study of Nanoparticle Aerosol Generation

机译:实时扫描电迁移率谱仪的设计及其在纳米气溶胶产生研究中的应用

摘要

A real-time, mobile Scanning Electrical Mobility Spectrometer (SEMS) was designed using a Condensation Particle Counter (CPC) and Differential Mobility Analyzer (DMA) to measure the size distribution of nanoparticles. The SEMS was calibrated using monodisperse Polystyrene Latex (PSL) particles, and was then applied to study the size distribution of TiO2 nanoparticle aerosols generated by spray drying water suspensions of the nanoparticles. The nanoparticle aerosol size distribution, the effect of surfactant, and the effect of residual solvent droplets were determined.The SEMS system was designed by integrating the Electrical System, the Fluid Flow System, and the SEMS Software. It was calibrated using aerosolized Polystyrene Latex (PSL) spheres with nominal diameters of 99 nm and 204 nm. TiO2 nanoparticle aerosols were generated by atomizing water suspensions of TiO2 nanoparticles using a Collison nebulizer. Size distribution of the TiO2 aerosol was measured by the SEMS, as well as by TEM. Furthermore, the effect of surfactant, Tween 20 at four different concentrations between 0.01mM and 0.80mM, and stability of aerosol concentration with time were studied. It was hypothesized that residual particles in DI water observed during the calibration process were a mixture of impurities in water and unevaporated droplets. Solid impurities were captured on TEM grids using a point-to-plane Electrostatic Precipitator (ESP) and analyzed by Energy Dispersive Spectroscopy (EDS) while the contribution of unevaporated liquid droplets to residual particles was confirmed by size distribution measurements of aerosolized DI water in different humidity conditions. The calibration indicated that the mode diameter was found to be at 92.5nm by TEM and 95.8nm by the SEMS for 99nm nominal diameter particles, a difference of 3.6%. Similarly, the mode diameter for 204nm nominal diameter particles was found to be 194.9nm by TEM and 191nm by SEMS, a difference of 2.0%. Measurements by SEMS for TiO2 aerosol generated by Collison nebulizer indicated the mode diameters of 3mM, 6mM, and 9mM concentrations of TiO2 suspension to be 197.5nm, 200.0nm and 195.2nm respectively. On the other hand, the mode diameter was found to be approximately 95nm from TEM analysis of TiO2 powder. Additionally, concentration of particles generated decreased with time. Dynamic Light Scattering (DLS) measurements indicated agglomeration of particles in the suspension. Furthermore, the emulation of single particle distribution was not possible even after using Tween 20 in concentrations between 0.01mM and 0.80mM. From the study of residual particles in DI water, it was found that residual particles observed during the aerosolization of suspensions of DI water were composed of impurities present in DI water and unevaporated droplets of DI water. Although it was possible to observe solid residual particles on the TEM grid, EDS was not able to determine the chemical composition of these particles.
机译:使用冷凝粒子计数器(CPC)和差分迁移率分析仪(DMA)设计了实时移动扫描电迁移率仪(SEMS),以测量纳米粒子的尺寸分布。使用单分散聚苯乙烯胶乳(PSL)颗粒对SEMS进行校准,然后将其用于研究通过喷雾干燥纳米颗粒的水悬浮液而生成的TiO2纳米颗粒气溶胶的尺寸分布。确定了纳米颗粒的气溶胶粒径分布,表面活性剂的作用以及残留的溶剂滴的作用。通过集成电气系统,流体流动系统和SEMS软件设计了SEMS系统。使用标称直径为99 nm和204 nm的雾化聚苯乙烯胶乳(PSL)球进行校准。通过使用Collison雾化器雾化TiO2纳米颗粒的水悬浮液来生成TiO2纳米颗粒气溶胶。通过SEMS和TEM测量TiO 2气雾剂的尺寸分布。此外,研究了表面活性剂,介于0.01mM和0.80mM之间的四个不同浓度的Tween 20的影响以及气溶胶浓度随时间的稳定性。假设在校准过程中观察到的去离子水中的残留颗粒是水中杂质和未蒸发液滴的混合物。使用点对面静电除尘器(ESP)将固体杂质捕获在TEM网格上,并通过能量色散谱(EDS)进行分析,同时通过不同浓度的雾化去离子水的尺寸分布测量证实了未蒸发的液滴对残留颗粒的贡献湿度条件。校准表明,对于99nm标称直径的颗粒,TEM的模直径为92.5nm,而SEMS的模直径为95.8nm,相差3.6%。类似地,通过TEM发现204nm标称直径颗粒的众数直径为194.9nm,通过SEMS发现为191nm,相差2.0%。通过SEMS对Collison雾化器产生的TiO2气溶胶进行的测量表明,浓度为3mM,6mM和9mM的TiO2悬浮液的众数直径分别为197.5nm,200.0nm和195.2nm。另一方面,从TiO 2粉末的TEM分析发现,模直径为约95nm。另外,产生的颗粒浓度随时间降低。动态光散射(DLS)测量表明悬浮液中的颗粒附聚。此外,即使使用浓度在0.01mM至0.80mM之间的Tween 20,也无法模拟单个粒子的分布。通过对去离子水中残留颗粒的研究,发现去离子水悬浮液雾化过程中观察到的残留颗粒由去离子水中存在的杂质和未蒸发的去离子水滴组成。尽管可以在TEM网格上观察到固体残留颗粒,但EDS不能确定这些颗粒的化学组成。

著录项

  • 作者

    Singh Gagan;

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  • 年度 2010
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  • 原文格式 PDF
  • 正文语种 en_US
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