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一种自制软X 射线颗粒中和器与同类商业化中和器的性能比较#br#
引用本文:梁宝玲,许汉冰∗,赵军,∗. 一种自制软X 射线颗粒中和器与同类商业化中和器的性能比较#br#[J]. 大气与环境光学学报, 2020, 15(6): 438-447
作者姓名:梁宝玲  许汉冰∗  赵军  
作者单位:1.中山大学大气科学学院, 广东 珠海 519082;2.中山大学公共实验教学中心, 广东 广州 510275;3.南方海洋科学与工程广东省实验室 (珠海), 广东 珠海 519082;4.广东省气候变化与自然灾害研究重点实验室, 广东 广州 510275;5.华南气候环境与全球变化综合观测开放实验站, 广东 广州 510275
基金项目:Supported by the National Key Research and Development Program of China (国家重点研发计划课题, 2017YFC0209502), Science andTechnology Innovation Committee of Guangzhou (广州市科技创新发展专项, 201803030010)
摘    要:运用扫描电迁移率粒径谱仪对比测试自制软 X 射线中和器 (CM-SXR) 与商业化 TSI 高级气溶胶中和器(TSI-SXR)。研究结果表明, 对于 20 nm 以上颗粒物, 在差分电迁移率分析仪 (SMPS) 筛分负电荷模式下, 对不同颗粒物 (聚苯乙烯乳胶颗粒、硫酸铵及氯化钠颗粒、室内空气颗粒) 的测试均显示, 使用自制中和器比使用 TSI 中和器测量所得的颗粒物数浓度要高, 浓度差异最大达 40%; 而在筛分正电荷模式下, 其结果正好相反, 最大浓度差达 77%。造成上述差异的原因可能是由于软 X 射线在两种中和器中放置位置不同而导致放射程度不同以及停留时间存在差异,从而最终导致中和器中颗粒物正负电荷分布不同。

关 键 词:软 X 射线  中和器;大气气溶胶  粒径分布  颗粒中和
  
收稿时间:2020-08-12
修稿时间:2020-09-24

Performance Comparison Between a Custom-Made SoftX-Ray Neutralizer and a Commercial Counterpart#br#
LIANG Baoling,XU Hanbing∗,ZHAO Jun,∗. Performance Comparison Between a Custom-Made SoftX-Ray Neutralizer and a Commercial Counterpart#br#[J]. Journal of Atmospheric and Environmental Optics, 2020, 15(6): 438-447
Authors:LIANG Baoling  XU Hanbing∗  ZHAO Jun  
Abstract:Performance comparison between a custom-made soft X-ray neutralizer (CM-SXR) and a commercialcounterpart (TSI-SXR, advanced aerosol neutralizer, model 3088, TSI, USA) is made by using a scanning mobilityparticle sizer (SMPS). The results show that for all the tested particles (i.e., Polystyrene latex particles, ammoniumsulfate particles, sodium chloride particles, and room air particles) with a size greater than 20 nm, the particle number concentration measured by CM-SXR is higher than that measured by TSI-SXR when the differential mobilityanalyzer (DMA) is operated under the negatively-charged particle mode, and the differences can be up to 40%. However, opposite results have been found when the DMA is operated at the positively-charged mode, that is the particlenumber concentration measured by TSI-SXR is higher than that measured by CM-SXR and the differences are upto 77%. Possible reasons accounting for the above differences are discussed, and it is deduced that the mountingposition of the soft X-ray in the two neutralizers, which results in different exposures of the X-ray and the differences of the residence time when the sample passes the two different neutralizers, is likely the main reason leadingto different positively- and negatively-charged particle distribution inside the neutralizers.
Keywords:soft X-ray  neutralizer  atmospheric aerosols  size distribution  particle neutralizing
  
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