Journal of Atmospheric and Environmental Optics ›› 2020, Vol. 15 ›› Issue (6): 438-447.

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Performance Comparison Between a Custom-Made Soft X-Ray Neutralizer and a Commercial Counterpart #br#

LIANG Baoling1, XU Hanbing2∗, ZHAO Jun1;3;4;5∗ #br#   

  1. 1 School of Atmospheric Sciences, Sun Yat-sen University, Zhuhai 519082, China; 2 Public Experimental Teaching Center, Sun Yat-sen University, Guangzhou 510275, China; 3 Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), Zhuhai 519082, China; 4 Guangdong Province Key Laboratory for Climate Change and Natural Disaster Studies, Guangzhou 510275, China; 5 Guangdong Provincial Observation and Research Station for Climate Environment and Air Quality Change in the Pearl River Estuary, Guangzhou 510275, China
  • Received:2020-08-12 Revised:2020-09-24 Online:2020-11-28 Published:2020-12-10
  • Contact: Jun Zhao E-mail:zhaojun23@mail.sysu.edu.cn
  • Supported by:
    Supported by the National Key Research and Development Program of China (国家重点研发计划课题, 2017YFC0209502), Science and Technology Innovation Committee of Guangzhou (广州市科技创新发展专项, 201803030010)


Abstract: Performance comparison between a custom-made soft X-ray neutralizer (CM-SXR) and a commercial counterpart (TSI-SXR, advanced aerosol neutralizer, model 3088, TSI, USA) is made by using a scanning mobility particle sizer (SMPS). The results show that for all the tested particles (i.e., Polystyrene latex particles, ammonium sulfate 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 mobility analyzer (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 particle number concentration measured by TSI-SXR is higher than that measured by CM-SXR and the differences are up to 77%. Possible reasons accounting for the above differences are discussed, and it is deduced that the mounting position 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 leading to different positively- and negatively-charged particle distribution inside the neutralizers.


Key words: soft X-ray, neutralizer, atmospheric aerosols, size distribution, particle neutralizing

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