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Pollutants identification of ambient aerosols by two types of aerosol mass spectrometers over southeast coastal area, China 被引量:1

Pollutants identification of ambient aerosols by two types of aerosol mass spectrometers over southeast coastal area, China
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摘要 Two different aerosol mass spectrometers, Aerodyne Aerosol Mass Spectrometer(AMS) and Single Particle Aerosol Mass Spectrometer(SPAMS) were deployed to identify the aerosol pollutants over Xiamen, representing the coastal urban area. Five obvious processes were classified during the whole observation period. Organics and sulfate were the dominant components in ambient aerosols over Xiamen. Most of the particles were in the size range of 0.2–1.0 μm, accounting for over 97% of the total particles measured by both instruments.Organics, as well as sulfate, measured by AMS were in good correlation with measured by SPAMS. However, high concentration of NH4+was obtained by AMS, while extremely low value of NH4+was detected by SPAMS. Contrarily, high particle number counts of NO3-and Clwere given by SPAMS while low concentrations of NO3-and Cl-were measured by AMS. The variations of POA and SOA obtained from SPAMS during event 1 and event 2 were in accordance with the analysis of HOA and OOA given by AMS, suggesting that both of AMS and SPAMS can well identify the organic clusters of aerosol particles. Overestimate or underestimate of the aerosol sources and acidity would be present in some circumstances when the measurement results were used to analyze the aerosol properties, because of the detection loss of some species for both instruments. Two different aerosol mass spectrometers, Aerodyne Aerosol Mass Spectrometer(AMS) and Single Particle Aerosol Mass Spectrometer(SPAMS) were deployed to identify the aerosol pollutants over Xiamen, representing the coastal urban area. Five obvious processes were classified during the whole observation period. Organics and sulfate were the dominant components in ambient aerosols over Xiamen. Most of the particles were in the size range of 0.2–1.0 μm, accounting for over 97% of the total particles measured by both instruments.Organics, as well as sulfate, measured by AMS were in good correlation with measured by SPAMS. However, high concentration of NH4+was obtained by AMS, while extremely low value of NH4+was detected by SPAMS. Contrarily, high particle number counts of NO3-and Clwere given by SPAMS while low concentrations of NO3-and Cl-were measured by AMS. The variations of POA and SOA obtained from SPAMS during event 1 and event 2 were in accordance with the analysis of HOA and OOA given by AMS, suggesting that both of AMS and SPAMS can well identify the organic clusters of aerosol particles. Overestimate or underestimate of the aerosol sources and acidity would be present in some circumstances when the measurement results were used to analyze the aerosol properties, because of the detection loss of some species for both instruments.
出处 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2018年第2期252-263,共12页 环境科学学报(英文版)
基金 supported by the Natural Science Foundation of Fujian Province,China(No.2015J05024) financially supported by Qingdao National Laboratory for marine science and technology(No.QNLM2016ORP0109) the National Natural Science Foundation of China(No.21106018,No.41305133) the Scientific Research Foundation of Third Institute of Oceanography,SOA(No.2014027) the Special Fund for Marine Researches in the Public Interest(No.2004DIB5J178)
关键词 AEROSOL Size distribution Chemical composition Aerosol mass spectrometer Aerosol source Aerosol Size distribution Chemical composition Aerosol mass spectrometer Aerosol source
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