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Using Hourly Measurements to Explore the Role of Secondary Inorganic Aerosol in PM_(2.5)during Haze and Fog in Hangzhou, China 被引量:15

Using Hourly Measurements to Explore the Role of Secondary Inorganic Aerosol in PM_(2.5)during Haze and Fog in Hangzhou, China
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摘要 This paper explores the role of the secondary inorganic aerosol (SIA) species ammonium,NH4+,nitrate,NO3-,and sulfate,SO24-,during haze and fog events using hourly mass concentrations of PM2.5 measured at a suburban site in Hangzhou,China.A total of 546 samples were collected between 1 April and 8 May 2012.The samples were analyzed and classified as clear,haze or fog depending on visibility and relative humidity (RH).The contribution of SIA species to PM2.5 mass increased to ~50% during haze and fog.The mass contribution of nitrate to PM2.5 increased from 11% during clear to 20% during haze episodes.Nitrate mass exceeded sulfate mass during haze,while near equal concentrations were observed during fog episodes.The role of RH on the correlation between concentrations of SIA and visibility was examined,with optimal correlation at 60%-70% RH.The total acidity during clear,haze and fog periods was 42.38,48.38 and 45.51 nmol m-3,respectively,indicating that sulfate,nitrate and chloride were not neutralized by ammonium during any period.The nitrate to sulfate molar ratio,as a function of the ammonium to sulfate molar ratio,indicated that nitrate formation during fog started at a higher ammonium to sulfate molar ratio compared to clear and haze periods.During haze and fog,the nitrate oxidation ratio increased by a factor of 1.6-1.7,while the sulfur oxidation ratio increased by a factor of 1.2-1.5,indicating that both gaseous NO2 and SO2 were involved in the reduced visibility. This paper explores the role of the secondary inorganic aerosol (SIA) species ammonium,NH4+,nitrate,NO3-,and sulfate,SO24-,during haze and fog events using hourly mass concentrations of PM2.5 measured at a suburban site in Hangzhou,China.A total of 546 samples were collected between 1 April and 8 May 2012.The samples were analyzed and classified as clear,haze or fog depending on visibility and relative humidity (RH).The contribution of SIA species to PM2.5 mass increased to ~50% during haze and fog.The mass contribution of nitrate to PM2.5 increased from 11% during clear to 20% during haze episodes.Nitrate mass exceeded sulfate mass during haze,while near equal concentrations were observed during fog episodes.The role of RH on the correlation between concentrations of SIA and visibility was examined,with optimal correlation at 60%-70% RH.The total acidity during clear,haze and fog periods was 42.38,48.38 and 45.51 nmol m-3,respectively,indicating that sulfate,nitrate and chloride were not neutralized by ammonium during any period.The nitrate to sulfate molar ratio,as a function of the ammonium to sulfate molar ratio,indicated that nitrate formation during fog started at a higher ammonium to sulfate molar ratio compared to clear and haze periods.During haze and fog,the nitrate oxidation ratio increased by a factor of 1.6-1.7,while the sulfur oxidation ratio increased by a factor of 1.2-1.5,indicating that both gaseous NO2 and SO2 were involved in the reduced visibility.
出处 《Advances in Atmospheric Sciences》 SCIE CAS CSCD 2014年第6期1427-1434,共8页 大气科学进展(英文版)
基金 supported by the National Natural Science Foundation of China (Grant Nos. 21190053 and 21177025) the Shanghai Science and Technology Commission of Shanghai Municipality (Grant Nos. 12DJ1400100 and 13XD 1400700) the Priority Fields for Ph.D. Programs Foundation of the Ministry of Education of China (Grant No.20110071130003)
关键词 HAZE secondary inorganic aerosol PM2.5 Yangtze River Delta haze secondary inorganic aerosol PM2.5 Yangtze River Delta
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  • 1WANGJing-li,ZHANGYuan-hang,SHAOMin,LiuXu-lin,ZENGLi-min,CHENGCong-lan,XUXiao-feng.Chemical composition and quantitative relationship between meteorological condition and fine particles in Beijing[J].Journal of Environmental Sciences,2004,16(5):860-864. 被引量:11
  • 2安俊岭,张仁健,韩志伟.北方15个大型城市总悬浮颗粒物的季节变化[J].气候与环境研究,2000,5(1):25-29. 被引量:67
  • 3Arimoto R, Duce R A, Savoie D L, Prospero J M, Talbot R, Cullen J D et al., 1996. Relationships among aerosol constituents from Asia and the North Pacific during PEM- West. Journal of Geophysical Research, 101:2011-2023.
  • 4Brown S G, Herckes P, Ashbaugh L, Hannigan M P, Kreidenweis S M, Collett Jr J L, 2002. Characterization of organic aerosol in Big Bend National Park, Texas. Atmospheric Environment, 36(38): 5807-5818.
  • 5Cao J J, Lee S C, Ho K F, Zou S C, Fung K, Li Yet al., 2004. Spatial and seasonal variations of atmospheric organic carbon and elemental carbon in Pearl River Delta Region, China. Atmospheric Environment, 38: 4447-4456.
  • 6Castro L M, Pio C A, Harrison R M, Smith D J T, 1999. Carbonaceous aerosol in urban and rural European atmospheres: estimation of secondary organic carbon concentrations. Atmospheric Environment, 33: 2771-2781.
  • 7Chen L W A, Chow J C, Doddridge B G, Dickerson R R, Ryan W F, Mueller P K, 2003. Analysis of a summertime PM2.5 and haze episode in the mid-Atlantic region. Journal of the Air & Waste Management Association, 53: 946-956.
  • 8Cheung H C, Wang T, Baumann K, Guo H, 2005. Influence of regional pollution outflow on the concentrations of fine particulate matter and visibility in the coastal area of southern China. Atmospheric Environment, 39: 6463-6474.
  • 9Chow J C, Watson J G, Fujita E M, Lu Z, Lawson D R, 1994. Temporal and spatial variations of PM2.5 and PM10 aerosol in the southern California air quality study. Atmospheric Environment, 28: 3773-3785.
  • 10Chow J C, Watson J G, Lu Z, Lowenthal D H, Frazier C A, Solomom P A et al., 1996. Descriptive analysis of PM2.5 and PM10 at regionally representative locations during SJVAQS/AUSPEX. Atmospheric Environment, 30: 2079- 2112.

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