Fractionation of inorganic nitrates in winter Arctic troposphere: Coarse aerosol particles containing inorganic nitrates

被引:30
作者
Hara, K
Osada, K
Hayashi, M
Matsunaga, K
Shibata, T
Iwasaka, Y
Furuya, K
机构
[1] Nagoya Univ, Solar Terr Environm Lab, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[2] Tokyo Univ Sci, Fac Sci, Dept Appl Chem, Shinjuku Ku, Tokyo 1628601, Japan
关键词
D O I
10.1029/1999JD900348
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Atmospheric aerosol particles and acidic gases were collected at Ny-Alesund, Norwegian high Arctic, in winter (December - March) of 1994/1995, 1995/1996 and 1996/1997 to understand the sink processes of atmospheric inorganic nitrate and reactive nitrogen or;ides. Atmospheric inorganic nitrates were mostly present as particulate NO3- in the coarse mode defined as diameter >2.3 mu m) of which major constituents were sea-salt compounds such as Nai and Cl-. The number fraction of coarse aerosol particles containing NO3- increased in aged oceanic air masses. The internal mixing between sea-salt particles and inorganic nitrates revealed by individual particle analysis implies that uptake of gaseous HNO3 and/or formation of particulate NO3- through heterogeneous processes occurs on sea-salt particles. A simple uptake model was used to estimate the production rate of particulate NO3- due to these processes. Model calculations showed that the formation of particulate NO3- was mainly due to the uptake of gaseous HNO3 on sea-salt particles in winter Arctic. However, the heterogeneous formation from N2O5 and NO3 also makes an important contribution to the formation of particulate NO3- under no and/or weak solar radiation in winter Arctic (polar night). Thus the heterogeneous formation of NO3- on sea-salt particles may play an important role as a sink of reactive nitrogen oxide in winter Arctic.
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收藏
页码:23671 / 23679
页数:9
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