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Field Survey of Trans-boundary Air Pollution with High Time Resolution at Coastal Sites on the Sea of Japan during Winter in Japan}
Authors:Masahide Aikawa  Takatoshi Hiraki  Motonori Tamaki  Mikio Kasahara  Akira Kondo  Itsushi Uno  Hitoshi Mukai  Atsushi Shimizu  Kentaro Murano
Institution:(1) Hyogo Prefectural Institute of Public Health and Environmental Sciences, 3-1-27 Yukihira-cho, Suma-ku, Kobe Hyogo, 654-0037, Japan;(2) Hyogo Environmental Advancement Association, 3-1-31 Yukihira-cho, Suma-ku, Kobe Hyogo, 654-0037, Japan;(3) Graduate School of Energy Science, Kyoto University, Yoshida-Honmachi, Sakyo-ku, Kyoto 606-8317, Japan;(4) Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita Osaka, 565-0871, Japan;(5) Research Institute for Applied Mechanics, Kyushu University, Kasuga Park 6-1, Kasuga Fukuoka, 816-8580, Japan;(6) National Institute for Environmental Studies, 16-2 Onogawa, Tukuba Ibaraki, 305-8506, Japan
Abstract:An intensive field survey, with 6-h measurement intervals, of concentrations of chemical species in particulate matter and gaseous compounds was carried out at coastal sites on the Sea of Japan during winter. The concentration variation of SO2(g) and HNO3(g) were well correlated, whereas the NH3(g) concentration variation had no correlation with those of SO2(g) and HNO3(g). The NH4 + (p)/non-sea-salt- (nss-)SO4 2 −(p) ratio in particulate matter was mainly affected by the location of the sampling site. One or more concentration peaks of nss-Ca2 + for survey period were observed. Backward trajectories analyses for the highest nss-Ca2 + concentration peaks showed some inconsistency in pathways. We consider that insufficient mixing of the atmosphere and/or insufficient time for the transported air pollutants to react with those discharged locally are the most likely explanations for the discrepancies between the measured products HNO3]NH3] and the calculated values.
Keywords:aerosol  ammonia  ammonium  filter pack  gases  nitrate  sulfate
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