Separate chemical characterizations of fog water, aerosol, and gas before, during, and after fog events near an industrialized area in Japan

• Published in: Atmospheric environment (1994) Vol. 41; no. 9; pp. 1950 - 1959
• Main Authors: Aikawa, Masahide, Hiraki, Takatoshi, Suzuki, Motoharu, Tamaki, Motonori, Kasahara, Mikio
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.03.2007; Elsevier Science
• Subjects: Aerosol; Applied sciences; Atmospheric pollution; Exact sciences and technology; Fog water; Gas; Pollutants physicochemistry study: properties, effects, reactions, transport and distribution; Pollution; Separate collection; Asia; Japan; Japan, Honshu, Hyogo Prefect., Kobe; Gas; Separate collection; Fog water; Aerosol; Sour gas; Water drop; Pollutant behavior; Scavenging; Troposphere; Nitrates; Sulfates; Nitric acid; Sulfur dioxide; Aerosols; Air pollution; Sampling; Fog; Hydrometeor
• ISSN: 1352-2310; 1873-2844
• DOI: 10.1016/j.atmosenv.2006.10.049

Fog water, aerosol, and gas were separately collected at Mt. Rokko (altitude 931 m) in Kobe, Japan, using a new sampling method at a mountainous site near a highly industrialized area. The fog water was collected by an active string-fog collector and the aerosol and gas by using the filter pack method. Using plural filter packs and controlling or switching the airflow before, during, and after a fog event made it possible to collect the fog water, aerosol, and gas separately. Nitrate species such as NO 3 −(p) and HNO 3(g) were effectively scavenged by fog water, while sulfur species such as SO 4 2−(p) and SO 2(g) could not be easily and effectively scavenged because of the poor solubility of SO 2(g). This difficulty was experimentally examined through an in situ investigation. Ion species (especially Na +(p) and Ca 2+(p)) which form coarse particles were easily and effectively scavenged by fog water. On the other hand, the difficulty of scavenging Mg 2+(p) could not be explained by particle size.