Author/Authors :
Kikuchi، نويسنده , , Ryoei and Takada، نويسنده , , Makoto and Hifumi، نويسنده , , Keita and Yoshimura، نويسنده , , Keiji and Ozeki، نويسنده , , Toru and Kimoto، نويسنده , , Takashi and Kajikawa، نويسنده , , Masahiro and Ogawa، نويسنده , , Nobuaki، نويسنده ,
Abstract :
It is well known that sea-salt aerosols in particulate matter (PM) react with acids such as H2SO4 and HNO3 during transportation and thereby lose chloride ions (Cl-loss). The PM and fog were sampled concurrently at different altitudes in the Hachimantai mountain range, northern Japan. The PM and fog sampled at different altitudes had nearly identical properties for the ion components. However, the PM was in a Cl-depleted state (more than 80% of all samples), but the fog water was not in so Cl-depleted state (less than 29%). As a result, it could be explained that this phenomenon caused because the fog droplets took up the gaseous state HCl other than sea-salt PM. After all Cl- in the fog water recovered and was rather rich compared with the sea-salt or the PM by the uptake of the gaseous state HCl. Moreover, it was found that for PMcoarse(2.5 < D < 10), 86% of the acid (H2SO4 and HNO3) was consumed for Cl-loss reactions and/or for dissolution of Ca and Mg in soil particles.
Keywords :
particulate matter (PM) , Sea-salt , Cl-loss , soil , fog