日本地球惑星科学連合2014年大会

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セッション記号 A (大気海洋・環境科学) » A-AS 大気科学・気象学・大気環境

[A-AS22_1AM2] 大気化学

2014年5月1日(木) 11:00 〜 12:45 511 (5F)

コンビーナ:*竹川 暢之(東京大学先端科学技術研究センター)、澤 庸介(気象研究所地球化学研究部)、金谷 有剛(独立行政法人海洋研究開発機構地球環境変動領域)、高橋 けんし(京都大学生存圏研究所)、谷本 浩志(国立環境研究所)、座長:坪井 一寛(気象研究所 海洋・地球化学研究部)

11:15 〜 11:30

[AAS22-16] 粗大粒子、微細粒子中の鉛化学種およびその形成過程に関して

*坂田 昂平1坂口 綾1谷水 雅治2高橋 嘉夫1 (1.広島大学大学院理学研究科、2.海洋開発研究機構)

There are very few studies on chemical speciation and atmospheric chemistry of trace elements. Among the trace elements in the aerosol particles, lead(Pb) has long been measured due to the toxicity of this element. The measurement of Pb isotope ratios in aerosol particles has also been employed as a powerful tracer for air-mass transportation because Pb isotope ratios differ significantly depending on the emission area/source. However the speciation of Pb has not been clarified, although their solubility is important to estimate the health effects for human/animal body. Furthermore, Pb in the aerosol particle is the dominant source of Pb, which is used as oceanic circulation tracer, in the surface seawater. Thus, the speciation of Pb in the aerosol particle is one of the important issue. In this study, we attempted to determine the Pb species in aerosol samples using X-ray absorption fine structure (XAFS) analysis. Size-fractionated aerosol particles were collected by a high-volume aerosol sampler with cascade impactor at Higashi-Hiroshima. Lead LIII-edge (absorption edge: 13.04 keV) X-ray absorption near-edge structure (XANES) spectra were recorded on SPring-8 on BL01B1 and at KEK PF-AR on NW10A to identify the Pb species. The analyzed sample-sets of size-fractionated aerosol particles are follows: Spring (Asian dust event), summer (two sample sets), fall, and winter (transboundary pollution event). Lead species in size-fractionated aerosol particles are different between fine and coarse aerosol particles. In the fine aerosol particles, the dominant Pb species were two or three components, PbSO4, Pb(NO3)2 and PbC2O4, in all seasons. That is, the seasonal variation of Pb species in the fine aerosol was not found. It is because the Pb species in the fine aerosol particles are formed by uniform chemical reaction with H2SO4, HNO3 and oxalic acid in droplet through a year. Pb species in the coarse aerosol particles, except for on Asian dust event, were 2PbCO3-Pb(OH)2, Pb(NO3)2 and PbC2O4. These 2PbCO3-Pb(OH)2 and partial PbC2O4 were derived from road dust, and Pb(NO3)2 in coarse aerosol particles was formed by chemical reactions with HNO3 on the surface of the particle. In Asian dust event, the coarse aerosol particles showed PbSiO3 as major Pb species, although other species, 2PbCO3-Pb(OH)2 and PbC2O4, were also obtained. Thus we could found the clear seasonal variation in the coarse aerosol particles. These results will be able to estimate the accurate estimation of Pb solubility to the surface seawater.