日本地球惑星科学連合2015年大会

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セッション記号 A (大気水圏科学) » A-AS 大気科学・気象学・大気環境

[A-AS21] 大気化学

2015年5月28日(木) 16:15 〜 17:00 201B (2F)

コンビーナ:*澤 庸介(気象研究所海洋・地球化学研究部)、竹川 暢之(首都大学東京 大学院理工学研究科)、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:中山 智喜(名古屋大学 太陽地球環境研究所)

16:45 〜 17:00

[AAS21-29] 塩素消失の新しい指標としての主要イオン化学組成の利用法

*坂田 昂平1坂口 綾2為則 雄祐3小川 雅裕4高橋 嘉夫5 (1.広島大学大学院理学研究科地球惑星システム学専攻、2.筑波大学大学院数理物質科学研究科、3.財団法人高輝度光科学研究センター、4.立命館大学SRセンター、5.東京大学大学院理学系研究科地球惑星科学専攻)

キーワード:大気化学, エアロゾル, ナトリウム, X線吸収微細構造法

A large part of sodium and chlorine in aerosol particles are derived from surface seawater as sodium chloride (sea-salt; NaCl). Sodium chloride in aerosol is altered to sodium nitrate (NaNO3) and sulfate (Na2SO4) by the reaction with nitric acid (HNO3) and sulfuric acid (H2SO4) in atmosphere, respectively. In these reactions, gaseous HCl is emitted from sea-salt particles to the atmosphere, which is is called as chlorine deficiency. These are important chemical reactions to anthropogenic N, in the process of transport from continent to open ocean, and to H2SO4 as scavenging process in atmosphere (Akimoto, 2014). However, detail processes of the chemical reaction and size-dependence of aerosol particles on this reaction are not clear. In order to clarify these reactions/processes in aerosol, we employed mass fractions (MF) parameter to size-fractionated aerosol particles obtained from land/continent and ocean. Direct speciation of Na was also conducted by soft X-ray absorption fine structure (XAFS) spectroscopy to intercompare the abundance ratio of Na species to those estimated by MF.
Size-fractionated aerosol particles on land were collected by a high volume cascade impactor at Higashi-Hiroshima from December 2012 to March 2014. Marine total suspended particulate (TSP) and size-fractionated aerosol particles were collected in the R/V Hakuho-Maru research cruises of KH-12-4 (the North Pacific Ocean: from 23th August to 3rd October 2012) and KH-13-4 Leg. 4 (the Bay of Bengal: from 31th July to 14th August 2013), respectively. Major ionic concentrations (Na+, NH4+, K+, Mg2+, Ca2+, Cl-, NO3- and SO42-) in aerosol samples were determined by an ion chromatography after appropriate pretreatment. MF parameters were calculated as [X]eq/[total anion]eq (X: Cl-, NO3- and nssSO42-). Direct speciation of Na in continental size-fractionated aerosol particles were conducted by XAFS spectroscopy on BL-10, SR-center, Ritsumeikan University.
MF[Cl-]eq was inversely correlated with both MF[NO3-]eq and MF[nssSO42-]eq in continental coarse aerosol particles. It can be said that the chlorine deficiency is explained by the reaction with NO3- and/or nssSO42-. The regression line for MF[Cl-]eq-MF[nssSO42-]eq was -2.16. As for MF[Cl-]eq-MF[NO3-]eq, the regression line shows -1.03, and this regression line satisfies the equation of y=1-x. Thus, HNO3 has large contribution as a reactant of NaCl in the urban atmosphere. Furthermore, chemical reaction of NaCl with HNO3 and H2SO4 preferentially occur on the small aerosol particles because further decrement of MF[Cl-]eq was found in smaller size of aerosols compared with that of large aerosol particles. The speciation analysis with XAFS spectroscopy showed comparable results with that obtained from MF analysis using the high reacted aerosol samples from continent (MF[Cl-]eq : MF[NO3-]eq : MF[nssSO42-]eq =18:56:23). As for marine aerosol samples from the North Pacific Ocean, dominant reactant of NaCl is H2SO4. On the other hand, the reaction of NaCl occurs with both NO3- and SO42- above the Bay of Bengal.
As a consequence, MF is very useful tools to find dominant reactant of NaCl and Na chemical species as a result of chlorine deficiency in both continental and marine aerosol particles.