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Evolution of mixing state of black carbon in polluted air from Tokyo
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作者:

Shiraiwa, M.
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机构: Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan

Kondo, Y.
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机构: Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan

Moteki, N.
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机构: Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan

Takegawa, N.
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机构: Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan

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Blake, D. R.
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机构: Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
机构:
[1] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
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D O I:
10.1029/2007GL029819
中图分类号:
P [天文学、地球科学];
学科分类号:
07 ;
摘要:
The evolution of the mixing state of black carbon aerosol ( BC) was investigated using a single-particle soot photometer ( SP2) in polluted air transported from Tokyo. Ground-based measurements of aerosols and trace gases were conducted at a suburban site ( Kisai) 50 km north of Tokyo during July -August 2004. The ratio of 2-pentyl nitrate ( 2-PeONO(2)) to n-pentane ( n-C5H12) was used to derive the photochemical age. According to the SP2 measurement, the number fraction of thickly coated BC ( Shell/ Corel Ratio > ca. 2) with a core diameter of 180 nm increased at the rate of 1.9% h(-1), as the photochemical clock proceeded under land-sea breeze circulation. Positive matrix factorization was applied to investigate the time-dependent contributions of different coating materials using the mass concentrations of sulfate, nitrate, and organics measured using an aerosol mass spectrometer. The main coating materials found in this study were sulfate and organics.
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