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  Quantification of environmentally persistent free radicals and reactive oxygen species in atmospheric aerosol particles

Arangio, A. M., Tong, H., Socorro, J., Pöschl, U., & Shiraiwa, M. (2016). Quantification of environmentally persistent free radicals and reactive oxygen species in atmospheric aerosol particles. Atmospheric Chemistry and Physics, 16(20), 13105-13119. doi:10.5194/acp-16-13105-2016.

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資料種別: 学術論文

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 作成者:
Arangio, Andrea M.1, 著者           
Tong, H.1, 著者           
Socorro, J.1, 著者           
Pöschl, U.1, 著者           
Shiraiwa, M.1, 著者           
所属:
1Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826290              

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 要旨: Fine particulate matter plays a central role in the adverse health effects of air pollution. Inhalation and deposition of aerosol particles in the respiratory tract can lead to the release of reactive oxygen species (ROS), which may cause oxidative stress. In this study, we have detected and quantified a wide range of particle-associated radicals using electron paramagnetic resonance (EPR) spectroscopy. Ambient particle samples were collected using a cascade impactor at a semi-urban site in central Europe, Mainz, Germany, in May-June 2015. Concentrations of environmentally persistent free radicals (EPFR), most likely semiquinone radicals, were found to be in the range of (1-7) x 10(11) spins mu g(-1) for particles in the accumulation mode, whereas coarse particles with a diameter larger than 1 mu m did not contain substantial amounts of EPFR. Using a spin trapping technique followed by deconvolution of EPR spectra, we have also characterized and quantified ROS, including OH, superoxide (O-2(-)/and carbon-and oxygen-centered organic radicals, which were formed upon extraction of the particle samples in water. Total ROS amounts of (0.1-3) x 10(11) spins mu g(-1) were released by submicron particle samples and the relative contributions of OH, O-2(-), C-centered and O-centered organic radicals were similar to 11-31, similar to 2-8, similar to 41-72 and similar to 0-25 %, respectively, depending on particle sizes. OH was the dominant species for coarse particles. Based on comparisons of the EPR spectra of ambient particulate matter with those of mixtures of organic hydroperoxides, quinones and iron ions followed by chemical analysis using liquid chromatography mass spectrometry (LC-MS), we suggest that the particle-associated ROS were formed by decomposition of organic hydroperoxides interacting with transition metal ions and quinones contained in atmospheric humic-like substances (HULIS).

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 日付: 2016
 出版の状態: 出版
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 識別子(DOI, ISBNなど): ISI: 000387112200002
DOI: 10.5194/acp-16-13105-2016
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出版物 1

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出版物名: Atmospheric Chemistry and Physics
種別: 学術雑誌
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出版社, 出版地: Katlenburg-Lindau, Germany : European Geosciences Union
ページ: - 巻号: 16 (20) 通巻号: - 開始・終了ページ: 13105 - 13119 識別子(ISBN, ISSN, DOIなど): ISSN: 1680-7316
CoNE: https://pure.mpg.de/cone/journals/resource/111030403014016