Alternativer Identifier:
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Verwandter Identifier:
Ersteller/in:
Jiang, Feng https://orcid.org/0000-0003-1399-5353 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Saathoff, Harald https://orcid.org/0000-0002-1301-8010 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Ezenobi, Uzoamaka [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Song, Junwei https://orcid.org/0000-0001-5573-3154 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Zhang, Hengheng https://orcid.org/0000-0001-5872-5985 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Gao, Linyu https://orcid.org/0000-0001-7080-6120 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]

Leisner, Thomas https://orcid.org/0000-0001-9693-7671 [Institut für Meteorologie und Klimaforschung Atmosphärische Aerosolforschung (IMKAAF), Karlsruher Institut für Technologie (KIT)]
Beitragende:
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Titel:
Dataset for the publication: Brown carbon aerosol in rural Germany: sources, chemistry, and diurnal variations
Weitere Titel:
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Beschreibung:
(Abstract) Brown carbon aerosol (BrC) is one major contributor to atmospheric air pollution in Europe, especially in winter. Therefore, we studied the chemical composition, diurnal variation, and sources of BrC from 17th February to 16th March at a rural location in southwest Germany. In total, 178 potential BrC molecules (including 7 nitro aromatic compounds, NACs) were identified in the particle phase comprising on average 63 ± 32 ng m−3, and 31 potential BrC (including 4 NACs) molecules were identified in the gas phase contributing on average 6.2 ± 5.0 ng m−3 during the whole campaign. The 178 potential BrC molecules only accounted for 2.3 ± 1.5 % of the total organic mass, but can explain 11 ± 11 % of the total BrC absorption at 370 nm, assuming an average mass absorption coefficient at 370 nm (MAC370) of 9.5 m2 g−1. A few BrC molecules dominated the total BrC absorption. In addition, diurnal variations show that gas phase BrC was higher at daytime and lower at night. It was mainly controlled by secondary formation (e.g. photooxidation) and particle-to-gas partitioning. Correspondingly, the particle phase BrC was lower at daytime and higher at nighttime. Secondary formation dominates the particle-phase BrC with 61 ± 21 %, while 39 ± 21 % originated from biomass burning. Furthermore, the particle-phase BrC showed decreasing light absorption due to photochemical aging. This study extends the current understanding of real-time behaviors of brown carbon aerosol in the gas and particle phase at a location characteristic for the central Europe.
(Abstract) Brown carbon aerosol (BrC) is one major contributor to atmospheric air pollution in Europe, especially in winter. Therefore, we studied the chemical composition, diurnal variation, and sources of BrC from 17th February to 16th March at a rural location in southwest Germany. In total, 178 potential BrC molecules (including 7 nitro aromatic compounds, NACs) were identified in the particle phase comprising on average 63 ± 32 ng m−3, and 31 potential BrC (including 4 NACs) molecules were identified in the gas phase contributing on average 6.2 ± 5.0 ng m−3 during the whole campaign. The 178 potential BrC molecules only accounted for 2.3 ± 1.5 % of the total organic mass, but can explain 11 ± 11 % of the total BrC absorption at 370 nm, assuming an average mass absorption coefficient at 370 nm (MAC370) of 9.5 m2 g−1. A few BrC molecules dominated the total BrC absorption. In addition, diurnal variations show that gas phase BrC was higher at daytime and lower at night. It was mainly controlled by secondary formation (e.g. photooxidation) and particle-to-gas partitioning. Correspondingly, the particle phase BrC was lower at daytime and higher at nighttime. Secondary formation dominates the particle-phase BrC with 61 ± 21 %, while 39 ± 21 % originated from biomass burning. Furthermore, the particle-phase BrC showed decreasing light absorption due to photochemical aging. This study extends the current understanding of real-time behaviors of brown carbon aerosol in the gas and particle phase at a location characteristic for the central Europe.
(Technical Remarks) The data in the Excel files are related to the publication Jiang et al., ACPD, 2024. Each sheet of the Excel files corresponds to one plot in the publication as repeated below. The data originates mainly from aethalometer and FIGAERO-CIMS. The figures and captions from the publication are shown in the following to allow for a good understanding of the data files. Jiang, F., Saathoff, H., Ezenobi, U., Song, J., Zhang, H., Gao, L., and Leisner, T.,: Measurement report: Brown carbon aerosol in rural Germany: sources, chemistry, and diurnal variations, EGUsphere, https://doi.org/10.5194/egusphere-2024-1848, 2024, in review, 2024.
Schlagworte:
Aerosol Chemistry Data
Brown Carbon at KIT
Zugehörige Informationen:
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Sprache:
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Erstellungsjahr:
Fachgebiet:
Geological Science
Objekttyp:
Dataset
Datenquelle:
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Verwendete Software:
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Datenverarbeitung:
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Erscheinungsjahr:
Förderung:
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Name Speichervolumen Metadaten Upload Aktion
Status:
Publiziert
Eingestellt von:
kitopen
Erstellt am:
Archivierungsdatum:
2024-11-21
Archivgröße:
3,0 MB
Archiversteller:
kitopen
Archiv-Prüfsumme:
47db0d502c155966d690a6a5bac1e95c (MD5)
Embargo-Zeitraum:
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