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Reactive uptake coefficients for multiphase reactions determined by a dynamic chamber system

MPS-Authors
/persons/resource/persons204129

Guo,  Li
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons101295

Su,  Hang
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons230378

Li,  Meng
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons203111

Kuhn,  Uwe
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons203184

Zheng,  Guangjie
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons280915

Han,  Lei
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons273233

Bao,  Fengxia
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons101189

Pöschl,  Ulrich
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons127588

Cheng,  Yafang
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Citation

Guo, L., Su, H., Li, M., Kuhn, U., Zheng, G., Han, L., et al. (2022). Reactive uptake coefficients for multiphase reactions determined by a dynamic chamber system. Atmospheric Measurement Techniques, 15(21), 6433-6446. doi:10.5194/amt-15-6433-2022.


Cite as: https://hdl.handle.net/21.11116/0000-000B-7B8A-0
Abstract
DDynamic flow-through chambers are frequently used to measure gas exchange rates between the atmosphere and biosphere on the Earth's surface such as vegetation and soils. Here, we explore the performance of a dynamic chamber system in determining the uptake coefficient γ of exemplary gases (O3 and SO2) on bulk solid-phase samples. After characterization of the dynamic chamber system, the derived γ is compared with that determined from a coated-wall flow tube system. Our results show that the dynamic chamber system and the flow tube method show a good agreement for γin the range of 10−8 to 10−3. The dynamic chamber technique can be used for liquid samples and real atmospheric aerosol samples without complicated coating procedures, which complements the existing techniques in atmospheric kinetic studies.