Abstract

Abstract. An improved aerosol flow tube system coupled with a detailed box model was developed to measure N2O5 heterogeneous uptake coefficients (γ(N2O5)) on ambient aerosols directly. This system features sequential measurements of N2O5 concentrations at both the entrance and exit of the flow tube to ensure an accurate retrieval of N2O5 loss in the flow tube. Simulation and laboratory tests demonstrate that this flow tube system is able to overcome the interference from side reactions led by varying reactants (e.g., NO2, O3 and NO) and to improve the robustness of results with the assistance of the box model method. Factors related to γ(N2O5) derivation – including particle transmission efficiency, mean residence time in the flow tube and the wall loss coefficient of N2O5 – were extensively characterized for normal operating conditions. The measured γ(N2O5) on (NH4)2SO4 model aerosols were in good agreement with literature values over a range of relative humidity (RH). The detection limit of γ(N2O5) was estimated to be 0.0016 at a low aerosol surface concentration (Sa) condition of 200 µm2 cm−3. Given the instrument uncertainties and potential fluctuation of air mass between successive sampling modes, we estimate the overall uncertainty of γ(N2O5) as ranging from 16 % to 43 % for different ambient conditions. This flow tube system was then successfully deployed for field observations at an urban site of Beijing that is influenced by anthropogenic emissions. The performance in field observations demonstrates that the current setup of this system is capable of obtaining robust γ(N2O5) amid the switch of air mass.

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