Abstract

Abstract. Hydroxymethanesulfonate (HMS) has recently been identified as an abundant organosulfur compound in aerosols during winter haze episodes in northern China. It has also been detected in other regions although the concentrations are low. Because of the sparse field measurements, the global significance of HMS and its spatial and seasonal patterns remain unclear. Here, we modify and add to the implementation of HMS chemistry in the GEOS-Chem chemical transport model and conduct multiple global simulations. The model accounts for cloud entrainment and gas–aqueous mass transfer within the rate expressions for heterogeneous sulfur chemistry. Our simulations can generally reproduce quantitative HMS observations from Beijing and show that East Asia has the highest HMS concentration, followed by Europe and North America. The simulated HMS shows a seasonal pattern with higher values in the colder period. Photochemical oxidizing capacity affects the competition of formaldehyde with oxidants (such as ozone and hydrogen peroxide) for sulfur dioxide and is a key factor influencing the seasonality of HMS. The highest average HMS concentration (1–3 µg m−3) and HMS ∕ sulfate molar ratio (0.1–0.2) are found in northern China in winter. The simulations suggest that aqueous clouds act as the major medium for HMS chemistry while aerosol liquid water may play a role if its rate constant for HMS formation is greatly enhanced compared to cloud water.

Highlights

  • Organosulfur (OS) compounds have been detected in secondary organic aerosols (SOAs)

  • SOT2(aq) is the sum of SO2 ·H2O, HSO−3, and SO23− (Eq 2). kf (M−1 s−1) and kd (s−1) represent the forward and backward reaction (HMS formation and decomposition) rate constants of Reaction (R8) and Keq (M−1) is its equilibrium constant (Eq 3). kf is a combination of k1 and k2 weighted by the fractions of HSO−3 and SO23− in SOT2(aq) (Eqs. 4–6)

  • The horizontal distributions of HMS concentration in the surface layer and the vertical profiles of its zonal average are shown in Fig. 4 (DJF: December–January–February and JJA: June–July–August) and Fig. S5 in the Supplement (MAM: March–April–May and SON: September–October– November)

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Summary

Introduction

Organosulfur (OS) compounds have been detected in secondary organic aerosols (SOAs). The identified OS compounds include organosulfates (ROSO−3 ), sulfoxides (RSOR ), sulfones (RSO2R ), and sulfonates (RSO−3 ) (Brüggemann et al, 2020). Sulfonates include methanesulfonate (CH3SO−3 , deprotonated MSA, methanesulfonic acid) and hydroxyalkylsulfonates (RCH (OH) SO−3 ) (Song et al, 2019a). These classes of OS compounds may differ widely in their formation mechanisms, concentration levels, and spatiotemporal distributions. Organosulfates and MSA are the two most studied OS species or classes

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