Abstract

Abstract Fog processing has a significant impact on sulfur chemistry in the atmosphere. This study analyzed three winter fog events in Hong Kong using single‐particle aerosol mass spectrometry (SPAMS) and a Monitor for AeRosols and GAses in ambient air (MARGA). Black carbon (BC)‐related carbonaceous particles with substantial sulfate amounts comprised the largest particle number fraction (56.7%). Sulfate mass concentration decreased during fog due to the cloud's effective scavenging, but fog processing notably promoted sulfate formation at the single‐particle level (average peak area increases of 31.2%). Hydroxymethanesulfonate (HMS), an important S(IV) compound and fog tracer, was identified accounting for up to 12% by particle number fraction. Although pH showed a positive correlation ( r = 0.53–0.69) with HMS particles in each fog scenario, a negative overall correlation ( r = −0.51) was observed. Further analysis revealed that the higher aerosol acidity (pH 0.65–3.11), promoted Fe dissolution, leading to 49% of HMS particles being mixed with Fe, which potentially facilitated sulfate formation via the Fenton reaction. Additionally, around 40% of HMS‐Fe particles are mixed with oxalate, thereby warranting further attention for their potential to cause more intricate sulfur oxidation processes. This study reveals the initial identification of a high mixed‐state of HMS‐Fe, which could potentially serve as a crucial avenue for the formation of sulfate on individual particulate matter. Considering the persistent augmentation of aerosol acidity in the Asian region, this phenomenon necessitates further investigation and attention.