Influence of acidity on liquid−liquid phase transitions of mixed SOA proxy–inorganic aerosol droplets

Abstract. Phase state and morphology of aerosol particles play a critical role in determining their effect on climate. While aerosol acidity has been identified as a key factor affecting the multiphase chemistry and phase transitions, the impact of acidity on phase transition of multicomponent aerosol particles has not been extensively studied in situ. In this work, we employ an aerosol optical tweezer (AOT) to probe the impact of acidity on the phase transition behavior of levitated aerosol particles. Our results reveal that higher acidity decreases the separation relative humidity (SRH) of aerosol droplets mixed with ammonium sulfate (AS) and secondary organic aerosol (SOA) proxy, such as 3-methylglutaric acid (3-MGA), 1,2,6-hexanetriol (HEXT) and 2,5-hexanediol (HEXD) across aerosol pH in atmospheric condition. Phase separation of organic acids was more sensitive to acidity compared to organic alcohols. We found the mixing relative humidity (MRH) was consistently higher than the SRH in several systems. Phase-separating systems, including 3-MGA/AS, HEXT/AS, and HEXD/AS, exhibited oxygen-to-carbon ratios (O:C) of 0.67, 0.50, and 0.33, respectively. In contrast, liquid-liquid phase separation (LLPS) did not occur in the high O:C system of glycerol/AS, which had an O:C of 1.00. Additionally, the morphology of 38 out of the 40 aerosol particles that underwent LLPS was observed to be a core-shell. Our findings provide a comprehensive understanding of the pH-dependent LLPS in individual suspended aerosol droplets and pave the way for future research on phase separation of atmospheric aerosol particles.