Aerosol Acidity Sensing via Polymer Degradation

Abstract

The acidity of atmospheric aerosols is a critical property that affects the chemistry and composition of the atmosphere. Many key multiphase chemical reactions are pH-dependent, impacting processes like secondary organic aerosol formation, and need to be understood at a single particle level due to differences in particle-to-particle composition that impact both climate and health. However, the analytical challenge of measuring aerosol acidity in individual particles has limited pH measurements for fine (<2.5 μm) and coarse (2.5-10 μm) particles. This has led to a reliance on indirect methods or thermodynamic modeling, which focus on average, not individual, particle pH. Thus, new approaches are needed to probe single particle pH. In this study, a novel method for pH measurement was explored using degradation of a pH-sensitive polymer, poly(ε-caprolactone), to determine the acidity of individual submicron particles. Submicron particles of known pH (0 or 6) were deposited on a polymer film (21-25 nm thick) and allowed to react. Particles were then rinsed off, and the degradation of the polymer was characterized using atomic force microscopy and Raman microspectroscopy. After degradation, holes in the PCL films exposed to pH 0 were observed, and the loss of the carbonyl stretch was monitored at 1723 cm^-1. As particle size decreased, polymer degradation increased, indicating an increase in aerosol acidity at smaller particle diameters. This study describes a new approach to determine individual particle acidity and is a step toward addressing a key measurement gap related to our understanding of atmospheric aerosol impacts on climate and health.