Predicting how stratospheric aerosol injection (SAI) will work in practice requires accurately modeling the evolution of sulfur dioxide (SO₂) plumes released by aircraft. Current climate models simplify this injection, assuming SO₂ instantly mixes throughout large grid cells (roughly 100 km across) rather than evolving in the narrow, concentrated plumes that aircraft produce. Because these concentrated aircraft plumes evolve through tightly coupled chemical, dynamical, and physical processes, the resulting aerosol size distribution (the range of particle sizes the plume produces) ultimately dictates both the radiative efficacy (cooling potential) and stratospheric residence time of the particles.
Because observational data for aircraft-injected SO₂ in the stratosphere does not exist, research cannot yet definitively validate a single aerosol model. Different aerosol microphysics models (simulations of particle-level interactions) predict different aerosol properties from the exact same injection scenario, sometimes differing by a factor of two or more in predicted cooling. To address this gap, this research activity funds a systematic aerosol box model intercomparison to quantify the structural uncertainties between competing models such as Modal Aerosol Module (MAM), Community Aerosol and Radiation Model for Atmospheres (CARMA), Global Model of Aerosol Processes (GloMAP) and TwO-Moment Aerosol Sectional (TOMAS).
While aerosol microphysics schemes directly simulate nucleation (the formation of new particles), condensation (particle growth as vapor collects on them), and coagulation (particles merging together), these mechanisms remain highly sensitive to surrounding chemistry (oxidation) and plume dynamics (dilution). Oxidation and dilution indirectly, but significantly, shape the microphysical outcomes. By comparing models across a range of realistic conditions, this project will isolate systemic differences in how models represent these coupled processes and will clarify which processes — nucleation, condensation, and coagulation — govern the final aerosol size distribution. These findings will directly inform the design and interpretation of future physical field experiments. This research contributes to understanding the aerosol size distribution uncertainties.