Heterogeneous
reactions occurring
between ozone and films or particles
containing skin oil or cooking oil can be a sink of ozone and a source
of organic compounds indoors with negative health effects. To predict
this heterogeneous chemistry, information on the phase behavior (number
and types of phases) within these films and particles, and its evolution
during ozone exposure, is needed. In this work, we used optical microscopy
to directly observe the phase behavior of proxies for skin oil and
cooking oil particles (diameters of 110–220 μm) during
exposure to O3. As a proxy for skin oil, we used a multicomponent
mixture of unsaturated lipids. For cooking oil, we used a commercially
available canola oil. We also studied single-component unsaturated
lipids (squalene, triolein, and oleic acid) and jojoba oil (mostly
unsaturated monoesters) as simpler proxies for skin oil and cooking
oil. Prior to reactions with ozone, the particles were all liquid.
Exposure to ozone led to the formation of a new phase within the particles.
For oleic acid, the new phase was most likely a high-molecular-weight
liquid formed by liquid–liquid phase separation. For all other
systems, the new phase was likely solid or semi-solid. Our results,
together with the resistor model and the reaction extent, were then
used to predict the time it takes for a new phase to form in skin
oil and cooking oil films indoors. Based on our results, we predict
that a new phase will form in skin oil films with a thickness of 0.1–1
μm after a timescale of 3 h to 7 days under typical indoor ozone
concentrations (6 ppb) and relative humidity (RH) conditions ranging
from 5 to 65%. In cooking oil films, we predict that a new phase will
form after 1.5–16 h for films of 0.1–1 μm thickness
under ozone concentrations of 6 ppb and RH conditions ranging from
5 to 65%. A new phase will likely impact diffusion rates and partitioning
coefficients within the films and hence ozone loss rates indoors,
production rates of respiratory irritants, and partitioning of these
irritants between films, particles, and the gas phase.