Lactic acid, a small α-hydroxyacid, is ubiquitous
in both
indoor and outdoor environments. Recently, the photochemistry of lactic
acid has garnered interest among the abiotic organic chemistry community
as it would have been present in abiotic settings and photoactive
with the high-energy solar radiation that would have been available
in the low oxygen early Earth environment. Additionally, we propose
that the photochemistry of lactic acid is relevant to modern Earth
during indoor ultraviolet-C (UVC) sterilization procedures as lactic
acid is emitted by humans and is thus prevalent in indoor environments
where UVC sterilization is increasingly being used. Here, we study
the oxygen effect on the gas phase photolysis of lactic acid using
Fourier-transform infrared (FTIR) spectroscopy and isotopically labeled
oxygen (18O2). We find that the major products
of gas phase lactic acid photolysis are CO2, CO, acetaldehyde,
and acetic acid. Furthermore, these products are the same with or
without added oxygen, but the partial pressures of produced CO2, CO, and acetaldehyde increase with the amount of added oxygen.
Notably, the added oxygen is primarily incorporated into produced
CO2 and CO, while little or none is incorporated into acetaldehyde.
We combine the results presented here with those in the literature
to propose a mechanism for the gas phase photolysis of lactic acid
and the role of oxygen in this mechanism. Finally, we compare the
output of a krypton-chloride excimer lamp (λ = 222 nm), one
of the lamps proposed for UVC sterilization procedures, to the absorption
of lactic acid. We show that lactic acid would be photoactive during
UVC sterilization procedures, and we use the gas phase results presented
here and aqueous lactic acid photolysis results previously published
to assess potential byproducts from lactic acid reactions during UVC
sterilization procedures.