posted on 2023-01-09, 19:03authored byCaroline C. Womack, Wyndom S. Chace, Siyuan Wang, Munkhbayar Baasandorj, Dorothy L. Fibiger, Alessandro Franchin, Lexie Goldberger, Colin Harkins, Duseong S. Jo, Ben H. Lee, John C. Lin, Brian C. McDonald, Erin E. McDuffie, Ann M. Middlebrook, Alexander Moravek, Jennifer G. Murphy, J. Andrew Neuman, Joel A. Thornton, Patrick R. Veres, Steven S. Brown
We report aircraft observations of extreme levels of
HCl and the
dihalogens Cl2, Br2, and BrCl in an industrial
plume near the Great Salt Lake, Utah. Complete depletion of O3 was observed concurrently with halogen enhancements as a
direct result of photochemically produced halogen radicals. Observed
fluxes for Cl2, HCl, and NOx agreed with facility-reported emissions inventories. Bromine emissions
are not required to be reported in the inventory, but are estimated
as 173 Mg year–1 Br2 and 949 Mg year–1 BrCl, representing a major uncounted oxidant source.
A zero-dimensional photochemical box model reproduced the observed
O3 depletions and demonstrated that bromine radical cycling
was principally responsible for the rapid O3 depletion.
Inclusion of observed halogen emissions in both the box model and
a 3D chemical model showed significant increases in oxidants and particulate
matter (PM2.5) in the populated regions of the Great Salt
Lake Basin, where winter PM2.5 is among the most severe
air quality issues in the U.S. The model shows regional PM2.5 increases of 10%–25% attributable to this single industrial
halogen source, demonstrating the impact of underreported industrial
bromine emissions on oxidation sources and air quality within a major
urban area of the western U.S.