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      Additional benefits of federal air quality rules: model estimates of controllable biogenic secondary organic aerosol

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          Abstract

          Atmospheric models that accurately describe the fate and transport of trace species for the right reasons aid in development of effective air quality management strategies that safeguard human health, in particular to mitigate the impacts of fine particulate matter (PM 2.5). Controllable emissions from human activity facilitate formation of biogenic secondary organic aerosol (BSOA) to enhance the atmospheric PM 2.5 burden. Previous modeling with EPA’s Community Multiscale Air Quality (CMAQ) model predicted that anthropogenic primary organic aerosol (POA) emissions had the greatest impact on BSOA. Those experiments included formation processes from semi-volatile partitioning, but not interactions with aerosol liquid water (ALW), a ubiquitous PM constituent that modulates BSOA. We conduct 17 CMAQ summertime simulations with updated chemistry and evaluate changes in predicted BSOA mass due to removal of individual pollutants and source sectors from model inputs for the continental U.S. Among individual sectors, CMAQ predicts that SO 2 emissions from electricity generating point sources and mobile source NO x emissions have the largest impact on BSOA. Removal of anthropogenic NO x, SO 2 and POA emissions during the simulated summertime period reduces nationally averaged BSOA by 23%, 14% and 8%, and PM 2.5 by 9.2%, 14% and 5.3% respectively. CMAQ-predicted ALW mass concentrations decrease by 10% and 35% in response to removal of NO x and SO 2 emissions. This work contributes to the understanding of ancillary benefits of existing and planned Federal NO x and SO 2 air quality rules through concurrent reductions in organic PM 2.5 mass.

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          Author and article information

          Journal
          0213155
          21768
          Environ Sci Technol
          Environ. Sci. Technol.
          Environmental science & technology
          0013-936X
          1520-5851
          4 September 2019
          30 July 2018
          21 August 2018
          17 September 2019
          : 52
          : 16
          : 9254-9265
          Affiliations
          [1 ]Department of Chemistry, University of California, Irvine, CA
          [2 ]US EPA, Office of Research and Development, Research Triangle Park, NC
          [3 ]US EPA, Office of Air Quality Planning and Standards, Research Triangle Park, NC
          [4 ]Department of Chemical, Biochemical and Environmental Eng., Univ. of Maryland, Baltimore County
          Author notes
          [* ]Corresponding author, agcarlto@ 123456uci.edu
          Article
          PMC6748392 PMC6748392 6748392 epapa997637
          10.1021/acs.est.8b01869
          6748392
          30005158
          e0a1e04a-b0da-453f-bf8d-259e591b2712
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