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Wintertime Formaldehyde: Airborne Observations and Source Apportionment Over the Eastern United States

  • Jaime R. Green
  • , Marc N. Fiddler
  • , Dorothy L. Fibiger
  • , Erin E. McDuffie
  • , Janine Aquino
  • , Teresa Campos
  • , Viral Shah
  • , Lyatt Jaeglé
  • , Joel A. Thornton
  • , Joshua P. DiGangi
  • , Glenn M. Wolfe
  • , Solomon Bililign
  • , Steven S. Brown
  • North Carolina Agricultural and Technical State University
  • University of North Carolina at Chapel Hill
  • NOAA Earth System Research Laboratory
  • University of Colorado Boulder
  • Now at California Air Resources Board
  • Washington University in St. Louis
  • National Center for Atmospheric Research
  • University of Washington
  • NASA Langley Research Center
  • NASA Goddard Space Flight Center
  • University of Maryland, Baltimore (UMB)

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Formaldehyde (HCHO) is generated from direct urban emission sources and secondary production from the photochemical reactions of urban smog. HCHO is linked to tropospheric ozone formation, and contributes to the photochemical reactions of other components of urban smog. In this study, pollution plume intercepts during the Wintertime INvestigation of Transport, Emissions, and Reactivity (WINTER) campaign were used to investigate and characterize the formation of HCHO in relation to several anthropogenic tracers. Analysis of aircraft intercepts combined with detailed chemical box modeling downwind of several cities suggests that the most important contribution to observed HCHO was primary emission. A box model analysis of a single plume suggested that secondary sources contribute to 21 ± 10% of the observed HCHO. Ratios of HCHO/CO observed in the northeast US, from Ohio to New York, ranging from 0.2% to 0.6%, are consistent with direct emissions combined with at most modest photochemical production. Analysis of the nocturnal boundary layer and residual layer from repeated vertical profiling over urban influenced areas indicate a direct HCHO emission flux of 1.3 × 1014 molecules cm−2 h−1. In a case study in Atlanta, GA, nighttime HCHO exhibited a ratio to CO (0.6%–1.8%) and was anti-correlated with O3. Observations were consistent with mixing between direct HCHO emissions in urban air masses with those influenced by more rapid HCHO photochemical production. The HCHO/CO emissions ratios determined from the measured data are 2.3–15 times greater than the NEI 2017 emissions database. The largest observed HCHO/CO was 1.7%–1.8%, located near co-generating power stations.
Original languageEnglish
Article numbere2020JD033518
JournalJournal of Geophysical Research Atmospheres
Volume126
Issue number5
DOIs
StatePublished - Mar 16 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 11 - Sustainable Cities and Communities
    SDG 11 Sustainable Cities and Communities

Keywords

  • Airborne observations
  • formaldehyde
  • primary production
  • secondary production
  • urban emissions
  • WINTER

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