Frank Keutsch

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Name: Keutsch, Frank
Organization: University of Wisconsin–Madison , USA
Department: Department of Chemistry
Title: Associate(PhD)
Co-reporter:Corey N. Olson, Melissa M. Galloway, Ge Yu, Curtis J. Hedman, Matthew R. Lockett, Tehshik P. Yoon, Elizabeth A. Stone, Lloyd M. Smith, and Frank N. Keutsch
Environmental Science & Technology 2011 Volume 45(Issue 20) pp:9111
Publication Date(Web):September 15, 2011
DOI:10.1021/es203122z
Co-reporter:Corey N. Olson, Melissa M. Galloway, Ge Yu, Curtis J. Hedman, Matthew R. Lockett, Tehshik Yoon, Elizabeth A. Stone, Lloyd M. Smith, and Frank N. Keutsch
Environmental Science & Technology 2011 Volume 45(Issue 15) pp:6468-6474
Publication Date(Web):June 17, 2011
DOI:10.1021/es201039p
Organosulfates have been proposed as contributors to aerosol growth and have been detected in both chamber and atmospheric aerosol samples. We present a simple method for the synthesis of quantitative analytical standards of two small hydroxycarboxylic acid-derived organosulfates, glycolic and lactic acid sulfate. Additionally, we discuss the stability of hydroxycarboxylic acid-derived organosulfates and their previously proposed sulfate hemiacetal isomers in commonly used solvents for filter extraction. The hydroxycarboxylic acid-derived organosulfates were found to be stable under acidic conditions comparable to those found in ambient aerosol. By using synthesized standards, quantitative organosulfate concentrations were measured from ambient particulate matter (PM2.5) collected in urban locations in the United States, Mexico City, and Pakistan. Lactic acid sulfate and glycolic acid sulfate concentrations ranged 0.4–3.8 ng/m3 and 1.9–11.3 ng/m3, respectively. We propose that glycolic acid sulfate represents an important tracer for atmospheric processes that form organosulfates in ambient particulate matter.
Co-reporter:Ge Yu, Amanda R. Bayer, Melissa M. Galloway, Kyle J. Korshavn, Charles G. Fry, and Frank N. Keutsch
Environmental Science & Technology 2011 Volume 45(Issue 15) pp:6336-6342
Publication Date(Web):July 1, 2011
DOI:10.1021/es200989n
Reactions and interactions between glyoxal and salts in aqueous solution were studied. Glyoxal was found to react with ammonium to form imidazole, imidazole-2-carboxaldehyde, formic acid, N-glyoxal substituted imidazole, and minor products at very low concentrations. Overall reaction orders and rates for each major product were measured. Sulfate ions have a strong and specific interaction with glyoxal in aqueous solution, which shifts the hydration equilibria of glyoxal from the unhydrated carbonyl form to the hydrated form. This ion-specific effect contributes to the observed enhancement of the effective Henry’s law coefficient for glyoxal in sulfate-containing solutions. The results of UV–vis absorption and NMR spectroscopy studies of solutions of glyoxal with ammonium, methylamine, and dimethylamine salts reveal that light absorbing compounds require the formation of nitrogen containing molecules. These findings have implications on the role of glyoxal in the atmosphere, both in models of the contribution of glyoxal to form secondary organic aerosol (SOA), the role of nitrogen containing species for aerosol optical properties and in predictions of the behavior of other carbonyls or dicarbonyls in the atmosphere.
2-Hexenal, 4-hydroperoxy-, (2E)-
Propanoic acid, 2-(sulfooxy)-
Propanoic acid, 2-(sulfooxy)-, (S)-
Sulfate (7CI,8CI,9CI)
Hydrogen cation
2-Butenedial, (2E)-
Hydroxyl
C2H5OO
Nitric acid, methylester (8CI,9CI)
ACETONITRILE