34 research outputs found

    Gas phase hydration of methyl glyoxal to form the gemdiol

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    Methylglyoxal is a known oxidation product of volatile organic compounds (VOCs) in Earth’s atmosphere. While the gas phase chemistry of methylglyoxal is fairly well understood, its modeled concentration and role in the formation of secondary organic aerosol (SOA) continues to be controversial. The gas phase hydration of methylglyoxal to form a gemdiol has not been widely considered for water-restricted environments such as the atmosphere. However, this process may have important consequences for the atmospheric processing of VOCs. We will report on spectroscopic work done in the Vaida laboratory studying the hydration of methylglyoxal and discuss the implications for understanding the atmospheric processing and fate of methylglyoxal and similar molecules

    Gas phase hydration of methyl glyoxal to form the gemdiol

    No full text
    Methylglyoxal is a known oxidation product of volatile organic compounds (VOCs) in Earth’s atmosphere. While the gas phase chemistry of methylglyoxal is fairly well understood, its modeled concentration and role in the formation of secondary organic aerosol (SOA) continues to be controversial. The gas phase hydration of methylglyoxal to form a gemdiol has not been widely considered for water-restricted environments such as the atmosphere. However, this process may have important consequences for the atmospheric processing of VOCs. We will report on spectroscopic work done in the Vaida laboratory studying the hydration of methylglyoxal and discuss the implications for understanding the atmospheric processing and fate of methylglyoxal and similar molecules.Made available in DSpace on 2017-01-26T21:39:35Z (GMT). No. of bitstreams: 4 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 1734.pdf: 13786 bytes, checksum: 957721fe8f56e250c3aa37f4a16306b7 (MD5) 636378.pdf: 8649741 bytes, checksum: 7d863d0cc582718f18dd0aec345e62fd (MD5) 636378.pptx: 7403766 bytes, checksum: c0340dbf0331344cef9e14a55446ce33 (MD5) Previous issue date: 2016-06-2

    Ultraviolet study of the gas phase hydration of methylglyoxal to form the gemdiol

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    Made available in DSpace on 2017-07-27T20:15:12Z (GMT). No. of bitstreams: 2 2503.pdf: 14721 bytes, checksum: 36b8649460c221041389bc73ca484882 (MD5) license.txt: 4814 bytes, checksum: a3dad671d2baf2db10a2bec0f2e0c408 (MD5) Previous issue date: 6Made available in DSpace on 2018-01-29T23:03:24Z (GMT). No. of bitstreams: 3 license.txt: 4814 bytes, checksum: a3dad671d2baf2db10a2bec0f2e0c408 (MD5) 2503.pdf: 14721 bytes, checksum: 36b8649460c221041389bc73ca484882 (MD5) 918601.pptx: 4083669 bytes, checksum: 3add38ff9674b9208b3bcc7816f9dae5 (MD5) Previous issue date: 6Methylglyoxal is a known oxidation product of volatile organic compounds (VOCs) in Earth’s atmosphere. While the gas phase chemistry of methylglyoxal is fairly well understood, its modeled concentration and role in the formation of secondary organic aerosol (SOA) continues to be controversial. The gas phase hydration of methylglyoxal to form a gemdiol has been shown to occur in infrared studies but has not been widely considered for water-restricted environments such as the atmosphere. However, this process may have important consequences for the atmospheric processing or VOCs. We have recorded UV spectroscopic measurements following the hydration of methylglyoxal and have compared these measurements to calculated spectra of the electronic transitions of methylglyoxal and methylglyoxal diol. We will report on these measurements and discuss the implications for understanding the atmospheric processing and fate of methylglyoxal and similar molecule

    Examining Interdisciplinary Sustainability Institutes at Major Research Universities: Innovations in Cross-Campus and Cross-Disciplinary Models.

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    This is a study of the distinctive characteristics, activities, challenges and opportunities of a specific type of sustainability institute, one that spans the many disciplines of the University and, to do so, reports to upper administration (Provost or Vice President.) Among research universities within the Association of American Universities (AAU), 19 are identified and 18 agreed to participate in this study. Directors were sent a 71-question survey in January 2017 that covered issues of Governance, Research, Education, Engagement, Campus Operations and Best Practiceshttps://deepblue.lib.umich.edu/bitstream/2027.42/136638/1/1366_Hoffman.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/136638/4/1366_Hoffman_June2017.pdfDescription of 1366_Hoffman_June2017.pdf : June 2017 revisio

    VIBRATIONAL SPECTROSCOPY OF PHOTOREACTIVE MOLECULES IN ATMOSPHERIC CHEMISTRY

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    Author Institution: Department of chemistry and Biochemistry, University of Colorado, Boulder, CO 80309Vibrational overtone spectra of oxidized atmospheric chromophores are presented and analyzed to energies where chemistry through vibrational overtone pumping is possible. Experimental near infrared and visible spectra complemented by dynamical theory are presented to elucidate the light initiated reaction dynamics of pyruvic and of glyoxilic acid photo-decarboxylation. The role of water is investigated by making use of vibrational spectra of hydrates of the title compounds. Consequences of water and sunlight mediated chemistry to formation of secondary organic aerosol in the atmosphere will be discussed.\\ \\ \noindent K. L. Plath, J. L. Axson, G. C. Nelson, K. Takahashi, R. T. Skodje and V. Vaida {em React. Kineti. Catal. Lett.} \textbf{96}, 209 (2009)\\ V. Vaida {\em J. Phys. Chem. A} \textbf{113}, 5 (2009)\\ K. Takahashi, K. L. Plath, R. T. Skodje and V. Vaida {\em J. Phys. Chem A} \textbf{112} 7321 (2008

    Detection of Active Microbial Enzymes in Nascent Sea Spray Aerosol: Implications for Atmospheric Chemistry and Climate

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    The oceans cover nearly three-quarters of the Earth’s surface and produce vast quantities of sea spray aerosols (SSA). Studies have shown that due to ocean biology SSA particles are comprised of much more than just sea salt and often include proteins, lipids, sugars, viruses, and bacteria. In this study, we show for the first time that a diverse array of microbial enzymes (protease, lipases, and alkaline phosphatase) are transferred from the ocean into the atmosphere and often become even more active with measured activities in SSA particles that are 1–2 orders of magnitude higher than those in bulk seawater. We hypothesize that these enzymatic reactions are enhanced in the interfacial environment of droplets and aerosols that can dynamically modify surface chemical species and properties. Simulations reveal that enzyme-containing SSA particles can rapidly coagulate with other preexisting aerosols, thus transferring the impact of enzyme reactions to a broad range of marine aerosols. These biotic reaction pathways are expected to profoundly change the composition of marine aerosols, particularly at the interface, and thus will impact cloud properties in marine environments. Future studies are needed to determine how photochemistry, changing ocean conditions in a warming climate, and other external factors will influence the activities of these enzymes and their impact on the composition of the marine atmosphere

    Advancing Model Systems for Fundamental Laboratory Studies of Sea Spray Aerosol Using the Microbial Loop

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    Sea spray aerosol (SSA) particles represent one of the most abundant surfaces available for heterogeneous reactions to occur upon and thus profoundly alter the composition of the troposphere. In an effort to better understand tropospheric heterogeneous reaction processes, fundamental laboratory studies must be able to accurately reproduce the chemical complexity of SSA. Here we describe a new approach that uses microbial processes to control the composition of seawater and SSA particle composition. By inducing a phytoplankton bloom, we are able to create dynamic ecosystem interactions between marine microorganisms, which serve to alter the organic mixtures present in seawater. Using this controlled approach, changes in seawater composition become reflected in the chemical composition of SSA particles 4 to 10 d after the peak in chlorophyll-a. This approach for producing and varying the chemical complexity of a dominant tropospheric aerosol provides the foundation for further investigations of the physical and chemical properties of realistic SSA particles under controlled conditions
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