Correlation of adsorption behavior for a gas-surface system to the molecular structure of the gas-phase molecule is necessary to better constrain atmospheric modeling. Despite the variety of compounds emitted into the atmosphere, the role of molecular structure on uptake probability, γ, for a compound adsorbing onto a surface is not well understood. A custom designed flow manifold coupled to a mass spectrometer provides the means to analyze changes in γ for gases at environmentally relevant low ppb concentrations. Studies have focused on the adsorption of two classes of compounds: singly substituted benzene derivatives and several terpenoid compounds for a silica surface composed of hydroxyl groups and bridging oxygen species. Results for benzene derivatives show an enhancement of the initial γ value of all functionalized compounds relative to benzene, with this initial value influenced by both the dipole and volatility of a compound. The time-dependent behavior of γ has been shown to depend on the interactions occurring between the adsorbate and surface with species capable of hydrogen bond interactions exhibiting a greater number of adsorbed species at equilibrium. The initial γ value for terpenoid species was observed to increase from isoprene to sesquiterpenes, with several monoterpene isomers exhibiting distinct adsorption behavior based on structural differences. The sesquiterpene examined, β-caryophyllene, exhibited continuous uptake onto the silica surface and such uptake behavior could contribute in part to the low concentrations of sesquiterpenes observed in the environment. Encapsulation of the hydroxyl groups resulted in decreased uptake of several aromatic and terpenoid species examined and indicates that hydroxyl groups represent the majority of adsorption sites for the systems examined. Comparison between observed uptake behavior to adsorption models exhibited the best agreement with a model depicting monolayer formation with cooperative adsorption due to interactions between adsorbates. Formulations for predicting initial γ values based on the volatility and dipole of the compound are provided. Overall, these results represent the first step towards a better understanding of gas-surface interactions that occur in the environment.
Sesquiterpenes represent one class of biogenic emissions not well constrained with regards to SOA influence due to their low volatility and concentrations relative to more abundant terpenoid species. Ambient measurements of sesquiterpenes through the Semi-Volatile Thermal desorption Aerosol Gas chromatography (SV-TAG) instrument presented total sesquiterpene concentrations that ranged from 0.8 to 2 ppt with no isomer dominating. Sesquiterpene contribution towards hydroxyl reactivity is negligible in comparison to more abundant terpenoid species while ozone reactivity was dominated by two isomers and could contribute to atmospheric reactivity during periods of high emissions. These measurements represent the first step in better constraining the contribution of sesquiterpenes towards secondary organic aerosol formation. / Doctor of Philosophy / A large variety of compounds are emitted into the atmosphere from natural and human sources. The molecular structures of these compounds are complex and differences in structure can alter the environmental fate of compounds, which can directly affect human health. While atmospheric modeling provides insight into the fate of compounds, it relies on experimentally determined values for accuracy. The probability that a gas-phase molecule "sticks" to a surface upon collision, defined as the uptake probability, represents one value that is not well understood. My research has primarily focused on the development and testing of an instrument capable of observing gas uptake onto a surface for environmentally relevant gas concentrations. This has included understanding how differences in structure of a molecule affect adsorption for a single surface. For example, α-pinene and β-pinene (both compounds emitted by plants and found in air fresheners!) exhibit distinct adsorption behavior that arises from the location of a single carbon-carbon double bond for the same structure. Similarly, making a "water-loving" surface into a "water-repelling" surface results in less α-pinene adsorbed, despite α-pinene being considered insoluble in water. The developed instrument represents a vital tool in improving the accuracy of atmospheric modeling.
In addition to understanding gas adsorption onto a surface, my research has focused on the detection and quantification of one class of naturally emitted compounds in Virginia: sesquiterpenes. These compounds are emitted by plants for a variety of reasons, and their influence on particle formation is not well understood. Measurement of sesquiterpenes at two sites in Virginia provides a better understanding of the abundance of sesquiterpenes in geographic regions not previously analyzed. These measurements contribute to an increased understanding of the role of different compound classes on particle formation in the atmosphere.
Identifer | oai:union.ndltd.org:VTETD/oai:vtechworks.lib.vt.edu:10919/115064 |
Date | 15 May 2023 |
Creators | Frazier, Graham Owen |
Contributors | Chemistry, Morris, John R., Isaacman-VanWertz, Gabriel, Esker, Alan R., Tanko, James M. |
Publisher | Virginia Tech |
Source Sets | Virginia Tech Theses and Dissertation |
Language | English |
Detected Language | English |
Type | Dissertation |
Format | ETD, application/pdf |
Rights | Creative Commons Attribution-NonCommercial 4.0 International, http://creativecommons.org/licenses/by-nc/4.0/ |
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