ETDs

This collection includes most of the ASU Theses and Dissertations from 2011 to present. ASU Theses and Dissertations are available in downloadable PDF format; however, a small percentage of items are under embargo. Information about the dissertations/theses includes degree information, committee members, an abstract, supporting data or media.

In addition to the electronic theses found in the ASU Digital Repository, ASU Theses and Dissertations can be found in the ASU Library Catalog.

Dissertations and Theses granted by Arizona State University are archived and made available through a joint effort of the ASU Graduate College and the ASU Libraries. For more information or questions about this collection contact or visit the Digital Repository ETD Library Guide or contact the ASU Graduate College at gradformat@asu.edu.

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Historical and future needs for geospatial iodide occurrence and sources in surface and ground waters of the United States of America

Description
Iodide (I-) in surface and groundwaters is a potential precursor for the formation of iodinated disinfection by-products (I-DBPs) during drinking water treatment. The aim of this thesis is to provide a perspective on the sources and occurrence of I- in United States (US) source waters based on ~9200 surface water…

Iodide (I-) in surface and groundwaters is a potential precursor for the formation of iodinated disinfection by-products (I-DBPs) during drinking water treatment. The aim of this thesis is to provide a perspective on the sources and occurrence of I- in United States (US) source waters based on ~9200 surface water (SW) and groundwater (GW) sampling locations. The median I- concentrations observed was 16 μg/l and 14 μg/l, respectively in SW and GW. However, these samples were rarely collected at water treatment plant (WTP) intakes, where such iodide occurrence data is needed to understand impacts on DBPs. Most samples were collected in association with geochemical studies. We conclude that I- occurrence appears to be influenced by geological features, including halite rock/river basin formations, saline aquifers and organic rich shale/oil formations. Halide ratios (Cl-/I-, Br-/I- and Cl-/Br-) were analyzed to determine the I- origin in source waters. SW and GW had median Cl-/I- ratios of ~3600 μg/μg and median Br-/I- ratios of ~15 μg/μg. For states with I- concentration >50 μg/l (e.g., Montana and North Dakota), a single source (i.e., organic rich formations) can be identified. However, for states like California and Texas that have wide-ranging I- concentration of below detection limit to >250 μg/l, I- occurrence can be attributed to a mixture of marine and organic signatures. The lack of information of organic iodine, inorganic I- and IO3- in source waters limits our ability to predict I-DBPs formed during drinking water treatment, and new occurrence studies are needed to fill these data gaps. This is first of its kind study to understand the I- occurrence through historical data, however we also identify the shortcomings of existing databases used to carry out this study.
ContributorsSharma, Naushita (Author) / Westerhoff, Paul (Thesis advisor) / Lackner, Klaus (Committee member) / Herckes, Pierre (Committee member) / Arizona State University (Publisher)
Created2018
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Numerical Simulation of Moisture Swing Absorption Model for Carbon Dioxide Capture

Description
The current level of carbon dioxide in ambient air is increasing and reinforcing the severity of global warming. Several techniques have been developed to capture the gas directly from the air. Moisture swing absorption (MSA) is a mechanism through which a reactive surface, namely resin beads, absorbs carbon dioxide…

The current level of carbon dioxide in ambient air is increasing and reinforcing the severity of global warming. Several techniques have been developed to capture the gas directly from the air. Moisture swing absorption (MSA) is a mechanism through which a reactive surface, namely resin beads, absorbs carbon dioxide when dry and releases it when wet. The ionic complexity of the surface of the bead interacts with CO2 when H2O contents are low, and CO2 diffuses as bicarbonate or carbonate. Hence, diffusion-drift-reaction equations describe the moving species behavior MS sorbent. A numerical model has been developed previously applying finite difference scheme (FDS) to estimate the evolution of species concentrations over uniform time and space intervals. The methodology was based on a specific membrane and bead geometry. In this study, FDS was employed again with modifications over the boundary conditions. Neumann boundary condition was replaced by Robin boundary condition which enforced diffusion and drift fluxes at the center of the sorbent. Furthermore, the generic equations were approximated by another numerical scheme, Finite volume scheme (FVS), which discretizes the spatial domain into cells that conserves the mass of species within. The model was predicted to reduce the total carbon mass loss within the system. Both schemes were accommodated with a simulated model of isolated chamber that contained arbitrary sorbent. Moreover, to derive the outcomes of absorption/desorption cycles and validate the performance of FVS, Langmuir curve was utilized to obtain CO2 saturation in the sorbent and examine two scenarios: one by varying the partial pressure of CO2 (PCO2) in the chamber at constant H2O (PH2O), or changing PH2O at constant PCO2. The results from FDS approximation, when adjusting the center with Robin boundary condition, show 0.11% lower carbon mass gain than when applying Neumann boundary condition. On the other hand, FVS minimizes the mass loss by 0.3% lower than the original total carbon mass and achieves sorbent saturation without any adjustment. Moreover, the isotherm curve demonstrates that increasing PH2O reduces CO2 saturation and is dependent on the linear and non-linear correlations used to estimate water concentration on the surface.
ContributorsMejbel, Meteb (Author) / Lackner, Klaus (Thesis advisor) / Boyer, Treavor (Committee member) / Wang, Zhihua (Committee member) / Arizona State University (Publisher)
Created2021
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Experimental Characterization of Sorbents for Direct Air Capture of Carbon Dioxide

Description
Climate change poses a serious challenge humankind. Society’s reliance on fossil fuels raises atmospheric CO2 concentrations causing global warming. Already, the planet has warmed by 1.1 °C making it nearly impossible to heed the advice of the IPCC (2022) and prevent warming in excess of 1.5 °C by 2050. Even…

Climate change poses a serious challenge humankind. Society’s reliance on fossil fuels raises atmospheric CO2 concentrations causing global warming. Already, the planet has warmed by 1.1 °C making it nearly impossible to heed the advice of the IPCC (2022) and prevent warming in excess of 1.5 °C by 2050. Even the current excess of CO2 in the atmosphere poses significant risks. Direct air capture (DAC) of CO2 offers one of the most scalable options to the drawdown of carbon. DAC can collect CO2 that is already diluted into the atmosphere for disposal or utilization. Central to most DAC are sorbents, i.e., materials that bind and release CO2 in a capture and release cycle. There are sorbents that cycle through a temperature swing. Others use a moisture swing, or a pressure swing or combinations of all of them. Since DAC is still a nascent technology, advancement of sorbents is an important part of DAC development. There is a nearly infinite combination of possible sorbents and form factors of sorbents that can be deployed in many different variations of DAC. Our goal is to develop a methodology for characterizing sorbents to facilitate rational choices among different options. Good sorbent characteristics include high capacity, fast sorption and desorption kinetics, low energy need for unloading, and longevity. This work presents the development of a systematic approach to evaluate sorbents from the milligram to tonne scale focusing on the important characteristics mentioned above. The work identified a good temperature swing sorbent whose characterization moved from the mg to kg scale without loss in performance. This work represents a first step in systematizing sorbent characterization for rational sorbent development programs.
ContributorsStangherlin Barbosa, Thiago (Author) / Lackner, Klaus (Thesis advisor) / Cirucci, John (Committee member) / Dirks, Gary (Committee member) / Arizona State University (Publisher)
Created2022
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Projection of PM2.5, BC, NOx and VOCs from the Future Vehicle Fleet: Impact of Alternative Vehicle Penetration Versus Continual Reductions in Emissions from Traditional Vehicles

Description
Mobile sources emit a number of different gases including nitrogen oxides (NOx) and volatile organic compounds (VOCs) as well as particulate matter (PM10, PM2.5). As a result, mobile sources are major contributors to urban air pollution and can be the dominant source of some local air pollution problems. In general,…

Mobile sources emit a number of different gases including nitrogen oxides (NOx) and volatile organic compounds (VOCs) as well as particulate matter (PM10, PM2.5). As a result, mobile sources are major contributors to urban air pollution and can be the dominant source of some local air pollution problems. In general, mobile sources are divided into two categories: on-road mobile sources and non-road mobile sources. In Maricopa County, the Maricopa County Air Quality Department prepares inventories of all local sources [11], [12]. These inventories report that for Maricopa County, on-road mobile sources emit about 23% of total PM2.5 annually, 58% of the total NOx, and 8% of the total VOCs. To understand how future changes how vehicles might impact local air quality, this work focuses on comparing current inventories of PM2.5, black carbon (BC), NOx, and VOCs to what may be expected emissions in future years based on different scenarios of penetration of hybrid gas-electric vehicles (HEV) and electric vehicles (EV) as well as continued reduction in emissions from conventional internal combustion (IC) vehicles. A range of scenarios has been developed as part of this thesis based on literature reports [6], [8], air quality improvement plan documentation [5], projected vehicle sales and registration [3], [4], as well as using EPA’s Motor Vehicle Emission Simulator (MOVES) [9]. Thus, these created scenarios can be used to evaluate what factors will make the most significant difference in improving local air quality through reduced emissions of PM2.5, BC, NOx and VOCs in the future. Specifically, the impact of a greater fraction of cleaner alternative vehicles such as hybrid-electric and electric vehicles will be compared to the impact of continual reductions in emissions from traditional internal combustion vehicles to reducing urban air pollution emissions in Maricopa County.
ContributorsAlboaijan, Fahad A M S (Author) / Fraser, Matthew (Thesis advisor) / Andino, Jean (Committee member) / Lackner, Klaus (Committee member) / Arizona State University (Publisher)
Created2020
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Occurrence and Speciation of Bromine and Iodine in Drinking Water Sources

Description

Halogens in drinking water sources, such as bromine (Br) and iodine (I) pose no direct health risk, but are critical precursors in formation of cyto- and genotoxic brominated and iodinated (Br-/I-) DBPs. However, few spatial or historic datasets exist for bromine and iodine species in drinking water sources. This dissertation…

Halogens in drinking water sources, such as bromine (Br) and iodine (I) pose no direct health risk, but are critical precursors in formation of cyto- and genotoxic brominated and iodinated (Br-/I-) DBPs. However, few spatial or historic datasets exist for bromine and iodine species in drinking water sources. This dissertation aims to quantify and understand the occurrence and speciation of Br and I in groundwater and surface water serving as source waters for drinking water treatment plants (DWTPs). Aggregation of data from >9000 non-drinking water sampling locations in USA collected from 1930-2017 on halides (bromide (Br-) and iodide (I-)) determined that Br- concentrations were 50 μg/L and 100 μg/L; and I- concentrations were 12 μg/L and 13 μg/L in surface and groundwater respectively. Although, these locations were not drinking water sources, this first of its kind analysis provides potential bounds for Br- and I-. To focus specifically on DWTP sources, a nationwide survey of >250 drinking water sources was conducted between 2018-2020. Br- ion is the only bromine specie, whereas both inorganic (iodide and iodate ions) and organic iodine occur. I- concentrations ranged from 1-250 μg/L and are 4 to 100 times lower than Br- concentrations (10-7800 μg/L, median=80 μg/L). No strong correlation exists between bromide and iodide occurrence (R<0.5, p<0.005). I- was detected in 50% of the samples (75th percentile=5 μg/L) and IO3- was detected in 40% (75th percentile=3 μg/L) of all the samples. To quantify iodine species, tandem ion chromatography and inductively coupled plasma mass spectrometry was applied for the first time in drinking water sources. I- and IO3- peaks were well resolved and have minimum detection limit of 0.4 μg/L and 0.7 μg/L respectively. Organic iodine (Org-I) peaks in select drinking water samples from the nationwide survey were partically resolved ranging from <5 to 40 μg/L. This dissertation provides updated nationwide Br- survey and first ever national I species survey. The data generated through this dissertation will be useful to further Br-/I-DBP formation and toxicity research by providing relevant drinking water sources information. Future research targeting Br- and I- removal is advocated for managing Br-/I-DBPs in watersheds.
ContributorsSharma, Naushita (Author) / Westerhoff, Paul (Thesis advisor) / Karanfil, Tanju (Committee member) / Herckes, Pierre (Committee member) / Lackner, Klaus (Committee member) / Arizona State University (Publisher)
Created2021