Current Search: Sulfide (x)
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Title
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PREDICTIVE MODELING OF SULFIDE REMOVAL IN TRAY AERATORS.
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Creator
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Faborode, Jumoke, Reddi, Lakshmi, University of Central Florida
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Abstract / Description
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Hydrogen sulfide is commonly found in many Florida potable groundwater supplies. Removing sulfur species, particularly hydrogen sulfide is important because if left untreated, sulfide can impact finished water quality, corrosivity, create undesirable taste and odor, and oxidize to form visible turbidity and color. This document presents the results of a study designed to investigate the removal efficiencies of a variety of tray aerators in Central Florida in order to develop a predictive...
Show moreHydrogen sulfide is commonly found in many Florida potable groundwater supplies. Removing sulfur species, particularly hydrogen sulfide is important because if left untreated, sulfide can impact finished water quality, corrosivity, create undesirable taste and odor, and oxidize to form visible turbidity and color. This document presents the results of a study designed to investigate the removal efficiencies of a variety of tray aerators in Central Florida in order to develop a predictive mathematical model that could be used to determine tray effectiveness for sulfide removal. A literature review was performed that indicated there was limited information regarding the removal of hydrogen sulfide using conventional tray aerators, and no information regarding the removal of total sulfide from tray aerators. There was significantly more information available in the literature regarding the usefulness of sulfide removal technologies from water supplies. Consequently, the lack of literature regarding sulfide removal using tray aerators suggested that there was a need for additional research focused on sulfide removal from water flowing thru tray aerators. Several water purveyors that relied on tray aerators as a part of their water treatment operations were contacted and requested to participate in the study; three water purveyors agreed to allow the University of Central Florida (UCF) to enter their secured sites to collect samples and conduct this study. The three facilities included the UCFÃÂ's water treatment plant located in Orlando and situated in eastern Orange County, the City of Lake HamiltonÃÂ's water treatment plant located in west-central Polk County, and the Sarasota-Verna water treatment plant located in western Sarasota County. An experimental plan was developed and field sampling protocols were implemented to evaluate sulfide removal in commonly used tray aerators at the three drinking water treatment facilities. Total sulfide concentrations passing through the trays were determined in the field at each site using a standard iodometric analytical technique. In addition, other water quality parameters collected included dissolved oxygen, pH, temperature, conductivity, turbidity, alkalinity, hardness, total dissolved solids and total suspended solids; these samples were collected and analyzed either in the field or at the UCF laboratory. A first-order empirical model was developed that predicted sulfide removal in tray aerators. The modelÃÂ's constant was evaluated with respect to the waterÃÂ's proton concentration , the tray aeratorÃÂ's surface area, and hydraulic flow rate thru the trays. The selected model took the form of Cn=C0 (10-kn) where Cn is the sulfide remaining after aeration in mg/L, C0 is the sulfide entering the distribution tray in mg/L, n is the number of tray stages in the aerator, and k=(0.00248)(H^+ )^(-0.397) (Area)^0.584 (Flow)^(-1.17). From the empirical model, it was shown that sulfide removal was negatively impacted as the proton concentration (H+) decreased, and flow increased. Conversely, it was observed that increased sulfide removal occurred as the available tray aerator surface area increased. The combined parameters of proton concentration, flow rate, and area were statistically evaluated and used to develop an empirical constant that could be used in a first order model to predict sulfide removal in tray aerators. Using a site-specific derived experimental (empirical) constant, a water purveyor could use the developed model from this work to accurately predict sulfide removal in a tray aerator by simply measuring the total sulfide content in any raw groundwater supply and then providing the desired number of tray stages available for treatment.
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Date Issued
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2010
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Identifier
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CFE0003518, ucf:48980
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003518
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Title
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CONTROL OF HYDROGEN SULFIDE EMISSIONSUSING AUTOTROPHIC DENITRIFICATIONLANDFILL BIOCOVERS.
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Creator
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Sungthong, Daoroong, Reinhart, Debra, University of Central Florida
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Abstract / Description
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Hydrogen sulfide (H2S), a major odorous component emitted from construction and demolition debris landfills, has received increasing attention. Besides its unpleasant odor, long-term exposure to a very low concentration of H2S can cause a public health issue. Although cover materials such as soil and compost are recommended to be used routinely to control an odor problem from the landfills, the problem still remains. Autotrophic denitrification may have environmental applications including...
Show moreHydrogen sulfide (H2S), a major odorous component emitted from construction and demolition debris landfills, has received increasing attention. Besides its unpleasant odor, long-term exposure to a very low concentration of H2S can cause a public health issue. Although cover materials such as soil and compost are recommended to be used routinely to control an odor problem from the landfills, the problem still remains. Autotrophic denitrification may have environmental applications including treatment of water, groundwater, wastewater or gaseous streams contaminated with sulfur and/or nitrogen compounds. However, there have been no studies reported in the literature on H2S removal using autotrophic denitrification from landfills. This study, therefore, investigated the application of autotrophic denitrification incorporated into landfill covers in order to evaluate the feasibility of controlling H2S emissions generated from landfills. Research was investigated by two techniques, microcosm and laboratory-scale column studies. The microcosm experiments were conducted to evaluate the kinetics of autotrophic denitrification in various cover materials with H2S-nitrate as electron donor-acceptor couple. Cover materials including soil, compost and sand were tested and nitrate was added. Based on the microcosm study results, the addition of nitrate into soil and compost can stimulate indigenous autotrophic denitrifying bacteria which are capable of H2S oxidation biologically under anoxic conditions. Results also demonstrated that some amount of H2S can be removed physically and chemically by soil or compost. There was no H2S removal observed in sand microcosms. Rapid H2S oxidation to sulfate was achieved, especially in soil. Zero-order kinetics described the H2S oxidation rate in soil and compost microcosms. The rates of sulfide oxidation under autotrophic denitrification in soil and compost were 2.57 mg H2S/d-g dry soil and 0.17 mg H2S/d-g dry compost, respectively. To further explore H2S removal in a landfill biocover, two sets of column experiments were run. The first set of columns contained seven cm of soil. The autotrophic column was prepared with 1.94 mg KNO3/g dry soil; an identical control column was prepared without nitrate. A gas stream was introduced to the columns with a H2S concentration of 930 ppm. The second set contained seven cm of soil, with both an autotrophic (0.499 mg KNO3/g dry soil) and a control column. Influent H2S concentration was 140 ppm for the second set. Column studies supported the results of microcosm studies; removal of H2S was observed in all columns due to the capacity for soil to absorb H2S, however autotrophic columns removed significantly more. The higher concentration of H2S resulted in partial oxidation to elemental sulfur, while sulfate was found at levels predicted by stoichiometric relationships at the lower concentration. H2S oxidation in the column with higher loading was found to follow zero-order kinetics. The rate of H2S oxidation was 0.46 mg H2S removed/d-g dry soil. Economic comparison of cover systems including autotrophic denitrification, soil amended with lime, fine concrete, and compost covers were analyzed. Based on a case-study landfill area of 0.04 km2, the estimated H2S emissions of 80,900 kg over the 15-year period and costs of active cover system components (ammonium nitrate fertilizer, lime, concrete and compost), autotrophic denitrification cover was determined to be the most cost-effective method for controlling H2S emissions from landfills.
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Date Issued
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2010
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Identifier
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CFE0003283, ucf:48537
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003283
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Title
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Coated Quantum Dots: Engineering of Surface Chemistry for Biomedical and Agricultural Applications.
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Creator
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Maxwell, Tyler, Santra, Swadeshmukul, Gesquiere, Andre, Harper, James, Zou, Shengli, Leon, Lorraine, University of Central Florida
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Abstract / Description
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Quantum dots (QDs) are crystalline nanoparticles made from semiconductor material with sizes ranging from 1 to 10 nm in diameter. QDs are attractive fluorophores for bioimaging and sensing due to their size-dependent optical properties, broad absorption bands, high extinction coefficients and superior photostability. The combination of imaging and drug delivery in a single particle can provide valuable information and improve the efficacy of existing treatments. This dissertation highlights...
Show moreQuantum dots (QDs) are crystalline nanoparticles made from semiconductor material with sizes ranging from 1 to 10 nm in diameter. QDs are attractive fluorophores for bioimaging and sensing due to their size-dependent optical properties, broad absorption bands, high extinction coefficients and superior photostability. The combination of imaging and drug delivery in a single particle can provide valuable information and improve the efficacy of existing treatments. This dissertation highlights the use of QDs for biomedical and agricultural applications. Chapter 1 of this dissertation presents a background of QDs and outlines the synthesis methods of producing and functionalizing QDs. A discussion of the advantages and limitations of each method for producing water-soluble QDs and the rationale for the proposed research is also presented. Chapter 2 describes an activatable QD design for tracking of drug delivery for cancer treatment. QDs synthesized by microemulsion (ME) were cross-linked in a one-step procedure. Enhanced binding affinity of the probe to cell lines overexpressing folate receptors was shown through fluorescence microscopy. However, this system is not practical for the large-scale synthesis due to its complexity and can not be translated for clinical development. Chapter 3 presents a sol-gel synthesis method for producing water-soluble QDs utilizing the thiol-based small molecule capping agent as the stabilizer as an alternative to ME technique. This method was designed to be a simple (one-step), cost-effective, and scalable for making both manganese doped CdS and ZnS QDs. QDs were synthesized through sol-gel method with a library of organic thiol coatings and characterized by size, surface charge, stability, and optical properties. These particles were compared to QDs produced from ME synthesis and were found to have similar properties. Chapter 4 reports the sol-gel QDs as slow-release antibiotic delivery system for application as agricultural bactericide. Utilizing electrostatic interactions, the QDs were shown to be capable of improving the leaf adhesion and slowing the rate of release of streptomycin. Chapter 5 presents a summary of the major findings of this research and discusses the future research directions.
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Date Issued
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2019
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Identifier
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CFE0007681, ucf:52476
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007681
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Title
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EVALUATION OF OXIDIZED MEDIA FILTRATION PROCESSES FOR THE TREATMENT OF HYDROGEN SULFIDE IN GROUNDWATER.
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Creator
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Trupiano, Vito, Duranceau, Steven, University of Central Florida
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Abstract / Description
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This study evaluated alternative sulfide treatment processes for potable water systems that rely on groundwater supplies. Research for this study was conducted at the Imperial Lakes (IL) and Turner Road (TR) water treatment plants (WTPs) in Polk County, Florida. These WTPs are in the process of refurbishment and expansion, and will require the installation of a new groundwater well. The IL and TR WTPs both rely upon groundwater sources that contain total sulfide at concentrations ranging from...
Show moreThis study evaluated alternative sulfide treatment processes for potable water systems that rely on groundwater supplies. Research for this study was conducted at the Imperial Lakes (IL) and Turner Road (TR) water treatment plants (WTPs) in Polk County, Florida. These WTPs are in the process of refurbishment and expansion, and will require the installation of a new groundwater well. The IL and TR WTPs both rely upon groundwater sources that contain total sulfide at concentrations ranging from 1.4 to 2.6 mg/L. Sulfide is a concern because if left untreated it can impact finished water quality, corrosivity, create undesirable taste and odor, and oxidize to form visible turbidity. For this reason, the raw water will require treatment per Florida Department of Environmental Protection (FDEP) "Sulfide Rule" 62-555.315(5)(a). This rule does not allow the use of conventional tray aeration (currently in use at the IL and TR WTPs) for wells that have significant total sulfide content (0.6 to 3.0 mg/L). This research was commissioned because the potential water treatment method identified in the Sulfide Rule (i.e. forced-draft aeration) would not adequately fit within the confines of the existing sites and would pose undue burden to neighboring residents. In addition, an effective sulfide treatment process was desired that offered a low profile, did not necessitate the need for additional complex chemical feed systems, minimized the extent of electrical infrastructure upgrades, and was inexpensive to construct and operate. To meet these goals, several alternative technologies were evaluated at the desktop and bench-scale; these included anion exchange, various oxidation methods, and alternative media filtration processes. From that effort, several processes were selected for evaluation at the pilot scale: bleach (NaOCl) oxidation preceding electromedia filtration; manganese (IV) oxide (MnO2) filtration continuously regenerated with bleach; and ferrate (Fe(VI)) oxidation. Electromedia and MnO2 filtration were shown to be effective for total sulfide treatment. Both processes reduced total sulfide content to below detection levels (< 0.1 mg/L) for groundwater supplies containing as much as 2.6 mg/L of total sulfide. The use of bleach oxidation ahead of media filtration also produced finished water with low turbidity (< 1.0 NTU) as compared to conventional tray aeration and chlorination processes (6-16 NTU, as observed in this study). It was determined that the media filtration approach (electromedia and MnO2) was effective for sulfide treatment and met the County's site objectives established at the outset of the project. Ferrate was also shown to reduce total sulfide content to below detection levels (< 0.1 mg/L) for groundwater supplies containing as much as 2.6 mg/L of total sulfide. An opinion of probable capital costs for installing a sulfide oxidation/filtration process at either the Imperial Lakes or Turner Road WTP was estimated to range from roughly $830,000 to $1,100,000. That equates to a $/kgal capital cost of $0.10 to $0.32 (at 8% for 20 years). An opinion of annual probable bleach chemical costs was estimated to range from $3,500 to $9,800 for the IL WTP and $3,500 to $5,800 for the TR WTP.
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Date Issued
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2010
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Identifier
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CFE0003370, ucf:48432
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0003370
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Title
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EXPERIMENTAL ANALYSIS OF THE HYDROGEN SULFIDE ABSORTION PHENOMENA IN BRINE/OIL MIXTURES AS A FUNCTION OF SYSTEM PRESSURE AND H2S CONCENTRATION.
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Creator
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Zea, Luis, Kumar, Ranganathan, University of Central Florida
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Abstract / Description
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In underground oil reservoirs, Hydrogen sulfide is usually found coexisting with the oil due to bacteria reduction over a long period of time. The amount of H2S in the oil varies from place to place around the globe. When the oil extraction process begins, the presence of Hydrogen sulfide becomes noticeable as drilling tools, piping and other equipment suffer from sulfide stress cracking, electrochemical corrosion and corrosion fatigue. For this reason, the oil industry invests millions of...
Show moreIn underground oil reservoirs, Hydrogen sulfide is usually found coexisting with the oil due to bacteria reduction over a long period of time. The amount of H2S in the oil varies from place to place around the globe. When the oil extraction process begins, the presence of Hydrogen sulfide becomes noticeable as drilling tools, piping and other equipment suffer from sulfide stress cracking, electrochemical corrosion and corrosion fatigue. For this reason, the oil industry invests millions of dollars per year trying to find better ways to reduce the amount of H2S in oil. An important part of the current investigations deals with brine (sea water)/oil mixtures. The reasons are two-fold: 1) one way of extracting the petroleum from the reservoir is by injecting brine into it and since it has a higher density than oil, the latter will be ejected up to the surface. Taking into account the complex fluid flow occurring within the reservoir it is easy to understand that some brine will also be present as part of the ejected fluid; 2) brine is already present in the reservoir, so independent of the extraction method used, there will be a brine/oil mixture in the ejected flow. When brine and oil have absorbed H2S under pressure in the reservoir and then suffer a decompression during the extraction process, a certain amount of H2S is released from the liquid phase. In order to have a better prediction of how much Hydrogen sulfide can be liberated a good understanding of H2S absorption by these liquids is necessary. The amount of gas a solvent absorbs is a function of pressure, original gas concentration and temperature as described by Henry's Law. The purpose of this thesis is to experimentally analyze how much of the corrosive gas is absorbed into different brine/oil mixtures, and brine and oil, separately. In order to find sufficient data for a thorough analysis, different reservoir simulation scenarios were created. The liquids were mixed from pure brine to pure oil, resulting in 33% and 66% water cuts. Data were obtained at 2 pressures of 20atm and 70atm at room temperature. H2S concentration was also a variable, changing the original gas concentration through different values: 50, 100, and 300ppm. These experiments were conducted in an autoclave system and will better explain the hydrostatic process that occurs inside the reservoir. It was found that throughout all the water cuts, the role that total pressure plays in the absorption phenomena is of less importance as the original H2S concentration is increased. In the same manner it was observed that the highest mass-absorption ratios are always found between 50 and 100ppm and the lowest at 300ppm, this is observed for all water cuts and total pressures. Another important finding was that the ability to absorb the corrosive gas decreases as the original H2S concentration increases and this proves to be true for all water cuts and system pressures. After conducting these different reservoir scenarios, tests were conducted to simulate 300m of the horizontal section of the pipe that connects the head of the well with the platform. This was done with a high pressure 300-meter long loop. It was found that the corrosive gas is absorbed at a higher rate when there is a flow, opposite to a hydrostatic case. Henry's Law constant was identified for each water cut and each pressure, however, the test procedure could not be validated since the gas being studied was not in its pure form. Understanding the absorption phenomena of Hydrogen sulfide in different water cuts will definitely be of great help to the oil industry to make better forecasts of H2S concentrations being ejected from each well.
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Date Issued
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2008
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Identifier
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CFE0002257, ucf:47824
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0002257
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Title
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HYDROGEN SULFIDE FLUX MEASUREMENTS AND DISPERSION MODELING FROM CONSTRUCTION AND DEMOLITION (C&D) DEBRIS LANDFILLS.
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Creator
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Eun, Sangho, Reinhart, Debra, University of Central Florida
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Abstract / Description
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Odor problems are a common complaint from residents living near landfills. Many compounds can cause malodorous conditions. However, hydrogen sulfide (h2s) has been identified as a principal odorous component from construction and demolition (c&d)debris landfills. Although several studies have reported the ambient concentrations of h2s near c&d landfills, few studies have quantified emission rates of h2s. The most widely used and proven technique for measuring gas emission rates from...
Show moreOdor problems are a common complaint from residents living near landfills. Many compounds can cause malodorous conditions. However, hydrogen sulfide (h2s) has been identified as a principal odorous component from construction and demolition (c&d)debris landfills. Although several studies have reported the ambient concentrations of h2s near c&d landfills, few studies have quantified emission rates of h2s. The most widely used and proven technique for measuring gas emission rates from landfills is the flux chamber method. Typically the flux chamber is a cylindrical enclosure device with a spherical top which limits the gas emission area. Pure zero grade air is introduced into the chamber, allowed to mix with emitting gases captured from the landfill surface, and then transported to the exit port where concentrations can be measured. Flux measurements using the flux chamber were performed at five different c&d landfills from june to august, 2003. The flux rates of h2s measured in this research were three to six orders of magnitude lower than the flux rates of methane reported in the literature. In addition to the h2s flux measurements, dispersion modeling was conducted, using the epa dispersion model, industrial source complex short term (iscst3), in order to evaluate impacts on landfill workers and communities around the landfills. The modeling results were analyzed to estimate the potential ground level maximum h2s concentrations for 1-hr and 3-min periods and the frequency (occurrences per year) above the h2s odor detection threshold for each landfill. Odor complaints could be expected from four among five landfills selected for this study, based on 0.5-ppb odor detection threshold.
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Date Issued
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2004
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Identifier
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CFE0000169, ucf:52837
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0000169
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Title
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Monitoring and Modeling to Estimate Hydrogen Sulfide Emissions and Dispersion from Florida Construction and Demolition Landfills to Construct Odor Buffering Distances.
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Creator
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Bolyard, Steven, Cooper, Charles, Mackie, Kevin, Randall, Andrew, Zhang, Husen, University of Central Florida
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Abstract / Description
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Emissions of hydrogen sulfide (H2S) from construction and demolition (C & D) landfills can result in odors that are a significant nuisance to nearby neighborhoods and businesses. As Florida's population continues to grow and create development pressures, housing is built closer to existing landfills. Additionally, new landfills will be created in the future. This research project was undertaken to develop a detailed modeling methodology for use by counties and other landfill owners to provide...
Show moreEmissions of hydrogen sulfide (H2S) from construction and demolition (C & D) landfills can result in odors that are a significant nuisance to nearby neighborhoods and businesses. As Florida's population continues to grow and create development pressures, housing is built closer to existing landfills. Additionally, new landfills will be created in the future. This research project was undertaken to develop a detailed modeling methodology for use by counties and other landfill owners to provide them with an objective and scientifically defensible means to establish odor buffer zones around C & D landfills. A technique for estimating methane (and odorous gas) emissions from municipal solid waste (MSW) landfills was recently developed by researchers at the University of Central Florida. This technique was based on measuring hundreds of ambient methane concentrations near the surface of the landfill, and combining that data with matrix inversion mathematics to back-solve the dispersion equations. The technique was fully documented in two peer-reviewed journal articles. This project extends that methodology. In this work the author measured ambient H2S concentrations at various locations in a C & D landfill, and applied those same matrix inversion techniques to determine the H2S emission rates from the landfill. The emission rates were then input into the AERMOD dispersion model to determine H2S odor buffer distances around the landfill.Three sampling trips to one C & D landfill were undertaken, data were taken, and the modeling techniques were applied. One problem encountered was that H2S emissions from C & D landfills are typically about 1000 times smaller than methane emissions (from MSW landfills). Thus, H2S ambient concentrations often are near the detection limits of the instruments, and the data may not be as reliable. However, this approach could be used for any particular C & D landfill if the appropriate amount of data were available to characterize its emissions with some certainty. The graphical tool developed in this work shows isopleths of (")H2S(") concentrations at various distances, and color codes the isopleths into a (")green-yellow-red(") scheme (analogous to a traffic signal) that depicts zones where private landowners likely will not detect odors, where they may experience some odors, or where they likely will experience odors. The (")likelihood(") can be quantified by selecting the Nth highest hourly concentrations in one year to form the plot. In this study, N was conservatively selected as 8. Requiring that concentrations be at or below the 8th highest concentration in a year corresponds to a 99.9% probability of not exceeding that concentration at that distance in any future year. The graphical tool can be applied to any C & D landfill but each landfill is different. So this technique depends on having a fairly good estimate of the rate of emissions of H2S from the landfill in question, and at least one year's worth of hourly meteorological data (wind speed, direction, and stability class) that is representative of the landfill location. The meteorological data can be obtained with relative ease for most locations in Florida; however, the emission data must be obtained from on-site measurements for any given landfill.
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Date Issued
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2012
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Identifier
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CFE0004272, ucf:52879
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004272
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Title
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Investigating Novel Water Treatment Methods and Monitoring Techniques for Sulfide-Laden Groundwater Supplies.
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Creator
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Yoakum, Benjamin, Duranceau, Steven, Lee, Woo Hyoung, Sadmani, A H M Anwar, Moore, Sean, University of Central Florida
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Abstract / Description
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This dissertation reports on research related to novel water treatment and monitoring techniques for sulfide-laden groundwater supplies. The dissertation is divided into several chapters with four core chapters focused on investigations studying a novel water treatment method or monitoring technique. The first investigation assessed the efficacy of multi-pass spray aeration treatment to remove trihalomethanes (THMs) and to reduce the total THM formation potential (TTHMFP) of an aerated water...
Show moreThis dissertation reports on research related to novel water treatment and monitoring techniques for sulfide-laden groundwater supplies. The dissertation is divided into several chapters with four core chapters focused on investigations studying a novel water treatment method or monitoring technique. The first investigation assessed the efficacy of multi-pass spray aeration treatment to remove trihalomethanes (THMs) and to reduce the total THM formation potential (TTHMFP) of an aerated water column post-aeration. A recirculating spray aeration pilot unit was constructed to make this assessment. To assess the effect of multi-pass spray aeration on the TTHMFP, water was recirculated through a fabricated spray nozzle for various lengths of time. Results showed that multi-pass spray aeration can remove chloroform, dichlorobromomethane, dibromochloromethane and bromoform to below detection levels ((<) 0.7 ppb) for the waters investigated. Additionally, spray aeration reduced the TTHMFP of chlorinated water. Results suggest multi-pass spray aeration may be a viable treatment option for some bromide container waters. Results also indicate that multi-pass spray aeration removes bromide from the bulk water in the form of organically bound volatile compounds.The second investigation assessed the efficacy of using pre-existing tray aeration infrastructure to comply with disinfection by-product (DBP) regulations. To assess the efficacy of tray aerators to reduce the concentration TTHMs a pilot tray aerator was constructed. Results showed that after five tray passes (each pass consisting of water being passed over five trays) the concentration of TTHMs was below the detection limit ((<) 0.7 ppb) for the water investigated. To assess the efficacy of tray aeration at full-scale, a water treatment plant and the distribution system it serves were monitored for eight months. Results showed an approximate 40 ppb reduction in the TTHM concentration at two on-site monitoring locations and the one off-site monitoring location (initial concentrations being approximately 54 ppb, 60 ppb and 73 ppb, respectively). Results suggest that the utility managing the full-scale system could comply with DBP regulations by using the pre-existing tray aeration infrastructure to reduce formed THMs on-site where regulated haloacetic acids are not predominant.The third investigation assessed the efficacy of using biological activated carbon (BAC) to remove disinfection by-product precursor matter to comply with DBP regulations. To research this method, a pilot scale BAC filter was operated for three independent test runs. In addition, two full-scale WTPs using BAC were monitored over time. Results showed an approximate 40 percent removal of dissolved organic carbon (DOC) during the three pilot runs and an approximate 55 percent removal of DOC during full-scale monitoring. Results showed that the reduction in DOC reduced the TTHMFP of BAC treated water. Results suggest that BAC treatment could be a viable treatment option to comply with DBP regulations in the sulfide-laden water studied.The fourth investigation assessed the suitability of oxidation reduction potential (ORP) to monitor the effectiveness of an oxidizing media filter used to remove sulfur from a sulfide-laden groundwater. Results showed that ORP was more useful as a measurement technique as compared to free chlorine residual when assessing filter bed health and regeneration effectiveness. It was determined that when the ORP measurement taken from within the oxidative media layer was below 500 mV, the filter bed was not providing treatment, and manganese could be released. Results showed a significant increase in turbidity ((>) 2 NTU) and total manganese ((>) 0.05 mg/L) occurred when the ORP within the filter bed dropped below 400 mV. More frequent cycling of the filters was found to be an effective treatment option to maintain ORP values above an identified 400 mV operational threshold.
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Date Issued
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2017
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Identifier
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CFE0007141, ucf:52317
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007141
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Title
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Ozone and GAC Treatment of a Central Florida Groundwater for Sulfide and Disinfectant By-Product Control.
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Creator
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Lamoureux, Tara, Duranceau, Steven, Randall, Andrew, Wang, Dingbao, University of Central Florida
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Abstract / Description
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This study evaluated the combination of ozone and granular activated carbon (GAC) treatment for the removal of sulfide and disinfection byproduct (DBP) precursors in drinking water at the pilot-scale. The research conducted was performed at the Auxiliary (Aux) and Main Water Treatment Plants (WTPs) in Sanford, Florida. Both WTPs rely upon groundwater sources that contain total sulfide ranging from 0.02 to 2.35 mg/L and total organic carbon (TOC) ranging from 0.61 to 2.20 mg/L. The Aux WTP's...
Show moreThis study evaluated the combination of ozone and granular activated carbon (GAC) treatment for the removal of sulfide and disinfection byproduct (DBP) precursors in drinking water at the pilot-scale. The research conducted was performed at the Auxiliary (Aux) and Main Water Treatment Plants (WTPs) in Sanford, Florida. Both WTPs rely upon groundwater sources that contain total sulfide ranging from 0.02 to 2.35 mg/L and total organic carbon (TOC) ranging from 0.61 to 2.20 mg/L. The Aux WTP's raw water contains, on average, 88% more sulfide and 24% more TOC than the Main WTP. Haloacetic acids (HAA5) and total trihalomethanes (TTHMs) comprise the regulated forms of DBPs. HAA5 are consistently below the maximum contaminant level (MCL) of 60 ?g/L, while TTHM ranges from 70 to 110 ?g/L, at times exceeding the MCL of 80 ?g/L in the distribution system. Ozone alone removed total sulfide and reduced UV-254 by about 60% at the Aux Plant and 35% at the Main Plant. Producing an ozone residual of 0.50 mg/L prevented the formation of bromate while removing approximately 35 to 60% concentration of DBP precursors as measured by UV-254. Operating the GAC unit at an empty bed contact time (EBCT) of 10 minutes for the Aux Plant and 5.5 minutes for the Main Plant resulted in 75% and 53% of UV-254 reduction, respectively. The average 120 hour TTHM formation potential for the Aux and Main Plants were 66 ?g/L and 52 ?g/L, respectively, after treatment by ozone and GAC. GAC exhaustion was deemed to have occurred after seven weeks for the Aux Plant and eleven weeks for the Main Plant. The GAC columns operated in three phases: an adsorption phase, a transitional phase, and a biologically activated carbon (BAC) phase. The GAC adsorption phase was found to produce the lowest TTHMs; however, TTHMs remained less than 80 ?g/L during the BAC stage at each plant. BAC exhaustion did not occur during the course of this study. Ozone-GAC reduced chlorine demand by 73% for the Aux Plant and 10% for the Main Plant.
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Date Issued
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2013
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Identifier
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CFE0004708, ucf:49824
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0004708
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Title
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Development of Novel Redox Sensors and Processes Towards Biological Applications.
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Creator
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Patel, Jigna, Yestrebsky, Cherie, Clausen, Christian, Hampton, Michael, Harper, James, Diaz, Diego, University of Central Florida
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Abstract / Description
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Research on the cure and early detection of diseases such as diabetes, Alzheimer's, and Parkinson's is becoming of great interest due to the increasing number of people affected by them every year. An accurate and quick detection of various damaging species is highly critical in treatments of such diseases not only for exploring possible cures but also for early detection. If these diseases are detected during the initial stages than the possibility of curing them is much higher. Motivated by...
Show moreResearch on the cure and early detection of diseases such as diabetes, Alzheimer's, and Parkinson's is becoming of great interest due to the increasing number of people affected by them every year. An accurate and quick detection of various damaging species is highly critical in treatments of such diseases not only for exploring possible cures but also for early detection. If these diseases are detected during the initial stages than the possibility of curing them is much higher. Motivated by this, many researchers today have developed numerous types of sensing devices that can detect various physiological and biological compounds. However, most of these sensors are enzyme based. They have several setbacks such as the lack of sensitivity, restricted selectivity, short shelf life, and biological fouling. To overcome these obstacles, we examine the use of nanoceria modified Pt and Au electrodes for the detection of glucose and reactive oxygen species such as hydrogen peroxide. Amperometric detection of glucose and hydrogen peroxide is critical for biological applications for diabetes and possible Alzheimer's and Parkinson's patients. This dissertation focuses on the exploration of non-enzymatic detection of glucose and reactive oxygen species which has the prospective to be used for biological applications, in addition to an investigation of an odor control technology that uses these reactive oxygen species for the treatment of wastewater plants. The combination of bi-metallic composites with nanoceria showed increased oxidation ability towards glucose and hydrogen peroxide. The following dissertation expands on the relationship between bi-metallic nanoceria composite materials and its electro-oxidation of glucose and hydrogen peroxide towards biological sensing along with an investigation of an odor control technology that utilizes generates hydroxyl radical fine particle mist for the degradation of hydrogen sulfide odor in wastewater treatment plants.
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Date Issued
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2013
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Identifier
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CFE0005227, ucf:50585
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0005227
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Title
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Experimental confirmation of ballistic nanofriction and quasiparticle interference in Dirac materials.
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Creator
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Lodge, Michael, Ishigami, Masahiro, Kaden, William, Schelling, Patrick, Del Barco, Enrique, Roy, Tania, University of Central Florida
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Abstract / Description
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This dissertation is broadly divided into two parts. The first part details the development and usage of an experimental apparatus to measure the dry nanofriction for a well-defined interface at high sliding speeds. I leverage the sensitivity of a quartz crystal microbalance (QCM) to determine the drag coefficient of an ensemble of gold nanocrystals sliding on graphene at speeds up to 11 cm/s. I discuss the theories of velocity-dependent friction, especially at high sliding speeds, and QCM...
Show moreThis dissertation is broadly divided into two parts. The first part details the development and usage of an experimental apparatus to measure the dry nanofriction for a well-defined interface at high sliding speeds. I leverage the sensitivity of a quartz crystal microbalance (QCM) to determine the drag coefficient of an ensemble of gold nanocrystals sliding on graphene at speeds up to 11 cm/s. I discuss the theories of velocity-dependent friction, especially at high sliding speeds, and QCM modeling. I also discuss our synthesis protocols for graphene and molybdenum disulfide, as well as our protocol for fabricating a clean, graphene-laminated QCM device and nanocrystal ensemble. The design and fabrication of our QCM oscillator circuit is presented in detail. The quantitatively-measured the drag coefficient is compared against molecular dynamics simulations at both low and high sliding speeds. We show evidence of a predicted ultra-low friction regime and find that the interaction energy between gold nanocrystals and graphene is lower than previously assumed. In the second part of this dissertation, I detail the band structure measurement of a novel semimetal using scanning tunneling microscopy. In particular, I measured the energy-dependenceof quasiparticle interference patterns at the surface of zirconium silicon sulfide (ZrSiS), a topological nodal line semimetal whose charge carrier quasiparticles possess a pseudospin degree offreedom. The aims of this study were to (1) discover the shape of the band structure above the Fermi level along a high-symmetry direction, (2) discover the energetic location of the line node inthe same high-symmetry direction, and (3) discover the selection rules for k transitions. This study confirms the predicted linearity in E(k) of the band structure above the Fermi level. Additionally,we observe an energy-dependent mechanism for pseudospin scattering. This study also provides the first experimentally-derived estimation of the line node position in E(k).
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Date Issued
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2018
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Identifier
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CFE0007218, ucf:52222
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Format
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Document (PDF)
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PURL
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http://purl.flvc.org/ucf/fd/CFE0007218