Coal preparation plants use large quantities of water for cleaning processes. Upon cleaning, the spent water must be removed such that the final product moisture level meets market constraints. However, removal of free water from the surface of fine particles is difficult and costly, and often the results are less than desirable. Fine particles inherently have very large surface areas, and hence retain large amounts of water. Increased amounts of fines also cause denser particle packing, which creates relatively small capillaries in filter cakes and, thus, cause slower dewatering kinetics. As a result, dewatering costs for fine particles are much higher than for dewatering coarse particles. Considering the technical and economic issues associated with dewatering coal and mineral fines, an extensive matrix of laboratory- and pilot-scale dewatering tests have been conducted to evaluate the use of novel dewatering aids. The reagents are designed to lower the surface tension of water, increase the hydrophobicity of the particles to be dewatered, and increase the capillary radius by hydrophobic coagulation. All of these are designed to lower the moisture of the filter cakes produced in mechanical dewatering processes. Laboratory-scale dewatering tests confirmed that using the novel dewatering aids can lower the final cake moisture of coal by 20-50%, while increasing the dewatering kinetics. Several on-site, pilot-scale tests were conducted to demonstrate that the process of using the novel dewatering aids can be scaled. Based on the laboratory- and pilot-scale tests conducted, a scale-up model for the process of using the novel dewatering aids has been developed. It can predict the final cake moistures as a function of vacuum pressure, filtration time and specific cake weight. The model can be useful for the scale-up of vacuum disc filters (VDF) and horizontal belt filters (HBF). Simulation results indicate that dewatering aids can be very effective, especially when used in conjunction with HBF due to its ability to control cake thickness and drying cycle time independently. In light of the promising laboratory- and pilot-scale test results, an industrial demonstration of the novel dewatering aids has been conducted at the Smith Branch impoundment site, which contains 2.9 million tons of recoverable coal. When the reagent was used for dewatering flotation products using a VDF, the moisture content was reduced from 26 to 20% at 0.5 lb/ton of reagent addition and to 17.5% at 1 lb/ton. The use of the dewatering aid also improved the kinetics of dewatering, increased the throughput, and reduced the power consumption of vacuum pumps by 30%. The novel dewatering aids were also tested successfully for dewatering of kaolin clays. In this case, the mineral was treated with a cationic surfactant before adding the dewatering aids. This two-step hydrophobization process was able to reduce the cake moisture and also increase the throughput. / Ph. D.

Vacuum-Assisted Resin Transfer Molding (VARTM) processes are becoming promising technologies in the manufacturing of primary composite structures in the aircraft industry as well as infrastructure. A great deal of work still needs to be done on efforts to reduce the costly trial-and-error methods of VARTM processing that are currently in practice today. A computer simulation model of the VARTM process would provide a cost-effective tool in the manufacturing of composites utilizing this technique. Therefore, the objective of this research was to modify an existing three-dimensional, Resin Film Infusion (RFI)/Resin Transfer Molding (RTM) model to include VARTM simulation capabilities and to verify this model with the fabrication of aircraft structural composites. An additional objective was to use the VARTM model as a process analysis tool, where this tool would enable the user to configure the best process for manufacturing quality composites. Experimental verification of the model was performed by processing several flat composite panels. The parameters verified included flow front patterns and infiltration times. The flow front patterns were determined to be qualitatively accurate, while the simulated infiltration times over predicted experimental times by 8 to 10%. Capillary and gravitational forces were incorporated into the existing RFI/RTM model in order to simulate VARTM processing physics more accurately. The theoretical capillary pressure showed the capability to reduce the simulated infiltration times by as great as 6%. The gravity, on the other hand, was found to be negligible for all cases. Finally, the VARTM model was used as a process analysis tool. This enabled the user to determine such important process constraints as the location and type of injection ports and the permeability and location of the high-permeable media. A process for a three-stiffener composite panel was proposed. This configuration evolved from the variation of the process constraints in the modeling of several different composite panels. The configuration was proposed by considering such factors as: infiltration time, the number of vacuum ports, and possible areas of void entrapment. / Ph. D.

Constructing a detailed understanding of the heterogeneous oxidation of atmospheric organic aerosols, both from a mechanistic and kinetic perspective, will enable researchers to predict the fate and lifetime of atmospheric gases and the particles with which they interact. In an effort to develop a more complete understanding of the interfacial reactions of ozone with vinyl-containing organic thin films, self-assembled monolayers that contain vinyl groups positioned precisely at the gas/surface interface were synthesized as model systems for atmospheric organic aerosols. To isolate the reactions of background gases with ozone or surface products, an ultrahigh vacuum surface analysis instrument was designed and constructed to explore the reactions of ozone with the atmospheric model systems. The surface reactions can be monitored in real-time with reflection absorption infrared spectroscopy (RAIRS) and mass spectrometry. The chemical identity of adsorbates on a surface can also be determined before or after a reaction with X-ray photoelectron spectroscopy (XPS). Disordering of the monolayers concurrent with the disappearance of the vinyl group was observed with RAIRS. New bands within the RAIR spectra were observed and assigned to carbonyl or carboxylic acids bound to the surface. Little oxidation of the sulfur head groups and no significant loss of carbon during the reaction was observed with XPS. A mechanism is proposed that includes the cross linking of the hydrocarbon chains within the monolayer, which impedes further oxidation of the sulfur head group and limits desorption of the chains. By RAIRS, the kinetics of the oxidation of the vinyl groups were tracked and an observed rate constant was determined by monitoring the changes in IR absorbance of the C=C bond. With the aid of the rate constant, an initial reaction probability for the collisions of ozone with vinyl groups positioned precisely at an interface was determined. The reaction probability is approximately three orders of magnitude greater than the reaction probability for an analogous gas-phase reaction, which demonstrates that the gas/surface interface plays an important role in this reaction. The results presented in this thesis should help develop a more detailed understanding of the interfacial reactions of pure ozone at surfaces. / Ph. D.

The Casimir force for charge-neutral, perfect conductors of non-planar geometric configurations have been investigated. The configurations were: (1) the plate-hemisphere, (2) the hemisphere-hemisphere and (3) the spherical shell. The resulting Casimir forces for these physical arrangements have been found to be attractive. The repulsive Casimir force found by Boyer for a spherical shell is a special case requiring stringent material property of the sphere, as well as the specific boundary conditions for the wave modes inside and outside of the sphere. The necessary criteria in detecting Boyer's repulsive Casimir force for a sphere are discussed at the end of this thesis. / Ph. D.

The advancements of chemists, engineers, and material scientists has yielded an enormous and diverse library of high-performance materials with varying chemical and physical properties that can be used in a wide array of applications. A molecular-level understanding of the nature of gas–surface interactions is critical to the development of next generation materials for applications such as gas storage and separation, chemical sensing, catalysis, energy conversion, and protective coatings. Quartz crystal microbalance (QCM) and in situ infrared (IR) spectroscopic techniques were employed to probe how topological features of a material as well as structural differences of the analytes affect gas sorption. Detailed studies of the interactions of three categories of molecules: aromatic hydrocarbons, triatomic ambient gases, and chemical warfare agents, with metal-organic frameworks (MOFs) and polyurethane coatings were conducted to build structure–property relationships for the nature and energetics of gas sorption within each material. Differences in the molecular structure of the guest compounds were found to greatly influence how, and to what extent each molecule interacts with the MOF or polyurethane film. Specifically, IR studies revealed that transport of aromatic compounds within the zirconium-based MOF, UiO-66 was limited by steric restrictions as molecules passed through small triangular apertures within the pore environment of the MOF. In contrast, the smaller triatomic molecules, CO2, SO2, and NO2, were able to pass freely through the MOF apertures and instead reversibly adsorbed inside the MOF cavities. Specifically, SO2 and NO2 were observed to preferentially bind to undercoordinated zirconium sites located on the MOF nodes. In addition, uptake of CO2, SO2, and NO2 was also aided by dispersion forces within the confined pore environments and by hydrogen bond formation with μ3 OH groups of the MOFs. Dimethyl chlorophosphate (DMCP), a nerve agent simulant that contains several electronegative moieties, was also found to strongly adsorb to undercoordinated zirconium; however, unlike in the aromatic and triatomic molecule systems, DMCP remained permanently bound to the MOFs, even at high temperatures. Finally, QCM studies of mustard gas simulant uptake into polyurethane films of varying hard:soft segment compositions revealed that dipole-dipole and dipole-induced dipole interactions were responsible for favorable absorption conditions. Furthermore, the ratio of hard and soft segment components of the polyurethane had a minor impact on simulant adsorption. Higher hard-segment content resulted in a more crystalline film that reduced simulant uptake, whereas the rubbery, high soft segment polyurethane allowed for greater vapor absorption. Ultimately, molecular-level insight into how the chemical identity of a guest molecule impacts the mechanism and energetics of vapor sorption into both MOFs and polymeric films can be extended to other relevant systems and may help identify how specific characteristics of each material, such as size, shape, and chemical functionality impact their potential use in targeted applications. / Doctor of Philosophy / The nature in which specific gases interact with materials will largely dictate how the material can be utilized. By understanding where and how strongly gas molecules interact with a material, scientists and engineers can rationally design new and improved systems for targeted applications. In the research described in this thesis, we examined how the chemical structure of three different groups of compounds, which have relevance in many industrial, environmental, and defense-related applications, affected the type and strength of interaction between the gas and material of interest. From these studies, we have identified how key properties and features within the examined materials such as size, shape, and chemical composition, lead to significant differences in how vapor molecules interacted with the materials. For example, benzene, toluene, and xylene, which are incredibly important chemicals in industry, were found to be restricted by narrow passageways as they moved through materials with small pores. In contrast, small gases present in the environment from combustion exhaust such as CO₂, SO₂, and NO₂ were able to freely traverse through the passageways, and instead weakly interacted with specific chemical groups inside the cavities of the material. On the same material however, a third class of compounds, organophosphorus-containing chemical warfare agent mimics, irreversibly reacted with chemical groups of the surface, and remained bound even after exposure to high temperatures. Ultimately, the work presented in this thesis is aimed at providing key fundamental insights about specific classes of materials on how, and how strongly they interact with targeted hazardous vapors, which can be utilized by synthetic chemists to design next generation materials.

Diborane (B2H6) is a hydride gas often employed in high-purity industrial surface processes such as chemical vapor deposition or epitaxial layer growth. The use of diborane at industrial scales is complicated by the formation of higher-order borane contaminants in pure diborane gas via a complex series of gas-phase reactions. An advanced, rationally designed sorbent could stabilize diborane through interfacial interactions, dramatically reducing the decomposition rate without permanently trapping the molecule. However, the design of such a sorbent would require a nuanced understanding of diborane's fundamental surface chemistry, about which little is known. In the work presented in this thesis, a novel ultra-high vacuum (UHV) system was designed and employed to characterize the fundamental interactions of diborane with a variety of surfaces. In situ Fourier-transform infrared (FTIR) spectroscopy and temperature-programmed desorption (TPD) experiments were used in conjunction with density-functional theory (DFT) calculations to elucidate binding geometries and interaction mechanisms. On non-functionalized model surfaces such as CaF2 or amorphous carbon, diborane adsorbed only at cryogenic temperatures. Hydroxylated surfaces such as amorphous silica (SiO2) adsorbed significantly more diborane, which remained at slightly higher temperatures. FTIR spectra indicated the presence of hydrogen bonding between diborane and surface hydroxyl groups. DFT calculations revealed that the interaction takes the form of a novel bifurcated dihydrogen bond. In contrast with previous reports, diborane exhibited only weak interactions with the surface hydroxyl groups of silica. DFT calculations further elucidated that the irreversible reaction of diborane with surface hydroxyls is only possible in the presence of a second nucleophile (such as adventitious water). On the metal-organic framework (MOF) UiO-66 NH2, unique chemistry was observed in which diborane reacted with the –NH2 groups of the MOF linkers, yielding stable surface-bound products. DFT calculations determined the reaction mechanism to be dissociative adsorption of diborane, resulting in two amine-bound –BH3 moieties. Importantly, it was found that these fragments persisted at room temperature and could only leave the surface via the reverse reaction. The discovery that diborane can be stored as separate fragments that re-combine to yield the parent molecule has important implications for the development of new diborane sorbents. We hypothesize that surfaces designed with fixed, precisely spaced nucleophiles could enable the reversible storage of diborane. / Doctor of Philosophy / Diborane (B2H6) is a useful but hazardous gas employed in both academia and industry, often in processes that require ultra-high-purity source gases. However, diborane reacts with itself at room temperature, making the contamination of pure diborane very difficult to avoid. This problem could potentially be solved with a specially designed solid material that would sequester diborane without destroying it, but the design of such a material would require a much better understanding of diborane's chemistry with surfaces than currently exists. In this work, we employed ultra-high vacuum (UHV) methods to study the interactions between diborane and a variety of surfaces, with the ultimate goal of determining guiding principles for the design of diborane-stabilizing sorbents. Among the materials we studied were inorganic carbon, silica (SiO2), and a class of advanced microporous materials known as metal-organic frameworks (MOFs). Inorganic materials were found not to interact meaningfully with diborane. A novel hydrogen bond was discovered between diborane and the surface of silica, but the interaction was found to be too weak to provide significant stabilization. Most MOFs behaved similarly to silica. The MOF UiO-66-NH2, however, was found to react with diborane. Through a combination of computer simulations and UHV experiments, the precise nature of the reaction was determined. On the surface of UiO 66 NH2, diborane splits into two surface-bound BH3 molecules, where it is trapped until the reaction reverses. Importantly, it was found that BH3 can only leave the surface by recombining into diborane—effectively storing diborane on the surface to be released later. We hypothesize that this useful chemistry is due to the fixed distance between chemical groups on the MOF surface. This discovery suggests a promising strategy for the design of advanced diborane sorbents.

This study describes the construction of a high vacuum station and the instrumentation and testing of two methods for obtaining the first derivative of the current-voltage characteristic of a Langmuir Probe, which is needed to determine the electron speed distribution in rare gases. The theory behind using a lock-in amplifier differentiator to obtain the derivative of the I-V characteristic of a Langmuir Probe is derived and discussed. A test was devised to check the instrumentation for correct operation. / M.S.

Detailed understanding of the kinetics and mechanisms of heterogeneous reactions between gas-phase nitrate radicals, a key nighttime atmospheric oxidant, and organic particles will enable scientists to predict the fate and lifetime of the particles in the atmosphere. In an effort to acquire knowledge of interfacial reactions of nitrate radical with organics, model surfaces are created by the spontaneous adsorption of methyl-/vinyl-/hydroxyl-terminated alkanethiols on to a polycrystalline gold substrate. The self-assembled monolayers provide a well-defined surface with the desired functional group (-CH3, H2C=CH-, or HO-) positioned precisely at the gas-surface interface. The experimental approach employs in situ reflection-absorption infrared spectroscopy (RAIRS) to monitor bond rupture and formation while a well-characterized flux of NO3 impinges on the organic surface. Overall, the reaction kinetics and mechanisms were found to depend on the terminal functional group of the SAM and incident energy of the nitrate radical (NO3). For reactions of the H2C=CH-SAM with NO3, the surface reaction kinetics obtained from RAIRS reveals that the consumption rate of the terminal vinyl groups is nearly identical to the formation rate of a surface-bound nitrate species and implies that the mechanism is one of direct addition to the vinyl group rather than hydrogen abstraction. Upon nitrate radical collisions with the surface, the initial reaction probability for consumption of carbon-carbon double bonds was determined to be (2.3 ± 0.5) -- 10-3. Studies of reactions of HO-SAM with the effusive source of NO3 suggest that the reaction between NO3 and the HO-SAM is initiated by hydrogen abstraction at the terminal - 'CH2OH groups with the initial reaction probability of (6 ± 1)-- 10-3. An Arrhenius plot was obtained to measure the activation energy of the H abstraction from the HO-SAM. Further, for reactions of the HO-SAM with the high incident energy of NO3 molecules created by molecular beam, the reaction probability for H abstraction at the hydroxyl terminus was determined to be ~0.4. The significant increase in the reaction probability was attributed to the promotion in the ability of NO3 abstracting hydrogen atom at the methylene groups along hydrocarbon chains. The reaction rates of NO3 with the model organic surfaces that have been investigated are orders of magnitude greater than the rate of ozone reactions on the same surfaces which suggests that oxidation of surface-bound organics by nighttime nitrate radicals may play an important role in atmospheric chemistry despite their relative low concentration. X-ray photoelectron spectroscopy (XPS) data suggests that oxidation of the model organic surfaces by NO3 leads to the production of organic nitrates, which are stable for a period time. In addition, the effect of background gases on reactions of NO3 with model organic surfaces needs further investigations at atmospheric pressures. The results presented in this thesis should help researchers to predict the fate and environmental impacts of organic particulates with which nitrate radicals interact. / Ph. D.

Current methods to reduce the native microbiota and potential pathogens on spices include steam treatments and ethylene oxide (EtO) fumigation. The objectives of this research were to identify the effectiveness of a lab-scale steam apparatus and a commercial EtO process on the inactivation of Salmonella enterica or Enterococcus faecium NRRL B-2354 inoculated whole black peppercorns and cumin seeds. Peppercorns and cumin seeds were inoculated with Salmonella or Enterococcus and processed in a lab-scale steam apparatus at 16.9 PSIA and two references temperatures (165°F and 180°F) and in a commercial ethylene oxide fumigation chamber using a standard commercial EtO fumigation process. Cells were enumerated by serial dilution and plating onto TSA with a thin overlay of selective media. Inoculation preparation influenced inactivation of Salmonella on peppercorns with greater reductions reported for TSA-grown cells compared to within a biofilm. To achieve an assured 5-log reduction of TSA-inoculated Salmonella on peppercorns exposure for 125s and 100s at 165°F and 180°F, respectively is required. For cumin seeds temperatures of 165°F for 110s were needed or 65s at 180°F to assure 5 log reduction. EtO fumigation significantly reduced both microorganisms on both spices (p<0.05), however significant variation existed between bags in the same process run. Reductions of Enterococcus were comparable or less than that of Salmonella under the majority of conditions, however a direct linear relationship cannot be used to compare the microbes. This study demonstrates that the effectiveness of Enterococcus faecium NRRL B-2354 as a surrogate for Salmonella can vary between spices and processes. / Master of Science in Life Sciences

Metal oxide and metal oxide-supported metal nanoparticles can adsorb and decompose chemical warfare agents (CWAs) and their simulants. Nanoparticle activity depends on several factors including chemical composition, particle size, and support, resulting in a vast number of materials with potential applications in CWA decontamination. Current instrumentation in our laboratory used to investigate fundamental gas-surface interactions require extensive time and effort to achieve operating conditions. This thesis describes the design and construction of a high-throughput, high vacuum surface analysis instrument capable of studying interactions between CWA simulants and nanoparticulate surfaces. The new instrument is small, relatively inexpensive, and easy to use, allowing for expeditious investigations of fundamental interactions between gasses and nanoparticulate samples. The instrument maintains the sample under high vacuum (10?⁷-10?⁹ torr) and can reach operating pressures in less than one hour. Thermal control of the sample from 150-800 K enables sample cleaning and thermal desorption experiments. Infrared spectroscopic and mass spectrometric methods are used concurrently to study gas-surface interactions. Temperature programmed desorption is used to estimate binding strength of adsorbed species. Initial studies were conducted to assess the performance of the instrument and to investigate interactions between the CWA simulant dimethyl methylphosphonate (DMMP) and nanoparticulate silicon dioxide. / Master of Science