Yes / This study examines experimentally and for the first time the effect of reduced air pressure on dynamic wetting. The purpose is to assess the role of air viscosity on dynamic wetting failure which hitherto has been speculated on but not measured. In this paper we used dip coating as the model experimental flow and report data on air entrainment velocity Vae we measured with a series of silicone oils in a range of viscosities in a vacuum chamber where the pressure can be reduced from atmospheric down to a few mbar when the mean molecular free path of air is large and air ceases to have a viscosity. To complement earlier work, we carried out the experiments with a range of substrates of varying roughness. The substrates were chosen so that for each one, their two sides differ in roughness. This enables simultaneous comparative observation of their wetting performance and reduces the experimental error in assessing the role of roughness. The data presented here capture the effects of viscosity, roughness and air pressure but the important result of this study is that Vae can be increased considerably (exponentially) when the pressure is reduced with the suggestion that Vae approaches infinity as pressure approaches zero. In other words, the role of the surrounding air viscosity is important in dynamic wetting. The data from this study have significant implication to the fundamental understanding of dynamic wetting. Indeed they form the missing data link to fully understand this phenomenon. The data presented in this work also confirm the complex role of roughness, in that it can increase or decrease the air entrainment speed depending on the value on the viscosity of the coating solution. The results presented in this paper are very useful in practice as they imply that if one chooses carefully roughness one can coat viscous formulation at unexpectedly very high speeds with a moderate vacuum (50 mbar typically).

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

Winds create forces on buildings, sometimes with disastrous results. Low-slope roofs are subjected to potentially high levels of suction pressure, especially when winds strike the corner of a building, creating vortices. Traditional methods of attaching roof membranes to substrates are prone to failure when the low pressure on the roof surface instigates a transfer of forces to the roof membrane. Existing pressure-equalized roof systems use the power of the wind to transmit low pressure to the space immediately beneath the roof membrane, pulling the membrane down to the roof surface. The object of this study is the design of a wind vent which, when coupled with a single-ply roof membrane in a complete roof assembly, will successfully equalize low pressure throughout the entire field of the roof. The proposed wind vent differs from existing equalizer valves in its use of the Bernoulli effect to create low pressure. Optimized for ease of manufacturing and installation, the vent is omni-directional and contains no moving parts. After the wind vent prototype is developed, future study will be required to determine the tributary area of each vent, the interaction with the insulation beneath the membrane, the response time of the system when subjected to dynamic wind loading, the effect on the vent of various weather conditions, and the permissible amount of infiltration into the roof system. Associated research will also investigate the benefits of incorporating the heat evacuating capacity of the pressure-equalizing roof vent system into a roof membrane containing an amorphous photovoltaic array. / Master of Science

Developing a fundamental understanding of the interactions of chemical warfare agents (CWAs) with surfaces is essential for the rational design of new sorbents, sensors, and decontamination strategies. The interactions of chemical warfare agent simulants, molecules which retain many of the same chemical or physical properties of the agent without the toxic effects, with amorphous silica were conducted to investigate how small changes in chemical structure affect the overall chemistry. Experiments investigating the surface chemistry of two classes of CWAs, nerve and blister agents, were performed in ultrahigh vacuum to provide a well-characterized system in the absence of background gases. Transmission infrared spectroscopy and temperature-programmed desorption techniques were used to learn about the adsorption mechanism and to measure the activation energy for desorption for each of the simulant studied. In the organophosphate series, the simulants diisopropyl methylphosphonate (DIMP), dimethyl methylphosphonate (DMMP), trimethyl phosphate (TMP), dimethyl chlorophosphate (DMCP), and methyl dichlorophosphate (MDCP) were all observed to interact with the silica surface through the formation of a hydrogen bond between the phosphoryl oxygen of the simulant and an isolated hydroxyl group on the surface. In the limit of zero coverage, and after defect effects were excluded, the activation energies for desorption were measured to be 57.9 ± 1, 54.5 ± 0.3, 52.4 ± 0.6, 48.4 ± 1, and 43.0 ± 0.8 kJ/mol for DIMP. DMMP, TMP, DMCP, and MDCP respectively. The adsorption strength was linearly correlated to the magnitude of the frequency shift of the ν(SiO-H) mode upon simulant adsorption. The interaction strength was also linearly correlated to the calculated negative charge on the phosphoryl oxygen, which is affected by the combined inductive effects of the simulants’ different substituents. From the structure-function relationship provided by the simulant studies, the CWA, Sarin is predicted to adsorb to isolated hydroxyl groups of the silica surface via the phosphoryl oxygen with a strength of 53 kJ/mol. The interactions of two common mustard simulants, 2-chloroethyl ethyl sulfide (2-CEES) and methyl salicylate (MeS), with amorphous silica were also studied. 2-CEES was observed to adsorb to form two different types of hydrogen bonds with isolated hydroxyl groups, one via the S moiety and another via the Cl moiety. The desorption energy depends strongly on the simulant coverage, suggesting that each 2-CEES adsorbate forms two hydrogen bonds. MeS interacts with the surface via a single hydrogen bond through either its hydroxyl or carbonyl functionality. While the simulant work has allowed us to make predictions agent-surface interactions, actual experiments with the live agents need to be conducted to fully understand this chemistry. To this end, a new surface science instrument specifically designed for agent-surface experiments has been developed, constructed, and tested. The instrument, located at Edgewood Chemical Biological Center, now makes it possible to make direct comparisons between simulants and agents that will aid in choosing which simulants best model live agent chemistry for a given system. These fundamental studies will also contribute to the development of new agent detection and decontamination strategies. / Ph. D.

A swept neutral pressure instrument(SNeuPI) is used to study the effect of gravity waves on the composition of the ionosphere. When mounted on a nanosatellite in the low earth orbit, changes in atmospheric pressure due to gravity waves are measured as the changes in neutral gas density. This measurement is achieved by use of micro-tip emitters as an electron source and micro channel plates(MCPs) as ion collectors. Ionization of the neutral gas produces a current at the output of the MCPs to quantify the pressure of the ionosphere. Traditionally, such measurements are made on larger satellites which enable the use of higher power equipment. This thesis describes the design and use of a low power instrument, to be used on a limited-resource satellite. The background and theoretical analysis is presented first, followed by descriptions of the mechanical and electrical designs. The laboratory tests are limited to a vacuum chamber setup that simulates the conditions of the ionosphere. / Master of Science

Understanding interfacial interactions at the molecular level is important for interpreting and predicting the dynamics and mechanisms of all chemistry processes. A thorough understanding of the interaction dynamics and energy transfer between gas molecules and surfaces is essential for the study of various chemical reactions. The collisions of diatomic molecules on organic surfaces are crucial to the study of atmospheric chemistry. Molecular beam scattering experiments performed in ultra-high vacuum chambers provide insight into the dynamics of gas-surface interactions. Many questions remain to be answered in the study of gas-surface interfacial chemistry. For example, what affects the energy transfer between gas molecules and surfaces? How do intermolecular forces affect the interfacial interaction dynamics? We have approached these questions by scattering diatomic gas molecules from functionalized self-assembled monolayers (SAMs). Our results indicate that the intermolecular forces between gas molecules and surfaces play an important role in the energy transfer processes. Moreover, the stronger the intermolecular forces, the more often the incident molecules come into thermal equilibrium with the surface. Furthermore, most of the previous approaches toward understanding gas-surface interaction dynamics considered the interactions as independent incidents. By scattering O2, N2, CO and NO on both CH3- and OH- terminated SAM, we found a correlation between the gas-surface interactions and a bulk property, solubility. Both being strongly affected by intermolecular forces, the gas-surface energy transfer and solubility of gases in surface-similar solvents (water for OH-SAM, n-hexane for CH3-SAM) have a positive correlation. This correlation facilitates the understanding of interfacial dynamics at the molecular level, and helps predict the outcome of the similar-size gas collisions on surfaces. / Master of Science

A molecular-level understanding of gas-surface energy exchange and reaction mechanisms will aid in the prediction of the environmental fate of pollutants and enable advances toward catalysts for the decomposition of toxic compounds. To this end, molecular beam scattering experiments performed in an ultra-high vacuum environment have provided key insights into the initial collision and outcome of critical interfacial processes on model systems. Results from these surface science experiments show that, upon gas-surface collisions, energy transfer depends, in subtle ways, on both the properties of the gas molecules and surfaces. Specifically, model organic surfaces, comprised of long-chain methyl- and hydroxyl-terminated self-assembled monolayers (SAMs) have been employed to test how an interfacial hydrogen bonding network may affect the ability of a gas-phase compound to thermally accommodate (typically, the first step in a reaction) with the surfaces. Results indeed show that small organic compounds transfer less energy to the interconnected hydroxyl-terminated SAM (OH-SAM) than to the organic surface with methyl groups at the interface. However, the dynamics also appear to depend on the polarizability of the impinging gas-phase molecule. The π electrons in the double bond of ethene (C2H4) and the triple bond in ethyne (C2H2) appear to act as hydrogen bond acceptors when the molecules collide with the OH-SAM. The molecular beam scattering studies have demonstrated that these weak attractive forces facilitate energy transfer. A positive correlation between energy transfer and solubilities for analogous solute-solvent combinations was observed for the CH3-SAM (TD fractions: C2H6 > C2H4 > C2H2), but not for the OH-SAM (TD fractions: C2H6 > C2H2 > C2H4). The extent of energy transfer between ethane, ethene, and ethyne and the CH3-SAM appears to be determined by the degrees of freedom or rigidity of the impinging compound, while gas-surface attractive forces play a more decisive role in controlling the scattering dynamics at the OH-SAM. Beyond fundamental studies of energy transfer, this thesis provides detailed surface-science-based studies of the mechanisms involved in the uptake and decomposition of chemical warfare agent (CWA) simulants on or within metal-organic frameworks (MOFs). The work presented here represents the first such study reported in with traditional surface-science based methods have been applied to the study of MOF chemistry. The mechanism and kinetics of interactions between dimethyl methylphosphonate (DMMP) or dimethyl chlorophosphate (DMCP), key CWA simulants, and Zr6-based metal-organic frameworks (MOFs) have been investigated with in situ infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (PXRD), and DFT calculations. DMMP and DMCP were found to adsorb molecularly (physisorption) to the MOFs through the formation of hydrogen bonds between the phosphoryl oxygen and the free hydroxyl groups associated with Zr6 nodes or dangling -COH groups on the surface of crystallites. Unlike UiO-66, the infrared spectra for UiO-67 and MOF-808, recorded during DMMP exposure, suggest that uptake occurs through both physisorption and chemisorption. The XPS spectra of MOF-808 zirconium 3d electrons reveal a charge redistribution following exposure to DMMP. Besides, the analysis of the phosphorus 2p electrons following exposure and thermal annealing to 600 K indicates that two types of stable phosphorus-containing species exist within the MOF. DFT calculations (performed by Professor Troya at Virginia Tech), were used to guide the IR band assignments and to help interpret the XPS features, suggest that uptake is driven by nucleophilic addition of a surface OH group to DMMP with subsequent elimination of a methoxy substituent to form strongly bound methyl methylphosphonic acid (MMPA). With similar IR features of MOF-808 upon DMCP exposure, the reaction pathway of DMCP in Zr6-MOFs may be similar to that for DMMP, but with the final product being methyl chlorophosphonic acid (elimination of the chlorine) or MMPA (elimination of a methoxy group). The rates of product formation upon DMMP exposure of the MOFs suggest that there are two distinct uptake processes. The rate constants for these processes were found to differ by approximately an order of magnitude. However, the rates of molecular uptake were found to be nearly identical to the rates of reaction, which strongly suggests that the reaction rates are diffusion limited. Overall, and perhaps most importantly, this research has demonstrated that the final products inhibit further reactions within the MOFs. The strongly bound products could not be thermally driven from the MOFs prior to the decomposition of the MOFs themselves. Therefore, new materials are needed before the ultimate goal of creating a catalyst for the air-based destruction of traditional chemical nerve agents is realized. / Doctor of Philosophy / A molecular-level understanding of gas-surface energy exchange and reaction mechanisms will aid in the prediction of the environmental fate of pollutants and enable advances toward catalysts for the decomposition of toxic compounds. Our gas-surface scattering experiments performed in an ultra-high vacuum environment have provided key insights into the outcome of critical interfacial processes on model systems. Results show that energy transfer upon gas-surface collisions depends on both the properties of the gas molecules and surfaces. Due to the formation of interfacial hydrogen bonding network in hydroxyl-terminated surface, the small organic compounds transfer less energy to it than to the organic surface with methyl groups at the interface. The dynamics also appear to depend on the properties of the impinging gas-phase molecule. The π electrons in the double bond of ethene and the triple bond in ethyne act as hydrogen bond acceptors when the molecules collide with the hydroxyl-terminated surface. The attractive forces facilitate energy transfer. A positive correlation between energy transfer and solubilities for analogous solute-solvent combinations was observed for the methyl-terminated surface, but not for the hydroxyl-terminated surface. The extent of energy transfer between ethane, ethene, and ethyne and the methyl-terminated surface appears to be determined by the degrees of freedom or rigidity of the gas, while gas-surface attractive forces play a more decisive role in controlling the scattering dynamics at the hydroxyl-terminated surface. Furthermore, this thesis provides detailed surface-science-based studies of the mechanisms involved in the uptake and decomposition of chemical warfare agent (CWA) simulants on or within metal-organic frameworks (MOFs). Dimethyl methylphosphonate (DMMP) and dimethyl chlorophosphate (DMCP), key CWA simulants, physisorbed to the MOFs through the formation of hydrogen bonds between the phosphoryl oxygen and the free hydroxyl groups associated with inorganic nodes or dangling -COH groups on the surface of crystallites. The infrared spectra for UiO-67 and MOF-808 suggest that uptake occurs through both physisorption and chemisorption. The XPS spectra of MOF-808 zirconium 3d electrons reveal a charge redistribution following exposure to DMMP. Besides, the analysis of the phosphorus 2p electrons following exposure and thermal annealing to 600 K indicates that two types of stable phosphorus-containing species exist within the MOF. DFT calculations suggest that uptake is driven by nucleophilic addition of a surface OH group to DMMP with subsequent elimination of a methoxy substituent to form strongly bound methyl methylphosphonic acid (MMPA). With similar IR features of MOF-808 upon DMCP exposure, the reaction pathway of DMCP in MOFs may be similar to that for DMMP, but with the final product being methyl chlorophosphonic acid (elimination of the chlorine) or MMPA (elimination of a methoxy group). The rates of product formation suggest that there are two distinct uptake processes. The rate constants for these processes were found to be nearly identical to the rates of physisorption, which suggests that the reaction rates are diffusion limited. Overall, this research has demonstrated that the final products inhibit further reactions within the MOFs. The strongly bound products could not be thermally driven from the MOFs prior to the decomposition of the MOFs themselves. Therefore, new materials are needed before the ultimate goal of creating a catalyst for the air-based destruction of traditional chemical nerve agents is realized.

<p dir="ltr">Following the development of laser technology in the 1960s, radiation pressure was soon employed to manipulate particles by Arthur Ashkin in the 1970s. Since then, levitated optomechanics has been widely studied across physics, engineering, chemistry, and biology. In this dissertation, we first experimentally demonstrate GHz rotation and sensing with an optically levitated nanodumbbell near a surface. Then, we propose achieving optical refrigeration below liquid nitrogen temperature using near-field Purcell enhancement.</p><p dir="ltr">The first part of this dissertation focuses on fast rotation and sensing with a non-spherical silica nanoparticle levitated near a surface. Specifically, we optically levitate a nanodumbbell at 430 nm away from a surface in high vacuum and drive it to rotate at 1.6 GHz. This corresponds to a relative linear velocity of 1.4 km/s between the tip of the nanodumbbell and the surface at sub-micrometer separation. The near-surface rotating nanodumbbell demonstrates a superior torque sensitivity of (5.0 +/- 1.1 ) x 10^-26 Nm at room temperature. Our numerical simulation shows that such an ultra-sensitive nanodumbbell levitated near nanostructures can be used to detect fundamental physics, such as Casimir torque and non-Newtonian gravity. </p><p dir="ltr">In the latter part of this dissertation, we propose that optical refrigeration of solid with anti-Stokes fluorescence can be enhanced by Purcell effect. The spontaneous emission rate of high-energy photons is Purcell enhanced by coupling with a near-field cavity. The enhanced emission shifts the mean emission wavelength and enables optical refrigeration with high-absorption cooling laser. We estimate a minimum achievable temperature of 38 K with a Yb³⁺:YLiF₄ nanocrystal near a cavity using our proposed Purcell enhanced optical refrigeration method. This method can be applied to other rare-earth ion doped materials and enable applications that require solid-state cooling below liquid nitrogen temperature.</p>