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This study deals with fibre suspension flows through cylindrical pipes. Thepresent work aims at measurements of opaque flows, which are common inindustries. Nuclear magnetic resonance imaging (NMRI) and ultrasound velocimetryprofiling (UVP) were employed as non-invasive and optic-independenttools to measure the velocity profiles. As a first experiment, a paper-pulp suspensionflow through a sudden contraction and expansion was investigated.The results show the NMRI technique can be used to measure the stronglyunsteady flow such as separated regions though the MR signal is attenuateddue to the turbulence in the flow. The flow loop had however an insufficientinlet length which caused asymmetric profiles at the test section. As a secondexperiment, a flow loop which provided fully developed flows at the test sectionwas designed. After that, the velocity profiles of rayon-fibre and micro-spheresuspension flows were measured by the NMRI and the UVP independently.In principle, these two techniques measure the different velocities of the fibresuspensionflows, i.e. the velocity of the water and the fibre. In dilute suspensionflows, where the velocities of the two phases were assumed to be thesame, the velocity profiles were in good agreement. This shows the validityof the two measurement techniques. However, it should be pointed out thatthere is a limitation of the current UVP method for highly concentrated flows.The velocity profiles obtained by the UVP at high concentrations seems notto represent physics while the NMRI is not affected by the concentrations. Itis argued that the advances of the NMRI for the measurement of the highlyconcentrated flows.

This thesis concerns the use of advanced solid-state NMR methods to investigate local structural features and ion dynamics in a series of paramagnetic cathode materials for lithium and sodium ion batteries. A variety of polyanionic phosphate and fluorophosphate derivatives were explored to identify characteristics that ultimately improve battery performance. Solid-state NMR is an excellent method to probe such materials, as it offers the unique ability to track the charge-carrying alkali ion (Li or Na) over the course of the electrochemical process, adding insight not obtainable by bulk characterization techniques. Selective inversion exchange experiments were used to elucidate ion diffusion pathways in low-mobility Li ion conductors Li2MnP2O7 and Li2SnO3. Contrasting experimental results highlight significant differences observed when the method is applied to paramagnetic versus diamagnetic systems, with the former being much more complicated to study with traditional exchange spectroscopy methods. Selective inversion was similarly applied to a new lithium iron vanadate framework, LiFeV2O7, where the changing ion dynamics as a function of electrochemical state of charge were quantified, allowing for the development of a model to explain the corresponding phase changes in the material. This represents the first example of an ex situ Li-Li exchange study for a cathode material, particularly where the conductivity changes are linked directly to a change of ion exchange rates. Additionally, 23Na NMR spectroscopy was additionally used to investigate Na2FePO4F as a potential Na ion battery cathode, where ex situ NMR measurements successfully determined the local Na ion distribution in the electrode as a function of electrochemical cycling. In combination with density functional theory (DFT) calculations, the NMR results lead to the construction of a biphasic desodiation model for Na2FePO4F cathodes. Finally, possible defect formation in sodium iron fluorophosphate was investigated with a variety of methods including 23Na NMR, DFT calculations, powder X-ray diffraction and Mössbauer spectroscopy. / Thesis / Doctor of Philosophy (PhD) / Lithium ion batteries are considered to be at the forefront of current energy storage development, offering high energy density in a small and lightweight package. This thesis delineates the investigation of materials for both lithium and sodium ion batteries via nuclear magnetic resonance methods. Slow Li ion dynamics were investigated and quantified in three lithium-conducting materials: Li2MnP2O7, Li2SnO3, and LiFeV2O7 via the use of selective inversion NMR experiments. In the case of the latter, the ion dynamics were probed ex situ during the course of battery cycling, where a maximum in Li mobility is observed approximately half way through the charge-discharge cycle. Additionally, a potential Na ion cathode material, Na2FePO4F, was found by ex situ methods to reveal a biphasic mechanism for the desodiation of the electrode during charging. This mechanism and the NMR data used to discover it were further supported by ab initio calculations.

Protein misfolding and the accumulation of insoluble aggregates is a hallmark of several neurodegenerative disorders, including Alzheimer’s (AD) and Parkinson’s disease (PD). In AD and PD patients, extracellular protein deposits consisting of amyloid beta (Aβ) and intraneuronal inclusions composed of alpha synuclein (αS) are observed, respectively. Notably, the spatiotemporal patterning of soluble protein oligomers of αS and Aβ closely follow disease progression, giving support to an emerging role of soluble oligomers in PD and AD pathogenesis. However, the structural features underlying the toxicity of Aβ and αS oligomers remain elusive. This doctoral dissertation aims at elucidating the structural determinants of oligomer toxicity by focusing on the development and application of multidisciplinary approaches based primarily on solution NMR in combination with electron microscopy, multi-angle light scattering, fluorescence microscopy, wide-angle x-ray diffraction and cellular biophysics. Using this interdisciplinary approach, in chapters 2 and 3, we identify at atomic resolution the key structural elements that facilitate the colocalization, interaction and subsequent insertion of soluble Aβ oligomers into membranes, which ultimately result in the loss of membrane integrity. Notably, we show that small molecules, such as green tea catechins, remodel these structural features and effectively perturb the interactions with membranes. In chapter 4, we extend these analyses to αS and identify how the chaperone, Human Serum Albumin (HSA), remodels toxic αS oligomers into non-toxic species and breaks the catalytic cycle that generates new toxic oligomers. Lastly, in chapter 5, we describe a novel solution NMR approach to map at atomic resolution the sites of early self-association, with minimal bias from monomer dynamics, an effect that frequently dominates residue-dependent variations in solution NMR measurements. Overall, given that Aβ and αS are archetypical amyloidogenic proteins, we anticipate that the structure – toxicity relationships established herein, and the related experimental approaches may be transferrable to other amyloidogenic systems. / Dissertation / Doctor of Philosophy (PhD)

A series of studies are presented in which fluorine tagging reagents are used to analyze complex mixtures for compounds containing active hydrogen functional groups (e.g., hydroxyl, amine, thiol, and carboxylic groups). The existence of these derivatized functional groups is determined by utilizing a number of solution and solid-state nuclear magnetic resonance (NMR) techniques. In solution NMR studies p-fluorobenzoyl chloride was the fluorine tagging reagent of choice because of a large ¹⁹F chemical shift range for the different derivatized substrates (~10 ppm) and generally good reaction yields. Various classes of sterol and amino acid p-fluorobenzoyl derivatives were characterized on the basis of their ¹⁹F NMR isotropic chemical shifts. The presence (or absence) of hydroxyl, amine, and carboxylic acid functional groups in coal extract and pyrolysis products was also determined. The versatility of the p-fluorobenzoyl chloride as the fluorine tagging reagent in ¹⁹F NMR was enhanced by: a) enriching the carbonyl carbon of the acid chloride with labeled ¹³C isotope, thus synthesizing a dual ¹⁹F and ¹³C NMR sensitive reagent and b) using the reagent in conjunction with LC-NMR. The extension to either technique added another dimension to the NMR spectral data obtained from the p-fluorobenzoyl tagging reagent in solution NMR. Finally, preliminary data is presented illustrating how fluorine tagging reagents may be used to study functional groups (and atoms present in the immediate proximity of the group) existing on solid material utilizing solid-state NMR. Functional groups on the solid material are tagged with a fluorinated reagent. The sample is then analyzed using solid-state NMR with cross-polarization (CP), magic angle spinning (MAS), and high-power proton decoupling. The ¹⁹F dipolar coupling interactions, created by the presence of the fluorine tag, attenuate signals for these nuclei in the immediate proximity of the tagged site. A series of 1-adamantanol, steroid, and silica gel fluorinated derivatives show that the effects of the ¹⁹F dipolar interactions were modulated by complex anisotropic molecular motions (i.e., solid system with little motion, exhibiting greater signal attenuations due to ¹⁹F dipolar coupling). / Ph. D. / incomplete_metadata

The limitations of previous dynamic nuclear polarization (DNP) experiments have been avoided by a transfer DNP approach whereby the nuclear spins are polarized by DNP at low magnetic field (0.33 T) and then quickly transferred to a high monitoring field (4.7 T). This approach provides an order of magnitude improvement in sensitivity when compared to the usual low field DNP experiment. Also high resolution spectra commonly obtainable at high magnetic fields are now possible for the DNP enhanced signals. Using this method, we have observed large ¹H, ²D, ¹³C, ²⁹Si, and ¹⁵N scalar and dipolar enhancements (2-60 times of signal strength at 4.7 T NMR). Among the results, ¹⁵N and ²⁹Si liquid DNP enhancements are the first to be reported. The selective ¹³C and ¹H DNP enhancements at 0.33 T for different nuclei on the same molecule were observed. A mathematical model describing the low to high magnetic field transfer DNP experiments has also been developed. In ¹³C DNP, we find that the three-spin effect can significantly degrade the dipolar dominated enhancements unless high radical concentrations are used. The scalar dominated ¹³C DNP enhancements can be very large. In addition, the nitroxide radical (TEMPO) used in the present study can induce large scalar enhancements at carbon or nitrogen atoms which have weakly acidic hydrogens. These results indicate DNP can be a very sensitive probe to study weak intermolecular interactions (e.g., hydrogen bonding). / Ph. D.

Investigation and characterization of polymeric materials are necessary to obtain in-depth understanding of their behavior and properties, which can fuel further development. To illuminate these molecular properties and their coupling to macroscopic behavior, we have performed nuclear magnetic resonance (NMR) studies on a variety of chemical systems. In addition to versatile "traditional" NMR measurements, we took advantage of specialized techniques, such as "rheo-NMR," 2H NMR, and NMR self-diffusion experiments to analyze alignment, orientational order, elaborate rheological behavior, and ion transport in polymer films and complex fluids. We employed self-diffusion and quadrupolar deuterium NMR methods to water-swollen channels in Nafion ionomer films commonly used in fuel cells and actuators. We also correlated water uptake and anisotropic diffusion with differing degrees and types of alignment in Nafion films based on membrane processing methods. Further, we made quantitative measurements of bulk channel alignment in Nafion membranes and determined anisotropic properties such as the biaxiality parameter using these methods. Additionally, our studies made the first direct comparison of directional transport (diffusion) with quantitative orientational order measurements for ionomer membranes. These results lend insight to the importance of water content in ionomer device performance, and showed that increased control over the direction and extent of orientational order of the hydrophilic channels could lead to improved materials design. We used the same techniques, with the addition of "rheo-NMR" and solution rheology measurements, to study the complex rheological behavior of cetyltrimethylammonium bromide wormlike micelle solutions, which behave as nematic liquid crystals at sufficiently high concentration. Amphiphilic solutions of this type are used in myriad applications, from fracturing fluids in oil fields to personal care products. We investigated the phase behavior and dynamics of shear and magnetic field alignment, and made the first observations of a novel bistable shear-activated phase in these solutions. Our first reports of the complex Leslie-Ericksen viscoelastic parameters in wormlike micelles and measurements of diffusion anisotropy show the potential for increased control and understanding of materials used in tissue engineering, oil extraction, personal care products, and advanced lubricants. / Ph. D.

In this study the applicability of Carbon-13 NMR and XPS to the detection of chemical changes in a solid composite rocket propellant was studied. Storage at elevated temperatures was used to simulate the propellant ageing process. In the XPS analysis, changes in the sources for the N(1s) and Cl(2p) photopeaks were investigated. The propellant loses "organic" nitrogen as it ages. Changes in the amount of Cl⁻ present are in doubt due to instrumental considerations. Carbon-13 NMR analysis showed that with increasing age of a sample there is a corresponding loss of vinylic groups from the binder. This loss of vinylic character is preferential in the order pendant>>cis>trans. Due to the long scan times involved this method is of limited utility for ageing analysis. / Master of Science

In this thesis, I traced the development of Nuclear Magnetic Resonance (NMR) Spectroscopy through the pages of the Journal of Organic Chemistry (JOC) from the year 1956 to 1969 to understand how organic chemists and Varian Associates?the makers of the first commercial NMR spectrometers?negotiated the identity of the NMR spectrometer. The work of the organic chemists was examined through their publications in the JOC. Examining the abstracts from the JOC between the years 1956 and 1969 developed an understanding of the ways in which organic chemists used the instrument. To understand the role Varian Associates played in the development of NMR, I examined the company?s advertisements in the JOC. I traced the changes in advertising style and format in order to see how Varian Associates expected their instruments to be used. I drew three conclusions from this work: 1) organic chemists and Varian Associates together determined what an NMR spectrometer was and how it could be used; 2) the identity of the instrument was negotiated by these two groups, and the novel use of the instrument by the organic chemists and new schemes in advertising on the part of Varian Associates were attempts to shift this identity; 3) NMR spectroscopy was a domain of knowledge that was embodied in the NMR spectrometer, and that could only be accessed through the instrument. / Master of Science