京都大学 / 新制・課程博士 / 博士(工学) / 甲第24297号 / 工博第5070号 / 新制||工||1791(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 陰山 洋, 教授 安部 武志, 教授 阿部 竜 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

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Since strain changes the interatomic spacing of matter and alters electron and phonon dispersion, an applied strain ϵ can modify the thermal conductivity κ of a material. This thesis shows how the strain induced by heteroepitaxy is a passive mechanism to change κ in a thin film and how the film thickness is key to the functional form of κ(ϵ). Molecular Dynamics simulations of the physical vapor deposition and epitaxial growth of ZnTe thin films provide insights into the role of interfacial strain on the thermal conductivity of a deposited film. ZnTe films grown on a lattice mismatched CdTe substrate exhibit ~6% in-plane biaxial tension and ~7% out-of-plane uniaxial compression. In the T=700 K to 1100 K temperature range, the conductivities of strained ZnTe layers that are 5 unit cells thick decrease by ~ 35%, a result that is relevant to thermoelectric devices since strain can also enhance charge mobility and increase their overall efficiency. The resulting understanding of dκ/dT shows that strain engineering can also be used to create a thermal rectifier in a material that is partly strained and partly relaxed, like at the junction of an axial nanowire heterostructure. To better isolate the role of strain, the study is extended to free-standing ZnTe films with thicknesses between 116 Å to 1149 Å under the application of both uniform and biaxial strain between -3% to 3% at 300 K. Since the boundaries of the film are diffuse, κ becomes size dependent when the film thickness approaches the order of the mean free path of the phonons. As this thickness is decreased, the magnitude of κ decreases until boundary scattering dominates so that κ(ϵ) depends on v_g (ϵ). This conclusion is important as it can be generalized to other materials and potential functions; it suggests that if a film is thin enough for boundary scattering to dominate, then the behavior of κ(ϵ) can be predicted based on the bulk dispersion curve alone, which should greatly simplify strain-based device design. / Thesis / Doctor of Philosophy (PhD) / Since strain changes the interatomic spacing of matter and alters electron and phonon dispersion, an applied strain ϵ can modify the thermal conductivity κ of a material. This thesis shows how the strain induced by heteroepitaxy is a passive mechanism to change κ in a thin film and how the film thickness is key to the functional form of κ(ϵ). Molecular Dynamics simulations of the physical vapor deposition and epitaxial growth of ZnTe thin films provide insights into the role of interfacial strain on the thermal conductivity of a deposited film. The result is relevant to thermoelectric devices since strain can also enhance charge mobility and increase their overall efficiency. The resulting understanding of dκ/dT shows that strain engineering can also be used to create a thermal rectifier in a material that is partly strained and partly relaxed, like at the junction of an axial nanowire heterostructure.

Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Earth and Planetary Science, 1981. / MICROFICHE COPY AVAILABLE IN ARCHIVES AND LINDGREN. / Bibliography: leaves 99-110. / by David Samuel Goldberg. / M.S.

The thermal conductivities of polystyrene in benzene solutions at concentrations of 0.l to 15 weight percent were measured at 25° C and atmospheric pressure. Osmotic pressure measurements and information supplied by the manufacturer indicated number average molecular weights (M̅_N) of 21,000, 264,000, and 660,000 for the three polystyrene polymers studied. The following equation was obtained by regression analysis of the results and predicts the measured thermal conductivity within ± 2 percent in the range of variables studied. K = 0.1088 - 0.1311 C + 0.57629 C² - 6.40 x 10⁻⁵ (M̅_N x 10⁻⁵)² - 4.2 x 10⁻³ C(M̅_N x 10⁻⁵) where: K = thermal conductivity of solution, Btu/hr-ft-°F C = weight fraction polymer M̅_N = number average molecular weight The conductivities were measured in a steady-state concentric cylinder apparatus developed for measuring the thermal conductivity of viscous liquids. The annular gap was 0.052 inches and guard heaters were employed to minimize end losses and distortion of the steady-state temperature distribution at the ends. The apparatus was calibrated with three liquids of known thermal conductivity, water, cyclohexanol and ethylene glycol. The calibration factor was found to be constant to within experimental error (± 3 percent) over the range of measurements. / Master of Science

Despite decades of research and thousands of studies on cardiac electrophysiology, cardiovascular disease remains among the leading causes of death in the United States today. Despite substantially beneficial advances, we have largely shifted cardiovascular disease from an acute to a chronic issue. It is therefore clear that our current understanding of the heart's functions remain inadequate and we must search for untapped therapeutic approaches to eliminate these deadly and costly ailments once and for all. This thesis will focus on the electrophysiology of the heart, specifically the mechanisms of cell-to-cell conduction. Canonically, the understood mechanism of cardiac conduction is through gap junctions (GJ) following a cable-like conduction model. While both experimentally and mathematically, this understanding of conduction has explained cardiac electrical behavior, it is also incomplete, as evidenced by recent conflicting modeling and experimental data. The overall goal of this thesis is to explore a structure modulating an ephaptic, or electric field, cellular coupling mechanism: the GJ-adjacent perinexus, with three specific aims. First, I identified the perinexus – a recently-established structure in rodent myocardium – in human atrial tissue. I also observed a significant tendency for open-heart surgery patients with pre-operative atrial fibrillation to have wider perinexi, indicating a possibly targetable mechanism of atrial fibrillation, one of the costliest, and most poorly-understood cardiac diseases. Next, I developed a high-throughput, high-resolution method for quantifying the perinexus. Finally, I sought to reconcile a major controversy in the field: whether cardiac edema could either be beneficial or harmful to cardiac conduction. Using a Langendorff perfusion model, I added osmotic agents of various sizes to guinea pig hearts and measured electrical and structural parameters. My findings suggest that while cardiac conduction is multifaceted and influenced by several parameters, the strongest correlation is an inverse relationship between conduction velocity and the width of the perinexus. This study is the first to osmotically expand and narrow the perinexus and show an inverse correlation with conduction. Importantly, my conduction data cannot be explained by factors consistent with a cable-like conduction mechanism, indicating once again that the perinexus could be a therapeutic target for a myriad of cardiac conduction diseases. / Doctor of Philosophy / The ways by which cells in the heart communicate have been studied extensively and are thought to be well-understood. However, despite decades of research, cardiovascular disease is a major problem in the developed world today and we remain unable to develop treatments to truly cure many major cardiac diseases. Because of this lack of clinical success in preventing or treating conditions such as atrial fibrillation, Brugada syndrome and sudden cardiac death, all of which are associated with disruptions in the heart’s electrical communication systems, I have sought to better understand the ways by which cellular communication is achieved. Currently, we think of cardiac tissue to propagate electrical signals as if it was a series of cables, just like the electrical wires over our streets and in our homes. However, we have seen experimental evidence, along with computer simulations, that supports the idea of a second mechanism of cellular electrical conduction. This second mechanism is called ephaptic, or electric field, coupling and relies on changes in charges inside and outside the cell to trigger the action potential – the electrical signal which tells the cell to contract. In order for ephaptic coupling to occur, two main conditions must be met. First, there must be a suitably-sized cleft, or ephapse, between adjacent cells. Models have estimated this space to be between 10-100 nm wide. Second, there must be a large concentration of sodium channels, as sodium ions are primarily used to set off the action potential. The region in which I am most interested is the cardiac perinexus, which is the space immediately adjacent to plaques of connexin proteins which link adjacent cells. The perinexus is both of an appropriate size (we’ve measured it between 10 and 25 nm on average) and rich in sodium channels, making it an ideal candidate to be a cardiac ephapse. In recent years, our lab has shown experimentally that expanding this space can disrupt cardiac conduction and my first study showed that clinically, patients with chronic atrial fibrillation (a-fib) prior to open-heart surgery have wider perinexi than patients without chronic a-fib. No one, however, has been able to demonstrate that narrowing the perinexus would be therapeutic by making it easier for cells to communicate via this ephaptic mechanism. Knowing I would need a better method for measuring the width of huge numbers of perinexi, I then developed a faster, more precise measurement program. Finally, I perfused several osmotic agents – substances which would theoretically draw fluid into or out of various compartments of cardiac tissue – into guinea pig hearts and observed changes to both their electrical behavior and tissue structure. Using my new perinexal measurement program, I found that changing the perinexus was the only factor that could explain the conduction changes I observed with each osmotic agent and that parameters associated with cable theory, such as gap junctional protein expression or interstitial resistance, could not explain conduction changes. Therefore, I have indicated, along with my clinical study, that the cardiac perinexus could be a therapeutic target for preventing, managing, or possibly even curing cardiac conduction diseases.

The ultimate capacity of offshore platform conductor strings is studied. The unique way in which conductors are loaded is described and the various design methods that exist are presented. Previous research in the field of tubular member behavior is also reviewed. The results of seven experimental tests are evaluated and compared with the existing conductor design criteria. The test matrix calls for various amounts of lateral loading to be imposed on the conductor system. Axial load, applied to simulate the weight of inner casings, is then applied until failure. Results indicate that internally applied axial loads do not induce stability related failure in the outer conductor. Additionally, the design internal moment, which is based on an inner casing being as eccentric as possible, accurately represents the upper limit for the bending moment observed in the experimental tests. The flexural stiffness of the inner casing serves to strengthen the conductor system. Therefore, a design method that considers the strength of the outer conductor and the inner casings is recommended. / Master of Science

There is scarce information on the fate of cardiac progenitor cells (CPC) in the embryonic heart after chamber specification. Furthermore, the role of acetylcholinesterase (AChE) during heart development is unknown, despite record of its presence in the myocardium. Although three molecular variants of AChE (R, H and T) exist due to alternate splicing, temporal and spatial distribution of these splice variants during cardiac ontogeny is not well characterized. We hypothesized that the AChE “R” splice variant (AChE-R) is involved in directing lineage commitment of mouse ventricular CPCs to the conduction cell phenotype. It is possible that AChE may promote the breakdown of ACh and block the effects of ligand-binding via M2 receptors present on the surface of CPCs. Our study has also provided a platform to suggest that AChE may play a role in the molecular mechanisms underlying functional diversification of myocardial cells into conduction system cells during ontogenesis.

Ce travail de thèse présente les résultats obtenus lors de l'étude des mécanismes élémentaires à l'origine de la forte conduction protonique mesurée dans le cas de clathrates hydrates d'acides forts. Une méthodologie combinant diffusion neutronique, résonance magnétique nucléaire et simulation de dynamique moléculaire "ab-initio" a permis de modéliser les différents processus dynamiques impliqués, se produisant sur des temps allant de la nanoseconde à la femtoseconde. Le modèle proposé explique la forte conduction de ces systèmes aqueux par la délocalisation à longue distance de leurs protons résultant d'un mécanisme de type Grotthuss gouverné par la relaxation des molécules aqueuses environnant les protons en excès. / This work shows the results obtain about the study of elementary mechanisms behind the high protonic conduction of strong acids clathrate hydrate. A method using quasiélastic neutron scattering and pulse field gradient NMR experiments both with DFT molecular dynamic simulations allowed to establish a model which describe the several dynamical processes involve occuring on timescales from nanosecond to femtosecond. The model deduced explain the high conduction property of ionic clathrate hydrate by a delocalization of their protons following a grotthuss type mecanism managed by the relaxation of water molecules around the excess protons.