Background: A negative fluid balance during bed rest (BR) is accompanied by decreased plasma volume (PV) which contributes to cardiovascular deconditioning. Hypothesis: We hypothesized that increasing dietary sodium while controlling fluid intake would increase plasma osmolality (POSM), stimulate fluid conserving hormones, and reduce fluid/electrolyte (F/E) losses during BR; conversely, decreasing dietary sodium would decrease POSM, suppress fluid conserving hormones, and increase F/E losses. Methods: We controlled fluid intake (30 ml · kg-1 · d-1) in 17 men who consumed either a 4.0 ± 0.06 g · d-1 (174 mmol · d-1) (CONT; n = 6), 1.0 ± 0.02 g · d-1 (43 mmol · d-1) (LS; n = 6), or 10.0 ± 0.04 g · d-1 (430 mmol · d-1) (HS; n = 5) sodium diet before, during, and after 21 d of 6° head-down BR. PV, total body water, urine volume and osmolality, POSM, and F/E controlling hormone concentrations were measured. Results: In HS subjects, plasma renin activity (-92%), plasma/urinary aldosterone (-59%; -64%), and PV (-15.0%; 6.0 ml · kg-1; p < 0.05) decreased while plasma atrial natriuretic peptide (+34%) and urine antidiuretic hormone (+24%) increased during BR (p < 0.05) compared with CONT. In LS, plasma renin activity (+166%), plasma aldosterone (+167%), plasma antidiuretic hormone (+19%), and urinary aldosterone (+335%) increased with no change in PV compared with CONT (p < 0.05). Total body water did not change in any of the subjects. Conclusions: Contrary to our hypothesis, increasing dietary sodium while controlling fluid intake during BR resulted in a greater loss of PV compared with the CONT subjects. Reducing dietary sodium while controlling fluid intake did not alter the PV response during BR compared with CONT subjects.

京都大学 / 新制・課程博士 / 博士(人間・環境学) / 甲第23288号 / 人博第1003号 / 新制||人||236(附属図書館) / 2020||人博||1003(吉田南総合図書館) / 京都大学大学院人間・環境学研究科相関環境学専攻 / (主査)教授 内本 喜晴, 教授 高木 紀明, 教授 中村 敏浩 / 学位規則第4条第1項該当 / Doctor of Human and Environmental Studies / Kyoto University / DFAM

Aqueous zinc ion storage system has been deemed as one of the most promising alternatives due to its high capacity of zinc metal anode, low cost, and high safety characteristics. Recently, significant attempts have been made to produce highperformance aqueous Zn batteries. (AZBs) and great progress has been achieved. Yet there are a lot of issues still exist and need to be further optimized. In this thesis, we proposed several strategies to tackle these challenges and finally optimize the overall battery performance, including metal anode protection, cathode structural engineering, and rational electrolyte design. In the present thesis, we first developed the ZnF2 layer coated Zn metal anode via a simple plasma treatment method. The plasma treated Zn anode leads to dendrite-free Zn electrodeposition with lower overpotential. Density function theory calculation results demonstrate that the Zn diffusion energy barrier can be greatly reduced on the ZnF2 surface. Benefiting from these merits, the symmetric cell and full cell exhibited much improved electrolchemical performance and stability. Afterthen, We synthesised a layered Mg2+-intercalated V2O5 as the cathode material for AZBs. The large interlayer spacing reachs up to 13.4 A, allowing for efficient Zn2+ (de)insertion. As a result, the porous Mg0.34V2O5・nH2O cathodes can provide high capacities as well as long-term durability. We then recongnized that most of the parasitic side reactions are related to the aqueous electrolyte. We therefore further designed a hybrid electrolyte to realize the anode-free Zn metal batteries. It is demonstrated that in the presence of propylene carbonate, triflate anions are involved in the Zn2+ solvation sheath structure. The unique solvation structure results in the reduction of anions, thus forming a hydrophobic solid electrolyte interphase. Consequently, in the hybrid electrolyte, both Zn anodes and cathodes show excellent stability and reversibility. More importantly, we design an anode-free Zn metal battery, which exhibits good cycling stability (80% capacity retention after 275 cycles at 0.5 mA cm–2).

京都大学 / 新制・課程博士 / 博士(工学) / 甲第23199号 / 工博第4843号 / 新制||工||1756(附属図書館) / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 邑瀬 邦明, 教授 宇田 哲也, 教授 作花 哲夫 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

No description available.

Techniques of capillary electrophoresis are essential for both the quantitative and qualitative analysis of a large variety of compounds. They find application in many areas of chemistry, from pharmacological industry and food processing, up to highly specialized biotechnological laboratories. Over the last hundred years, their mathematical model has been described with precision. Thus, current research mainly aims for the development of more advanced and more specialized applications. During the greatest boom of affinity capillary electrophoresis within the nineties, many authors would describe similar phenomena under different names. The first part of this work focuses on the consolidation and unification of the problematics and terminology of this method. It also discusses the phenomena which can affect electromigration and separation during electrophoretic processes. We will focus on a specific subset of affinity capillary electrophoresis, partial filling capillary electrophoresis, which, to our knowledge, has not been fully theoretically explored yet, and present a mathematical model allowing the determination of complexation constants and state some limitations of this approach. The second part of this thesis focuses on the development and application of computer softwares, which are meant...

Indiana University-Purdue University Indianapolis (IUPUI) / The geometric and electrochemical characteristics of different lithium ion batteries (LIBs) are investigated in this study. The core work is to study the impact of the calendering process on NMC cathode electrodes performance. X-ray CT image processing by Python, MATLAB, ImageJ and Avizo is utilized in this study. NMC electrodes with different calendering conditions were fabricated to calculate electrochemical properties of the cells. Charge/discharge of the electrodes under 0.1C, 0.2C, 0.4C, 1C, 2C, 4C and 0.1C (retention test) rates were cycled for three times respectively between 4.2 V and 3.0 V. Electrochemical impedance spectroscopy testing was used to further explain the effects of NMC density on rate capability. Geometric properties of NMC electrodes with different calendering conditions were calculated from the computed tomography data of the electrodes. A synchrotron transmission X-ray microscopy tomography system at the Advanced Photon Source of the Argonne National Laboratory was employed to obtain the tomography data. X-ray CT image processing before the data analysis was introduced. Python based Tomopy and ASTRA toolbox were used to filter the original HDF5 data and reconstruction. ImageJ was used to help remove noise, adjust contrast and cropping. Iso2mesh and image processing tool box were used in MATLAB to generate meshed 3D structure of CT data. Geometric properties of NMC electrodes including porosity, pore size distribution, particle size distribution, specific surface area and tortuosity were calculated from the computed tomography data of the electrodes. The geometric and electrochemical analysis show that calendering can increase the electrochemically active area, which lead to improving of the rate capability. However, more calendering will result in crushing of NMC particles, which can reduce the electrode capacity at relatively high C rates. This study shows that the optimum electrochemical performance of NMC electrode at 94:3:3 weight ratio of NMC:binder:carbon black can be achieved by calendering to 3.0 g/cm3 NMC density. LTAP solid electrolyte and NMC cathode material mix electrode-electrolyte X-ray CT data was studied in last chapter. By using 8 kev X-ray energy, we could distinguish NMC active material, LTAP solid electrolyte and the others three phase. On the basis of NMC electrode image processing method, dilation and multiply threshold method is applied to get three-phase 3D geometry. A comparing of connection area between NMC and LTAP of 700psi and 1300psi electrode was analyzed. Geometric properties like tortuosity, di_usion length and e_ective di_usivity were generated from the CT data.

The doctoral theses deal with electrochemical deposition of lead, tin, silicon and germanium from aprotic electrolytes in anhydrous inert atmosphere. Deposited layers are studied from the perspective of their surface and of electrochemical characteristics.

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第17888号 / 工博第3797号 / 新制||工||1581(附属図書館) / 30708 / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 田中 功, 教授 酒井 明, 教授 邑瀬 邦明 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第18278号 / 工博第3870号 / 新制||工||1594(附属図書館) / 31136 / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 田中 功, 教授 邑瀬 邦明, 教授 酒井 明 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM