QC 20101203

High entropy alloys (HEAs) or complex concentrated alloys (CCAs) represent a new paradigm in structural alloy design. Molten salt corrosion behavior was studied for single-phase HEAs such as TaTiVWZr and HfTaTiVZr, and multi-phase HEAs such as AlCoCrFeNi2.1. De-alloying with porosity formation along the exposed surface and fluxing of unstable oxides were found to be primary corrosion mechanisms. Potentiodynamic polarization study was combined with systematic mass–loss study for TaTiVWZr, HfTaTiVZr, and AlCoCrFeNi2.1 as a function of temperature. Electrochemical impedance spectroscopy (EIS) was used for monitoring the corrosion of TaTiVWZr and HfTaTiVZr in molten fluoride salt at 650 oC. TaTiVWZr and AlCoCrFeNi2.1 showed low corrosion rate in the range of 5.5-7.5 mm/year and low mass-loss in the range of 35-40 mg/cm2 in molten chloride salt at 650 oC. Both TaTiVWZr and HfTaTiVZr showed similar mass loss in the range of 31-33 mg/cm2, which was slightly higher than IN 718 (~ 28 mg/cm2) in molten fluoride salt at 650 oC. Ta-W rich dendrite region in TaTiVWZr showed higher corrosion resistance against dissolution of alloying elements in the molten salt environment. AlCoCrFeNi2.1 showed higher resistance to galvanic corrosion compared to Duplex steel 2205 in molten chloride salt environment. These results suggest the potential use of HEAs/CCAs as structural materials in the molten salt environment for concentrating solar power and nuclear reactor systems.

In the near future, Gen II, III, and IV nuclear reactors will be in operation. UO2 is a common fuel for reactors in each of these generations and molten salts are used as coolant/fuel in Gen IV molten salt reactors. This thesis investigates potential ways to measure thermal conductivity for these materials: Raman thermometry for UO2 and a needle probe for molten salts. Four Raman thermometry techniques are investigated in this thesis: The Two Laser Raman (TLR), Time Differential Domain Raman (TDDR), Frequency Resolved Raman (FRR), and Frequency Domain Raman (FDR). The TLR is a steady state method used with a thin film. The TDDR and FRR are both time domain methods used with thin cantilever samples. The FDR is a frequency domain method used with a thermally thick sample. Monte Carlo like simulations are performed for each technique. In the simulations, the affect introduced uncertainty has on the measurement of thermal conductivity and thermal diffusivity is measured. From the results, it is recommended that the TLR should be used for measuring thermal conductivity and the FRR used for measuring thermal diffusivity. The TDDR and FDR were heavily affected by the uncertainty which resulted in inconsistent measured thermal properties. For measuring the thermal conductivity of molten salt, a needle probe was designed and manufactured to withstand the corrosive environment found in using molten salts. The probe uses modulated joule heating and measures the temperature rise in a thermocouple. The phase delay and temperature amplitude of the thermocouple are used in determining the thermal conductivity. A new thermal quadrupole based analytical solution, which takes into consideration convection and radiation, to the temperature rise of the probe is presented. The analytical solution is verified using a numerical solution found using COMSOL. Preliminary data was obtained with the probe in water.

Colicin A is a water-soluble toxin that forms a voltage-gated channel in the cytoplasmic membrane of target bacteria. In the present thesis, we aimed at studying the closed channel state, the membrane insertion mechanism, the acidic pH induced molten globule state and the interaction of colicin A in living E. coli cells. For that, we used Electron Paramagnetic Resonance (EPR) spectroscopy in combination with site-directed spin labeling (SDSL) method to explore the structural details of colicin A. The EPR studies of the membrane-bound colicin A (reconstituted into proteoliposomes) suggest the transmembrane orientation of the hydrophobic hairpin in the closed channel state. The pH dependent membrane insertion studies indicate that the membrane binding efficiency is significantly enhanced at pH < 3. Moreover, in the presence of a membrane potential, the pH induced membrane-bound state is able to open channels in the liposomes. The membrane-bound conformation (induced by acidic pH) is similar to the conformation of reconstituted colicin A which support the umbrella model for the closed channel state of colicin A. The studies on pH dependent conformational changes suggest that colicin A forms a molten globule at pH 2. The molecular details of pH induced conformational changes were analyzed by molecular dynamic simulations. The results of the MD simulations agree with the EPR results. Conformational changes of colicin A upon interaction with living E. coli cells could also be followed. Comparison between colicin A in wild type (WT) cells and tolB knock-out mutants suggest that the observed conformational changes originate from colicin A which has been already translocated to the inner membrane.

京都大学 / 0048 / 新制・課程博士 / 博士(エネルギー科学) / 甲第21192号 / エネ博第366号 / 新制||エネ||72(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻 / (主査)教授 野平 俊之, 教授 萩原 理加, 教授 佐川 尚 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DFAM

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CLIC1 is an intracellular membrane protein that is unusual in that it can exist in both a soluble and an integral membrane form. The manner in which this protein inserts into membranes is unknown although it is proposed to undergo a change in structure whereby it initially experiences a degree of unfolding and then refolds into its new membrane-bound conformation. This study focuses on the characterisation of CLIC1 in terms of its secondary, tertiary and quaternary structure, the determination of its conformational stability at equilibrium and the establishment of its unfolding kinetics, all under conditions of varying pH, polarity, redox conditions, temperature and ionic strength. CLIC1 was found to be most stable at pH 7.0 / 20oC. The unfolding process is two-state and cooperative, producing a DG(H2O) of ~10 kcal/mol and a m-value of ~2 kcal/mol per molar urea. A decrease in pH to 5.5 or an increase in temperature to 37oC resulted in the stabilisation of an equilibrium intermediate species under mild denaturing conditions and a destabilisation of the native state. This was further evidenced by an increase in the rate of unfolding of CLIC1 from the native state to the denatured state under these conditions. A state with similar properties to the intermediate species was detected in the absence of urea at pH 5.5 / 37oC and under non-reducing conditions at both pH 7.0 / 20oC and pH 5.5 / 20oC. The intermediate species is more hydrophobic than either the native or denatured state; it is stabilised by salts, has a reduced secondary structure, increased flexibility and a buried Trp35 relative to the native state. The rate of formation of the intermediate species is a slow process which may involve an oligomerisation step. The results from this study provide an interpretation for the structure and mechanism of CLIC1 pore formation in vivo by comparing the effects of the environment on the structure and stability of the protein.

Supercapacitor is the best potential candidate of the energy storage system due to the superior charge or discharge efficiency, high power density (>10 kW kg-1), and long cycling life. Porous carbon materials as the promising electrode material have been widely used in supercapacitor. In fact, conventional porous carbon supercapacitor electrodes cannot fulfil the growing demand of high energy and power densities of supercapacitor. A large number of studies show that nitrogen doping can change the surface electronic structure of carbon materials, thus significantly improving the electrochemical properties. In addition to, the pore structure and morphology of carbon materials have great influence on the electrochemical performance. In this work, we firstly fabricated nitrogen-doped porous carbon nanotubes by using a simple mixed salts (NaCl/ZnCl2) activation strategy. The as-obtained porous carbon nanotubes exhibited excellent electrochemical performance in supercapacitor. Furthermore, two- dimension nitrogen-doping porous nanosheets were prepared by a salt template-assisted monomer deposition method. In this study, by optimizing the synthesis conditions, the as-obtained carbon nanosheets showed a high specific capacitance of 277 F g-1 at 1 A g-1 and excellent cycle stability retained 91 % after 10,000 cycles. / College of Engineering, Science and Technology / M. Tech.( Civil and Chemical Engineering

Molten salt reactors (MSRs) using chloride-based salt-matrixes as coolants or fuels are a promising option for advanced nuclear reactors, but the extreme temperatures and corrosivity of molten salts pose a challenge for implementation. Molten MgCl2-NaCl-KCl is a viable candidate for MSRs that is considered in this work. Thermochemical properties are derived from electrochemical tests that aid in characterizing the properties of salts. To study these properties, some work has proposed using a three-electrode system with a reference electrode housed in a ceramic membrane. This research aims to develop a stable high-temperature reference electrode using a ceramic membrane that is then applied to develop an on-line monitoring system of Ni-Cr alloy corrosion in chloride salt. A mullite tube used as the membrane of a Ni(II)/Ni reference electrode in molten MgCl2-NaCl-KCl is studied. The performance of two different membrane thicknesses (1.325mm and 0.255mm) was studied in temperature ranges from 635oC to 835oC and data collected on the calculated formal potential of the Ni(II)/Ni system. Tests indicated that the results were stable and repeatable, and the formal potential for both systems differed from the previous experimental data by 0.12V at most, indicating that the system can be applied as an effective reference electrode. Using the reference electrode, on-line monitoring the corrosion of Ni-15wt.%Cr, Ni-20wt.%Cr, and Ni-30wt.%Cr was studied for 120 hours in MgCl2-NaCl-KCl. The on-line measurements showed the concentration changes of dissolved Cr and Ni by corrosion in the bulk molten salt. This work confirms that Ni(II)/Ni reference electrodes with a mullite tube membrane are stable and effective in molten chloride salt systems, particularly MgCl2-NaCl-KCl. The mullite membrane prepared by the manufacturer may be used directly for electrochemical applications without polishing, simplifying the reference electrode manufacturing process, and making it easier to replicate. The use of a Ni(II)/Ni reference electrode provides an avenue to study a different range of salt systems than previous reference electrodes allowed, particularly alloys in chloride salts at high temperatures. This work also confirms that the mullite tube may be used to perform on-line analysis of alloy corrosion in high temperature molten chloride salts. The study of Ni-Cr alloys in chloride salts better prepares the nuclear industry to select coolant salts and alloy containers with the best set of thermochemical and corrosion resistant characteristics for MSRs. / Master of Science / The United States receives approximately 18% of its energy from nuclear technology. Many of the reactors supplying this energy are at the end of their lifecycle and the decommissioning of some of these plants has already begun. In order to replace this older generation of nuclear reactors, a safer and cheaper option has been suggested: Molten Salt Reactors. Molten salt reactors (MSRs) using high temperature salts as a fuel or coolant are a promising option, but the extreme conditions of molten salts pose a challenge for construction and use of MSRs. Molten MgCl2-NaCl-KCl is a salt being considered for MSR application, and is considered in this work. Properties of the salts considered for MSRs are being studied diligently before implementation of these reactors. Electrochemical tests are used to study and monitor these properties. These electrochemical tests use a three-electrode system with a reference electrode housed in a membrane. In this work, a mullite tube is used as a ceramic membrane for a reference electrode in molten MgCl2-NaCl-KCl. The performance of two different membrane thicknesses (1.325mm and 0.255mm) was studied in temperature ranges from 635oC to 835oC. Results indicate that the system is an effective reference electrode. Using this innovative reference electrode, a method of monitoring on-line corrosion of Ni-15wt.%Cr, Ni-20wt.%Cr, and Ni-30wt.%Cr alloys was studied for 120-hour time periods during exposure to MgCl2-NaCl-KCl. This work confirms that reference electrodes with a mullite membrane may be used for electrochemical applications when studying molten chloride salts. The use of a Ni(II)/Ni reference electrode with a mullite membrane provides an avenue to study a different range of salt systems than previous reference electrodes and ceramics allowed, particularly chloride salts. Additionally, this mullite membrane Ni(II)/Ni reference electrode system may be used for monitoring on-line corrosion of Ni-Cr alloys in chloride salt systems.

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