This study encompasses various aspects of corrosion in chloride molten salt environments, employing electrochemical techniques and a forced convection loop. It explores corrosion thermodynamic properties, electrochemical corrosion kinetics, and flow-induced dynamic corrosion. The study developed a novel electrochemical method for measuring thermodynamic properties of corrosion products and develops a new analysis theory for potentiodynamic polarization data obtained from cathodic diffusion-controlled reactions. Additionally, the design and operation experience of a forced convection chloride molten salt loop is shared. Particularly, the study presents novel findings on the turbulent flow-induced corrosion phenomenon and mechanism of Fe-based alloys in Mg-based chloride molten salt. These outcomes provide valuable insights into the corrosion mechanisms and flow-induced corrosion of Fe-based alloys in chloride molten salt. The results and experiences shared in this paper have implications for the successful implementation of molten salt as an advanced heat transfer fluid and thermal energy storage material in high-temperature applications, benefiting the nuclear and concentrating solar communities. / Doctor of Philosophy / This study explores the corrosion behavior of materials chloride molten salt, which is used in advanced energy systems. By using advanced techniques, the researchers investigated how these materials react and corrode in different conditions. They developed new methods to measure the properties of the corrosion products and analyzed how different factors affect the corrosion process. Additionally, they shared their experiences in building and operating a flow loop to simulate these conditions. The study discovered interesting phenomena, such as how the flow of molten salt can cause corrosion in certain types of metals. These findings provide important insights for improving the use of molten salt as a heat transfer fluid and energy storage material in advanced energy technologies.

Transition-metal chemistry in ionic liquids (IL) has achieved intrinsic fascination in the last few years. The use of an IL as environmental friendly solvent, offers many advantages over traditional materials synthesis methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room-temperature IL have been found to be excellent media for stabilising transition-metal clusters in solution and to crystallise homo- and heteronuclear transition-metal complexes and clusters. Furthermore, the use of IL as solvent provides the option to replace high-temperature routes, such as crystallisation from the melt or gas-phase deposition, by convenient room- or low-temperature syntheses. Inorganic IL composed of alkali metal cations and polynuclear transition-metal cluster anions are also known. Each of these areas will be discussed briefly in this contribution. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.

Transition-metal chemistry in ionic liquids (IL) has achieved intrinsic fascination in the last few years. The use of an IL as environmental friendly solvent, offers many advantages over traditional materials synthesis methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room-temperature IL have been found to be excellent media for stabilising transition-metal clusters in solution and to crystallise homo- and heteronuclear transition-metal complexes and clusters. Furthermore, the use of IL as solvent provides the option to replace high-temperature routes, such as crystallisation from the melt or gas-phase deposition, by convenient room- or low-temperature syntheses. Inorganic IL composed of alkali metal cations and polynuclear transition-metal cluster anions are also known. Each of these areas will be discussed briefly in this contribution. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.