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IUPAC-NIST Solubility Data Series. 100. Rare Earth Metal Fluorides in Water and Aqueous Systems. Part 3. Heavy Lanthanides (Gd–Lu)

This is the third part of the volume devoted to solubility data for the rare earth metal (REM) fluorides in water and in aqueous ternary and multicomponent systems. It covers experimental results of trivalent fluorides of Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu (so-called heavy lanthanides), since no quantitative data on solubilities of TbF{sub 4} and YbF{sub 2} (the most stable compounds at these valencies) are available. The related literature has been covered through the end of 2014. Compilations of all available papers with the solubility data are introduced for each REM fluoride with a corresponding critical evaluation. Every such assessment contains a collection of all solubility results in aqueous solution, a selection of suggested solubility data, a solubility equation, and a brief discussion of the multicomponent systems. Only simple fluorides (no complexes or double salts) are treated as the input substances in this report. General features of the systems, such as nature of the equilibrium solid phases, solubility as a function of temperature, influence of ionic strength, solution pH, mixed solvent medium on the solubility, quality of the solubility results, and the solubility as a function of REM atomic number, have already been presented in Part 1 of the volume.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Interactions between fluoride ions and cement paste containing superplasticizer

Fluoride compounds are used as fluxes in the low-temperature calcination of cement. Elution of fluoride ions after calcination decreases the fluidity of cement paste containing superplasticizers, but the mechanism of fluidity decrease is unclear. Authors investigated the effects of fluoride on cement pastes containing superplasticizers and the fluidity decrease mechanism. KF addition to cement paste containing a polycarboxylate- or naphthalenesulfonate-based superplasticizer increased the yield stress, the amount of adsorbed superplasticizer, and the solid-phase specific surface area. KF addition increased the amount of adsorbed superplasticizer for alite paste but not for Ca{sub 3}Al{sub 2}O{sub 6}-CaSO{sub 4} paste. Transmission electron microscopy found SiO{sub 2} fine particles after KF addition. In the absence of water, the increase in specific surface area with fluoride was larger in hydrated than in unhydrated cement. It is supposed that the fluidity decrease results from the preferential adsorption of superplasticizer on SiO{sub 2} particles generated by reactions between hydrated calcium silicate and fluoride ions.

36 MATERIALS SCIENCE↗

Rapid Crystallization of Zeolites with Controllable Defects: Disentangling Fluoride Concentration and pH Using NH 4 F

Zeolite synthesis is typically conducted either under basic conditions or in neutral fluoride media using hydrofluoric acid (HF). While basic (OH − ) conditions generally result in faster zeolite crystallization, they can also increase the likelihood of framework defects and crystal intergrowths. In contrast, synthesis in neutral fluoride media tends to produce fewer defects because fluoride balances positive charges from structure-directing agents. However, this method often requires significantly longer crystallization times and involves the handling of dangerous HF. In the present study, we pursue the best of both synthesis conditions, rapid syntheses with controllable defect concentrations, by disentangling of mineralizing agent and chargebalancing agent using ammonium fluoride (NH 4 F) as an alternative to HF. We have investigated the use of NH 4 F in the syntheses of siliceous and aluminum-containing zeolite A (LTA, small pore), ZSM-5 (MFI, medium pore), and siliceous Beta(*BEA, large pore). The crystallization times of all four zeolites decreased substantially with an increasing NH 4 F concentration. Crystallization times were reduced from 24 to 4 h (Si-LTA), 96 to 36 h (Al-LTA), 240 to 6 h (ZSM-5), and 24 to 3 h (Si-*BEA). Additionally, increasing the NH 4 F concentration in the synthesis mixtures decreases the defect densities of siliceous zeolites. Raman spectroscopy, along with 29 Si MAS NMR, 19 F MAS NMR, 13 C MAS NMR, and fluorine elemental analysis of Si-LTA samples confirms that the reduction in charged defects (Si−O − ) is due to the higher incorporation of F − within the double four-membered ring (D4R) present in the LTA samples. We show that the accelerated crystallization is due to the role of F − in enhancing the silica mineralization rate (formation of silicon hexafluoride species) and stabilizing D4Rs under basic conditions. As a result, combining basic and fluoride-mediated synthesis could therefore be advantageous for faster zeolite production and improved control over structural properties for a wide variety of zeolite structures.

Anions↗

Integrated Approach to Fluoride High Temperature Reactor Technology and Licensing Challenges (FHR-IRP)

This document constitutes progress made on this project by the Georgia Tech led Integrated Approach to Fluoride High Temperature Reactor Technology and Licensing Challenges (FHR-IRP). This is the first draft of the project final report. Chapter 3 is focused on Tritium management. Tritium management in Fluoride-salt High-temperature Reactors (FHRs) presents a major operational concern and a significant challenge. Tritium is generated via multiple pathways including various interactions in fuel and structural materials, as well as coolant (primarily interaction with lithium and beryllium), leading to a complex evolution and spatial distribution of tritium generation rate. FHR generates orders of magnitude more tritium than in LWRs, and has potential for a significant release, via permeation through structural materials (due to high temperature), and through heat exchanger(s). Therefore, accurate estimate is necessary. For that purpose relevant tritium production pathways were identified. A methodology to obtain space-time dependent tritium generation rate was developed and implemented, employing SCALE and MCNP codes. Detailed models of the reference Advanced High Temperature Reactor (AHTR) design were developed. A multi-parametric metrics was introduced to capture relevant tritium production indicators, including the instantaneous tritium production rate, total tritium production (neglecting subsequent decay), and accumulated tritium production (accounting for the decay). The obtained results will inform tritium management, including the sizing of the components, and to gain insight on the impact of the core design parameters on tritium generation rates. Research effort on Liquid Salt Impurity Removal, Redox and Corrosion Control is discussed in Chapter 4. Section 4.1 is an introduction chapter. Based on the current available knowledge and operation experience on previous MSRs and other types of nuclear reactors, the report identifies the major impurities that are related to either material compatibility, salt properties or radioactive source terms, and the potential contamination sources of these impurities, their transport in the primary coolant loop and available cleanup methodologies for a particular group of impurity. In section 4.2, the available purification methods were discussed, including the liquid/liquid extraction using liquid Bi-Li which has been applied in MSBR and electrochemical purification which is developed based on Pyroprocessing. In this section, the new multi-stage and multi-salt-component was developed and discussed. Section 4.3 discussed the redox potential control for salt chemistry and corrosion mitigation, including the control theory and the soluble/soluble buffer control method. The section also developed method on how to analyze soluble/soluble redox reaction in a molten salt system and designed an electrochemical sensor for redox potential control. Corrosion models were also reported in this section. Section 4.4 focused on how to measure the fundamental properties in a molten salt. As an example, the section focused on La fluoride in the molten salt. The section developed methods on how analyze electrochemical measurement data to obtain the fundamental properties including the redox potential, diffusion coefficient and exchange current density. All these fundamental information is important for salt purification system development. Section 4.5 focused on measurements of corrosion products in the salts. Because of the different behaviors between Cr and La in the salt, new analysis method for Cr fluorides in the salt was developed. Some results for Fe fluoride in the salt and corrosion measurements were also reported. Section 4.6 demonstrated the separation of oxide from the salt. This section also measured the solubility of La 2 O 3 in the salt as function of temperature. Section 4.7 focused on the separation of La and Ce from the molten salt. These two elements were selected because La was found to be separated by using inert electrode, while for separation of Ce, reactive electrode must be selected. Section 4.8 demonstrated the separation iodine ions from the molten salt. Two kinds of working electrode materials (metal W and graphite) were investigated. Section 4.9 focused on the fundamental data of fission products and actinides in liquid Bi. The chapter reviewed the available data, then based a CALPHAD model, the available data were broadened to the concentration-dependent cases.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗

Phosphate and Fluoride Processing Options for Hanford Sludge

The Direct Feed High-Level Waste (DFHLW) strategy represents an alternative flowsheet to bypass the Hanford Waste Treatment and Immobilization Plant (WTP) Pretreatment Facility. Key processing functions previously captured during baseline pretreatment operations include leaching and washing prior to solids concentration and should be considered in the new DFHLW flowsheet to maximize waste feed loading, minimize high-level waste (HLW) volume, and mitigate corrosion challenges associated with vitrification of high phosphate and fluoride concentrations. The effectiveness and efficiency of sludge washing can have a substantial impact on DST space and mission duration. Two target species that benefit significantly from washing are phosphate and fluoride. Commonly present in many high-level wastes at Hanford, phosphate and fluoride are found predominately in the form of salt precipitates and can have adverse and detrimental effects on glass waste loading. Additionally, fluoride produces melter off-gas that creates corrosion risks in the off-gas system piping. Determining the solubilities of fluoride and phosphate salts, as well as the dissolution kinetics under potential HLW processing conditions will help to mitigate future operational risks and mature flowsheet technical bases.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

The Infrared Spectroscopy of Equilibrium Mixtures of Vapor-Phase Water and Hydrogen Fluoride

Hydrogen fluoride readily associates with water vapor in the air to form the H 2 O-HF complex, which has optical absorption properties that are different from those of unassociated hydrogen fluoride. Consequently, to accurately quantify the total amount of hydrogen fluoride coming from an industrial stack or vent, for example, requires that the complexed amount of hydrogen fluoride be accounted for. To do this, the equilibrium constant for the association reaction is needed. Using statistical mechanical methods, Adebayo and coworkers [Adebayo SLA, AC Legon and DJ Millen. 1991. J. Chem. Soc. Faraday Trans. 87:443-447.] made an estimate of this equilibrium constant based on measured and estimated spectroscopic values for the complex. This value is K eq = 84(18) but has never been confirmed experimentally. In the research described herein, we have measured the equilibrium constant for the formation of H 2 O-HF by monitoring the decrease in the infrared absorption features of water vapor and hydrogen fluoride in mixtures of these two vapors in a temperature-regulated cell. Our experimental values for K eq at 25 °C, based on the diminution of the water vapor and HF transitions, are 77(46) and 51(24), respectively. The decay of the spectral features continues long after (hours) the two vapors are mixed in the gas cell. This suggests that other reactions (the growth of a film of hydrofluoric acid, perhaps) are taking place. While the experimental results agree reasonably well with the calculated equilibrium value of Adebayo et al., further improvements in experimental and analysis techniques are needed to reduce the uncertainties in the experimental results.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The Role of Process-Directing Agents on Enamel Lesion Remineralization: Fluoride Boosters

The aim of this study was to investigate the effects of two process-directing agents (polyaspartic acid and osteopontin) used in a polymer-induced liquid-precursor (PILP) process on the remineralization of bacteria-induced enamel demineralization. Enamel demineralization lesions (depths of about 180–200 µm) were created and exposed to Streptococcus mutans, cultured with a 10% sucrose solution for 21 days, and remineralized using a PILP process (pH = 7.4, 14 days) with a calcium phosphate solution containing either polyaspartic acid or osteopontin in the presence or absence of fluoride (0.5 ppm). The specimens were examined under scanning electron microscopy. The fluoride was successfully incorporated into the PILP remineralization process for both polyaspartic acid and osteopontin. When the fluoride was added to the PILP remineralization solution, there was more uniform remineralization throughout the lesion than with either polyaspartic acid or osteopontin alone. However, in the absence of these process-directing agents, fluoride alone showed less remineralization with the formation of a predominantly surface-only layer. The PILP remineralization process relies on the ability of process-directing agents to stabilize calcium phosphate ions and holds promise for enamel lesion remineralization, and these agents, in the presence of fluoride, seem to play an important role as a booster or supplement in the continuation of remineralization by reducing the mineral gains at the surface layer.

59 BASIC BIOLOGICAL SCIENCES↗

Discrimination of fluoride and phosphate contamination in central Florida for analyses of environmental effects

A study was made of the spatial registration of fluoride and phosphate pollution parameters in central Florida by utilizing remote sensing techniques. Multispectral remote sensing data were collected over the area and processed to produce multispectral recognition maps. These processed data were used to map land areas and waters containing concentrations of fluoride and phosphate. Maps showing distribution of affected and unaffected vegetation were produced. In addition, the multispectral data were processed by single band radiometric slicing to produce radiometric maps used to delineate areas of high ultraviolet radiance, which indicates high fluoride concentrations. The multispectral parameter maps and radiometric maps in combination showed distinctive patterns, which are correlated with areas known to be affected by fluoride and phosphate contamination. These remote sensing techniques have the potential for regional use to assess the environmental impact of fluoride and phosphate wastes in central Florida.

Coker, A. E.↗

Direct measurements of stratospheric fluoride

Stratospheric fluoride mass mixing ratios were measured by passing stratospheric air through filters half of which is impregnated in a base. Measurements of stratospheric fluoride were obtained at altitudes from 15 to 40 km at latitude 30-33 N and longitude 95-105 W at different months of the year. The significant amount of fluoride collected on the base-impregnated portion of the filters suggests that fluoride is present in the stratosphere as an acid gas. The mixing ratios decrease markedly at altitudes less than 20-25 km, suggesting the troposphere as the major sink for stratospheric fluoride.

Mroz, E. J.↗

Hot filament technique for measuring the thermal conductivity of molten lithium fluoride

Molten salts, such as lithium fluoride, are attractive candidates for thermal energy storage in solar dynamic space power systems because of their high latent heat of fusion. However, these same salts have poor thermal conductivities which inhibit the transfer of heat into the solid phase and out of the liquid phase. One concept for improving the thermal conductivity of the thermal energy storage system is to add a conductive filler material to the molten salt. High thermal conductivity pitch-based graphite fibers are being considered for this application. Although there is some information available on the thermal conductivity of lithium fluoride solid, there is very little information on lithium fluoride liquid, and no information on molten salt graphite fiber composites. This paper describes a hot filament technique for determining the thermal conductivity of molten salts. The hot filament technique was used to find the thermal conductivity of molten lithium fluoride at 930 C, and the thermal conductivity values ranged from 1.2 to 1.6 W/mK. These values are comparable to the slightly larger value of 5.0 W/mK for lithium fluoride solid. In addition, two molten salt graphite fiber composites were characterized with the hot filament technique and these results are also presented.

Jaworske, Donald A.↗

Towards green synthesis of Mn 4+ -doped fluoride phosphors: a review

Mn 4+ -doped fluoride phosphors are attractive for application in white solid-state lighting devices because their distinct red emission can improve the color rendering index, while the earth-abundance of Mn 4+ ions can reduce the production cost. However, highly hazardous HF is used as the fluoride source in the synthesis processes, which requires extreme caution. In this review, we introduce various methods for synthesizing Mn 4+ -doped fluoride phosphors, categorized according to the presence or absence of HF in the synthesis. The underlying optical properties of the phosphors fabricated using the various methods are discussed. In addition, in the discussion of each method, we emphasize on the key factors and strategies for developing phosphors. Finally, this review highlights perspectives on and future directions for the safe synthesis of Mn 4+ -doped fluoride phosphors to achieve solid-state lighting devices with superior optical properties.

36 MATERIALS SCIENCE↗

Advantages of liquid fluoride thorium reactor in comparison with light water reactor

Liquid Fluoride Thorium Reactor (LFTR) is an innovative design for the thermal breeder reactor that has important potential benefits over the traditional reactor design. LFTR is fluoride based liquid fuel, that use the thorium dissolved in salt mixture of lithium fluoride and beryllium fluoride. Therefore, LFTR technology is fundamentally different from the solid fuel technology currently in use. Although the traditional nuclear reactor technology has been proven, it has perceptual problems with safety and nuclear waste products. The aim of this paper is to discuss the potential advantages of LFTR in three aspects such as safety, fuel efficiency and nuclear waste as an alternative energy generator in the future. Comparisons between LFTR and Light Water Reactor (LWR), on general principles of fuel cycle, resource availability, radiotoxicity and nuclear weapon proliferation shall be elaborated.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗

Novel gas exposure system for the controlled exposure of plants to gaseous hydrogen fluoride

Abstract Plants can serve as sensitive bioindicators of the presence of contaminant vapors in the atmosphere. This work describes a novel laboratory-based gas exposure system capable of calibrating plants as bioindicators for the detection and delineation of the atmospheric contaminant hydrogen fluoride (HF) as a preparatory step for monitoring release emissions. To evaluate changes in plant phenotype and stress-induced physiological effects attributed to HF alone, the gas exposure chamber must have additional controls to simulate otherwise optimal plant growth conditions including variables such as light intensity, photoperiod, temperature, and irrigation. The exposure system was designed to maintain constant growth conditions during a series of independent experiments that varied between optimal (control) and stressful (HF exposure) conditions. The system was also designed to ensure the safe handling and application of HF. An initial system calibration introduced HF gas into the exposure chamber and monitored HF concentrations by cavity ring-down spectroscopy for a 48-h period. Stable concentrations inside the exposure chamber were observed after approximately 15 h, and losses of HF to the system ranged from 88 to 91%. A model plant species ( Festuca arundinacea ) was then exposed to HF for 48 h. Visual phenotype stress-induced responses aligned with symptoms reported in the literature for fluoride exposure (tip dieback and discoloration along the dieback transition margin). Fluoride concentrations in exposed tissues compared to control tissues confirmed enhanced fluoride uptake due to HF exposure. The system described herein can be applied to other reactive atmospheric pollutants of interest in support of bioindicator research.

54 ENVIRONMENTAL SCIENCES↗

Effect of metal fluorides on the corrosion of structural materials in molten LiF-NaF-KF

The corrosion of structural materials in molten fluoride salts is predominantly caused by the presence of impurities in the salt. Here, this study focuses on understanding the corrosion behavior of selected alloys in molten FLiNaK salt with addition of similar quantities of metal fluoride impurities such as CrF 2 , CrF 3 , FeF 2 , FeF 3 , and NiF 2 . The results show that the presence of selected metal fluoride impurities increases the extent of corrosion of the selected alloys in molten FLiNaK salt, with the exact effect depending on the thermodynamic stability of the fluoride impurity added as well as the composition of the structural alloy studied.

36 MATERIALS SCIENCE↗

Enhanced Tooth Structure Via Silver Microwires Following Treatment with 38 Percent Silver Diamine Fluoride.

The American Academy of Pediatric Dentistry guidelines recommend treatment of primary teeth with 38 percent silver diamine fluoride (SDF) as a noninvasive option to arrest active dental caries lesions. A significant outcome of SDF treatment are lesions that clinically harden and become more resistant to further decay. Many practicing dentists believe that this increased hardening is due to the reaction of silver and fluoride with carious dentin. The purpose of this study was to focus on the structural and chemical effects of silver diamine fluoride treatment on the native tooth. In SDF-treated cavitated dentin lesions in teeth subsequently extracted for orthodontic reasons, the authors observed continuous, filamentous silver densities formed in situ from 50 to 2,100 μm in length and 0.25 to 7.0 μm in diameter using high-resolution synchrotron X-ray microcomputer tomography and field emission scanning electron microscopy. These "microwires" fill voids in the lesion caused by disease and permeate through surrounding dentinal tubules. Spectroscopy confirmed that the chemical composition of the observed microwires is predominantly silver. These observations suggest mechanistic explanations for the structural reinforcement of carious dentin in addition to remineralization. It is hypothesized that silver diamine fluoride may achieve its antimicrobial functions by biochemical interactions and through its inherent ability to integrate into the native tooth structure.

60 APPLIED LIFE SCIENCES↗

Corrosion of Candidate Materials in Molten FLiBe Salt for Fluoride-Salt-Cooled High-Temperature Reactor (FHR)

Molten fluoride salts have attracted considerable attention because of their desirable thermophysical properties that lead to superior heat transfer. Recently, fluoride salts are being considered as coolants in the fluoride salt-cooled high temperature reactors (FHRs). The successes of the molten salt reactor experiment (MSRE) program in 1950's-70's at Oak Ridge National Laboratory (ORNL) has also driven the pursuit of molten salt nuclear reactor as one of the lead next generation nuclear reactor concepts. Unlike MSRE where the uranium fuel was dissolved in the molten fluoride salt, the FHR concept is expected to use molten salt (2LiF-BeF{sub 2}, FLiBe) only as coolant in conjunction with solid TRISO fuel particles immersed in the molten salt. One of the important challenges in FHR development is corrosion of structural materials in high-temperature molten 2LiF-BeF{sub 2} (FLiBe) salt. Currently, 316 stainless steel (nominal composition: Fe-12Ni-17Cr-2.5Mo-1Si-2Mn-0.03C) and Hastelloy N (nominal composition: Ni-7Cr-16Mo-5Fe-1Si-0.8Mn) are deemed as promising candidate alloys for the construction of some of the structural components of FHR. 316 stainless steel is ASME code certified for high temperatures (up to 760 deg. C) applications. Hastelloy N has been shown to have outstanding corrosion resistance in molten FLiBe but present code certification data limit the use of this alloy to only about 704 deg. C. Modifications of Hastelloy N with higher creep strength are presently being developed at ORNL. Other materials such graphite, SiC/SiCf and C/Cf composites, are also considered for structural applications in the FHR. The presence of these multiple materials in a molten FLiBe salt medium can further exacerbate and complicate corrosion effects. Therefore, it is necessary to understand the corrosion behavior of these materials in molten FLiBe salt. The corrosion behavior of Hastelloy N, 316 stainless steel, and CVD SiC and two types of SiC-SiC{sub f} composites have been tested in molten FLiBe salt at 700 deg. C. When tested in metal-lined crucibles both Hastelloy N and 316 stainless steel showed very good corrosion resistance. Samples tested in graphite crucibles showed greater propensity for corrosion and carburization was observed in the near surface regions of the alloys. CVD SiC showed outstanding corrosion resistance. However, the two SiC-SiC{sub f} composites exhibited corrosion attack implying that the manufacturing process may play a role in the corrosion of these composites. (authors)

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗

Enhanced Tooth Structure Via Silver Microwires Following Treatment with 38 Percent Silver Diamine Fluoride.

Purpose: American Academy of Pediatric Dentistry guidelines recommend treatment of primary teeth with 38 percent silver diamine fluoride (SDF) as a noninvasive option to arrest active dental caries lesions. A significant outcome of SDF treatment are lesions that clinically harden and become more resistant to further decay. Many practicing dentists believe that this increased hardening is due to the reaction of silver and fluoride with carious dentin. The purpose of this study was to focus on the structural and chemical effects of silver diamine fluoride treatment on the native tooth. Methods: In SDF-treated cavitated dentin lesions in teeth subsequently extracted for orthodontic reasons, the authors observed continuous, filamentous silver densities formed in situ from 50 to 2,100 μm in length and 0.25 to 7.0 μm in diameter using high-resolution synchrotron X-ray microcomputer tomography and field emission scanning electron microscopy. These microwires fill voids in the lesion caused by disease and permeate through surrounding dentinal tubules. Results: Spectroscopy confirmed that the chemical composition of the observed microwires is predominantly silver. Conclusions: These observations suggest mechanistic explanations for the structural reinforcement of carious dentin in addition to remineralization. It is hypothesized that silver diamine fluoride may achieve its antimicrobial functions by biochemical interactions and through its inherent ability to integrate into the native tooth structure.

60 APPLIED LIFE SCIENCES↗

Fluoride salt static freezing study

Molten salt reactor designs such as the FHR must consider the safety implications of freezing, requiring the development of thermal hydraulics models that account for freezing behavior. Pipe models that couple heat transfer, fluid dynamics, and phase change physics will require verification and validation. A static freezing study is being conducted to provide an initial set of validation data with LiF-BeF{sub 2} (FLiBe). The study will also be performed with LiF-NaF-KF (FLiNaK) in order to quantify the distortion that arises from using FLiNaK as a non-toxic surrogate salt for thermal-hydraulic studies. In order to develop the numerical model, accurate inputs for the thermal hydraulic properties of the two salts of interest need to be measured near the freezing point. For this reason, a series of three experiments including Differential Scanning Calorimetry (DSC) measurements, the Density Measurement Experiment, and the Static Freezing Experiment are being conducted to determine these thermo-physical properties at temperatures near the freezing point. The Static Freezing Experiment is also designed to determine the degree of supercooling that FLiBe and FLiNaK experience. Supercooling is a temperature depression below the freezing point that the liquid experiences before freezing initiates. Increased supercooling in a liquid flowing through a pipe leads to increased dendritic freezing and an increased likelihood of pipe blockage and freeze-shut. Based on previous research on supercooling in water and non-fluoride salts, supercooling is likely affected most strongly by cooling rate and sample size (as well as salt purity). No data has been generated previously on supercooling in fluoride salts such as FLiBe and FLiNaK. The results of this set of DSC, Density Measurement and Static Freezing experiments will be used in an ongoing fluoride salt freezing study being conducted to develop pipe freezing models for molten salts to be used in safety analysis. The thermal hydraulic properties measured in this study will serve as inputs for all future models. With the supercooling behavior of both salts quantified, it can be assessed whether supercooling must be included in future thermal hydraulic models. The validated Static Freezing Experiment model can then serve as the framework for a pipe freezing model and eventually a 1D system code.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗