Enthalpy Of Fusion Research Articles

Development of an applied variant of the kolmogorov–johnson–mehl theory of crystallization for processing thermal analysis data. Temperatures and enthalpies of melting germanium isotopes

An applied kinetic model has been developed for processing DSC peaks of transitions between states, determining the temperature–time dependence of the degree of transition and combining the fundamental theory of Kolmogorov–Johnson–Mehl crystallization, simplified for practice, with the semi-empirical Erofeev model. In the development of this applied model, the concept of a “thermodynamic factor” is introduced, which allows a transition in the kinetics of phase transformations of condensed matter. The application of the new approach is demonstrated by the example of studying the dependences of temperature and enthalpy of fusion on the average atomic mass of stable germanium isotopes, data on which, as new chemical individuals, are of a fundamental nature and can serve as reference information.

Thermophysical properties of AlxCoCrCuFeNi high entropy alloys

The AlxCoCrCuFeNi (x = 0.25, 0.5, 1, 2) high entropy alloys (HEAs) were prepared by arc melting and spray casting techniques. Their microstructures, hardness, and thermophysical properties such as fusion enthalpy, entropy, thermal diffusion coefficients, thermal expansion coefficients, were investigated. XRD results indicated that AlxCoCrCuFeNi (x = 0.25 and 0.5) alloys were composed of a high-entropy FCC phase and Cu-rich nanophase. As the Al content increased to 1 and 2, the phase structures included the AlNi-rich B2 phase, FeCr-rich A2 phase and Cu-rich nanophase. With the increased Al content, the microstructures of AlxCoCrCuFeNi HEAs transitioned from coarse dendrites to petal-like dendrites, and the grains were continuously refined. Moreover, the Al additions reduced the density whereas increased the Vickers hardness of the alloys. The maximum hardness observed in Al2CoCrCuFeNi HEA was approximately 2.4 times greater than that of the Al0.25CoCrCuFeNi HEA. The thermal diffusion coefficients of alloys initially increased and subsequently decreased as the temperature elevated. The phase transformation induced by Al content was an effective method for rapidly homogenizing the internal temperature of alloys. Furthermore, the crystal structure, elemental segregation, lattice distortion, enthalpy and entropy of fusion, and lattice vibration frequency all mutually affected the thermal diffusion and expansion coefficients of AlxCoCrCuFeNi HEAs.

Electro-optical and thermal characterization of copper tartrate crystals grown in silica gel

Copper Tartrate crystals were grown by Gel Growth technique by single diffusion. Silica gel of Optimum specific gravity was set with tartaric acid at optimum pH and aging period. Band gap of copper tartrate crystal is determined using UV-Visible spectroscopy to be 5.24 eV. In PL spectra broad peak is observed at nearly 367.44186 nm in the range 287 nm to 458 nm along with the sharp, intense transmission maxima peak at wavelength nearly 505.03876 nm which is characteristic of a material composition and electronic band structure. This shows the transparency in UV-visible region and material is a filter in this range .TGA analysis concluded that Copper tartrate has one half water molecule as crystalline water and is stable up to 85.02 0 C.DSC analysis assigns the temperature value 314.5 0C as melting point and apparent enthalpy of fusion determined is 10.18 mW.

Temperature and Enthalpy of Fusion of Nanooxides UO2 and ThO2 of Different Morphologies

Temperature and Enthalpy of Fusion of Nanooxides UO2 and ThO2 of Different Morphologies

Heat capacities and thermodynamic functions of three 1-benzyl-4-aryl-1H-1,2,3-triazoles in the temperature range of (0 – Tm) K

In this paper, we present the results of comprehensive thermodynamic study of some functionally substituted triazoles such as 1-benzyl-4-phenyl-1H-1,2,3-triazole, 1-benzyl-4-(m-tolyl)-1H-1,2,3-triazole and 1-benzyl-4-(4‑tert-butylphenyl)-1H-1,2,3-triazole. The temperature dependences of heat capacities of 1-benzyl-4-(m-tolyl)-1H-1,2,3-triazole and 1-benzyl-4-(4‑tert-butylphenyl)-1H-1,2,3-triazole were measured in a wide temperature range of ∼(5 – 370) K using the adiabatic calorimetry. Those of 1-benzyl-4-phenyl-1H-1,2,3-triazole were determined at the range of ∼(5 – 80) K, supplementing the previous measurements at the more elevated temperatures. The melting parameters and thermal stability (melting temperature, enthalpy of fusion, temperature of thermal destruction) of the compounds were determined using the differential scanning calorimetry. Also, the standard thermodynamic functions (absolute entropies, reduced enthalpies and Gibbs energies) were calculated in the temperature range of (0 – Tm) K.

The morphology and thermo-regulating properties of electrospun PVA/PEG/Ag nanofibers of water and formic acid solvents

The solvent utilized in the electrospinning solution significantly impacts the morphology and thermal properties of PVA/PEG/Ag nanofibers. To prevent leakage of PEG, solid-liquid phase change, a suitable encapsulation method involves utilizing a combined single-phase electrospinning that incorporates PEG and supporting polymer of PVA. This study aims to investigate the production of thermal-regulating nanofibers from a solution containing PEG 6000, PVA, and AgNO3 precursor using electrospinning method. The influence of water and formic acid as a solvent on the morphology of the nanofibers was examined using SEM. The selected nanofiber characteristics and thermal performance were evaluated through FE-SEM, FT-IR, XRD, DSC, PCM leakage, and DTG tests. SEM images revealed that the formic acid-based nanofibers, consisting of two polymers and two polymer/Ag NPs, exhibited a nanoporous membrane, possibly due to enhanced cross-linking compared to water-based nanofibers. The results of the DSC indicated that fusion and solidification enthalpies of the selected water-based nanofibers were measured as 70.09 and −85.43 J/g, respectively. Unexpectedly, the DSC results indicated higher enthalpies compared to unheated samples. SEM image after thermal cycles, leakage results, and DTG of water-based nanofibers demonstrated their production with thermal stability, reliability, and the potential for creating shape-stable, thermally regulating fabricated nanofibers for various applications.

Thermal analysis, flexural mechanical properties and FTIR analysis of an HDPE matrix composite reinforced with alumina and silicon carbide

This research developed an HDPE composite reinforced with Al2O3 and 1% SiC in the proportions of pure HDPE, 40 %, 50 % and 60 % of ceramic load. The mechanical flexural test showed results of sMAX 19.09 ± 2.89 MPa and E 1806 ± 400 MPa for the A60 group and concluded that with ceramic loadings above 60 % contribute to crystallization in the regions around the particles. TGA analysis showed initial degradation at 409 °C and final degradation between 499 and 504 °C, with a residue in pure HDPE of 0.46%. The DSC curves showed an endothermic peak at 132 °C and crystallization around 119 °C, and the crystallinity of the HDPE was 95.29 %, and the analyses showed a decrease in the enthalpy of fusion and crystallization with increasing ceramic loading due to the decrease in the polymer fraction in the composite. DMA analysis showed that temperatures above the Tg of the crystalline phases were the mechanism that contributed most to the storage modulus. FTIR analysis showed several interactions in different bands between the 3 compounds in the composite.

A Novel Method for Increasing Phase‐Change Microcapsules in Nanofiber Textile through Electrospinning

AbstractPhase‐change textiles can achieve temperature regulation in variable ambient environments, however, augmenting the amounts of phase‐change materials (PCMs) in textiles remains a significant challenge due to the occurrence of leakage with higher amounts. Herein, a novel approach is proposed for the fabrication of a hierarchical nanofiber textile embedded with a substantial quantity of phase‐change microcapsules (PCMC) using electrospinning. Such nanofiber textile is composed of a polyvinylidene fluoride‐hexafluoropropylene fibers (PVDF‐HFP) layer and a polyvinyl butyral fibers doped with 60 wt% of PCMC (PVB/PCMC‐60) layer. Gratifyingly, doped PCMC shows no signs of rupture and exhibits excellent cycling stability. Furthermore, the incorporation of the PCMC does not affect the spectral characteristics of the PVDF‐HFP layer while providing a substantial enthalpy of fusion (92.6 J g−1) to the PVB/PCMC‐60 layer. This serves to compensate for the deficiency in radiative cooling capacity and effectively mitigates temperature fluctuations and overheating of the textile. Outdoor test results indicate that the nanofiber textile can achieve temperature drops of 3.7 and 14.8 °C compared to textile without the PCMC (namely PVDF‐HFP/PVB) and cotton, and attains a subambient temperature drop of 6.5 °C. Additionally, the nanofiber textile exhibits desirable mechanical strength, flexibility, washability, breathability, moisture permeability, and sun protection.

Investigation of Solid Polymer Electrolytes for NASICON-Type Solid-State Symmetric Sodium-Ion Battery.

The inevitable shift toward renewable energy and electrification necessitates earth-abundant sodium reserves for next-generation Na-based energy storage technologies. By coupling the benefits of solid electrolytes over traditional nonaqueous electrolytes due to their safety hazards, solid-state sodium-ion batteries hold huge prospects in the future. This work presents a comprehensively developed solid-state sodium-ion symmetric full cell operating at room temperature enabled through a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based polymer electrolyte and modified NASICON-structured positive and negative electrodes. Among the investigated polymer electrolytes, PVDF-HFP-NaTFSI was found to outperform other counterparts by achieving a higher ionic conductivity and delivered an appreciable electrochemical stability window. By further delving into the properties of PVDF-HFP-NaTFSI, it was found to possess the least crystallinity, minimal porous structure, lowest melting point, and fusion enthalpy, indicating better ion transport than other investigated polymer electrolytes. The as-assembled solid-state battery revealed a storage capacity of 74 mAh g-1 at 0.1 C with a specific energy density of 130 Wh kgcathode_active_material-1 and demonstrated an impressive capacity retention of 84% of the initial capacity after 200 cycles. The structure and morphology retention of the cycled electrode and electrolyte through postmortem analysis bolster the electrochemo-mechanical stability of the developed solid cell. The findings reported here on polymer electrolytes persuade expedient solutions for developing ambient temperature solid-state sodium-ion batteries with promising electrochemical performance for commercialization in the near future.

Magnetohydrodynamic double diffusion natural convection of power-law Non-Newtonian Nano-Encapsulated phase change materials in a trapezoidal enclosure

PurposeThe present numerical investigation examines the magnetohydrodynamic (MHD) double diffusion natural convection of power-law non-Newtonian nano-encapsulated phase change materials (NEPCMs) in a trapezoidal cavity.Design/methodology/approachThe governing Navier-Stokes, energy and concentration equations based on the Cartesian curvilinear coordinates are solved using the collocated grid arrangement’s finite volume method. The in-house FORTRAN code is validated with the different benchmark problems. The NEPCM nanoparticles consist of a core-shell structure with Phase Change Material (PCM) at the core. The enclosure, shaped as a trapezoidal hollow, features a warmed (Th) left wall and a cold (Tc) right wall. Various parameters are considered, including the power law index (0.6 ≤ n ≤ 1.4), Hartmann number (0 ≤ Ha ≤ 30), Rayleigh number (104 ≤ Ra ≤ 105) and fixed variables such as buoyancy ratio (Br = 0.8), Prandtl number (Pr = 6.2), Lewis number (Le = 5), fusion temperature (Θf = 0.5) and volume fraction (ϕ = 0.04).FindingsThe findings indicate a decrease in local Nusselt (Nu) and Sherwood (Sh) numbers with increasing Hartmann numbers (Ha). Additionally, for a shear-thinning fluid (n = 0.6) results in the maximum local Nu and Sh values. As the Rayleigh number (Ra) increases from 104 to 105, the structured vortex in the streamline pattern is disturbed. Furthermore, for different Ra values, an increase in n from 0.6 to 1.4 leads to a 67.43% to 76.88% decrease in average Nu and a 70% to 77% decrease in average Sh.Research limitations/implicationsThis research is for two-dimensioal laminar flow only.Practical implicationsPCMs represent a class of practical substances that behave as a function of temperature and have the innate ability to absorb, release and store heated energy in the form of hidden fusion enthalpy, or heat. They are valuable in these systems as they can store significant energy at a relatively constant temperature through their latent heat phase change.Originality/valueAs per the literature review and the authors’ understanding, an examination has never been conducted on MHD double diffusion natural convection of power-law non-Newtonian NEPCMs within a trapezoidal enclosure. The current work is innovative since it combines NEPCMs with the effect of magnetic field Double diffusion Natural Convection of power-law non-Newtonian NEPCMs in a Trapezoidal enclosure. This outcome can be used to improve thermal management in energy storage systems, increasing safety and effectiveness.

Electrospun nanofibers incorporating lactobionic acid as novel active packaging materials: biological activities and toxicological evaluation

In this study, lactobionic acid (LBA) was incorporated into poly(vinyl alcohol) (PVA) and poly(ε-caprolactone) (PCL) by electrospinning. The antimicrobial effects of the nanofibers were tested using the agar diffusion method. Only the PVA formulations showed antimicrobial activity against Staphylococcus aureus. The PVA and PCL nanofibers containing LBA showed antioxidant activity ranging from 690.33 to 798.67 µM TEAC when tested by the ABTS method. The characterization of nanofibers was performed by scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, and mechanical analysis. The nanofibers showed a uniform morphology and their average diameters ranged from 295.5 to 2778.2 nm. The LBA addition induced a decrease in the enthalpy of fusion (ΔHm) of PVA and PCL nanofibers, while the Young’s modulus was reduced from 20 to 10 MPa in PCL and PCL-LBA nanofibers, respectively. No relevant differences were observed between the FTIR spectra of the control nanofibers and the nanofibers containing LBA. All nanofibers presented hemolysis rate below 2%, thus can be considered as non-hemolytic materials. Further toxicological assessment was performed with the selected formulation PVA10 + LBA. The evaluations by mutagenicity assay, cell survival measurement, cell viability analysis and agar diffusion cytotoxicity test indicated that there are no significant toxic effects. Electrospun nanofibers PVA-LBA and PCL-LBA were successfully produced, showing good thermal and mechanical properties and non-toxic effects. Furthermore, the nanofibers showed antimicrobial activity and antioxidant activity. The findings of this study indicate that PVA and PCL electrospun nanofibers incorporating LBA are promising for use in packaging applications.

Freeze-Vulnerable Plastic Crystal to Cryogenic Liquid Electrolyte for Lithium Batteries by Deep Freezing-Point Depression.

Low-Tf solvents (Tf = freezing point) are considered and employed for low-temperature lithium-ion battery (LIB) electrolytes to keep electrolytes in the liquid phase at low temperatures. Unfortunately, Tf is synchronized with Tb (boiling point) so low Tf brings Tb down and therefore discourages the thermal stability of electrolytes using low-Tf solvents. In this work, 1) the hot wing of LIB-working temperature by employing a high-Tb (inevitably high-Tf) solvent and 2) the cold wing by using a significant Tf depression is secured. Sulfolane is employed as the high-Tf (therefore, high-Tb) and high-Kf (Kf = cryoscopic constant) solvent since its mesomorphic state between solid and liquid. That abnormally and significantly decreases the enthalpy of fusion, and resultantly grants extremely high Kf at 66.4Km-1. By employing sulfolane with 2m lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), the liquid-phase temperature window down to <-80°C for the cold wing and simultaneously guaranteed its flash point at >+150°C for the hot wing is successfully extended. LIB cells with lithium iron phosphate and lithium metal worked in a good stand with 2m LiTFSI/sulfolane at room temperature, -30°C as an ambient cold, -74°C as a deep cold, and +80°C as a deep hot.

A novel approach on artificial aging of nylon 12 powder for laser powder bed fusion

PurposeThis study aims to address challenges in the Laser Powder Bed Fusion process of polymers, focusing on the considerable amount of unsintered powder left post-printing. The objective is to understand the altered properties of this powder and find solutions to improve the process, reduce waste and explore reusing reprocessed powder.Design/methodology/approachA novel methodology is used to generate reprocessed powder without traditional printing, reducing time, cost and waste. The approach mimics the ageing effects during the printing process, providing insights into particle size distribution and thermal behaviour.FindingsResults reveal insights into artificial ageing, showing an 8.2% decrease in particle size (60.256–69.183 µm) and a 9.1% increase in particle size (17.378–19.953 µm) compared to unsintered powder. Thermal behaviour closely mirrors used powders, with variations in enthalpy of fusion (−0.55% to 2.69%) and degree of crystallinity (0.19% to 2.64%). The proposed methodology produces results that differ from those due to printing under 3% from a thermal point of view. The new process reduces the time needed for aged powder, contributing to cost savings and waste reduction.Originality/valueThe study introduces a novel method for reprocessed powder generation, deviating from traditional printing. The originality lies in artificially ageing powders, providing comparable results to actual printing. This approach offers efficiency, time savings and waste reduction in the Laser Powder Bed Fusion process, presenting a valuable avenue for further research.

Effect of heat treatment on microstructure of near-eutectic Al-Ni-Mn alloy, and determination of mechanical and thermoelectrical properties

This study examined the impact of solution heat treatment on the microstructure, mechanical characteristics, thermophysical properties, and electrical resistivity of an Al-Ni-Mn near-eutectic alloy. The investigation focused on varying temperatures and holding periods. The composition of the Al-Ni-Mn near-eutectic alloy system was chosen as Al-5.3%Ni-1.0%Mn (wt). In the non-heat-treated sample, the matrix phase (α-Al) is in equilibrium with the intermetallic Al9(Mn,Ni)2 and Al3Ni phases. The hardness value of the non-heat-treated sample (49.8 kg mm−2) increased to 70.1 kg mm−2 with 2 h of solution heat treatment at 570 °C and then 8 h of artificial aging at 180 °C. The hardness value increased by approximately 41%. TE: 651.81 °C for the non-heat-treated sample and TE:648.79 °C for the heat-treated sample. Fusion enthalpy (ΔH) value was determined as 336.79 (J g−1) for the non-heat-treated sample and 516.36 (J g−1) for the heat-treated sample. Heat Capacity (Cpl) value was found to be 0.364 J g−1.K for the non-heat-treated sample and 0.560 J g−1.K for the heat-treated sample. The electrical resistivity value of the 2 h’ solution heat-treated sample at 600 °C reached its highest value.

Solid–Liquid Phase Equilibrium of the n-Nonane + n-Undecane System for Low-Temperature Thermal Energy Storage

The current article presents an exploration of the solid–liquid phase diagram for a binary system comprising n-alkanes with an odd number of carbon atoms, specifically n-nonane (n-C9) and n-undecane (n-C11). This binary system exhibits promising characteristics for application as a phase change material (PCM) in low-temperature thermal energy storage (TES), due to the fusion temperatures of the individual components, thereby motivating an in-depth investigation of the solid–liquid phase diagram of their mixtures. The n-nonane (n-C9) + n-undecane (n-C11) solid–liquid phase equilibrium study herein reported includes the construction of the phase diagram using Differential Scanning Calorimetry (DSC) data, complemented with Hot–Stage Microscopy (HSM) and low-temperature Raman Spectroscopy results. From the DSC analysis, both the temperature and the enthalpy of solid–solid and solid–liquid transitions were obtained. The binary system n-C9 + n-C11 has evidenced a congruent melting solid solution at low temperatures. In particular, the blend with a molar composition xundecane = 0.10 shows to be a congruent melting solid solution with a melting point at 215.84 K and an enthalpy of fusion of 13.6 kJ·mol–1. For this reason, this system has confirmed the initial signs to be a candidate with good potential to be applied as a PCM in low-temperature TES applications. This work aims not only to contribute to gather information on the solid–liquid phase equilibrium on the system n-C9 + n-C11, which presently are not available in the literature, but especially to obtain essential and practical information on the possibility to use this system as PCM at low temperatures. The solid–liquid phase diagram of the system n-C9 + n-C11 is being published for the first time, as far as the authors are aware.

1-Ethyl (butyl)-3-methylimidazolium methanesulfonaties: Low-temperature heat capacity and standard thermodynamic functions of formation

A comprehensive study of the thermodynamic properties of two ionic liquids 1-ethyl-3-methylimidazolium (EmimMS) and 1-butyl-3-methylimidazolium methanesulfonate (BmimMS) was carried out. The isobaric heat capacity of the crystal and liquid phases of EmimMS and BmimMS was determined in the temperature range from 80 to 380 K by vacuum adiabatic calorimetry. The heat capacities of EmimMS and BmimMS were assessed at temperatures from 5 to 80 K by the Kelly method. The temperature dependencies of EmimMS and BmimMS main thermodynamic functions were determined in the temperature range from 5 to 380 K (isobaric heat capacity Cp,m(T), standard entropy Som(T), heat content Hom(T) – Hom(0), Gibbs energy content Gom(T) – Hom(0). Melting points and fusion enthalpies of EmimMS and BmimMS have been refined by DSC. The enthalpies of dissolution in water of EmimMS and BmimMS at 298.15 K were measured by the dissolution calorimetry. The standard enthalpies, entropies and Gibbs energies of EmimMS and BmimMS formation in the crystal and liquid state at 298.15 K were calculated from the experimental data. Comparison of the obtained thermodynamic characteristics with the literature data was carried out.

Phase transition study of bathophenanthroline and bathocuproine: A multitechnique approach

The thermal behaviour of bathophenanthroline and bathocuproine has been studied using several techniques, namely, differential scanning calorimetry and thermogravimetry. To determine their respective enthalpies of sublimation, vapor pressure measurements were carried out using different methods, such as Knudsen effusion mass loss/mass spectrometry, isothermal thermogravimetry, and a quartz crystal microbalance technique. Furthermore, the enthalpies of sublimation were determined by measuring the heat change of the sublimation process using high-temperature Calvet microcalorimetry.The results obtained in this work allowed the determination of the standard molar enthalpies of sublimation at 298.15 K, for bathophenanthroline and bathocuproine. The values obtained were (183.8 ± 2.2) kJ⋅mol−1 and (206.2 ± 2.8) kJ⋅mol−1, respectively. Additionally, the standard molar enthalpies of fusion were determined to be (30.4 ± 0.4) kJ⋅mol−1 and (26.5 ± 1.6) kJ⋅mol−1 for bathophenanthroline and bathocuproine, respectively. The analysis of the results allows a deeper understanding of the phase transition behavior for these compounds from the condensed to the gaseous phases, elucidating molecular decomposition and the inherent intermolecular forces governing the species.

Study of phase equilibria in a two-component system diphenyloxide &lt;i&gt;- n -&lt;/i&gt; nonadecane

Using the Schroeder, UNIFAC and UNIFAC Dortmund methods, the fusibility diagram of the diphenyloxide – n –nonadecane system was calculated and it was shown that it belongs to the eutectic type. Individual substances and their mixtures were studied experimentally using a differential scanning microcalorimeter. On the DTA heating curve of the eutectic alloy, two endo-effects are noted, corresponding to the polymorphic transition of n–nonadecane and the melting of the eutectic. A comparison of the eutectic coordinates calculated by these methods with experimental data is presented. For a eutectic alloy, the specific enthalpy of fusion, molar values of entropy and enthalpy of fusion, volumetric specific enthalpy of fusion and density for standard conditions are calculated. The eutectic mixture can be recommended for use as a coolant, as well as the working fluid of a heat accumulator.

Printability and Thermophysical Properties of Three-Dimensional-Printed Food Based on "Cochayuyo" Durvillaea antarctica Seaweed Flour.

This research assessed the feasibility of adding Cochayuyo seaweed flour (at 30, 50, and 70% levels) to rice flour-based paste to improve its 3D printing quality. The paste's rheological properties, printing quality, texture profile, thermal properties, and color of 3D-printed foods were explored. Results showed that pastes with Cochayuyo addition exhibited shear-thinning behavior, and viscosity increased with increased Cochayuyo concentration. Viscoelastic properties and a Texture Profile Analysis (TPA) revealed that Cochayuyo improved mechanical strength and made the paste easier to flow, improving printed food's extrudability, fidelity, and shape retention, which was better observed in RC50 and RC70 printed at 15 mm s-1. A differential scanning calorimetry (DSC) analysis showed a partial substitution of rice flour for Cochayuyo flour in the formulation. This increased the onset and melting peak temperatures and reduced the enthalpy of fusion. CIE color parameters a*, b*, and L* showed that Cochayuyo addition increased the color to yellow and red; however, lightness was considerably reduced. Therefore, Cochayuyo flour could have the potential to be used for the manufacture improvement of 3D-printed food with better rheological, mechanical, thermal, printing quality, and nutritional properties, making possible the exploitation of the native Cochayuyo seaweed, which is highly available in Chile.

Thermophysical Properties of FUNaK (NaF-KF-UF4) Eutectics.

General interest in the deployment of molten salt reactors (MSRs) is growing, while the available data on uranium-containing fuel salt candidates remains scarce. Thermophysical data are one of the key parameters for reactor design and understanding reactor operability. Hence, filling in the gap of the missing data is crucial to allow for the advancement of MSRs. This study provides novel data for two eutectic compositions within the NaF-KF-UF4 ternary system which serve as potential fuel candidates for MSRs. Experimental measurements include their melting point, density, fusion enthalpy, and vapor pressure. Additionally, their boiling point was extrapolated from the vapor pressure data, which were, at the same time, used to determine the enthalpy of vaporization. The obtained thermodynamic values were compared with available data from the literature but also with results from thermochemical equilibrium calculations using the JRCMSD database, finding a good correlation, which thus contributed to database validation. Preliminary thoughts on fluoride salt reactor operability based on the obtained results are discussed in this study.