Viscosity Deviations Research Articles

Glutinous rice gel as all-natural ink supply for extrusion-based food 3D printing – the chemical basis of gel printability

In this study, four varieties of glutinous rice were screened out of 18 varieties as representative model inks. Gel prepared using variety WN9612 of high amylose content displayed high viscosity and large overall print deviation (OPD = 17.4 ± 0.4 %) due to difficulties in extrusion. Printed item by variety 19,415 of medium amylose content showed good printability (OPD = 4.4 ± 0.4 %) and highest hardness (197.5 ± 7.3 N). Similarly good printability was demonstrated by variety 19,416 (OPD = 4.1 ± 0.2 %) containing low amylose content but abundant protein and bound-water. Variety WN9446 lacking protein and moisture created item with fluid structure, lowest gel strength (738.5 ± 20.9 Pa) and standing ability. Therefore, low to medium amylose content rendered suitable viscosity, extrudability and printability of rice gel while non-starchy components predominated water mobility and texture of 3D printed items. This study for the first time establishes theoretical groundwork of selecting glutinous rice varieties with appropriate chemical composition as all-natural materials in 3D printing and food customization.

Excess properties, intermolecular interaction, and CO2 capture performance of diethylene glycol monomethyl ether + ethylenediamine binary mixed solutions

In this work, the density (ρ) and viscosity (η) values of diethylene glycol monomethyl ether (DEGME) (1) + ethylenediamine (EDA) (2) binary mixed solutions were experimentally measured over the temperature span of 298.15–318.15 K and at a constant pressure of 100.5 kPa. To delve into the physicochemical properties of the binary mixed solutions, the excess properties, including excess molar volume, viscosity deviation, and excess molar activation Gibbs free energy, and thermodynamic values, including activation Gibbs free energy, enthalpy change, entropy change, and activation energy, were systemically calculated. Furthermore, the relationship between mole fraction and temperature was modeled using the Jouyban-Acree (J-A) model and a least squares method. Additionally, the three-body McAllister, the four-body McAllister, the Eyring-Margules, and the Heric viscosity models were employed to establish a relationship between viscosity and mole fraction. The relationship between viscosity and temperature was determined utilizing the Arrhenius equation, and the Redlich-Kister (R-K) polynomial was applied to fit the excess molar volume, viscosity deviation, and excess molar activation Gibbs free energy values of the binary mixed solutions. To further validate the intermolecular interactions within the binary mixed solutions, Raman, UV, and 1H NMR spectroscopic analyses, and density-functional theory (DFT) calculations were also conducted. These comprehensive analyses collectively confirmed the presence of significant intermolecular hydrogen bonds (IHBs) between the DEGME and EDA molecules, which are characterized as the –OH⋯NH2– interaction. Ultimately, the CO2 absorption capacity of the binary mixed solutions was examined, revealing that diethylene glycol monomethyl ether (DEGME) (1) + ethylenediamine (EDA) (2) binary mixed solutions owned superior CO2 absorption efficiency, thus offering a promising approach for CO2 capture.

Estimation of some important thermodynamic properties of organic liquid mixtures at various temperatures (3-pentanol, benzyl salicylate, ethyl salicylate and methyl salicylate)

ABSTRACT This study investigates the thermodynamic and transport properties of binary mixtures of 3-pentanol with methyl salicylate, ethyl salicylate, and benzyl salicylate at selected compositions and temperatures from 303.15 K to 313.15 K. The excess molar volume, excess isentropic compressibility, deviation in viscosity, and excess Gibbs free energy of activation of viscous flow were determined from measured values of densities, viscosities, and speeds of sound. The results reveal the strength of hydrogen bonding interactions between the 3-pentanol molecules hydroxyl group and the salicylate derivative molecules’ -OH groups. Furthermore, the Prigogine-Flory-Patterson (PFP) theory is applied to identify the most predominant molecular interaction, and the Jouyban-Acree model results are discussed in terms of mean relative deviation (MRDs) and individual relative deviation (IRD) between calculated and experimental densities, speeds of sound and viscosities as an accuracy criterion

Improvement of the properties of ionic liquids for the absorption refrigeration cycle

Ionic liquids (ILs), recognized as environmentally friendly green reagents, have good application prospects in many fields. However, their high viscosity has hindered their widespread application. Currently, an effective solution is to introduce a solvent as an additive. In this work, ethanol with different molar fractions was chosen to form working pairs with three ILs ([emim]BF4, [bmim]BF4 and [hmim]BF4), to reduce their viscosities. The densities and viscosities of the three working pairs were obtained in a temperature range of 293.15∼338.15 K, thereby determining the thermal expansion coefficients. The effects of ethanol on the volumetric and viscometric characteristics of the three ILs are discussed. To further analyze the interactions between ethanol and the ILs, excess mole volume and viscosity deviations were introduced. The interactions between different molecules were stronger than those between the same molecules in the working pairs. This is the main reason why the addition of ethanol reduces the viscosity of the three ILs. Finally, the hard-sphere model was applied to predict the viscosities of the working pairs. Upon introducing an adjustable argument, the average absolute relative deviation of the prediction for the aforementioned three ILs decreased to 4.4%, 5.9%, and 5.0%, respectively.

Temperature-dependent thermophysical characterisation of N,N-Dimethylbenzylamine binary mixtures with acetophenone derivatives (propiophenone, p-chloroacetophenone and p-methyl acetophenone)

ABSTRACT This study reports the density (ρ), speed of sound (u), and viscosity (η) of N,N-dimethyl benzyl amine (DMBA) binary mixtures with propiophenone, p-methylacetophenone, and p-chloroacetophenone in a temperature range of 303.15–313.15 K for various compositions. Excess thermodynamic properties (excess molar volume, V E ; excess isentropic compressibility, κ s E ; viscosity deviation, Δη; and excess Gibbs free energy of activation of viscous flow, ΔG *E ) were derived from the experimental data. The analysis focused on understanding intermolecular interactions, particularly the influence of the inductive effect on hydrogen bonding and dipole–dipole interactions within the mixtures. The Jouyban-Acree model was employed to predict the densities, speeds of sound, and viscosities. The model’s accuracy was assessed using the mean relative deviations (MRDs) and individual relative deviations (IRDs) between the calculated and experimental values. To further support these findings, Fourier Transform Infrared (FT-IR) spectroscopy was conducted to provide complementary insights into the intermolecular interactions within the mixtures.

Physicochemical analysis on molecular interactions in binary liquid mixtures at various temperatures and correlation with the Jouyban–Acree model (3-pentanol with allyl amine, allyl alcohol, and allyl chloride)

ABSTRACT This study investigates the molecular interactions in binary mixtures of 3-pentanol with three allyl compounds (allyl amine, allyl alcohol, and allyl chloride) at various temperatures. The excess molar volume, excess isentropic compressibility, deviation in viscosity, and excess Gibbs free energy of activation of viscous flow were determined from measured values of densities, speeds of sound, and viscosities. The data were analysed to determine excess properties and deviations from ideal behaviour, highlighting the predominance of molecular interactions such as geometrical packing effects and free volume effects. The experimental results were correlated with the Jouyban−Acree model, which effectively relates the observed thermodynamic properties to the composition of the mixtures. This correlation allows for a deeper understanding of molecular interactions that influence the properties of these binary mixtures across different temperatures.

Effect of water on the excess properties of eutectic solvents

Three eutectic solvents were created utilizing a heating and stirring process. The solvents consist of tetrabutylammonium bromide and levulinic acid, as well as tetrabutylammonium chloride with either levulinic acid or lactic acid. The characterization of the samples was conducted using 1H NMR and IR techniques. The density and viscosity of three different low eutectic solvent and water binary mixture systems were determined within the temperature range of 293.15 to 333.15 K. The volume properties (excess molar volume, coefficient of expansion, coefficient of excess expansion) of the binary mixtures with different amounts of water were thoroughly investigated across the complete range of mole fraction. The study also investigated the impact of viscosity parameters, such as viscosity deviation and Excess activation Gibbs free energy of viscous flow. Furthermore, an analysis was conducted on the interaction between the eutectic solvent and the solvent molecules in the binary mixture. This analysis revealed the presence of hydrogen bonds between the eutectic solvent and water molecules. Moreover, it was confirmed that the excess properties could be fitted with the Redlich-Kister equation with r2 ≥ 0.99,demonstrating high suitability for binary mixes consisting of low eutectic solvents and water.

Investigation of intermolecular interactions in binary mixtures of N,N-dimethyl benzyl amine with higher alkanols (N,N-dimethyl benzyl amine with 1-octanol, 1-nonanol, 1-decanol)

ABSTRACT Measurements of densities (ρ), speeds of sound (u), and viscosities (η) for binary mixtures of N,N-dimethyl benzyl amine (DMBA) with 1-octanol (D1), 1-nonanol (D2), and 1-decanol (D3) were performed across temperatures from 303.15 K to 313.15 K under atmospheric pressure, covering all composition ranges. These experimental results were utilised to calculate the excess molar volume, excess isentropic compressibility, viscosity deviation, and the excess Gibbs free energy of activation for viscous flow. Calculations for partial molar properties and infinite dilution partial molar properties were also carried out for each binary mixture. The dominant intermolecular interactions within these mixtures were analysed using the PFP theory. Additionally, the Jouyban−Acree model was applied to predict the thermo physical properties such as density, speed of sound, and viscosity. The model’s accuracy was evaluated by comparing predicted values with experimental data through mean relative deviations (MRDs) and individual relative deviations (IRDs).

Thermodynamic and spectroscopic analyses of N-Methyl benzylamine-isomeric amyl alcohol binary mixtures: Jouyban-Acree model correlation and experimental validation

ABSTRACT Excess molar volume, excess isentropic compressibility, deviation in viscosity, and excess Gibbs free energy of activation for viscous flow for binary mixtures of N-Methyl benzyl amine (NMBA) with 2-Methyl-2-butanol (2M2B), 2-Methyl-1-butanol (2M1B), and 3-Methyl-1-butanol (3M1B) were determined from measured densities (ρ), viscosities (η) and speeds of sound (u) at 303.15 K to 313.15 K. Influence Structural disparities on excess properties is discussed concerning intermolecular forces. The Prigogine – Flory – Patterson (PFP) theory identifies predominant molecular interactions, and the Jouyban – Acree model correlates density, speed of sound, and viscosity with composition. Thermodynamic activation parameters were calculated using the Eyring equation to study viscous flow thermodynamics. FT-IR and 1H NMR spectra of equimolar binary mixtures were analysed to confirm experimental findings through absorption bands (cm−1) and chemical shifts.

Excess Thermodynamic Properties and FTIR Studies of Binary Mixtures of Toluene with 2-Propanol or 2-Methyl-1-Propanol

Physical properties of the binary solutions, toluene with 2-propanol and 2-methyl-1-propanol, were measured at T = 293.15, 298.15, 303.15, 308.15, and 313.15 K and P = 100 kPa. The experimental density values were tested with the Emmerling et al. and Gonzalez-Olmos–Iglesias equations. The results indicate that the equation by Emmerling et al. is the best to correlate the density for toluene + 2-methyl-1-propanol system, while for toluene + 2-propanol, both proposed equations are proper to correlate the density with composition and temperature. The viscosity results were verified with different models containing two adjustable parameters. The values of viscosity deviation (∆η), excess molar volume (VE), excess Gibbs energy (ΔG*E), partial molar volumes (V1¯ and V2¯), and apparent molar volume (Vφ,1 and Vφ,2) were calculated. The values of the excess molar volume were positive for both systems, while negative values were obtained for the viscosity deviation and the excess Gibbs energy. The excess properties of the mixtures were adjusted to the Redlich–Kister equation. The values of thermodynamic functions of activation of viscous flow were computed and analyzed. Additionally, the Prigogine–Flory–Patterson (PFP) theory was applied to calculate VE and then compared with experimental values. The values of the percentage absolute average deviation obtained suggest the validity of this theory. The Fourier transform infrared spectroscopy (FTIR) spectra of the binary solutions studied in this work allowed for the understanding of the interactions between the molecules of these systems.

Investigation of the Physicochemical Behaviour of Homoeopathic Dilutions of Glycerol (Glycerinum) at the Temperatures (293.15 - 318.15) K: Volumetric, Acoustic and ViscometricStudy

The physicochemical studies of homoeopathic medicines provide better understanding regarding the presence and mechanism of their action in ultra-dilutions. The physicochemical behaviour of glycerol dilutions homoeopathic dilutions has been investigated from the measurements of densities, , ultrasonic speeds, u and viscosities,  of pure ethanol control (91% ethanol in water) and 33 dilutions of glycerol dilutions of potencies ranging from 1C to 200C at ambient temperatures and atmospheric pressure. From the experimental data, a number of physicochemical parameters, viz., the isentropic compressibilities, s , intermolecular free length, Lf , acoustic impedance, Z, relative association, RA, relaxation time, , ultrasonic absorption, /f 2 , pseudoGrüneisen parameter, , deviations in isentropic compressibility, s , deviations in intermolecular free length, Lf , deviations in acoustic impedance, Z, deviations in viscosity,  and deviations in pseudo-Grüneisen parameter, have been evaluated. These parameters showed diverse behaviour at certain potencies of these homoeopathic dilutions. The results have been qualitatively discussed in terms of prevailing interactions of these glycerol dilutions dilutions. The results indicated that that even in extreme dilutions (50C, 110C, 150C and 160C) the molecules of glycerol dilutions may be present in these homoeopathic formulations

Excess Molar Volume and Deviations in Viscosity of the Binary Liquid Mixtures Containing 1,3-Dioxolane + Alkanols at T = 298.15k

Thermodynamic and transport properties of liquid and liquid mixtures have been used to understand the intermolecular interactions between the components of the mixture. The sound velocity, density and viscosity of binary liquid mixtures are important from practical and theoretical point of view to understand the liquid theory. In the present study sound velocity, density and viscosity have been measured of binary mixtures of 1, 3-dioxolane with pentanol, hexanol, heptanol, octanol, nonanol and decanol over the entire range of mole fraction at 298.15K, and atmospheric pressure. From these experimental measurements the excess molar volume (V<sub>m</sub><SUP>E</SUP>), excess viscosity (η<SUP>E</SUP>), acoustic impedance (Z<SUP>E</SUP>) and excess adiabatic compressibility (β<sub>ad</sub><SUP>E</SUP>), have been calculated. The excess molar volume (V<sub>m</sub><SUP>E</SUP>), excess viscosity (η<SUP>E</SUP>), acoustic impedance (Z<SUP>E</SUP>) and excess adiabatic compressibility (β<sub>ad</sub><SUP>E</SUP>), have been analyzed in terms of interactions arising due to structural effect, charge-transfer complexes and dipole-dipole interaction between unlike molecules. These deviations have been correlated by a polynomial Redlich-Kister equation. The excess properties are found to be eighter negative or positive depending on the molecular interactions and nature of the liquid mixtures. Excess properties provide important information in understanding the solute-solvent interaction in a solution. The excess molar volume (V<sub>m</sub><SUP>E</SUP>), excess viscosity (η<SUP>E</SUP>), acoustic impedance (Z<SUP>E</SUP>) and excess adiabatic compressibility (β<sub>ad</sub><SUP>E</SUP>), values have been interpreted to terms of the nature of intermolecular interactions between constituent molecules of mixtures.

Insight into behaviors of internal interactions and thermodynamic properties of binary mixtures composed of ether-functionalized ionic liquids and 1,4-butyrolactone or propylene carbonate

A deeper comprehension of the mechanism behind various internal interactions and their influence on system properties encourages the utilization of ionic liquid mixture systems. In this work, the excess molar volume, viscosity deviation, change of electrical conductivity, and ionicity of both binary mixtures for N-methyl-N-methoxyethylpyrrolidinium bis(trifluoromethanesulfonyl)imide ([MOEMPYrr][TFSI]) ether-functionalized ionic liquids (ILs) with 1,4-butyrolactone (GBL) or propylene carbonate (PC) were systematically studied. The specific interactions between ILs and solvent molecules were investigated by using the COSMO-RS model in terms of DFT calculation. The results indicate that [MOEMPYrr]+ tends to act as a hydrogen bond donor and [TFSI]- tends to act as a hydrogen bond acceptor, and GBL (or PC) has a strong hydrogen bond acceptance ability. Furthermore, based on the radial distribution functions (RDFs) from molecular dynamics (MD) simulations, the H1 atom in [MOEMPYrr]+, the O2 atom in [TFSI]-, the O3 atom in GBL, and the O4 atom in PC are selected as reference sites to study the interaction between cations and anions (or solvent molecules). It is found that the interaction between anions and cations in the [MOEMPYrr][TFSI] + PC system is stronger than that in the [MOEMPYrr][TFSI] + GBL system, and the interaction between cations and GBL is stronger than that between cations and PC. This result further explains why the excess molar volumes (VE) of [MOMPYrr][TFSI] + GBL binary mixtures are greater than that of [MOMPYrr][TFSI] + PC binary mixtures from a microscopic perspective.

Exploring molecular interactions in active amyl alcohol-haloalkane systems through thermodynamic properties and Jouyban–Acree correlation

ABSTRACT A comprehensive study on the thermodynamic and transport properties of binary mixtures composed of active amyl alcohol (AAA) and haloalkane’s was conducted within a temperature range of 303.15 K to 313.15 K. Experimental data on densities (ρ), viscosities (η), and speeds of sound (u) were employed to calculate excess molar volume (V E ), isentropic compressibility (K s E ), viscosity deviation (Δη), and excess Gibbs free energy for viscous flow (∆G* E ). The impact of dipole moment on these excess properties was investigated to gain insights into the prevailing intermolecular interactions within the mixtures. The Prigogine – Flory – Patterson (PFP) theory is applied to identify the predominant molecular interaction. The accuracy of the Jouyban–Acree model in correlating densities (ρ), viscosities (η), and speeds of sound (u) with composition were evaluated, demonstrating satisfactory agreement with experimental data.

Thermodynamic and transport properties of binary mixtures containing 1,2-propanediol with 2-methoxyethanol and 2-ethoxyethanol at different temperatures

In the present investigation density, speed of sound, and viscosity have been reported for binary liquid mixtures of 1,2-propanediol (1,2-PD) with 2-methoxyethanol (2-ME) and 2-ethoxyethanol (2-EE) over the entire composition range at T= (298.15–323.15) K. From the experimental data, excess molar volume, (VmE), excess isentropic compressibility, (κsE), excess molar isentropic compressibility, (κs,mE), excess speed of sound, (uE), excess isobaric thermal expansion,αpE, and deviation in viscosity (Δη) of liquid mixtures have been calculated. The excess partial molar volume,V¯m,1E, V¯m,2E , excess partial molar isentropic compressibility, K¯s,m,1EK¯s,m,2E over the whole composition range together with partial molar volume,V¯m,10, V¯m,20, partial molar isentropic compressibility K¯s,m,10,K¯s,m,20, excess partial molar volume,V¯m,10E, V¯m,20E and excess partial molar isentropic compressibility, K¯s,m,10E,K¯s,m,20E at infinite dilution have also been calculated. All excess properties have been correlated using the Redlich-Kister smoothing polynomial equation. The VmE results are analysed in the light of Prigogine-Flory-Patterson theory. Analysis of each of the three contributions viz. interactional, free volume, and P* to VmE has shown that interactional contribution and free volume effect are negative for all the mixtures, and P* contribution is positive for the mixtures of 2-ME. The variations of these parameters with changes in composition and temperature have been discussed in terms of intermolecular interactions prevailing in these mixtures. Further, the viscosities of these binary mixtures were correlated theoretically by using various empirical and semi-empirical models and the results were compared with the experimental findings.

Insight into molecular interactions prevailing in N,N-dimethylformamide + alkyl acrylates mixtures at different temperatures: An experimental and theoretical investigation

The excess isentropic compressibility, excess speed of sound, excess molar isentropic compressibility and deviation in viscosity were evaluated from the experimental values of speeds of sound and viscosities of N,N-dimethylformamide + methyl acrylate/ethyl acrylate/n-butyl acrylate binary mixtures over the entire composition range at temperatures (288.15–318.15) K and pressure (101 kPa). Further, the partial molar isentropic compressibility; excess partial molar isentropic compressibility of the components over the entire composition range and also at infinite dilution have been calculated. These evaluated parameters have been interpreted in relations to prevailing interactions in these mixtures. These interactions were found dependent on the size of alkyl group in acrylate molecules and the amide-acrylate interactions decline with increase in size of the alkyl group. Moreover, the speeds of sound for the mixtures were calculated by scaled particle theory and the results compared well with the experimental results. Also, the viscosities of these mixtures were correlated by means of various empirical relations and the results were found in good agreement with the experimental results.

Fundamental physicochemical properties, intermolecular interactions and CO2 absorption properties of binary mixed solutions of monoethanolamine + diethylenetriamine

This work presents experimental data on the density (ρ), viscosity (η), and surface tension (γ) of monoethanolamine (MEA), diethylenetriamine (DETA), and their binary mixed solutions across 298.15–318.15 K. Using these physicochemical data, the work also explored properties like excess molar volume (VmE) and viscosity deviation (Δη) of the solutions. The experimental results were modeled using the Jouyban-Acree model, McAllister four-body model, and Redlich-Kister (R-K) equation. The application of these parametric models confirmed strong intermolecular interactions (The length (1.911 Å) and energy (HF value: −2237.54 kJ/mol and Des: −21.61 kJ/mol) of hydrogen bond) within the MEA + DETA binary mixed solutions. Spectroscopic analyses, including Raman and nuclear magnetic resonance hydrogen spectroscopy, revealed the presence of intermolecular hydrogen bonding (OH⋯N(H2)) in the MEA + DETA binary mixed solutions. Lastly, the CO2 absorption capacity of the solutions was experimentally studied, providing a theoretical foundation and reference data for future experiments and process design of CO2 capture.

The impact of rotation on the onset of cellular convective movement in a casson fluid saturated permeable layer with temperature dependent thermal conductivity and viscosity deviations

In this effort, we examined the impact of rotation on the arrival of cellular convective motion in a Casson fluid saturated permeable layer with temperature dependent thermal conductivity and viscosity deviations. The problem is important to cellular foams prepared from plastics, ceramics, and metallic where radiation conductivity is revealed as a power function of temperature. The altered Darcy model is used to characterize the rheological performance of Casson fluid flow in permeable medium. The approximate analytical solution and numerical solution correct to one decimal place are presented utilizing the Galerkin method. The analysis reveals that the influence of thermal conductivity disparity parameter and the rotation is to delay the convective motion whereas; the viscosity disparity parameter and the Casson parameter have dual impact on the convective motion in the presence of rotation. The range of the convective cell drops with increasing the thermal conductivity disparity parameter, the viscosity disparity parameter, the Casson parameter and rotation parameter. In the absence of rotation, the range of the convective cell does not depend on the Casson parameter and the viscosity disparity parameter. Further, the existing results are compared with the existing literature under the particular case of this study.

Physico-chemical studies of non-aqueous binary liquid mixtures of N-methyl aniline with amino alcohols at various temperatures

ABSTRACT Densities (ρ), speeds of sound (u) and viscosities (η) for three binary mixtures of N-methyl aniline with amino alcohols (3-amino-propan-1-ol, 2-amino-2-methyl-propan-1-ol and 1-amino propan-2-ol) were measured at temperatures ranging from 303.15 to 313.15 K and at atmospheric pressure across the entire composition range. Excess molar volume, excess isentropic compressibility, deviation in viscosity, and excess Gibbs free energy of activation of viscous flow were calculated using experimental data. Partial molar properties and infinite dilution molar partial properties were also determined for each binary system. The Prigogine-Flory-Patterson theory is used to identify the most important interaction. The results of the Jouyban-Acree model are discussed in terms of the mean relative deviation and individual relative deviation between the calculated and experimental densities, speed of sound, and viscosities as an accuracy criterion. FTIR studies have also been added to confirm the experimental findings of the investigated mixtures.

Molecular dynamics simulation on thermal and transport properties of LiF-KF

Molten fluoride is considered as an attractive heat transfer and storage medium in advanced energy utilization facilities, but it is short of the necessary thermal and transport properties at high temperature. In this paper, the thermal and transport properties of the binary LiF-KF mixtures at 1073–1473 K are obtained by classical molecular dynamics. The deviation of simulated thermal conductivity of binary LiF-KF at 1073 K from experimental value is less than 19 %. Moreover, the deviation of simulated viscosity of pure LiF at different temperatures from experimental value is around 10 %. It is indicated that reverse non-equilibrium molecular dynamics (RNEMD) is acceptable for describing fluoride salts. An exponential correlation is established between molar fraction of LiF and thermal conductivity at different temperatures. Furthermore, the macroscopic thermal and transport properties correlated with local structure are analyzed, especially the dependence of local structure on temperature and composition of LiF is discussed deeply. With temperature increasing, ion clusters are considered to be formed and overall structure become loose, which leads to reductions in density, thermal conductivity and viscosity. An increase in composition of LiF results in higher specific heat capacity, thermal conductivity and viscosity, which is related to the reduction of Li-Li bond length and the enhancement of interactions between F−. The comparison of properties enhancement of different compositions is completed through the analysis of the synergy coefficient of macroscopic properties. This work provides the basic data for the accurate design of high-temperature heat transfer system.