scholarly journals The ISM equation of state for nano-fluids: the quantum effects analysis and volumetric properties assessment of the systems

2020 ◽  
Vol 49 (3) ◽  
pp. 261-278
Author(s):  
MASOUMEH KIANI

In this study, the density of nanoparticles, nanofluids containing a base fluid and nanofluids containing a mixture of two base fluids in the compressive range of 0.1-45 MPa and a temperature range of 273-363 K were calculated and predicted. The equation of state used in this work is the Ihm-Sang-Mason equation of state. According to the quantum properties of nanoparticles, a part of quantum correction was used to calculate the second virial coefficient. The potential function of Morse three-parameters was used which is more flexible than the usual potential functions of two-parameters such as Lenard Jones 12-6.

2001 ◽  
Vol 66 (6) ◽  
pp. 833-854 ◽  
Author(s):  
Ivan Cibulka ◽  
Lubomír Hnědkovský ◽  
Květoslav Růžička

Values of adjustable parameters of the Bender equation of state evaluated for chloromethane, dichloromethane, trichloromethane, tetrachloromethane, and chlorobenzene from published experimental data are presented. Experimental data employed in the evaluation included the data on state behaviour (p-ρ-T) of fluid phases, vapour-liquid equilibrium data (saturated vapour pressures and orthobaric densities), second virial coefficients, and the coordinates of the gas-liquid critical point. The description of second virial coefficient by the equation of state is examined.


1954 ◽  
Vol 32 (12) ◽  
pp. 759-763 ◽  
Author(s):  
C. F. A. Beaumont

A new potential function for liquid helium is obtained by modifying the Margenau potential function and summing over a suggested structure for the liquid. The new potential function leads to fair agreement with the first peak of the radial distribution curve for liquid helium, with the isothermal compressibility, and with second virial coefficient data at high temperatures.


2020 ◽  
Vol 1 (4) ◽  
pp. 175-180
Author(s):  
M. Sivakumar ◽  
R. Balasubramanian

The present study aims to determine the second virial coefficient of gold over a wide range of temperatures from the boiling point to the critical point. A three - parameter modified Berthelot equation of state has been employed to determine the second virial coefficient of gold. The parameters of the equation of state are determined through the critical - point parameters of gold. The temperature -dependence of the second virial coefficient of gold has been investigated. The obtained results are compared with that of the van der Waals equation of state, Berthelot equation of state, Tsonopoulus correlation, and McGlashan correlation. The results of this work agree well with that of other correlations in the vicinity of the critical point. It is also established that gold obeys the single - parameter law of corresponding states. And, the new parameter introduced in the attractive term of the equation of state is found to be a thermodynamic similarity parameter. Doi: 10.28991/HEF-2020-01-04-02 Full Text: PDF


2016 ◽  
Vol 423 ◽  
pp. 181-189 ◽  
Author(s):  
Sayed Mostafa Hosseini ◽  
Mohammad Mehdi Alavianmehr ◽  
Jalil Moghadasi

1975 ◽  
Vol 189 (1) ◽  
pp. 427-436 ◽  
Author(s):  
F. Bakhtar ◽  
D. J. Ryley ◽  
K. A. Tubman ◽  
J. B. Young

A description is given of a theoretical treatment of nucleation in flowing steam employing an equation of state based on the second virial coefficient. Comparison is made with experimental observations of reversion in the pressure range 2–35 bars of steam in a convergent-divergent nozzle of expansion rate P = 104 s-1. The agreement obtained is moderate.


1971 ◽  
Vol 24 (8) ◽  
pp. 1567 ◽  
Author(s):  
CHJ Johnson ◽  
TH Spurling

Pairwise additive third virial coefficients for axially symmetric multipolar molecules have been calculated using a non-product multidimensional integration formula. Results for the Stockmayer potential agree with the corrected results of Rowlinson. It is found that the inclusion of the dipole-quadrupole and quadrupole-quadrupole terms in the potential function has a marked qualitative effect on the shape of the C-T curve. Values of the third virial coefficient for water vapour calculated using a potential function derived from gaseous viscosity and second virial coefficient data are in good agreement with the experimental values.


2013 ◽  
Vol 2013 ◽  
pp. 1-29 ◽  
Author(s):  
Seung-Kyo Oh

The three-parameter Lennard-Jones (12-6) potential function is proposed to calculate thermodynamic property (second virial coefficient) and transport properties (viscosity, thermal conductivity, and diffusion coefficient) of noble gases (He, Ne, Ar, Kr, and Xe) and their mixtures at low density. Empirical modification is made by introducing a reduced temperature-correction parameter τ to the Lennard-Jones potential function for this purpose. Potential parameters (σ, ε, and τ) are determined individually for each species when the second virial coefficient and viscosity data are fitted together within the experimental uncertainties. Calculated thermodynamic and transport properties are compared with experimental data by using a single set of parameters. The present study yields parameter sets that have more physical significance than those of second virial coefficient methods and is more discriminative than the existing transport property methods in most cases of pure gases and of gas mixtures. In particular, the proposed model is proved with better results than those of the two-parameter Lennard-Jones (12-6) potential, Kihara Potential with group contribution concepts, and other existing methods.


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