The Prediction of Volumes, Compressibilities and Thermal Expansion Coefficients of Hydrocarbon Mixtures

1968 ◽  
Vol 8 (02) ◽  
pp. 95-106
Author(s):  
Surjit M. Avasthi ◽  
Harvey T. Kennedy

Abstract An equation developed for gaseous hydrocarbon mixtures predicts molal volumes with an average absolute deviation of 0.73 percent when applied to 264 natural gas and condensate systems including 2,043 PVT points. Another equation developed for liquid hydrocarbon mixtures predicts molal volumes with an average absolute deviation of 1.12 percent when applied to 346 crude oil systems including 1,759 PVT points. Both equations require composition of the mixture to be expressed as mole fraction of methane through heptanes-plus, hydrogen sulfide, nitrogen and carbon dioxide, together with the characteristics of the heptanes-plus fraction in addition to the temperature and pressure. The equations cover wide ranges of the variables involved, and their accuracy is considerably better Than that of other available methods. The equations were differentiated to allow calculation of the coefficients of isothermal compressibility and isobaric thermal expansion. (In this paper the coefficient of isothermal compressibility and the coefficient of isobaric thermal expansion will be expressed as compressibility and thermal expansion coefficient, respectively.) Equations to calculate these quantities are presented. Introduction Calculations of reservoir performance for petroleum reservoirs require accurate knowledge of the volumetric behavior of hydrocarbon mixtures, both liquid and gaseous. Compressibilities are required in transient fluid flow problems, and thermal expansion coefficients are important in thermal methods of production. An accurate laboratory investigation of the PVT behavior of each reservoir fluid encountered would be costly and time consuming. For this reason various correlations for predicting fluid properties have been developed and recorded and recent literature. Correlations have been presented in the form of graphs, tables and equations. Since an increasing number of studies are being conducted with the aid of electronic computers, recent efforts have been directed toward development of correlations suitable for computer programming. Application of computers permits the use of more complex correlations which otherwise are not feasible. Moreover, methods for predicting reservoir performance, particularly those based on the compositional material balance, depend upon the capability of accurately expressing the molal volumes and other fluid properties as functions of pressure, temperature and composition. The coefficient of isothermal compressibility c is defined by(1) and can be computed from the slope of isothermal specific volume curve for each pressure. The compressibility is a point function and has the dimension of reciprocal pressure. The coefficient of isobaric thermal expansion beta is defined as(2) It is a point function and has the dimension of reciprocal temperature. The thermal expansion coefficient can be obtained from the slope of an isobaric specific volume curve for any temperature. SPEJ P. 95ˆ

1999 ◽  
Vol 77 (12) ◽  
pp. 2046-2052 ◽  
Author(s):  
Carmen Jarne ◽  
Manuela Artal ◽  
José Muñoz Embid ◽  
Inmaculada Velasco ◽  
Santos Otín

Densities of binary mixtures of 1,1,2-trichlorotrifluoroethane + dibromomethane, + bromochloromethane, or + bromotrichloromethane were measured over their entire composition ranges at 288.15 and 308.15 K. Thermal expansion coefficients (α) and excess molar volumes (VEm) were calculated. Moreover, densities at 298.15 K and pressures up to 80 bar (1 bar = 100 kPa) were determined for these same mixtures. Isothermal compressibilities (KT) of the pure liquids and their mixtures were obtained.Key words: density, excess volume, thermal expansion coefficient, isothermal compressibility.


2004 ◽  
Vol 82 (8) ◽  
pp. 1271-1279 ◽  
Author(s):  
M JP Comuñas ◽  
C Boned ◽  
A Baylaucq ◽  
E R López ◽  
J Fernández

In this work we report several derived thermodynamic properties, the isothermal compressibility (κT), the isobaric thermal expansion coefficient (αp), and the internal pressure (π), and their excess functions (κTE, αpE, and πE) for the refrigerant + lubricant mixtures HFC-134a + triethylene glycol dimethyl ether and HFC-134a + tetraethylene glycol dimethyl ether. These properties have been determined in wide temperature (293.15–373.15 K) and pressure (10–60 MPa) ranges in an effort to better understand the behaviour of these kinds of mixtures and their thermophysical properties as functions of temperature, pressure, and composition. The analysis of the thermodynamic excess properties (negative values for κTE and αpE, positive values for πE) for both systems shows a high degree of interaction between the refrigerant and the synthetic lubricant molecules. Key words: HFC-134a, high pressure, internal pressure, isobaric thermal expansion coefficient, isothermal compressibility, polyglycol ethers, refrigerant–lubricant mixtures.


1994 ◽  
Vol 59 (7) ◽  
pp. 1511-1524 ◽  
Author(s):  
Tejraj M. Aminabhavi ◽  
Hemant T. S. Phayde ◽  
Rajashekhar S. Khinnavar

Densities, refractive indices, speeds of sound and viscosities of the diethylene glycol dimethyl ether - methyl salicylate system were measured as a function of mole fraction at 298.15, 303.15, 308.15, 313.15 and 318.15 K. The results are fitted by a power series equation involving both the temperature and mole fraction variables. The basic physical data of the mixtures are further used to calculate the excess molar volume VE, changes in isentropic compressibility ∆β, changes in refractivity ∆R and changes in viscosity ∆η. The results are fitted by the Redlich-Kister polynomial relation. The isobaric thermal expansion coefficients of the mixtures are also determined from density measurements. The data are compared with those obtained from equations derived by differentiation of the Lorentz-Lorenz and Eykman relations. Refractive indices of the mixture are used to test the validity of mixing relations. The changes in isobaric thermal expansion coefficients ∆α of the mixtures were examined. Viscosity data were tested in terms of the McAllister, Heric and Auslaender relations.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Qazi Mohammed Omar ◽  
Jean-Noël Jaubert ◽  
Javeed A. Awan

The properties of 3 binary mixtures containing piperazine were investigated in this work. In a first step, the densities for the two binary mixtures (piperazine + methanol) and (piperazine + acetone) were measured in the temperature range of 293.15 to 328.15 K and 293.15 to 323.15 K, respectively, at atmospheric pressure by using a Rudolph research analytical density meter (DDM 2911). The concentration of piperazine in the (piperazine + methanol) mixture was varied from 0.6978 to 14.007 mol/kg, and the concentration of piperazine in the (piperazine + acetone) mixture was varied from 0.3478 to 1.8834 mol/kg. On the other hand, the density data for the (piperazine + water) mixture were taken from the literature in the temperature range of 298.15 to 328.15 K. In a second step, for the 3 investigated systems, the apparent molar volume (Vϕ) and the limiting apparent molar volume (Vϕ0) at infinite dilution were calculated using the Redlich–Mayer equation. The limiting apparent molar volumes (Vϕ0) were used to study the influence of the solute-solvent and solute-solute interactions. The temperature dependency of the apparent molar volumes was used to estimate the apparent molar expansibility, Hepler’s constant ∂2Vϕ0/∂T2P, and isobaric thermal expansion coefficients αP.


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