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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 10 (1989), S. 857-870 
    ISSN: 1572-9567
    Keywords: compressibility ; density ; fluorocarbon oil ; free-volume equation ; high pressure ; perfluoropolyether ; specific volume ; Tait equation ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract New experimental data on the density and viscosity of linear, unbranched perfluoropolyethers are presented at temperatures from 273 to 333 K and pressures up to 180 MPa. The measurements were carried out by a high-pressure burrette apparatus and a falling-cylinder viscometer. The uncertainties of the measurements are estimated to be less than 0.09% for the specific volume and 2.5% for the viscosity. The P-V data at each temperature are correlated satisfactorily by the Tait equation. The viscosity data are also analyzed and correlated with pressure or molar volume by several empirical and theoretical equations.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 12 (1991), S. 245-264 
    ISSN: 1572-9567
    Keywords: alkanes ; cyclohexane ; density ; dodecane ; hexadecane ; mixtures ; octane ; Tait equation ; viscometer ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The viscosity and density of three binary mixtures of cyclohexane with n-octane, n-dodecane, and n-hexadecane have been measured at 298, 323, and 348 K at pressures up to 150 MPa or freezing pressures. The measurements of the viscosity were performed by a torsionally vibrating crystal viscometer on a relative basis using benzene and cyclohexane as reference materials. The density was measured using a high-pressure burette apparatus. The uncertainties of the measurements are estimated to be less than 2% for viscosity and 0.1% for density, respectively. The effects of temperature, pressure, density, and composition on the viscosity are discussed. Applicabilities of several empirical correlating equations to the viscosity data were examined.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 9 (1988), S. 465-479 
    ISSN: 1572-9567
    Keywords: fluorocarbon ; halogenated ethane ; liquid ; high pressure ; refrigerant ; thermal conductivity ; transient hot-wire method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract New experimental data on the thermal conductivity of liquid halogenated ethanes, R112 (CCl2F-CCl2F), R113 (CCl2F-CClF2), R114 (CClF2-CClF2), R114B2 (CBrF2-CBrF2), and R123 (CHCl2-CF3), are presented in the temperature range from 283 to 348 K at pressures up to 200 MPa or the freezing pressures. The measurements were carried out by a transient hot-wire apparatus within an uncertainty of ±1.0%. The thermal conductivity data obtained have been analyzed by means of the corresponding-states principle and other empirical methods. It is found that the corresponding-states correlation λ=f(Tr, Pr) holds well for R112, R113, and R114. The thermal conductivity can also be correlated satisfactorily with temperature, pressure, and molar volume by a similar expression to the Tait equation and the dense hard-sphere model presented by Dymond.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 2 (1981), S. 249-268 
    ISSN: 1572-9567
    Keywords: chorotrifluoromethane (R 13) ; chlorodifluoromethane (R 22) ; dichlorodifluoromethane (R 12) ; fluorocarbon ; pressure effect on thermal conductivity ; thermal conductivity ; trifluoromethane (R 23)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The thermal conductivity of four gaseous fluorocarbon refrigerants has been measured by a vertical coaxial cylinder apparatus on a relative basis. The fluorocarbon refrigerants used and the ranges of temperature and pressure covered are as follows: R 12 (Dichlorodifluoromethane CCl2F2): 298.15–393.15 K, 0.1–4.28 MPa R 13 (Chlorotrifluoromethane CClF3): 283.15–373.15 K, 0.1–6.96 MPa R 22 (Chlorodifluoromethane CHClF2): 298.15–393.15 K, 0.1–5.76 MPa R 23 (Trifluoromethane CHF3): 283.15–373.15 K, 0.1–6.96 MPa The apparatus was calibrated using Ar, N2, and CO2 as the standard gases. The uncertainty of the experimental data is estimated to be within 2%, except in the critical region. The behavior of the thermal conductivity for these fluorocarbons is quite similar; thermal conductivity increases with increasing pressure. The temperature coefficient of thermal conductivity at constant pressure, (∂λ/∂T) p , is positive at low pressures and becomes negative at high pressures. Therefore, the thermal conductivity isotherms of each refrigerant intersect each other in a specific range of pressure. A steep enhancement of thermal conductivity is observed near the critical point. The experimental results are statistically analyzed and the thermal conductivities are expressed as functions of temperature and pressure and of temperature and density.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 3 (1982), S. 201-215 
    ISSN: 1572-9567
    Keywords: density ; isothermal compressibility ; Tait equation ; thermal conductivity ; thermal expansion coefficient ; toluene ; transient hot-wire method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract New experimental data on the thermal conductivity and the density of liquid toluene are presented in the temperature range 0–100°C at pressures up to 250 MPa. The measurements of thermal conductivity were performed with a transient hot-wire apparatus on an absolute basis with an inaccuracy less than 1.0%. The density was measured with a high-pressure burette method with an uncertainty within 0.1%. The experimental results for both properties are represented satisfactorily by the Tait-type equations, as well as empirical polynomials, covering the entire ranges of temperature and pressure. Furthermore, it is found that simple relations exist between the temperature dependence of thermal conductivity and the thermal expansion coefficient, and also between the pressure dependence of thermal conductivity and the isothermal compressibility, as are suggested theoretically.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 7 (1986), S. 1023-1031 
    ISSN: 1572-9567
    Keywords: dimensional analysis ; fluorocarbon ; gas mixture ; generalized correlation ; principle of corresponding states ; refrigerant ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A new generalized correlation is presented for the low-pressure gaseous viscosity of fluorocarbon refrigerants. The following empirical equation is obtained based on the most reliable experimental data for 16 fluorocarbons: $$\eta \xi = \left( {0.5124T_r - 0.0517} \right)^{0.82} Z_c ^{ - 0.81}$$ where η is the viscosity in μPa·s and ξ is the viscosity parameter defined using the critical temperature T c in K, the critical pressure P c in MPa, and the molar mass M in g·mol−1 as follows: $$\xi = T_c ^{1/6} M^{ - 1/2} P_c ^{ - 2/3}$$ The applicable ranges are 0.6〈T r〈1.8 and 0.253〈Z c〈0.282. The availability of the correlating equation for both pure fluorocarbons and their mixtures has been investigated based on the experimental data of these authors and those in the literature. It is found that the present correlation is useful for the prediction of the viscosity of pure fluorocarbons and their binary mixtures at atmospheric pressure with mean deviations less than 1.6%.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 8 (1987), S. 147-163 
    ISSN: 1572-9567
    Keywords: alcohols ; aqueous alcohol solutions ; ethanol ; free-volume theory ; methanol ; 2-methyl-2-propanol ; pressure effect ; propanol ; Tait equation ; t-butyl alcohol ; viscosity ; water
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract New experimental viscosity data are presented for aqueous solutions of methanol, ethanol, 1-propanol, 2-propanol, and 2-methyl-2-propanol (t-butyl alcohol) in the temperature range from 283 to 348 K and pressures up to 120 MPa. The viscosity measurements were performed using a falling-cylinder viscometer on a relative basis with an uncertainty of less than 2%. The viscosity of pure alcohols and aqueous solutions is found to increase almost linearly with increasing pressure, whereas that of water decreases slightly with pressure at temperatures below 298 K. As for the composition dependence of the viscosity, a distinct maximum appears near 0.3–0.4 mole fraction of alcohol on all isobars at each temperature. The viscosity maximum shifts gradually to a higher alcohol concentration with increasing temperature and pressure. The isobars of aqueous 2-propanol and 2-methyl-2-propanol solutions have another shallow minimum near 0.9 mole fraction of alcohol below 323 K. The experimental results were analized empirically by a Tait-type equation and a free-volume theory. It was found that the isothermal viscosity data were satisfactorily correlated by these equations as functions of pressure and composition or of density and composition.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 10 (1989), S. 885-897 
    ISSN: 1572-9567
    Keywords: decanol ; density ; dodecanol ; hexadecanol ; hexanol ; high pressure ; isothermal compressibility ; octanol ; Tait equation ; tetradecanol ; thermal expansion coefficient
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Molar volumes, thermal expansion coefficients, and isothermal compressibilities of six higher 1-alkanols (1-hexanol, 1-octanol, 1-decanol, 1-dodecanol, 1-tetradecanol, and 1-hexadecanol) have been determined at temperatures from 298 to 348 K and pressures up to 40 MPa. The density measurements were performed using a vibrating densitometer with an uncertainty of ±0.06%. The relationship between the properties and the structures of these alkanols is discussed in terms of the carbon-chain lengths.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 8 (1987), S. 47-70 
    ISSN: 1572-9567
    Keywords: alcohols ; aqueous mixtures ; butanols ; compressibility ; ethanol ; excess volume ; high pressure ; methanol ; propanols ; specific volume ; Tait equation ; water
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The specific volumes of C1-C4 alcohols and binary mixtures of water with methanol, ethanol, 1-propanol, 2-propanol, and 2-methyl-2-propanol are presented as functions of temperature, pressure, and composition. The measurements were carried out using a modified Adams piezometer and a high-pressure burette method in a temperature range from 283.15 to 348.15 K at pressures up to 350 MPa. The uncertainties in the specific volume obtained are estimated to be less than 0.09%. The specific volumes of the pure alcohols and their mixtures with water are found to decrease monotonously with increasing pressure. The numerical P-V relations at each temperature and composition are correlated satisfactorily as a function of pressure by the Tait equation. Definite inflections appear on the isobars of isothermal compressibility or partial molar volume versus composition of alcohol + water mixtures.
    Type of Medium: Electronic Resource
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