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  • viscosity  (12)
  • cyclohexane  (5)
  • methanol  (3)
  • aromatic hydrocarbons  (2)
  • compressibility  (2)
Materialart
Erscheinungszeitraum
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 10 (1989), S. 857-870 
    ISSN: 1572-9567
    Schlagwort(e): compressibility ; density ; fluorocarbon oil ; free-volume equation ; high pressure ; perfluoropolyether ; specific volume ; Tait equation ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: 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.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 12 (1991), S. 245-264 
    ISSN: 1572-9567
    Schlagwort(e): alkanes ; cyclohexane ; density ; dodecane ; hexadecane ; mixtures ; octane ; Tait equation ; viscometer ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: 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.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 3 (1982), S. 101-116 
    ISSN: 1572-9567
    Schlagwort(e): aromatic hydrocarbons ; cyclohexane ; n-alkanes ; phenyl halides ; thermal conductivity ; toluene ; transient hot-wire method
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract New experimental data on the thermal conductivity of 14 organic liquids at atmospheric pressure are presented in the temperature range from 25 to 100°C. The liquids measured are five n-alkanes (C6, C7, C8, C10, C12), cyclohexane, six aromatic hydrocarbons (benzene, ethylbenzene, o-, m-, p-xylenes, isopropylbenzene) and two phenyl halides (chloro-, bromobenzenes). The measurements were performed by a transient hot-wire method on a relative basis. The thermal conductivity of toluene, which was selected as a reference liquid, was determined on an absolute basis with another transient apparatus. The precision of the present experimental results is within ±1.2%. The uncertainty of the thermal conductivity values is estimated to be within ±2%; this includes the uncertainty of the values of toluene as the reference liquid. The experimental results for each liquid are represented satisfactorily by a linear equation in temperature. At a reduced temperature T/T c=0.5, thermal conductivity has a simple relation with the molar density for each homologous series of liquids.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 8 (1987), S. 415-424 
    ISSN: 1572-9567
    Schlagwort(e): benzene ; cyclohexane ; eutectic point ; high pressure ; solid-liquid phase equilibrium
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Solid-liquid phase equilibria of the benzene + cyclohexane system have been investigated experimentally at temperatures from 278 to 323 K and pressures up to 500 MPa using a newly designed optical vessel. The uncertainties of the measurements of temperature, pressure, and composition are within ±0.1 K, ±0.5 MPa, and ±0.001 mole fraction, respectively. The solid-liquid equilibrium pressure at a constant composition increases almost linearly with increasin temperature. The eutectic point shifts to a higher temperature and to a benzenerich composition with increasing pressure. This trend is found to agree with the direction predicted by the van Laar equation. The solid-liquid coexistence curves can be expressed by the Wilson equation with a mean deviation of 0.007 and a maximum deviation of 0.029 in mole fraction.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 9 (1988), S. 511-523 
    ISSN: 1572-9567
    Schlagwort(e): aqueous alcohol solution ; ethanediol ; ethylene glycol ; falling-cylinder viscometer ; free-volume theory ; high pressure ; pressure effect ; propanediol ; propylene glycol ; viscosity ; water
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract New experimental data on the viscosity of aqueous solutions of 1,2-ethanediol (ethylene glycol) and 1,2-propanediol (propylene glycol) are presented at 298 and 323 K under pressures up to 120 MPa. The measurements were performed by a falling-cylinder viscometer on a relative basis with an uncertainty of less than ±2%. The viscosity of these aqueous solutions at a constant temperature and pressure increases monotonously with increasing concentrations of diols (glycols) and is slightly lower than the mole fraction average value at each composition. The viscosity also increases almost linearly with pressure at a constant temperature and composition. The pressure coefficient of the viscosity, (∂η/∂P)T,x, increases with decreasing temperature and increasing concentrations of diols. The experimental results are correlated with pressure, density, and composition by several empirical equations.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 3 (1982), S. 289-305 
    ISSN: 1572-9567
    Schlagwort(e): aromatic hydrocarbons ; cyclohexane ; free volume expression ; hard-sphere theory ; high pressure ; n-alkanes ; torsionally vibrating crystal method ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract New experimental data on the viscosity of 12 organic liquids are presented at temperatures of 25, 30, 50, and 75°C and at pressures up to 110 MPa. The liquids measured are five n-alkanes (C6, C7, C8, C10, C12), cyclohexane, and six aromatic hydrocarbons (benzene, toluene, ethylbenzene, o-, m-, p-xylenes). The measurements were performed using a torsionally vibrating crystal method on a relative basis with an uncertainty less than 2%. A linear relationship between fluidity and molar volume, which is predicted from the hard-sphere theory, fails at pressures above 50 MPa. The rough hard-sphere model proposed by Chandler provides a reasonable representation of the data for aromatic hydrocarbons, while for n-alkanes the agreement is not satisfactory because of an aspherical shape of molecules. The viscosity data can be correlated well with the molar volume by a free-volume expression and also can be represented as a function of pressure by a similar expression to the Tait equation.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 12 (1991), S. 459-468 
    ISSN: 1572-9567
    Schlagwort(e): alcohols ; capillary viscometer ; methanol ; 2-methyl-2-propanol ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract A new capillary viscometer has been constructed and the viscosities of methanol, 2-methyl-2-propanol, and their mixtures have been measured at two temperatures, 303 and 323 K, and at pressures up to 30 MPa. Simple empirical equations are given to represent the pressure and composition dependences of the viscosity within the experimental uncertainty of ±2%.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 14 (1993), S. 67-77 
    ISSN: 1572-9567
    Schlagwort(e): benzene ; cyclohexane ; deuteriobenzene ; isotope effect ; molar volume ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Viscosities of binary mixtures of cyclohexane with protiobenzene, C6H6, or deuteriobenzene, C6D6, have been measured at 298 and 323 K and at pressures up to 50 MPa using a capillary viscometer. The viscosities of these mixtures obtained were represented by a empirical Tait-type equation within the experimental uncertainty of ±2%. The effect of the isotopic substitution on the viscosity has been discussed.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 7 (1986), S. 1023-1031 
    ISSN: 1572-9567
    Schlagwort(e): dimensional analysis ; fluorocarbon ; gas mixture ; generalized correlation ; principle of corresponding states ; refrigerant ; viscosity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: 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%.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 8 (1987), S. 147-163 
    ISSN: 1572-9567
    Schlagwort(e): alcohols ; aqueous alcohol solutions ; ethanol ; free-volume theory ; methanol ; 2-methyl-2-propanol ; pressure effect ; propanol ; Tait equation ; t-butyl alcohol ; viscosity ; water
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: 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.
    Materialart: Digitale Medien
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