2012
DOI: 10.1016/j.fluid.2011.11.022
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Experimental study of the density and viscosity of polyethylene glycols and their mixtures at temperatures from 293K to 465K and at high pressures up to 245MPa

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Cited by 49 publications
(43 citation statements)
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“…We estimate the uncertainty is 4 % for the liquid phase between 288 K and 373 K at atmospheric pressure. The data of Sagdeev et al (Sagdeev, Fomina, Mukhamedzyanov, & Abdulagatov, 2012) extend to very high pressures (245 MPa) and we show comparisons up to 50 MPa. The highpressure data were not used in the regression, as we were unable to find parameters that fit the high-pressure data, and we limit the use of the equation to 10 MPa.…”
Section: Ethylene Glycolsupporting
confidence: 68%
“…We estimate the uncertainty is 4 % for the liquid phase between 288 K and 373 K at atmospheric pressure. The data of Sagdeev et al (Sagdeev, Fomina, Mukhamedzyanov, & Abdulagatov, 2012) extend to very high pressures (245 MPa) and we show comparisons up to 50 MPa. The highpressure data were not used in the regression, as we were unable to find parameters that fit the high-pressure data, and we limit the use of the equation to 10 MPa.…”
Section: Ethylene Glycolsupporting
confidence: 68%
“…, the measured values of the viscosity of oleic acid decrease rapidly as the temperature initially increases above 293 K. At high temperatures, the viscosity asymptotically approaches a high‐temperature limit ( η → η ∞ ). In general, the same temperature behavior of the viscosity was found for all studied liquids (see, for example, our previous studies Sagdeev et al, , , , , , , , , , , ; Usmanov et al, ).…”
Section: Resultssupporting
confidence: 81%
“…where b 0 is the viscosity (mPa s), η = η ∞ , at the high temperature limit ( T → ∞, i.e., viscosity of the system in the vapor state); b 1 = ε a / R (viscosity Arrhenius energy), and ε a = Δ H are the flow activation energy (enthalpy of activation, related to the enthalpy of vaporization), where T is in K. This equation was used previously by many authors to represent the temperature dependence of the experimental viscosity data for different types of molecular liquids and liquid mixtures (see, for example our previous publications Sagdeev et al, , , , , , , , , , , ; Usmanov et al, ). However, very limited simple pure and binary systems obey the linear Arrhenius behavior (Eq. )…”
Section: Resultsmentioning
confidence: 99%
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