J.T. Sipowska
Brigham Young University
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The Journal of Chemical Thermodynamics | 1989
J.T. Sipowska; R.C Graham; B.J. Neely; J.B. Ott; Reed M. Izatt
Abstract Excess molar enthalpies HmE have been determined for (ethane + methanol) at 298.15, 323.15, and 348.15 K and at pressures of 7.5 and 15 MPa. Measurements were also made at 323.15 K at 10 MPa. (Ethane + methanol) is a type-III system (Scott and van Konynenburgs classification) which is distinguished by a discontinuous critical curve. The results reported in this paper span the critical locus so that miscible mixtures form at the highest pressure, but (liquid + liquid) or (vapor + liquid) phase separations are present at the lower pressures. The HmE results correlate well with the phase-equilibria description and are used to predict the (vapor + liquid) equilibrium curve at 7.5 MPa.
The Journal of Chemical Thermodynamics | 1990
J.T. Sipowska; J.B. Ott; A.T. Woolley; Reed M. Izatt
Abstract Excess molar enthalpies H m E are reported for (propane + propan-1-ol) at temperatures of (298.15, 323.15, 363.15, and 368.15) K and pressures of 5 MPa and 15 MPa. The results are explained in terms of chemical, physical, and structural effects and compared with the UNIFAC-2 prediction.
The Journal of Chemical Thermodynamics | 1991
J.B. Ott; J.T. Sipowska; Reed M. Izatt
Excess molar enthalpies H E m have been determined for (propane + acetonitrile) at the temperatures (298.15, 313.15, 323.15, 333.15, 338.15, and 348.15) K and at the pressures (5, 10, and 15) MPa. The linear regions of H E m against x at 298.15 K, 313.15 K, and 323.15 K at all three pressures and at 333.15 K at 5 MPa and 10 MPa, are due to (liquid + liquid) phase separation. The T ( x ) values obtained from the discontinuity in the H E m curves were used to construct the (liquid + liquid) phase diagram.
The Journal of Chemical Thermodynamics | 1991
J.T. Sipowska; J.B. Ott; B.J. Neely; Reed M. Izatt
Excess molar enthalpies HEm for (propane + methanol) have been determined at the temperatures (298.15, 323.15, 348.15, and 373.15) K and at the pressures (5, 10, and 15) MPa. Measurements were also made at 363.15 K and (5 and 15) MPa. (Propane + methanol) is a type-II mixture (Scott and van Konynenburgs classification) with a (liquid + liquid) phase separation at lower temperatures. The measurements reported in this paper were performed at temperatures and pressures at which both components were liquids and where phase separation does not occur.
The Journal of Chemical Thermodynamics | 1990
J.T. Sipowska; J.B. Ott; A.T. Woolley; Reed M. Izatt
Abstract Excess molar enthalpies H m E are reported for (ethane + ethanol) at the temperatures (298.15, 323.15, and 348.15) K and at pressures of (5, 10, and 15) MPa. According to Scott and van Konynenburgs classification, (ethane + ethanol) is a type V mixture which is distinguished by a discontinuous critical curve and a miscibility gap with upper and lower critical end points. The measurements have been made at temperatures and pressures that span the critical locus. At 10 MPa and 15 MPa, miscible mixtures are formed at all three temperatures over the entire range of composition, but (vapor + liquid) phase separation occurs at the higher temperatures at 5 MPa. The results are explained in terms of chemical, physical, and structural effects.
The Journal of Chemical Thermodynamics | 1992
J.T. Sipowska; J.B. Ott; A.T. Woolley; Reed M. Izatt
Excess molar enthalpies H E m for (butane + methanol) have been measured at the temperatures (298.15, 323.15, and 348.15) K and at the pressures (5 and 15) MPa. (Liquid + liquid) phase separation occurs for this mixture at lower temperatures with the (liquid + liquid) and (liquid + gas) critical lines separated. Reported measurements were performed at temperatures and pressures at which the two liquid components form a homogenous liquid mixture.
The Journal of Chemical Thermodynamics | 1992
J.B. Ott; J.T. Sipowska; A.T. Woolley; Reed M. Izatt
Excess molar enthalpies are reported for (propane + butan-1-ol) at the temperatures 298.15 K and 323.15 K, and the pressures 5 MPa and 15 MPa, and at 348.15 K and 363.15 K, and 5 MPa, 10 MPa, and 15 MPa. The results are explained in terms of chemical, physical, and structural effects and compared with the UNIFAC-2 prediction.
The Journal of Chemical Thermodynamics | 1992
A.T. Woolley; J.T. Sipowska; J.B. Ott; Reed M. Izatt
Excess molar enthalpies HEm have been determined for (butane + acetonitrile) at the temperatures T = (298.15, 323.15, and 348.15) K and at the pressures p = (5, 10, and 15) MPa. The linear regions of HEm as a function of x at T = 298.15 K and 323.15 K at all three pressures are caused by (liquid + liquid) phase separation.
Thermochimica Acta | 1994
M.S. Gruszkiewicz; J.B. Ott; J.T. Sipowska
Abstract A thermostated sapphire capillary was inserted into the exit line of a flow calorimeter. This capillary is used to visually determine the upper critical solution temperature (UCST) for acetonitrile + cyclohexane, + propane, and + butane at several pressures. The UCST results were combined with liquid + liquid results obtained earlier from breaks in the excess molar enthalpy versus mole fraction curves to obtain the liquid + liquid phase diagrams for acetonitrile + propane, and + butane at 5 and 10 MPa.
The Journal of Chemical Thermodynamics | 1996
J.B. Ott; P.R. Brown; J.T. Sipowska