Liquid phase PVTx properties of (water+tert-butanol) binary mixtures at temperatures from 278.15 to 323.15K and pressures from 0.1 to 100MPa. II. Molar isothermal compressions, molar isobaric expansions, molar thermal pressure coefficients, and internal pressure

2013 ◽  
Vol 61 ◽  
pp. 169-179 ◽  
Author(s):  
Gennadiy I. Egorov ◽  
Dmitriy M. Makarov ◽  
Arkadiy M. Kolker
1979 ◽  
Vol 57 (23) ◽  
pp. 3135-3139
Author(s):  
R. Philippe ◽  
Z. Ferhat-Hamida ◽  
J. C. Merlin

An apparatus for the measurement of thermal pressure coefficients of pure compounds is described. The thermal pressure coefficient β of n-thiaalkanes R2S (R = CH3, C2H5, n-C3H7, n-C4H9, n-C7H15) and of dithiaalkanes R2S2 (R = CH3, C2H5, iso-C3H7) were measured at 298.15 K and at zero pressure. These experimental results in conjunction with data from literature for other compounds are compared using the reduced parameter of pressure P* proposed by Flory. The P* do not have regular values for the lower members of thiaalkanes series. One explanation of these irregularities is the different size of the molecules.


1979 ◽  
Vol 44 (8) ◽  
pp. 2378-2383 ◽  
Author(s):  
Libor Červený ◽  
Radka Junová ◽  
Vlastimil Růžička

Hydrogenation of olefinic substrates in binary and ternary mixtures using 5% Pt on silica gel as the catalyst was studied in normal conditions in the liquid phase with methanol or cyclohexane or in solvent-free systems. The effect of the solvent concentration on the selectivity of hydrogenation of the unsaturated alcohol-olefin binary mixtures was investigated. In ternary systems of unsaturated substrates, the effect of each of the substrates on the selectivity of hydrogenation of the remaining two substances was examined. Another system was found in which a jump change of the hydrogenation selectivity occurred on the vanishing of the fastest reacting substance.


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