Enthalpies of Mixing of Multicomponent Alkane Mixtures

1988 ◽  
Vol 41 (11) ◽  
pp. 1763 ◽  
Author(s):  
TJ Brady ◽  
S Weiguo ◽  
AG Williamson
Keyword(s):  
Chain Length ◽  
Binary Mixtures ◽  
Ternary Mixtures ◽  
Enthalpies Of Mixing

Enthalpies of mixing are reported for ternary n-alkane mixtures prepared from binary mixtures with large chain-length differences and at temperatures where the enthalpies of mixing of simple binary mixtures show changes of sign. In neither case does the behaviour of the ternary mixtures deviate significantly from that of the congruent binaries.

Catalytic hydrogenation of binary and ternary mixtures of unsaturated substances in the liquid phase on platinum

1979 ◽  
Vol 44 (8) ◽  
pp. 2378-2383 ◽  
Author(s):  
Libor Červený ◽  
Radka Junová ◽  
Vlastimil Růžička
Keyword(s):  
Liquid Phase ◽  
Binary Mixtures ◽  
Silica Gel ◽  
Catalytic Hydrogenation ◽  
Ternary Systems ◽  
Ternary Mixtures ◽  
Unsaturated Alcohol ◽  
Solvent Concentration ◽  
Binary And Ternary Mixtures ◽  
Hydrogenation Selectivity

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.

Solvation of ions by dipolar aprotic solvents and water. A CNDO/2 study

1985 ◽  
Vol 50 (11) ◽  
pp. 2493-2508 ◽  
Author(s):  
Petr Kyselka ◽  
Zdeněk Havlas ◽  
Ivo Sláma
Keyword(s):  
Binary Mixtures ◽  
Quantum Chemical ◽  
Chemical Method ◽  
Molecular Structures ◽  
Dimethyl Sulphoxide ◽  
Ternary Mixtures ◽  
Aprotic Solvents ◽  
Quantum Chemical Method ◽  
Solvation Of Ions ◽  
Dipolar Aprotic Solvents

Solvation of Li+, Be2+, Na+, Mg2+, and Al3+ ions has been studied in binary mixtures with dimethyl sulphoxide, dimethylformamide, acetonitrile and water, and in ternary mixtures of the organic solvents with water. The CNDO/2 quantum chemical method was used to calculate the energies of solvation, molecular structures and charge distributions for the complexes acetonitrile...ion (1:1, 2:1, 4:1), dimethyl sulphoxide...ion (1:1), dimethylformamide...ion (1:1), and acetonitrile (dimethyl sulphoxide, dimethylformamide)...ion...water (1:1:1).

Induced Smectic Phases I. Polymorphism in Binary Mixtures of Alkyloxybenzylidene-alkylanilines with Alkyl- and Alkyloxy- cyanobiphenyls

1981 ◽  
Vol 36 (1) ◽  
pp. 62-67 ◽  
Author(s):  
F. Schneider ◽  
N. K. Sharma
Keyword(s):  
Chain Length ◽  
Binary Mixtures ◽  
Transition Temperatures ◽  
Mean Values ◽  
Smectic Phases ◽  
The Mean ◽  
Induced Smectic Phases

The diagrams of state of mixtures of 4-n-alkyloxybenzylidene-4'-n-butylanilines with 4-n- alkyl- and 4-n-alkyloxy-4'-cyanobiphenyls are studied. The mixtures form induced smectic phases of type SA, SB and SE. In all three smectic phases the thickness of the smectic layers agrees with the mean values of the molecular lengths. In most cases the induced SA phases do not show uninterrupted miscibility with the SA phases of the pure components. For instance, the system 40 • 4/8 CBP exhibits three separate SA phase areas. The maximum transition temperatures of the induced smectic phases increase with increasing chain length of the azomethines, but remain constant in case of the SA and SB phases or even decrease in case of the SE phases with increasing chain length of the cyanobiphenyls

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