Excess volumes, viscosities, enthalpies, and Gibbs free energies for mixtures of methyl isobutyl ketone + n-pentanol and methyl isobutyl ketone + isoamyl alcohol at 298.15 K

1986 ◽  
Vol 64 (8) ◽  
pp. 1595-1598 ◽  
Author(s):  
Roque Riggio ◽  
Hector E. Martinez ◽  
Horacio N. Solimo

Three excess functions (molar volumes, viscosities, and molar enthalpies) for the methyl isobutyl ketone + n-pentanol and methyl isobutyl ketone + isoamyl alcohol systems at 298.15 K were calculated from measured densities, viscosities, and enthalpies, respectively. The UNIFAC group contribution method was used in order to estimate the activity coefficients which were then employed to calculate the excess molar Gibbs free energy. An attempt to explain the experimental results in terms of molecular interactions was made.

1992 ◽  
Vol 70 (12) ◽  
pp. 2859-2863 ◽  
Author(s):  
Roque Riggio ◽  
Hector E. Martinez ◽  
Norma Z. de Salas

From experimental densities, viscosities, and refractive indexes for the acetylacetone + 1-pentanol, + 2-Pentanol, + isoamyl alcohol, and + tert-amyl alcohol systems at 298.15 K, the excess molar volumes, excess viscosities, excess molar free energies of activation of flow, and excess internal pressures were calculated over the whole concentration range. Conclusions about the molecular interactions in these mixtures were drawn from the variations of the excess functions with the composition.


1994 ◽  
Vol 59 (10) ◽  
pp. 2227-2234 ◽  
Author(s):  
Václav Stužka ◽  
Jaromír Souček

A new method has been developed for the indirect determination of nitroso- and nitrophenols by atomic absorption spectrometry (AAS) after extraction of ionic associates involving bipyridylocopper(II) (CuDP) or phenanthrolinocopper(II) (CuPH) complexes. Nitrobenzene and methyl isobutyl ketone appeared to be suitable for the extraction. It was possible to determine several tenths to hundredths of a milligram of nitrophenol in a litre. Extractable associates with CuDP and CuPH are formed by phenols possessing two substituents or by higher molecular weight phenols such as naphthol or hydroxyquinoline. Monosubstituted phenols fail to form associates of this kind.


Author(s):  
Kalina Grzelak ◽  
Rouzana Pulikkal Thumbayil ◽  
Søren Kegnæs ◽  
Maciej Trejda ◽  
Anders Riisager

1958 ◽  
Vol 9 (1) ◽  
pp. 69-73 ◽  
Author(s):  
P. Dakshinamurty ◽  
G. Jayarama Rao ◽  
M.V.R. Acharya ◽  
C. Venkata Rao

Sign in / Sign up

Export Citation Format

Share Document