Excess volumes of binary mixtures of cyclohexanone with some monosubstituted benzenes at 298.15 K

1983 ◽  
Vol 61 (9) ◽  
pp. 2147-2150 ◽  
Author(s):  
B. Chawla ◽  
S. K. Mehta ◽  
R. V. Jasra ◽  
S. K. Suri
Keyword(s):  
Binary Mixtures ◽  
Molecular Interactions ◽  
Composition Range ◽  
Excess Volumes ◽  
Entire Composition Range ◽  
Density Data ◽  
Molar Excess ◽  
Monosubstituted Benzenes ◽  
Molar Excess Volumes ◽  
Experimental Density

Molar excess volumes for the binary mixtures of cyclohexanone with benzene and some monosubstituted benzenes, namely, toluene, ethylbenzene, isopropylbenzene, tertiary butylbenzene, chlorobenzene, bromobenzene, iodobenzene, N,N-dimethylaniline, nitrobenzene, benzaldehyde, and benzonitrile have been calculated from the precise and accurate experimental density data at 298.15 K over the entire composition range. The results have been discussed in terms of the strength of molecular interactions in the binary mixtures.

Excess volumes of binary mixtures of tetrahydrofuran with various hydrocarbons at 313.15 K

1981 ◽  
Vol 59 (19) ◽  
pp. 2839-2844 ◽  
Author(s):  
S. K. Suri
Keyword(s):  
Binary Mixtures ◽  
Molecular Geometry ◽  
Excess Volumes ◽  
Systematic Variation ◽  
Density Data ◽  
Molar Excess ◽  
Molar Excess Volumes ◽  
Experimental Density

Molar excess volumes of binary mixtures of tetrahydrofuran with n-propylbenzene, isopropylbenzene, 1,3,5-trimethylbenzene, 1,2,3,4-tetramethylbenzene, diphenylmethane, n-hexane, n-octane, 2,2,4-trimethylpentane, n-nonane, 3,3-diethylpentane, n-dodecane, 2,2,4,6,6-pentamethylheptane, cyclohexane, and methylcyclohexane at 313.5 K have been computed from the experimental density data. The systematic variation of VE with the change in size, substitution, and molecular geometry of the hydrocarbon has been discussed.

Volumetric studies on binary mixtures of some furan derivatives with benzene, chlorobenzene, and bromobenzene at 298.15 K

1989 ◽  
Vol 67 (10) ◽  
pp. 1672-1675 ◽  
Author(s):  
Homendra Naorem ◽  
S. K. Suri
Keyword(s):  
Aromatic Ring ◽  
Binary Mixtures ◽  
Furfuryl Alcohol ◽  
Composition Range ◽  
Heterocyclic Ring ◽  
Excess Volumes ◽  
Furan Derivatives ◽  
Π Interactions ◽  
Molar Excess Volumes ◽  
Experimental Density

Molar excess volumes for the binary mixtures of tetrahydrofuran, furan, furfural, and furfuryl alcohol with benzene, chlorobenzene, and bromobenzene have been calculated from precise experimental density data at 298.15 K over the entire composition range. The results have been discussed in light of unlike n–π interactions between the π-electron cloud of the aromatic ring and the oxygen atom of the heterocyclic ring. The substitution of a halogen atom in the aromatic ring activates the molecule for n–π interactions in tetrahydrofuran and furan solutions and deactivates the molecule in furfural and furfuryl alcohol solutions. Keywords: furan derivatives, binary mixtures, excess volumes, n–π interactions, π–π interactions.

Topological and thermodynamic investigations of molecular interactions in binary mixtures: Molar excess volumes and molar excess enthalpies

2005 ◽  
Vol 235 (1) ◽  
pp. 42-49 ◽  
Author(s):  
Sanjeev Maken ◽  
Bal Raj Deshwal ◽  
Renu Chadha ◽  
Anu ◽  
Krishan Chander Singh ◽  
...  
Keyword(s):  
Binary Mixtures ◽  
Molecular Interactions ◽  
Excess Volumes ◽  
Excess Enthalpies ◽  
Molar Excess ◽  
Molar Excess Volumes

Thermodynamics of binary mixtures of 1,2-dichloroethane with aromatic hydrocarbons

1980 ◽  
Vol 58 (18) ◽  
pp. 1902-1905 ◽  
Author(s):  
Ram K. Nigam ◽  
Prem P. Singh ◽  
Krishan C. Singh ◽  
Mohan Singh ◽  
Ruchi Mishra
Keyword(s):  
Binary Mixtures ◽  
Aromatic Hydrocarbons ◽  
Vapour Pressure ◽  
Excess Volumes ◽  
Equimolar Mixture ◽  
Excess Enthalpies ◽  
Molar Excess ◽  
Experimental Values ◽  
Molar Excess Volumes

Molar excess volumes, VE at 298.15 and 308.15 K, molar excess enthalpies HE at 308.15 K, and total vapour pressure at 298.15 and 308.15 K. have been measured for binary mixtures of 1,2-dichloroethane with aromatic hydrocarbons. The VE and HE data for an equimolar mixture at 308.15 K only have been utilized to predict VE, HE, and TSE values (using Sanchez and Lacombe theory) for these mixtures as a function of temperature and composition. The agreement between the predicted and the corresponding experimental values is good so far as VE and HE data are concerned but the same is not true of the TSE values.

Pycnometric determination of densities and excess volumes of binary mixtures containing at least one associating component

1990 ◽  
Vol 55 (10) ◽  
pp. 2395-2403 ◽  
Author(s):  
Kamila Chýlková ◽  
Ivona Malijevská
Keyword(s):  
Acetic Acid ◽  
Propionic Acid ◽  
Binary Mixtures ◽  
Trifluoroacetic Acid ◽  
Excess Volume ◽  
Excess Volumes ◽  
Molar Excess ◽  
Molar Excess Volumes

Densities at 20 °C and molar excess volumes calculated from them are reported in the work for the mixtures of the substances: propionic acid-n-heptane, propionic acid-benzene, trifluoroacetic acid-benzene, propionic acid-cyclohexane, acetic acid-cyclohexane, acetic acid-trifluoroacetic acid, acetic acid-propionic acid, and propionic acid-trifluoroacetic acid. For the last system mentioned, a strange dependence of excess volume on composition was found which is noted for three local extremes. The dependences of excess volume on composition are correlated by the Redlich-Kister polynomial.

Excess volumes of toluene mixtures with some alcohols at 303.15 K

1980 ◽  
Vol 58 (3) ◽  
pp. 229-230 ◽  
Author(s):  
Goolla Narayana Swamy ◽  
Golla Dharmaraju ◽  
Gurajala Kodanda Raman
Keyword(s):  
Binary Mixtures ◽  
Excess Volume ◽  
Composition Range ◽  
Excess Volumes ◽  
Entire Composition Range ◽  
Dilatometric Method

Excess volumes for binary mixtures of toluene with 1-propanol, 2-propanol, 1-butanol, 2-methyl-1-propanol, 1-pentanol, 1-hexanol, 1-heptanol, and cyclohexanol have been measured as a function of composition at 303.15 K by a dilatometric method. The excess volume curves for 1-propanol and 1-butanol are sigmoid. For other alcohols VE values are positive over the entire composition range.

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