Molar heat capacities of solvents used in CO2 capture: A group additivity and molecular connectivity analysis

2011 ◽  
Vol 90 (2) ◽  
pp. 367-376 ◽  
Author(s):  
Aravind V. Rayer ◽  
Amr Henni ◽  
Paitoon Tontiwachwuthikul
Keyword(s):  
Co2 Capture ◽  
Heat Capacities ◽  
Group Additivity ◽  
Connectivity Analysis ◽  
Molecular Connectivity

Molar heat capacities of alkanolamines from 299.1 to 397.8 K Group additivity and molecular connectivity analyses

1997 ◽  
Vol 93 (9) ◽  
pp. 1747-1750 ◽  
Author(s):  
Yadollah Maham ◽  
Loren G. Hepler ◽  
Alan E. Mather ◽  
Andrew W. Hakin ◽  
Robert A. Marriott
Keyword(s):  
Heat Capacities ◽  
Group Additivity ◽  
Molecular Connectivity

Heats of vaporization and gaseous heats of formation of some five- and six-membered ring alkenes

1979 ◽  
Vol 57 (17) ◽  
pp. 2302-2304 ◽  
Author(s):  
Richard Fuchs ◽  
L. Alan Peacock
Keyword(s):  
Gas Chromatography ◽  
Double Bond ◽  
Heat Capacities ◽  
Membered Ring ◽  
Heats Of Formation ◽  
Group Additivity ◽  
Liquid Heat ◽  
Heats Of Vaporization

The heats of vaporization of 1-methylcyclopentene, 3-methylcyclopentene, ethylidenecyclopentane, 1-ethylcyclopentene, methylenecyclohexane, allylcyclopentane, vinylcyclohexane, ethylidenecyclohexane, allylcyclohexane, 3,3-diethylpentane, 2,2,4,4-tetramethylpentane, and trans-2,2,5,5-tetramethyl-3-hexene have been measured by the gas chromatography – calorimetry method. These values have been combined with previously reported liquid heats of formation to give gaseous values of ΔHf. The results indicate that the internal double bond is favored by about 0.5 kcal over the exo in both 5- and 6-membered rings, but the endo–exo differences are much smaller than previously believed. Several of the liquid heat capacities that were measured were not well predicted by group additivity schemes.

Molecular Connectivity Analysis of Hallucinogenic Mescaline Analogs

1979 ◽  
Vol 68 (7) ◽  
pp. 906-907 ◽  
Author(s):  
R.A. Glennon ◽  
L.B. Kier ◽  
A.T. Shulgin
Keyword(s):  
Connectivity Analysis ◽  
Molecular Connectivity

Heat Capacities of Some Alkyl Acetates at 295-323 K

1997 ◽  
Vol 62 (10) ◽  
pp. 1527-1532 ◽  
Author(s):  
Václav Svoboda ◽  
Kornelia Gottmanová ◽  
Vladimír Hynek ◽  
Bohumír Koutek
Keyword(s):  
Experimental Data ◽  
Linear Function ◽  
Atmospheric Pressure ◽  
Heat Capacities ◽  
Group Additivity ◽  
Temperature Range ◽  
Alkyl Acetates

Molar heat capacities Cp,m at constant atmospheric pressure have been determined with a typical uncertainty of about 0.3% for eight liquid alkyl acetates H(CH2)nOCOCH3 (n = 6-12, 14), over the temperature range 295-323 K. The Cp,m values were found to be a linear function of temperature. A comparison of experimental data with those predicted by the group additivity method demonstrated a rather limited capability of the additivity scheme to predict correctly the Cp,m values for higher (n > 10) homologues in the series.

Apparent molar heat capacities and volumes of unsaturated heterocyclic solutes in aqueous solution at 25 °C

1980 ◽  
Vol 58 (7) ◽  
pp. 704-707 ◽  
Author(s):  
Octavian Enea ◽  
Carmel Jolicoeur ◽  
Loren G. Hepler
Keyword(s):  
Aqueous Solution ◽  
Aqueous Solutions ◽  
Heterocyclic Compounds ◽  
Infinite Dilution ◽  
Heat Capacities ◽  
Group Additivity ◽  
Standard State ◽  
Apparent Molar Heat Capacities ◽  
Partial Molar Heat Capacities

Measurements at 25 °C with flow calorimeters and densimeters have led to heat capacities and densities of aqueous solutions of 15 unsaturated heterocyclic compounds containing nitrogen. From the results of these measurements we have obtained apparent molar heat capacities and volumes of the solutes. Extrapolations to infinite dilution have led to corresponding standard state apparent and partial molar heat capacities and volumes, which have been analyzed in terms of atomic and group additivity relationships.

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