Standard free energy, enthalpy, and entropy of formation of titanium hydride

1979 ◽  
Vol 24 (4) ◽  
pp. 277-279 ◽  
Author(s):  
Minoru Arita ◽  
Mayumi Someno
Keyword(s):  
Free Energy ◽  
Titanium Hydride ◽  
Standard Free Energy ◽  
Entropy Of Formation ◽  
Enthalpy And Entropy

Adsorption of Liquids and Swelling of Wood. Part VI. Saturated Amounts and Some Thermodynamic Values of Adsorption

Holzforschung ◽  
2002 ◽  
Vol 56 (1) ◽  
pp. 91-97
Author(s):  
Kei Morisato ◽  
Yutaka Ishimaru ◽  
Hiroyuki Urakami
Keyword(s):  
Free Energy ◽  
Standard Free Energy ◽  
Molecular Size ◽  
Free Energy Change ◽  
Energy Change ◽  
Multilayer Adsorption ◽  
Monolayer Adsorption ◽  
Wood Part ◽  
Cohesive Interaction

Summary To understand the swelling phenomenon of wood in liquids,the saturated amount of adsorption of liquids onto wood and the standard free energy changes of the adsorption were determined. The saturated amount of adsorption obtained by regression for several liquids decreased with increasing molecular size of the solvents. The mechanism of wood swelling is discussed systematically taking all the liquids examined in previous experiments into account. Since methanol molecules require more energy for release from cohesive interactions within bulk liquids in the adsorption onto pre-swollen wood,the values of free energy change of adsorption for methanol were lower than the values for acetone,although the relative swelling with methanol was higher. These results suggest that although the cohesive interaction within the bulk liquids reduces adsorptivity,the phenomenon of wood swelling is influenced not only by monolayer adsorption but also by multilayer adsorption. Therefore,the cohesive interaction within the bulk liquids reduces adsorptivity but enhances the condensation which strongly influences the swelling of wood.

The Equilibrium and the Determination of D00 (H—CN)

1975 ◽  
Vol 53 (16) ◽  
pp. 2365-2370 ◽  
Author(s):  
Don Betowski ◽  
Gervase Mackay ◽  
John Payzant ◽  
Diethard Bohme
Keyword(s):  
Free Energy ◽  
Standard Enthalpy ◽  
Transfer Reaction ◽  
Standard Free Energy ◽  
Proton Transfer Reaction ◽  
Enthalpy Change ◽  
Standard Free Energy Change ◽  
Flowing Afterglow ◽  
Standard Enthalpy Change

The rate constants and equilibrium constant for the proton transfer reaction [Formula: see text] have been measured at 296 ± 2 K using the flowing afterglow technique: kforward = (2.9 ± 0.6) × 10−9 cm3molecule−1s−1, kreverse = (1.8 ± 0.4) × 10−10 cm3 molecule1 s−1, and K = 16 ± 2. The measured value of K corresponds to a standard free energy change, ΔG296°, of −1.6 ± 0.1 kcal mol−1 which provides values for the standard enthalpy change, ΔH298°= −1.0 ± 0.2 kcal mol−1, the bond dissociation energy, D00(H—CN) = 124 ± 2 kcal mol−1, and the proton affinity, p.a.(CN−) = 350 ± 1 kcal mol−1.

Dielectric relaxation of some aliphatic ketones in dilute solutions

1976 ◽  
Vol 54 (7) ◽  
pp. 794-799 ◽  
Author(s):  
M. P. Madan
Keyword(s):  
Free Energy ◽  
Relaxation Time ◽  
Dielectric Relaxation ◽  
Relaxation Mechanism ◽  
Relaxation Data ◽  
Nonpolar Solvents ◽  
Aliphatic Ketones ◽  
Entropy Of Activation ◽  
Enthalpy And Entropy ◽  
Dielectric Relaxation Behavior

The dielectric relaxation behavior of 2-butanone, 2-pentanone, 2-heptanone, and 3-nonanone in dilute nonpolar solvents, n-heptane, cyclohexane, benzene, and carbon tetrachloride has been studied in the microwave region at a number of temperatures. The relaxation data have been used to estimate the free energy, enthalpy, and entropy of activation for the relaxation mechanism. The values of the relaxation time for those solutions for which there are available known data agree well with other determinations. The results have been discussed in terms of dipole reorientation by intramolecular and overall molecular rotation and compared, wherever possible, with other similar studies on aliphatic molecules.

Standard Free Energy of Adsorption at Liquid Interfaces

1991 ◽  
pp. 277-292 ◽  
Author(s):  
D. K. Chattoraj ◽  
L. N. Ghosh ◽  
P. K. Mahapatra
Keyword(s):  
Free Energy ◽  
Standard Free Energy ◽  
Liquid Interfaces ◽  
Free Energy Of Adsorption

scholarly journals Conductivity Study of DTAB in Water and Ethanol-Water Mixture in the Presence and Absence of ZnSO4

2020 ◽  
Vol 17 (4) ◽  
pp. 1207
Author(s):  
Sangita Acharya ◽  
Tulasi Niraula ◽  
Ajaya Bhattarai
Keyword(s):  
Free Energy ◽  
Critical Micelle Concentration ◽  
Volume Fraction ◽  
Standard Free Energy ◽  
Water Mixture ◽  
Dodecyltrimethylammonium Bromide ◽  
Degree Of Dissociation ◽  
Ethanol Content ◽  
Presence And Absence ◽  
Free Energy Of Micellization

The physicochemical behaviour of dodecyltrimethylammonium bromide (DTAB) in water and ethanol-water mixture in the presence and absence of ZnSO4 were studied by measuring the conductivity at 298.15 K. The pre-micellar (S1) and post-micellar slopes (S2) were obtained and calculated the degree of dissociation (α) and the critical micelle concentration (cmc). With an increase in ethanol content, the cmc and α of DTAB increased whereas, in the presence of ZnSO4, the cmc and α decreased. By using cmc and α, thermodynamic properties as the standard free energy of micellization ( ) were evaluated. With an increase in ethanol content, the negative values of  are decreased indicating less spontaneous in the micellization which makes micellization less favourable. The correlation of the pre-micellar and post-micellar slopes with the volume fraction of ethanol were discussed. DTAB micellization was tested in contexts of specific solvent parameters and solvophobic parameter.

scholarly journals Rationalisation of the activities of phenolic (vitamin E-type) antioxidants

2003 ◽  
Vol 17 (4) ◽  
pp. 753-762
Author(s):  
Christopher J. Rhodes ◽  
Thuy T. Tran ◽  
Philip Denton ◽  
Harry Morris
Keyword(s):  
Free Energy ◽  
Vitamin E ◽  
Gibbs Free Energy ◽  
State Theory ◽  
Linear Free Energy Relationship ◽  
Free Energies ◽  
Gibbs Free Energy Change ◽  
Linear Free Energy ◽  
Free Energy Of Activation ◽  
Enthalpy And Entropy

Using Transition-State Theory, experimental rate constants, determined over a range of temperatures, for reactions of vitamin E type antioxidants are analysed in terms of their enthalpies and entropies of activation. It is further shown that computational methods may be employed to calculate enthalpies and entropies, and hence Gibbs Free Energies, for the overall reactions. Within the Linear Free Energy Relationship (LFER) assumption, that the Gibbs Free Energy of activation is proportional to the overall Gibbs Free Energy change for the reaction, it is possible to rationalise, and even to predict, the relative contributions of enthalpy and entropy for reactions of interest, involving potential antioxidants.

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