Comparison of two methods to estimate the standard free energy of adsorption

2002 ◽  
Vol 5 (3) ◽  
pp. 281-286 ◽  
Author(s):  
R. Miller ◽  
V. B. Fainerman ◽  
H. Möhwald
1991 ◽  
pp. 277-292 ◽  
Author(s):  
D. K. Chattoraj ◽  
L. N. Ghosh ◽  
P. K. Mahapatra

Author(s):  
Magdalena Bielawska ◽  
Anna Zdziennicka ◽  
Bronisław Jańczuk

<p>Measurements of the dynamic surface tension of the aqueous solutions of methanol, ethanol, propanol, CTAB and SDDS at their given concentrations were made. From the obtained results and the literature data it was concluded that the adsorption of short-chain alcohols at the water-air interface is somewhat similar to that of classical surfactants. For that reason the relationship between the Gibbs standard free energy of adsorption of short-chain alcohols and classical surfactants at that interface was established. The correlation between the chemical potential of mixing of alcohols and surfactants was also analysed. This analysis concerned the critical aggregation concentration (CAC) of alcohols and the critical micelle concentration (CMC) of surfactants. The chemical potential of surfactant mixing was calculated from the literature CMC data for the homologous series of alkyl sulfates, alkyl sulfonates, alkyl ammonium chlorides, alkyl trimethylammonium bromides, and alkyl pyridinium bromides. The influence of the hydrophobic chain length of alcohol and surfactant molecules on the Gibbs standard free energy of their adsorption at the water-air interface and their chemical potential of mixing were considered. It appeared that there is a linear dependence between these thermodynamic functions and the number of carbon atoms increased by 1 in the hydrocarbon chains of these compounds. This confirms clearly our conclusion that the behaviour of short-chain alcohols and classical surfactants at the water-air interface and in the bulk phase of aqueous solutions is similar. </p>


1985 ◽  
Vol 63 (10) ◽  
pp. 2742-2746 ◽  
Author(s):  
Robert Aveyard ◽  
Neil Carr ◽  
Helen Slezok

Surface pressure–area isotherms have been obtained for mono- and dioxyethylene dodecyl ethers both spread at the air–water surface and adsorbed at the heptane–water interface and results are compared with those for straight chain alkanols. At the heptane–water interface it appears that the ethyleneoxy groups are disposed parallel to the interface in fairly dilute films. The dual hydrophilic/hydrophobic nature of isolated CH2CH2O groups is demonstrated by showing that they give a negative contribution to the standard free energy of adsorption from both water and heptane to the heptane–water interface.


1995 ◽  
Vol 10 (2) ◽  
pp. 339-344 ◽  
Author(s):  
C. Galassi ◽  
E. Rastelli ◽  
E. Roncari ◽  
S. Ardizzone ◽  
M.G. Cattania

Two commercial Si3N4 powders were mixed with Al2O3 and Y2O3 through coprecipitation of the oxides from solutions of nitrates. The samples were characterized by XPS spectroscopy and electrophoretic mobility determinations on the suspensions. Sedimentation tests indicated that an oxylignin-based polyelectrolyte proved effective in the dispersion of the powders. The adsorption of the deflocculant followed Langmuir type isotherms characterized by values of the standard free energy of adsorption in the range typical of physisorption processes. The results of the different characterizations are discussed point by point, and different localizations of the dispersant in the interfacial region of the different samples are proposed.


Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4313
Author(s):  
Bronisław Jańczuk ◽  
Katarzyna Szymczyk ◽  
Anna Zdziennicka

Measurements were made of the surface tension of the aqueous solutions of p-(1,1,3,3-tetramethylbutyl) phenoxypoly(ethylene glycols) having 10 oxyethylene groups in the molecule (Triton X-100, TX100) and cetyltrimethylammonium bromide (CTAB) with Zonyl FSN-100 (FC6EO14, FC1) as well as with Zonyl FSO-100 (FC5EO10, FC2) ternary mixtures. The obtained results were compared to those provided by the Fainerman and Miller equation and to the values of the solution surface tension calculated, based on the contribution of a particular surfactant in the mixture to the reduction of water surface tension. The changes of the aqueous solution ternary surfactants mixture surface tension at the constant concentration of TX100 and CTAB mixture at which the water surface tension was reduced to 60 and 50 mN/m as a function of fluorocarbon surfactant concentration, were considered with regard to the composition of the mixed monolayer at the water-air interface. Next, this composition was applied for the calculation of the concentration of the particular surfactants in the monolayer using the Frumkin equation. On the other hand, the Gibbs surface excess concentration was determined only for the fluorocarbon surfactants. The tendency of the particular surfactants to adsorb at the water-air interface was discussed, based on the Gibbs standard free energy of adsorption which was determined using different methods. This energy was also deduced, based on the surfactant tail surface tension and tail-water interface tension.


Holzforschung ◽  
2002 ◽  
Vol 56 (1) ◽  
pp. 91-97
Author(s):  
Kei Morisato ◽  
Yutaka Ishimaru ◽  
Hiroyuki Urakami

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.


1998 ◽  
Vol 120 (5) ◽  
pp. 1062-1069 ◽  
Author(s):  
David W. Hatchett ◽  
Rory H. Uibel ◽  
Keith J. Stevenson ◽  
Joel M. Harris ◽  
Henry S. White

Sign in / Sign up

Export Citation Format

Share Document