scholarly journals Comparison between surface and volumetric properties of short-chain alcohols and some classical surfactants

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>

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.


1979 ◽  
Vol 24 (6) ◽  
pp. 1022-1030 ◽  
Author(s):  
Dj. Dragcevic ◽  
M. Vukovic ◽  
D. Cukman ◽  
V. Pravdic

1991 ◽  
pp. 277-292 ◽  
Author(s):  
D. K. Chattoraj ◽  
L. N. Ghosh ◽  
P. K. Mahapatra

Clay Minerals ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 499-510 ◽  
Author(s):  
Ph. Refait ◽  
C. Bon ◽  
L. Simon ◽  
G. Bourrié ◽  
F. Trolard ◽  
...  

AbstractThe redox potential and pH of aerated suspensions of iron(II) hydroxide in sulphate–containing aqueous solutions are measured during the oxidation process. Plateaux corresponding to the equilibrium conditions between Fe(OH)2(s) and Fe(II)-Fe(III) hydroxysulphate GR2(SO2-4)(s) on the one hand, and between GR2(SO2-4)(s) and FeOOH(s) on the other hand, are displayed. Potentiometry, voltammetry, pH-metry and Mössbauer spectroscopy are applied to follow all reactions. The thermodynamic meaning of the measured potential of the first plateau which corresponds to the GR2(SO2-4)(s)/Fe(OH)2(s) equilibrium is demonstrated. The chemical composition of GR2(SO2-4)(s) is found to be FeII4 FeIII2(OH)12SO4·nH2O all along the oxidation process, implying that this compound must be considered as a pure phase with a well-defined composition. The Gibbs standard free energy of formation or chemical potential μ°[GR2(SO2-4)(s)] in ‘anhydrous form’ (n = 0) is determined at −3790±10 kJ mol-1. A consistent value of μ°[Fe(OH)2(s)] at −490±1 kJ mol-1 is obtained.


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