Molecular simulation of the surface tension of simple aqueous electrolytes and the Gibbs adsorption equation

2004 ◽  
Vol 9 (1-2) ◽  
pp. 145-148 ◽  
Author(s):  
Divesh Bhatt ◽  
Raymen Chee ◽  
John Newman ◽  
C.J. Radke
Holzforschung ◽  
2004 ◽  
Vol 58 (6) ◽  
pp. 631-639 ◽  
Author(s):  
Rui Wang ◽  
Chen-Loung Chen ◽  
Josef S. Gratzl

Abstract The surface tension and interfacial tension of the F-1000, F-1800, F-5000 and F-15000 fractions obtained by ultrafiltration of the Oz-25-KL, Oz-30-KL and Oz-40-KL preparations (ozonated kraft lignin, KL, preparations with ozone consumption of 25, 30 and 40% per KL) were determined with the concentration range of 1–30 g l-1 at pH of 6, 9 and 11. The surface tension of these ozonated KL preparations decreased with increasing concentration and pH according to the simplified Gibbs adsorption equation for dilute aqueous solution, ∂γ= -RTΓ∂(ln C). The results were discussed in term of functional group contents and weight average molecular mass (Mw) of the ozonated KL preparations. The surface tension of the ozonated KL preparations decreased with increasing carboxylic acid content and, to some extent, phenolic hydroxyl content, but increased with increasing Mw. The synergistic effect of the ozonated KL preparations with a commercial surfactant was then investigated. The oil-water interfacial tension was determined in the ozonated KL preparations in an aqueous solution containing 1.5% Petrostep B-120R and 1.5% sodium chloride with hexane as oil phase by spinning drop technique. The interfacial tension of the system also decreased with increasing the concentration of ozonated KL preparations in the range of 1–16 g l-1 according to the simplified Gibbs adsorption equation. Thus, the addition of a small amount of ozonated KL preparations to the aqueous solution containing 1.5% Petrostep B-120R and 1.5% sodium chloride showed a remarkable synergistic effect on reducing the interfacial tension.


1960 ◽  
Vol 13 (2) ◽  
pp. 210 ◽  
Author(s):  
JA Allen

The Gibbs adsorption equation has been used in conjunction with surface tension measurements on silver wires to determine the adsorption isobar of oxygen on silver at a pressure of 16 cmHg over the temperature range 650-850 �C. The results show the existence of a surface concentration of oxygen of 2 x 1015 atoms oxygen per cm2. The value of ΔH for the equilibrium between adsorbed and dissolved oxygen has been estimated as 20.6 kcal. This value in conjunction with the heats of formation and solution of Ag2O in silver permit the h3at of adsorption to be determined as 10.5 kcal per g-atom of oxygen.


Author(s):  
A.M. Ovrutsky ◽  
A.S. Prokhoda ◽  
M.S. Rasshchupkyna

Electrochem ◽  
2020 ◽  
Vol 1 (2) ◽  
pp. 104-123 ◽  
Author(s):  
Gyözö G. Láng

On the basis of a survey on the relevant literature it can be stated that some views and approaches concerning the charged state of adsorbed species and the charge transfer processes occurring with them are far from being unambiguous even in some respect they contradict fundamental physical and physicochemical principles. The meaning of the electrosorption valency, the misleading formulation of the Gibbs adsorption equation, and the interpretation of redox processes occurring with adsorbed species, is discussed in detail. It has been concluded that although the electrosorption valency of an adsorbed species as usually defined is an extra-thermodynamic and self-contradictory concept, experimental determined formal partial charge numbers can be a useful tool for scientists investigating adsorption phenomena, since the observed deviation between its value and the charge number of the same species in the solution phase unequivocally indicates a non-simple mechanism of the adsorption process, which should be taken into account in theoretical interpretation of the experimental data. It has been emphasized that the evaluation of voltammetric curves obtained in the presence of adsorbed redox partners requires a cautious analysis of the accompanying chemical transformations. In the framework of a critical analysis it is demonstrated that probably one of the most important sources of the misinterpretations and misunderstandings is the inadequate approach to the concept of electrode charge. The possibility of a general and straightforward presentation of the Gibbs adsorption equation has also been discussed.


2017 ◽  
Vol 235 ◽  
pp. 126-134 ◽  
Author(s):  
Stephan Werth ◽  
Martin Horsch ◽  
Hans Hasse

Sign in / Sign up

Export Citation Format

Share Document