The Solubility of Silver Acetate in Mixed Solvents and the Incomplete Disso ciation of Ternary Electrolytes

1937 ◽  
Vol 41 (3) ◽  
pp. 417-429 ◽  
Author(s):  
F. H. MacDougall ◽  
William D. Larson
Keyword(s):  
Mixed Solvents ◽  
Silver Acetate ◽  
Disso Ciation

The Solubility and Activity Coefficient of Silver Acetate in Mixed Solvents.

1936 ◽  
Vol 40 (5) ◽  
pp. 649-659 ◽  
Author(s):  
F. H. MacDougall ◽  
Charles Edward Bartsch
Keyword(s):  
Activity Coefficient ◽  
Mixed Solvents ◽  
Silver Acetate

The Equivalent Conductance of Electrolytes in Mixed Solvents

1958 ◽  
Vol 17 (5_6) ◽  
pp. 300-314 ◽  
Author(s):  
Rayburn Whorton ◽  
Edward S. Amis
Keyword(s):  
Mixed Solvents ◽  
Equivalent Conductance

A description of effect of composition of mixed binary solvents on processes in solutions

1988 ◽  
Vol 53 (4) ◽  
pp. 671-685 ◽  
Author(s):  
Oldřich Pytela ◽  
Miroslav Ludwig
Keyword(s):  
Gibbs Energy ◽  
Mixed Solvents ◽  
Theoretical Description ◽  
Energy Change ◽  
Binary Solvents ◽  
Gibbs Energy Change ◽  
Order Model ◽  
Significant Difference

A theoretical description of the effect of changed composition of mixed solvents on processes in solutions has been suggested on the basis of the proportionality between the Gibbs energy change of the process and that of the solvent due to the transition from pure components to the mixture. The additional Gibbs energy has been expressed by means of the so-called classical functions by Margules, van Laar-Wohl, and van Laar-Null. The application to 115 various processes (pK, IR, UV-VIS, NMR, log k, and others) has confirmed that the theoretical presumptions are justified, the most suitable being Margules' 4th order model which shows a statistically significant difference from the models of lower orders.

Conductivity of Silver Nitrate in Nonaqueous and Mixed Solvents.

1965 ◽  
Vol 10 (1) ◽  
pp. 29-31 ◽  
Author(s):  
R. E. Busby ◽  
V. S. Griffiths
Keyword(s):  
Silver Nitrate ◽  
Mixed Solvents

scholarly journals The Additive Influence of Propane-1,2-Diol on SDS Micellar Structure and Properties

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3773
Author(s):  
Martina Gudelj ◽  
Paola Šurina ◽  
Lucija Jurko ◽  
Ante Prkić ◽  
Perica Bošković
Keyword(s):  
Mixed Solvents ◽  
Sodium Dodecyl ◽  
Shielding Effect ◽  
Bulk Solution ◽  
Structure And Properties ◽  
Micellar Structure ◽  
Related Substances ◽  
Micellar Systems ◽  
Small Change ◽  
Additive Influence

Micellar systems are colloids with significant properties for pharmaceutical and food applications. They can be used to formulate thermodynamically stable mixtures to solubilize hydrophobic food-related substances. Furthermore, micellar formation is a complex process in which a variety of intermolecular interactions determine the course of formation and most important are the hydrophobic and hydrophilic interactions between surfactant–solvent and solvent–solvent. Glycols are organic compounds that belong to the group of alcohols. Among them, propane-1,2-diol (PG) is a substance commonly used as a food additive or ingredient in many cosmetic and hygiene products. The nature of the additive influences the micellar structure and properties of sodium dodecyl sulfate (SDS). When increasing the mass fraction of propane-1,2-diol in binary mixtures, the c.m.c. values decrease because propane-1,2-diol is a polar solvent, which gives it the ability to form hydrogen bonds, decreasing the cohesivity of water and reducing the dielectric constant of the aqueous phase. The values of ΔGm0 are negative in all mixed solvents according to the reduction in solvophobic interactions and increase in electrostatic interaction. With the rising concentration of cosolvent, the equilibrium between cosolvent in bulk solution and in the formed micelles is on the side of micelles, leading to the formation of micelles at a lower concentration with a small change in micellar size. According to the 1H NMR, with the addition of propylene glycol, there is a slight shift of SDS peaks towards lower ppm regions in comparison to the D2O peak. The shift is more evident with the increase in the amount of added propane-1,2-diol in comparison to the NMR spectra of pure SDS. Addition of propane-1,2-diol causes the upfield shift of the protons associated with hydrophilic groups, causing the shielding effect. This signifies that the alcohol is linked with the polar head groups of SDS due to its proximity to the SDS molecules.

scholarly journals An interplay of excluded-volume and polymer–(co)solvent attractive interactions regulates polymer collapse in mixed solvents

2021 ◽  
Vol 154 (13) ◽  
pp. 134903
Author(s):  
Swaminath Bharadwaj ◽  
Divya Nayar ◽  
Cahit Dalgicdir ◽  
Nico F. A. van der Vegt
Keyword(s):  
Mixed Solvents ◽  
Excluded Volume ◽  
Polymer Collapse

scholarly journals THE PHYSICAL CHEMISTRY OF THE PROTEINS IN NON-AQUEOUS AND MIXED SOLVENTS

1930 ◽  
Vol 87 (2) ◽  
pp. 197-238
Author(s):  
Norval F. Burk ◽  
David M. Greenberg
Keyword(s):  
Physical Chemistry ◽  
Mixed Solvents
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