scholarly journals Solute-Solvent Interaction in Aqueous Solutions Studied by Optical Kerr Effect

1997 ◽  
Vol 91 (3) ◽  
pp. 531-541 ◽  
Author(s):  
Z. Błaszczak ◽  
M. Farhoud
1997 ◽  
Vol 101 (38) ◽  
pp. 7029-7035 ◽  
Author(s):  
Paolo Foggi ◽  
Marco Bellini ◽  
Dany P. Kien ◽  
Isabelle Vercuque ◽  
Roberto Righini

2019 ◽  
Vol 35 (2) ◽  
pp. 901-904
Author(s):  
Sandhya Sharma ◽  
N. D. Kandpal ◽  
R. Joshi

Viscosities (ƞ) of solutions of 1- propanol and 2-propanol have been determined in aqueous systems of varying composition (0.16-3.64 mol dm-3) at 298 K. The ƞ/ƞ0 data have been analyzed in the light of reduced Jone-Dole equation ƞ/ƞ0 = BC+1. The results in the regards to solute-solvent interaction in aqueous solutions of both the alcohols have been discussed in the terms of the value B. The result of study reveals that both the alcohols behave as the structure makers in the water. The result shows that solute-solvent type interaction of same magnitude exists in water-alcohol system.


2011 ◽  
Vol 115 (11) ◽  
pp. 2563-2573 ◽  
Author(s):  
Kamila Mazur ◽  
Ismael A. Heisler ◽  
Stephen R. Meech

2010 ◽  
Vol 7 (s1) ◽  
pp. S223-S230 ◽  
Author(s):  
Chandravir S. Solanki ◽  
Sushree Tripathy ◽  
Minaketan Tripathy ◽  
Upendra N. Dash

The present study deals with experiments so as to highlight the solute (drug nimesulide) - solvent(water) interactions and related modifications in case of the presence of hydrotropic agents at different temperatures T(=298.15 to 313.15)K. Density and viscosity values of nimesulide have been determined in water in (0.1, 0.2, 0.4, 0.6, 0.8, 1 and 2) mol dm-3aqueous solutions of hydrotropic agents (sodium benzoate, sodium salicylate, sodium bromide and nicotinamide) at temperatures 298.15, 303.15, 308.15 and 313.15 K where as the solubility was studied at 308.15 K. From the density values, the limiting partial molar volumes and expansibilities have been calculated. The experimental viscosity values have been analyzed in terms of jones-dole equation and on the basis of transition theory for relative viscosity.


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