Dependence of the Second Virial Coefficient of Aqueous Solutions of Small Non-Electrolytes on Partial Molar Volume and Molecular Weight of the Solutes

1993 ◽  
Vol 46 (6) ◽  
pp. 929 ◽  
Author(s):  
K Kiyosawa

The osmotic pressures of aqueous solutions of small non-electrolytes, namely ethane-1,2-diol, propane-1,2,3-triol, sucrose and raffinose , were found to be expressible by quadratic equations of the molar concentration, which indicate that these aqueous systems involve no term higher than the second virial coefficient A2. Analysis has shown that A2 mainly does not arise from non-ideality of the aqueous solutions, but its magnitude depends on the partial molar volume of the solute, more precisely on the molecular weight or van der Waals radius or volume of the solute in the aqueous solution.


1983 ◽  
Vol 48 (8) ◽  
pp. 2327-2334
Author(s):  
Otakar Söhnel ◽  
Petr Novotný ◽  
Zdeněk Šolc

Two methods are given for assessment of density of binary aqueous solutions of electrolytes; one is based on partial molar volume of the dissolved electrolyte at infinite dilution, and the other is based on additivity of apparent molar volumes at a given concentration. The density estimates of aqueous solutions by means of the two methods are compared with experimental values for some electrolytes of the type 1-1 to 4 and 2-2. In all cases the estimates agree with experimental densities up to concentrations of the saturated solutions.



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.



2008 ◽  
Vol 86 (6) ◽  
pp. 503-511 ◽  
Author(s):  
Stephanie Beck-Candanedo ◽  
David Viet ◽  
Derek G Gray

The partitioning behaviour of dye-labeled dextrans of high molecular weight in aqueous suspensions of native cellulose nanocrystals was studied. Cellulose concentrations lie in the isotropic–nematic coexistence region. Blue dextrans of various molecular weights and degrees of substitution of dye molecules (anionic Cibacron blue 3G-A) were investigated. Increasing the total concentration of blue dextran and degree of dye substitution led to increasing partition coefficients. Increasing dextran molecular weight resulted in higher partition coefficients, in agreement with theory. Partition coefficients were larger than predicted theoretically using a second virial coefficient approximation. Electrostatic and entropic contributions to the partition coefficient of blue dextran are discussed. Dextrans labeled with neutral fluorescein isothiocyanate did not partition preferentially in this system.Key words: partition coefficient, cellulose nanocrystals, dextrans, degree of substitution, polyelectrolyte.



1957 ◽  
Vol 35 (3) ◽  
pp. 202-206 ◽  
Author(s):  
A. M. Couture ◽  
K. J. Laidler

The entropies of oxy-anions in aqueous solution are shown to obey the empirical relationship[Formula: see text]with a mean deviation of 3.6 e.u. In this equation [Formula: see text] is the entropy relative to a value of −5.5 e.u. for the proton, M is the molecular weight, z the number of charges on the ion, n the number of charge-bearing ligands, r is equal to r12 + 1.40, where r12 is the interatomic distance between the central atom and the surrounding oxygens, and 1.40 is the van der Waals radius of oxygen. The significance of the empirical equation is discussed.





2002 ◽  
Vol 106 (21) ◽  
pp. 5500-5505 ◽  
Author(s):  
A. Striolo ◽  
J. Ward ◽  
J. M. Prausnitz ◽  
W. J. Parak ◽  
D. Zanchet ◽  
...  






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