Surface Tension and Bubble Coalescence Phenomena of Aqueous Solutions of Electrolytes

Langmuir ◽  
1995 ◽  
Vol 11 (5) ◽  
pp. 1422-1426 ◽  
Author(s):  
Peter K. Weissenborn ◽  
Robert J. Pugh
Keyword(s):  
Surface Tension ◽  
Aqueous Solutions ◽  
Bubble Coalescence ◽  
Solutions Of Electrolytes

Additivity of molar metachors of chlorides in aqueous solutions

1989 ◽  
Vol 54 (10) ◽  
pp. 2657-2666
Author(s):  
Jiří Čeleda ◽  
Jana Žilková
Keyword(s):  
Surface Tension ◽  
Aqueous Solutions ◽  
Ion Pairs ◽  
Chloro Complexes ◽  
Divalent Metals ◽  
Degree Of Dissociation ◽  
Molar Ratios ◽  
Mixed Solutions ◽  
Solutions Of Electrolytes ◽  
Electrostatic Contribution

For the molar metachor, a quantity expressing the electrostatic contribution from free (nonassociated and noncomplexed) ions to the surface tension of aqueous solutions of electrolytes, its additivity was verified for completely dissociating chlorides of univalent and divalent metals at concentrations up to 5 mol dm-3. Owing to this property, the degree of dissociation could be estimated for associating components of solutions containing also completely dissociated electrolytes. Measurements revealed that NaCl, LiCl, MgCl2 and CaCl2 in mixed solutions are completely dissociated whereas ZnCl2, CdCl2 and UO2Cl2 at molar ratios NaCl:MeCl = 2:1 and higher ( at cCl- = 5 mol dm-3) are completely transformed into electroneutral and anionic chloro complexes, the latter forming ion pairs and triplets with Na+ ions.

Gas holdup in bubbled beds of aqueous solutions of electrolytes

1977 ◽  
Vol 42 (9) ◽  
pp. 2642-2650
Author(s):  
F. Kaštánek ◽  
J. Kratochvíl ◽  
J. Pata ◽  
M. Rylek
Keyword(s):  
Aqueous Solutions ◽  
Gas Holdup ◽  
Solutions Of Electrolytes

The metachor as a characteristic of the association of electrolytes in aqueous solutions

1984 ◽  
Vol 49 (5) ◽  
pp. 1061-1078 ◽  
Author(s):  
Jiří Čeleda ◽  
Stanislav Škramovský
Keyword(s):  
Aqueous Solutions ◽  
Apparent Volume ◽  
Solutions Of Electrolytes ◽  
Molal Volumes ◽  
The Difference ◽  
High Concentrations ◽  
Experimental Values ◽  
Suitable Characteristic ◽  
Association Of Ions ◽  
Very High

Based on the earlier paper introducing a concept of the apparent parachor of a solute in the solution, we have eliminated in the present work algebraically the effect which is introduced into this quantity by the additivity of the apparent molal volumes. The difference remaining from the apparent parachor after substracting the contribution corresponding to the apparent volume ( for which the present authors suggest the name metachor) was evaluated from the experimental values of the surface tension of aqueous solutions for a set of 1,1-, 1,2- and 2,1-valent electrolytes. This difference showed to be independent of concentration up to the very high values of the order of units mol dm-3 but it was directly proportional to the number of the free charges (with a proportionality factor 5 ± 1 cm3 mol-1 identical for all studied electrolytes). The metachor can be, for this reason, a suitable characteristic for detection of the association of ions and formation of complexes in the solutions of electrolytes, up to high concentrations where other methods are failing.

scholarly journals Surface Thermodynamics, Viscosity, Activation Energy of N-Methyldiethanolamine Aqueous Solutions Promoted by Tetramethylammonium Arginate

Entropy ◽  
2020 ◽  
Vol 22 (12) ◽  
pp. 1337
Author(s):  
Xiangfeng Tian ◽  
Lemeng Wang ◽  
Pan Zhang ◽  
Dong Fu
Keyword(s):  
Activation Energy ◽  
Surface Tension ◽  
Diffusion Coefficient ◽  
Aqueous Solutions ◽  
Quantitative Relationship ◽  
Viscosity Data ◽  
Surface Thermodynamics ◽  
Surface Entropy ◽  
Operation Conditions ◽  
Surface Enthalpy

The surface tension and viscosity values of N-methyldiethanolamine (MDEA) aqueous solutions promoted by tetramethylammonium arginate ([N1111][Arg]) were measured and modeled. The experimental temperatures were 303.2 to 323.2 K. The mass fractions of MDEA (wMDEA) and [N1111][Arg] (w[N1111][Arg]) were 0.300 to 0.500 and 0.025 to 0.075, respectively. The measured surface tension and viscosity values were satisfactorily fitted to thermodynamic models. With the aid of experimentally viscosity data, the activation energy (Ea) and H2S diffusion coefficient (DH2S) of MDEA-[N1111][Arg] aqueous solution were deduced. The surface entropy and surface enthalpy of the solutions were calculated using the fitted model of the surface tension. The quantitative relationship between the calculated values (surface tension, surface entropy, surface enthalpy, viscosity, activation energy, and H2S diffusion coefficient) and the operation conditions (mass fraction and temperature) was demonstrated.

Physico-chemical study of aqueous solutions of electrolytes in mixed solvents

2006 ◽  
Vol 38 (11) ◽  
pp. 1474-1478 ◽  
Author(s):  
Monimul Huque ◽  
Iqbal Ahmed Siddiquey ◽  
Md. Nizam Uddin
Keyword(s):  
Aqueous Solutions ◽  
Mixed Solvents ◽  
Chemical Study ◽  
Physico Chemical ◽  
Solutions Of Electrolytes
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