scholarly journals Model for estimating activity coefficients in binary and ternary ionic surfactant solutions

2020 ◽  
Vol 77 (4) ◽  
pp. 141-168
Author(s):  
Silvia M. Calderón ◽  
Jussi Malila ◽  
Nønne L. Prisle

AbstractWe introduce the CMC based Ionic Surfactant Activity model (CISA) to calculate activity coefficients in ternary aqueous solutions of an ionic surfactant and an inorganic salt. The surfactant can be either anionic or cationic and in the present development, the surfactant and inorganic salts share a common counterion. CISA incorporates micellization into the Pitzer–Debye–Hückel (PDH) framework for activities of mixed electrolyte solutions. To reduce computing requirements, a parametrization of the critical micelle concentration (CMC) is used to estimate the degree of micellization instead of explicit equilibrium calculations. For both binary and ternary systems, CISA only requires binary experimentally-based parameters to describe water–ion interactions and temperature–composition dependency of the CMC. The CISA model is intended in particular for atmospheric applications, where higher-order solution interaction parameters are typically not constrained by experiments and the description must be reliable across a wide range of compositions. We evaluate the model against experimental activity data for binary aqueous solutions of ionic surfactants sodium octanoate and sodium decanoate, as common components of atmospheric aerosols, and sodium dodecylsulfate, the most commonly used model compound for atmospheric surfactants. Capabilities of the CISA model to describe ternary systems are tested for the water–sodium decanoate–sodium chloride system, a common surrogate for marine background cloud condensation nuclei and to our knowledge the only atmospherically relevant system for which ternary activity data is available. For these systems, CISA is able to provide continuous predictions of activity coefficients both below and above CMC and in all cases gives an improved description of the water activity above the CMC, compared to the alternative model of Burchfield and Wolley [J. Phys. Chem., 88(10), 2149–2155 (1984)]. The water activity is a key parameter governing the formation and equilibrium growth of cloud droplets. The CISA model can be extended from the current form to include the effect of other inorganic salts with the existing database of binary PDH parameters and using appropriate mixing rules to account for ion specificity in the micellization process.

1981 ◽  
Vol 59 (13) ◽  
pp. 1865-1871 ◽  
Author(s):  
Rosario De Lisi ◽  
Gérald Perron ◽  
Jean Paquette ◽  
Jacques E. Desnoyers

The freezing-point depressions of aqueous solutions of the homologous series RNH3Br, where R varies from ethyl to n-octyl, and of sodium decanoate were determined and used to calculate osmotic and mean activity coefficients. In the case of the surfactants octylamine hydrobromide and sodium decanoate, the pre- and post-micellar regions were covered. Activity data at higher temperatures were calculated using previously published thermochemical data. Some difficulties arise in the critical micellar region of sodium decanoate at high temperatures as a result of the large concentration and temperature dependence of the heat capacity data. The activities from freezing point data are compared with those obtained from specific electrodes.


1975 ◽  
Vol 53 (20) ◽  
pp. 3133-3140 ◽  
Author(s):  
Fabio Lenzi ◽  
Tuong-Tu Tran ◽  
Tjoon-Tow Teng

Reverse application of the Reilly–Wood-Robinson and Zdanovskii–Stokes–Robinson equations to the water-activity data of various ternary aqueous systems containing NaCl, KCl, K2SO4 as one of the components yields self-consistent estimates of the water-activity of binary aqueous supersaturated solutions of the individual salts; these can be further extended by curvilinear extrapolation to give: [Formula: see text] with A1 = −3.28806 × 10−2, A2 = 1.12512 × 10−4, A3 = −4.30034 × 10−4, A4 = 2.70506 × 10−5, A5 = 1.43435 × 10−6, A6 = 1.30209 ×10−7, A7 = −1.51941 × 10−8, A8 = 1.00520 × 10−9, A9 = −4.21593 × 10−10, A10 = 2.62532 × 10−11, valid to aw(NaCl) = 0.5422, [Formula: see text][Formula: see text]with B1 = −3.21884 × 10−2, B2 = 9.77773 × 10−4, B3 = −6.05349 × 10−4, B4 = 1.18422 × 10−4, B5 = −7.91572 × 10−6, B6 = −3.88125 × 10−8, B7 = 1.55125 × 10−8, valid to aw(KCl) = 0.7115, [Formula: see text][Formula: see text] with C1 = −4.16810 × 10−2, C2 = 1.16033 × 10−2, C3 = −4.80543 × 10−3, C4 = 7.15536 x 10−4, valid to [Formula: see text][Formula: see text]


1996 ◽  
Vol 61 (11) ◽  
pp. 1549-1562 ◽  
Author(s):  
Jan Balej

Up to now, there exist a quite wide temperature interval between 70 or 80 and 150 °C with no sufficiently reliable experimental data of mean activity coefficients for aqueous NaOH as well as KOH solutions. In order to fill this gap, it was tried to derive suitable correlation equations for this quantity in dependence on the molality (for NaOH in the range mNaOH = 2-25 mol kg-1, for KOH in the range mKOH = 2-18 mol kg-1) and temperature (in the range 0-200 °C for both kinds of solutions) on the basis of the available data of this quantity and with the use of the previously derived correlation equations for the water activity in aqueous solutions of NaOH and KOH under the same conditions. The comparison between the calculated and experimental data was discussed.


1973 ◽  
Vol 51 (16) ◽  
pp. 2626-2631 ◽  
Author(s):  
J. Sangster ◽  
T. T. Teng ◽  
F. Lenzi

Recently developed methods of predicting water activities of multicomponent aqueous solutions use binary data. At high concentrations these methods are limited inasmuch as they require binary data beyond the solubility limit of individual solutes. A method is proposed whereby ternary water activity data may be used to calculate water activities of supersaturated binary solutions. The new method is compared with two extrapolation procedures on a known system and gives the best agreement. Values of the water activities for supersaturated solutions of KNO3 (3.8 to 7.6 m) and K2SO4 (0.7 to 2.3 m) at 25 °C are obtained.


1977 ◽  
Vol 55 (10) ◽  
pp. 1713-1719 ◽  
Author(s):  
Marie-Christine Trudelle ◽  
Maurice Abraham ◽  
James Sangster

Vapour pressures of the system (Ag,Tl)NO3 + H2O have been measured at 98.5 °C by the static method over the complete concentration range for Ag/Tl mole ratio = 1.14. The water activity data can be represented by a modified BET isotherm in the range 0.1 < aw < 0.7. The derived BET constants indicate that the salts in this system are very weakly hydrated, probably less so than (for example) CsNO3. The linearity of vapour pressure with water mole ratio RH, found previously by Tripp and Braunstein for (Li,K)NO3 + H2O, is absent in the present system. The Henry's law constant for water dissolved in molten (Ag,Tl)NO3 has been deduced. The excess free energy of the system is positive at all concentrations and shows a maximum of 117 cal/mol at water mole fraction 0.66.


1977 ◽  
Vol 24 (1) ◽  
pp. 673-677 ◽  
Author(s):  
J. J. Lipsett ◽  
I. L. Fowler ◽  
R. J. Dinger ◽  
H. L. Malm

Sign in / Sign up

Export Citation Format

Share Document