scholarly journals Composition dependent density of ternary aqueous solutions of ionic surfactants and salts

Author(s):  
Silvia M. Calderón ◽  
Nønne L. Prisle

AbstractSurfactants exist in atmospheric aerosols mixed with inorganic salts and can significantly influence the formation of cloud droplets due to bulk–surface partitioning and surface tension depression. To model these processes, we need continuous parametrizations of the concentration dependent properties of aqueous surfactant–salt solutions for the full composition range from pure water to pure surfactant or salt. We have developed density functions based on the pseudo-separation method and Young’s mixing rule for apparent partial molal volumes for solutions that mimic atmospheric droplets of marine environments. The developed framework requires only model parameters from binary water–salt and water–surfactant systems and includes the effect of salinity on micellization with composition-dependent functions for the critical micelle concentration (CMC). We evaluate different models and data available in the literature to find the most suitable representations of the apparent partial molal volume of sodium chloride (NaCl) in aqueous solutions and the CMC of selected atmospheric and model surfactants in pure water and aqueous NaCl solutions. We compare model results to experimental density data, available in the literature and obtained from additional measurements, for aqueous solutions containing one of the ionic surfactants sodium octanoate, sodium decanoate, sodium dodecanoate or sodium dodecylsulfate mixed with NaCl in different relative ratios. Our model follows the experimental trends of increasing densities with increasing surfactant concentrations or increasing surfactant–salt mixing ratios both, below and above the CMC, capturing the effect of the inorganic salt on the surfactant micellization.

1993 ◽  
Vol 48 (11) ◽  
pp. 1073-1080
Author(s):  
B. A. Bilal ◽  
E. Müller

Abstract The equilibrium constant, partial molal volume, entropy and enthalpy of the formation of HSO4- ion in aqueous solutions have been determined up to 473 K and 975 bar at the ionic strengths 1 = 0 as well as in NaCl solutions having I = 1, 0.5 and 0.1 mol kg-1 At 473 K, for instance, the thermodynamic formation constant K0 decreases by ≈ 0.75 log units from saturation pressure to 975 bar. The corresponding decrease of the apparent formation constant Q at I = 1 m is ≈ 0.6 log units. The increased dissociation at higher pressure leads to a decrease of the partial molal volume and entropy due to the resulting higher electrostriction in the system.


1981 ◽  
Vol 34 (9) ◽  
pp. 1785 ◽  
Author(s):  
JV Leyendekkers

The Tammann-Tait-Gibson (TTG) model was used to derive and analyse an equation for the isothermal compressibility of aqueous electrolyte solutions as a function of temperature and pressure. The linear equation of Φk in c½ (Φk is the apparent molal compressibility, c is in mol 1-1) is shown to be inadequate. The best function in the square-root of the concentration [either in (mol kg-1) or c] is degree three. This gives the correct limiting slope predicted by the TTG model, viz., Sv/(BT + 1), where S, is the Masson slope for apparent molal volumes and BT is the Tait parameter for pure water. This slope was verified previously by comparison with the limiting slope obtained experi- mentally, and can be predicted from the standard ionic entropies. The difference in the TTG slope and the Debye-Hiickel point-charge slope is proportional to changes in the reorientation motion of water molecules close to the ionic surface. The electrostriction component, Vcelect, of the limiting partial molal volume is equal to - K°(BT+ 1), where K° is the limiting partial molal compressibility. Values of V°elect calculated from this relationship are compared with values from other models. The TTG model was used to derive internal pressure functions which could be used to analyse deviations of V°elect from the NIH (non-interacting homomorph) model. The TTG equations were used to calculate the isothermal compressibilities of 15 electrolytes. The agreement with experimental values is good (deviations are less than 0.1 × 10-6cm3 g-1 bar-1 for βv for the most reliable data). Values of Φk at 200 bar were calculated also and are in good agreement with the corresponding experimental values.


2021 ◽  
Vol 13 (13) ◽  
pp. 7509
Author(s):  
Ana M. Ferreira ◽  
Hugo M. D. Gomes ◽  
João A. P. Coutinho ◽  
Mara G. Freire

Spent coffee grounds (SCGs) are a waste product with no relevant commercial value. However, SCGs are rich in extractable compounds with biological activity. To add value to this coffee byproduct, water and aqueous solutions of cholinium-based ionic liquids (ILs) were studied to extract caffeine from SCGs. In general, all IL aqueous solutions lead to higher extraction efficiencies of caffeine than pure water, with aqueous solutions of cholinium bicarbonate being the most efficient. A factorial planning was applied to optimize operational conditions. Aqueous solutions of cholinium bicarbonate, at a temperature of 80 °C for 30 min of extraction, a biomass–solvent weight ratio of 0.05 and at an IL concentration of 1.5 M, made it possible to extract 3.29 wt% of caffeine (against 1.50 wt% obtained at the best conditions obtained with pure water). Furthermore, to improve the sustainability of the process, the same IL aqueous solution was consecutively applied to extract caffeine from six samples of fresh biomass, where an increase in the extraction yield from 3.29 to 13.10 wt% was achieved. Finally, the cholinium bicarbonate was converted to cholinium chloride by titration with hydrochloric acid envisioning the direct application of the IL-caffeine extract in food, cosmetic and nutraceutical products. The results obtained prove that aqueous solutions of cholinium-based ILs are improved solvents for the extraction of caffeine from SCGs, paving the way for their use in the valorization of other waste rich in high-value compounds.


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