Surface tension aqueous mixtures

We have considered the surface tension behavior of several types of systems, and now it is desirable to discuss in slightly more detail the very important case of aqueous mixtures. If the surface tensions of the separate pure liquids differ appreciably, as in the case of alcohol-water mixtures, then the addition of small amounts of the second component generally results in a marked decrease in surface tension from that of the pure water. The case of ethanol and water is shown in Fig. III-9c. As seen in Section III-5, this effect may be accounted for in terms of selective adsorption of the alcohol at the interface. Dilute aqueous solutions of organic substances can be treated with a semiempirical equation attributed to von Szyszkowski [89,90]... 

Surface tensions for aqueous solutions are more difficult to predict than those for nonaqueous mixtures because of the nonlinear dependence on mole fraction. Small concentrations of the organic material may significantly affect the mixture surface tension value. For many binary organic-water mixtures, the method of Tamura, Kurata, and Odanfi maybe used ... 

The bulk properties of mixed solvents, especially of binary solvent mixtures of water and organic solvents, are often needed. Many dielectric constant measurements have been made on such binary mixtures. The surface tension of aqueous binary mixtures can be quantitatively related to composition. ... 

Separation of phases is sometimes a problem, especially in the case of mixtures of alkaline aqueous solutions and organic liquids. Addition of materials that decrease the surface tension, filtration of the emulsion to remove interfacial contamination, and the use of sedimentation centrifuges should be considered if the separation time is too long. 

Equation (87) and analogous equations for AG , AHm, and for surface tensions apply to molten salt mixtures in which the interaction potential can be classed as conformal. These relations may also be used to test whether the ionic interaction potential in aqueous solutions may be considered as conformal. Thus, as will be shown in one simple example, the limits of usefulness of some interionic interaction potentials may be tested in ranges of concentration of salts in water too high to obtain absolute values for the partition functions. A similar test may be made for associations in salt vapors such as... 

So far only aqueous solutions have been considered however, mixtures of HF and ethanol or methanol are quite common, because this addition reduces the surface tension and thereby the sticking probability of hydrogen bubbles. While substantial quantities of ethanol or methanol are needed to reduce the surface tension, cationic or anionic surfactants fulfill the same purpose in concentrations as low as 0.01 M [So3, Chl6]. 

Raney K, Benton W, Miller CA (1987) Optimum detergency conditions with nonionic siufactants II. Effect of hydrophobic additives. J Colloid Interface Sci 119 539-549 Rosen MJ, Wu Y (2001) Superspreading of trisiloxane surfactant mixtures on hydrophobic siufaces 1. Interfacial adsorption of aqueous trisiloxane surfactant -M-alkyl pyrrolidinone mixtures on polyethylene. Langmuir 17 7296-7305 Stevens PJG, Kimberely MO, Mimphy DS, Policello GA (1993) Adhesion of spray droplets to foliage - the role of dynamic surface tension and advantages of organosil-icone surfactants. Pesticide Sci 38 237-245... 

The conditions for synergism in surface tension reduction efficiency, mixed micelle formation, and Surface tension reduction effectiveness in aqueous solution have been derived mathematically together with the properties of the surfactant mixture at the point of maximum synergism. This treatment has been extended to liquid-liquid (aqueous solution/hydrocarbon) systems at low surfactant concentrations.) The effect of chemical structure and molecular environment on the value of B is demonstrated and discussed. 

The surface tension of the aqueous solution of dode-cylaitunonium chloride (DAC) — decylairanonium chloride (DeAC) mixture was measured as a function of the total molality m of surfactants and the mole fraction X of DeAC in the total surfactant in the neighborhood of the critical micelle concentration (CMC). By use of the thermodynamic equations derived previously, the mole fraction in the mixed adsorbed film was evaluated from the y vs. X and m vs. X curves. Further, the mole fraction in the mixed micelle was evaluated from the CMC vs. X curve. By comparing these values at the CMC, it was concluded that the behavior of DAC and DeAC molecules in the mixed micelle is fairly similar to that in the mixed adsorbed film. 

The surface tension y of the aqueous solution of dodecylammonium chloride — decylammonium chloride mixture was measured as a function of m at a given value of the mole fraction X of DeAC at 298.15 K under atmospheric pressure. The results are shown in Figure 1. It is seen that the y vs. m curves are similar in appearance. This behavior is in harmony with that observed previously in a low concentration range (9). Moreover, the formation of micelle is found to cause the curves to break sharply at the CMC which increases with X. It should be noted, however, that the y vs. m curve of a mixture has a very shallow minimum in the immediate vicinity of the CMC. 

Figure 4, Surface tension of aqueous solutions of RDH-Cio SNa mixtures at 30 C(with NaCl, ionic strength =...

Shinoda, K. Yamaguchi, T. and Hori, R. (1961) The surface tension and the critical micelle concentration in aqueous solution of/3-D-alkylglucosides and their mixtures. Bull. Chem. Soc. Japan, 34(2), 237-41. 

Conventional water-based and non-aqueous inkjet inks are mixtures of several components, including volatile solvents, dissolved materials, and dispersed solids (for pigment inks). When the ink reaches the nozzles prior to jetting, the volatile components may evaporate from the nozzle. Therefore, the liquid in the vicinity of the nozzle can have a composition which differs from that of the bulk ink which is further back in the print head supply channels. This disparity causes differences in the physicochemical properties of the ink (e.g., an increase in viscosity or decrease in surface tension)... 

Relationship between the variation of surface tension of aqueous phase of reaction mixture and the number of polymer particles produced ... 

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