Surfactant sodium dodecyl sulfate

Xu Z H, Ducker W and Israelachvili J N 1996 Forces between crystalline alumina (sapphire) surfaces in aqueous sodium dodecyl sulfate surfactant solutions Langmuir 12 2263-70... 

Choi PK, Funayama K (2007) Multibubble sonoluminescence and Na atom emission in sodium dodecyl sulfate surfactant solutions. Jpn J Appl Phys 46 4768 1770... 

The self-diffusion of the individual components is strongly affected by the formation of micelles in the solution. This applies to the surfactant, the counterion, the water, and to solubilized molecules. As illustrated in Fig. 2.11 for sodium dodecyl sulfate, surfactant and counterion diffusion are very weakly dependent on concentration below the CMC while a marked decrease in the micellar region is observed for the surfactant and a less marked one for the counterion37. Water diffusion shows a stronger concentration dependence below the CMC than above it. Self-diffusion studies using radioactive tracers have been performed to obtain information on CMC, on counterion binding, on hydration and on intermicellar interactions and shape changes. 

Figure 14. Stratification of horizontal foam film from 0.1 mol/L sodium dodecyl sulfate surfactant solution.

To elucidate the mechanism of chain association, we prepared three series of N-alkylacrylamide-acrylamide copolymers containing up to 0.75 mol % of Cg, Cio, and C12 N-alkylacrylamide monomers. The copolymerizations were conducted with potassium persulfate as the initiator in an aqueous medium containing a high concentration of sodium dodecyl sulfate surfactant (28). The reaction parameters and solubility of the resulting copolymers are given in Table I. Table I indicates solubility in water of all... 

The presence of surfactants, besides altering the latex particle surface, can also interact with the water-soluble polymer. For instance, poly(ethylene oxide) homopolymer and block copolymers interact with sodium dodecyl sulfate surfactant [109], and hence alter the latex viscosity behaviour [110]. Other water-soluble polymers are also capable of interacting with specifle surfactants [111]. When pigmented latex dispersions are thickened with associative thickeners one must consider the interactions with some of the pigment stabilizers [112] and other additives, like coalescing aids [113]. 

Emulsion polymerization of methyl methacrylate macromonomer latex (30 g, 28% solids prepared with 0.3% sodium dodecyl sulfate surfactant) was heated to 80 °C under nitrogen. Potassium persulfate solution (0.4 wt% in water, 19mLh ) and butyl methacrylate (10gh ) were added by syringe pumps. 

This form is obeyed fairly well above x values of 5-10 dyn/cm in Fig. Ill-15c. Limiting areas or a values of about 22 per molecule result, nearly independent of chain length, as would be expected if the molecules assume a final orientation that is perpendicular to the surface. Larger A values are found for longer-chain surfactants, such as sodium dodecyl sulfate, and this has been attributed to the hydrocarbon tails having a variety of conformations [127]. 

Surface heterogeneity may be inferred from emission studies such as those studies by de Schrijver and co-workers on P and on R adsorbed on clay minerals [197,198]. In the case of adsorbed pyrene and its derivatives, there is considerable evidence for surface mobility (on clays, metal oxides, sulfides), as from the work of Thomas [199], de Mayo and co-workers [200], Singer [201] and Stahlberg et al. [202]. There has also been evidence for ground-state bimolecular association of adsorbed pyrene [66,203]. The sensitivity of pyrene to the polarity of its environment allows its use as a probe of surface polarity [204,205]. Pyrene or ofter emitters may be used as probes to study the structure of an adsorbate film, as in the case of Triton X-100 on silica [206], sodium dodecyl sulfate at the alumina surface [207] and hexadecyltrimethylammonium chloride adsorbed onto silver electrodes from water and dimethylformamide [208]. In all cases progressive structural changes were concluded to occur with increasing surfactant adsorption. 

The kinetics of vinyl acetate emulsion polymeriza tion in the presence of alkyl phenyl ethoxylate surfactants of various chain lengths indicate that part of the emulsion polymerization occurs in the aqueous phase and part in the particles (115). A study of the emulsion polymerization of vinyl acetate in the presence of sodium lauryl sulfate reveals that a water-soluble poly(vinyl acetate)—sodium dodecyl sulfate polyelectrolyte complex forms, and that latex stabihty, polymer hydrolysis, and molecular weight are controlled by this phenomenon (116). 

Removal of general organic fouling is best achieved by alkaline cleaning based on caustic, EDTA, and a surfactant such as sodium dodecyl sulfate or sodium lauryl sulfate. 

If the coupling component is not ionic, however, more dramatic effects occur, as found by Hashida et al. (1979) and by Tentorio et al. (1985). Hashida used N,N-bis(2-hydroxyethyl)aniline, while Tentorio and coworkers took 1-naphthylamine and l-amino-2-methylnaphthalene as coupling components. With cationic arenediazo-nium salts and addition of sodium dodecyl sulfate (SDS), rate increases up to 1100-fold were measured in cases where the surfactant concentration was higher than the critical micelle concentration (cmc). Under the same conditions the reaction... 

The curve shown in Fig. 6 for sodium dodecyl sulfate is characteristic of ionic surfactants, which present a discontinuous and sharp increase of solubility at a particular temperature [80]. This temperature is known as the Krafft temperature. The Krafft temperature is defined by ISO as the temperature [in practice, a narrow range of temperatures] at which the solubility of ionic surface active agents rises sharply. At this temperature the solubility becomes equal to the critical micelle concentration (cmc). The curve of solubility vs. temperature intersects with the curve of the CMC vs. temperature at the Krafft temperature. 

The influence of the presence of alcohols on the CMC is also well known. In 1943 Miles and Shedlovsky [117] studied the effect of dodecanol on the surface tension of solutions of sodium dodecyl sulfate detecting a significant decrease of the surface tension and a displacement of the CMC toward lower surfactant concentrations. Schwuger studied the influence of different alcohols, such as hexanol, octanol, and decanol, on the surface tension of sodium hexa-decyl sulfate [118]. The effect of dodecyl alcohol on the surface tension, CMC, and adsorption behavior of sodium dodecyl sulfate was studied in detail by Batina et al. [119]. 

FIG. 10 Surface tension vs. surfactant concentration for sodium dodecyl sulfate and sodium dodecyl ether (m EO) sulfates at 25 °C [124],... 

FIG. 11 Surface tension vs. log surfactant concentration for (O) sodium decyl ether (2 EO) sulfate, (A) sodium dodecyl sulfate, (A) sodium dodecyl ether (1 EO) sulfate, ( ) sodium dodecyl ether (2 EO) sulfate, and ( ) sodium tetradecyl ether (2 EO) sulfate at 25 °C [94]. 

Sodium dodecyl sulfate is commonly used as the standard surfactant in many chemical and physicochemical determinations. It is often taken as the surfactant of reference when comparing surfactants. This can be explained by the fact that sodium dodecyl sulfate is the surfactant that can be obtained with the highest degree of purity. It can easily be produced by chlorosulfation or sulfation of pure dodecanol and purified by crystallization to obtain crystals of purity near to 100%. In addition, sodium dodecyl sulfate has outstanding surfactant properties. 

Sodium dodecyl sulfate is the universal analytical standard for the determination of anionic and cationic active matter. It is used to determine the analytical concentration factor of the cationic surfactant in the titration of anionic active matter and as titrant to determine the cationic active matter. 

Sodium dodecyl sulfate and hydrogen dodecyl sulfate have been used as catalysts in the denitrosation iV-nitroso-iV-methyl-p-toluenesulfonamide [138]. The kinetics of condensation of benzidine and p-anisidine with p-dimethylamino-benzaldehyde was studied by spectrophotometry in the presence of micelles of sodium dodecyl sulfate, with the result that the surfactant increases the rate of reaction [188]. The kinetics of reversible complexation of Ni(II) and Fe(III) with oxalatopentaaminecobalt(III) has been investigated in aqueous micellar medium of sodium dodecyl sulfate. The reaction occurs exclusively on the micellar surface [189]. Vitamin E reacts rapidly with the peroxidized linoleic acid present in linoleic acid in micellar sodium dodecyl sulfate solutions, whereas no significant reaction occurs in ethanol solution [190]. 

Mechanisms of micellar reactions have been studied by a kinetic study of the state of the proton at the surface of dodecyl sulfate micelles [191]. Surface diffusion constants of Ni(II) on a sodium dodecyl sulfate micelle were studied by electron spin resonance (ESR). The lateral diffusion constant of Ni(II) was found to be three orders of magnitude less than that in ordinary aqueous solutions [192]. Migration and self-diffusion coefficients of divalent counterions in micellar solutions containing monovalent counterions were studied for solutions of Be2+ in lithium dodecyl sulfate and for solutions of Ca2+ in sodium dodecyl sulfate [193]. The structural disposition of the porphyrin complex and the conformation of the surfactant molecules inside the micellar cavity was studied by NMR on aqueous sodium dodecyl sulfate micelles [194]. 

Sodium dodecyl sulfate has been used to modify polypyrrole film electrodes. Electrodes synthesized in the presence of sodium dodecyl sulfate have improved redox processes which are faster and more reversible than those prepared without this surfactant. The electrochemical behavior of these electrodes was investigated by cyclic voltametry and frequence response analysis. The electrodes used in lithium/organic electrolyte batteries show improved performance [195]. 

Sodium alcohol sulfates are also used in the formulation of synthetic soaps and paste hand cleaners, commonly together with other surfactants and as tablet disintegrators in the case of sodium dodecyl sulfate. Sodium, but preferably ammonium and alkanolamine salts, is also used in liquid soaps. 

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