Surfactants sodium dodecyl

In an extensive study by Read et al. [93], 10 anionic surfactants were evaluated for their ability to remove pyritic sulfur and ash from ultrafine Illinois no. 5 coal by flotation processes. The authors observed that of the commercially available surfactants, sodium dodecyl sulfate was the most effective on either a weight or a molar basis, followed by a linear AOS (average molweight 272) and alkylpolyethoxylated sulfonates. Of the noncommercial surfactants tested, -(E -b-dodecene-b-suIfonate (f0) was the most effective and better than any commercial surfactant on a dosage/recovery basis. 

The Diels-Alder reaction of methyl methacrylate with cyclopentadiene was studied [72] with solutions from three different regions of the pseudophase diagram for toluene, water and 2-propanol, in the absence and in the presence of surfactant [sodium dodecyl sulfate (SDS) and hexadecyltrimethylammonium bromide (HTAB)]. The composition of the three solutions (Table 6.11) corresponds to a W/O-fiE (A), a solution of small aggregates (B) and a normal ternary solution (C). The diastereoselectivity was practically constant in the absence and in the presence of surfactant a slight increase of endo adduct was observed in the C medium in the presence of surfactant. This suggests that the reaction probably occurs in the interphase and that the transition state has a similar environment in all three media. 

GL 19] ]R 9] ]P 20] The rate of reaction is proportional to decreasing surfactant (sodium dodecyl sulfate) concentration [63]. No change in the enantiomeric excess was observed. These results are an indication of operation in a chemical regime. 

A further interesting application of CLM involves the fluorescence quenching reaction between (5,10,15,20-tetraphenylporphyrinato) zinc (II) and methylviologen at a dode-cane-water interface. [62] This study demonstrated that the quenching reaction could occur only in the presence of an anionic surfactant, sodium dodecyl sulfate (SDS). The quenching efficiency depended on the concentration of SDS in the aqueous phase with a maximum value of 13.5%... 

By asserting that the film thickness remains proportional to the 2/3 power of the capillary number, they establish that the dynamic pressure drop for surfactant-laden bubbles also varies with the capillary number to the 2/3 power but with an unknown constant of proportionality. New pressure-drop data for a 1 wt% commercial surfactant, sodium dodecyl benzene sulfonate (Siponate DS-10), in water, after correction for the liquid indices between the bubbles, confirmed the 2/3 power dependence on Ca and revealed significant increases over the Bretherton theory due to the soluble surfactant. 

Homogeneous LaMn03 nanopowder with the size of 19-55 nm and with the specific surface area of 17-22 m2/g has been synthesized using a surfactant, sodium dodecyl sulphate (SDS) to prevent agglomeration [47], The sonochemically prepared LaMn03 showed a lower phase transformation temperature of 700°C, as compared to the LaMn03 prepared by other conventional methods which has been attributed to the homogenization caused by sonication. Also, a sintered density of 97% of the powders was achieved for the sonochemically prepared powders at low temperature than that of conventionally prepared powders. 

Wilkins. S.J., Coles, B.A., Compton, R.G., and Cowley, A. Mechanism and kinetics of salicylic acid dissolution in aqueous solutionunder defined hydrod3mamic conditions via atortric force trricrosopy the effects of the ionic additives NaCl, LiCl, and MgCb, the organic additives 1-propanol, 2-propanol, and the surfactant sodium dodecyl sulfate. J. Rhys. Chem. B, 1061(106) 4763-4774, 2002. 

The surfactant sodium dodecyl sulphonate (Ci2H2sS03Na) and its sulphate adsorb electrostatically on hematite at low solute concentrations (Han et al., 1973). Hydro-phobic effects operate at high concentrations due to the incompatibility of the hydrocarbon part of the molecule with water. This involves condensation of the alkyl chains at the surface (hemi-micelle interactions), which lowers the free energy of the system and reverses the surface charge. 

In a recent paper, the interaction of various simple flavonoids with an anionic surfactant, sodium dodecyl sulfate (SDS) in aqueous solution, has been studied through absorption spectroscopy as a function of the concentration of the surfactant above and below the critical micelle concentration.The approximate number of additive molecules (flavonoids) incorporated per micelle was estimated at a particular concentration of SDS. Incorporation of flavonoids in micelles shifted the UV absorption bands toward higher wavelengths, and the bathochromic shifts also depended upon the nature of the surfactant head group. 

Anionic surfactant Sodium dodecyl sulfate (SDS, C] 2 25 3 supplied by Nihon Surfactant Industries Co., Ltd Tokyo, Japan. It was extracted with ether and recrystallized from ethanol. The purity was ascertained by surface tension measurement. Nonionic surfactant Alkyl poly(oxyethylene) ether (CjjPOEjj, CmH2nhPlO(CH2CH20)2oH, m=12, 14, 16, and 18 Ci6H330(CH2CH20) H, n=10, 20, 30, and 40) were supplied by Nihon Surfactant Industries Co., Ltd. These have a narrow molecular weight distribution. 

Surfactant (sodium dodecyl sulphate) Distilled water... 

Also shown in Figure 7 is the theoretical curve based upon Equation 16, and taking into account particle swelling by monomer and growth by polymerization. In contrast to it, both experimental curves rise much more steeply. The experiment run in the absence of surfactant, sodium dodecyl sulfate (SDS), has the steeper slope. This pronounced difference due to surfactant concentration, even at levels as low as the 6 X 10 molar used here, has always been found in the many experiments which have been run (33). 

A sample of poly(L-ornithine) containing 48 mol% azo units was found to adopt the a-helix structure in HFP/water = 1/1. In this solvent mixture, however, irradiation at 360 nm followed by irradiation at 460 nm produced the trans-cis photoisomerization of the azo moieties, but did not induce any change of the backbone conformation. When the surfactant sodium dodecyl sulfate was added to the HFP/water solvent mixture, the CD spectrum displayed an intense side chain CD couplet and a negative band at about 225 nm which was assigned to the presence of a P-structure. The CD bands were almost completely abolished upon trans-cis photoisomerization. 

The phase separation behavior of a sample of poly(N-vinyl-2.pyrrolidone) (PVP) in aqueous Na2S04 (0.55 M) containing a surfactant, sodium dodecyl sulfate (SDS), was reported [83], This phenomenon was studied in function of temperature and surfactant concentration as independent variables. Without surfactant, the polymer exhibits a lower solution temperature (LCST) of 28°C, above which it precipitates. At SDS concentrations of only 300 mg L-1, aggregation was prevented and the behavior of isolated polymer molecules could be studied. 

There is evidence that protein structures are also responsible for cell cohesion in nonpalmo-plantar stratum corneum. When punch biopsies of normal human gluteal skin were incubated in a buffer containing a mixture of the zwitterionic surfactant /V,/V,-dimethyldodecylamine and the anionic surfactant sodium dodecyl sulfate,11 there was dissociation of cells in the stratum corneum but not in the rest of the epidermis. The cell dissociation took place only in the presence of EDTA and was inhibited by the serine protease inhibitor aprotinin.12 Suzuki et al.13,14 presented evidence that spontaneous cell dissociation in nonpalmo-plantar stratum corneum could be inhibited by a combination of inhibitors of trypsin-like and chymotrypsin-like enzymes. Thus, nonpalmo-plantar stratum corneum contains endogenous proteases that mediate cell dissociation. 

Calculations were carried out for a system consisting of the anionic surfactant sodium dodecyl sulfate, 1-pen-tanol (cosurfactant), cyclohexane, and water containing 0.3 M NaCl. As mentioned atthe very beginning, thechoice of this system was dictated by the possibility of identifying various types of phase behaviors for the same chemical components by merely changing the amount of added alcohol. In all calculations, we assumed the coexistence of an excess dispersed phase. This means that the droplet microemulsion phase is part of a two-phase system and that the amount of dispersed phase present in the droplet is the maximum achievable. 

Recent molecular dynamics simulations of water between two surfactant (sodium dodecyl sulfate) layers, reported by Faraudo and Bresme,14 revealed oscillatory behaviors for both the polarization and the electric fields near a surface and that the two fields are not proportional to each other. While the nonmonotonic behavior again invalidated the Gruen—Marcelja model for the polarization, the nonproportionality suggested that a more complex dielectric response of water might, be at the origin of the hydration force. The latter conclusion was also supported by recent molecular dynamics simulations of Far audo and Bresme, who reported interactions between surfactant surfaces with a nonmonotonic dependence on distance.15... 

Abstract Investigations of alternate adsorption regularities of cationic polyelectrolytes a) copolymer of styrene and dimethylaminopropyl-maleimide (CSDAPM) and b) poly(diallyldimethylammonium chloride) (PDADMAC) and anionic surfactant - sodium dodecyl sulfate (SDS) on fused quartz surface were carried out by capillary electrokinetic method. The adsorption/desorption kinetics, structure and properties of adsorbed layers for both polyelectrolytes and also for the second adsorbed layer were studied in dependence on different conditions molecular weight of polyelectrolyte, surfactant and polyelectrolyte concentration, the solution flow rate through the capillary during the adsorption, adsorbed layer formation... 

Aqueous phase (2.7 mm3) was placed in the thin lower compartment of the microcell and the Dil dodecane solution (63 mm3) was added on top of the aqueous layer. Fluorescence of the interfacial Dil was observed in the range of 571-575 nm. The influence of two kinds of surfactants, sodium dodecyl sulfate (SDS) and dimyristoyl phosphatidylcholine (DMPC), on the lateral diffusion dynamics of single molecules at the interface was investigated. DMPC was dissolved in chloroform, and the solution was mixed with pure diethyl ether at a ratio of 1 19 (chloroform diethyl ether) by volume. Pure water was placed in the lower container, and the DMPC solution was subsequently (5 mm3) spread carefully on the water. After evaporation of chloroform and diethyl ether, the Dil dodecane solution was added on the DMPC layer. Since Dil has a high... 

It has been shown that the addition of a small amount of the anionic surfactant sodium dodecyl sulfate (SDS) to a microemulsion based on nonionic surfactant increased the rate of decyl sulfonate formation from decyl bromide and sodium sulfite (Scheme 1 of Fig. 2) [59,60]. Addition of minor amounts of the cationic surfactant tetradecyltrimethylammonium gave either a rate increase or a rate decrease depending on the surfactant counterion. A poorly polarizable counterion, such as acetate, accelerated the reaction. A large, polarizable counterion, such as bromide, on the other hand, gave a slight decrease in reaction rate. The reaction profiles for the different systems are shown in Fig. 12. More recent studies indicate that when chloride is used as surfactant counterion the reaction may at least partly proceed in two steps, first chloride substitutes bromide to give decyl chloride, which reacts with the sulfite ion to give the final product [61]. 

In this context also, the electrochemical oxidation was proposed as effective process of wastewater treatment. Among surfactants, sodium dodecyl benzenesulfonate is generally assumed to represent anionic surfactants, whereas hexadecyltrimethy-lammonium chloride is assumed as representing the cationic class. 

The lanthanide triflate remains in the aqueous phase and can be re-used after concentration. From a green chemistry viewpoint it would be more attractive to perform the reactions in water as the only solvent. This was achieved by adding the surfactant sodium dodecyl sulfate (SDS 20 mol%) to the aqueous solution of e.g. Sc(OTf)3 (10 mol%) [145]. A further extension of this concept resulted in the development of lanthanide salts of dodecyl sulfate, so-called Lewis acid-surfactant combined catalysts (LASC) which combine the Lewis acidity of the cation with the surfactant properties of the anion [148]. These LASCs, e.g. Sc(DS)3, exhibited much higher activities in water than in organic solvents. They were shown to catalyze a variety of reactions, such as Michael additions and a three component a-aminophosphonate synthesis (see Fig. 2.44) in water [145]. 

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