Twin surfactants

The term gemini surfactant was coined by Menger inl991. A gemini surfactant may be viewed as a surfactant dimer, i.e. two amphiphilic molecules connected by a spacer. Figure 17.1 shows the general structure. Gemini surfactants are also referred to as twin surfactants , dimeric surfactants or bis-surfactants . 

The effect of concentration of cationic (cetylpyridinium chloride, CPC), anionic (sodium dodecylsulfate, SDS) and nonionic (Twin-80) surfactants as well as effect of pH value on the characteristics of TLC separ ation has been investigated. The best separ ation of three components has been achieved with 210 M CPC and LIO M Twin-80 solutions, at pH 7 (phosphate buffer). Individual solution of SDS didn t provide effective separation of caffeine, theophylline, theobromine, the rate of separ ation was low. The separ ation factor and rate of separ ation was increase by adding of modifiers - alcohol 1- propanol (6 % vol.) or 1-butanol (0.1 % vol.) in SDS solution. The optimal concentration of SDS is 210 M. 

It was found that the effect of solvents and various surfactants Triton X-100, Twin-80, Brij-35 sodium laurylsulfate, sodium cetylsulfate, cetylpyridinium chloride, cetyltrimethylammonium bromide on the luminescence intensity is insignificant. 

The effect of mixtures of surfactants and polyelectrolytes on spontaneous, water-catalysed hydrolysis (Fadnavis and Engberts, 1982) was mentioned in Section 4, but mixtures of functionalized polyelectrolytes and cationic surfacants are effective deacylating agents (Visser et al., 1983). Polymerized isocyanides were functionalized with an imidazole group and the deacylation of 2,4-dinitrophenyl acetate in the polyelectrolyte was speeded by addition of single or twin chain quaternary ammonium ion surfactants, up to a plateau value. Anionic surfactants had essentially no effect. It is probable that the cationic surfactants accelerate the reaction by increasing the deprotonation of the imidazole groups. 

The relation between head-group area and extended chain length and volume of the apolar groups favors formation of vesicles or bilayers from these twin-tailed surfactants. However, it seems that DDDAOH forms vesicles only in dilute solution, because the solution becomes viscous with increasing [surfactant] which is incompatible with the presence of approximately spherical vesicles. It appears that the solution then contains long, non-vesicular aggregates (Ninham et al., 1983). 

Fig. 22. ETEM at 180°C in N2, illustrating the stability of gold nanorods, for nanoelectronics and catalysis applications. Gold atomic layers and surface atomic structures are visible. Surface of gold nanorod at room temperature showing twin defect lamellae on the atomic scale. They indicate interaction of the surfactant with the (110) surface forming twins to accommodate the shape misfit between the two.

Rouse, J. D., Sabatini, D. A., and Harwell, J. H. (1993). Minimizing Surfactant Losses Using Twin Head Anionic Surfactants in Subsurface Remediation. Environmental Science and Technology, 27, 2072-2078. 

Ethoxylation is carried out in the same manner as for primary alcohols described earlier but, in general, only up to the 3-mol ethoxylate as a feedstock for some specialised ether sulphates. These products show some advantages in wetting and foaming applications compared to the straight alcohol sulphates. These twin tail surfactants require less co-surfactant to make microemulsions and emulsify 3-5 times more oil than sulphates made from linear hydrophobes. 

The positively charged nitrogen aids in the deposition of the surfactant onto the fabric and the twin tails provide the lubricity and hand-feel desired by consumers [20]. From this basic structure a medley of materials arise each with its particular exigency being satisfied. 

The new structures place a cleavable functionality within the twin tails of the cationic surfactant which aids in biodegradation by separating the positively charged nitrogen hy-drophile from the hydrophobic portion as shown in Figure 6.2. 

In emulsions, amine hydrochloride constitutes the aqueous phase and acrylic ester the organic phase. Cetyltrimethylanunonium bromide (CTAB) or span/twin (S/T)-type surfactants are used for emulsion polymerization. Solid dispersants such as talc and colloidal silica are often used to stabilize emulsions which are difficult to stabilize with usual surfactants. HydrophiUc colloidal silica (Aerosil 200) drastically increases the stability of some emulsions provided high amounts (up to 10%) of Aerosil are used. Random copolymers containing 10% hydroxyl groups can be used as polymeric dispersants for preparing w/o emulsions. 

For multifetal pregnancies, separate specimens should be analyzed for each fetus. Infrequently, more than one fetus shares an amniotic fluid cavity. In such a case, a mature result is less predictive of maturity, because it represents a mixture of pulmonary surfactant from multiple fetuses. In the case of twins, the smaller is more likely to develop RDS than the larger. ... 

All types of micro emulsions were obtained in salinity scans with mixtures of Aerosol MA (sodium dihexyl sulphosuccinate) and twin-tailed (Guerbet and Exxon type) alcohol ethoxy and propoxy sulphates for perchloroethylene (PCE), carbon tetrachloride, 1,2-dichlorobenzene and trichloroethylene [59] at 25°C. At lower temperatures, however, stable macro emulsions are formed. Chloroform, 1,2-dichloroethane and other chlorinated hydrocarbons were found to be too polar for those anionic surfactants. Extremely hydrophilic and temperature-insensitive surfactants are necessary for effective solubilisation of chlorinated hydrocarbons yielding Winsor III systems. N-methyl-N-D-glucalkaneamide surfactants showed good performance for DNAPL solubilisation even at 16°C [56]. 

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