Surfactants anionic

Anionic surfactants are those which bear a negative charge and migrate toward the anode or positive charge in solution. This class of salt like compounds include the soaps and many of the popular synthetics (Fig. 4-6). When fats are hydrolysed 

Anionic surfactants are amphiphilic substances that include an anionic group as an obligatory component attached directly or through intermediates to a long hydrocarbon chain. The most commercial anionic surfactants are generally inhomogeneous mixtures with respect to both the composition and hydrocarbon chain length since the purity is often not crucial for their 

Dissociating in water, anionic surfactants form the surface-active anions and hydrated cations, for example, cations of alkali metals or ammonium  

The hydrocarbon part of the surfactant can be a straight-chain aliphatic radical, as in the case of sodium dodecyl sulphate given above, as well as a branched-chain, unsaturated radical, and can involve benzene or phenolic residues and polar groups  

0(CH2CH20)6C3H6S03NH4 Ammonium o-nonylphenol hexa(ethoxy)propanesulphonate 

About 75 % of anionic surfactants (other than soaps) in the world are based on synthetic raw materials. Recent tendencies however let expect that in the 3 millennium renewable materials of biological and botanical origin will be more and more preferred. 

These are the most widely used class of surfactants in agrochemical applications [8,9). This is due to their relatively low cost of manufacture and they are used in practically every type of formulation. Linear chains are preferred since they are more effective and more degradable than the branched chains. The most commonly used hydrophilic groups are carboxylates, sulfates, sulfonates and phosphates. A general formula may be ascribed to anionic surfactants as follows  

Several other anionic surfactants are commercially available such as sulfosuccinates, isethionates and taurates and these are sometimes used for special applications. A brief description of the above anionic classes is given below with some of their applications. 

Sodium Lauryl Sulfate BP is a mixture of sodium alkyl sulfates, the chief of which is sodium dodecyl sulfate, Cj2H25S04Na. it is very soluble in water and is used pharmaceutically as a preoperative skin cleaner, having bacteriostatic action against Gram-positive 

The degree of branching of the alkyl chain can be analysed from the intensity of CH3 bands at 2960 and 1380 cm Hard ABS—highly branched and therefore less biodegradable—exhibits more intense CH3 bands than does soft linear ABS. 

Alkyl and alkoxy sulphates. Alkyl sulphates can be distinguished from sulphonates by the position of the S=0 stretch this is above 1200 cm for sulphates but just below 1200 cm for sulphonates. The SO4 deformation is also shifted higher (to approximately 1080 cm ). 

Alkyl ether sulphates feature bands characteristic of ethoxy groups (see section 10.6.2) and alkyl sulphate functionality, with additional bands at 1030 and 780 cm  

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Results can sometimes be unexpected. The first study of this type made use of labeled Aerosol OTN [111], an anionic surfactant, also known as di-n-octylsodium sulfosuccinate. The measured F was twice that in Eq. III-93 and it was realized that hydrolysis had occurred, that is, X + H2O = HX + OH , and that it was the undissociated acid HX that was surface-active. Since pH was essentially constant, the activity of HX was just proportional to C. A similar behavior was found for aqueous sodium stearate [112]. 

A selection of important anionic surfactants is displayed in table C2.3.1. Carboxylic acid salts or tire soaps are tire best known anionic surfactants. These materials were originally derived from animal fats by saponification. The ionized carboxyl group provides tire anionic charge. Examples witlr hydrocarbon chains of fewer tlran ten carbon atoms are too soluble and tliose witlr chains longer tlran 20 carbon atoms are too insoluble to be useful in aqueous applications. They may be prepared witlr cations otlrer tlran sodium. 

This ordering is the same as discussed above for anionic surfactants and follows from the charge density of the particular acid group. 

Fonnation of a complex with a copper cation only further stimulates this behaviour. As a result, S.lg is almost completely bound to the micelles, even at low concentrations of Cu(DS)2. By contrast, the reaction of 5.1 f still benefits from an increasing surfactant concentration at 10 mM of Cu(DS)2. In fact, it is surprising that the reaction of this anionic compound is catalysed at all by an anionic surfactant. Probably it is the copper complex of 5.If, being overall cationic, that binds to the micelle. Not surprisingly, the neutral substrate S.lc shows intermediate behaviour. 

The concentration of anionic surfactants at the sub-ppm level in natural waters and industrial waters are determined spectrophotometrically. The anionic surfactants are extracted into a nonaqueous solvent following the formation of an ion association complex with a suitable cation. 

Anionic polymers Anionic starches Anionic surfactants... 

Eigure 6 illustrates how the three tensions among the top, middle, and bottom phases depend on temperature for a system of nonionic surfactant—oil—water (38), or on salinity for a representative system of anionic surfactant—cosurfactant—oil—water and electrolyte (39). As T approaches from lower temperatures, the composition of M approaches the composition of T, and the iaterfacial teasioa betweea them, goes to 2ero at T =. ... 

The surfactants used in the emulsion polymerization of acryhc monomers are classified as anionic, cationic, or nonionic. Anionic surfactants, such as salts of alkyl sulfates and alkylarene sulfates and phosphates, or nonionic surfactants, such as alkyl or aryl polyoxyethylenes, are most common (87,98—101). Mixed anionic—nonionic surfactant systems are also widely utilized (102—105). 

Aqueous Dispersions. The dispersion is made by the polymerization process used to produce fine powders of different average particle sizes (58). The most common dispersion has an average particle size of about 0.2 p.m, probably the optimum particle size for most appHcations. The raw dispersion is stabilized with a nonionic or anionic surfactant and concentrated to 60—65 wt % soHds by electrodecantation, evaporation, or thermal concentration (59). The concentrated dispersion can be modified further with chemical additives. The fabrication characteristics of these dispersions depend on polymerization conditions and additives. 

Anionic Surfactants. In terms of general usage in cosmetic products, the anionics are by far the most widely used and are chiefly found in shampoo systems. They provide the formulator with the basic conditions for preparing these products, ie, foaming, cleansing, and solubiHty. 

A.lkyl Sulfosuccinate Half Asters. These detergents are prepared by reaction of maleic anhydride and a primary fatty alcohol, followed by sulfonation with sodium bisulfite. A typical member of this group is disodium lauryl sulfosucciaate [26838-05-1]. Although not known as effective foamers, these surfactants can boost foams and act as stabilizers when used ia combination with other anionic surfactants. In combination with alkyl sulfates, they are said to reduce the irritation effects of the latter (6). 

Many different types of foaming agents are used, but nonionic surfactants are the most common, eg, ethoxylated fatty alcohols, fatty acid alkanolamides, fatty amine oxides, nonylphenol ethoxylates, and octylphenol ethoxylates, to name a few (see Alkylphenols). Anionic surfactants can be used, but with caution, due to potential complexing with cationic polymers commonly used in mousses. 

Three generations of latices as characterized by the type of surfactant used in manufacture have been defined (53). The first generation includes latices made with conventional (/) anionic surfactants like fatty acid soaps, alkyl carboxylates, alkyl sulfates, and alkyl sulfonates (54) (2) nonionic surfactants like poly(ethylene oxide) or poly(vinyl alcohol) used to improve freeze—thaw and shear stabiUty and (J) cationic surfactants like amines, nitriles, and other nitrogen bases, rarely used because of incompatibiUty problems. Portiand cement latex modifiers are one example where cationic surfactants are used. Anionic surfactants yield smaller particles than nonionic surfactants (55). Often a combination of anionic surfactants or anionic and nonionic surfactants are used to provide improved stabiUty. The stabilizing abiUty of anionic fatty acid soaps diminishes at lower pH as the soaps revert to their acids. First-generation latices also suffer from the presence of soap on the polymer particles at the end of the polymerization. Steam and vacuum stripping methods are often used to remove the soap and unreacted monomer from the final product (56). 

Lignites and lignosulfonates can act as o/w emulsifiers, but generally are added for other purposes. Various anionic surfactants, including alkylarylsulfonates and alkylaryl sulfates and poly(ethylene oxide) derivatives of fatty acids, esters, and others, are used. Very Httle oil is added to water-base muds in use offshore for environmental reasons. A nonionic poly(ethylene oxide) derivative of nonylphenol [9016-45-9] is used in calcium-treated muds (126). 

In the 1990s, the thmst of surfactant flooding work has been to develop surfactants which provide low interfacial tensions in saline media, particularly seawater require less cosurfactant are effective at low concentrations and exhibit lower adsorption on rock. Nonionic surfactants such as alcohol ethoxylates, alkylphenol ethoxylates (215) and propoxylates (216), and alcohol propoxylates (216) have been evaluated for this appHcation. More recently, anionic surfactants have been used (216—230). 

Including a surfactant in the caustic formulation (surfactant-enhanced alkaline flooding) can increase optimal salinity of a saline alkaline formulation. This can reduce iaterfacial tension and increase oil recovery (255,257,258). Encouraging field test results have been reported (259). Both nonionic and anionic surfactants have been evaluated in this appHcation (260,261). 

Surfactants evaluated in surfactant-enhanced alkaline flooding include internal olefin sulfonates (259,261), linear alkyl xylene sulfonates (262), petroleum sulfonates (262), alcohol ethoxysulfates (258,261,263), and alcohol ethoxylates/anionic surfactants (257). Water-thickening polymers, either xanthan or polyacrylamide, can reduce injected fluid mobiHty in alkaline flooding (264) and surfactant-enhanced alkaline flooding (259,263). The combined use of alkah, surfactant, and water-thickening polymer has been termed the alkaH—surfactant—polymer (ASP) process. Cross-linked polymers have been used to increase volumetric sweep efficiency of surfactant—polymer—alkaline agent formulations (265). 

In the presence of an anionic surfactant such as sodium dodecyl-benzenesulfonate [25155-30-0] any protonated amine salt present forms an insoluble salt (4). Salt formation results in an increase in the pH of the solution. 

Anionic surfactants are the most commonly used class of surfactant. Anionic surfactants include sulfates such as sodium alkylsulfate and the homologous ethoxylated versions and sulfonates, eg, sodium alkylglycerol ether sulfonate and sodium cocoyl isethionate. Nonionic surfactants are commonly used at low levels ( 1 2%) to reduce soap scum formation of the product, especially in hard water. These nonionic surfactants are usually ethoxylated fatty materials, such as H0CH2CH20(CH2CH20) R. These are commonly based on triglycerides or fatty alcohols. Amphoteric surfactants, such as cocamidopropyl betaine and cocoamphoacetate, are more recent surfactants in the bar soap area and are typically used at low levels (<2%) as secondary surfactants. These materials can have a dramatic impact on both the lathering and mildness of products (26). 

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