Cationic soluble surfactant

In a recent study, the influence of indifferent electrolytes on the adsorption behaviour of cationic soluble surfactant solutions has been investigated by surface tension measurements, ellipsometry and surface second harmonic generation (SHG). ° Each technique addresses different structural aspects and the combined data provide a detailed picture of the interfacial architecture. The analysis gives an indirect proof of the existence of a phase transition between the free and condensed state of the counterions caused by a small increase of surface charge close to the critical micelle concentration (cmc). 

In spite of the good calcium and magnesium tolerance of AOS systems, situations can arise whereby too many exchangeable hardness ions present themselves to the surfactant formulation. One way to overcome this is by blending AOS with a divalent cation-tolerant surfactant. A product which has been field-tested [87] is a blend of AOS and a disulfonated alkyldiphenyloxide (DPOS). Calcium and magnesium salts of DPOS are water-soluble and remain soluble even in solutions which are very concentrated in calcium and magnesium salts. 

The solubility of numerous ionic surfactants in water is strongly reduced in the presence of divalent cations. Stability in hard water is thus an important fact for surfactants used as detergents. Their stability can be measured as the amount of divalent cations at which the formation of a poorly soluble surfactant salt leads to permanent turbidity. The values given in the literature can only be... 

Quaternary alkylammonium salts are generally water-soluble surfactants. The sol-gel-derived anion-sensing membranes encapsulating a quaternary alkylammonium salt, especially with high contents, are easy to deteriorate due to the exudation of the cationic site from the membrane to aqueous sample phases. Moreover, another issue concerning the dispersibility of ammonium salts in sol-gel-derived membranes may happen when high... 

The surface active agents (surfactants) may be cationic, anionic or non-ionic. Surfactants commonly used are cetyltrimethyl ammonium bromide (CTABr), sodium lauryl sulphate (NaLS) and triton-X, etc. The surfactants help to lower the surface tension at the monomer-water interface and also facilitate emulsification of the monomer in water. Because of their low solubility surfactants get fully dissolved or molecularly dispersed only at low concentrations and at higher concentrations micelles are formed. The highest concentration where in all the molecules are in dispersed state is known as critical micelle concentration (CMC). The CMC values of some surfactants are listed in table below. 

The application of surfactants can enhance remediation or recovery of contaminants by increasing their mobility and solubility. Surfactants can thus be used to enhance ex situ soil washing, in situsoil flushing, non-aqueous-phase liquid (NAPE) pump-and-treat applications, and in situbiodegradation. Cationic surfactants have been shown to improve the capacity of soil... 

Detergent In relationship to fuel technology, a detergent is an oil-soluble surfactant added to fuel aiding in the prevention and removal of deposits. Examples include anionic alkyl aryl sulfonates, cationic fatty acid amides, or nonionic polyol condensates. 

Oil-in-water creams, for topical use, generally contain mixed emulsifiers/surfactants one of which is a water soluble surfactant with a high HLB, the other being an amphiphile, usually a long chain fatty alcohol (e.g., of chain length C14 to Cig) or acid (e.g., palmitic or stearic). The water soluble surfactant may be anionic (e.g., sodium lauryl sulphate), cationic (e.g., cetri-mide), or non-ionic (e.g., cetomacrogol. Tweens). 

In hard water, insoluble salts may form owing to interaction with calcium and magnesium cations. Solubility may be enhanced by the inclusion of surfactants such as cetrimide. 

Aminimides also offer processing advantages because of their water solubility. Aminimide predips are easily prepared in water, so a variety of water-soluble surfactants, both anionic and cationic, can be used to enhance performance. 

In addition to all of these components, a modern commercial detergent may also contain antistatic agents (cationic surfactants added to reduce static cling) hydro-tropes (compounds added to liquid detergents to hold less-soluble surfactants and other compounds in solution) and, of course, fragrances and perfumes and inert fillers and formulation aids that keep powdered detergents free flowing. 

Features Low foaming stable In addle, hot, alkaline systems good stability In hard water good solubility In aq. tems without any solubilizers, hydrotropes misc. with all anionic, cationic, nonlonic surfactants Properties Coloriess to It. yellowish, cl. liq. doud pt. 32-35 C (In 5% NaCI) 100% act. 

Konig and Waldorf discuss analysis of hair and body shampoos (32). The shampoo is first evaporated to dryness and extracted with isopropanol or 95% ethanol to separate the surfactant, which is qualitatively identified by IR. The alcohol-insoluble residue is also examined by IR in case a less-soluble surfactant remains there. The alcohol extract is then separated into anionic, cationic, nonionic, and amphoteric surfactant fractions by ion exchange. Anionics can be separated into sulfonates and carboxylates by use of strongly basic anion exchange resins in the Cl" and OH" form, respectively. Anionics are further characterized by TLC. Nonionics are likewise characterized by TLC. Once the components are identified, quantitative analysis is by the usual methods, described elsewhere in this volume. 

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. 

Sequestration forms the basis for detergent and water-treatment appHcations of polyphosphates. Sequestration of hardness ions by sodium tripolyphosphate used in detergent formulations prevents the precipitation of surfactants by the hardness ions. Sodium polyphosphate glass (SHMP) may be added to water system to prevent the formation of calcium or magnesium scales by reducing the activity of the hardness ions. However, if the ratio of cation to polyphosphate is too high at a given pH, insoluble precipitates such as may result instead of the soluble polyphosphate complexes. The... 

Microscopic sheets of amorphous silica have been prepared in the laboratory by either (/) hydrolysis of gaseous SiCl or SiF to form monosilicic acid [10193-36-9] (orthosihcic acid), Si(OH)4, with simultaneous polymerisation in water of the monosilicic acid that is formed (7) (2) freesing of colloidal silica or polysilicic acid (8—10) (J) hydrolysis of HSiCl in ether, followed by solvent evaporation (11) or (4) coagulation of silica in the presence of cationic surfactants (12). Amorphous silica fibers are prepared by drying thin films of sols or oxidising silicon monoxide (13). Hydrated amorphous silica differs in solubility from anhydrous or surface-hydrated amorphous sdica forms (1) in that the former is generally stable up to 60°C, and water is not lost by evaporation at room temperature. Hydrated sdica gel can be prepared by reaction of hydrated sodium siUcate crystals and anhydrous acid, followed by polymerisation of the monosilicic acid that is formed into a dense state (14). This process can result in a water content of approximately one molecule of H2O for each sdanol group present. 

Physical and ionic adsorption may be either monolayer or multilayer (12). Capillary stmctures in which the diameters of the capillaries are small, ie, one to two molecular diameters, exhibit a marked hysteresis effect on desorption. Sorbed surfactant solutes do not necessarily cover ah. of a sohd iaterface and their presence does not preclude adsorption of solvent molecules. The strength of surfactant sorption generally foUows the order cationic > anionic > nonionic. Surfaces to which this rule apphes include metals, glass, plastics, textiles (13), paper, and many minerals. The pH is an important modifying factor in the adsorption of all ionic surfactants but especially for amphoteric surfactants which are least soluble at their isoelectric point. The speed and degree of adsorption are increased by the presence of dissolved inorganic salts in surfactant solutions (14). 

Ethoxylation of alkyl amine ethoxylates is an economical route to obtain the variety of properties required by numerous and sometimes smaH-volume industrial uses of cationic surfactants. Commercial amine ethoxylates shown in Tables 27 and 28 are derived from linear alkyl amines, ahphatic /-alkyl amines, and rosin (dehydroabietyl) amines. Despite the variety of chemical stmctures, the amine ethoxylates tend to have similar properties. In general, they are yellow or amber Hquids or yellowish low melting soHds. Specific gravity at room temperature ranges from 0.9 to 1.15, and they are soluble in acidic media. Higher ethoxylation promotes solubiUty in neutral and alkaline media. The lower ethoxylates form insoluble salts with fatty acids and other anionic surfactants. Salts of higher ethoxylates are soluble, however. Oil solubiUty decreases with increasing ethylene oxide content but many ethoxylates with a fairly even hydrophilic—hydrophobic balance show appreciable oil solubiUty and are used as solutes in the oil phase. 

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