Detergency anionic surfactants

Formation of ineffective neutral salts with detergent anionic surfactants... 

Oxidation of the precursor anion in these models can be catalysed by cobalt (and other transition metals) [25]. The enzyme can also be modelled to some extent by surfactant solutions [26]. Quaternary ammonium salts (e. g. cetyl trimethylammonium bromide) are better than neutral detergents. Anionic surfactants are ineffective. The reason for the activity is two-fold. The rate of oxidation is increased, and the fluorescence of the product, which is very weak in pure water, is considerably enhanced in the hydrophobic micelles. 

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). 

Amphoteric Detergents. These surfactants, also known as ampholytics, have both cationic and anionic charged groups ki thek composition. The cationic groups are usually amino or quaternary forms while the anionic sites consist of carboxylates, sulfates, or sulfonates. Amphoterics have compatibihty with anionics, nonionics, and cationics. The pH of the surfactant solution determines the charge exhibited by the amphoteric under alkaline conditions it behaves anionically while ki an acidic condition it has a cationic behavior. Most amphoterics are derivatives of imidazoline or betaine. Sodium lauroamphoacetate [68647-44-9] has been recommended for use ki non-eye stinging shampoos (12). Combkiations of amphoterics with cationics have provided the basis for conditioning shampoos (13). 

In acidic media, amine oxides and anionic surfactants form precipitates the CMC is much greater than in neutral or alkaline media. Change in CMC parallels change from ionic to nonionic form. Amine oxides are stable in formulated detergent products and do not act as oxidizing agents. Composition and function of representative commercial amine oxides are given in Table 26. 

Anionic Surfactants. PVP also interacts with anionic detergents, another class of large anions (108). This interaction has generated considerable interest because addition of PVP results in the formation of micelles at lower concentration than the critical micelle concentration (CMC) of the free surfactant the mechanism is described as a "necklace" of hemimicelles along the polymer chain, the hemimicelles being surrounded to some extent with PVP (109). The effective lowering of the CMC increases the surfactant s apparent activity at interfaces. PVP will increase foaming of anionic surfactants for this reason. 

Protease performance is strongly influenced by detergent pH and ionic strength. Surfactants influence both protease performance and stabiUty in the wash solution. In general, anionic surfactants are more aggressive than amphoteric surfactants, which again are more aggressive than nonionic surfactants. 

AH detergent proteases are destabilized by linear alkylbenzenesulfonate (LAS), the most common type of anionic surfactant in detergents. The higher the LAS concentration and wash temperature, the greater the inactivation of the enzyme. The presence of nonionic surfactants, however, counteracts the negative effect of LAS. Almost aH detergents contain some nonionic surfactant therefore, the stabHity of proteases in a washing context is not problematic. 

The system of anionic surfactants is another example of organic compounds mixtures. The procedure of their determination is proposed using coordinate pH in two-dimensional spectra of ionic associates anionic surfactants with rhodamine 6G. This procedure was tested on the analysis of surfactant waters and domestic detergents. 

Sodium dodecylbenzenesulfonate is undoubtedly the anionic surfactant used in the greatest amount because it is the basic component in almost all laundry and dishwashing detergents in powder and liquid forms. However, alcohol and alcohol ether sulfates are the more versatile anionic surfactants because their properties vary, with the alkyl chain, with the number of moles of ethylene oxide added to the base alcohol and with the cation. Consequently, alcohol and alcohol ether sulfates are used in almost all scientific, consumer, and industrial applications. 

Ether carboxylates are used not only in powdered detergents but in liquid laundry detergents for their hard water stability, lime soap dispersibility, and electrolyte stability they improve the suspension stability and rheology of the electrolyte builder [130,131]. Formulations based particularly on lauryl ether carboxylate + 4.5 EO combined with fatty acid salt and other anionic surfactants are described [132], sometimes in combination with quaternary compounds as softeners [133,163]. Ether carboxylates show improved cleaning properties as suds-controlling agents in formulations with ethoxylated alkylphenol or fatty alcohol, alkyl phosphate esters or alkoxylate phosphate esters, and water-soluble builders [134]. 

This chapter deals with sodium a-olefinsulfonate (AOS) and with sodium internal olefmsulfonate (IOS). AOS is a well-established product and is being applied in many household and industrial formulations. IOS of a sufficiently high quality has only recently been made on laboratory scale and pilot plant scale and has not yet been applied in commercial formulations. AOS and IOS have not only good wetting and detergency properties, but also good tolerance toward water hardness ions, a combination not always observed for other anionic surfactants. 

The composition of a typical IOS system prepared by Stapersma et al. [4] is shown in Table 2, along with the analytical data of an AOS with the same chain length. Compositions containing IOS, a nonionic surfactant, glycols, and another salt-tolerant anionic surfactant which are pourable and pumpable at 20°C and can be used in the manufacturing of detergent compositions, have also been described by Stapersma et al. [36]. 

The types of analyses discussed in this section can be divided into two groups active matter and impurities. Several methods assess the anionic surfactant (active matter) content of the AOS product. These are particularly important since detergent performance is directly related to surfactant concentration. The different types of anionic active material are identified and quantified. 

Also the a-ester sulfonates are less important today. In the Federal Republic of Germany, for example, the total production of surfactants was about 700,000 t/a in 1993. For a more detailed analysis of different types of surfactants, use must be made of data collected before the unification of Germany. In 1988 the consumption of surfactants in detergents was about 227,500 t/a, the consumption of anionic surfactants was about 116,000 t/a and less than 1000 t/a of a-sulfo fatty acid esters [5] (the values refer to German Detergent Law). 

Stable liquid detergents are obtained by polyacetalcarboxylate builders, ionic or nonionic surfactants, and common ingredients of detergents. If esters of phosphoric acid are used as anionic surfactants a detergent of this kind with 62% of water retained a single phase after a 30-day storage [213]. 

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