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Surfactants alkyl sulfates

Ammonium Lauryl Sulfate Water-White Liquid Activity, % 27-29 [Pg.113]

Detergent, foaming and suspending agent for liquid cleaners. Produces copious rich foam. Stable in products at pH range 4 to 7 buffering is recommended. Good viscosity response to the additions of salt and alkanolamides. [Pg.113]


Anionic surfactant Alkyl sulfate, alkylbenzene sulfonate, ethoxylated alkyl sulfate, soap 0-10 0-0.3... [Pg.601]

Ion flotation in the presence of surfactants for the treatment of rinses and separation of metal ions is of interest since the sixties [327, 328]. Here, we take only a few examples. The recovery of silver ions from highly diluted solutions is possible by forming a silver-thiourea complex in form of a colloidal precipitate (sublate) followed by sublate flotation with sodium dodecyl benzene sulfonate [329]. Skiylev [330] has developed methods for the removal of non-ferrous metal salts from waste waters. Subject of the investigations were 0.01 - 0.001% solutions of ferrous metal salts. Typical anionic surfactants (alkyl sulfates, alkyl phosphates, alkyl xanthogenates of potassium) or cationic surfactants (quaternary ammonium salts) were used as collectors in ion flotation from diluted solutions. At certain pH, a sublate containing a non-ferrous metal ion was formed, followed by a sublate film formation at the surface due to the rise of the complexes with air bubbles stabilised by the surfactants. [Pg.600]

Surfactant alkyl sulfate, soap, linear benzene Cleaning, wetting, thickening 1-15... [Pg.95]

Surfactants Alkyl sulfate, alkyl polyglucoside, alkyl polyethylene glycol ether 2-5 2-5... [Pg.249]

Anionic surfactants. The main anionic surfactants, alkyl sulfates and alkyl sulfonates as well as ethoxylate derivatives were analysed. C12 and C14 homologues of alkyl sulfates... [Pg.307]

Uses Intermediate for mfg. of surfactants, alkyl sulfates and ethoxylates, alkyl halides, esters, alkyl amines, aluminum rolling lubricants, tertiaty amines, cosmetics, ethoxylales, halldes/mercaptans, polymerization stabilizers, sulfation Properties Wh. waxy solid mild, soapy odor negligible sol. In water sp.gr. 0.811 (K C) vapor pressure < 1 mm Hg m.p. 56-M C b.p. > 248.9 C flash pt. (PMCC) 172 C acid no. 0.5 max. iodine no. 2 max. sapon. no. 1 max. hyd. no. 200-215 100% cone. [Pg.266]

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). [Pg.168]

The detergent range alcohols and their derivatives have a wide variety of uses ia consumer and iadustrial products either because of surface-active properties, or as a means of iatroduciag a long chain moiety iato a chemical compound. The major use is as surfactants (qv) ia detergents and cleaning products. Only a small amount of the alcohol is used as-is rather most is used as derivatives such as the poly(oxyethylene) ethers and the sulfated ethers, the alkyl sulfates, and the esters of other acids, eg, phosphoric acid and monocarboxyhc and dicarboxyhc acids. Major use areas are given ia Table 11. [Pg.449]

Shampoos based on lauryl sulfates can range from 6—17% of the active surfactant. However, though they are effective cleansers, the alkyl sulfates tend to be defatting. In an effort to make these shampoos more mild, many shampoos are now based on blends of amphoterics and alkyl sulfates or the less irritating alkyl ether sulfates. [Pg.449]

AlkylPtherSulfates. These surfactants are also found in shampoo appHcations. They are prepared similarly to alkyl sulfates except that the fatty alcohol is... [Pg.449]

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). [Pg.450]

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). [Pg.25]

Sodium fatty acid ester sulfonates are known to be highly attractive as surfactants. These have good wetting abiHty and exceUent calcium ion stabiHty as weU as high detergency without phosphates, and are used in powders or Hquids. They can also be used in the textile industry, emulsion polymerization, cosmetics, and metal surface fields. Moreover, they are attractive because they are produced from renewable natural resources and their biodegradabiHty is almost as good as alkyl sulfates (134—137). [Pg.80]

The solubihty characteristics of sodium acyl isethionates allow them to be used in synthetic detergent (syndet) bars. Complex blends of an isethionate and various soaps, free fatty acids, and small amounts of other surfactants reportedly are essentially nonirritant skin cleansers (66). As a rule, the more detersive surfactants, for example alkyl sulfates, a-olefin sulfonates, and alkylaryl sulfonates, are used in limited amounts in skin cleansers. Most skin cleansers are compounded to leave an emollient residue on the skin after rinsing with water. Free fatty acids, alkyl betaines, and some compatible cationic or quaternary compounds have been found to be especially useful. A mildly acidic environment on the skin helps control the growth of resident microbial species. Detergent-based skin cleansers can be formulated with abrasives to remove scaly or hard-to-remove materials from the skin. [Pg.299]

Until the 1950s ether carboxylates were almost in very limited amounts in the textile industry. It was only in 1957 [9] that the first ethercarobxylates were mentioned, in combination with other surfactants such as alkyl sulfates and ether sulfates, for use in shampoos. In spite of the special properties of ether carboxylates, their use was low in the industry as well as in cosmetics at that time. This was also due to the fact that at that time properties such as toxicity, biodegradability, and mildness to the skin did not have the high priority they do now. [Pg.314]

All of the aspects and applications described in papers can be traced back to the patent literature [73]. The special or synergistic effect of ether carboxylates in combination with other surfactants is very often the basis, like combinations with alkyl ether sulfates or alkyl sulfates, for shampoos, foambaths, showerbaths, and liquid soaps [9,70,81-85], and the same for amidether carboxylates [71]. [Pg.337]

AOS is a complex mixture of different chemical species. A typical product composition is as follows [1-7] sodium alkenesulfonate (60-70%) sodium hydroxyalkanesulfonate (30%) sodium disulfonate (0-10%) 6- or 1, 4-sultone (50 ppm) unsulfonated matter (less than 2%) and inorganic salt (mainly sodium sulfate, less than 2.5%). AOS can therefore be regarded as a surfactant system in contrast with other common surfactants such as alkyl sulfates, alkyle-thoxy sulfates, alkanesulfonates, and alkylbenzenesulfonates, which consist of mixtures of their isomers and/or homologs. [Pg.364]

The CMC of commercial AOS and other surfactants at 40°C has been determined by Gafa and Lattanzi [6] who plotted the surface tension of aqueous surfactant solutions against concentration. The surface tensions were determined with the ring method according to du Nouy. Table 5 gives their CMC values in mmol/L and the surface tension at the CMC in mN/m. Table 5 also contains CMC values of isomerically pure sodium alkyl sulfates, sodium alkylbenzene-sulfonates, sodium hydroxyalkanesulfonate, and sodium alkenesulfonates at 40°C, taken from the literature [39 and references cited therein]. [Pg.372]

Alkyl sulfates and alcohol ether sulfates have been established for use in emulsion polymerization. AOS, although it has been used for many detergent applications during the past four decades, does not find any large-scale use as a primary surfactant system in emulsion polymerization. A study by Kreis [92] has shown that AOS surfactants are very well able to produce a small size latex and have excellent foaming characteristics (i.e., foam height and stability) in latex. They should therefore be able to compete with alkyl sulfates and alcohol ether sulfates. [Pg.429]

More recent publications on sulfosuccinates have confirmed the minimal or close to zero skin and eye irritation caused by these products. In a general screening of product safety evaluation methods the authors [16] rejected the sulfosuccinate from further consideration in the statistical analysis of experimental data (variance analysis) because the product had not shown any irritation in the Duhring-Chamber test. The sulfosuccinate (based on fatty alcohol ethoxy late) was tested in a screening with 14 other surfactants, namely, alkyl sulfates, sulfonates, ether sulfates, and a protein fatty acid condensation product. [Pg.505]

In the simplest case a surfactant is composed of an organic hydrophobic part and a hydrophilic part (Fig. 3). In an alkyl sulfate the hydrophobic part is derived from a fatty alcohol and the sodium sulfate moiety as the hydrophilic counterpart. (Only small variations concerning the fatty chain are possible in this special kind of structure.)... [Pg.505]

Phosphoric acid esters of alcohols or ethoxylated alcohols are recommended as surfactants which are mild to the skin. Thus they are successfully used in cosmetics such as shampoos and lotions. In analogy to alkyl sulfates and alkyl ether... [Pg.609]

Ellis AW, SG Hales, NGA Ur-Rehman, GF White (2002) Novel alkylsulfatases required for biodegradation of the branched primary alkyl sulfate surfactant 2-butyloctyl sulfate. Appl Environ Microbiol 68 31-36. [Pg.572]

Ethoxylated methylcarboxylates Propoxyethoxy glyceryl sulfonate Alkylpropoxyethoxy sulfate as surfactant, xanthan, and a copolymer of acrylamide and sodium 2-acrylamido-2-methylpropane sulfonate Carboxymethylated ethoxylated surfactants (CME) Polyethylene oxide (PEG) as a sacrificial adsorbate Polyethylene glycols, propoxylated/ethoxylated alkyl sulfates Mixtures of sulfonates and nonionic alcohols Combination of lignosulfonates and fatty amines Alkyl xylene sulfonates, polyethoxylated alkyl phenols, octaethylene glycol mono n-decyl ether, and tetradecyl trimethyl ammonium chloride Anionic sodium dodecyl sulfate (SDS), cationic tetradecyl trimethyl ammonium chloride (TTAC), nonionic pentadecylethoxylated nonylphenol (NP-15), and nonionic octaethylene glycol N-dodecyl ether Dimethylalkylamine oxides as cosurfactants and viscosifiers (N-Dodecyl)trimethylammonium bromide Petrochemical sulfonate and propane sulfonate of an ethoxylated alcohol or phenol Petrochemical sulfonate and a-olefin sulfonate... [Pg.198]

Steinbrech, B., Neugebauer, D., Zulauf, G. (1986). Determination of surfactants by liquid chromatography (HPLC). Reversed phase ion-pair chromatography of alkyl sulfates and alkyl sulfosuccinates. Analytische Chemie 324(2), 154—157. [Pg.445]


See other pages where Surfactants alkyl sulfates is mentioned: [Pg.325]    [Pg.807]    [Pg.113]    [Pg.666]    [Pg.308]    [Pg.325]    [Pg.807]    [Pg.113]    [Pg.666]    [Pg.308]    [Pg.488]    [Pg.449]    [Pg.158]    [Pg.233]    [Pg.299]    [Pg.529]    [Pg.168]    [Pg.200]    [Pg.217]    [Pg.337]    [Pg.475]    [Pg.482]    [Pg.606]    [Pg.637]    [Pg.569]    [Pg.232]    [Pg.197]    [Pg.256]    [Pg.434]   
See also in sourсe #XX -- [ Pg.2 , Pg.211 ]




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Alkyl sulfates

Alkyl surfactants

Alkylated surfactants

Anionic surfactants alkyl ether sulfate

Anionic surfactants alkyl sulfate

Sulfate surfactants

Sulfated surfactants

Surfactants Alkyl Ether Sulfates

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