Detergent properties

Chemistry produces many materials, other than drugs, that have to be optimized in their properties and preparation. Chemoinformatics methods will be used more and more for the elucidation and modeling of the relationships between chemical structure, or chemical composition, and many physical and chemical properties, be they nonlinear optical properties, adhesive power, conversion of light into electrical energy, detergent properties, hair-coloring suitabHty, or whatever. 

A.lpha-Olefm Sulfonates. Sulfonation of alpha-olefins yields a mixture of alkene sulfonates, hydroxyalkane sulfonates, and some amount of various disulfonates. These detergents are excellent foamers with good detergency properties. They are unaffected ia hard water and thek effects are considered superior to the alkyl ether sulfates (9). 

Step 2 A mixture of 118 parts of the product of Step 1, having hydroxyl number of 260, 2 parts of solid NaH, and 100 parts of toluene was heated to 125° to 150°C In an autoclave. Ethylene oxide was added slowly over a period of 2 /2 hours until 261 parts of ethylene oxide were absorbed. This corresponds to 11 mols of ethylene oxide per mol of phenol in the product of Step 1. The toluene was then removed by steam distillation and the water by vacuum distillation at 10°C. The product was obtained as a viscous paste having a corrected hydroxyl number of 97. It was readily soluble in water and had marked detergent properties. 

Metal surface cleaning, by virtue of (limited) sequestration, dispersing, surface-acting, and detergent properties. 

Already in 1943 M. Schuler [2] described the comparison of the surface-active properties of sodium palmitate with several ether carboxylates based on a constant amount of C atoms. The results showed that with more O bridges the optimal surface activity and emulsifying properties can be achieved at lower temperature, with the detergent properties decreasing and solubility increasing. 

Low-foaming liquid or powdered machine detergents are described using a surfactant system prepared from naturally based raw materials with good biodegradability and detergent properties [135]. These formulations are based on 5-30% alkylpolyglucoside, 5-30% alkyl ether carboxylate, 5-35% soap, and 0-3% of another surfactant. 

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. 

There has been considerable discussion regarding the mode of action of the sea cucumber and starfish saponins. Both the triterpene and steroidal glycosides inhibit both Na/K ATPase and Ca/Mg ATPase 06) possibly as a result of their aglycone structures. However, their detergent properties cause membrane disruption which will influence the activity of membrane-bound enzymes such as the ATPases. In investigating the actions of saponins on multilamellar liposomes, it was found that cholesterol serves as the binding site for such saponins and that cholesterol-free lip-somes are not lysed by saponins 107). 

Even if this class covers the smallest market segment, amphoteric surfactants still remain useful because of their unique properties, which justifies their comparably high manufacturing costs. Since they have partial anionic and cationic character, they can be compatible, under specific conditions, with both anionic and cationic surfactants. They can function in acid or basic pH systems and, at their isoelectric point, they exhibit special behaviour. Many amphoteric surfactants demonstrate exceptional foaming and detergency properties combined with antistatic effects. 

Step 1 The dominant quality factors here are convenience and the ability to deliver the precise dosage for applications. Optimum HLB is an important factor for convenience (Table 2). As in example 1, an HLB value between 3 and 15 is desirable for the detergency property, preferably towards the high end to give clear appearance (Figure 1). Thus, HLB0p is set to be 15. 

Trace aromatics removal from linear paraffins in the Ciq-Cis range is an important step in producing linear alkylbenzene (LAB) which in turn is used to make linear alkylbenzene sulfonate (LAS) an important constituent of detergents. High purity linear paraffins are required to produce superior detergent properties. For this application, MgY and NaX adsorbents are reported to be effective adsorbents in removing aromatics from Cio-C n-paraffins [265-267]. 

Representing >20% of bile, are strong sulphonic acids with detergent properties. They are soluble in the normal acidic stomach, with pKa values of <2. Thus they can partially enter the gastric epithelium. It is also known that epithelial diffusion barriers can be broken by BAs, which further allow them entry into the epithelium. 

Bile helps in the digestion and absorption of fats. Its constituent bile acids (BAs) have detergent properties, and some can be carcinogenic. BAs can act as signalling molecules, entering the nuclei and reacting with the nuclear receptors and this could enhance or reduce BA synthesis. In this way, they control their own levels as well as those of their precursor, cholesterol. This controls cholesterol homeostasis and BA and lipid synthesis. 

Base hydrolysis of fats with sodium or potassium hydroxide liberates glycerol and the salt of the carboxylic acid(s). This reaction was the basis of soap making the salt, or mixture of salts, is a soap with characteristic detergent properties. The relationship of ester hydrolysis to soap-making remains, in that base hydrolysis of esters is still commonly referred to as saponification. 

While synthetic oil-soluble sulfonates have also been made by reacting high molecular weight olefins or chlorinated wax with selected aromatics and sulfonating the resulting compound, the oil detergent properties of these materials have been reported to be inferior to those made by conventional acid-treating procedures on petroleum distillates. 

The detergent properties of the alkyl sulfonates approach those of the alkyl aryl sulfonates, but the commercial processing problems have placed these materials at an economic disadvantage. 

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