Potassium acid-soaps

The potassium acid-soaps were made by two methods. 

Table I. Per Cent Acid in Potassium Acid-Soaps...

Figure I. Differential thermograms of potassium acid-soaps (Hormel and Baker fatty acids) prepared from ethanol and petroleum ether...

Upper and lower lines. Those of Piper (18) for potassium acid-soaps and potassium soaps, respectively... 

In soap bar processing free fatty acid is usually added in formulations to create so-called super-fatted soap. An acid-soap complex with a fixed stoichiometric ratio between alkaline soap and the fatty acid is formed. For example, the ratio of potassium acid soap is 1 1 while sodium soap forms acid soaps with various ratios. The fixed ratio complex exits not only in anhydrous crystalline phase but also in a hydrous liquid crystalline phase (11, 12). Oleic acid and its potassium soap form a 1 1 complex acid soap when equal molar acid and soap are mixed. Above the Krafft boundary, the acid soap in water forms a lamellar liquid crystal phase at low surfactant concentration, from a few percent, and the lamellar liquid crystal phase extends to ca 60% surfactant concentration. A hexagonal liquid crystal phase is formed after the lamellar liquid crystal phase with further increasing the surfactant concentration. This phase behavior is different from the soap and water phase behavior, in which the hexagonal liquid crystalline phase is formed first followed by the lamellar liquid crystalline phase. Below the Krafft boundary the acid soap complex forms a solid crystal and separates from water (4). 

In the other market areas, lead naphthenates are used on a limited basis in extreme pressure additives for lubricating oils and greases. Sodium and potassium naphthenates are used in emulsiftable oils, where they have the advantage over fatty acid soaps of having improved disinfectant properties. Catalyst uses include cobalt naphthenate as a cross-linking catalyst in adhesives (52) and manganese naphthenate as an oxidation catalyst (35). Metal naphthenates are also being used in the hydroconversion of heavy petroleum fractions (53,54) and bitumens (55). 

Oxalate Acid Number. A metal soap solution is treated with a measured excess of organic acid. Potassium oxalate solution is added to precipitate the metal and the total sample is back-titrated with alkaU to determine its acidity. Acidity is expressed ia acid number units, equivalent to mg KOH per g. A neutral soap gives a 2ero acid number, an acidic soap solution a positive acid number, and a basic soap solution a negative acid number. 

Latex Types. Latexes are differentiated both by the nature of the coUoidal system and by the type of polymer present. Nearly aU of the coUoidal systems are similar to those used in the manufacture of dry types. That is, they are anionic and contain either a sodium or potassium salt of a rosin acid or derivative. In addition, they may also contain a strong acid soap to provide additional stabUity. Those having polymer soUds around 60% contain a very finely tuned soap system to avoid excessive emulsion viscosity during polymeri2ation (162—164). Du Pont also offers a carboxylated nonionic latex stabili2ed with poly(vinyl alcohol). This latex type is especiaUy resistant to flocculation by electrolytes, heat, and mechanical shear, surviving conditions which would easUy flocculate ionic latexes. The differences between anionic and nonionic latexes are outlined in Table 11. 

Vinyl monomers may be polymerized at favorable rates in an aqueous medium containing an emulsifier and a water-soluble initiator. A typical simple Tecipe would consist of the following ingredients with their proportions indicated in parts by weight 100 of monomer, 180 of water, 2 to 5 of a fatty acid soap, and 0.1 to 0.5 of potassium persulfate. Cationic soaps (e.g., dodecylamine hydrochloride) may be used instead of the fatty acid soap, and various other initiators may replace the persulfate (e.g., hydrogen peroxide and ferrous ion, or a water-soluble organic hydroperoxide). 

Soaps are salts of fatty acids (weak acids) and strong bases such as sodium hydroxide or potassium hydroxide. Soaps therefore dissolve in water to form alkaline solutions. 

Soaps are the detergents used since long. Soaps used for cleaning purpose are sodium or potassium salts of long chain fatty acids, e.g., stearic, oleic and palmitic acids. Soaps containing sodium salts are formed by heating fat (i.e., glyceryl ester of fatty acid) with aqueous sodium hydroxide solution. This reaction is known as saponification. 

Anionic surfactants are the most commonly used surfactants in emulsion polymerization [Blackley, 1975 Gardon, 1977]. These include fatty acid soaps (sodium or potassium... 

Table II lists the absorption peaks observed in the 6-micron region for the acid-soaps. With the exception of potassium acid-butyrate all members up to Ci2 have their major absorption peak (underlined in Table II) at 5.82 to 5.9 microns. On the other hand, the acid-soaps of chain length Ci4 or greater have their major C=0 absorption band at 6.1 microns. A sole exception in Table II is the potassium acid-stearate prepared from Eastman fatty acid, whose major absorption peak falls in the range 5.82 to 5.9 microns again.

The composition data obtained for the series of mixed fatty acid-potassium soap systems, prepared by both the ethanol and petroleum ether routes, lend strong support to the formation of 1 to 1 acid-soap complexes. It is of interest to inquire into the phase relationships in these two-component systems. A phase diagram presented by McBain and Field (15) for the lauric acid-potassium laurate system shows that compound formation takes place between the two components at the 1 to 1 molar ratio, but the compound undergoes melting with decomposition at 91.3 °C. [A similar type of phase behavior has been reported by us for the sodium alkyl sulfate-alkyl alcohol (9) and sodium alkyl sulfonate-alkyl alcohol (12) systems, but in these cases the stoichiometry is 2 to 1]. 

Saturated straight-chain fatty-acid soaps (1). Figure 1 shows the effects of increasing levels of various potassium saturated straight-chain fatty-acid soaps upon the mechanical stability of natural rubber latex. For convenience of making comparisons between the various soaps, the levels of added soap are expressed as moles per 100 g. of latex solids. 

The results summarised in Table I show the effect of equal parts by weight of each of the potassium fatty-acid soaps upon the mechanical stability of each of the three chemically-destabilised latices. For convenience in making comparisons, estimates of the corresponding results for unmodified natural rubber latex are also included. It is clear from these results that the ability of added potassium fatty-acid soaps to enhance the stability of chemically-destabilised natural rubber latex roughly parallels their abilities to enhance the mechanical stability of unmodified natural rubber latex. 

Figure 1. Effect of added straight-chain potassium fatty-acid soaps upon mechanical stability of natural rubber latex (1). Numbers appended to curves are number of carbon atoms in alkyl chain of soap.

The effects of a range of sodium n-alkyl sulphates and sodium n-alkyl sulphonates upon the mechanical stability of natural rubber latex are summarised in Figures 4 and 5 respectively. As in the case of added potassium fatty-acid soaps, small additions of... 

Table Ii Effect of 0.1 part by weight per 100 parts latex solids of various potassium fatty-acid soaps upon mechanical stability of unmodified and chemically-destabilised natural rubber 1atices (1 )...

A surfactant molecule is an amphiphile, which means it has a hydrophilic (water-soluble) moiety and a hydrophobic (water-insoluble) moiety separable by a mathematical surface. The hydrophobic tails of the most common surfactants are hydrocarbons. Fluorocarbon and perfluorocarbon tails are, however, not unusual. Because of the hydrophobic tail, a surfactant resists forming a molecular solution in water. The molecules will tend to migrate to any water-vapor interface available or, at sufficiently high concentration, the surfactant molecules will spontaneously aggregate into association colloids, i.e., into micelles or liquid crystals. Because of the hydrophilic head, a surfactant (with a hydrocarbon tail) will behave similarly when placed in oil or when put in solution with oil and water mixtures. Some common surfactants are sodium or potassium salts of long-chained fatty acids (soaps), sodium ethyl sulfates and sulfonates (detergents), alkyl polyethoxy alcohols, alkyl ammonium halides, and lecithins or phospholipids. 

Builders are formulated into detergents mainly to sequester hardness ions (Ca2+, Mg2+) found in water, as well as to disperse the dirt and soil particulates in the wash water. Common builders used in liquid detergents are sodium and potassium polyphosphates (except in the U.S.), carbonates, aluminosilicates (zeolite A), silicates, citrates, and fatty acid soaps [5],... 

Fatty acids, potassium salts Potassium fatty acid soap Potassium salts of fatty acids Potassium soap Soap, potassium Soaps, potassium. 

Cocoa fatty acids, potassium salts Coconut fatty acid, potassium salt Coconut oil acids, potassium salt Coconut oil fatty acid, potassium salt Coconut oil, potassium salts Coconut Oil po sium soap EINECS 263-049-9 Fatty acids, coco, potassium salts Fatty acids, coconut oil, potassium salts Potassium cocoate Potassium coconut oil soap Potassium coconut soap Soap, potassium coconut. 

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