Solubilisation Solubility

The maximum additive concentration (MAC) is defined as the maximum amount of solubilisate, at a given concentration of surfactant, that produces a clear solution. Different amounts of solubilisates, in ascending order, are added to a series of vials containing the known concentration of surfactant and mixed until equilibrium is reached. The maximum concentration of solubilisate that forms a clear solution is then determined visually. This same procedure can be repeated for the different concentrations of surfactant in a known amount of solubilisate in order to determine the optimum concentration of surfactant (Figure 4.24). Based on this information, one can construct a ternary phase diagram that describes the effects of three constituents (i.e., solubilisate, surfactant, and water) on the micelle system. Note that unwanted phase transitions can be avoided by ignoring the formulation compositions near the boundary. In general, the MAC increases with an increase in temperature. This may be due to the combination of the increase of solubilisate solubility in the aqueous phase and the micellar phase rather than an increased solubilization by the micelles alone. 

Detergents are made by, for example, treating petroleum hydrocarbons with sulphuric acid, yielding sulphonated products which are water soluble. These can also solubilise fats and oils since, like the stearate ion, they have an oil-miscible hydrocarbon chain and a water-soluble ionic end. The calcium salts of these substances, however, are soiu u-ic in water and, therefore, remove hardness without scum formation. 

Paint strippers are also formulated to have high viscosity, otherwise they run off vertical surfaces and thereby fail to penetrate or solubilise the paint to which they have been applied. Hydroxypropyl methylcellulose is the main thickener for paint strippers, which use methylene chloride (dicldoromethane) as the principal component. Hydroxypropyl methylcellulose is useful for this purpose because it is soluble in the orgaiuc component but is not sensitive to the presence of any water that may also be present in the paint stripper. 

Positive photoresists, by contrast, are based on water-soluble novolak resins with naphthalene diazoquinone sulfonate (NDS) as the photosensi-tiser. On photolysis the NDS causes a rearrangement in the polymer to yield nitrogen gas plus an indene carboxylic acid. This latter functional group considerably increases the solubility of the polymer, hence solubilising those areas of the polymer that had been exposed to light. 

Analysis of the products which become water-soluble after extrusioncooking showed that feroylated heteroxylans and glucans were solubilised from wheat bran (10), arabinans, heteroxyalans and pectins from pea hulls (11,12), and pectins from the other sources (13,14). 

Extrusion-cooking increased very significantly the water-solubility of plant cell wall rich-materials. High amounts of pectins can be solubilised from sugar-beet pulp, citrus peels or apple pomace. 

Pectins from different tissue zones, namely epidermis, the outer parenchyma, the parenchyma of the Ccirpels zone, the carpels and the core line, were isolated firom alcohol-insoluble solids (AIS. In both zones of parenchyma, the cell-wall material represented about 80% of the total cell-wall material from the whole fruit. The pectins from the outer parenchyma accounted for 70% of the total. However, there was no change in galacturonic acid concentration. The enzymatic solubilisation of tissues or AIS was higher in the parenchyma zones than in the others. Nevertheless, the depolymerisation of the soluble pectins from parenchyma zones with an endopolygacturonase required the action of pectin methylesterase. The depoiymerisation of pectins from the other zones, however, did not. 

The ability of SFE-FTIR to perform a variety of extraction methods is a definite advantage, especially for the study of complex mixtures containing analytes of varying solubility. For analytes which are readily solubilised in C02, direct dynamic and direct static-dynamic SFE-FTIR methods are quite successful. Elimination of the trapping process reduces both analysis time and potential analyte loss arising from... 

A surfactant was defined in Chapter 8 as an agent, soluble or dispersible in a liquid, which reduces the surface tension of the liquid [1]. It is helpful to visualise surfactant molecules as being composed of opposing solubility tendencies. Thus, those effective in aqueous media typically contain an oil-soluble hydrocarbon-based chain (the hydrophobe) and a smaller water-solubilising moiety which may or may not confer ionic character (the hydrophile). The limitations of space do not permit a comprehensive detailed treatment of the chemistry of surfactants. The emphasis is therefore on a broad-brush discussion of the principal types of surfactant encountered in textile preparation and coloration processes. Comprehensive accounts of the chemistry and properties of surfactants are available [2-13]. A useful and lucid account of the chemistry and technology of surfactant manufacturing processes is given by Davidsohn and Milwidsky [ 14] ... 

Desizing by chemical decomposition is applicable to starch-based sizes. Since starch and its hydrophilic derivatives are soluble in water, it might be assumed that a simple alkaline rinse with surfactant would be sufficient to effect removal from the fibre. As is also the case with some other size polymers, however, once the starch solution has dried to a film on the fibre surface it is much more difficult to effect rehydration and dissolution. Thus controlled chemical degradation is required to disintegrate and solubilise the size film without damaging the cellulosic fibre. Enzymatic, oxidative and hydrolytic degradation methods can be used. 

Many acrylic acid copolymers are water-soluble but unlike poly(vinyl alcohol) they are not degraded by alkali. In fact they need alkali for effective desizing as they are more soluble at alkaline pH than in neutral solutions. They are sensitive to acidic media, which should not be used. Solubilisation occurs by the formation of sodium carboxylate groups from the anionic polyacid. The polyelectrolyte formed in this way is readily soluble and shows a rapid rate of dissolution. However, the presence of electrolytes such as magnesium or calcium salts from hard water can inhibit removal [191]. 

Normal rhombic sulphur has differing degrees of solubility in the different rubber types. In NR and SBR the required proportion for crosslinking dissolves relatively rapidly at room temperature. In stereospecific rubbers such as polybutadiene and nitrile it does not solubilise so readily. As one would expect, the solubility of the sulphur within the rubber increases with temperature increase. 

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