Anion compatibility

If we use the values for polytethylene, we see that Nc is smaller than the value of N corresponding to the mathematical minimum of the total free energy. This fact is still true for other values of V, as long as y is large enough. The conclusion is straightforward the hydrophobicity of neutral monomers causes the vesicle to be coated with the maximum Nr of anions, compatible with their cross-section. 

A unique, liquid cationic exhibiting excellent substantivity and conditioning properties. Its anionic compatibility is ideal in formulating true conditioning shampoos. Its solubility properties create new possibilities for sprays, mousses, setting gels and conditioners. 

Uses Surfactant, conditioner, softener and emulsifier for shampoos, body washes Features Mod, foaming anionic-compat. no adverse foam or detergent performance... 

Uses Patented surfactant providing copious dense foam softener for personai care prods. anionic-compat. 

Quats are usually moderately soluble ia water, but this varies widely owiag to the range of groups bonded to the nitrogen. They are fundamentally nonreactive but act as surface—active cations. Compatibility with anionic detergents and activity ia the presence of hard water have been claimed for some quats (19). 

Emulsifiers. Removing the remover is just as important as removing the finish. For water rinse removers, a detergent that is compatible with the remover formula must be selected. Many organic solvents used in removers are not water soluble, so emulsifiers are often added (see Emulsions). Anionic types such as alkyl aryl sulfonates or tolyl fatty acid salts are used. In other appHcations, nonionic surfactants are preferred and hydrophilic—lipophilic balance is an important consideration. 

A detergent that is compatible with the remover formula must be developed for water rinse removers. Anionic or nonionic surfactants should be selected, depending on the pH and intended application of the remover. 

HEC is generally compatible with other ceUulosic water-soluble polymers to give clear, homogeneous solutions. When mixed with an anionic polymer such as CMC, however, interactions between the two polymers may result in synergistic behavior, ie, viscosities higher than predicted and calculated. HEC has excellent compatibiUty with natural gums. 

HPC is compatible with many natural and synthetic water-soluble polymers and gums (50). Generally, blends of HPC with another nonionic polymer such as HEC yield water solutions having viscosities in agreement with the calculated value. Blends of HPC and anionic CMC, however, produce solution viscosities greater than calculated. This synergistic effect may be reduced in the presence of dissolved salts or if the pH is below 3 or above 10. 

Polyacrjiates (3), where R = H, CH n < 100, 000 and Y = OH, OCH, O, etc, or copolymers with compatible monomers, are probably the most flexible dispersant products, because they are produced in a variety of molecular weights and degrees of anionic charge. Moreover, reaction of acryflc acid with other monomers confers additional properties that make them more adaptable for niche appHcations. 

The earliest SIS block copolymers used in PSAs were nominally 15 wt% styrene, with an overall molecular weight on the order of 200,000 Da. The preparation by living anionic polymerization starts with the formation of polystyryl lithium, followed by isoprene addition to form the diblock anion, which is then coupled with a difunctional agent, such as 1,2-dibromoethane to form the triblock (Fig. 5a, path i). Some diblock material is inherently present in the final polymer due to inefficient coupling. The diblock is compatible with the triblock and acts... 

In an ideal SEC separation, the mechanism is purely sieving, with no chemical interaction between the column matrix and the sample molecules. In practice, however, a small number of weakly charged groups on the surface of all TSK-GEL PW type packings can cause changes in elution order from that of an ideal system. Fortunately, the eluent composition can be varied greatly with TSK-GEL PW columns to be compatible with a wide range of neutral, polar, anionic, and cationic samples. Table 4.8 lists appropriate eluents for GFC of all polymer types on TSK-GEL PW type columns (11). 

Incorporation of a carbonyl group into the alkyl side chain also proved compatible with biologic activity. The key intermediate (76) is obtainable by Michael addition of the anion from diethyl malonate to methylvinyl ketone followed by ketalization with ethylene glycol. Condensation of 76 with hydrazobenzene leads to the pyrazolodione hydrolysis of the ketal group affords ketasone (78). ... 

The addition of co-solvents to ionic liquids can result in dramatic reductions in the viscosity without alteration of the cations or anions in the system. The haloaluminate ionic liquids present a challenge, due to the reactivity of the ionic liquid. Nonetheless, several compatible co-solvents including benzene, dichloromethane, and acetonitrile have been investigated [33-37]. The addition of as little as 5 wt. % acetonitrile or 15 wt. % benzene or methylene chloride was able to reduce the... 

As a polycation, chitosan spontaneously forms macromolecular complexes upon reaction with anionic polyelectrolytes. These complexes are generally water-insoluble and form hydrogels [90,91]. A variety of polyelectrolytes can be obtained by changing the chemical structure of component polymers, such as molecular weight, flexibility, fimctional group structure, charge density, hydrophilicity and hydrophobicity, stereoregularity, and compatibility, as... 

The condensation of nitro compounds and imines, the so-called aza-Henry or nitro-Mannich reaction, has recently emerged as a powerful tool for the enantioselective synthesis of 1,2-diamines through the intermediate /3-amino nitro compounds. The method is based on the addition of a nitronate ion (a-nitro carbanion), generated from nitroalkanes, to an imine. The addition of a nitronate ion to an imine is thermodynamically disfavored, so that the presence of a protic species or a Lewis acid is required, to activate the imine and/or to quench the adduct. The acidic medium is compatible with the existence of the nitronate anion, as acetic acid and nitromethane have comparable acidities. Moreover, the products are often unstable, either for the reversibility of the addition or for the possible /3-elimination of the nitro group, and the crude products are generally reduced, avoiding purification to give the desired 1,2-diamines. Hence, the nitronate ion is an equivalent of an a-amino carbanion. 

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