Stearic acid functionality

Monoalkoxy titanate Chelate titanate Quat titanate Neoalkoxy titanate Cycloheteroatom titanate Stearic acid functionality aids in dispersion of mineral fillers in polyolefins Greater stability in wet environments Water-soluble, aids adhesion of water-soluble coatings and adhesives Eliminates pretreatment associated with fillers, can be used as a concentrated solid additive Ultrahigh thermal properties for specialty applications... 

Chemical properties of deposited monolayers have been studied in various ways. The degree of ionization of a substituted coumarin film deposited on quartz was determined as a function of the pH of a solution in contact with the film, from which comparison with Gouy-Chapman theory (see Section V-2) could be made [151]. Several studies have been made of the UV-induced polymerization of monolayers (as well as of multilayers) of diacetylene amphiphiles (see Refs. 168, 169). Excitation energy transfer has been observed in a mixed monolayer of donor and acceptor molecules in stearic acid [170]. Electrical properties have been of interest, particularly the possibility that a suitably asymmetric film might be a unidirectional conductor, that is, a rectifier (see Refs. 171, 172). Optical properties of interest include the ability to make planar optical waveguides of thick LB films [173, 174]. 

The most commonly used amphiphiles to build L-B hlms for tribological applications are the straight chain hydrocarbon compounds with simple functional groups such as the fatty acids, including stearic acids, arachidic acids, and behenic acids [32], but other amphiphilic molecules, e.g., 2,4-heneicosanedione and 2-docosylamina-5-nitropyridine, are also applied in some cases. There are two major systems of self-assembled monolayers, namely the alkylsilance derivatives (e.g., OTS, octadecyltrichlorosilane) on hydroxylated surfaces and the alkanethiols on metal substrates, which have been investigated extensively to examine their properties as solid lubricants and protective surface films [31 ]. 

An analytical solution for molecules with alkaline functionality is acid/base titration. In this technique, the polymer is dissolved, but not precipitated prior to analysis. In this way, the additive, even if polymer-bound, is still in solution and titratable. This principle has also been applied for the determination of 0.01 % stearic acid and sodium stearate in SBR solutions. The polymer was diluted with toluene/absolute ethanol mixed solvent and stearic acid was determined by titration with 0.1 M ethanolic NaOH solution to the m-cresol purple endpoint similarly, sodium stearate was titrated with 0.05 M ethanolic HC1 solution [83]. Also long-chain acid lubricants (e.g. stearic acid) in acrylic polyesters were quantitatively determined by titration of the extract. 

Fig. 8 Optimizing values of stearic acid and starch as a function of restrictions on tablet friability (A) percent starch (B) percent stearic acid. (From Ref. 15.)...

A dusting agent which is soluble in rubber and thus does not impair the vulcanised bond between rubber components of a composite product. It is also an activator combining the functions of zinc oxide and stearic acid, of particular value in transparent rubbers since it does not produce the same opacity as zinc oxide. 

Triacylglycerols, commonly refered to as fats and oils, consist of three fatty acids linked to a molecule of glycerol, a three-carbon alcohol. Fatty acids are long-carbon-chain molecules, each with a single carboxyl functional group. Common examples are stearic acid and palmitic acid, shown in Figure 16.3. 

The hyperbranched polyesteramides described above can also easily be functionalized by esterification with various mono carboxylic acids like acetic acid, benzoic acid, 2-ethylhexanoic acid, stearic acid, (un)satuxated fatty acids, or (meth)acrylic acid. With the exception of the latter mentioned acids, which give highly temperature sensitive products, the synthesis of these functionalized hyperbranched polyesteramides can be performed in two different ways ... 

Fig. 13. Idealized structure of the product of hydroxyl/stearic ester functionalized hyperbranched polyesteramides based on adipic acid and diisopro-panolamine functionalized with octenyl succinic anhydride... 

A 50% functionalization evokes the interesting question, bearing in mind facile transesterification, of how the fluoroalkyl chains will be distributed over the molecules and how they will be distributed on one particular molecule This question has been examined in detail for dendrimers of the poly(propyleneimine) type functionalized with stearic acid [33]. It was proven that the compositional heterogeneity (distribution of degree of substitution) is random, but the positional heterogeneity (spatial distribution of the substituents over the dendrimer molecule) is not random. However, due to flexibility, no particular effect of the spatial distribution can be observed. Unlike the dendrimers, we expect the hyperbranched polyesteramides to be stiffer, so that spatial distribution could lead to interesting effects if the molecule were composed of a functionalized side and a non-func-tionalized side (Fig. 28), as shown possible for dendrimers via a convergent synthesis [34]. 

Dampproofing admixtures are formulated to affect the properties of the hardened concrete, and not those of concrete in its plastic state. In the case of materials based solely on calcium and aluminum stearates, stearic acid in solid or emulsion form, bitumens and hydrocarbon resins, there will be no effect on the properties of the plastic concrete with regard to air content, workability, mix design parameters, etc. When water-reducing admixtures or accelerators are included in the formulation, the effect on the concrete will be a function of the particular type of material used (see relevant section). The wax emulsions do appear to have an effect on the properties of the plastic concrete because of the lubrication effect of the very small... 

Compacting of specific materials can be facilitated with certain kinds of additives. Binders are additives that confer strength to the agglomerates, and lubricants reduce friction during the operation. Some additives may function both ways. A few of the hundreds of binders that have been tried or proposed are listed in Table 12.12. Lubricants include the liquids water, glycerine, and lubricating oils and typical solids are waxes, stearic acid, metallic stearates, starch, and talc. 

An aliphatic ketone (9-heptadecanone) and two keto derivatives of stearic acid (as potassium salts) containing a ketone functionality either at position 5 or 12 were incorporated into bilayers of the phospholipid l,2-dihexadecyl-sn-glycero-3-phosphocholine. Infrared spectra of these mixtures were measured as a function of temperature and amount of added cholesterol. It was found that the presence of cholesterol in these bilayers induces changes in the location of the guest ketone and that these changes are dependent on both temperature and cholesterol concentration. It is also demonstrated that, in the gel phase, the presence of cholesterol induces larger intersheadgroup separations and, therefore, water penetrates deeper into the lipid bilayer. 

The effect of the particular functional group on adsorption, however, is not always the same as seen on oxide surfaces. For example, carboxylic acids adsorb strongly on metal oxide surfaces, and the heat of adsorption of stearic acid is higher than that of the corresponding ester, methyl stearate (Hironaka et al., 1978). For adsorption on the nascent surface, however, propionic acid is a poor adsorbate, and the adsorption activity of propionic acid is lower than that of methyl propionate. Although propyl amine adsorbs easily on metal oxide surfaces, the adsorption activity of propyl amine is low on the fresh steel surfaces. Also, the heat of adsorption of organic sulfides on iron oxide is less than that of esters (Forbes et al., 1970b), but the results of adsorption activity on the nascent surface were the opposite. It is thus noteworthy that the chemical nature of the nascent surface of steel is often opposite to that of oxide-covered metal surfaces, with respect to adsorption. 

Figure 7 Plot of the change in the product of the coupling and maximum saturation factors as a function of macromolecular structure. At lower pH values, the spin-labelled lipids are present as vesicles and vesicular aggregates, while at higher pH values, micelles are formed. The higher psmax values for the micelles imply greater water accessibility to the radical site. The solid circles represent 16-DS (16-doxyl stearic acid, spin-labelled at the end of the lipid tail) while the open circles represent 5-DS (5-doxyl stearic acid, spin-labelled near the polar head group). Reproduced with permission from Ref. [70].

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