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Polarity, relative

It is clear from our discussion of contact angle hysteresis that there is some degree of variability in reported contact angle values. The data collected in Table X-2, therefore, are intended mainly as a guide to the type of behavior to be expected. The older data comprise mainly results for refractory and relatively polar solids, while newer data are for polymeric surfaces. [Pg.364]

Most LB-forming amphiphiles have hydrophobic tails, leaving a very hydrophobic surface. In order to introduce polarity to the final surface, one needs to incorporate bipolar components that would not normally form LB films on their own. Berg and co-workers have partly surmounted this problem with two- and three-component mixtures of fatty acids, amines, and bipolar alcohols [175, 176]. Interestingly, the type of deposition depends on the contact angle of the substrate, and, thus, when relatively polar monolayers are formed, they are deposited as Z-type multilayers. Phase-separated LB films of hydrocarbon-fluorocarbon mixtures provide selective adsorption sites for macromolecules, due to the formation of a step site at the domain boundary [177]. [Pg.560]

An interesting aspect of two-photon spectroscopy is that some polarization infonnation is obtainable even for randomly oriented molecules in solution by studymg the effect of the relative polarization of die two photons. This is readily done by comparing linearly and circularly polarized light. Transitions to A states will absorb linearly polarized light more strongly than circularly polarized light. The reverse is true of transitions to B ... [Pg.1146]

Solution Properties. Typically, if a polymer is soluble ia a solvent, it is soluble ia all proportions. As solvent evaporates from the solution, no phase separation or precipitation occurs. The solution viscosity iacreases continually until a coherent film is formed. The film is held together by molecular entanglements and secondary bonding forces. The solubiUty of the acrylate polymers is affected by the nature of the side group. Polymers that contain short side chaias are relatively polar and are soluble ia polar solvents such as ketones, esters, or ether alcohols. As the side chaia iacreases ia length the polymers are less polar and dissolve ia relatively nonpolar solvents, such as aromatic or aUphatic hydrocarbons. [Pg.164]

One of the important attributes of alkyds is their good compatibiUty with a wide variety of other coating polymers. This good compatibiUty comes from the relatively low molecular weight of the alkyds, and the fact that the resin stmcture contains, on the one hand, a relatively polar and aromatic backbone, and, on the other hand, many aUphatic side chains with low polarity. An alkyd resin in a blend with another coating polymer may serve as a modifier for the other film-former, or it may be the principal film-former and the other polymer may serve as the modifier for the alkyd to enhance certain properties. Examples of compatible blends foUow. [Pg.41]

Identification of the pesticides is based on retention time on at least two dissimilar glc columns. A nonpolar and a relatively polar packing are generaUy used, for example, OV-17 and a mixture of QE-1 and DC-200. [Pg.233]

Binary Mixtures—Low Pressure—Polar Components The Brokaw correlation was based on the Chapman-Enskog equation, but 0 g and were evaluated with a modified Stockmayer potential for polar molecules. Hence, slightly different symbols are used. That potential model reduces to the Lennard-Jones 6-12 potential for interactions between nonpolar molecules. As a result, the method should yield accurate predictions for polar as well as nonpolar gas mixtures. Brokaw presented data for 9 relatively polar pairs along with the prediction. The agreement was good an average absolute error of 6.4 percent, considering the complexity of some of... [Pg.595]

Polarity test to check the connections through the potential transformer to ensure that the connections between the transformer and the meters or relays have a correct relative polarity. Otherwise the meters would show erratic readings, while the relays would transmit wrong signals. This test may also be conducted with a low-voltage source of 10 V by ob.serving the deflection of the instruments. [Pg.434]

Ionic interactions 20 0.25 Strength also depends on the relative polarity of the interacting charged species. Some ionic interactions are also H bonds —NH3+. . . ooc—... [Pg.15]

The coupling of SEC to GC is not an easy process and in order to avoid addiRonal LC interacRons that could effect the predominate size exclusion separation relatively polar solvents such as THF are usually employed. The drawback is that polar... [Pg.309]

Chlorophenoxy acids are relatively polar pesticides which are usually determined by LC because volatile derivatives have to be prepared for GC analysis. This group of herbicides can be detected by multiresidue methods combined with automated procedures for sample clean-up, although selectivity and sensitivity can be enhanced by coupled-column chromatographic techniques (52). The experimental conditions for Such analyses are shown in Table 13.1. [Pg.353]

As a matter of fact, the main advantage in comparison with HPLC is the reduction of solvent consumption, which is limited to the organic modifiers, and that will be nonexistent when no modifier is used. Usually, one of the drawbacks of HPLC applied at large scale is that the product must be recovered from dilute solution and the solvent recycled in order to make the process less expensive. In that sense, SFC can be advantageous because it requires fewer manipulations of the sample after the chromatographic process. This facilitates recovery of the products after the separation. Although SFC is usually superior to HPLC with respect to enantioselectivity, efficiency and time of analysis [136], its use is limited to compounds which are soluble in nonpolar solvents (carbon dioxide, CO,). This represents a major drawback, as many of the chemical and pharmaceutical products of interest are relatively polar. [Pg.12]

The free radical initiators are more suitable for the monomers having electron-withdrawing substituents directed to the ethylene nucleus. The monomers having electron-supplying groups can be polymerized better with the ionic initiators. The water solubility of the monomer is another important consideration. Highly water-soluble (relatively polar) monomers are not suitable for the emulsion polymerization process since most of the monomer polymerizes within the continuous medium, The detailed emulsion polymerization procedures for various monomers, including styrene [59-64], butadiene [61,63,64], vinyl acetate [62,64], vinyl chloride [62,64,65], alkyl acrylates [61-63,65], alkyl methacrylates [62,64], chloroprene [63], and isoprene [61,63] are available in the literature. [Pg.198]

The relative polarities of iron and tin are considered in Sections 4.6 and 14.5 and will not be discussed here. [Pg.232]

On the other hand there are polymers that are capable of being degraded, generally in a controlled way, to yield low molar mass molecules that can be safely metabolised by living organisms. Polymers of this type need to have relatively polar substituents, preferably ester and hydroxyl groups. One such... [Pg.125]

A number of different retention mechanisms operate in HPLC and interested readers may find further details elsewhere [2-4]. It is sufficient to say here that the interaction may be considered in terms of the relative polarities of the species involved. As indicated in Section 2.1 above, there are two extremes of interaction, neither of which is desirable if separation is to be achieved. [Pg.29]

In this section we describe a cellular automata model of a semipermeable membrane separating two compartments [5]. A solute in one compartment has varied parameters to reflect its relative polarity or lipophilicity. The passage of this solute into and through the membrane is observed, as this property is varied. [Pg.100]

With notable exceptions, the application of HPLC to clinical chemistry has not as yet been extensive. This is somewhat surprising in view of the potential the method has for this area. This potential arises, in part, from the fact that HPLC is well suited to the types of substances that must be analyzed in the biomedical field. Ionic, relatively polar species can be directly chromatographed, without the need to make volatile derivatives as in gas chromatography. Typically, columns are operated at room temperature so that thermally labile substances can be separated. Finally, certain modes of HPLC allow fractionation of high molecular weight species, such as biopolymers. [Pg.226]

By far the most popular phase system at the present time is the one in which R n-octadecyl. Since the stationary phase is hydrophobic and nonpolar, while the mobile phase is relatively polar, this mode of operation is frequently called reverse phase... [Pg.227]

Celluloses (native or microcrystalline) are organic sorbents. They have a low specific surface area and are applied mainly in partition chromatography, especially for the separation of relatively polar compounds. Works on the topic include those by Whitton and coworkers [8], who examined biosynthetic pathways for the formation of taurine in vertebrates. Taurine and its precursor amino acids were extracted from tissues, and the purified supernatant was spotted onto cellulose plates. The... [Pg.201]


See other pages where Polarity, relative is mentioned: [Pg.1208]    [Pg.583]    [Pg.282]    [Pg.1318]    [Pg.61]    [Pg.399]    [Pg.110]    [Pg.110]    [Pg.76]    [Pg.214]    [Pg.196]    [Pg.198]    [Pg.373]    [Pg.502]    [Pg.504]    [Pg.217]    [Pg.66]    [Pg.219]    [Pg.476]    [Pg.320]    [Pg.52]    [Pg.158]    [Pg.406]    [Pg.23]    [Pg.51]    [Pg.118]    [Pg.62]    [Pg.97]    [Pg.101]    [Pg.181]    [Pg.301]   
See also in sourсe #XX -- [ Pg.167 ]

See also in sourсe #XX -- [ Pg.167 ]




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