INDEX preferential

The general or universal effects in intermolecular interactions are determined by the electronic polarizability of solvent (refraction index n0) and the molecular polarity (which results from the reorientation of solvent dipoles in solution) described by dielectric constant z. These parameters describe collective effects in solvate s shell. In contrast, specific interactions are produced by one or few neighboring molecules, and are determined by the specific chemical properties of both the solute and the solvent. Specific effects can be due to hydrogen bonding, preferential solvation, acid-base chemistry, or charge transfer interactions. 

Special care has to be taken if the polymer is only soluble in a solvent mixture or if a certain property, e.g., a definite value of the second virial coefficient, needs to be adjusted by adding another solvent. In this case the analysis is complicated due to the different refractive indices of the solvent components [32]. In case of a binary solvent mixture we find, that formally Equation (42) is still valid. The refractive index increment needs to be replaced by an increment accounting for a complex formation of the polymer and the solvent mixture, when one of the solvents adsorbs preferentially on the polymer. Instead of measuring the true molar mass Mw the apparent molar mass Mapp is measured. How large the difference is depends on the difference between the refractive index increments ([dn/dc) — (dn/dc)A>0. (dn/dc)fl is the increment determined in the mixed solvents in osmotic equilibrium, while (dn/dc)A0 is determined for infinite dilution of the polymer in solvent A. For clarity we omitted the fixed parameters such as temperature, T, and pressure, p. 

If the optically active medium is not transparent at the wavelength of the incident radiation, the transmitted intensity may be further reduced by an absorptive contribution to the index of refraction. Because of preferential absorption of either the left or the right circularly polarized component, the emerging beam would no longer be the sum of equal amplitudes and trace out an ellipse with ellipticity tp = (kt — kr). Practical details of the measurement and chemical applications of optical activity are discussed by Charney[34],... 

Identification of Peaks for Hydrogen Adsorption on the Disordered Low Index Planes. Besides the major objective for studying electrocatalysis on single crystal stepped surfaces mentioned above, these studies offer a wealth of information on the behaviour of polycrystalline surfaces, of preferentially oriented surfaces and, as we suggested recently (12), of disordered low-index surface. 

Polymers formed from two or more monomers such as condensation polymers and copolymers, as well as homopolymers are indexed at each inverted monomer name with the modifying term polymer with followed by the other monomer names in uninverted alphabetical order. The preferential listing for identical heading parents is in the order (1) maximum number of substituents (2) lowest locants for substituents (3) maximum number of occurrences of index heading parent and (4) earliest index position of the index heading. Examples are ... 

The results on olefin isomers (Table Vll) can also be explained by the observation that the constraint index of ZSM-5 is approximately unity under the conditions of this study. Shape selectivity or preferential conversion of straight chain olefins by ZSM-5 cannot be expected at 500 C. Thus, under the conditions of this study, olefin isomer distribution was not significantly affected by deactivated ZSM-5. At temperatures lower than that employed in the present study, it is conceivable that distribution of olefin isomers could be altered by steam deactivated ZSM-5. 

A quantitative measure of interaction between polymer and monomer in solution can be expressed by a value of preferential solvation. Preferential solvation can be calculated from the measurements of refractive index increments in dialysis experiments. This experiment can be illustrated as in Figure 3.1. 

Sulfurized Vat Dyes. These dyes occupy an intermediate position between the true vat colors and sulfur dyes because, like vat dyes, they are dyed preferentially from a sodium dithionite—caustic soda bath. However, some dyes of this class can also be dyed from an alkali sulfide bath or a combination of the two, depending on the dyeing method used and the nature of the substrate to be dyed. This has led to some confusion because Cl Vat Blue 42 and 43 are listed in the constitution section of the Colour Index under sulfur dyes. Although inferior to true vat dyes in fastness properties, they offer the advantage of better fastness, especially to chlorine, than conventional sulfur dyes. 

There are numerous properties of materials which can be used as measures of composition, e.g. preferential adsorption of components (as in chromatography), absorption of electromagnetic waves (infra-red, ultra-violet, etc.), refractive index, pH, density, etc. In many cases, however, the property will not give a unique result if there are more than two components, e.g. there may be a number of different compositions of a particular ternary liquid mixture which will have the same refractive index or will exhibit the same infra-red radiation absorption characteristics. Other difficulties can make a particular physical property unsuitable as a measure of composition for a particular system, e.g. the dielectric constant cannot be used if water is present as the dielectric constant of water is very much greater than that of most other liquids. Instruments containing optical systems (e.g. refractometers) and/or electromechanical feedback systems (e.g. some infra-red analysers) can be sensitive to mechanical vibration. In cases where it is not practicable to measure composition directly, then indirect or inferential means of obtaining a measurement which itself is a function of composition may be employed (e.g. the use of boiling temperature in a distillation column as a measure of the liquid composition—see Section 7.3.1). 

Extensive theoretical work in support of both models of thermal etching was produced before 1970. The theoretical basis for the thermodynamic model was the concept of reduction in total surface energy by the preferential formation of low-energy, low-index planes. The true equilibrium shape of a crystal is the shape with the lowest surface energy, as noted by Curie (36) and Gibbs (37). The thermodynamic models provide no information regarding the process of surface rearrangement. 

Microscopy. This is a powerful tool for studying visually the distribution of the two phases in the polyblend. One can tell not only the domain size of the dispersed phase but also which polymer forms the dispersed phase from refractive index. A phase contrast light microscope can detect heterogeneity at the 0.2-10 /x level. If the sample can be stained preferentially and sectioned with microtome, then under favorable conditions electron microscopy can show heterogeneity to a very fine scale. In a study of PVC-poly(butadiene-co-acrylonitrile) blend,... 

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