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Compound molar mass

Conformation in the Melt and in Solution 4.3.1. Low-Molar Mass Compounds [Pg.104]

The conformation of molecules is determined in the gaseous state completely, and in the crystalline state almost completely by intracatenary forces. Solvents interact with solutes, and, thus, can alter their conformations. The effect of this interaction, however, is weak when the solute is surrounded by like molecules. Thus, butane has practically the same conformation energy in the gaseous state, 3.35 kJ/mol, as in the liquid state, 3.22 kJ/mol. [Pg.104]

The increase in gauche conformations in polar solvents caused by the gauche effect is also seen with w 5o-2,4-pentane diol (Table 4-4). The proportion of TT diads with this compound decreases with increasing solvent polarity, and the proportions of TG and G T diads increase. It is noteworthy that the proportion of pure gauche diads is practically zero in all solvents. [Pg.104]

Solvent Relative permittivity Percentage of conformative diads  [Pg.105]

In principle, the same effects are observed on dissolving crystalline helical polymers. In addition, the interaction of the solvent with the polymer may be observed, as well as changes in the population and sequence lengths of conformations caused by this interaction. Two limiting cases may be distinguished according to the strength of the interaction  [Pg.106]


Ideally, the sample should be injected onto the column as an infinitely thin disc, which covers the total cross section of the column. Because this is impossible, PSS has injected finite volumes onto the columns. In theory, these injection volumes should be as low as possible. In order to be able to detect the sample with significance, a certain (high) concentration of the sample has to be injected. This concept works well for low molar mass compounds, which do not generate much sample viscosity. However, when working with samples... [Pg.282]

FIGURE 9.9 Definition of column test parameters using a SEC chromatogram of a polymer standard mixture (PSS Polystyrene ReadyCal) and a low molar mass compound (BHT). [Pg.286]

HPLC is limited to relatively low molar mass compounds, Le. below 3000. In practice this tends to restrict the technique to dendrons rather than fully formed dendrimers, but it is nonetheless a useful technique, given the importance of establishing high analytical purity of products at each step in a dendrimer synthesis. [Pg.139]

When estimating the remaining service life of a polymer material for a particular application, the limiting value should be established of some material property such as tensile strength, elongation at break, electrical conductivity, permeability to low molar mass compounds, the average polymerization degree, etc., at which the polymer does not fail. [Pg.461]

The model calculations in Figure 4 represent an idealised situation, as the diffusion coefficient Dw of anthracene in aqueous solution was used. Diffusion coefficients of low molar-mass-compounds in water at ambient temperature are in the range of 5 x 10-10 to 1 x 10 9 m2 s [2,18], Due to physical restriction... [Pg.410]

Fraction I, which is less hydrophobic than fractions III and V (Fig. 8), contains lower molar mass compounds than fraction III, which in turn contains lower molar mass compounds than the most hydrophobic fraction (fraction IV). [Pg.190]

Fraction I, which consists mainly of low molar mass compounds, also contains a small amount of high molar mass lignin derivatives eluting with relative retention volumes of 0-0.1. These derivatives are polar and some may be bound to carbohydrates, or otherwise they would have been eluted by RPC along with the hydrophobic fractions II-IV. [Pg.190]

Watanabe et al. [Ill] have used an electrostatic layer - by - layer deposition technique to fabricate self - assembled films from alternating molecular layers of oppositely charged PAMAM dendrimers and low molar mass compounds. [Pg.229]

Bouteiller, L. "Assembly via hydrogen bonds of low molar mass compounds into supramolecular polymers". Adv. Polym Sci. 207, 79112 (2007). [Pg.73]

The absorption positions of the pendants in the polymers are slightly red-shifted compared with those of corresponding low molar mass compounds [31]. The absorption positions corresponding to 7t-7t transitions of the backbone of... [Pg.211]

Bouteiller, L. Assembly via Hydrogen Bonds of Low Molar Mass Compounds into Supramolecular Polymers. Vol. 207, pp. 79-112... [Pg.229]

In Chapter 6 we talked about the ability of solvent molecules to interact with and surround amorphous polymer chains, leading to the formation of polymer solutions. A closely related phenomenon utilizes a low-molar mass compound to penetrate a polymer and reduce the forces of attraction between chains. Such a compound is called a plasticizer. It must be compatible with the polymer and is almost always nonvolatile. Solvent molecules actually plasticize a polymer sample before forming a solution. However most solvents are not good permanent plasticizers because they diffuse to the surface and evaporate. [Pg.150]

It is evident from the above discussion that the threshold voltage, current density, power efficiency, luminous efficiency and, to some extent, device lifetime of OLEDs using organic low-molar-mass compounds, oligomers and polymers depends on intrinsic molecular properties, such as HOMO and LUMO energy levels, efficiency of hole and electron injection and subsequent transport, efficiency of singlet formation and fluorescence efficiency. The... [Pg.141]

In the 1920s, it was not feasible to accurately measure the molecu-f lar weight of natural or synthetic polymers. Classical methods 1 of molecular weight determina-V tion, those based upon colligative x properties, elevation of boiling point, depression of freezing point and lowering of vapor pressure, worked very well for low-molar-mass compounds, but were essentially useless for macromolecules. Modern instrumental methods that... [Pg.360]

Assembly via Hydrogen Bonds of Low Molar Mass Compounds into Supramolecular Polymers... [Pg.79]

In the absence of solvent, low molar mass compounds tend to crystalhze. Therefore, if polymer-like properties are desired, it is necessary to reduce at least partly their crystalhzation tendency, through adequate molecular design. The following examples were chosen to illustrate the range of properties currently achieved with HBSPs. [Pg.91]

NMR is not only applicable to the solutions of the isolated polysaccharide, but also can be used for the study of human body fluids, e.g., the synovial fluids from patients suffering from RA [246] Subsequent to y-irradiation, increased peak intensities of the A-acetyl groups of HA (at about 2.04 ppm) could be clearly monitored [247]. Concomitantly, the intensity of another peak at 8.44 ppm increased. This resonance is stemming from formate and represents another important (low molecular) degradation product of HA in the synovial fluid. It is one of the major advantages of NMR that both high and low molar mass compounds can be simultaneously detected. Of course, NMR offers also the additional advantage that even completely unexpected metabolites can be monitored [248]. [Pg.838]

Part of the rationale for investigating liquid crystal polyphosphazenes is for nonlinear optical (NLO) applications. In general, for NLO activity, polymers must either contain noncentrosymmetric side chains (eg., side-chain liquid crystal polymers) or highly delocalized (conjugated) backbones (16). Alternatively, polymers can be doped with low molar mass compounds to obtain NLO activity. [Pg.194]

Despite the theoretical advantages of the power compensated approach, the associated instrumentation is much more complex and, therefore, there are circumstances where the simpUcity of DTA has much to recommend it. DTA requires just two thermocouples and can, therefore, be used under demanding conditions. For example, high-pressure DTA experiments have been used extensively to generate phase diagrams of polyethylene and related low molar mass compounds— high-pressure DSC is rather more complex. [Pg.19]

In gas chromatography (GC), the separation of analytes is based on a distribution between a mobile gas phase and a stationary phase. It is a technique with high resolution, high selectivity and high sensitivity. A range of different detectors can be used. This technique has nevertheless certain limitations in the characterization of antioxidants, since many antioxidants are thermally sensitive. GC analysis is also limited to lower molar mass compounds, additives, oligomers, etc., since the analytes must have a boiling point below... [Pg.125]

One important aspect is solution condition. In most laboratory experiments dilute protein solutions are used in dilute salt or cosolvent conditions. These conditions are widely different from those found in the living cell. In the cell molecular crowding from the presence of macromolecules may have a profound influence on protein-protein interactions [99]. In addition low molar mass compounds may accumulate under certain conditions in the cells of certain plants, animals and microorganisms to cope with environmental stresses. The presence of these molecules may have important contributions to the dynamics, the stability and the interactions of proteins [100]. While the effect of these molecules has been studied widely on the temperature stability of proteins, their detailed study on the effect of the pressure stability is just at a beginning [101]. [Pg.16]

A polymer sample can be made more pliable by lowering its 7g, and this can be achieved by incorporating quantities of high-boiling, low-molar-mass compounds in the material. These are called plasticizers and must be compatible with the polymer. The extent to which 7g is depressed depends on the amount of plasticizer present and can be predicted from the relation... [Pg.419]


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See also in sourсe #XX -- [ Pg.46 ]




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Molar Mass and Chemical Compounds

Molar mass

Molar mass of compound

Molarity molar masses

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