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Molecular weights absolute

The universal calibration, derived from GPC viscosimetry online coupling, has further confirmed the predicted molecular weights. Absolute verification of this calibration principle, which neglects differences in viscosity of molecules of equal molecular weight but with different architectures, is still underway [16]. [Pg.49]

Molecular weight Absolute methods end group analysis, membrane osmometry, vapor pressure osmometry, static light scattering, mass spectrometry, sedimentation measurements... [Pg.67]

Xj = mole fraction of component i Xw, = weight fraction of component i M- = molecular weight of the component i = molecular weight of the mixture = absolute viscosity of the mixture... [Pg.130]

The high sodium ion concentration results in facile crystallisation of the sodium salt. This process of salting out with common salt may be used for recrystallisation, but sodium benzenesulphonate (and salts of other acids of comparable molecular weight) is so very soluble in water that the solution must be almost saturated with sodium chloride and consequently the product is likely to be contaminated with it. In such a case a pure product may be obtained by crystallisation from, or Soxhlet extraction with, absolute alcohol the sul-phonate is slightly soluble but the inorganic salts are almost insoluble. Very small amounts of sulphones are formed as by-products, but since these are insoluble in water, they separate when the reaction mixture is poured into water ... [Pg.548]

Scale of Operation Coulometric methods of analysis can be used to analyze small absolute amounts of analyte. In controlled-current coulometry, for example, the moles of analyte consumed during an exhaustive electrolysis is given by equation 11.32. An electrolysis carried out with a constant current of 100 pA for 100 s, therefore, consumes only 1 X 10 mol of analyte if = 1. For an analyte with a molecular weight of 100 g/mol, 1 X 10 mol corresponds to only 10 pg. The concentration of analyte in the electrochemical cell, however, must be sufficient to allow an accurate determination of the end point. When using visual end points, coulometric titrations require solution concentrations greater than 10 M and, as with conventional titrations, are limited to major and minor analytes. A coulometric titration to a preset potentiometric end point is feasible even with solution concentrations of 10 M, making possible the analysis of trace analytes. [Pg.507]

The viscosity average molecular weight is not an absolute value, but a relative molecular weight based on prior calibration with known molecular weights for the same polymer-solvent-temperature conditions. The parameter a depends on all three of these it is called the Mark-Houwink exponent, and tables of experimental values are available for different systems. [Pg.42]

The phenomena we discuss, phase separation and osmotic pressure, are developed with particular attention to their applications in polymer characterization. Phase separation can be used to fractionate poly disperse polymer specimens into samples in which the molecular weight distribution is more narrow. Osmostic pressure experiments can be used to provide absolute values for the number average molecular weight of a polymer. Alternative methods for both fractionation and molecular weight determination exist, but the methods discussed in this chapter occupy a place of prominence among the alternatives, both historically and in contemporary practice. [Pg.505]

Concretes and absolutes, both obtained by total extraction of the plant material and not subject to any form of distillation other than solvent removal, are complex mixtures containing many chemical types over wide molecular weight ranges. In some cases, gas chromatographic analysis shows httle volatile material. Yet these products have powerful odors and contribute in important ways to the perfumes in which they are used. [Pg.76]

In early hterature, the molecular weights of PVDC and VDC copolymers were characterized by the absolute viscosity of a 2 wt % solution in (9-dichlorobenzene at 140°C. The exact correlation between this viscosity value and molecular weight is not known. Gel-permeation chromatography is the... [Pg.433]

Table 6. Absolute Molecular Weights and Molecular Weight Distributions of Gantrez AN (PMVEMA) ... Table 6. Absolute Molecular Weights and Molecular Weight Distributions of Gantrez AN (PMVEMA) ...
Pi = upstream absolute pressure p2 = downstream absolute pressure R = gas constant T = absolute temperature M,, = molecular weight Di = upstream specific volume of gas Vo = downstream specific volume of gas... [Pg.665]

Absolute humidity H equals the pounds of water vapor carried by 1 lb of diy air. If ideal-gas behavior is assumed, H = M p/[M P — p)], where M,, = molecular weight of water = molecular weight of air p = partial pressure of water vapor, atm and P = total pressure, atm. [Pg.1151]


See other pages where Molecular weights absolute is mentioned: [Pg.232]    [Pg.18]    [Pg.239]    [Pg.46]    [Pg.358]    [Pg.232]    [Pg.18]    [Pg.239]    [Pg.46]    [Pg.358]    [Pg.247]    [Pg.3000]    [Pg.8]    [Pg.189]    [Pg.121]    [Pg.360]    [Pg.1059]    [Pg.621]    [Pg.660]    [Pg.663]    [Pg.282]    [Pg.7]    [Pg.220]    [Pg.350]    [Pg.259]    [Pg.318]    [Pg.368]    [Pg.85]    [Pg.598]    [Pg.599]    [Pg.648]    [Pg.788]    [Pg.893]    [Pg.915]    [Pg.917]    [Pg.1161]    [Pg.1161]    [Pg.1175]    [Pg.1428]    [Pg.1511]    [Pg.6]   
See also in sourсe #XX -- [ Pg.145 ]

See also in sourсe #XX -- [ Pg.215 ]




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Weight absolute

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