Polymer molecular weight averages

Kataoka,T. Onset of non-newtonian flow a correlation with an average molecular weight. Polymer Letters 5,1063-1068 (1967). 

Mw,H high weight-average molecular weight polymer... 

Number average molecular weight (polymer) DPn X molecular weight (monomer)... 

A decrease in the observed value of rj may therefore occur by depletion of the polymer (decrease in cP) or a decrease in [rj] which may be caused either by an increase in I (if the polymer is a polyelectrolyte) or a decrease in the average molecular weight (polymer degradation). 

A 200,000-amu average molecular weight polymer is contaminated with 0.5% of a 100-amu impurity, presumably the monomer. Determine the error in the molecular weight determination if a 1.000 x lO molal aqueous solution is used. Assume a temperature of 25.0°C. 

The terminal groups of a polymer chain are different in some way from the repeat units that characterize the rest of the molecule. If some technique of analytical chemistry can be applied to determine the number of these end groups in a polymer sample, then the average molecular weight of the polymer is readily evaluated. In essence, the concept is no different than the equivalent procedure applied to low molecular weight compounds. The latter is often included as an experiment in general chemistry laboratory classes. The following steps outline the experimental and computational essence of this procedure ... 

This result shows that the square root of the amount by which the ratio M /M exceeds unity equals the standard deviation of the distribution relative to the number average molecular weight. Thus if a distribution is characterized by M = 10,000 and a = 3000, then M /M = 1.09. Alternatively, if M / n then the standard deviation is 71% of the value of M. This shows that reporting the mean and standard deviation of a distribution or the values of and Mw/Mn gives equivalent information about the distribution. We shall see in a moment that the second alternative is more easily accomplished for samples of polymers. First, however, consider the following example in which we apply some of the equations of this section to some numerical data. 

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. 

An important application of Eq. (3.39) is the evaluation of M, . Flory et al.t measured the tensile force required for 100% elongation of synthetic rubber with variable crosslinking at 25°C. The molecular weight of the un-cross-linked polymer was 225,000, its density was 0.92 g cm , and the average molecular weight of a repeat unit was 68. Use Eq. (3.39) to estimate M. for each of the following samples and compare the calculated value with that obtained from the known fraction of repeat units cross-linked ... 

An equivalent way of looking at the conclusion of item (2) is to recall that Eq. (5.40) gives the (number average) number of monomers of both kinds in the polymer and multiply this quantity by the average molecular weight of the two kinds of units in the structure (88 + 112)/2 = 100. 

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. 

In the next section we shall describe the use of Eq. (8.83) to determine the number average molecular weight of a polymer, and in subsequent sections we shall examine models which offer interpretations of the second virial coefficient. 

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