Gel permeation chromatography and cellulose. II. Application of universal calibration
โ Scribed by Segal, L. ;Timpa, J. D. ;Wadsworth, J. I.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1970
- Tongue
- English
- Weight
- 703 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0449-296X
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
In previously reported work concerning the chainโlength distributions obtained by gel permeation chromatography (GPC) in celluloses, degrees of polymerization (DP) of unusually high magnitude were reported. Later work in GPC has shown that the concept of relating extended nolecular chain length of different polymers to elution volume for obtaining molecular weight is not theoretically sound. Correlation of molecular hydrodynamic volume (indicated by the product of intrinsic viscosity and molecular weight) with elution volume has been found to place polymers of vastly different natures on a single curve, such is now designated universal calibration. Application of universal calibration to the determination of DP distributions in celluloses required a different method of converting counts to DP. This new procedure is described in detail. Weightโaverage DP's given by the procedure for samples of cellulose I, II, III, and IV were 5190, 4520, 4795, and 3390, respectively. These are decreases of 74โ75% from the results obtained by the extendedโchain procedure. The results compare favorably with the viscosityโDP's of the samples. Numberโaverage DP's were 1580, 1040, 1140, and 490 for the four samples, respectively, these being decreases of 87โ93% from the values formerly reported. The polymolecularity ratios for the samples are now unusually large, being 3.4, 4.7, 4.2, and 7.1, respectively.
๐ SIMILAR VOLUMES
Well-characterized fractions of linear poly(vinylacetate) have been used to establish the validity of universal calibration for that polymer in gel permeation chromatography. Viscosity parameters have been determined and comparisons made with earlier work.