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Small-angle X-ray scattering as a useful supplementary technique to determine molecular masses of polyelectrolytes in solution.


ABSTRACT: Determination of molecular masses of charged polymers is often nontrivial and most methods have their drawbacks. For polyelectrolytes, a new possibility for the determination of number-average molecular masses is represented by small-angle X-ray scattering (SAXS) which allows fast determinations with a 10% accuracy. This is done by relating the mass to the position of a characteristic peak feature which arises in SAXS due to the local ordering caused by charge-repulsions between polyelectrolytes. Advantages of the technique are the simplicity of data analysis, the independency from polymer architecture, and the low sample and time consumption. The method was tested on polyelectrolytes of various structures and chemical compositions, and the results were compared with those obtained from more conventional techniques, such as asymmetric flow field-flow fractionation, gel permeation chromatography, and classical SAXS data analysis, showing that the accuracy of the suggested method is similar to that of the other techniques. © 2016 The Authors. Journal of Polymer Science Part B: Polymer Physics Published by Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 1913-1917.

SUBMITTER: Plazzotta B 

PROVIDER: S-EPMC5094539 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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Small-angle X-ray scattering as a useful supplementary technique to determine molecular masses of polyelectrolytes in solution.

Plazzotta Beatrice B   Diget Jakob Stensgaard JS   Zhu Kaizheng K   Nyström Bo B   Pedersen Jan Skov JS  

Journal of polymer science. Part B, Polymer physics 20160622 19


Determination of molecular masses of charged polymers is often nontrivial and most methods have their drawbacks. For polyelectrolytes, a new possibility for the determination of number-average molecular masses is represented by small-angle X-ray scattering (SAXS) which allows fast determinations with a 10% accuracy. This is done by relating the mass to the position of a characteristic peak feature which arises in SAXS due to the local ordering caused by charge-repulsions between polyelectrolytes  ...[more]

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