Abstract
SEC separates complex branched polymers by hydrodynamic volume, rather than by molecular weight or branching characteristics. Equations relating the response of different types of detectors are derived including band broadening, by defining a distribution function Nââ"šÂ¬Ã¢"žÂ¢(M, Vh), the number of chains with molecular weight M and hydrodynamic volume Vh. While the true molecular weight distribution of complex polymers cannot be determined by SEC, irrespective of the detector used, the formalism enables multiple detection SEC data to be processed to both analyze the polymer sample and reveal mechanistic information about polymer synthesis. The formalism also shows how the true weight- and number-average molecular weight, Mw andMn, can be obtained from correct processing of the hydrodynamic volume distributions.
| Original language | English |
|---|---|
| Pages (from-to) | 13-28 |
| Number of pages | 16 |
| Journal | Macromolecular Theory and Simulations |
| Volume | 16 |
| Publication status | Published - 2007 |
Keywords
- gel permeation chromatography
- polymers
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