## Abstract Dextran and random dextran‐based copolymers containing different molar fractions __f__ of charged units are studied in aqueous solution and in the pure state. The specific volumes of the solutions decrease linearly with increasing weight fraction of the polymer. Extrapolation to the pur
Dextran-Based Polycations: Thermodynamic Interaction with Water as Compared With Unsubstituted Dextran, 2 – Flory/Huggins Interaction Parameter
✍ Scribed by Maria Bercea; Marieta Nichifor; John Eckelt; Bernhard A. Wolf
- Book ID
- 102485160
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 343 KB
- Volume
- 212
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The Flory‐Huggins interaction parameter χ is determined as a function of volume fraction of polymer φ by vapor‐pressure measurements at 25, 37.5 and 50 °C for five dextran samples that differ in f, the fraction of randomly distributed charged monomer units. The function χ(φ) has a minimum that is shifted towards lower χ values as f increases. The higher the temperature, the more the individual curves fan out. The heats of dilution at high polymer concentrations change from exothermal to endothermal as f increases. The results can be well modeled by an approach accounting explicitly for chain connectivity and conformational changes. A smooth transition of the solution properties upon the random introduction of charged units into dextran is observed.
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