## Abstract In a previous paper we reported the enthalpies of mixing of oligomers of ethylene oxide with different end groups in tetrachloromethane. This paper shows the applicability of the modified theoretical treatment, based on a quasichemical equilibrium of the contacting segmental surfaces or
Thermodynamics of mixing of propylene oxide oligomers with different end groups and of statistical and block cooligomers of ethylene oxide and propylene oxide in tetrachloromethane
✍ Scribed by Erwin Killmann; Frank Cordt; Friedrich Möller; Helmut Zellner
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 704 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Mixing enthalpies and Gibbs energies of liquid propylene oxide oligomers with hydroxyl and methoxy end groups and of block and statistical cooligomers of ethylene oxide and propylene oxide in tetrachloromethane are obtained by microcalorimetry and vapour pressure measurements. The thermodynamic excess quantities AH, AGE and ASE of mixing are influenced by induced dipol interactions of the ether segments with CCI, and by the hydrogen bond interactions of the OH end groups. An expanded theoretical treatment using the Huggins approach of quasichemical equilibrium between the contacting segment surfaces is successfully applied on the experimental results.
📜 SIMILAR VOLUMES
In addition to associating into (''normal'') micelles in aqueous blocks (1). Many of these copolymers associate in aqueous solutions, amphiphilic polyoxyalkylene block copolymers can form solutions to form spherical micelles (with a ''core'' made ''reverse'' micelles in organic solvents at sufficien