Carbon dioxide–poly(vinylidene fluoride) interactions at high pressure
✍ Scribed by B. J. Briscoe; O. Lorge; A. Wajs; P. Dang
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 201 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-6266
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✦ Synopsis
The article reports on the behaviour of poly(vinylidene fluoride) in carbon dioxide at 42°C and 80°C and in a pressure range of 0.1-30 MPa. Experimental techniques for the measurement of gas mass uptake and polymer dilatation are described and the corresponding data are reported as mass sorption and dilatation isotherms, respectively. The mass uptake experiment was also used to follow the evolution of the coefficient of diffusion of carbon dioxide into the polymer as a function of pressure or concentration. An analysis for the calculation of the partial molar volume of carbon dioxide as a function of pressure is also given, which shows that the 'apparent' partial molar volume of the carbon dioxide decreases with pressure to very low values, at high pressure. The computed values are significantly less than those for either the liquid or the solid phases of pure carbon dioxide, and also lower than some data previously reported for silicone elastomers. A consideration of the origins of this apparent anomaly is given in the conclusions.
📜 SIMILAR VOLUMES
Knowledge of the sorption rate and solubility of CO 2 in polymers are of great importance for developing technologies utilizing high-pressure and supercritical CO 2 -assisted processes. Many conventional techniques for measuring gas sorption have inherent complications when used at elevated pressure
Glass transition in the system poly(methy1 methacrylate)/compressed gas was studied as a function of the gas pressure p using a high-pressure Tian-Calvet heat flow calorimeter. Measurements were made on PMMA-CHI, ;-C&, and ;-C02 at pressures to 200 atm. All three gases plasticize the polymer leading