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Journal ArticleDOI

Crystallization of bisphenol a polycarbonate induced by supercritical carbon dioxide

01 Jul 1987-Journal of Polymer Science Part B (John Wiley & Sons, Inc.)-Vol. 25, Iss: 7, pp 1511-1517
TL;DR: In this paper, supercritical carbon dioxide readily induces crystallization in bisphenol A polycarbonate and the degree of crystallinity increases sharply as the CO2 pressure is raised from 100 to 300 atm but levels off thereafter.
Abstract: Supercritical carbon dioxide readily induces crystallization in bisphenol A polycarbonate. Crystallization begins within one h of exposure to the CO2 at temperatures and pressures as low as 75°C and 100 atm. The degree of crystallinity increases sharply as the CO2 pressure is raised from 100 to 300 atm but levels off thereafter. This behavior is likely due to a minimum in the Tg of the polycarbonate/CO2 mixture owing to the opposite effects of the pressure on the Tg of the polymer and on the equilibrium weight fraction of CO2 absorbed. Percent crystallinities of over 20%, comparable to that achieved using acetone or other organic liquids, have been obtained after 2 h exposure to supercritical CO2. Since polycarbonate degasses quickly and quantitatively at ambient temperature and pressure, the high Tg of bisphenol A polycarbonate can be regained in the crystallized material without further vacuum treatment.
Citations
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Journal ArticleDOI
TL;DR: The use of supercritical carbon dioxide as a processing solvent for the physical processing of polymeric materials is reviewed in this article, with an emphasis on available data and measurement techniques, the development of theory or models for a particular property, and an evaluation of the current state of understanding for that property.
Abstract: The use of supercritical carbon dioxide as a processing solvent for the physical processing of polymeric materials is reviewed. Fundamental properties of CO2/polymer systems are discussed with an emphasis on available data and measurement techniques, the development of theory or models for a particular property, and an evaluation of the current state of understanding for that property. Applications such as impregnation, particle formation, foaming, blending, and injection molding are described in detail including practical operating information for selected topics. The review concludes with some forward-looking discussion on the future of CO2 in polymer processing.

646 citations

Journal ArticleDOI
Wentao Zhai1, Jian Yu1, Lichuan Wu1, Weiming Ma1, Jiasong He1 
04 Oct 2006-Polymer
TL;DR: In this paper, the energy-barrier for heterogeneous nucleation was three orders of magnitude lower than that of homogeneous one for polycarbonate/nano-silica nanocomposites.

186 citations

Journal ArticleDOI
Wentao Zhai1, Yoorim Ko, Wenli Zhu, Anson Wong, Chul B. Park 
TL;DR: It was found that foaming clearly reduced the needed time for PLA’s crystallization equilibrium, and this exhibited a slight dependency on treatment times, temperatures, and pressures.
Abstract: The crystallization and melting behaviors of linear polylactic acid (PLA) treated by compressed CO2 was investigated. The isothermal crystallization test indicated that while PLA exhibited very low crystallization kinetics under atmospheric pressure, CO2 exposure significantly increased PLA’s crystallization rate; a high crystallinity of 16.5% was achieved after CO2 treatment for only 1 min at 100 °C and 6.89 MPa. One melting peak could be found in the DSC curve, and this exhibited a slight dependency on treatment times, temperatures, and pressures. PLA samples tended to foam during the gas release process, and a foaming window as a function of time and temperature was established. Based on the foaming window, crystallinity, and cell morphology, it was found that foaming clearly reduced the needed time for PLA’s crystallization equilibrium.

182 citations

Journal ArticleDOI
TL;DR: Small changes in temperature and pressure cause dramatic changes in the density, viscosity, and dielectric properties of CO2, making it a tunable solvent that can be tailored for various applications.
Abstract: CO(2) is a good solvent for many substances when compressed into its liquid or supercritical fluid state. Above the critical temperature and critical pressure (T(c)=31 degrees C, P(c)=73.8 bar, see Figure 1 for the phase diagram for CO(2)), CO(2) has both gaslike viscosities and liquidlike densities. These moderate critical conditions allow CO(2) to be used within safe commercial and laboratory operating conditions. Small changes in temperature and pressure cause dramatic changes in the density, viscosity, and dielectric properties of CO(2), making it a tunable solvent that can be tailored for various applications. Combined, these unique properties make CO(2) a "solvent of choice" for the new millennium.

165 citations