Phase behavior of biodegradable polymers in dimethyl ether and dimethyl ether plus carbon dioxide

Citation
Ym. Kuk et al., Phase behavior of biodegradable polymers in dimethyl ether and dimethyl ether plus carbon dioxide, J CHEM EN D, 46(5), 2001, pp. 1344-1348
Citations number
12
Categorie Soggetti
Chemistry,"Chemical Engineering
Journal title
JOURNAL OF CHEMICAL AND ENGINEERING DATA
ISSN journal
00219568 → ACNP
Volume
46
Issue
5
Year of publication
2001
Pages
1344 - 1348
Database
ISI
SICI code
0021-9568(200109/10)46:5<1344:PBOBPI>2.0.ZU;2-9
Abstract
Phase behavior data are presented for biodegradable polymers in high-pressu re dimethyl ether (DME) and in supercritical mixtures of DME and carbon dio xide (CO2). The cloud point curves of poly(D,L-lactide) MW = 30000) in DME were measured at polymer concentrations up to similar to 15 mass % and at t emperatures to 373.15 K and pressures to 14 MPa using a variable-volume vie w cell apparatus. This system exhibited the characteristics of a lower crit ical solution temperature phase behavior and showed the pressure-polymer co ncentration isotherms with the maximum cloud point pressure at the polymer concentration of similar to5 mass %. The cloud point pressure increased wit h increasing molecular weight of the poly(D,L-lactide). For poly(D,L-lactid e-co-glycolide) copolymers in DME, decreasing the D,L-lactide content in th e copolymer caused the single-phase region to shrink and changed the cloud point curve from a lower critical solution temperature behavior to an upper critical solution temperature behavior. The cloud points of poly(D,L-lacti de) in the solvent mixtures of DME and CO2 were measured at various CO2 Com positions up to similar to 73 mass % (on a polymer-free basis) and at tempe ratures up to similar to 373.15 K. As the CO2 Composition in the mixed solv ent increased, the cloud point pressure at a fixed temperature increased si gnificantly. Addition Of CO2 to DME caused a lowering of the dissolving pow er of the mixed solvent due to the decrease of the solvent polarity.