Phase behavior of poly(L-lactide) in supercritical mixtures of carbon dioxide and chlorodifluoromethane

Jae Min Lee, Byung Chul Lee, Sung Joo Hwang

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Phase behavior data are presented for poly(L-lactide) (L-PLA: MW = 2000 g·mol-1), a biodegradable polymer, in supercritical solvent mixtures of carbon dioxide (CO2) and chlorodifluoromethane (HCFC-22). Experimental cloud point curves, which were the phase boundaries between single and liquid-liquid phases, were measured using a variable-volume view cell apparatus for various CO2 compositions up to about 82 mass % (on a polymer-free basis) and for temperatures up to about 393.15 K. The location of the phase transition boundaries between liquid (L) and liquid-vapor (LV) and between liquid-liquid (LL) and liquid-liquid-vapor (LLV) was also investigated as a function of solvent composition for the L-PLA dissolved in mixed solvents of CO2 and HCFC-22. The cloud point curves exhibited a lower critical solution temperature phase behavior. As the CO2 content in the solvent mixture increased, the cloud point pressure at a fixed temperature increased significantly. Addition of CO2 to HCFC-22 caused a lowering of dissolving power of the mixed solvent. A lower critical end point (LCEP) was estimated from the cloud point curve and the L-to-LV and LL-to-LLV phase transition curves. The LCEPs were shifted to lower temperatures as the CO2 content in the mixed solvent increased.

Original languageEnglish
Pages (from-to)1162-1166
Number of pages5
JournalJournal of Chemical and Engineering Data
Volume45
Issue number6
DOIs
Publication statusPublished - 2000 Nov 1

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Phase behavior
Carbon Dioxide
Carbon dioxide
Liquids
Vapors
fluorocarbon 22
poly(lactide)
Phase transitions
Temperature
Biodegradable polymers
Phase boundaries
Chemical analysis
Polymers

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

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title = "Phase behavior of poly(L-lactide) in supercritical mixtures of carbon dioxide and chlorodifluoromethane",
abstract = "Phase behavior data are presented for poly(L-lactide) (L-PLA: MW = 2000 g·mol-1), a biodegradable polymer, in supercritical solvent mixtures of carbon dioxide (CO2) and chlorodifluoromethane (HCFC-22). Experimental cloud point curves, which were the phase boundaries between single and liquid-liquid phases, were measured using a variable-volume view cell apparatus for various CO2 compositions up to about 82 mass {\%} (on a polymer-free basis) and for temperatures up to about 393.15 K. The location of the phase transition boundaries between liquid (L) and liquid-vapor (LV) and between liquid-liquid (LL) and liquid-liquid-vapor (LLV) was also investigated as a function of solvent composition for the L-PLA dissolved in mixed solvents of CO2 and HCFC-22. The cloud point curves exhibited a lower critical solution temperature phase behavior. As the CO2 content in the solvent mixture increased, the cloud point pressure at a fixed temperature increased significantly. Addition of CO2 to HCFC-22 caused a lowering of dissolving power of the mixed solvent. A lower critical end point (LCEP) was estimated from the cloud point curve and the L-to-LV and LL-to-LLV phase transition curves. The LCEPs were shifted to lower temperatures as the CO2 content in the mixed solvent increased.",
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Phase behavior of poly(L-lactide) in supercritical mixtures of carbon dioxide and chlorodifluoromethane. / Lee, Jae Min; Lee, Byung Chul; Hwang, Sung Joo.

In: Journal of Chemical and Engineering Data, Vol. 45, No. 6, 01.11.2000, p. 1162-1166.

Research output: Contribution to journalArticle

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AB - Phase behavior data are presented for poly(L-lactide) (L-PLA: MW = 2000 g·mol-1), a biodegradable polymer, in supercritical solvent mixtures of carbon dioxide (CO2) and chlorodifluoromethane (HCFC-22). Experimental cloud point curves, which were the phase boundaries between single and liquid-liquid phases, were measured using a variable-volume view cell apparatus for various CO2 compositions up to about 82 mass % (on a polymer-free basis) and for temperatures up to about 393.15 K. The location of the phase transition boundaries between liquid (L) and liquid-vapor (LV) and between liquid-liquid (LL) and liquid-liquid-vapor (LLV) was also investigated as a function of solvent composition for the L-PLA dissolved in mixed solvents of CO2 and HCFC-22. The cloud point curves exhibited a lower critical solution temperature phase behavior. As the CO2 content in the solvent mixture increased, the cloud point pressure at a fixed temperature increased significantly. Addition of CO2 to HCFC-22 caused a lowering of dissolving power of the mixed solvent. A lower critical end point (LCEP) was estimated from the cloud point curve and the L-to-LV and LL-to-LLV phase transition curves. The LCEPs were shifted to lower temperatures as the CO2 content in the mixed solvent increased.

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