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Received April 28, 2004
Accepted June 24, 2004
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Thermodynamic Phase Behavior of Fluoropolymer Mixtures with Supercritical Fluid Solvents
Department of Chemical Engineering, Yosu National University, Yosu, Chonnam 550-749, Korea
Korean Journal of Chemical Engineering, November 2004, 21(6), 1193-1198(6), 10.1007/BF02719493
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Abstract
Cloud-point experimental data were presented at temperatures up to 260 ℃ and pressures up to 2,500 bar for poly(vinylidene fluoride) (PVDF) [Mw=180,000 and 275,000] in CO2, CHF3, CHClF2, and dimethyl ether (DME). Also, phase behavior curves were shown for the PVDF [Mw=180,000] in CO2 with 1-propanol and 1-pentanol. Poly(vinyl fluoride) does not dissolve in CO2 even at 215 ℃ and 2,500 bar, while poly(vinylidene fluoride) does dissolve in CO2 at 220 ℃ and pressures of 1,700 bar. To dissolve poly(vinylidene fluoride) in dimethyl ether, pressures in excess of 200 bar and temperatures in excess of 165 ℃ are needed. The cloud-point behavior between the ternary PVDF [Mw=180,000]-CO2-DME mixture shows a temperature range of 100-195 ℃ and pressure range of 350-1,360 bar by adding the 11, 29, and 60 wt% DME in cosolvent. The phase behavior for PVDF [Mw=180,000]-CHF3-9, 19, and 40 wt% CHClF2 system shows a temperature at below 200 ℃ and pressure up to 1,700 bar. The effect of CHClF2 as a cosolvent for PVDF [Mw=275,000] in CO2 decreased with the pressure increasing 10, 26, 40 and 61 wt% of cosolvent (CHClF2) contents. Also, the effect of 15 and 40 wt% DME for the PVDF [Mw=275,000]-CHF3 mixture shows temperature ranges of 120-206 ℃ and pressures up to 1,570 bar.
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References
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Chun SW, Kim JD, Korean J. Chem. Eng., 19(5), 803 (2002)
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DeSimone JM, Guan Z, Elsbernd CS, Science, 257, 945 (1992)
Hsu CC, Geil PH, J. Appl. Phys., 56, 2404 (1984)
Lora M, Lim JS, McHugh MA, J. Phys. Chem. B, 103(14), 2818 (1999)
Mertdogan CA, Byun HS, McHugh MA, Tuminello WH, Macromolecules, 29(20), 6548 (1996)
Mertdogan CA, DiNoia TP, McHugh MA, Macromolecules, 30(24), 7511 (1997)
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