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Phase behavior of a ternary system of poly[ p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene] and poly[ p-decyl(oxy, thio, sulfonyl)methyl styrene] in supercritical solvents
The high-pressure phase behavior of poly[ p-decyl(oxy, thio, sulfonyl)methyl styrene] and poly[ p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene] in supercritical solvents comprised of CO 2 and DME were measured using a variable volume view cell. The focus of this study is to determine t...
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Published in: | The Journal of supercritical fluids 2008-11, Vol.47 (1), p.1-7 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The high-pressure phase behavior of poly[
p-decyl(oxy, thio, sulfonyl)methyl styrene] and poly[
p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene] in supercritical solvents comprised of CO
2 and DME were measured using a variable volume view cell. The focus of this study is to determine the impact of substitution of the functional group (oxy, thio, sulfonyl) next to the styrene and the appearance when the connected alkyl group was changed to a perfluoro alkyl group by measuring the phase behavior of poly[
p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene] and poly[
p-decyl(oxy, thio, sulfonyl)methyl styrene] in supercritical solvents, CO
2 and/or DME.
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In this study, the high-pressure phase behavior of poly[
p-decyl(oxy, thio, sulfonyl)methyl styrene] and poly[
p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene] in supercritical solvents comprised of carbon dioxide (CO
2) and dimethyl ether (DME) were examined. When the poly[
p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene]
+
CO
2 systems were evaluated, cloud-point pressures were obtained at temperatures ranging from 60 to 180
°C and pressures of up to 1300
bar. In addition, the poly[
p-perfluorooctyl-ethylene(oxy, thio, sulfonyl)methyl styrene]
+
DME mixtures dissolved at temperatures under 180
°C and pressures under 200
bar, but the poly[
p-decyl(oxy, thio, sulfonyl)methyl styrene]
+
CO
2 mixtures did not dissolve, even at 230
°C and 2800
bar. However, the poly[
p-decyl(oxy, thio, sulfonyl)methyl styrene]
+
DME mixtures readily dissolved at temperatures and pressures under 180
°C and 200
bar, respectively. Furthermore, the cloud-point curves for the poly(
p-decyl sulfonyl methyl styrene)
+
DME mixtures with 15.6, 44.3 and 56.4
wt% CO
2 changed the
P–
T curve from a lower critical solution temperature (LCST) type to an upper critical solution temperature (UCST) type at increased CO
2 concentrations. |
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ISSN: | 0896-8446 1872-8162 |
DOI: | 10.1016/j.supflu.2008.06.003 |