TY - JOUR
T1 - Poly(vinyl acetate), poly((1-O-(vinyloxy) ethyl-2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside) and amorphous poly(lactic acid) are the most CO2-soluble oxygenated hydrocarbon-based polymers
AU - Tapriyal, D.
AU - Wang, Y.
AU - Enick, R. M.
AU - Johnson, J. K.
AU - Crosthwaite, J.
AU - Thies, M. C.
AU - Paik, I. H.
AU - Hamilton, A. D.
N1 - Funding Information:
Funding for this work has also been provided by the U.S. Department of Energy through the National Energy Technology Laboratory under grant no. RDS 41817M2239 and Contract DE-FC26-04NT 15533. The authors would also like to thank the U.S. Environmental Protection Agency Grant EPA-RD-83150401-1 for providing the financial support for this research. We would like to thank Dr. Mark A. McHugh and L. Jun, Department of Chemical Engineering, Virginia Commonwealth University, for their measurement of the CO 2 /PLA cloud point data for high molecular weight PLA samples (Mw = 55,400 and 94,500).
PY - 2008/10
Y1 - 2008/10
N2 - Poly(vinyl acetate), PVAc, remains the most CO2-soluble non-fluorous polymer identified to date. Small sugar acetates are known to be extraordinarily CO2-philic, but cellulose triacetate, a crystalline high molecule weight polymer is CO2 insoluble. Therefore, an amorphous high molecular weight polymer with pendant sugar acetates was synthesized. This polymer, poly(1-O-(vinyloxy) ethyl-2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside, P(AcGIcVE), was indeed CO2-soluble, however cloud point pressures of P(AcGIcVE) at 5 wt% polymer and 298 K were greater than that required for the dissolution of PVAc. Finally, the solubility of amorphous poly(lactic acid), PLA, was determined over a wide range of molecular weight. The corresponding cloud point pressures were much greater than either PVAc or P(AcGIcVE). Ab initio calculations for the CO2/PVAc dimer and CO2/PLA dimer mixtures were conducted in an attempt to elucidate the dramatic differences in the cloud point values of PVAc and PLA. Our calculations indicate that there is little difference in the average interaction energies for the CO2/PLA and the CO2/IPA systems. The only indication that PVAc would be expected to be more CO2-soluble that PLA was that the vinyl acetate dimer has binding modes that will readily accept multiple CO2 molecules, whereas the binding modes for the lactic acid dimer can apparently only accommodate a single CO2 molecule at a time.
AB - Poly(vinyl acetate), PVAc, remains the most CO2-soluble non-fluorous polymer identified to date. Small sugar acetates are known to be extraordinarily CO2-philic, but cellulose triacetate, a crystalline high molecule weight polymer is CO2 insoluble. Therefore, an amorphous high molecular weight polymer with pendant sugar acetates was synthesized. This polymer, poly(1-O-(vinyloxy) ethyl-2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside, P(AcGIcVE), was indeed CO2-soluble, however cloud point pressures of P(AcGIcVE) at 5 wt% polymer and 298 K were greater than that required for the dissolution of PVAc. Finally, the solubility of amorphous poly(lactic acid), PLA, was determined over a wide range of molecular weight. The corresponding cloud point pressures were much greater than either PVAc or P(AcGIcVE). Ab initio calculations for the CO2/PVAc dimer and CO2/PLA dimer mixtures were conducted in an attempt to elucidate the dramatic differences in the cloud point values of PVAc and PLA. Our calculations indicate that there is little difference in the average interaction energies for the CO2/PLA and the CO2/IPA systems. The only indication that PVAc would be expected to be more CO2-soluble that PLA was that the vinyl acetate dimer has binding modes that will readily accept multiple CO2 molecules, whereas the binding modes for the lactic acid dimer can apparently only accommodate a single CO2 molecule at a time.
KW - CO
KW - Cloud point pressure
KW - Poly(lactic acid)
KW - Poly(vinyl acetate)
KW - Sugar acetates
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U2 - 10.1016/j.supflu.2008.05.001
DO - 10.1016/j.supflu.2008.05.001
M3 - Article
AN - SCOPUS:49449085784
SN - 0896-8446
VL - 46
SP - 252
EP - 257
JO - Journal of Supercritical Fluids
JF - Journal of Supercritical Fluids
IS - 3
ER -