Phase diagrams, densities, and refractive indexes of aqueous two-phase systems comprising (F68, L64, or PEO1500) + (ammonium, sodium, or potassium thiocyanate salts) +water : effect of cation and type of macromolecule.

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In extraction procedures, the more commonly used aqueous two-phase systems (ATPS) comprise mainly water, salt, and macromolecule, particularly the macromolecule poly(ethylene oxide) (PEO). However, one limitation of such ATPS is their capacity to separate compounds that are more hydrophobic. One possible solution to overcome this restriction is the use of ATPS formed with triblock copolymers, which are more hydrophobic and therefore enable the extraction of hydrophobic solutes. In addition, the range of applications of ATPS formed with thiocyanate salts can be broader, mainly to extract metal ions. In view of this, equilibrium data were acquired in this work by constructing phase diagrams for ATPS comprising macromolecules [poly(ethylene oxide), PEO, or (poly(ethylene oxide))-(poly(propylene oxide))-(poly(ethylene oxide)) triblock copolymers, F68 or L64] + thiocyanate salts (ammonium, sodium, or potassium) + water at 25.0 °C. The influence of the nature of the cation on the formation of the ATPS was investigated and followed the order K+ > Na+ > NH4+. The capacity of different macromolecules to enable ATPS formation was also examined and followed the order L64 > F68 > PEO1500. Phase inversion occurred with the (L64 or F68) + NH4SCN + water ATPS, in that the top phase is rich in salt and the bottom phase is rich in macromolecule. This aspect is different in most ATPS that are typically described in the literature.

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SILVA, M. C. H. et al. Phase diagrams, densities, and refractive indexes of aqueous two-phase systems comprising (F68, L64, or PEO1500) + (ammonium, sodium, or potassium thiocyanate salts) +water: effect of cation and type of macromolecule. Journal of Chemical and Engineering Data, v. 64, n. 5, p. 1991-1998, abr. 2019. Disponível em: <https://pubs.acs.org/doi/10.1021/acs.jced.8b01005>. Acesso em: 10 fev. 2020.

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