TY - JOUR
T1 - Determination of the distribution constants of aromatic compounds and steroids in biphasic micellar phosphonium ionic liquid/aqueous buffer systems by capillary electrokinetic chromatography
AU - Lokajová, Jana
AU - Railila, Annika
AU - King, Alistair W.T.
AU - Wiedmer, Susanne K.
N1 - Funding Information:
Financial support from the Magnus Ehrnrooth foundation (SKW) and Academy of Sciences of the Czech Republic (RVO: 61388963 ), and Technology Agency of the Czech Republic (TACR alfa, project number TA02010760 ) is acknowledged.
PY - 2013/9/20
Y1 - 2013/9/20
N2 - The distribution constants of some analytes, closely connected to the petrochemical industry, between an aqueous phase and a phosphonium ionic liquid phase, were determined by ionic liquid micellar electrokinetic chromatography (MEKC). The phosphonium ionic liquids studied were the water-soluble tributyl(tetradecyl)phosphonium with chloride or acetate as the counter ion. The retention factors were calculated and used for determination of the distribution constants. For calculating the retention factors the electrophoretic mobilities of the ionic liquids were required, thus, we adopted the iterative process, based on a homologous series of alkyl benzoates. Calculation of the distribution constants required information on the phase-ratio of the systems. For this the critical micelle concentrations (CMC) of the ionic liquids were needed. The CMCs were calculated using a method based on PeakMaster simulations, using the electrophoretic mobilities of system peaks. The resulting distribution constants for the neutral analytes between the ionic liquid and the aqueous (buffer) phase were compared with octanol-water partitioning coefficients. The results indicate that there are other factors affecting the distribution of analytes between phases, than just simple hydrophobic interactions.
AB - The distribution constants of some analytes, closely connected to the petrochemical industry, between an aqueous phase and a phosphonium ionic liquid phase, were determined by ionic liquid micellar electrokinetic chromatography (MEKC). The phosphonium ionic liquids studied were the water-soluble tributyl(tetradecyl)phosphonium with chloride or acetate as the counter ion. The retention factors were calculated and used for determination of the distribution constants. For calculating the retention factors the electrophoretic mobilities of the ionic liquids were required, thus, we adopted the iterative process, based on a homologous series of alkyl benzoates. Calculation of the distribution constants required information on the phase-ratio of the systems. For this the critical micelle concentrations (CMC) of the ionic liquids were needed. The CMCs were calculated using a method based on PeakMaster simulations, using the electrophoretic mobilities of system peaks. The resulting distribution constants for the neutral analytes between the ionic liquid and the aqueous (buffer) phase were compared with octanol-water partitioning coefficients. The results indicate that there are other factors affecting the distribution of analytes between phases, than just simple hydrophobic interactions.
KW - Critical micelle concentration
KW - Distribution constant
KW - Electrokinetic chromatography
KW - PeakMaster
KW - Phosphonium ionic liquid
UR - http://www.scopus.com/inward/record.url?scp=84883051272&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2013.07.109
DO - 10.1016/j.chroma.2013.07.109
M3 - Article
AN - SCOPUS:84883051272
SN - 0021-9673
VL - 1308
SP - 144
EP - 151
JO - Journal of Chromatography A
JF - Journal of Chromatography A
ER -