Naphthalene sulphonic acids -: new test compounds for characterization of the columns for reversed-phase chromatography

被引:24
作者
Jandera, P
Bunceková, S
Halama, M
Novotná, K
Nepras, M
机构
[1] Univ Pardubice, Fac Chem Technol, Dept Analyt Chem, CZ-53210 Pardubice, Czech Republic
[2] Univ Pardubice, Fac Chem Technol, Dept Organ Technol, CZ-53210 Pardubice, Czech Republic
关键词
naphthalene sulphonic acids; stationary phases; separation selectivity; column characterisation;
D O I
10.1016/j.chroma.2004.10.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Non-substituted naphthalene sulphonic acids are strong acids, which are completely ionised in aqueous and aqueous-organic solutions. Because of repulsive electrostatic interactions, they are more or less excluded from the pores of the column packing materials commonly used in reversed-phase chromatography. The ionic exclusion can be suppressed by increasing the ionic strength of the mobile phase. In aqueous sodium sulphate solutions, very good selectivity was observed for isomeric naphthalene di- and tri-sulphonic acids, allowing reversed-phase separations of these strongly ionic compounds without addition of ion-pairing reagents to the mobile phase. The retention of the isomeric acids increases proportionally to the dipole moment, which can be explained by its effect on increasing exposure of the naphthalene ring to hydrophobic interactions with the non-polar stationary phases. Chromatographic behaviour of isomeric naphthalene di- and trisulphonic acids was investigated on 25 different columns for reversed-phase chromatography. The elution order of the isomers is the same on all the columns, but very strong stationary phase effects were observed on the retention and on the band asymmetry, depending on polar interactions with residual silanol groups and other polar adsorption centres in the stationary phases. These effects are independent of the organic solvents, as the tests are performed in purely aqueous mobile phases and allow classification of the columns into several groups. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 72
页数:12
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