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  • Capillary electrophoresis  (3)
  • 42.75
  • Computational Chemistry and Molecular Modeling
  • Inorganic Chemistry
  • Nederland
  • Springer  (3)
  • 1995-1999  (3)
  • 1960-1964
Collection
Years
Year
  • 1
    ISSN: 1612-1112
    Keywords: Capillary electrophoresis ; Chiral separtions ; Chromane ; Cyclodextrin ; Screening design
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Six different cyclodextrins with varying cavity size and rim substitution were used as chiral agents for the enantiomeric separation of eight chromane compounds or analogues using capillary electrophoresis. It is shown that the cyclodextrin type and concentration have a large influence on the enantiomeric separation obtained for these compounds. A chiral resolution of 1.4 or better could be obtained for all the substances with either substituted heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin or unsubstituted γ-cyclodextrin as the chiral selector. The influence of the γ-cyclodextrin concentration, ionic strength and pH on the chiral separations was also investigated with a multivariate screening design. The detection limit and resolution of the present method allow determinations of the investigated compounds down to a chiral impurity of less than 0.1 % (area/area).
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1612-1112
    Keywords: Capillary electrophoresis ; Aldehydes ; Hydrazino benzene sulfonic acid ; Water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method has been developed for the analysis of environmentally important aldehydes in rain water. The method is based on the derivatization of the aldehydes with hydrazino benzene sulfonic acid, separation of the hydrazones formed by capillary electrophoresis and UV detection at 280 nm. Derivatization was shown to be complete in 15 min at 50°C. The aldehyde derivatives could be separated from each other and from the excess of reagent using a pH 9 borate buffer as background electrolyte, with an analysis time of less than 6 min. The repeatability was better than 0.5% for the peak mobilities and in the order of 2–5% for the peak areas. Detection limits of 0.8–3 μmol L−1 (0.02–0.2 ppm) were obtained. The method was applied for the determination of formaldehyde and acetaldehyde in rain water samples.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Capillary electrophoresis ; On-line LC-CE ; Sample pretreatment ; Matrix effects ; Benzoic acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Various methods are currently under investigation to improve concentration detection limits in capillary electrophoresis (CE). Stacking and isotachophoresis coupled in-line with free-solution electrophoresis are the techniques most frequently used. Samples containing a high and/or varying salt concentration, such as urine and serum, are difficult to handle: usually a significant loss in electrophoretic efficiency is observed compared with samples possessing a low electric conductivity. In the present paper an alternative approach is developed, i.e. a liquid chromatographic (LC)-type of sample pretreatment is coupled on-line with CE. To demonstrate the feasibility of this approach, the separation of three model compounds (benzoates) in water containing up to 400 mM of sodium chloride is studied using a 50 mM borate CE buffer of pH 9.5. The direct injection of samples with high salt concentrations in CE results in peak splitting and/or serious band broadening. These problems are not encountered when using the present LC-CE system. In addition, the detection limits are hardly influenced by the salt concentration of the sample; this underlines the robustness of the system.
    Type of Medium: Electronic Resource
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