An ion chromatographic method has been developed for the determination of alkali (Li+, Na+, K+), alkaline earths (Ca2+, Mg2+, Ba2+, Sr2+) and ammonium ion in waters. The usual difficulties encountered during traditional cation-exchange separations (incomplete resolution for Na+ and NH4+ present in disproportionate concentration ratios) have been overcome tuning the selectivity of the separation by the introduction of 18-crown-6 ether in the mobile phase using an IonPac CS12A (150 × 3 mm id) column. After a detailed study of the effect of mobile phase components on separation, a gradient elution from 26 mM methanesulphonic acid (MSA) with a step change at 9 min to 60 mM MSA (0.5 mM 18-crown-6) provided the required baseline separation for the eight selected analytes. The method developed provides the advantage of the determination, in the same analytical run, also of strontium and barium, which is usually performed by spectroscopic techniques. Within-day and between-day repeatability have been assessed, observing between-day RSD included between 0.3 and 1.8% for retention times and 0.6 and 7.2% for peak areas. The method has been finally tested for the analysis of water samples of different provenience (well, tanks, water system) and results compared with those obtained by the laboratory in charge of the control of drinking water for the city of Torino (Italy).
SIMULTANEOUS DETERMINATION OF ALKALI, ALKALINE EARTHS AND AMMONIUM IN NATURAL WATERS BY ION CHROMATOGRAPHY
BRUZZONITI, Maria Concetta;DE CARLO, Rosa Maria;
2008-01-01
Abstract
An ion chromatographic method has been developed for the determination of alkali (Li+, Na+, K+), alkaline earths (Ca2+, Mg2+, Ba2+, Sr2+) and ammonium ion in waters. The usual difficulties encountered during traditional cation-exchange separations (incomplete resolution for Na+ and NH4+ present in disproportionate concentration ratios) have been overcome tuning the selectivity of the separation by the introduction of 18-crown-6 ether in the mobile phase using an IonPac CS12A (150 × 3 mm id) column. After a detailed study of the effect of mobile phase components on separation, a gradient elution from 26 mM methanesulphonic acid (MSA) with a step change at 9 min to 60 mM MSA (0.5 mM 18-crown-6) provided the required baseline separation for the eight selected analytes. The method developed provides the advantage of the determination, in the same analytical run, also of strontium and barium, which is usually performed by spectroscopic techniques. Within-day and between-day repeatability have been assessed, observing between-day RSD included between 0.3 and 1.8% for retention times and 0.6 and 7.2% for peak areas. The method has been finally tested for the analysis of water samples of different provenience (well, tanks, water system) and results compared with those obtained by the laboratory in charge of the control of drinking water for the city of Torino (Italy).
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