Eluent systems carbonate based

Other eluent systems in suppressed ion chromatography are typically chosen based on specific separation requirements. For routine analysis of monovalent and divalent anions, carbonate-based eluents represent a reasonable alternative to hydroxide-based eluent systems. Carbonate eluents are simple to prepare and can be useful in cases where anion analysis is only occasionally performed. It must be kept in mind, however, that carbonate lowers the detection sensitivity for anionic species and introduces significant nonlinearity into the analysis. ... 

The unique selectivity of modern hyperbranched condensation polymers such as lonPac AS22 allows the simultaneous analysis of mineral acids and a wide variety of polarizable anions with a carbonate-based eluent under isocratic conditions in less than 30 min (Figure 3.131). Even strongly retained analytes such as perchlorate, thiosulfate, and chromate elute as symmetric peaks from this column. In contrast to the respective separation on an acrylate-based anion exchanger in Figure 3.130, fluoride is well separated from the system void. 

Uranium ores are leached with dilute sulfuric acid or an alkaline carbonate [3812-32-6] solution. Hexavalent uranium forms anionic complexes, such as uranyl sulfate [56959-61-6], U02(S0 3, which are more selectively adsorbed by strong base anion exchangers than are other anions in the leach Hquors. Sulfate complexes are eluted with an acidified NaCl or ammonium nitrate [6484-52-2], NH NO, solution. Carbonate complexes are eluted with a neutral brine solution. Uranium is precipitated from the eluent and shipped to other locations for enrichment. Columnar recovery systems were popular in South Africa and Canada. Continuous resin-in-pulp (RIP) systems gained popularity in the United States since they eliminated a difficult and cosdy ore particle/leach hquor separation step. 

The knots based on neutral, purely organic molecules are obviously not prone to classical diastereomer resolution, and, while chromatographic methods were not suitable for the separation of the two enantiomers of the metal-templated trefoil knot, they have been proved successful in the amide-containing knots. As far as these knotted molecules are concerned, it must be noted that they incorporate classical stereogenic centers (carbon atoms), which makes them very different from the copper-based systems in terms of chirality. In the first instance, the separation of the two enantiomers of six different knots was achieved with a colunm that was not conunercially available (chiral-AD type). Trichloromethane was needed to obtain an optimal separation. The silica gel and the chiral stationary phase were covalently bound so that the material did not bleed out when the lipophilic eluent was used. Moreover, comparison of the experimental CD of the pure enantiomers of a knot with a theoretically calculated CD (based on X-ray structure and a fiiUy optimized AMI geometry) permitted assignment of the absolute configuration of this knot. The latter preparation of soluble knots based on substitution of the 5-position of the pyridine moieties in 13 afforded molecules that were soluble in solvents which could be used in commercially available chiral columns." On the other hand, the substitution of a racemic mixture of knots with chiral auxiliaries allows the separation of the diastereomeric product." ... 

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