<mods:mods xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:mods="http://www.loc.gov/mods/v3" version="3.0" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-0.xsd"><mods:titleInfo><mods:title>Determination of inorganic anions at parts per billion levels using single-column ion chromatography without sample preconcentration</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">AL</mods:namePart><mods:namePart type="family">Heckenberg</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">PR</mods:namePart><mods:namePart type="family">Haddad</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Single-column ion chromatography using low-capacity ion-exchange columns and dilute eluents contaioning an aromatic acid {ref. 1-9} have proved to be a popular alternative to suppressed ion chromatography {ref. 10} for the determination of inorganic anions. The single-column methods appear to be readily adaptable to conventional high-performance liquid chromatography (HPLC) instrumentation and have been employed with conductivity {ref. 1-8}, indirect refractive index {ref. 9}, or indirect UV absorbance {ref. 8-9} detection methods.&#13;
Detection limits are comparable for the above detection methods and are typically in the range 0.2-1.0 ppm, depending on the particular ion being determined. Lower detection limits are possible if sample pre-concentration methods are employed {ref. 11}, such as the use of an ion-exchange pre-column onto which a relatively large volume of sample is loaded before elution onto the analytical column. The utility of this sample pre-concentration procedure is strongly dependent on the sample composition, the procedure used to load the concentrator column, and preconditioning of the concentrator column. For example, samples containing a mixture of strongly adsorbed ion (such as sulphate) and a weakly adsorbed ion (such as chloride) must be preconcentrated with care to avoid loss of chloride through displacement by sulphate.&#13;
One possible alternative to sample preconcentration is the use of large injection volumes (up to 2 ml), and this approach has been reported for the determination of chloride and sulphate using conductivity detection {ref. 2}. In our experience, conductivity detection is not optimal with large injection volumes due to severe baseline instability following injection. We have found that indirect UV absorbance detection {ref. 8,9,12} is superior and in this paper, we report the use of this detection method for the determination of a mixture of inorganic anions at low ppb* levels.&#13;
*Throughout this article, the American billion (10^9) is meant.</mods:abstract><mods:classification authority="lcc">250000 Chemical Sciences</mods:classification><mods:classification authority="lcc">250401 Separation Science</mods:classification><mods:classification authority="lcc">250400 Analytical Chemistry</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">1984</mods:dateIssued></mods:originInfo><mods:genre>Article</mods:genre></mods:mods>