Lookabaugh M, Krull I S, LaCourse W R
J Chromatogr. 1987 Jan 30;387:301-12. doi: 10.1016/s0021-9673(01)94533-9.
Inorganic anions are typically determined by ion chromatography, ion-selective electrodes, or by "wet chemical" procedures. An alternative to these approaches is afforded by paired-ion, reversed-phase high-performance liquid chromatography (HPLC), and the application of this technique to the determination of iodide and thiosulfate is discussed. Each analyte can be determined using ultraviolet (UV) absorbance detection and oxidative, amperometric electrochemical detection (ED). Furthermore, in the case of iodide, an additional and quite selective ED scheme is available through the use of series-configured dual glassy carbon electrodes. The dual-series ED approach utilizes an upstream electrode which is maintained at an oxidative potential. This results in the formation of an electroactive species, which may be detected at a downstream electrode held at a reductive potential. Finally, it is demonstrated that non-suppressed conductimetric detection is also perfectly viable within the context of paired-ion, reversed-phase HPLC, provided the overall conductance of the mobile phase is not excessive.
无机阴离子通常通过离子色谱法、离子选择性电极或“湿化学”方法来测定。离子对反相高效液相色谱法(HPLC)为这些方法提供了一种替代方案,并讨论了该技术在碘化物和硫代硫酸盐测定中的应用。每种分析物都可以使用紫外(UV)吸光度检测和氧化型安培电化学检测(ED)来测定。此外,对于碘化物,通过使用串联配置的双玻碳电极,可以获得一种额外且具有相当选择性的ED方案。双串联ED方法利用一个保持在氧化电位的上游电极。这会导致形成一种电活性物质,该物质可以在保持在还原电位的下游电极上被检测到。最后证明,在离子对反相HPLC的背景下,只要流动相的总电导率不过高,非抑制型电导检测也是完全可行的。