14.4: Ion Chromatography
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In ion-exchange chromatography (IEC) the stationary phase is a cross-linked polymer resin, usually divinylbenzene cross-linked polystyrene, with covalently attached ionic functional groups. As shown in Figure 1 for a styrene–divinylbenzene co-polymer modified for use as an ion-exchange resin, the ion-exchange sites—indicated here by R and shown in blue—are mostly in the para position and are not necessarily bound to all styrene units. The cross-linking is shown in red. The counterions to these fixed charges are mobile and can be displaced by ions that compete more favorably for the exchange sites.
Figure 1: (left) styrene–divinylbenzene co-polymer modified for use as an ion-exchange resin. (right) The photo here shows an example of ion-exchange polymer beads. These beads are approximately 0.30–0.85 mm in diameter. Resins for use in ion-exchange chromatography are smaller, typically 5–11 mm in diameter.
Imagine if we had a tube whose surfaces were coated with an immobilized cation. These would have electrostatic attraction for anions. If a solution containing a mixture of positively and negatively charged groups flows through this tube, the anions would preferentially bind, and the cations in the solution would flow through (Figure 2).
Figure 2: Separating action of amino acids in an anion exchange column.
- This is the basis of ion exchange chromatography. The example above is termed "anion exchange" because the inert surface is interacting with anions
- If the immobile surface was coated with anions, then the chromatography would be termed "cation exchange" chromatography (and cations would selectively bind and be removed from the solution flowing through
- Strength of binding can be affected by pH, and salt concentration of the buffer. The ionic species "stuck" to the column can be removed (i.e. "eluted") and collected by changing one of these conditions. For example, we could lower the pH of the buffer and protonate anions. This would eliminate their electrostatic attraction to the immobilized cation surface. Or, we could increase the salt concentration of the buffer, the anions in the salt would "compete off" bound anions on the cation surface.
A common detector used exclusively in liquid chromatography for ion chromatography is the conductivity detector. In this detector two closely spaced electrodes are placed after the separation column and changes in the conductivity of the solution passing between the two electrodes is monitored. In order to improve the sensitivity of this simple detector and ion suppressor is typically placed between the separation column and the conductivity detector. Pictures in Figure 3 is a schematic of an ion suppressor used , in this example for improving the detectability of a series of anions, X-.
Figure 3. An ion suppressor used in ion chromatography. Image source currently unknown
As evident in Figure 3 an ion suppressor is based on simple acid base neutralization chemistry, i.e. H+ + OH- → H2O or 2H+ + CO32- → H2CO3. In the example in Figure 3, hydronium ions generated at the anode of an electroylsis cell pass through the ion exchange membrane where sodium ions exit due to charge balance and the hydronium ions neutralize the hydroxide ions in the mobile phase, thus reducing the net ion concentration and conductivity of the solution passing to the conductivity detector.
An example of the effect of an ion suppressor is illustrated in Figure 4 for a separation of a series of anions.
Figure 5: An example of the expected improvement in detectability in the separation of a series of anions with an ion suppressor. Image source currently unknown.
Ion-exchange chromatography is an important technique for the analysis of anions and cations in environmental samples. For example, an IEC analysis for the anions F–, Cl–, Br–, NO2–, NO3–, PO43–, and SO42– takes approximately 15 minutes. A complete analysis of the same set of anions by a combination of potentiometry and spectrophotometry requires 1–2 days.
Contributors and Attributions
Mike Blaber (Florida State University)