Editing High-performance liquid chromatography (section)

===Ion-exchange chromatography===
{{further|Ion-exchange chromatography}}
'''Ion-exchange chromatography''' ('''IEC''') or '''ion chromatography''' ('''IC''')<ref>{{Cite book |last1=Fritz |first1=James S. |url=https://onlinelibrary.wiley.com/doi/book/10.1002/9783527613243 |title=Ion Chromatography |last2=Gjerde |first2=Douglas T. |date=2000-04-25 |publisher=Wiley |isbn=978-3-527-29914-0 |edition=1 |language=en |doi=10.1002/9783527613243}}</ref> is an analytical technique for the separation and determination of ionic solutes in aqueous samples from environmental and industrial origins such as metal industry, industrial waste water, in biological systems, pharmaceutical samples, food, etc. Retention is based on the attraction between solute ions and charged sites bound to the stationary phase. Solute ions charged the same as the ions on the column are repulsed and elute without retention, while solute ions charged oppositely to the charged sites of the column are retained on it. Solute ions that are retained on the column can be eluted from it by changing the mobile phase composition, such as increasing its salt concentration and pH or increasing the column temperature, etc.

Types of ion exchangers include [[polystyrene]] [[resin]]s, [[cellulose]] and [[dextran]] ion exchangers (gels), and controlled-pore glass or porous [[silica gel]]. Polystyrene resins allow cross linkage, which increases the stability of the chain. Higher cross linkage reduces swerving, which increases the equilibration time and ultimately improves selectivity. Cellulose and dextran ion exchangers possess larger pore sizes and low charge densities making them suitable for protein separation.

In general, ion exchangers favor the binding of ions of higher charge and smaller radius.

An increase in [[counter ion]] (with respect to the functional groups in resins) concentration reduces the retention time, as it creates a strong competition with the solute ions. A decrease in pH reduces the retention time in cation exchange while an increase in pH reduces the retention time in anion exchange. By lowering the pH of the solvent in a cation exchange column, for instance, more hydrogen ions are available to compete for positions on the anionic stationary phase, thereby eluting weakly bound cations.

This form of chromatography is widely used in the following applications: water purification, preconcentration of trace components, ligand-exchange chromatography, ion-exchange chromatography of proteins, high-pH [[anion-exchange chromatography]] of carbohydrates and oligosaccharides, and others.