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Reversed Phase Chromatography
Reversed Phase Chromatography (RP) is the most commonly used method of liquid chromatography. It is characterised by stationary phases with non-polar surface properties and a mobile phase of polar character - exactly the opposite of normal phase chromatography.
You will find an introduction to the basics of reversed-phase chromatography on this page as well as an overview of HPLC columns suitable for this separation technique.
We will be happy to help you select the right column for your analytical problem.
Technical Data
Basics
Stationary phases of reversed-phase chromatography
Surface-modified (C30, C18, C8, C4,C1, C6H5,...) silica gels are often used as stationary phases. These can be produced comparatively easily and in large quantities and have high mechanical and chemical stability as well as reproducibility.
Other materials used as stationary phases in reversed phase chromatography are
- Hydrophobic polymers, e.g. styrene-divinylbenzene copolymer (PS-DVB)
- Modified hydrophilic polymers, e.g. C18-modified polyvinyl alcohol
- Graphitised carbon, e.g. Hypercarbâ„¢
- Modified metal oxide particles, e.g. zirconium oxide particles coated with carbon
Surface modification of silica gel
When modifying silica gel, the silanols present on the surface (free Si-OH groups) are chemically reacted with non-polar groups. This process inevitably always leaves free residual silanols, as it is not possible to get all silanols to react due to steric reasons. These residual silanols sometimes lead to unwanted interactions between analyte and stationary phase, which - if conditions are not adapted - can result in insufficient separation performance, adsorption or peaktailing.
In addition to free silanols, impurities in the base silica gel, e.g. metal ions, can also lead to undesirable polar interactions. For this reason, almost all stationary phases today are based on high-purity silica gel ("Type B silica").
The simplest approach to minimise the proportion of residual silanols is so-called end-capping. The remaining residual silanols are reacted with small alkylating reagents, such as trimethylsilyl (TMS) groups. In addition to conventional endcapping, other methods are also used to shield residual silanols. The aim is always to ensure that the analytes do not come into contact with free silanols.
Figure 1: Schematic representation of silica modification and subsequent end capping.
The separation mechanism of reversed-phase chromatography
In classical reversed-phase chromatography, the separation mechanism is mainly based on the different distribution of analytes between the stationary and mobile phases. This phenomenon can also be understood as a kind of extraction of the analytes between the stationary and mobile phases. This means that a non-polar analyte dissolves preferentially in the stationary phase, remains there and is thus eluted slowly from the column. Polar compounds, on the other hand, are rinsed from the column very quickly, as they prefer to remain in the mobile phase.
With negligibly small proportions of free residual silanols, only hydrophobic interactions (van der Waals forces) contribute to the separation. Depending on the silica modification, other interactions can also contribute to the separation, e.g. π-π interactions in phenyl-modified stationary phases or weak ion exchange interactions in the presence of free silanols.
Mobile phases of reversed-phase chromatography
The mobile phase used in reversed-phase chromatography almost always contains water as the component with the lowest elution power and a water-miscible solvent, which increases the elution power of the mobile phase. Methanol, acetonitrile or tetrahydrofuran are usually used for this purpose, which differ from each other not only in their elution power, but also in the selectivity of the interactions they have with the analytes and the stationary phase.
Manufacturers and columns for reversed-phase chromatography
Almost all manufacturers or suppliers of HPLC columns now have several reversed-phase columns in their range. The variety of available phases and selectivities is enormous. We are happy to support you in finding and selecting a suitable column for your analysis. Below you will find a small selection of reversed phase HPLC columns that are frequently used.
The right column for you - we will be happy to support you individually
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