
August 8, 2025
Author: Duilio Romanello
Gas chromatography (GC) is a fast and sensitive technique used to separate and analyze volatile and semivolatiles compounds. In GC, the sample is first dissolved in a suitable solvent, vaporized, and then introduced into the system. Separation occurs as the components interact with a stationary phase. The stationary phase in gas chromatography plays a critical role in determining the separation efficiency and resolution of analytes. A thorough understanding of the stationary phase is essential for optimizing GC performance.
The stationary phase in GC refers to a non-volatile, heat-resistant material that is either coated on the inner walls of the column or packed within it. Analytes interact with the stationary phase, which impacts their retention and separation. The choice of stationary phase depends on the polarity and chemical properties of the analytes. Polar stationary phases retain polar compounds longer, while non-polar phases retain non-polar compounds longer. A clear understanding of stationary phases is essential for developing reliable and efficient gas chromatography solutions.
In GC, stationary phases can be categorized based on physical state, column type, and polarity.
Based on their physical state, stationary phases for gas chromatography are categorized into solid and liquid stationary phases.
In gas-solid chromatography (GSC), the stationary phase consists of a column packed with finely divided solid materials such as silica, alumina, or activated carbon. Separation occurs through adsorption, where analytes adhere to the solid surface; stronger adsorption leads to longer retention times. Solid stationary phases are commonly used to separate gases like oxygen, nitrogen, and carbon dioxide, as well as small volatile hydrocarbons. However, strong interactions between analytes and the solid surface can sometimes cause peak tailing.
In gas-liquid chromatography (GLC), the stationary phase consists of a thin liquid film coated onto an inert solid support or the inner surface of capillary columns. Separation occurs through a partitioning mechanism, where analytes dissolve into the liquid phase based on their solubility; compounds with higher solubility exhibit longer retention times. Liquid stationary phases can be either polar or non-polar, depending on the properties of the liquid used. GLC is commonly employed to separate organic compounds such as alcohols, amines, acids, and hydrocarbons.
Classification based on column type is determined by how the stationary phase is incorporated within the column.
Packed columns are filled with an inert solid support, which may be coated with a liquid stationary phase, such as silicone oil on diatomaceous earth. In some cases, solid materials like alumina or activated charcoal are used directly as the stationary phase. Packed columns are particularly effective for separating and analyzing gases and low molecular weight compounds but they are still very common in compendial pharmacopeia methods and industrial application.
Capillary columns are long, narrow hollow tubes with the stationary phase coated along their inner surfaces. They are available in two types: wall-coated open tubular (WCOT) columns and support-coated open tubular (SCOT) columns.
Stationary phases used in gas chromatography can be categorized into non-polar, mid-polar, and polar types. The polarity of the stationary phase is important as it impacts analyte retention times and separation.
Non-polar stationary phases are hydrophobic or only weakly polar. Analytes interact primarily through dispersion forces, such as van der Waals interactions, with non-polar compounds exhibiting longer retention times. Common examples of non-polar stationary phases include polydimethylsiloxane (PDMS) and squalane.
Mid-polar stationary phases, such as phenyl-methylpolysiloxane and trifluoro propyl methyl polysiloxane, allow analyte separation based on a combination of dipole-dipole interactions and dispersion forces. They are well-suited for separating moderately polar compounds, including aromatics, alcohols, and esters.
Polar stationary phases consist of highly polar materials like polyethylene glycol (PEG) or cyanopropylsiloxane. Separation occurs through hydrogen bonding, dipole-dipole interactions, or ionic interactions, leading to longer retention of polar analytes. These phases are ideal for separating polar compounds such as acids, alcohols, and amines.
Several factors influence the performance of the stationary phase in gas chromatography, and understanding these variables, along with practical GC technical tips, is key to achieving optimal separation and analysis.
No, you cannot use one stationary phase for all kinds of samples. Different samples have different polarity, volatility, boiling points, and reactivity. For a good resolution, the stationary phase needs to match the sample’s polarity. Gas chromatography is not ideal for analyzing samples that are thermally unstable or possess extremely high boiling points.
In a GC packed column, the stationary phase consists of either uncoated solid particles or solid particles coated with a liquid. The separation of analytes in GC takes place through partition or adsorption, depending on the type of stationary phase.
