Chromatography is an analytical technique widely used in fields such as chemistry, biology, environmental science, and pharmaceuticals to separate the components of a mixture and identify substances between them. The process of chromatography is based on the interactions between two distinct phases: the stationary phase and the mobile phase. The stationary phase is fixed in place by a supporting material, while the mobile phase moves over it, carrying the solutes. As the mobile phase travels, it interacts differently with each mixture component, leading to their separation.

Chromatography can be classified into several types based on the nature of the mobile and stationary phases, such as gas chromatography (GC), liquid chromatography (LC), and thin-layer chromatography (TLC). Each type is suited for specific applications, depending on the physical state of the substances being analyzed and the desired resolution of the separation.

The liquid that flows out of the chromatography column goes past a detector, which creates a signal when it detects the solute being separated. This signal is then plotted against the elution time or the volume of solution eluted, resulting in a series of peaks known as a chromatogram.

In chromatography, several key terms help describe the process and results. The retention volume refers to the mobile phase required to carry an analyte from the injection point to the peak maximum in the chromatogram. Closely related is the retention time, which is the duration of time it takes for an analyte to travel through the system. This is calculated by dividing the retention volume by the flow rate of the mobile phase. Another important concept is the retention factor (often called the capacity factor), which measures the ratio of the time the analyte spends in the stationary phase to the time it spends in the mobile phase.

Additionally, void time indicates the time taken for unretained solutes to elute from the system. The corresponding void volume is the amount of mobile phase needed to elute these unretained solutes. When discussing the peaks in a chromatogram, the peak width, also known as the baseline width, is defined as the width of the peak at its baseline, measured where the peak starts to rise and where it returns to the baseline. Finally, resolution measures the degree of separation between two adjacent peaks, reflecting how well the components of a mixture are distinguished from one another.