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Main Similarities and Differences Between Liquid Chromatography and Gas Chromatography

Authors

Chromatography is a common separation technique based on the principle that components to be separated have different partition coefficients between two phases. The mobile phase elutes the mixture through the stationary phase, and different substances in the mixture move at different speeds along the stationary phase, ultimately achieving separation.

Based on the physical states of the two phases, chromatography can be divided into gas chromatography (GC) and liquid chromatography (LC). In modern sample analysis, both gas and liquid chromatography are widely used methods, but they have many differences and unique characteristics, which determine their distinct applications.

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Figure 1: GC
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Figure 2: LC

Main Differences Between GC and LC

1. Difference in Mobile Phase

  • GC (Gas Chromatography): The mobile phase is an inert gas. The mobile phase does not interact with the components and only interacts with the stationary phase.

  • LC (Liquid Chromatography): The mobile phase is a liquid, which interacts with the components.

2. Difference in Column Length

  • GC: The column length ranges from a few meters to several dozen meters. Due to the relatively low density and high mobility of the carrier gas, the components move quickly in the gas phase, allowing for longer columns to improve column efficiency.

  • LC: The column length is typically between a few dozen to a few hundred millimeters.

3. Sample Selection

  • GC: Best suited for analyzing samples with relatively low molecular weights (generally less than 1000), low boiling points (typically below 500°C), high volatility, and good thermal stability.

  • LC: More suitable for analyzing high boiling point, low volatility, thermally unstable, and larger molecular weight compounds (1000-2000).

    According to statistics, GC can analyze only 15%-20% of all organic compounds, so its application range is narrower than LC. However, advancements like headspace sampling and pyrolysis injection have expanded GC’s analytical capabilities.

4. Differences in Detectors

  • GC: Common detectors include Flame Ionization Detector (FID), Thermal Conductivity Detector (TCD), Electron Capture Detector (ECD), Flame Photometric Detector (FPD), and Nitrogen-Phosphorus Detector (NPD).

  • LC: Common detectors include UV detectors, fluorescence detectors, and differential refractive index detectors.

5. Other Differences

  • GC: Samples must be vaporized in the injection port and analyzed at higher temperatures, using a sharp-tip syringe for injection.

  • LC: No need to vaporize samples; detection can be done at room temperature, using a flat-tip syringe for injection.

Main Similarities Between GC and LC

Both GC and LC share the fundamental principle of adsorption-desorption equilibrium. They achieve separation by exploiting the different partition coefficients of components between the stationary and mobile phases. This repeated partitioning (occurring thousands to millions of times) allows even components with small differences in partition coefficients to be separated. Essentially, both techniques rely on the principle of "like dissolves like" for separation via chromatographic columns.

Summary

GC offers high separation efficiency, fast analysis speed, low sample consumption, good selectivity, and high detection sensitivity, making it widely used in fields such as food, environment, and chemical industries.

LC has a broader application range, providing accurate analysis for difficult-to-separate mixtures and easy sample recovery. Thus, LC is used not only as an analytical method but also as a separation technique in industries like food and pharmaceuticals.

With the increasing demands in various application fields, single chromatographic techniques may not fully meet market needs. This has led to the development of new analytical technologies such as Gas Chromatography-Mass Spectrometry (GC-MS) and Liquid Chromatography-Mass Spectrometry (LC-MS) for better separation and analysis of samples.