LimsPulse
Chromatography

Gas Chromatography–Mass Spectrometry (GC-MS)

Couples a gas chromatograph to a mass spectrometer so each volatile compound is separated and then identified from its fragmentation pattern. Used for unknown volatile impurities, nitrosamines, residual solvent confirmation and extractables.

  • Pharmaceutical
  • Environmental
  • Forensic and toxicology
  • Food & flavour
  • Petrochemical
  • Packaging
Photo of a Gas Chromatography–Mass Spectrometry (GC-MS)
Photo: Polimerek, CC BY-SA 4.0 (cropped), via Wikimedia Commons
WORKING PRINCIPLE

How GC-MS works

Volatile compounds are separated on a capillary GC column and enter the ion source, where 70 eV electrons ionise and fragment them. A quadrupole (most commonly) filters ions by m/z, either scanning a mass range to record full spectra or monitoring selected ions for sensitivity. The total ion chromatogram shows every compound; extracted ion chromatograms show only selected masses.

FLOW

The path of a sample

  1. 01

    Injection

    The sample is vaporised in a heated split / splitless inlet, or introduced by headspace or thermal desorption.

  2. 02

    GC separation

    Compounds separate on a low-bleed capillary column (often 30 m × 0.25 mm) under a temperature programme.

  3. 03

    Transfer line

    A heated line carries the column outlet into the MS vacuum without condensation.

  4. 04

    EI ion source

    A filament emits electrons at 70 eV that ionise and fragment the molecules.

  5. 05

    Quadrupole analyser

    Filters ions by m/z, either scanning (e.g. m/z 35–500) or in SIM mode.

  6. 06

    Detector and library search

    An electron multiplier records ions; spectra are compared with a reference library to suggest an identity.

COMPONENTS

Main parts and what they do

1

Gas chromatograph with inlet and oven

Separates the sample; the inlet liner and septum must be clean and inert.

2

Low-bleed MS capillary column

Separates compounds with minimal stationary-phase bleed into the MS.

3

Heated transfer line

Delivers the column effluent into the ion source at a controlled temperature.

4

Ion source (EI, optionally CI)

Filament and repeller ionise and push ions toward the analyser.

5

Quadrupole mass filter

Four rods with RF and DC voltages that pass only ions of a chosen m/z.

6

Electron multiplier detector

Amplifies the ion signal; its voltage rises as it ages.

7

Vacuum system

Rough pump plus turbomolecular (or diffusion) pump maintain high vacuum.

8

Calibrant vial (PFTBA)

Supplies the reference compound for tuning and mass-axis calibration.

9

Data system and spectral library

Controls acquisition, processes data and searches spectra against reference libraries.

KEY CONCEPTS

Terms every analyst should know

Electron ionisation (EI)

A hard ionisation method at a standard 70 eV that gives reproducible fragment patterns, the basis of library searching.

Total ion chromatogram (TIC)

The sum of all ion currents at each time point; it looks like an ordinary chromatogram.

Selected ion monitoring (SIM)

The quadrupole monitors only a few chosen m/z values, giving much higher sensitivity than full scan.

Base peak and molecular ion

The base peak is the most intense ion (set to 100%); the molecular ion (M⁺•) shows the molecular weight if it survives.

Library match

A similarity score between the measured and library spectra. A good match supports, but does not prove, identity; confirm with a reference standard.

Autotune

An automatic routine that uses a reference compound (usually PFTBA) to set lens voltages and calibrate the mass axis.

In LimsPulse · Calibration Management

Keep every GC-MS in control: usage logs, calibration and maintenance schedules, and automatic blocking of overdue instruments.

See how