Collision Cell [GC/GC-MS]

Main
Glossary

WHAT IT IS

The collision cell is a component in triple quadrupole or tandem mass spectrometers. It is located between the first and third mass analyzers (Q1 and Q3) and is responsible for fragmenting selected ions from the sample to create smaller ions (called product ions) for further analysis.

This process – called Collision-Induced Dissociation (CID) – allows the instrument to perform Multiple Reaction Monitoring (MRM), which is widely used for highly specific and sensitive quantification of known compounds.

HOW IT WORKS

Ion Selection (Q1) – The first quadrupole selects a specific precursor ion (an ion from the target compound).

Collision Cell (Q2) – This ion enters the collision cell, which contains an inert gas such as argon or nitrogen. The ions collide with the gas molecules, breaking into predictable product ions.

Product Ion Filtering (Q3) – The third quadrupole then selects one or more of these fragments (product ions) for detection.

MRM Pathway – The entire path precursor ion → collision → product ion is used in an MRM transition for targeted quantification.

IMPACT ON PERFORMANCE

Selective Fragmentation: The collision cell helps isolate and generate specific product ions that are unique to each compound, improving selectivity.

High Sensitivity: By focusing only on the ions of interest, the system reduces background noise and allows for detection of very low concentrations (pg or ppt levels).

Compound Confirmation: The unique pattern of product ions helps confirm the identity of the compound, reducing the chance of false positives.

Cleaner Spectra: Because only selected ions are fragmented, the mass spectrum is less crowded, making quantification easier and more accurate.

TYPES AND CONFIGURATIONS

Standard Collision Cell: A simple chamber with collision gas. Common in traditional triple quadrupole instruments.

Linear Collision Cell: A more advanced design that improves ion transfer efficiency and reduces signal loss.

Axial or Orthogonal Designs: Some systems adjust how ions flow through the cell to optimize speed and sensitivity.

CID Mode vs. MS³ (Advanced MS/MS): In some instruments, collision cells can be used in multi-stage fragmentation (MS³) to increase selectivity for very complex samples.

CHALLENGES AND LIMITATIONS

Collision Energy Tuning: The energy used in the collision must be optimized. Too low = poor fragmentation; too high = too many fragments or loss of sensitivity.

Ion Loss: Inefficient cell design or poor tuning may cause reduced ion transmission, lowering signal intensity.

Interference from Background Ions: In complex matrices, co-eluting ions can still cause interference if transitions are not carefully selected.

Maintenance: Over time, the collision cell may become contaminated with residue or non-volatile compounds, which can affect performance.