

Pyrolysis GC-MS System
裂解气质联用仪
- SKU GCM-0005
- GC-MS
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Pyrolysis temperature range | ambient to 1050 °C (furnace) |
|---|---|
| Temperature reproducibility | ±1 °C |
| Sample amount | 10–500 µg |
| Autosampler capacity | 48–80 samples |
| Interface temperature | up to 400 °C |
| Mass range (MS) | m/z 1.6–1050 |
By Lab Manufacturers China Technical TeamLast reviewed Standards: EPA Method 8270, EPA Method 524.2, EPA Method 8260
What is the Pyrolysis GC-MS System?
A pyrolysis GC-MS thermally decomposes solid or polymeric samples in an inert atmosphere and sends the fragments to a GC-MS for identification. It is used to characterize polymers, rubbers, coatings, microplastics, paints and other materials that cannot be dissolved or volatilized directly.
What is the Pyrolysis GC-MS System?
A pyrolysis GC-MS thermally decomposes solid or polymeric samples in an inert atmosphere and sends the fragments to a GC-MS for identification. It is used to characterize polymers, rubbers, coatings, microplastics, paints and other materials that cannot be dissolved or volatilized directly.
Overview
Pyrolysis GC-MS attaches a micro-furnace, filament or Curie-point pyrolyzer to the GC inlet. A sample of 50 to 500 µg is rapidly heated, often to 500 to 800 °C, in helium. Macromolecules break into characteristic fragments, known as a pyrogram, which are separated by the GC column and identified by MS. Polymer type, monomer ratio, additives and degradation products can be determined. Multi-shot and evolved gas analysis modes allow step-wise thermal desorption followed by pyrolysis, separating additives from the polymer backbone. Reactive pyrolysis using tetramethylammonium hydroxide improves analysis of polyesters, resins and natural products. Pyrolyzer temperature reproducibility of ±1 °C is important for comparable pyrograms. The technique needs very little sample preparation and handles insoluble materials, but quantitation is more difficult than for extractable analytes.
How does it work?
In GC-MS, a liquid or gas sample is vaporized in a heated inlet and carried by helium or hydrogen through a capillary column, typically 15 to 60 m long with a 0.25 mm internal diameter. Compounds separate according to boiling point and interaction with the stationary phase and elute at characteristic retention times. The column exit feeds an ion source, most often electron ionization at 70 eV, which produces reproducible fragmentation patterns that can be matched against libraries such as NIST. Ions are filtered by a mass analyzer, commonly a quadrupole, and counted by an electron multiplier. Acquisition can run in full scan for identification or selected ion monitoring for higher sensitivity. A turbomolecular pump maintains the high vacuum required in the analyzer.
What are the key features?
- Micro-furnace or Curie-point pyrolyzer with temperature reproducibility of ±1 °C
- Multi-shot mode for thermal desorption followed by pyrolysis of the same sample
- Evolved gas analysis mode directly coupling the furnace to MS through a deactivated tube
- Sample cups and autosampler for 48 or more unattended samples
- Reactive pyrolysis support with derivatization reagents for polar polymers and resins
- Pyrogram libraries for polymers, additives and plasticizers in the data system
What are the technical specifications?
A typical pyrolysis gc-ms system configuration offers pyrolysis temperature range of ambient to 1050 °C (furnace), temperature reproducibility of ±1 °C, sample amount of 10–500 µg, autosampler capacity of 48–80 samples, interface temperature of up to 400 °C and mass range (MS) of m/z 1.6–1050. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Pyrolysis GC-MS System is used in polymer identification and copolymer composition, microplastics identification in environmental samples, forensic analysis of paint, fibers and tape, rubber and elastomer characterization and additives and residual monomer in plastics. Across the wider GC-MS class, laboratories also deploy it for environmental VOC and semi-volatile analysis, pesticide residue testing in food and forensic toxicology and drug screening.
Which standards and certifications apply?
Relevant standards and methods include EPA Method 8270, EPA Method 524.2, EPA Method 8260, ASTM D5769, USP <467> Residual Solvents, ISO 11423, EN 15662, ISO/IEC 17025 and IEC 61010-1. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 safety; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the GC-MS on a level bench with a dedicated power outlet, a vented exhaust for the rotary pump, and stable room temperature. Use high-purity carrier gas of at least 99.999 percent with moisture and oxygen traps, since contamination shortens column and filament life. Perform an autotune with perfluorotributylamine before each batch and verify mass accuracy and isotope ratios. Routine maintenance includes replacing inlet liners, septa and gold seals, trimming the column, cleaning the ion source and changing pump oil. Keep leak checks in the daily routine, as air peaks at m/z 28 and 32 indicate a leak. Regulated laboratories should require audit trails, electronic signatures and access control that support 21 CFR Part 11.
How do I select the right Pyrolysis GC-MS System?
Select pyrolysis GC-MS for insoluble polymers, coatings, rubber and microplastics where solvent extraction is impractical. Choose headspace for purely volatile analytes, since pyrolysis adds thermal fragmentation that is unnecessary for them. In an RFQ, specify temperature range, reproducibility, multi-shot and EGA capability, autosampler capacity and the polymer libraries to be supplied.
How does it compare with other GC-MS variants?
Select a GC-MS by matching the detector to the task. A single quadrupole is the economical choice for routine identification and quantitation of residues, volatiles and unknowns using library matching. A triple quadrupole configuration is needed when matrix interference limits sensitivity, as in pesticide multi-residue or dioxin-related work. Time-of-flight offers fast acquisition and accurate mass for non-targeted screening. Headspace and pyrolysis configurations suit specific sample types without solvent extraction. Check the scan speed, mass range, source cleanliness tolerance, and whether the ion source can be changed without venting. Verify support for helium alternatives such as hydrogen, autosampler capacity, and library and data-integrity software. Ask vendors for detection-limit data, such as octafluoronaphthalene instrument detection limit, measured on the exact configuration quoted.
Full specifications
| Pyrolysis temperature range | ambient to 1050 °C (furnace) |
|---|---|
| Temperature reproducibility | ±1 °C |
| Sample amount | 10–500 µg |
| Autosampler capacity | 48–80 samples |
| Interface temperature | up to 400 °C |
| Mass range (MS) | m/z 1.6–1050 |
| Scan speed (MS) | up to 10000 Da/s |
| Operating modes | Single-shot, multi-shot, EGA, reactive pyrolysis |
| Heating rate | up to 20 °C/ms (Curie-point models) |
| Carrier gas | Helium, 99.999% |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Polymer identification and copolymer composition
- Microplastics identification in environmental samples
- Forensic analysis of paint, fibers and tape
- Rubber and elastomer characterization
- Additives and residual monomer in plastics
Key features
- Micro-furnace or Curie-point pyrolyzer with temperature reproducibility of ±1 °C
- Multi-shot mode for thermal desorption followed by pyrolysis of the same sample
- Evolved gas analysis mode directly coupling the furnace to MS through a deactivated tube
- Sample cups and autosampler for 48 or more unattended samples
- Reactive pyrolysis support with derivatization reagents for polar polymers and resins
- Pyrogram libraries for polymers, additives and plasticizers in the data system
Frequently asked questions about Pyrolysis GC-MS System
A pyrogram is the chromatogram produced when a sample is pyrolyzed and its fragments are separated by GC. Each polymer generates a reproducible pattern of monomers, dimers and other fragments, so the pyrogram serves as a fingerprint that can be compared with reference libraries.
Yes. Individual particles or filtered residues are pyrolyzed and identified by marker fragments of polymers such as polyethylene, polypropylene, polystyrene and PET. It gives polymer type and mass-based quantitation, but not particle size or shape, which require microscopy or spectroscopy.
Typically 10 to 500 micrograms, which is a small fragment or a fraction of a milligram. Samples should be homogeneous and representative. Because the amount is tiny, inhomogeneous materials may require cryogenic grinding or multiple replicates for reliable results.
GC-MS analyzes compounds that can be vaporized without decomposition, generally with molecular weights below about 500 Da. Examples are solvents, pesticides, hydrocarbons, fatty acid methyl esters, flavors and many drugs. Polar or non-volatile analytes can be made suitable by derivatization, for example silylation.
Full scan records the whole mass range, for example m/z 35 to 550, and gives spectra for library identification of unknowns. Selected ion monitoring records only chosen ions, which increases dwell time per ion and typically improves sensitivity by ten to one hundred times, but it loses information about unexpected compounds.
Yes, with conditions. Hydrogen gives faster separations and lower cost, but it can react with some analytes, change spectra in electron ionization sources, and requires safety measures. Many systems need a hydrogen-compatible ion source and method revalidation before replacing helium in regulated work.




