

Pyrolysis GC-MS System for Rubber Analysis
橡胶分析用裂解气质联用仪
- SKU RCA-0003
- Rubber Composition Analysis
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Pyrolysis temperature | 400–800 °C programmable |
|---|---|
| Sample mass | 0.1–2 mg |
| Column type | Capillary, 30 m, 5% phenyl phase |
| GC oven temperature | Ambient to 350 °C with programming |
| Mass range | m/z 10–500 |
| Carrier gas | Helium, ≥ 99.999% |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9924-1, ISO 9924-2, ISO 1407
What is the Pyrolysis GC-MS System for Rubber Analysis?
A pyrolysis GC-MS system fragments a rubber sample thermally and separates the products chromatographically with mass spectrometric detection. It identifies elastomer blends, plasticisers, antioxidants and vulcanising agents that infrared cannot resolve in cured, filled compounds.
What is the Pyrolysis GC-MS System for Rubber Analysis?
A pyrolysis GC-MS system fragments a rubber sample thermally and separates the products chromatographically with mass spectrometric detection. It identifies elastomer blends, plasticisers, antioxidants and vulcanising agents that infrared cannot resolve in cured, filled compounds.
Overview
A small specimen is pyrolysed at a defined temperature, usually between 500 and 700 °C, and the fragments are separated on a capillary column and identified by mass spectrometry against reference libraries. Because the fragments reflect the monomer units of each polymer, blends such as natural rubber with butadiene rubber can be distinguished more reliably than by infrared, and the presence of specific antioxidants, accelerators or plasticisers can be confirmed from their characteristic fragments. Programmed pyrolysis and evolved gas analysis modes allow volatiles to be examined separately from the polymer fragments. Quantification requires calibration with pure standards in a comparable matrix, since fragment yields depend on temperature and on interactions with fillers such as carbon black.
How does it work?
Rubber is a complex mixture, so several techniques are combined. Thermogravimetric analysis decomposes the sample in a staged nitrogen and oxygen atmosphere, giving the polymer fraction, carbon black and the inorganic residue in one run. Infrared spectrometry identifies the elastomer through its characteristic absorption bands and is standardised for rubber identification. Pyrolysis gas chromatography separates the products of thermal fragmentation and identifies copolymers and additives that spectroscopy cannot resolve. Solvent extraction removes plasticisers, process oils, waxes and free sulfur, which are then quantified by mass difference or by chromatography. X-ray fluorescence or elemental analysis measures the inorganic components, including zinc oxide, silica and sulfur-containing additives, that remain in the ash.
What are the key features?
- Pyrolysis temperature range from 400 to 800 °C
- Capillary column with temperature programming
- Mass spectrometric detection and library search
- Programmed pyrolysis for volatile additives
- Identification of elastomer blends
- Calibration for quantitative additive work
What are the technical specifications?
A typical pyrolysis gc-ms system for rubber analysis configuration offers pyrolysis temperature of 400–800 °C programmable, sample mass of 0.1–2 mg, column type of Capillary, 30 m, 5% phenyl phase, GC oven temperature of Ambient to 350 °C with programming, mass range of m/z 10–500 and carrier gas of Helium, ≥ 99.999%. 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 for Rubber Analysis is used in identification of elastomer blends in compounds, plasticiser and antioxidant identification, investigation of odour and staining problems and verification of reclaimed rubber composition. Across the wider Rubber Composition Analysis class, laboratories also deploy it for filler, carbon black and polymer content determination, elastomer identification in incoming inspection and plasticiser and process oil content testing.
Which standards and certifications apply?
Relevant standards and methods include ISO 9924-1, ISO 9924-2, ISO 1407, ISO 4650, ASTM D6370, ASTM D297, ASTM D3452, ASTM D3677 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Sampling is the dominant source of error, because fillers and oils are distributed unevenly in a finished rubber article. Cut specimens from several locations, or mill and homogenise the sample before taking portions, and record the sampling plan. For thermogravimetric analysis, fix the temperature programme and atmosphere switching, and subtract a crucible blank, since incomplete carbon burn-off is the commonest cause of inflated filler results. Clean infrared crystals after every measurement, since migrated oil and wax contaminate the surface. Solvent extraction requires maintenance of the extraction thimble and solvent purity, and the extracted mass must be measured after conditioning, because these materials are volatile and hygroscopic.
How do I select the right Pyrolysis GC-MS System for Rubber Analysis?
Select pyrolysis GC-MS when infrared cannot resolve the polymer blend, or when a specific plasticiser, antioxidant or curing agent must be identified. Confirm the pyrolysis modes and mass range needed, and budget for reference standards, because meaningful quantitative work requires calibration in a similar rubber matrix.
How does it compare with other Rubber Composition Analysis variants?
Begin with the question. Thermogravimetric analysis is the fastest route to filler, carbon black and polymer content and can be run on any compound, so it suits routine incoming checks and rubber process control. Infrared identification is the standard first step for polymer type and is fast and cheap. Where the identity of a plasticiser or an unknown additive matters, pyrolysis gas chromatography is required for separation. Solvent extraction is used when the content of extractable material is the specification parameter, for example in rubber products with limits on plasticiser or on free sulfur. Elemental methods complete the picture for zinc, sulfur and other inorganic components, and are also the confirmation step for results that a screening technique suggests.
Full specifications
| Pyrolysis temperature | 400–800 °C programmable |
|---|---|
| Sample mass | 0.1–2 mg |
| Column type | Capillary, 30 m, 5% phenyl phase |
| GC oven temperature | Ambient to 350 °C with programming |
| Mass range | m/z 10–500 |
| Carrier gas | Helium, ≥ 99.999% |
| Detector | Electron ionisation quadrupole |
| Data output | Pyrograms and mass spectra with library matches |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Identification of elastomer blends in compounds
- Plasticiser and antioxidant identification
- Investigation of odour and staining problems
- Verification of reclaimed rubber composition
Key features
- Pyrolysis temperature range from 400 to 800 °C
- Capillary column with temperature programming
- Mass spectrometric detection and library search
- Programmed pyrolysis for volatile additives
- Identification of elastomer blends
- Calibration for quantitative additive work
Frequently asked questions about Pyrolysis GC-MS System for Rubber Analysis
It can distinguish the synthetic polymer from the natural product only through minor components associated with natural rubber, such as proteins or fatty acid residues, which requires careful comparison with reference materials. Routine identification of the elastomer family is straightforward, but sourcing claims usually require supporting techniques.
At lower pyrolysis temperatures, or in evolved gas mode, additives desorb or decompose into recognisable fragments that are separated by the column. Characteristic ions from mass spectral library matching then identify the antioxidant, accelerator or plasticiser, and comparison with a pure standard confirms the assignment.
It can be. Carbon black adsorbs some fragments and can alter the ratios between them, so a compound containing carbon black may give a different fragment pattern from an unfilled one of the same polymer. Comparisons intended as quantitative should therefore use compounds with similar filler content.
Thermogravimetric analysis gives the most information per run: polymer content from the first weight loss, carbon black from the oxidative stage and inorganic filler as the residue. The result is available in under an hour and requires only a few milligrams, which is why it is the usual starting point for compound verification.
It measures the material soluble in hot acetone, which includes plasticisers, some process oils, waxes, accelerators, antioxidants and free sulfur. The amount is expressed as a percentage of the specimen mass, and the extract can be analysed further by chromatography to identify individual components.
Fillers, oils and curatives are not uniformly distributed in a finished part, and the surface may differ from the core because of migration and moulding flow. Several specimens from defined locations, or a milled and homogenised sample, are needed for a representative result, and the sampling plan should be reported with the data.




