

Thermogravimetric Analyzer for Rubber Compound Analysis
橡胶胶料分析用热重分析仪
- SKU RCA-0001
- 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
| Temperature range | Ambient to 1000 °C |
|---|---|
| Heating rate | 0.1–50 °C/min |
| Balance resolution | 0.1 µg |
| Weighing accuracy | ±0.1% |
| Typical sample mass | 5–20 mg |
| Atmosphere control | Nitrogen to air or oxygen switching |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9924-1, ISO 9924-2, ISO 1407
What is the Thermogravimetric Analyzer for Rubber Compound Analysis?
A thermogravimetric analyzer for rubber decomposes a specimen in staged inert and oxidising atmospheres, giving polymer, carbon black and inorganic filler content in one run. It is the fastest general method for compound verification.
What is the Thermogravimetric Analyzer for Rubber Compound Analysis?
A thermogravimetric analyzer for rubber decomposes a specimen in staged inert and oxidising atmospheres, giving polymer, carbon black and inorganic filler content in one run. It is the fastest general method for compound verification.
Overview
Specimens of 5 to 20 mg are heated in nitrogen so the elastomer decomposes and volatilises, then the atmosphere is switched to air or oxygen to burn off carbon black, leaving zinc oxide, silica, clay and other inorganic fillers as residue. Each stage is quantified from the mass loss, and the derivative curve helps separate overlapping steps such as oil volatilisation from rubber decomposition. Typical instrumentation covers ambient to 1000 °C with a balance resolution of 0.1 µg and programmed gas switching, and the method is standardised for rubber in ISO 9924 and ASTM D6370. Because only a few milligrams are used, specimens should be cut from several locations or from a milled sample so that the result represents the compound rather than one small region.
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?
- Staged nitrogen and oxygen atmosphere programme
- Balance resolution of 0.1 µg
- Temperature range to 1000 °C
- Derivative curve for step separation
- Residue reporting for inorganic fillers
- Alumina and quartz crucible options
What are the technical specifications?
A typical thermogravimetric analyzer for rubber compound analysis configuration offers temperature range of Ambient to 1000 °C, heating rate of 0.1–50 °C/min, balance resolution of 0.1 µg, weighing accuracy of ±0.1%, typical sample mass of 5–20 mg and atmosphere control of Nitrogen to air or oxygen switching. 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 Thermogravimetric Analyzer for Rubber Compound Analysis is used in polymer, carbon black and filler content of compounds, incoming verification of rubber deliveries, comparison of supplier formulations and control of recycled 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 Thermogravimetric Analyzer for Rubber Compound Analysis?
Specify thermogravimetric analysis as the first composition method for rubber, because it quantifies three important components in one short run. Confirm the atmosphere switching capability and the crucible type, and agree the temperature programme with the standard you follow, since different programmes shift the boundaries between carbon black and inorganic residue.
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
| Temperature range | Ambient to 1000 °C |
|---|---|
| Heating rate | 0.1–50 °C/min |
| Balance resolution | 0.1 µg |
| Weighing accuracy | ±0.1% |
| Typical sample mass | 5–20 mg |
| Atmosphere control | Nitrogen to air or oxygen switching |
| Crucible volume | 70–150 µL |
| Data output | Mass curve, derivative and residue percentage |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Polymer, carbon black and filler content of compounds
- Incoming verification of rubber deliveries
- Comparison of supplier formulations
- Control of recycled rubber composition
Key features
- Staged nitrogen and oxygen atmosphere programme
- Balance resolution of 0.1 µg
- Temperature range to 1000 °C
- Derivative curve for step separation
- Residue reporting for inorganic fillers
- Alumina and quartz crucible options
Frequently asked questions about Thermogravimetric Analyzer for Rubber Compound Analysis
A typical programme heats to about 550 °C in nitrogen to decompose the elastomer, switches to air or oxygen and continues to 700 or 900 °C to burn off carbon black, then cools. ISO 9924 and ASTM D6370 define specific programmes, and results should only be compared when the same programme is used.
Incomplete combustion of carbon in the oxidative stage leaves char behind, which is then counted as inorganic filler, or the residue is simply misassigned between stages. Higher oxygen flow, a longer hold at the oxidative temperature and confirmation that the mass stabilises before the step ends all reduce this error.
Cut small pieces of a few milligrams from several parts of the article, or mill the sample and take a representative portion, avoiding steel wire or textile reinforcement. Do not use the surface layer alone unless the surface is the subject of the investigation, since migrated waxes and oils concentrate there.
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.




