

TGA-FTIR Coupled Analyzer for Polymer Decomposition
聚合物分解分析用热重-红外联用仪
- SKU TGAA-0004
- TGA
- 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
| Coupling interface | Heated transfer line, 200–250 °C |
|---|---|
| Spectral range | 4000–600 cm⁻¹ |
| Spectral resolution | 4 cm⁻¹ typical |
| Spectra per minute | Up to 10 spectra/min |
| TGA temperature range | Ambient to 1000 °C |
| Heating rate | 0.1–50 °C/min |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 11358-1, ISO 11358-2, ASTM E1131
What is the TGA-FTIR Coupled Analyzer for Polymer Decomposition?
A TGA-FTIR system passes the gases released during thermal decomposition through a heated infrared gas cell, identifying functional groups of the evolved products. It is used to establish decomposition mechanisms, verify additives and investigate failures in polymer compounds.
What is the TGA-FTIR Coupled Analyzer for Polymer Decomposition?
A TGA-FTIR system passes the gases released during thermal decomposition through a heated infrared gas cell, identifying functional groups of the evolved products. It is used to establish decomposition mechanisms, verify additives and investigate failures in polymer compounds.
Overview
A heated transfer line carries the furnace off-gas to a temperature-controlled gas cell, typically at 200 to 250 °C, where an infrared spectrometer records spectra in the mid-infrared region as often as every few seconds. Linking each spectrum to the corresponding point on the TGA curve shows which functional groups appear in each weight-loss step: carbon dioxide and carbonyl bands for oxidation, hydrogen chloride for polyvinyl chloride, ammonia or amine bands for polyamides, or aromatic bands for polystyrene. The technique is qualitative to semi-quantitative, with detection limited by cell volume and purge dilution. Because the transfer line must stay hot to prevent condensation, the system needs careful maintenance, and the coupling reduces sample throughput relative to a plain thermobalance.
How does it work?
A thermogravimetric analyzer suspends the sample from a sensitive balance inside a furnace whose temperature is programmed. The balance continuously records mass, and the derivative curve shows the rate of change, which makes overlapping steps easier to resolve. Atmosphere, heating rate, purge flow and crucible type determine the temperature at which a step occurs, so standards fix these conditions. In an inert atmosphere the polymer matrix decomposes and leaves a residue of filler, ash or carbon black; switching to air or oxygen then burns off the carbon and leaves the inorganic ash. A TGA can also be coupled to an infrared spectrometer or a mass spectrometer through a heated transfer line, so the gases released at each step are identified, which turns a mass-loss curve into evidence about the chemical structure of the sample.
What are the key features?
- Heated transfer line at 200–250 °C
- Gas cell with mid-infrared spectral range
- Spectra recorded every few seconds
- Gram-Schmidt or spectral library identification
- Time-resolved correlation with weight-loss steps
- Purge dilution control for quantitative trends
What are the technical specifications?
A typical tga-ftir coupled analyzer for polymer decomposition configuration offers coupling interface of Heated transfer line, 200–250 °C, spectral range of 4000–600 cm⁻¹, spectral resolution of 4 cm⁻¹ typical, spectra per minute of Up to 10 spectra/min, TGA temperature range of Ambient to 1000 °C and heating rate of 0.1–50 °C/min. 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 TGA-FTIR Coupled Analyzer for Polymer Decomposition is used in decomposition mechanism studies of thermoplastics, gas-phase action of flame retardants, identification of plasticisers and process residues, failure analysis of degraded polymer parts and verification of additive release temperatures. Across the wider TGA class, laboratories also deploy it for thermal stability ranking of polymer grades, filler, glass fibre and ash content determination and carbon black content in crosslinked compounds.
Which standards and certifications apply?
Relevant standards and methods include ISO 11358-1, ISO 11358-2, ASTM E1131, ASTM E2550, ASTM D6370 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.
Calibrate the balance with certified masses and verify the temperature scale with a Curie-point or melting-point standard, since a temperature offset shifts every step. Use a purge flow high enough to remove volatiles but stable enough not to disturb the balance, and buoyancy-corrected blank runs for accurate small mass changes. Crucibles must be matched to the sample: platinum for oxidative work, alumina for most polymer programmes, and open crucibles for combustion steps. Crucibles must be cleaned or replaced because residue from a previous run adds mass. Finally, record heating rate, atmosphere and sample mass with every result, since the same polymer can give quite different decomposition temperatures under other conditions.
How do I select the right TGA-FTIR Coupled Analyzer for Polymer Decomposition?
Choose TGA-FTIR when the goal is to know which chemical groups are released, for example when establishing whether a flame retardant acts in the gas phase or when identifying an unknown additive. Confirm the maximum transfer line temperature needed for your analytes, and provide the required purge gas supply and a dry environment. Plan for a daily or weekly check that the transfer line is at temperature before a run, since condensation can ruin a sequence.
How does it compare with other TGA variants?
First define the question. For thermal stability ranking, a standard thermobalance with inert and oxidative gas switching is enough. For filler and carbon black content in filled compounds, choose an instrument with a wide temperature range, precise balance and a staged atmosphere programme, and add an autosampler if many samples are run. When the identity of evolved products matters, for example in failure analysis or in verifying flame-retardant mechanisms, select a coupled TGA-FTIR or TGA-MS system, noting that coupling reduces sample throughput and requires a heated interface. For composites that contain glass, mineral or ceramic fillers, confirm the furnace reaches the temperature needed to fully burn off the matrix.
Full specifications
| Coupling interface | Heated transfer line, 200–250 °C |
|---|---|
| Spectral range | 4000–600 cm⁻¹ |
| Spectral resolution | 4 cm⁻¹ typical |
| Spectra per minute | Up to 10 spectra/min |
| TGA temperature range | Ambient to 1000 °C |
| Heating rate | 0.1–50 °C/min |
| Balance resolution | 0.1 µg |
| Typical sample mass | 5–20 mg |
| Purge gas flow | 20–80 mL/min |
| Detector | Deuterated triglycine sulfate, cooled option |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Decomposition mechanism studies of thermoplastics
- Gas-phase action of flame retardants
- Identification of plasticisers and process residues
- Failure analysis of degraded polymer parts
- Verification of additive release temperatures
Key features
- Heated transfer line at 200–250 °C
- Gas cell with mid-infrared spectral range
- Spectra recorded every few seconds
- Gram-Schmidt or spectral library identification
- Time-resolved correlation with weight-loss steps
- Purge dilution control for quantitative trends
Frequently asked questions about TGA-FTIR Coupled Analyzer for Polymer Decomposition
It is qualitative to semi-quantitative. Detectability depends on the amount released, the purge flow that dilutes it and the gas-cell path length, so an additive present at a fraction of a percent may still be identifiable if it is volatile. For quantification of a specific compound, a calibration with known standards in the same system is required.
Many decomposition products condense or adsorb on cool surfaces between about 150 and 250 °C, so an unheated line would lose the very compounds of interest and also become contaminated. The line is therefore held at a temperature above the dew point of the expected species, typically 200 to 250 °C, and is checked before each run.
It provides strong evidence for class identification, since characteristic bands reveal polyvinyl chloride, polyamide, polyester, polyurethane or polyolefin decomposition products. Confirming an exact grade may still require FTIR of the solid sample or pyrolysis gas chromatography, and blends with overlapping bands should be interpreted together with the mass-loss steps.
The sample is heated in nitrogen so the polymer matrix decomposes and leaves the filler, then the atmosphere is switched to air or oxygen to burn off any carbon black or char. The residue after the oxidative stage is the inorganic filler or ash, and its mass percentage is reported against the initial sample mass, with a blank crucible run subtracted.
Heat transfer through the sample and the kinetics of bond scission both need time, so a faster heating rate shifts decomposition to higher temperature and can merge two steps into one. Standards therefore fix a heating rate, commonly 10 °C per minute, and results should only be compared when the rate and atmosphere are identical.
Coupling is justified when the identity of the evolved species matters, for example to confirm that a flame retardant acts in the gas phase, to identify a plasticiser or solvent, or to determine which component of a blend decomposes first. Coupling needs a heated transfer line and reduces sample throughput, so routine composition testing does not require it.
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