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TGA-FTIR Coupled Analyzer for Polymer Decomposition — product photo

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

Key specifications
Coupling interfaceHeated transfer line, 200–250 °C
Spectral range4000–600 cm⁻¹
Spectral resolution4 cm⁻¹ typical
Spectra per minuteUp to 10 spectra/min
TGA temperature rangeAmbient to 1000 °C
Heating rate0.1–50 °C/min
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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

Full specifications
Coupling interfaceHeated transfer line, 200–250 °C
Spectral range4000–600 cm⁻¹
Spectral resolution4 cm⁻¹ typical
Spectra per minuteUp to 10 spectra/min
TGA temperature rangeAmbient to 1000 °C
Heating rate0.1–50 °C/min
Balance resolution0.1 µg
Typical sample mass5–20 mg
Purge gas flow20–80 mL/min
DetectorDeuterated 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.

Related models

All TGA

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