

TGA-MS Coupled Analyzer for Polymer Analysis
聚合物分析用热重-质谱联用仪
- SKU TGAA-0005
- 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
| Mass range | m/z 1–300 |
|---|---|
| Coupling interface | Heated capillary at 200–300 °C |
| Scan rate | Up to 1000 amu/s |
| Detector | Electron multiplier |
| 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-MS Coupled Analyzer for Polymer Analysis?
A TGA-MS system transfers evolved gases into a mass spectrometer, identifying individual species by mass-to-charge ratio with high sensitivity. It is chosen for trace-level evolved-gas analysis, isotope or fragment studies and detailed decomposition pathway work on polymers.
What is the TGA-MS Coupled Analyzer for Polymer Analysis?
A TGA-MS system transfers evolved gases into a mass spectrometer, identifying individual species by mass-to-charge ratio with high sensitivity. It is chosen for trace-level evolved-gas analysis, isotope or fragment studies and detailed decomposition pathway work on polymers.
Overview
Evolved gases from the thermobalance pass through a heated capillary or a two-stage skimmer interface into the ion source of a quadrupole mass spectrometer, which scans a chosen mass range continuously, often from m/z 1 to 200 or 300. Mass-to-charge ratios identify species directly, so water, carbon dioxide, hydrocarbons, hydrogen chloride and amine fragments can be followed separately and traced back to specific weight-loss steps. Sensitivity is higher than with infrared coupling and the signal is linear over several decades, which supports semi-quantitative comparison of release profiles. Requirements include a high-vacuum system, careful capillary maintenance and a purge gas that does not overload the source; helium is often used because it is light and does not interfere with most analyte masses.
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?
- Quadrupole mass range from m/z 1 to 300
- Heated capillary or skimmer interface
- Multiple ion monitoring for chosen species
- Traces individual species to weight-loss steps
- Helium purge to avoid mass interference
- Detection limits in the low microgram range
What are the technical specifications?
A typical tga-ms coupled analyzer for polymer analysis configuration offers mass range of m/z 1–300, coupling interface of Heated capillary at 200–300 °C, scan rate of Up to 1000 amu/s, detector of Electron multiplier, 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-MS Coupled Analyzer for Polymer Analysis is used in trace evolved-gas identification in polymer degradation, water and solvent release profiling, flame-retardant decomposition pathway analysis, residual monomer and oligomer detection and comparative studies of stabiliser effectiveness. 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-MS Coupled Analyzer for Polymer Analysis?
Specify TGA-MS when detection limits matter, when several species with overlapping infrared bands must be separated, or when specific fragments must be monitored. Confirm the mass range needed for your analytes, the gas supply purity and the vacuum maintenance interval. Because helium is the usual purge gas, check that the instrument's mass-flow control supports it and that no target analyte mass coincides with the residual helium or nitrogen background.
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
| Mass range | m/z 1–300 |
|---|---|
| Coupling interface | Heated capillary at 200–300 °C |
| Scan rate | Up to 1000 amu/s |
| Detector | Electron multiplier |
| TGA temperature range | Ambient to 1000 °C |
| Heating rate | 0.1–50 °C/min |
| Balance resolution | 0.1 µg |
| Typical sample mass | 2–10 mg |
| Purge gas | Helium, ≥ 99.999% |
| Vacuum system | Turbomolecular pump, two-stage |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Trace evolved-gas identification in polymer degradation
- Water and solvent release profiling
- Flame-retardant decomposition pathway analysis
- Residual monomer and oligomer detection
- Comparative studies of stabiliser effectiveness
Key features
- Quadrupole mass range from m/z 1 to 300
- Heated capillary or skimmer interface
- Multiple ion monitoring for chosen species
- Traces individual species to weight-loss steps
- Helium purge to avoid mass interference
- Detection limits in the low microgram range
Frequently asked questions about TGA-MS Coupled Analyzer for Polymer Analysis
Detection depends on the species, the sample mass and the dilution by purge gas, but evolved masses corresponding to a few micrograms of material can often be detected with multiple ion monitoring. As with any evolved-gas method, quantification requires calibration of the specific species in the same system and under the same purge conditions.
Helium is light, so it is pumped away efficiently and does not produce intense background peaks in the mass range of most interest. Nitrogen and oxygen would interfere with the m/z 28 and 32 signals used for nitrogen and oxygen-containing fragments. Purity of at least 99.999% is normally specified.
Each ion current is plotted against the same time base as the mass curve, so a rise in a given m/z signal coincides with a particular weight-loss step. This time correlation identifies which step releases water, carbon dioxide, hydrogen chloride or hydrocarbon fragments, and overlapping release profiles can be deconvoluted as long as the scan rate is fast enough.
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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