

X-Ray Fluorescence Analyzer for Plastic Elemental Analysis
塑料元素分析用 X 射线荧光光谱仪
- SKU PCA-0005
- Plastic 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
| Element range | Na to U (light elements in vacuum) |
|---|---|
| Detector | Silicon drift detector, 25–50 mm² |
| Energy resolution | About 130–150 eV at Mn Kα |
| Tube voltage | Up to 50 kV |
| Measurement spot | 1–10 mm selectable |
| Detection limit | 1–50 ppm depending on element |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 3451-1, ASTM D5630, ASTM D1603
What is the X-Ray Fluorescence Analyzer for Plastic Elemental Analysis?
An X-ray fluorescence analyzer excites a plastic sample and records characteristic element radiation, giving rapid non-destructive elemental screening. It is used for restricted substance checks and for verifying filler and additive elements such as bromine, zinc and titanium.
What is the X-Ray Fluorescence Analyzer for Plastic Elemental Analysis?
An X-ray fluorescence analyzer excites a plastic sample and records characteristic element radiation, giving rapid non-destructive elemental screening. It is used for restricted substance checks and for verifying filler and additive elements such as bromine, zinc and titanium.
Overview
An X-ray tube irradiates the sample, and atoms emit fluorescence at wavelengths or energies characteristic of each element, which a silicon drift detector records and the software converts into concentrations using calibration curves. Energy-dispersive instruments are compact and rapid and can measure a whole small part directly, while wavelength-dispersive instruments offer better resolution and lower detection limits for heavier elements. Measurements are usually made in air, under helium or in vacuum, and the effective sampling depth varies from tens of micrometres for light elements to millimetres for heavier ones, so a surface layer can dominate the result. Plastic parts are often screened for lead, cadmium, mercury, chromium and bromine, and fillers containing calcium, magnesium, silicon and titanium are readily identified by their element pattern.
How does it work?
Different questions require different physical principles. Ashing and combustion methods remove the organic matrix by heating in air or oxygen, leaving the inorganic filler or ash as a residue that is weighed, which quantifies mineral content and glass fibre. Carbon black is measured by pyrolysing the polymer in nitrogen and then burning the carbon in oxygen. Infrared spectrometry identifies the polymer and detects functional-group changes caused by oxidation or additives. X-ray fluorescence excites the sample with X-rays and records the emitted characteristic radiation, giving rapid elemental screening for restricted substances. Pyrolysis gas chromatography with mass spectrometry thermally fragments the polymer in an inert atmosphere and separates the fragments, which identifies copolymers, plasticisers and additives that spectroscopy alone cannot resolve.
What are the key features?
- X-ray tube with rhodium or tungsten anode
- Silicon drift detector for rapid analysis
- Measurement in air, helium or vacuum
- Preloaded restricted substance methods
- Fundamental parameter or empirical calibration
- Whole-part measurement without preparation
What are the technical specifications?
A typical x-ray fluorescence analyzer for plastic elemental analysis configuration offers element range of Na to U (light elements in vacuum), detector of Silicon drift detector, 25–50 mm², energy resolution of About 130–150 eV at Mn Kα, tube voltage of Up to 50 kV, measurement spot of 1–10 mm selectable and detection limit of 1–50 ppm depending on element. 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 X-Ray Fluorescence Analyzer for Plastic Elemental Analysis is used in restricted substance screening of plastic parts, filler element identification and verification, brominated flame retardant checks and recycled plastic contaminant screening. Across the wider Plastic Composition Analysis class, laboratories also deploy it for filler and glass fibre content determination, carbon black content in pipe and cable compounds and polymer identification in incoming inspection.
Which standards and certifications apply?
Relevant standards and methods include ISO 3451-1, ASTM D5630, ASTM D1603, ASTM E1131, ASTM D5576, ASTM D3452, ASTM F2617 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.
Representative sampling matters more than instrument precision, because fillers and additives are rarely distributed perfectly evenly. Grind or cryo-mill specimens, or take several portions from different locations, and record the sampling plan. Control the ashing temperature and time exactly, since mineral fillers may lose mass at high temperature and glass fibre can sinter. Keep crucibles clean and run a blank. For X-ray fluorescence, check the measurement area against the sample size and confirm whether the result reflects the surface layer only. Calibrate all equipment with certified reference materials and retain the raw data with the report.
How do I select the right X-Ray Fluorescence Analyzer for Plastic Elemental Analysis?
Choose X-ray fluorescence when quick elemental screening is required on many samples or on whole parts, and when the question concerns elements rather than organic additives. Confirm the element range and detection limits against your specification thresholds, and note that screening results above a limit must be confirmed by a laboratory reference method before a compliance decision.
How does it compare with other Plastic Composition Analysis variants?
Choose by the question and the number of samples. Filler or glass content is measured by ashing in a muffle furnace or by thermogravimetry, and carbon black by a dedicated tube furnace with controlled atmospheres. Polymer identification is fastest by infrared, while X-ray fluorescence gives the quickest elemental screen for compliance work and can be used on a whole part without preparation. Pyrolysis gas chromatography is reserved for cases where the polymer or additive must be identified rather than quantified quickly, for example in a competitor product study or in a contamination investigation. For surface-specific questions such as filler dispersion or the composition of a single particle, microscopy with elemental analysis is added.
Full specifications
| Element range | Na to U (light elements in vacuum) |
|---|---|
| Detector | Silicon drift detector, 25–50 mm² |
| Energy resolution | About 130–150 eV at Mn Kα |
| Tube voltage | Up to 50 kV |
| Measurement spot | 1–10 mm selectable |
| Detection limit | 1–50 ppm depending on element |
| Measurement time | 60–300 s per sample |
| Atmosphere | Air, helium or vacuum |
| Power supply | 220 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Restricted substance screening of plastic parts
- Filler element identification and verification
- Brominated flame retardant checks
- Recycled plastic contaminant screening
Key features
- X-ray tube with rhodium or tungsten anode
- Silicon drift detector for rapid analysis
- Measurement in air, helium or vacuum
- Preloaded restricted substance methods
- Fundamental parameter or empirical calibration
- Whole-part measurement without preparation
Frequently asked questions about X-Ray Fluorescence Analyzer for Plastic Elemental Analysis
Depth depends on the element and the plastic matrix, ranging from tens of micrometres for light elements to several millimetres for heavy elements such as lead. A painted or plated surface, or a concentrated surface layer of additive, can therefore dominate the result, and layered parts should be measured separately.
X-ray fluorescence measures total elemental content and cannot distinguish oxidation states, so it cannot tell whether chromium is hexavalent, which is the restricted form. Limits are also expressed on the homogeneous material, so a positive screen must be confirmed by a wet chemical method on the appropriate material portion.
It can estimate filler content when the filler is characterised by a distinctive element, such as calcium in calcium carbonate or silicon in talc, provided a calibration exists for that filler in the same polymer matrix. Ashing remains the reference method for total filler content.
A weighed specimen is ashed at 625 °C under the conditions of ISO 3451-1, and the residue is weighed as total filler. For glass content alone, the ash is further treated by acid digestion or ignition at higher temperature to remove mineral fillers, and the remaining glass is weighed. Cryo-milling improves repeatability.
Carbon black burns away at ashing temperatures, so it is not included in the ash residue, and it is a separately specified additive in cable, pipe and geosynthetic compounds. It is determined by pyrolysing the polymer under nitrogen and then oxidising the carbon, so the mass loss in the oxidising stage gives the carbon black content.
Infrared identifies the main polymer and shows additive bands, but it cannot easily separate chemically similar additives or distinguish a copolymer composition in detail. Pyrolysis gas chromatography with mass spectrometry separates the fragments, so plasticisers, stabilisers, flame retardants and comonomer ratios can be identified even in a complex compound.




