

X-Ray Fluorescence Analyzer for Rubber Compound Analysis
橡胶胶料分析用 X 射线荧光光谱仪
- SKU RCA-0005
- 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
| 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 |
| Detection limit | 5–100 ppm depending on element |
| Measurement time | 60–300 s per sample |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9924-1, ISO 9924-2, ISO 1407
What is the X-Ray Fluorescence Analyzer for Rubber Compound Analysis?
An X-ray fluorescence analyzer measures the inorganic elements in a rubber compound, including zinc, sulfur, silicon, calcium and bromine, without dissolving the sample. It verifies filler and curing system composition and screens for restricted elements.
What is the X-Ray Fluorescence Analyzer for Rubber Compound Analysis?
An X-ray fluorescence analyzer measures the inorganic elements in a rubber compound, including zinc, sulfur, silicon, calcium and bromine, without dissolving the sample. It verifies filler and curing system composition and screens for restricted elements.
Overview
The specimen is irradiated by X-rays from a tube and the emitted fluorescence is recorded by a silicon drift detector, giving intensities that are converted to concentrations through calibration curves. Because rubber is a light matrix, a pressed disc or a ground and pelletised sample gives the most stable geometry, while a whole part can be screened for restricted elements directly. Typical applications include checking zinc oxide content as an activator, verifying silica or clay filler levels through the silicon and aluminium signals, estimating sulfur content from the curing system and screening for brominated flame retardants in rubber parts. Detection limits are element dependent, and results are reported on the specimen as measured, so the thickness and surface condition must be recorded.
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?
- Element range from sodium to uranium
- Silicon drift detector for fast measurement
- Pressed disc and whole-part measurement
- Preloaded restricted substance methods
- Zinc, sulfur and silicon quantification
- Measurement in air, helium or vacuum
What are the technical specifications?
A typical x-ray fluorescence analyzer for rubber compound 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, detection limit of 5–100 ppm depending on element and measurement time of 60–300 s per sample. 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 Rubber Compound Analysis is used in zinc oxide activator content verification, silica and clay filler level checking, restricted element screening of rubber parts and comparison of curing systems between suppliers. 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 X-Ray Fluorescence Analyzer for Rubber Compound Analysis?
Choose X-ray fluorescence for rapid verification of the inorganic part of a rubber formulation, and for restricted element screening across many parts. Confirm the detection limits against your specification thresholds, and follow up any screening result above a limit with a laboratory reference method before making a compliance decision.
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
| 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 |
| Detection limit | 5–100 ppm depending on element |
| Measurement time | 60–300 s per sample |
| Sample preparation | Pressed disc, pellet or whole part |
| Measurement atmosphere | Air, helium or vacuum |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Zinc oxide activator content verification
- Silica and clay filler level checking
- Restricted element screening of rubber parts
- Comparison of curing systems between suppliers
Key features
- Element range from sodium to uranium
- Silicon drift detector for fast measurement
- Pressed disc and whole-part measurement
- Preloaded restricted substance methods
- Zinc, sulfur and silicon quantification
- Measurement in air, helium or vacuum
Frequently asked questions about X-Ray Fluorescence Analyzer for Rubber Compound Analysis
It can measure total sulfur, but it cannot distinguish sulfur in the crosslink network from sulfur in accelerators, sulfate fillers or free sulfur, and calibration is strongly matrix dependent. For total sulfur with higher accuracy a combustion method with infrared or titrimetric detection is preferred, and for crosslink density a swelling test is used.
Grinding the rubber and pressing it into a disc of controlled thickness gives the most reproducible geometry and is preferred for quantitative work on fillers. Whole parts can be measured for screening, but curved or varying surfaces change the effective path length and should be noted as a limitation of the result.
Air absorbs the low-energy fluorescence of light elements such as sodium, magnesium, aluminium and silicon, which are the very elements that indicate clay and silica fillers. Replacing air with helium or evacuating the chamber raises the intensity of these signals and lowers their detection limits considerably.
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.
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