X-Ray Fluorescence ( XRF)

X-Ray Fluorescence (XRF) spectrometry is a non-destructive analytical technique based on the characteristic emission of X-Ray photons by atoms when returning to the ground state after an excitation. This property is used to obtain elemental information from different types of materials in several fields.

The basic Energy-Dispersive XRF analyzer (ED-XRF) set-up consists of an X-Ray tube as the excitation source, a sample housing and a semi-conductor detector which allows to discriminate between different energy photons. The angles between the incident X-Ray beam, the sample and detector are equal to 45 degrees to minimize the scattered background.

TXRF is founded on the same principles of the EDXRF however there is one significant difference. In contrast to EDXRF where the primary beam strikes the sample at an angle of 45°, TXRF uses a glancing angle of a few milliradians with the detector positioned just above the sample at 90 degrees.

Primary beam is totally reflected by a flat substrate (carrier) because of low incidence angle to which the sample in dried liquid/slurry form to leave only a thin residue film ideally few nanometres thick. The total reflection condition provides an enhanced fluorescence excitation, while the reduced thickness allows to get rid of any matrix effect: thus, the signal to background ratio is enhanced and for each element a simple linear relationship between its characteristics fluorescence peak intensity and concentration exists.

Quantitative analysis can be performed by adding an internal standard to the sample solution/suspension, i.e. an element which is not present in the original sample (usually Ga, Sc, Co or Y). Then a small droplet, about 5-100 ml is taken from the solution/suspension with the internal standard and deposited onto the carrier.

The technique is generally non-destructive and it is suitable for solids, liquids, powders and alloys. Depending on the sample, analysis can be carried out on the “as is” specimen or after a treatment step, e.g. dilution, digestion, ashing, on-site enrichment etc. In many cases the correct sample preparation is instrumental in getting low LOD and accurate qualification.

Advantages of the TXRF

  • No matrix effects
  • A single internal standard greatly simplifies quantitative analyses
  • Calibration and quantification independent from any sample matrix
  • Simultaneous multi-element ultra-trace analysis
  • Several different sample types and applications
  • Minimal quantity of sample required for the measurement (5 ml)
  • Unique microanalytical applications for liquid and solid samples
  • Excellent detection limits (ppt or pg) for all elements from sodium to plutonium
  • Excellent dynamic ranges from ppt to percent
  • Possibility to analyse the sample directly without chemical pre-treatment
  • No memory effects
  • Non-destructive analysis
  • Low running cost

Products Portfolio

TX 2000 State of the art  TXRF Spectrometer

ProSpector is non-destructive handheld ED XRF elemental analysis solution for quantification on the field of nearly any element (from Magnesium to Uranium).

Simultaneous multi-element analysis from Na to Pu

Confirms to ISO/TS 18507:2015, ISO 20289:2018

No matrix effect

No matrix-dependent calibration curves

Microanalysis capabilities

Improved detection limits (LOD) down to ng/g or lower

ProSpector Handheld XRF  Analyzer

ProSpector is non-destructive handheld ED XRF elemental analysis solution for quantification on the field of nearly any element (from Magnesium to Uranium).

High speed of operation @ above 500 000 CPS count rate

Ambient temperature and pressure corrections for highest stability

Over 10 hours operation from the battery

Detector protection

Extensive and editable alloy grade library

Radiation safety: IR proximity sensor and low count detection

Horizon benchtop TXRF Analyzer

Horizon is Ultra Trace Benchtop EDXRF Spectrometer (TXRF) for multi elemental qualitative and quantitative analyses for major constituents and ultra-trace in suspension as well as liquid samples.

Simultaneous multi-element analysis from Na to Pu

Confirms to ISO/TS 18507:2015, ISO 20289:2018

No matrix effect

No matrix-dependent calibration curves

Microanalysis capabilities

Improved detection limits (LOD) down to ng/g or lower