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Particle analysis quality

10 Common Particle Analysis Errors to Review

Particle-analysis errors can begin before a sample reaches the analyzer. Review sampling, dispersion and the meaning of the reported distribution before changing instrument settings or treating a result as a product difference.

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Can a repeatable particle result still be misleading?

Yes. Repeatability does not rule out biased sampling, inappropriate dispersion or an unsuitable size definition. Review the complete measurement method, not just repeated scans of the same sample.

A useful investigation separates the material selected for testing from the way it was dispersed and measured. Changing several steps at once makes the cause harder to identify. Keep the original result and conditions, then compare one defined change using representative portions and the same reporting basis.

Ten error areas to check

  1. Sampling bias
  2. Unrepresentative sample division
  3. Unsuitable dispersion
  4. Inconsistent size definitions
  5. Incorrect sample amount
  6. Ignored measurement tolerances
  7. Assumed oversize sensitivity
  8. Misread distribution density
  9. Mixed number, volume or intensity weighting
  10. Undocumented procedures

How can a lab locate a sampling error?

Start with the same prepared portion and repeat its measurement. Then divide fresh portions from the bulk material and prepare each independently. If the fresh portions scatter more widely, investigate division and dispersion before adjusting the analyzer.

Method details to record

10 Common Particle Analysis Errors to Review: method checklist
ConsiderationWhat to record
Sampling from one locationCollect increments across the bulk material to account for segregation
Taking a convenient scoopDivide the laboratory sample reproducibly before choosing the test portion
Changing the dispersion stateCheck for remaining agglomerates or unintended particle breakage
Comparing different dimensionsState which particle dimension each method reports
Using an unsuitable test amountSelect a loading appropriate to the sample and instrument
Overlooking method variabilityEstimate the variation between independently prepared portions
Expecting detection of every rare particleCheck whether the sampled quantity and method can reveal the fraction of interest
Misreading distribution densityCheck the size intervals and axis scale before comparing peak heights
Mixing distribution basesIdentify whether results are weighted by number, volume or intensity
Leaving the method undocumentedRecord preparation, measurement and evaluation steps in the laboratory procedure

Which report details can hide an apparent difference?

Check whether both reports show density or cumulative values and use the same weighting. A change from a number distribution to a volume distribution can make a coarse fraction appear more prominent even when the particles are unchanged.

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