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Diss Factsheets

Physical & Chemical properties

Particle size distribution (Granulometry)

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Link to relevant study record(s)

Reference
Endpoint:
particle size distribution (granulometry)
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 110 (Particle Size Distribution / Fibre Length and Diameter Distributions - Method A: Particle Size Distribution (effective hydrodynamic radius)
Deviations:
no
Qualifier:
according to guideline
Guideline:
ISO 13320 (Particle size analysis - Laser diffraction methods)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
Laser scattering/diffraction
Type of particle tested:
primary particle
Type of distribution:
volumetric distribution
Percentile:
D10
Remarks on result:
other: results not yet available
Key result
Percentile:
D50
Remarks on result:
other: results not yet available
Percentile:
D90
Remarks on result:
other: results not yet available
No.:
#1
Remarks on result:
other: results not yet available
Conclusions:
The particle size distribution D50 of the test item will be determined.
Executive summary:

A study will be performed in accordance with OECD TG 110 and ISO 13320 in order to determine the particle size distribution of the the test item. Two test series of three measurements each will be performed. The particle size distibution will be determined of the test item. The results will be updated as soon as available.

Description of key information

The particle size distribution D50 will be determined.

Additional information

A study will be performed in accordance with OECD TG 110 and ISO 13320 in order to determine the particle size distribution of the the test item. Two test series of three measurements each will be performed. The particle size distibution will be determined for D50 of the test item. The study was initiated before 31 March 2018 but was not completed by the CRO in due time to complete the registration dossier. The study record will be updated as soon as the results will become available.