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Physical & Chemical properties

Particle size distribution (Granulometry)

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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)
Version / remarks:
Screening Test
Deviations:
no
Principles of method if other than guideline:
The method used is based on a procedure designed to comply with that given in 'Particle size distribution, fibre length and diameter distribution', June 1996 European Commission technical guidance document, which satifies the requirements of OECD Guideline 110.
Test item was sieved for approximately 30 minutes on an Inclyno sieve shaker using a sieve with an aperture size of 100 µm. The mass of the test item passing through the sieve was measured.
GLP compliance:
yes (incl. QA statement)
Type of method:
determination of fibre length and diameter distributions
Percentile:
D50
Remarks on result:
other: Migrated from fields under 'Mass median diameter' as D50 percentile. No source field for Standard deviation.
No.:
#1
Size:
< 100 µm
Distribution:
0.1 %

The results of the sieving procedure are shown below:

Measurement

Result 

Mass of test item transferred to sieve 

10.95g

Mass of test item passed through sieve

0.01g

Proportion of test item <100µm 

0.1%
Conclusions:
The proportion of diammonium hexachloroiridate < 100 μm was determined to be.0.1%
Executive summary:

This result is from a GLP compliant study following OECD guideline 110, which is considered suitable for use as the key study for this endpoint (Harlan 2011). The proportion of diammonium hexachloroiridate < 100 μm was determined to be 0.1 %.

Description of key information

The proportion of diammonium hexachloroiridate < 100 μm was determined to be 0.1%.

Additional information

This result is from a GLP compliant study following OECD guideline 110, which is considered suitable for use as the key study for this endpoint (Harlan 2011). The proportion of diammonium hexachloroiridate < 100 μm was determined to be 0.1 %.