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EC number: - | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
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- Toxicokinetics, metabolism and distribution
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- Specific investigations
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- Additional toxicological data

Particle size distribution (Granulometry)
Administrative data
Link to relevant study record(s)
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From July 18, 2017 to September 14, 2017
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: ISO 2591-1
- Version / remarks:
- ISO 2591-1:1988, Test sieving -- Part 1: Methods using test sieves of woven wire cloth and perforated metal plate
- Deviations:
- not specified
- Principles of method if other than guideline:
- To characterise the particle size distribution of the test substance powder, the analysis was conducted initially using an optical microscope analysis and was then undertaken more formally using a manual sieve analysis.
- GLP compliance:
- yes
- Type of method:
- sieving
- Remarks:
- Microscopic examination also was performed
- Type of particle tested:
- other: Sample tested as received (white solid block)
- Type of distribution:
- mass based distribution
- No.:
- #1
- Size:
- > 2 000 µm
- Distribution:
- ca. 100 %
- Remarks on result:
- other: The test susbtance was found to be a solid block with few broken bits. During sieve analysis, only 3.3 g of the test substance poured into the sieve. The remaining portion of the test susbtance remained as a solid block.
- Remarks:
- All the particles that went into the sieve were greater than 2000 μm. Because these particles were greater than the upper limit of detection for the distribution analysis, no further testing was performed.
- Conclusions:
- Under the study conditions, the particle size of the test substance was considered to be >2000 µm.
- Executive summary:
A study was conducted to determine particle size distribution of the test substance, by optical microscopic and manual sieve analysis according to ISO 2591 -1 Method, in compliance with GLP. The test susbtance was found to be a solid block with few broken bits. During sieve analysis, only 3.3 g of the test substance was poured into the sieve. The remaining portion of the test susbtance remained as a solid block. All the particles that went into the sieve were greater than 2000 μm. Because test substance particles were greater than the upper limit of detection for the distribution analysis, the author concluded that no further testing was required. Under study conditions, the particle size of the test substance was considered to be >2000 µm (Chilworth, 2017).
Reference
1) Optical microscope analysis
In standard visual observation, test substance was observed to be a white block with few broken bits. All the particles were greater that 2000 μm. In observation using 3.2 objective lens, the particles were appeared to be irregular shaped crystals. Whereas in observation using 40 objective lens, all of the particles were greater than 2000 μm.
2) Manual sieve analysis
Full test results
Sieve size (μm) |
Sieve weight (g) |
Sieve + powder weight (g) |
Powder weight (g) |
% by weight |
|
> 2000 |
325.88 |
326.65 |
0.8 |
100.0 |
|
< 2000 |
352.25 |
352.25 |
0.0 |
0.0 |
|
Total |
0.8 |
100.0 |
|||
The test susbtance was found to be a solid block with few broken bits. During sieve analysis, only 3.3 g of the test substance poured into the sieve. The remaining portion of the test susbtance remained as a solid block. All the particles that went into the sieve were greater than 2000 μm. Because test substance particles were greater than the upper limit of detection for the distribution analysis, no further testing was performed
Description of key information
The particle size distribution of the test substance was determined by optical microscopic and manual sieve analysis method (Chilworth, 2017).
Additional information
The particle size of the test substance was determined to be >2000 µm.
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