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EC number: 935-756-9 | CAS number: 1344-95-2
- 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
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Hydrolysis
Administrative data
Link to relevant study record(s)
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23/08/2010 - 28/09/2010
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Extrapolation from water solubility study according to international guideline under GLP.
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- other: water solubility
- Principles of method if other than guideline:
- Extrapolation of results obtained from water solubility study according to OECD guideline 105 using the shake-flask method (see chapter 4.8).
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
Not relevant - Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- Samples were taken on days 1, 2, 3, 6, 7, 8, 9 and 13.
- Buffers:
- Not relevant
- Estimation method (if used):
- Not relevant
- Details on test conditions:
- Preliminary test
In 10 mL centrifuge vials, 0.1171 g of the test item was weighed. Different volumes of water were added, ranging from 0.1 mL to 10 mL. No complete dissolution was observed. 10.7 mg of the test item were mixed with 1000 mL water and the mixture was shaken for 72 hours. After this time, undissolved particles could be detected in the flask; therefore solubility was estimated as < 10 mg/L. The resulting solution was filtrated and measured. Ca concentration lay by 2.36 mg/L Ca. Therefore, the column elution method was chosen for the determination of the solubility of crystalline calcium silicate hydrates (xonotlite – tobermorite). The measurements of the overnight collected solution by AAS gave a Ca concentration of 4.8 mg/L. Therefore, the column elution method was aborted, and the flask method was used for the determination of the solubility of the test item in water. Si pre-test of this solution was also performed, but not described in the final report.
As no Ca content in the test item was known at that moment, secondary pre-test after the determination of the Ca content was performed. 100 mg of the test item mixed with 30 ml water and the mixture was shaken for 22 hours. After this time the solution was filtrated, diluted (1 : 10 and 1: 100) and measured via AAS for Ca. Ca concentration of the first dilution (1 : 10) lay at 1.7 mg/L Ca, corresponding to the approx. 100 mg/L test item (from the Ca content of 17.19%). Therefore, the flask method was chosen for the determination of the solubility of crystalline calcium silicate hydrates (xonotlite – tobermorite).
Main test
The value which was detected in the preliminary study was used to calculate the amount of test item which is necessary to saturate 1000 ml as approx. 100 mg. Six vessels were used. 25 – 65 mg crystalline calcium silicate hydrates (xonotlite – tobermorite) were weighed into the six vessels, 50 mL water (p.A.) was added to each vessel. The sealed flasks were put on the orbital shaker.
Shaking was performed for 24 hours, then, vessel 1 was taken from the shaker and left to stand at 20 ± 0.5°C for equilibration, followed by the first sampling. The flask was put back on the shaker, and the sample was prepared for analysis and measured Ca, giving the value for day 1. The following samples were taken in the same manner on the days 2, 3, 6, 7, 8, 9 and 13. - Duration:
- 14 d
- pH:
- 10
- Temp.:
- 20 °C
- Initial conc. measured:
- 100 mg/L
- Remarks:
- details described in test conditions
- Number of replicates:
- Not relevant
- Positive controls:
- no
- Negative controls:
- no
- Statistical methods:
- No data
- Preliminary study:
- No data
- Test performance:
- No data
- Transformation products:
- not specified
- Details on hydrolysis and appearance of transformation product(s):
- The substance decomposes for a small part in Ca2+ and SiO3(2-) which in water transforms into the solid SiO2
- Key result
- pH:
- 10
- Temp.:
- 20 °C
- DT50:
- < 6 d
- Type:
- not specified
- Other kinetic parameters:
- No data
- Details on results:
- It was shown that after 14 days, 37 mg of the substance was transformed in water. This plateau was reached after 6 days. This resulted in a hydrolyis rate half-life of less than 6 days.
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- The hydrolysis rate of crystalline calcium silicate hydrate (xonotlite - tobermorite) is < 6 days.
- Executive summary:
Information on the hydrolysis rate of crystalline calciium silicate hydrate (xonotlite - tobermorite) was derived from a water solubility study (see chapter 4.8). It was shown that after 14 days, 37 mg of the substance was transformed in water. This plateau was reached after 6 days. This resulted in a hydrolyis rate half-life of less than 6 days.
Reference
No data
Description of key information
Hydrolysis DT50: <6 days
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 6 d
- at the temperature of:
- 20 °C
Additional information
Information on the hydrolysis rate of silicic acid, calcium salt was derived from a water solubility study (see chapter 4.8). It was shown that after 14 days, 37 mg of the substance was transformed in water. This plateau was reached after 6 days. This resulted in a hydrolyis rate half-life of less than 6 days.
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