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EC number: 215-138-9 | CAS number: 1305-78-8
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 13 - 14 June 2007
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- According to OECD 209. Well documented GLP study. Validity criteria fulfilled. Rationale for read-across: in the environment, lime substances rapidly dissociate or react with water. These reactions, together with the equivalent amount of hydroxyl ions set free when considering 100mg of the lime compound (hypothetic example), are illustrated below: Ca(OH)2 <-> Ca2+ + 2OH- 100 mg Ca(OH)2 or 1.35 mmol sets free 2.70 mmol OH- CaO + H2O <-> Ca2+ + 2OH- 100 mg CaO or 1.78 mmol sets free 3.56 mmol OH- From these reactions it is clear that the effect of calcium oxide will be caused either by calcium or hydroxyl ions. Since calcium is abundantly present in the environment and since the effect concentrations are within the same order of magnitude of its natural concentration, it can be assumed that the adverse effects are mainly caused by the pH increase caused by the hydroxyl ions. Furthermore, the above mentioned calculations show that the base equivalents are within a factor 2 for calcium oxide and calcium hydroxide. As such, it can be reasonably expected that the effect on pH of calcium oxide is comparable to calcium hydroxide for a same application on a weight basis. Consequently, read-across from calcium hydroxide to calcium oxide is justified.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- not required
- Details on sampling:
- After the test, the contents of the test vessels were poured into flat bottom flasks. Then oxygen measurements were conducted.
- Vehicle:
- no
- Details on test solutions:
- The dilution medium (deionised water) will be adapted to test temperature. For each test concentration, the dilution medium will be combined with the synthetic sewage feed (16 mL) in a way that a total volume of 300 ml will be obtained. The test item is weighed into a vessel and transferred to the test medium. The volume of the test solution will be large enough to prepare each test concentration level. Then 200 ml of the microbial inoculum were added. The total mixture for each concentration and the two controls was 500 mL.
- Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- Activated sludge from a sewage treatment plant will be used as the microbial inoculum for the test. The activated sludge is obtained preferentially from a sewage work treating predominantly domestic sewage.
On the day the activated sludge is obtained from the sewage treatment plant it was washed with reconstituted water. After centrifugation of the sludge the supernatant was decanted. This procedure was repeated three times.
The final concentration of active sludge in the test medium was 1.6 g/l.
If the activated sludge was not used the day of the collection, 50 ml synthetic sewage feed was added to each litre of the activated sludge and it was aerated with clean, oil-free air and kept at a temperature of 20 ± 2°C. At the end of every storage day the sludge will be fed with 50 ml/l of synthetic sewage feed (maximum storage = 4 days).
The used microbial inoculum had a mixed liquor suspended solids level of 3.6 g/l. The final level in the test solustions was 1.44 g/l.
RECONSTITUTED WATER
According to OECD Guideline No. 203, prepared according the ECT-Standard Operation Procedure (SOP) A 2.1.
Used to keep the microbial inoculum before the period of the test.
Concentration of salts: 294.0 mg/l CaCl2.2H2O, 123.0 mg/l MgSO4.7H2O, 64.8 mg/l NaHCO3 and 5.75 mg/l KCl.
Water was prepared not longer than 4 weeks before it was used. During storage water was aerated.
SYNTHETIC SEWAGE FEED
Contains peptone, meat extract, urea, NaCl, CaCl2.2H2O, MgSO4.7H2O and K2HPO4.
Prepared not longer than 1 week before it was used. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Hardness:
- 235.8 mg/l CaCO3
- Test temperature:
- 19.1-19.7 °C
- pH:
- 7.4-12.6 (before contact time)
7.8-10.6 (after contact time) - Dissolved oxygen:
- 8.7 mg/l (at the beginning of the test)
- Salinity:
- not applicable
- Nominal and measured concentrations:
- Nominal: 0, 62.5, 125, 250, 500 and 1000 mg/l
- Details on test conditions:
- Before use the pH of the activated sludge will be checked and adjusted if necessary to a pH 6.0-8.0 using sodium hydrogen carbonate (NaHCO3) solution.
Every 15 minutes one test vessel containing the test item will be prepared (starting with control 1 and ending with control 2):
- 16 ml of synthetic sewage feed was added to each test vessel.
- deionised water and/or the prepared stock solution was added to the test vessels to a total volume of 300 ml.
- the amount of test item necessary to result in the desired test concentration was added to the test medium and stirred.
- the pH was measured in the test medium.
- 200 ml microbial inoculum was added to each test vessel.
Test vessels: 1000 ml glass beakers.
Number of replicates per test item concentration: 1
Number of replicates in the control: 2
After 3 hours of incubation, the pH was measured. Afterwards the content of the vessels was poured into the measuring apparatus and the respiration rate was determined. - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
- Duration:
- 3 h
- Dose descriptor:
- other: EC20
- Effect conc.:
- 229.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Lower 95%: 192.4 mg/l. Upper 95%: 252.6 mg/l.
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 300.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Lower 95%: 273.4 mg/l. Upper 95%: 348.9 mg/l.
- Duration:
- 3 h
- Dose descriptor:
- other: EC80
- Effect conc.:
- 393.9 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Lower 95%: 341.6 mg/l. Upper 95%: 548.1 mg/l.
- Details on results:
- The biological findings were closely related to the initial pH of the test solutions, which increased from 7.4 in the controls to pH 9.2, 10.0, 11.6, 12.2, 12.6 at 62.5, 125, 250, 500 and 1000 mg/L, respectively. Within the contact time of 3 hours, the initial pH was considerably lowered which is likely attributable to the reaction of the test item with CO2 in the medium to CaCO3. Therefore the initial pH is considered to be the main reason for the effects of the test item on the test organisms.
- Results with reference substance (positive control):
- The 3h- EC50 was in the accepted range of 5-30 mg/L : namely 7.8 mg/L.
- Validity criteria fulfilled:
- yes
- Remarks:
- The two control respiration rates within 15 per cent of each other: 0,4%. The EC50 (3 hours) of 3,5-dichlorophenol was in the accepted range of 5 to 30 mg/l: 7,8 mg/l.
- Conclusions:
- The biological findings (inhibition of respiration) were closely related to the initial pH of the test solutions.
Within the contact time of 3 hours, the initial pH was considerably lowered which is likely attributable to the reaction of the test item with CO2 in the medium to Calcium carbonate. Therefore the initial pH is considered to be the main reason for the effects of the test item in the test organisms.
Reference
Description of key information
Klimisch 1 study (Egeler et al. (2007): activated sludge respiration inhibition test for Ca(OH)2 according to OECD 209; nominal EC50(3h) = 300.4 mg Ca(OH)2/L .
Rationale for read-across: in the environment, lime substances rapidly dissociate or react with water. These reactions, together with the equivalent amount of hydroxyl ions set free when considering 100mg of the lime compound (hypothetic example), are illustrated below:
Ca(OH)2 <-> Ca2+ + 2OH-
100 mg Ca(OH)2 or 1.35 mmol sets free 2.70 mmol OH-
CaO + H2O <-> Ca2+ + 2OH-
100 mg CaO or 1.78 mmol sets free 3.56 mmol OH-
From these reactions it is clear that the effect of calcium oxide will be caused either by calcium or hydroxyl ions. Since calcium is abundantly present in the environment and since the effect concentrations are within the same order of magnitude of its natural concentration, it can be assumed that the adverse effects are mainly caused by the pH increase caused by the hydroxyl ions. Furthermore, the above mentioned calculations show that the base equivalents are within a factor 2 for calcium oxide and calcium hydroxide. As such, it can be reasonably expected that the effect on pH of calcium oxide is comparable to calcium hydroxide for a same application on a weight basis. Consequently, read-across from calcium hydroxide to calcium oxide is justified.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 300.4 mg/L
Additional information
The toxicity to aquatic microorganisms of calcium dihydroxide was assessed in a study performed to OECD TG 209 under GLP (Egeler et al. 2007). Activated sewage sludge was exposed to calcium dihydroxide at nominal test concentrations of 0, 62.5, 125, 250, 500 and 1000 mg/L for 3 hours. The biological findings were closely related to the initial pH of the test solutions, which increased from 7.4 in the controls to pH 9.2, 10.0, 11.6, 12.2, 12.6 at 62.5, 125, 250, 500 and 1000 mg/L, respectively. Within the contact time of 3 hours, the initial pH was considerably lowered which is likely attributable to the reaction of the test item with CO2 in the medium to CaCO3. Therefore the initial pH is considered to be the main reason for the effects of the test item on the test organisms. The 3-h EC50 was 300.4 mg/L.
The toxicity to aquatic micro-organisms of calcium carbonate (nano) was assessed in a study performed according to OECD TG 209 under GLP (Youngs, 2010). Activated sewage sludge was exposed to calcium carbonate at nominal test concentrations of 0, 10, 32, 100, 320 and 1000 mg/L for 3 hours. No toxic effects were seen at any concentration of calcium carbonate (nano) tested. Hence the 3-h EC50 was >1000 mg/L and the NOEC was 1000 mg/L. Calcium carbonate (nano) is therefore not toxic to aquatic microorganisms at concentrations up to 1000 mg/L. Evidence of undissolved test material was observed in some of the test vessels suggesting that the concentrations tested exceeded the maximum solubility of calcium carbonate in water.
Based on the results of the studies performed on the read-across substance calcium dihydroxide and on calcium carbonate, it may be concluded that the acute toxicity to microorganisms of grades of calcium oxide containing up to 35% calcium carbonate will be driven by the calcium oxide content and hence the results available for the read-across substance calcium dihydroxide represent the worse-case for all grades of calcium oxide.
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