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EC number: 500-107-7 | CAS number: 40039-93-8
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 02/04/2012-11/07/2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP comparable to OECD guideline
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-C (Determination of the "Ready" Biodegradability - Carbon Dioxide Evolution Test)
- Principles of method if other than guideline:
- /
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
/ - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure):collected from the Cambridge Wastewater Treatment Facility, Cambridge, Maryland, 19/04/2012
- Storage conditions:at 20°C for
- Storage length:48h
- Preparation of inoculum for exposure: A total suspended solids measurement and standard plate count were performed on the inoculum on the day of use in the test.
- Pretreatment: sludge was sieved using a 2-mm screen, adjusted to approximately 1,000mg total suspended solids/L with mineral media and then aerated at test temperature until use.
- Concentration of sludge: 1000mg/L suspended solids/L mineral media
- Water filtered: yes
- Type and size of filter used, if any:2-mm screen - Duration of test (contact time):
- 28 d
- Initial conc.:
- 10 mg/L
- Based on:
- other: mg C of test material
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Composition of medium:
a modified biochemical oxygen demand (BOD) test dilution water
- Test temperature:20°C
- Suspended solids concentration: <=30mg/l
TEST SYSTEM
- Culturing apparatus:amber 4-liter bottles
- Number of culture flasks/concentration: 3
- Method used to create aerobic conditions:All chambers were aerated with CO2-free air for approximately 24 hours at a rate of 50 to 100 mL per minute to purge the systems of CO2.
- Measuring equipment:Shimadzu Model TOC-Vcsh carbon analyzer to measure CO2 trapped as K2CO3 in the KOH solution
- Details of trap for CO2 and volatile organics if used: CO2 trap, contains approximately 100 mL of 0.5 M KOH, connected to the exit air lines of each chamber.
SAMPLING
- Sampling frequency:3, 6, 9, 13, 17, 20, 23 and 27 days
- Sampling method: removing the Co2 trap nearest the test chamber
CONTROL AND BLANK SYSTEM
- Inoculum blank: not dosed with a carbon source
- Other:Reference group: a reference substance sodium benzoate, a substance known to be biodegradable, was used to check the viability of the inoculum - Preliminary study:
- /
- Test performance:
- The control chambers evolved an average of 65.0 mg CO2 over the test period. This value has been corrected for the amount of CO2 in the trapping solution since potassium hydroxide solution, even when freshly prepared, contains carbonates. The amount of CO2 evolved by the blank control chambers did not exceed the 40 mg/L (120 mg total) value considered the acceptable limit for CO2 evolution tests.
- Parameter:
- % degradation (CO2 evolution)
- Value:
- -2.4
- Sampling time:
- 28 d
- Details on results:
- /
- Results with reference substance:
- The viability of the inoculum and validity of the test were supported by the results of the reference substance, sodium benzoate, from which an average of 101.8% of theoretical CO2 was evolved. An average percent biodegradation of greater than 60% was achieved by Day 6, thereby fulfilling the criteria for a valid test by reaching the pass level by Day 14. The final mean percent biodegradation for Brominated Epoxy was -2.4%. Brominated Epoxy may not be considered readily biodegradable, since the pass level of 60% ThCO2 was not achieved.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- Evidence of ready biodegradability in a Carbon Dioxide Evolution Test is 60% ThCO2 within the 28-day test period. In addition, the pass level must be reached within 10 days of achieving 10% ThCO2. The final mean percent biodegradation for Brominated Epoxy was –2.4%. Brominated Epoxy may not be considered readily biodegradable since the pass level of 60% ThCO2 was not achieved.
- Executive summary:
The ready biodegradability of Brominated Epoxy was determined by the Carbon Dioxide Evolution Test Method (OECD Guideline 301B). Tests of ready biodegradability are stringent tests that provide limited opportunity for acclimation and biodegradation to occur. In the CO2 test, inoculated mineral medium was dosed with a known amount of test substance as the nominal sole source of organic carbon and aerated with CO2-free air. The CO2 produced from the mineralization of organic carbon within the test chambers was displaced by the flow of CO2-free air and trapped as K2CO3 in KOH trapping solution. The amount of CO2 produced by the test substance (corrected for that evolved by the blank inoculum) is expressed as a percentage of the theoretical amount of CO2 (ThCO2) that could have been produced if complete biodegradation of the test substance occurred. The test contained a blank control group, a reference group and a treatment group. Each group contained three replicate test chambers. The blank control was used to measure the background CO2 production of the inoculum and was not dosed with a carbon source. The reference chambers were dosed with sodium benzoate, a substance known to be biodegradable, at a nominal concentration of 10 mg C/L. The treatment group test chambers were used to evaluate Brominated Epoxy at a nominal concentration of 10 mg C/L. The results indicated that the activated sludge inoculum was active, degrading the reference substance an average of 101.8%. The average cumulative percent biodegradation for Brominated Epoxy was –2.4%.
Reference
The temperature range recorded during the test was 19.3-20.8°C and was within the protocol specified range throughout the test. The average TSS of the activated sludge on the day of collection was 12,687 mg/L. The results of the standard plate count and TSS measurement performed on the inoculum were 1.1 x 106 CFU/mL and 900 mg/L, respectively.
The measured dissolved organic carbon (DOC) on Day 29 and pH values of the test chamber contents on Day 28 are presented in Table 1. The measured concentrations of inorganic carbon in the carbon dioxide trapping solutions are presented in Table 2. The cumulative amounts of CO2 produced over the test period are presented in Table 3. The cumulative percent of theoretical carbon dioxide (% TCO2) evolved is presented in tabular and graphical forms in Table 4 and Figure 1, respectively.
Description of key information
Biodegradation for Brominated Epoxy
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
Additional information
Evidence of ready biodegradability in a Carbon Dioxide Evolution Test is 60% ThCO2 within the 28-day test period. In addition, the pass level must be reached within 10 days of achieving 10% ThCO2. The final mean percent biodegradation for Brominated Epoxy was –2.4%. Brominated Epoxy may not be considered readily biodegradable since the pass level of 60% ThCO2 was not achieved.
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