Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Ecotoxicological information

Toxicity to microorganisms

Currently viewing:

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
key study
Study period:
06 Feb - 23 Feb 2012
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
Deviations:
yes
Remarks:
The temperature in the pre-test was in a range of 16.9 - 18.8 °C instead of 20 ± 2 °C as recommeded by the guideline.
GLP compliance:
yes (incl. QA statement)
Remarks:
Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Mainz
Analytical monitoring:
no
Vehicle:
no
Test organisms (species):
activated sludge of a predominantly domestic sewage
Details on inoculum:
- Pretreatment: Upon arrival in the test facility, the sludge was filtrated, washed with tap water and resuspended in tap water. The activated sludge was aerated until usage in the test and fed daily with 50 mL/L synthetic sewage feed. On the day before the experiment, the inoculum was taken from its source, washed, aerated and the dry matter was determined. The volume was adapted to the desired content of dry matter. The nutrient solution was thawed and the sludge was fed with 50 mL/L sludge
- Dry matter of sludge: 2.50 g suspended solids/L
- Dry matter in the test: 1.25 g suspended solids/L
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h
Hardness:
1.08 mmol/L
Test temperature:
16.9 - 18.8 °C
pH:
7.7 - 7.8
Nominal and measured concentrations:
nominal: 0, 1.2, 12.2, 100, 999.4, 1000 and 1001.2 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel:
- Material, size, fill volume: glass beaker, 1000 mL, fill volume: 500 mL
- Aeration: purified air, using Pasteur pipettes, flow approx. 0.75 L/min
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 6
- Biomass loading rate: 1.25 g suspended solids/L

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: deionised tap water
- Total organic carbon: 0.5 mg/L
- Pesticides: < limit of detection
- Chloride: 12.0 mg/L
- Ca: 35.7 mg/L
- Mg: 0.007 mg/L
- Conductivity: 223 µS/cm

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : respiration rate, at the end of the test

TEST CONCENTRATIONS
- Spacing factor for test concentrations: 8 to 10
Reference substance (positive control):
yes
Remarks:
3,5-Dichloro-phenole
Duration:
3 h
Dose descriptor:
NOEC
Effect conc.:
>= 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Duration:
3 h
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Details on results:
No statistically significant inhibition of respiration was observed at any of the treatments.
Results with reference substance (positive control):
- Results with reference substance valid? yes
- Relevant effect levels: EC50 of 8.1 mg/L

Description of key information

NOEC >= 1000 mg/L (activated sludge, OECD 209)

Key value for chemical safety assessment

Additional information

One study on the toxicity of Zinc aluminium oxide to microorganisms is available. This key study was performed as a limit test according to OECD Guideline 209, using activated sludge as inoculum (2012). The sludge was exposed to nominal concentrations of 0 (control), 1.2, 12.2, 100, 999.4, 1000 and 1001.2 mg/L during 3 hours. As no significant inhibition was observed in any of the treatments, the NOEC was determined to be 1000 mg/L and the EC50 > 1000 mg/L.