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Environmental fate & pathways

Biodegradation in water: screening tests

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Reference
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
EU Method C.4-E (Determination of the "Ready" Biodegradability - Closed Bottle Test)
Version / remarks:
published in O.J. L 142 (2008)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Oxygen conditions:
aerobic
Inoculum or test system:
sewage, predominantly domestic (adaptation not specified)
Details on inoculum:
- Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): secondary effluent of the waste water treatment plant of Pardubice processing predominantly municipal sewage- Laboratory culture: fresh collected waste water was filtered through paper filter, COD was determined and waste water was aerated till using
Duration of test (contact time):
28 d
Initial conc.:
2.99 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation:
O2 consumption
Details on study design:
TEST SYSTEMThe inoculum contained a mixed population of microorganisms obtained from the secondary effluent of the waste water treatment plant of Pardubice processing predominantly municipal sewage. Preparation of the inoculum:The fresh collected waste water was filtered through paper filter. COD was determined and waste water was aerated till using. Justification of the test system:The inoculum preparation is in conformity with the recommendations of the test guideline.SOLUTIONS AND CHEMICALSThe deionized water with conductivity less than 5 S·cm-1 was used for the preparation of all solutions. The same batch of water was used for each set of the experiments. Analytical grade reagents were used. Stock solutions for the preparation of mineral medium:- Solution a)Monopotassium dihydrogen phosphate, (KH2PO4): 8.50 gDipotassium monohydrogen phosphate, (K2HPO4): 21.75 gDisodium monohydrogen phosphate dodekahydrate, (Na2HPO4·12H2O): 67.21 gAmmonium chloride (NH4Cl): 0.50 g Water up to the volume of 1 000 mL. The right composition of medium was checked by the determination of pH value, which must be 7.4.- Solution b) 22.50 g Magnesium sulphate heptahydrate, (MgSO4·7H2O) in 1 000 mL of water- Solution c)27.50 g Calcium chloride, anhydrous, (CaCl2) in 1 000 mL of water- Solution d)0.25 g Iron (III) chloride hexahydrate, (FeCl3·6H2O) in 1 000 mL of water Preparation of mineral mediumPreparation of 1 litre of mineral medium: 1 mL of solutions a), b), c) and d) were mixed with approx. 500 mL of water, the mixture was replenished with water up to 1 000 mL. The solution was prepared from aerated water. Chemicals for the determination of COD:- Sulfuric acid, (H2SO4) - Silver sulfate, (Ag2SO4) - Ammonium iron(II) sulfate hexahydrate, (NH4)2Fe(SO4)2.6H2O - Potassium dichromate, (K2Cr2O7) - Ferroin solution (C36H24FeN6O4S) - Mercury (II) sulfate, (HgSO4) - Sodium thiosulfate pentahydrate, (Na2S2O3·5H2O) Chemicals for the determination of BOD:- Potassium dihydrogen phosphate, (KH2PO4) - Dipotassium hydrogen phosphate, (K2HPO4) - Disodium hydrogen phosphate dodecahydrate), (Na2 HPO4.12H 2O)- Ammonium chloride, (NH4Cl) - Magnesium sulfate heptahydrate, (MgSO4.7H2O) - Calcium chloride anhydrous, (CaCl2) - Potassium iodide, (KI) - Starch soluble, (C6H10O5)n - Iron (III) chloride hexahydrate, (FeCl3.6H2O) - N-allylthiourea, (C4H8N2S) Chemicals for the determination of nitrites:- Phosphoric acid, (H3PO4) - Sulfanilamide (C6H8N2O2S)- N-(1-Naphtyl) ethylene-diamine dihydrochloride (C12H14N2·2HCl)INSTRUMENTS AND EQUIPMENT- oxygen vessels with glass stopper, volume of approx. 280 mL - large glass bottles of 5 and 10 L volume for the preparation and inoculation of medium- closed thermostat- pH meter WTW Inolab pH 730- oximetr WTW Oxi 730 with membrane probe CellOx 325- analytical balance XS 105 DU (Mettler Toledo)- UV/VIS spectrophotometer Helios Alpha- equipment for the determination of nitrite- volumetric flasks, flasks, beakers, pipettes and further common laboratory equipmentPREPARATION OF SOLUTIONS FOR THE TEST Inoculated mediumThe volume of waste water for the inoculation of mineral medium was chosen 1.8 mL per 1 L of medium (COD of waste water: 93 mg/L). 30 L aerated mineral medium was prepared for the test and before the beginning of the test it was inoculated with 54 mL of modified waste water. The pH value of medium: 7.4. Test substance The stock solution of the test substance was prepared in concentration 0.1021 g/L of deionized water. From this stock solution 175.8 mL (29.3 mL/L) were transferred to a large glass bottle and completed with the inoculated medium to the volume of 6 L. The solution prepared in this way contained 2.99 mg/L of the test substance. The pH value of solution: 7.5. Reference substanceThe stock solution of sodium benzoate was prepared in concentration 1.0000 g/L of deionized water. From this solution, the 12.6 mL (2.1 mL/L) were transferred to a large glass bottle and completed with the inoculated medium to the volume of 6 L. The solution prepared in this way contained 2.10 mg/L of sodium benzoate. The pH value of solution: 7.5. Test substance for nitrification determination The stock solution of the test substance for nitrification determination was prepared in concentration 0.1021 g/L of deionized water. From this solution 117.2 mL (29.3 mL/L) were transferred to a large glass bottle and completed with the inoculated medium to the volume of 4 L. The solution prepared in this way contained 2.99 mg/L of the test substance. Toxicity testThe solution was prepared by dosing 117.2 mL of stock solution of the test substance and 8.4 mL of stock solution of the reference substance into inoculated medium and completed with this medium to the volume of 4 L. The mixture prepared in this way contained 2.99 mg/L of the test substance and 2.10 mg/L of sodium benzoate. Control (blank) determinationThe inoculated mineral medium without test substance was used for the blank determination.TEST CONDITIONS- Temperature: 20 ± 1.0°C - Illumination: no illumination, in the dark- Exposition time: 28 daysTEST PROCEDUREThe number of bottles for individual series: - Test substance series: 2 × 9 bottles with test substance and inoculum- Reference substance series: 2 × 9 bottles with reference substance and inoculum - Blank series: 2 × 9 bottles with inoculated medium only- Toxicity test series: 2 × 5 bottles with test substance, reference substance and inoculum Series for nitrification determination:- 1 × 9 bottles with test substance and inoculumThe prepared dosing solutions for each series was filled in two parallel bottle replicates (except series for nitrification determination). The bottles were placed into thermostat.MEASUREMENTThe first two bottles from each series were immediately submitted to analysis for dissolved oxygen (zero-time) and other bottles were placed in the thermostat. On the 3rd, 7th, 10th, 14th, 17th, 21st, 24th and 28th day of the test, two bottles (parallel replicate) from the test substance series, from the reference substance series and from the blank series were taken off and the same determinations were performed.On the 3rd, 7th, 10th, 14th day of the test, two bottles from the toxicity test series were taken off and the same determination was performed.The analysis of dissolved oxygen was performed electrochemically using oximeter device (oximeter WTW OXI 730).On the 3rd, 7th, 10th, 14th, 17th, 21st, 24th and 28th day of the test, one bottle from the series for nitrification determination was taken off and the determinations of nitrite-N concentration was carried out by spectrophotometric method.The determination of nitrate-nitrogen concentration was carried out by ion chromatography.
Reference substance:
benzoic acid, sodium salt
Key result
Parameter:
% degradation (O2 consumption)
Value:
0
Sampling time:
28 d
Details on results:
see Table 1 and 2
Validity criteria fulfilled:
yes
Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
In this 28-day study of ready biological degradability, the degradation of 0% of the test substance, Direct Yellow 28, was attained in the end of study.
Executive summary:

The test substance, Direct Yellow 28, was tested for the ready biological degradability in Closed Bottle Test.

The test was performed according to Method C.4E - Closed Bottle Test, Council Regulation (EC) No. 440/2008, published in O.J.L 142, 2008.

The results of biological degradation are related to experimentally determined COD values of the test and reference substance at the beginning of the test. The test substance was sufficiently soluble in used mineral medium so the dosage from the stock solution was carried out. Sodium benzoate was used as the reference substance. The dosage was carried out from the stock solution.

Specific COD of the test substance in medium: 1.136 mg/mg

Specific COD of the reference substance in medium: 1.643 mg/mg

In parallel to the main test the toxicity test was performed. Based on the test substance contains nitrogen in the chemical composition, the oxidized nitrogen forms were determined and the correction for nitrification was carried out. The test was performed at temperature of 20 ± 1°C with the pH values of solutions 7 – 8 at the beginning of the test.

The prescribed validity criteria in the test were fulfilled. The test substance was not inhibiting for the used inoculum. Since all criteria of acceptability were met, this study is considered to be valid.

In this 28-day study of ready biological degradability, the degradation of 0% of the test substance, Direct Yellow 28, was attained in the end of study.

Description of key information

In the 28 day study of ready biological degradability, the degradation of 0% of the test substance, Direct Yellow 28, was attained in the end of study.

Key value for chemical safety assessment

Biodegradation in water:
under test conditions no biodegradation observed

Additional information