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Diss Factsheets

Environmental fate & pathways

Biodegradation in water: screening tests

Administrative data

Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Study period:
21 March 2017 - 28 April 2017
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2017
Report date:
2017

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
Version / remarks:
17 July 1992
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: ISO International Standard 10634. "Water Quality - Guidance for the preparation and treatment of poorly water-soluble organic compounds for the subsequent evaluation of their biodegradability in an aqueous medium"
Version / remarks:
1995
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Remarks:
dd. 03 November 2015

Test material

Constituent 1
Reference substance name:
Reaction products of Resin acids and Rosin acids, sodium salts and barium chloride
Molecular formula:
not applicable
IUPAC Name:
Reaction products of Resin acids and Rosin acids, sodium salts and barium chloride
Test material form:
solid: particulate/powder
Details on test material:
Name as cited in the report: Barium salts of resin acids and rosin acids
Appearance: light tan powder
Storage conditions: at room temperature desiccated
Specific details on test material used for the study:
Solubility in water: not indicated
Stability in water: stable

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: municipal sewage treatment plant Waterschap Aa en Maas', 's-Hertogenbosch, The Netherlands, receiving predominantly domestic sewage.
- Storage: not applicable, the freshly obtained sludge was used immediately.
- Preparation of inoculum for exposure: the sludge was allowed to settle (31 minutes) and the supernatant liquid was used as inoculum at the amount of 10 mL/L of mineral medium.
- Pretreatment: the day before the start of the test mineral components, Milli-RO water (ca. 80% of final volume) and inoculum (1% of final volume) were added to each bottle. This mixture was aerated with synthetic air overnight to purge the system of CO2.
- Concentration of sludge: 3.6 g/L
- Water filtered: no
Duration of test (contact time):
28 d
Initial test substance concentrationopen allclose all
Initial conc.:
12 mg/L
Based on:
TOC
Initial conc.:
17 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
CO2 evolution
Details on study design:
TEST CONDITIONS
- Composition of medium: mineral medium according to OECD 301
- Test temperature: 22.2 - 23.7°C
- pH: between 7.4 and 7.8 in different test bottles throughout the test
- pH adjusted: no
- Aeration of dilution water: not indicated; tap-water purified by reverse osmosis (Milli-RO) and subsequently passed over activated carbon.
- Continuous darkness: yes
- Other: Test solutions were continuously stirred. Furthermore, the test medium was daily swirled around since the test item tended to float on the water surface.

TEST SYSTEM
- Culturing apparatus: 2 litre brown coloured glass bottles
- Number of culture flasks/concentration: 2
- Method used to create aerobic conditions: synthetic air (CO2 < 1 ppm) sparged through scrubbing solutions at a rate of approximately 1-2 bubbles per second (ca. 30-100 mL/min).
- Measuring method: produced CO2 reacted with barium hydroxide Ba(OH)2 in the gas scrubbing bottle and precipitated out as barium carbonate. The amount of CO2 produced was determined by titrating the remaining Ba(OH)2 with 0.05 M standardized HCl.

SAMPLING
- Sampling frequency: Titrations were made every second or third day during the first 10 days, and thereafter at least every fifth day until day 28, for the inoculum blank and test suspension. Titrations for the positive and toxicity control were made over a period of at least 14 days.
- Sampling method: Each time the CO2-absorber nearest to the test bottle was removed for titration; each of the remaining two absorbers was moved one position in the direction of the test bottle. A new CO2-absorber was placed at the far end of the series. Phenolphthalein (1% solution in ethanol, Merck) was used as pH-indicator.
On the penultimate day, the pH of respective test suspensions was measured and 1 mL of concentrated HCl (37%, Merck) was added to the bottles of the inoculum blank and test suspension. The bottles were aerated overnight to drive off CO2 present in the test suspension.

CONTROL AND BLANK SYSTEM
- Inoculum blank: yes, containing only inoculum (2 bottles)
- Abiotic sterile control: no
- Toxicity control: yes, containing test item, reference item and inoculum (1 bottle).
- Other: positive control: containing reference item and inoculum (1 bottle).

STATISTICAL METHODS: no statistics were used

TEST CONCENTRATIONS:
Test substance (added as weighed amounts to the bottles): bottle A: 16.93 mg/L test substance; bottle B: 17.04 mg/L test substance
Reference control: 40 mg/L reference substance
Toxicity control: 17 mg/L test substance and 40 mg/L reference substance
Reference substance
Reference substance:
acetic acid, sodium salt
Remarks:
purity: 99.5%

Results and discussion

% Degradationopen allclose all
Key result
Parameter:
% degradation (CO2 evolution)
Remarks:
Replicate 1
Value:
63
Sampling time:
28 d
Parameter:
% degradation (CO2 evolution)
Remarks:
Replicate 2
Value:
47
Sampling time:
28 d
Details on results:
- The relative biodegradation values were 63% and 47% biodegradation of the test substance (based on ThCO2), for the duplicate bottles tested. Since the test item is a UVCB the 10-day criterion need not be applied since a sequential biodegradation of the separate constituents can be anticipated. In one of the two bottles, the criterion for ready biodegradability was met.
- In the toxicity control, more than 25% biodegradation occurred within 14 days (56%, based on ThCO2). Therefore, the test item was assumed not to inhibit microbial activity.
- Functioning of the test system was checked by testing the reference item sodium acetate, which showed a normal biodegradation curve (85% biodegradation within 14 days).
- The theoretical CO2 production of the test substance was calculated to be 2.55 mg CO2/mg and that of the reference substance was calculated to be 1.07 mg CO2/mg.

BOD5 / COD results

Results with reference substance:
85% within 14 days

Any other information on results incl. tables

For details on results, see tables in attached illustration.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Remarks:
see 'overall remarks' section for details.
Interpretation of results:
not readily biodegradable
Conclusions:
A ready biodegradation test (Modified Sturm test), performed according to OECD 301B and GLP principles, showed that barium salts of resin acids and rosin acids biodegraded 63% and 47% in duplicate bottles tested. Based on this result, the substance is classified as readily biodegradable.
Executive summary:

In a Modified Sturm Test, according to OECD guideline 301 B and GLP principles, barium salts of resin acids and rosin acids was assessed for its ready biodegradability. The test substance was tested in duplicate at a target concentration of 17 mg/L, corresponding to 12 mg TOC/L. The exposure period was 28 days and two inoculum blanks, a positive control and a toxicity control were included. The test substance was not sufficiently soluble to prepare an aqueous solution of 1 g/L. Therefore, weighed amounts were directly added to medium containing sludge and Milli-RO water was added. After vigorous mixing, the suspension was added o the test medium. The test solutions were continuously stirred during the test to ensure optimal contact between the test item and test organisms. Furthermore, the test medium was daily swirled around, since the test item tended to float on the water surface. CO2 measurements showed that the test substances biodegraded for 63% and 47%, in the duplicate bottles measured. Because the test substance is a UVCB, the 10 -day window does not apply. Based on the degradation of 63% in one of the replicates, the substance is classified as readily biodegradable in the Modified Sturm Test. The test substance was found not to inhibit microbial activity and all validity criteria were met, thus the study was considered to be valid.