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Environmental fate & pathways

Biodegradation in water: screening tests

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Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
Deviations:
yes
Remarks:
Concentration of test material was reduced to 0.2 and 1.0 mg/L.
GLP compliance:
yes
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: A sample of activated sludge mixed Iiquor was obtained from the Midland Municipal Wastewater Treatment Plant (Midland, Michigan. USA) on April 28, 1997.
- Concentration of sludge: mixed liquor suspended solids (MLSS) concentration of the activated sludge sample was determined to be 2190 ± 160 mg/L: Based on this determination, the mineral medium (3 liters) was inoculated with 41 ml of activated sludge to yield a final MLSS concentration of 30 ± 1 mg/L.


Duration of test (contact time):
28 d
Initial conc.:
0.2 mg/L
Based on:
test mat.
Initial conc.:
1 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation:
CO2 evolution
Details on study design:
TEST CONDITIONS
- Composition of medium: according to guideline
- Test temperature: 23 ± 1°C
- pH adjusted: yes, the pH of the inoculated mineral medium was adjusted from 7.01 to 7.37 with 5N NaOH.

TEST SYSTEM
- Culturing apparatus: 1 L flasks were sealed with rubber stoppers fitted with CO2 traps containing 4 ml of 1N NaOH.


CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Abiotic sterile control: yes
- Toxicity control: yes
- Other: non labelled control

Reference substance:
benzoic acid, sodium salt
Parameter:
% degradation (CO2 evolution)
Value:
33.5
St. dev.:
1.5
Sampling time:
3 d
Remarks on result:
other: 0.2 mg [14C]-OPP
Parameter:
% degradation (CO2 evolution)
Value:
62.5
St. dev.:
0.5
Sampling time:
11 d
Remarks on result:
other: 0.2 mg [14C]-OPP
Parameter:
% degradation (CO2 evolution)
Value:
70.8
St. dev.:
0.3
Sampling time:
28 h
Remarks on result:
other: 0.2 mg [14C]-OPP
Parameter:
% degradation (CO2 evolution)
Value:
35.2
St. dev.:
0.2
Sampling time:
3 d
Remarks on result:
other: 1.0 mg [14C]-OPP
Parameter:
% degradation (CO2 evolution)
Value:
67.7
St. dev.:
0.8
Sampling time:
11 d
Remarks on result:
other: 1.0 mg [14C]-OPP
Parameter:
% degradation (CO2 evolution)
Value:
75.7
St. dev.:
0.5
Sampling time:
28 d
Remarks on result:
other: 1.0 mg [14C]-OPP
Details on results:
70.8 and 75.7% biodegradation (CO2 formation as percentage of theoretical value) after 28 days at low (0.2 mg/L) and high (1.0 mg/L) concentration
Results with reference substance:
Kinetic of control substance: 81% after 2 days

Biodegradation rates of o-phenylphenol (percentage of added radioactivity mineralized to 14CO2):

 

Day

Abiotic control

Biodegradation at different OPP concentrations

1.0 mg [14C]-OPP

0.2 mg [14C]-OPP

1.0 mg [14C]-OPP

0

0.0%

0.0%

0.0%

3

0.2%

33.5% (± 1.5)

35.2% (± 0.2)

11

0.3%

62.5% (± 0.5)

67.7% (± 0.8)

28

0.6%

70.8% (± 0.3)

75.7% (± 0.5)

Validity criteria fulfilled:
yes
Interpretation of results:
readily biodegradable
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: GLP guideline study modified (no activated sludge used, Rhine river water used instead)
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 E (Ready biodegradability: Modified OECD Screening Test)
Deviations:
yes
Remarks:
instead of deionised water, Rhine river water was used
GLP compliance:
yes
Oxygen conditions:
aerobic
Inoculum or test system:
other: inoculum from Rhine river water
Duration of test (contact time):
28 d
Parameter:
% degradation (DOC removal)
Value:
100
Sampling time:
6 d
Validity criteria fulfilled:
yes
Interpretation of results:
readily biodegradable
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP guideline study, some test details are missing
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method C.4-D (Determination of the "Ready" Biodegradability - Manometric Respirometry Test)
GLP compliance:
no
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Duration of test (contact time):
28 d
Parameter:
% degradation (O2 consumption)
Value:
ca. 96
Sampling time:
28 d
Details on results:
All ten participants in a ring test reported > 60% biodegradation of 2-phenylphenol after 28 days (mean value = 96%).
Validity criteria fulfilled:
not specified
Interpretation of results:
readily biodegradable
Endpoint:
biodegradation in water: inherent biodegradability
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP guideline study, with some reporting deficiencies: the pH, temperature, purity of test and reference substance, batch numbers are not described.
Qualifier:
according to guideline
Guideline:
OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
Qualifier:
equivalent or similar to guideline
Guideline:
other: DIN 38412
GLP compliance:
no
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, industrial, adapted
Initial conc.:
50 - 400 mg/L
Based on:
DOC
Initial conc.:
200 - 1 000 mg/L
Based on:
COD
Parameter followed for biodegradation estimation:
DOC removal
Parameter:
% degradation (DOC removal)
Value:
100
Sampling time:
10 d
Validity criteria fulfilled:
not specified
Interpretation of results:
inherently biodegradable
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 E (Ready biodegradability: Modified OECD Screening Test)
GLP compliance:
not specified
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: domestic sewage from 10 L laboratory system
- Laboratory culture: yes
Duration of test (contact time):
16 d
Initial conc.:
20 mg/L
Based on:
DOC
Initial conc.:
41.3 other: ml/900ml medium
Based on:
test mat.
Parameter followed for biodegradation estimation:
DOC removal
Details on study design:
TEST CONDITIONS
- Composition of medium: according to guideline

TEST SYSTEM
- Number of culture flasks/concentration: 2


SAMPLING
- Sampling frequency: Sampling after 0 h, 1 d, 2 d, 3 d, 4 d, 8 d, 9 d, 11 d, 14 d, 15 d and 16 d


CONTROL AND BLANK SYSTEM
- Inoculum blank: 2

Reference substance:
aniline
Parameter:
% degradation (DOC removal)
Value:
12
Sampling time:
2 d
Parameter:
% degradation (DOC removal)
Value:
88
Sampling time:
9 d
Parameter:
% degradation (DOC removal)
Value:
94
Sampling time:
9 d
Parameter:
% degradation (DOC removal)
Value:
100
Sampling time:
14 d
Results with reference substance:
Kinetic of control substance (in %):
= 25 after 2 day(s)
= 100 after 9 day(s)
Validity criteria fulfilled:
yes
Interpretation of results:
readily biodegradable

Description of key information

Readily biodegradable: 70.8-75.7% (CO2 evolution) in 28 days (OECD 301B)

Key value for chemical safety assessment

Biodegradation in water:
readily biodegradable

Additional information

Five studies investigating the biodegradability of OPP (CAS-No. 90-43-7) are available. Ready biodegradability was tested in four studies. The key study was carried out according to OECD guideline 301 B and GLP compliance. Using domestic sludge a biodegradation of 70.8 – 75.7% after 28 days was observed (Gonsior and Tryska, 1997).

The rapid biodegradation of OPP is supported by the results of the three other biodegradation studies. These studies were performed according to OECD guideline 301 F, and EU method C.4-D, respectively. In the test conducted according to OECD guideline 301 F 100% biodegradation was reached between 6 and 9 days (Kanne, 1989). In the test following the procedures of the EU method C.4-D, 96% biodegradation after 28 days was observed (Painter, 1985).

An inherent biodegradation study, which was performed according to OECD guideline 302 B shows a DOC removal of 100% after 10 days (Wellens, 1990).

Based on the results above it can be concluded that OPP is readily biodegradable.