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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:
05 January 1991 to 14 June 1991
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I))
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: MITI as described in "Chemical Substances Control Law" (Japanese Law No. 117,1974)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Oxygen conditions:
anaerobic
Inoculum or test system:
activated sludge (adaptation not specified)
Details on inoculum:
Activated sludge, which was purchased from a reputable supplier and was cultured in accordance with SOP T-201, was used for the test.
Concentration of activated sludge: 30 mg/L.
Duration of test (contact time):
14 d
Initial conc.:
100 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation:
TOC removal
Details on study design:
CULTIVATION
Cultivation of test solutions for the biodegradability test was carried our according to the following conditions:
Concentration of test material: 100 mg/L
Concentration of activated sludge: 30 mg/L
Cultivating temparature: 25 °C
Cultivating period: 14 days

ACTIVATED SLUDGE
Activated sludge, which was purchased from Chemical Inspection & Testing Institute, Japan on January 17, 1991 and was cultured in accordance with SOP T-201, was used for the test.

CONCENTRATION OF SUSPENDED SOLIDS IN THE ACTIVATED SLUDGE (MLSS)
MLSS: 4808 mg/L
Volume of activated sludge solution added to each test vessel: 1.87 mL

INSTRUMENT FOR CULTIVATION
Closed system oxgen consumption measuring apparatus No.2 (Coulometer : Ohkura Electric Co.,Ltd.). There was no abnormality of function of this apparatus when inspections (periodic and before-using) were carried out.

INITIATION OF CULTIVATION
Following test solution were prepared and cultivated under the aforementioned cultvating conditions:

1. Sludge + aniline
2. Control blank
3. Water + test material (1)
4. Water + test material (2)
5. Sludge + test material (1)
6. Sludge + test material (2)

RECOVERY TEST
Duplicate test solutions of (sludge + test substance) (water + test substance) for recovery test were prepared by reference to the above. Simultaneously duplicate control blanks which did not contain the test substance were prepared in a similar manner. Test vessels were closed with glass plugs and sealed with grease. The test solutions were mixed for 1 hour with a stirrer.
After test solutions were pre-treated by the method above, and analysed according to the procedures above.
Reference substance:
aniline
Key result
Parameter:
% degradation (TOC removal)
Value:
0
Sampling time:
14 d
Details on results:
Percentages degradations calculated on the basis of SOP T-208 are shown below:

Percentage degradation by BOD:
Test substance = 0 %
Aniline:
63.2 % at 7th day
>75 % at 14th day

Percentage degradation by HPLC:
No.1 peak component = 1.74 %
No.2 peak component = 0.95 %
No.3 peak component = 0 %
No.4 peak component = 0 %

Percentage degradation by TOC = 0 %
Parameter:
BOD5
Value:
0 other: %
Results with reference substance:
Aniline:
Day 7 = >40 %
Day 14 = >65 %

Results of biodegradation test

Number

Sample

Initial content (mg)

TOD (mg)

BOD (mg)

 

7 days        14 days

Percentage biodegradation

7 days        14 days

1

Aniline

30

90.3

61.5

>75

63.2

74.2

2

Control blank

0

0

4.4

7.4

0.0

0.0

3

Test substance + water -1

29.7

95.6

0.9

1.9

-

-

4

Test substance + water - 2

30.9

99.6

0.8

1.7

-

-

5

Test substance + sludge - 1

30.9

99.5

0.7

1.5

0.0

0.0

6

Test substance + sludge - 2

30.7

98.9

1.2

2.6

0.0

0.0

Test substance concentration (mg/L): 100

Activated sludge concentration (mg/L): 30

Temperature (°C): 25 ± 1

TOD of test substance: 3.22 (g/g)

Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
Percentage biodegradations of aniline calculated from BOD were over 40 % and 65 % at the 7th and 14th day, respectively. Therefore, this test condition was valid. Percentage biodegradations of test material calculated fron BOD and TOC were both 0 %. In HPLC Method, percentage biodegradations for peak components of No.1 and No. 2 of test material were approxinately 1~ 2 %, on the other hand, other conponents were 0 %.
Consequently it was concluded that the test substance was almost not biodegraded by microorganisms.



Executive summary:

The ready biodegradability of the test material was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I)).

Under the conditions of the study, the test material attained 0 % degradation, as calculated from BOD and TOC. Furthermore, in the HPLC method the test material attained 0 - 2 % degradation.

It is subsequently concluded that the substance is not readily biodegradable.

Description of key information

Not readily biodegradable, OECD 301C, M Sato (1991).

Key value for chemical safety assessment

Biodegradation in water:
under test conditions no biodegradation observed

Additional information

The ready biodegradability of the test material was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I)).

Under the conditions of the study, the test material attained 0 % degradation, as calculated from BOD and TOC. Furthermore, in the HPLC method the test material attained 0 - 2 % degradation.

It is subsequently concluded that the substance is not readily biodegradable.