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AR226-3106 H n tin g d o n
V
CONFIDENTIAL
DPT 437/984087 i
ACTIVATED SLUDGE - RESPIRATION INHIBITION TEST
Sponsor
Dupont Speciality Chemicals, Jackson Laboratory, Chambers Works, Deepwater, NJ 08023, USA.
Research Laboratory
Huntingdon Life Sciences Limited, Eye, S u ffo lk , IP23 7PX, ENGLAND.
Final report issued: 5 November 1998
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CONTENTS COMPLIANCE WITH GOOD LABORATORY PRACTICE STANDARDS QUALITY ASSURANCE STATEMENT........................................................ RESPONSIBLE PERSONNEL........................................................................ SUMMARY..... ................................................................................................ INTRODUCTION..................................................................... ....................... TEST SUBSTANCE......................................................................................... EXPERIMENTAL PROCEDURE................................................................... MAINTENANCE OF RECORDS..................................................... .............. RESULTS.......................................................................................................... CONCLUSIONS............................................................................................... REFERENCE....................................................................................................
DPT 437/984087 Page 3 4 5 6 7 8 9 13 14 15 16
TABLE 1. Temperature, pH and measurements o f respiration rate..........................
17
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DPT 437/984087 COMPLIANCE W ITH GOOD LABORATORY PRACTICE STANDARDS
The study described in this report was conducted in compliance with the following Good Laboratory Practice standards and I consider die data generated to be valid. United Kingdom Good Laboratory Practice Regulations (1997), Statutory Instrument No. 654. OECD Principles o f Good Laboratory Practice (as revised in 1997), ENV/MC/CHEM(98)17. EC Council Directive, 87/18/EEC o f 18 December 1986, (No. L 15/29).
Christine E. Burwood, B.Sc. (Hons.), Study Director, Huntingdon Life Sciences Ltd.
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QUALITY ASSURANCE STATEMENT The following have been inspected or audited in relation to this study.
DPT 437/984087
Study Phases Inspected
Protocol
Process Based Inspections Formulation Measurement o f dissolved oxygen Collection o f activated sludge' Audit
R ep o rt
Date of Inspection 11.08.98
16.09.98 18.08.98 24.06.98 12.05.98 14.10.98
Date of Reporting
1108.98
16.09.98 18.08.98 24:06:98 12.05.98 15.10.98
Protocol: An audit o f the protocol for this study was conducted and reported to the Study Director and Company Management as indicated above.
Process based inspections: At or about the time this study was in progress inspections and audits of routine and repetitive procedures employed on this type o f study were earned out. These were conducted and reported to appropriate Company Management as indicated above.
Report A udit: This report has been audited by the Quality Assurance Department. This audit was conducted and reported to the Study Director and Company Management as indicated above.
The methods, procedures and observations were found to be accurately described and the reported results to reflect the raw data.
Gregg I. Goddard, Senior Auditor, Department o f Quality Assurance, Huntingdon Life Sciences Ltd.
3 O ^. OC JofS&L.'..(, S $ Date
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RESPONSIBLE PERSONNEL
Christine E. Burwood, B.Sc. (Hons.) (Study Director)
Faye O. Shanahan (Laboratory Technician)
DPT 437/984087
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SUMMARY
DPT 437/984087
The effect o l |H f l ^ H H |> n the respiration rate o f activated sludge was assessed by the methods detailed in EC birective 80^02, `Biodegradation - Activated Sludge Respiration Inhibition test' and OECD Test Guideline 209, `Activated Sludge, Respiration Inhibition test'.
Samples of activated sludge (suspended solids 1.6 g/1), fed with synthetic sewage, were exposed to the test substance at nominal concentrations o f 1,10 and 100 mg/1 for three hours. Single mixtures were prepared at 1 and 10 mg/1 and the highest level was prepared in triplicate. Their rates o f oxygen consumption were determined using an oxygen electrode and compared with those o f controls, containing activated sludge and synthetic sewage alone, which were established at the beginning and end of the culture series.
The reference inhibitor 3,5-dichlorophenol (3,5-DGP) was employed at 3.0, 10.0 and 32.0 mg/1; as a positive control.
The specific respiration rate o f the control culture established at the end o f the test series (32.6 mgCVg/h) was 96% o f the rate o f that established at the start (34.1 m gO/g/h). The three-hour 50% effect concentration (EC50) for 3,5-DCP was calculated to be 15.1 mg/1 (95% confidence limits 12.2 -19.5 mg/1). These results show that the test was valid and that the sample of activated sludge employed was sensitive to inhibition.
id no significant inhibitory effect on the respiration rate o f activated sludge at any of j e concentrations employed in the test. At nominal concentrations o f 1 and 10 mg/1, respiration rates were reduced by 4% when compared to the mean control value; no effect on respiration was observed at 100 mg/1. The EC20, EC50 and ECgo o f the test substance could not, therefore, be . calculated but these must be greater than 100 mg/1, the highest level tested.
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INTRODUCTION
DPT 437/984087
The objective of this study was to assess the effects o
[on sewage micro-organisms by
mpacuring the rate of oxygen uptake of activated sluclge at 20 T&Z in its presence at a range o f
concentrations.
The methods employed were designed to meet the requirements o f EC Directive 88/302, `Biodegradation - Activated Sludge Respiration Inhibition test' and OECD test guideline 209, `Activated Sludge, Respiration Inhibition test* adopted 4 April 1984.
The dechlorinated tap water used to prepare test mixtures had a measured hardness o f 184 mg/1 as CaC03. This deviated from the hardness specified in the protocol (200 - 250 mg/1 as CaC03) but this is not considered to be significant, nor to have affected the integrity of the test.
The protocol was approved by Huntingdon Life Sciences Management on 7 July 1998, by the Sponsor on 17 July 1998, and by the Study Director on 10 August 1998.
The experimental phase of the study was conducted between 12 and 14 August 1998.
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Identity: Chemical name:
TEST SUBSTANCE
DPT 437/984087
Lot number / Batch number: Expiry date: Purity / Composition: Appearance: Storage conditions: Date received:
J 2 years from date of receipt 25% Pale Yellow Slurry Room temperature 23 June 1998
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EXPERIMENTAL PROCEDURE
DPT 437/984087
REFERENCE INHIBITOR
3 5-DCP, >97%, product number D7,060-0, was obtained from the Aldrich Chemical Company Ltd.
DILUTION WATER
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The water used to prepare test mixtures was decblorinated tap water (measured hardness, 184 mg/1 as CaC0 3 ).
The dilution water used to prepare synthetic sewage was tap water that had been softened and treated by reverse osmosis (Elga Ltd,- Prima 4 reverse osmosis unit) and then purified (Elga Ltd, UHP) to give a resistivity o f 18 Megohm/cm. This water complies with the relevant standards (British Standard (BS) 3978 :1987 (ISO 3696 :1987)).
SYNTHETIC SEWAGE
Synthetic sewage feed for activated sludge was prepared by dissolving the following in one litre of ultrapure water (resistivity 18 Megohm/cm):
peptone
- 16.0g
meat extract
- ll.O g
urea - 3.0g
sodium chloride
- 0.7g
calcium chloride dihydrate
- 0.4g
magnesium sulphate heptahydrate -
0.2g
di-potassium hydrogen phosphate -
2.8g
PREPARATION OF THE MICROBIAL INOCULUM
A sample o f activated sludge was obtained the day before the start o f the test from Oakley Sewage Treatment Works, a sewage plant treating predominantly domestic waste. In the laboratory, the sample was maintained under aerobic conditions until required.
The concentration o f suspended solids in a homogenised sample was determined on the day of collection and immediately before the start of the test.
On the day of collection, aliquots (25 ml) o f the activated sludge were filtered through dried and preweighed Whatman's GFC filter papers which were then dried again at approximately 105C for at least one hour, allowed to cool in a desiccator and reweighed. The mixed liquor suspended solids (MLSS) content o f the activated sludge was then calculated. Synthetic sewage (50 ml/1) was added and the mixture aerated overnight. On the day o f the test, the MLSS content of the sludge was determined and adjusted to 4 g/1 by the addition o f dechlorinated tap water. The pH of the sludge was also measured.
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DPT 437/984087
PREPARATION OF SOLUTIONS OF THE REFERENCE SUBSTANCE (3,5DICHLOROPHENOL)
A concentrated solution of 3,5-DCP (500 mg/1) was prepared by dissolving 0.5 g in 10 ml of IN sodium hydroxide and diluting to approximately 30 ml with ultrapure water. Sulphuric acid (IN ) was added to the point of incipient precipitation and the solution made up to a final volume of one litre with ultrapure water. The pH of this solution was then measured.
I Nominal concentrations of 3.0, 10.0 and 32.0 mg/1 were prepared by dilution o f this concentrated
l
solution.
TEST METHODS
The results o f a preliminary solubility trial showed t h a j y p l l H g w a s insufficiently soluble in water at room temperature to allow the preparation oF a suitable Slock solution, so appropriate weights contained in glass weighboats, were added directly to test beakers. The test material was provided as an aqueous slurry containing 25% active ingredient (A.I.) and 75% water. To promote dissolution, the slurry was gently heated in a water bath at 37.5C until the solids had dissolved and a clear solution was obtained. An approximate amount o f die warm test substance was transferred to a glass weighboat. The material was allowed to cool and die final weight recorded once a stable balance readingcouldbe.obtained. Dechlorinated tap water (284 ml) was added to each test beaker c o n ta in in a B H |H ^ B p n d the mixtures were treated with ultrasound for 10 minutes. Additions of sy n th ed ^ ^rag ^ m S n icro b ial inoculum were then made as detailed in the schedule below. The
D mixtures were prepared at 15 minute intervals.
Test mixture
Control (1)
Test substance* (mg) or reference (ml)
0
Synthetic sewage (ml)
16
Test substance (mg/1) 1 10 100 100 100
2.0 20 200 200 200
16 16 16 16 16
3,5-DCP (mg/1) 3.0 10.0 32.0
Control (2)
3.0 10 32
0
16 16 16
16
The table quotes the intended addition o f the test substance.
Water (ml)
284
M icrobial inoculum (ml)
200
284 200 284 200 284 200 284 200 284 200
281 200 274 200 252 200
284 200
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DPT 437/984087
An allowance was made for the concentration of the active ingredient during the formulation o f test mixtures. The actual weights of test substance added to each mixture were recorded and the achieved concentrations calculated. Prepared mixtures were then aerated using a Pasteur pipette connected to a laboratory supply of oilfree compressed air for three hours. Following the exposure period, a well-mixed sample o f each mixture was transferred to a biochemical oxygen demand (BOD) bottle (capacity; 270 ml) and its rate of oxygen consumption over a period o f approximately ten minutes was measured using a Yellow Springs Instruments (YSI) dissolved oxygen meter, with temperature probe and self-stirring bottle probe, connected to a chart recorder. The pH and temperature o f the samples were measured at the start and end of the te st
CALCULATION OF RESULTS The respiration rate o f each te st reference and control mixture was calculated from oxygen levels in the following way: Respiration rate (r) = DO(i ) - DO?) mg02/l/minute
D O (i) = initial oxygen level DO(2) = final oxygen level t = time over which measurements were made in minutes The specific respiration rate o f each mixture was calculated from respiration rate in the following way: SRR (mg02/g/h) = r (meCb/l/min) x 60
MLSS where: SRR = specific respiration rate MLSS = concentration of mixed liquor suspended solids in the sample of activated sludge (g/1)
in the test or control mixture.
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DPT 437/984087
The inhibitory effect o f the test or reference substance at a particular concentration was calculated by expressing the specific respiration rate as a percentage o f the mean of the respiration rates o f the two controls in the following way:
% inhibition where:
1 - ( 2 Rs ) x 100 Rcj + Rc2
Rs = rate of oxygen consumption of test or reference substance
Rc i = rate of oxygen consumption of control 1
Rc2 = rate o f oxygen consumption of control 2
The EC50 and 95% confidence limits of die reference substance were calculated using the computer program o f Stephan et al (1982).
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DPT 437/984087
MAINTENANCE OF RECORDS
All specimens, raw data and study related documents generated during the course o f the study at Huntingdon Life Sciences, together with a copy of the final report will be lodged in the Huntingdon Life Sciences Archive.
Specimens and records will be retained for a minimum of five years from the date o f issue of the final report. At the end of die five year retention period the Sponsor will be contacted and advice sought on their future requirements. Under no circumstances will any item be discarded without the Sponsor's knowledge.
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RESULTS
DPT 437/984087
Temperature, pH and measurements of respiration rate in the test are given in Table 1.
Measurements of the pH of the aqueous stock solution o f the reference substance and o f the activated sludge before the start o f the test, are given below.
Preparation 3,5-DCP stock solution
activated sludge
pH measurement 8.0 7.4
The weights of the test substance added to test beakers and the actual concentrations achieved are given below:
Beaker No.
1 2 3 4 5
Nominal Concentration
(mg/1)
1 10 100 100 100
Weight Added (mg)
Actual Concentration
(mg/1)
2.19 19.63 205.24 209.08 215.12
1.095 9.815 102.63 104.54 107.56
Actual as a Percentage of Nominal
(%) 109.5 98.2 102.6 104.5 107.6
Sludge respiration rates were progressively reduced in the presence of increasing concentrations of 3,5-DCP. The three-hour 50% effect concentrations (EC50) for 3,5-DCP was calculated, by the Moving Average method, to be 15.1 mg/1 (95% confidence limits 12.2 - 19.5 mg/1).
The specific respiration rate o f the control culture established at the end of the test (32.6 mg02/g/h) was 96% o f the rate o f that established at the start (34.1 mgC>2/g/h).
These results show that the test was valid and that the sample o f activated sludge employed was sensitive to inhibition.
l a d no significant inhibitory effect on the respiration ra te g factiv ate^ k jjg e att any of
Jie concenntrtSrtTrTftomns concentrations o f 1
aenmdp1lo0_ymedg/1-i,nretmshpei.rartet.i.sotn.,
raiIt.nes
mwieAxrte_iu_mrr_eecjds_u_cc_eojd ntb__yt. aA4Oi%/n
iwnh^enHco| |m| MparWfSrtaot+t1hnAeoommtiiaernaanl
control value; no effect on respiration rate was observed at 100 mg/1. The EC20. EC50 and ECgo of
the test substance could not, therefore, be calculated but these must be greater than 100 mg/1, the
highest level tested.
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CONCLUSIONS
DPT 437/984087
m ^ l ^ K i a d no significant inhibitory effect on the respiration rate of activated sludge at any of employed in the test The EC20EC50 and ECso of the test substance could not,
therefore, be calculated but these must be greater than 100 mg/1, the highest level tested.
The three-hour EC50 for 3,5-DCP (15.1 mg/1) fulfilled the validity criterion relating to sensitivity to inhibition (acceptable EC50 range; 5 to 30 mg/1), and that relating to the respiration rates in the control (variation not greater than 15%) was also satisfied.
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REFERENCE
DPT 437/984087
STEPHAN et al (1982). A computer program for calculating an LC50. US Environmental Protection Agency.
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DPT 437/984087 TABLEI Temperature, pH and measurements of respiration rate
Test mixture
C on trolli!
1 10 100 100 100 3.5-DCP lme/11 3.0 10.0 32.0 Control 12!
Temperature (C)
Initial
22.0
Final 19.8
PH
Initial
7.5
Final 8.1
Respiration rate
mgCVg/h
34.1
% inhibition
-
21.2 19.6 7.5 8.1 21.0 19.8 7.5 8.0 22.0 20.8 7.2 7.8 21.6 19.6 7.1 7.9 21.2 20.0 7.1 7.9
31.9 32.0 33.8 34.1 35.6
4 4 0 0 0
20.8 20.5 7.5 8.1 20.9 20.0 7.5 8.2 20.9 19.8 7.5 8-2 20.9 20.0 7.5 8.1
30.0 20.6 9.7 32.6
10 38 71 -
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