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1.0 Objective
To determine the chemical oxygen demand of the samples
2.0 Apparatus
1. Digestion reactor / COD reactor
2. Spectrophotometer
3. Pipette, 0.1-1ml +tips
4. COD vials rack
4.0 Procedure
Digestion of sample:
1.100 ml of sample was been blended for 30 sec in order to get the homogenize sample.
2. The homogenized sample was poured into 250 ml beaker and been stirred by using a magnetic
stir plate.
3. The sample then was pipetted into 3 bottles of vial (each vial about 2.0 ml)
4. All vials were capped tightly and been inverted gently for several times to make sure that the
content was mixed. The exterior of all the COD were rinsed with deionised water and wiped by
using paper towel. The vials then were placed in the preheated COD reactor
5. A blank and standard solution were prepared by repeating steps 3-4.(but only 1 bottle of vial
for each solution)
6. The exterior wall of all the vials were wiped , cleaned ,before been heated simultaneously in
the digestion reactor for two hours.
7. The reactor was turn off and let it cool to about 120 Celsius
8. Each vial was inverted for several times while still warm
9. The process then was proceeded to colorimetric determination in order to measure COD.
5.0 Results
READING (mg/L)
A
average
SEK 2
75
166
71
104
U 12
50
19
47
116
SEK 7
173
155
108
145
Botanical
18
16
13
Sources of
water sample
(lake)
garden
Table 5.1: Spectrophotometers reading of water sample
Reading of
(lake)
SEK 2
76
U 12
132
SEK 7
114
Botanical garden
11
Parameters
Reading
19.2
1.41
Temperature
31.58
Salinity
0.03
pH
10.66
0.046
ORP
149.3
Table 5.3: YSIs reading meter at the U12