Error Analysis Final
Error Analysis Final
This experiment has several steps and each one gives potential for error.
Possible errors in this experiment are in the following steps; dilution,
pipetting and measurement. Systematic errors found in this experiment
are poor timing of taking/recording results and the uv-vis spectrometer
was not calibrated after being used by different groups. Another
systematic error is; a wrong reading was recorded due to cuvette being
placed wrongly in the uv-vis spectrometer and it took an extra two
minutes to rectify the mistake.
It is not possible to determine random error; because only one reading
was taken for each step. The random error is based on a set of readings.
It is equal to the standard deviation.
There are several other errors which contributed to the result obtained
being different from the expected pattern. These include;
The sample took about 3 – 4 minutes to reach the last bench on
which this experiment was conducted. In this case the flask
containing the culture had been opened several times; this might
have contributed to replication of bacteria starting earlier than
expected.
Sometimes the shake flask was brought out of the incubator
before the correct time for the sample to be taken out.
Random Errors
Random errors are errors in measurement that leads to measurable
values being inconsistent, thus measured values are subject to small
fluctuations over time. The random error of a set of readings is equal to
the standard deviation.
Detailed error analysis calculations are shown in the appendices.
n
1 1
T́ = ∑ Ti ¿ ( 0.24+ 0.32+ 0.52+ 0.96 )=0.51
n i=1 4
n
Random Error=ε R=
√ 1
n∑i=1
( T i −T́ )
2