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18
DILUTION PROCEDURES
Appendix A
The software program for dilution (2
nd
icon from the right on the SuperCount
homepage) makes it extremely easy to enter dilution factors. See manual for
more details.
ONE STEP DILUTION
Since the path length of the laser through the sample is at least 2 inches, the
sample may need to be diluted in order to avoid coincident counts. Ideally, one
should aim at < 1,000 particles per mL. A fairly simple procedure is outlined here.
Pour the raw sample into a 140 mL beaker and place on the particle counter. If
the counts exceed 800-900 particles/mL at 1
µm, use the following dilution
procedure:
STEP 1
Fill a clean 140mL beaker with 100mL of clean diluent and take a count.
There should not be more than 30 particles/mL greater than
1µm.
STEP 2
Thoroughly redisperse the sample.
STEP 3
Draw 1 mL of sample by glass pipette and begin adding a controlled
proportion of sample to the diluent. Stir carefully with clean spatula or
magnetic stir bar.
STEP 4
Take a count. If a 0.5 mL addition takes the counts above 1,000/mL we
suggest you use the two step dilution procedure (below).
STEP 5
If Step 3 is done carefully, the counts should increase by
100-200 particles/mL. Add more sample until total counts are between
500-600 particles/mL. This is a good place to stop and indicates that
you are safely below the “1,000 count”, coincident count state.
STEP 6
Calculate the dilution ratio as follows: (assuming you start with 100mL
diluent).
If 1mL of sample is added, dilution ratio is 100 = 100:1 (Dilution factor is 101)
1
If 0.1mL of sample is added, dilution ratio is 100 =1000:1 (Dilution factor is 1,001)
0.1
If 5mL of sample are added, dilution ratio is 100 = 20:1 (Dilution factor is 21)
5
Summary of Contents for PC-2300
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