Standard additions – LaMotte SMART Spectro Spectrophotometer User Manual

Page 16

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PREPARING DILUTE STANDARD SOLUTIONS

Standard solutions should be prepared to create a calibration curve. Standard
solutions can be prepared by diluting a known concentrated standard by
specified amounts. A chart or computer spreadsheet can be created to
determine the proper dilutions. Use volumetric flasks and volumetric pipets for
all dilutions.

1. In Column A – Record the maximum concentration of test as determined

by the range and path length.

2. In Column B – Record the percent of the maximum concentration the

standard solution will be.

3. In Column C – Calculate the final concentration of the diluted standard

solutions by multiplying the maximum concentration (In Column A) by the
% of maximum concentration divided by 100. (C = A x

B

100

).

4. In Column D – Record the final volume of the diluted sample (i.e. volume

of volumetric flask).

5. In Column E – Record the concentration of the original standard.

6. In Column F – Calculate the milliliters of original standard required

(C x

D

E

= F).

A sample chart appears below:

A

B

C = A x

B

I 00

D

E

F = C x

D

E

Maximum

concentration

of test

% of

Maximum

concentration

Final

concentration

of Diluted

Standard

Volume of

Standard

Concentration

of Original

Standard

mL of

Original

Standard

Required

10.0 ppm

90

9.0 ppm

100 mL

1000 ppm

0.90 mL

10.0 ppm

70

7.0 ppm

100 mL

1000 ppm

0.70 mL

10.0 ppm

50

5.0 ppm

100 mL

1000 ppm

0.50 mL

10.0 ppm

30

3.0 ppm

100 mL

1000 ppm

0.30 mL

10.0 ppm

10

1.0 ppm

100 mL

1000 ppm

0.10 mL

10.0 ppm

0

0 ppm

100 mL

1000 ppm

0 mL

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STANDARD ADDITIONS

A common method to check the accuracy and precision of a test is by standard
additions. In this method a sample is tested to determine the concentration of
the test substance. A second sample is then “spiked” by the addition of a known
quantity of the test substance. The second sample is then tested. The
determined concentration of the spiked sample should equal the concentration
of the first plus the amount added with the spike. The procedure can be
repeated with larger and larger “spikes.” If the determined concentrations do not
equal the concentration of the sample plus that added with the “spike”, then an
interference may exist.

16

SMART SPECTRO SPECTROPHOTOMETER 05.04

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