AC 16 Colorimetric Analysis For Lab Notebook
AC 16 Colorimetric Analysis For Lab Notebook
Period
Date
Pre-Lab Activity
Setting the stage for the activity
When light interacts with light-absorbing particles, some of the light is removed. Consequently, objects with many
light-absorbing particles appear darker than objects with fewer light-absorbing particles. The ability to absorb color,
as well as what color is to be absorbed, depends on the type of particle present.
One can vary the number of particles with which light interacts in two ways. If you compare two solutions of the
same colored substance with different concentrations, you see that the one with the higher concentration appears
darker because it has more absorbing particles and it absorbs more of the incident light. Also, if you pour the same
solution into a test tube and a 100-mL beaker, the solution in the beaker appears darker. Even though the
concentration in the two solutions is the same, the light has to travel a longer path in the beaker. Therefore, photons
have a higher probability of being absorbed so less light will leave the beaker and the solution appears darker.
Next, if you pour a little bit of the 1 M copper(II) sulfate solution into a 1-L beaker nearly full with water, why is the
original beaker so much darker? It is darker because the "light catching" particles in the more diluted solution are
much farther apart. From this we see that concentration is another variable to consider when looking at absorbed
light.
To measure the amount of light absorbed, we use a colorimeter. Like all electronic measuring devices, the
colorimeter produces a voltage based on the amount of light that hits it. The voltage is converted to an absorbance
level in optical density units (o.d.).
Sample
Concentration
Absorbance
0.20
0.062
0.50
0.156
0.70
0.218
0.90
0.281
(M)
y = (3.119 10-1)x
If a solution of unknown concentration has a absorbance A of .200, the concentration c of the unknown can be found
on the graph, which looks to be between 0.63 M and 0.64 M or calculated from the obtained equation:
The equation of the line is
y 0.3119x
Where y = absorbance A, and x = concentration
Solving for the concentration:
A 0.3119 M 1 c
0.200 0.3119 M 1 c
c
0.200
0.3119 M 1
0.641 M
Colorimeter
Cuvette
Distilled water, 30 mL
Marking pen
Safety
Follow all standard laboratory procedures.
Procedure
After you complete a step (or answer a question), place a check mark in the box () next to that step.
Set Up
1. Connect the colorimeter to the data collection system using the extension cable.
2. Start a new experiment on the data collection system. Click on Sparkvue and then Build.
*
Colorimeter
Unknown
Stock
9. Deliver 8.0, 6.0, 4.0, and 2.0 mL of distilled water into test tubes 1 through 4 so that each test tube has
10.0 mL of solution.
10. Thoroughly mix each solution with a stirring rod.
Note: Clean and dry the stirring rod before stirring a different solution.
Trial #
H2O (mL)
Concentration (M)
2.0
8.0
0.08
4.0
6.0
0.16
6.0
4.0
0.24
8.0
2.0
0.32
10.0
0.40
Collect Data
11. Start a new, manually sampled data set. Click on
Note: The data for test tube 6 is not yet recorded because it has an unknown molarity and it will not be part of the
standardization curve.
Data Analysis
1. Create a data table to record the concentration an absorbance of the 5 solutions. Also include a place to
record the unknown (to be done later in the lab)
2. To graph your data start a new page by clicking on
. Select the absorbance orange and
concentration again, but now click on the graph button and ok.
3. Adjust the scale of the graph to show all data, if needed.
and then