Determining the Concentration of a Solution: Beer’s Law
Purpose
To determine the wavelength
(color) of maximum absorbance for a copper (II) sulfate solution.
To examine the relationship between the absorbance and concentration of a
copper (II) sulfate solution.
To determine the concentration of an unknown copper (II) sulfate solution.
Introduction
You will be using the
Colorimeter shown in Figure 1. In this device, light from an LED light
source will pass through the solution and strike a photocell. The CuSO4
solution used in this experiment has a deep blue color. A higher concentration
of a colored solution will absorb more light and transmit less light than a
solution of lower concentration. The colorimeter will interpret the light
received by the photocell and express it both as an absorbance and a percent
transmittance value.
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Figure 1 | Figure 2 |
You will prepare five copper (II) sulfate solutions of known concentration (standard solutions). Each solution will be transferred to a small, rectangular cuvette that is placed into the colorimeter. The absorbance of each solution will be measured and recorded. When a graph of absorbance vs. concentration is plotted for the standard solutions, a direct relationship should result, as shown in Figure 2. The direct relationship between absorbance and concentration for a solution is known as Beer’s Law. The concentration of an unknown CuSO4 solution will then be determined by measuring its absorbance with the colorimeter and using the equation of the best-fit line to determine its concentration.
Materials | |
computer with Logger Pro 3.2 and Interface | 30 mL of 0.50 M CuSO4 |
Vernier Colorimeter | 5 mL of an unknown CuSO4 solution |
two 1-mL, two 2-mL pipets (or a micropipet) | pipet pump(s) or bulb(s) |
a set of matched cuvettes | Kimwipes® |
stirring rod | two 100-mL beakers |
five small, labeled test tubes | test tube rack |
Procedure
Table 1 |
|
Test Tube | CuSO4 concentration (M) |
1 | 0.10 |
2 | 0.20 |
3 | 0.30 |
4 | 0.40 |
5 | 0.50 |
HANDLING CUVETTES: Cuvettes should be wiped clean and dry on the outside with a Kimwipe®. Do not use a paper towel! Handle the cuvettes near the top of the ribbed sides. Solutions should be free of bubbles. If a cuvette is not dry on the inside, a small amount of the solution to be used should be used to rinse the cuvette before filling. Always align the reference mark on the cuvette with the reference mark on the slot of the colorimeter. |
FINDING THE WAVELENGTH OF MAXIMUM ABSORBANCE (lmax): Before making any measurements with the colorimeter, the wavelength (color) of maximum absorbance must be determined. This may be done by following the calibration procedure below for each of the wavelengths available on the colorimeter. Once the colorimeter is calibrated at a particular wavelength, place a cuvette containing the most concentrated sample into the colorimeter. The wavelength that yields the greatest absorbance reading for this sample is called lmax and is the wavelength you should use for all of your measurements. |
CALIBRATION: Click the "LabPro" icon on the toolbar. Then click on the "CH1" icon and select "calibrate". Then click on the "Calibrate Now" button. Place the blank cuvette in the cuvette slot of the colorimeter and close the lid. Turn the wavelength knob of the colorimeter to the 0%T position. In this position, the light source is turned off, so no light is received by the photocell. Type "0" in the Reading 1 Value box. When the voltage stabilizes, click "Keep". Turn the knob of the colorimeter to the desired wavelength. In this position, the sample transmits 100% of the light. Type "100" in the Reading 2 Value box. When the voltage stabilizes, click "Keep", then click "Done". |
Assignment
Written by Lance S. Lund, Anoka-Ramsey Community College. Portions of this lab courtesy of Kirk Boraas, Minneapolis Community and Technical College, and Vernier Software, "Chemistry With Computers". Updated October 22, 2007.