![]() |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Experiment
16 PROCEDURES 1.Obtain and wear goggles. 2. Pour about 30 mL of 0.00200 M Fe(NO3 )3 into a clean, dry 100-mL beaker. Label five 50-mL beakers 1-5. Pipette about 5 mL of the solution into each of the first four labeled beakers. Record the actual volume of solution used. The pipettes can be read to hundredths of a milliliter, so each volume should have 2 decimal places. Use a pipette bulb to pipette all solutions.
Pour about 25 mL of the 0.00200 M KSCN into another clean, dry 100-mL beaker. Pipette 2, 3, 4 and 5 mL of this solution into Beakers 1-4, respectively. Record volumes to hundredths of a milliliter. Obtain about 25 mL of distilled water in a 100-mL beaker. Then pipette 3, 2, 1, and 0 mL of distilled water into Beakers 1-4, respectively, to bring the total volume of each beaker to 10.00 mL. Again, be sure to record to hundredths of a milliliter. Mix each solution thoroughly with a stirring rod. Be sure to clean and dry the stirring rod after each mixing. Volumes added to each test beaker are summarized below, but remember that your exact volumes may vary from those shown and should be recorded to hundredths of a mL:
4. Examine the layout of the computer screen for this experiment. There is just a live display and a data table. A graph is not necessary, because you are just trying to determine the absorbance values of each solution. They will be recorded in the data table versus Trial Number. 5.
You are now ready to calibrate the colorimeter. Prepare a blank by
filling a cuvette 3/4 full with distilled water. To correctly use
a colorimeter cuvette, remember:
Choose "Calibrate" from the "EXPERIMENT" menu and then click "Perform Now". 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. When Input 1 in the column labeled Reading 1, stabilizes, click the "KEEP" button. Turn the wavelength knob of the colorimeter to the Blue LED position (470 nm). In this position, the colorimeter is calibrated to show 100% of the blue light being transmitted through the blank cuvette. When Input 1 in the column labeled Reading 2 stabilizes, click the "KEEP" button. Click on the "OK" button. Leave the colorimeter set to the Blue LED position for the remainder of your measurements. 6. You are now ready to collect absorbance data for the four equilibrium systems and the standard solution. Keep your solutions identified by writing their numbers on a paper towel and placing the cuvette and beaker on the number. Fill each of five clean, dry cuvettes about 3/4 full with each solution from the test beakers. Wipe the outside of each cuvette with a tissue and then place the first cuvette (Beaker 1) in the colorimeter. Click on the "Collect" button. Close the lid and wait for the absorbance value to stabilize. Click on the "Keep" button and then type 1 in the edit box. Press the "ENTER button. Your data will be recorded in the data table . 7. Repeat the Step 6 procedure for each of the remaining solutions. 8. Click the "Stop" button after completing the last solution. 9. Copy the absorbance values from the data table into your data table on Page 13-9. 10. Waste disposal: Keep a beaker at your lab station to collect waste. At the end of the experiment, pour the waste into the labeled container at the side bench designated for this waste. Your instructor must neutralize the acid before flushing the solution down the drain. PROCESSING THE DATA
This should be the same for Beakers 1 - 4. 3. Calculate the initial concentration of SCN-, based on its dilution by Fe(NO3)3 and water:
In Beaker 1, [SCN-]i =
(2 mL / 10 mL)(.00200 M) = .000400 M. Calculate this for the other three
beakers.
7. [SCN-]eq: Calculate the concentration of SCN- at equilibrium for Trials 1-4 using the equation:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||