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Computer-Interfaced Experiments - Temperature Measurement

Kinetics
Decomposition of Hydrogen Peroxide catalyzed by Potassium Iodide

Objective: Dependance of the Reaction Rate upon the Concentration of the Catalyst

Peter Keusch


Datalogging and data analysis using the Program CHEMEX and the Analog-Digital-Converter CHEMBOX
IBK electronic + informatic


German version




Chemicals:
0.43 M aqueous potassium iodide solution
hydrogen peroxide 10 %
0.1075, 0.215 and 0.3225 molar iodide solutions are prepared by diluting appropriate aliquots of the 0.43 molar stock potassium iodide solution.

Apparatus and glass wares:
magnetic stirring bar
stirring bar remover
Dewar vessel (500 mL) with plastic cover, suitable for magnetic stirrer
temperature sensor
volumetric pipette 8 mL
volumetric pipette 25 mL
volumetric pipette 50 mL
3 pipette bulbs
disposal container


Hazards and safety precautions:

Inhalation of potassium iodide dust may irritate respiratory tract. May act as a skin or eye irritant. May cause sensitization or allergic reaction.
Hydrogenperoxide is toxic, corrosive - can cause serious burns. Eye contact can cause serious injury, possibly blindness. Harmful by inhalation, ingestion and skin contact.

Safety glasses and gloves, suitable ventilation.



Theoretical background:

The iodide-catalyzed decomposition of hydrogen peroxide produces oxygen gas:


The experimental rate law is first order in both peroxide and iodide.



Hydrogen peroxide reacts vigorously with potassium iodide. Energy is liberated and the reaction takes place so rapidly that the temperature of the reaction solution rises. Hence the decompostion of hydrogenperoxide can be monitored by following the change in the temperature of the reaction mixture with time.


Experimental procedure:

experimental set-up
Fig. 1: Experiment set-up
The temperature sensor is connected to the input Sensor2 of the CHEMBOX.

The Dewar vessel is fitted with a magnetic stirring bar. 75 mL of 10 % hydrogen peroxide solution are pipetted into the Dewar vessel and 8 mL of the 0.215 molar potassium iodide solution are added. The magnetic stirrer is started. On the Dewar vessel is placed a plastic cover, whose hole is fitted with a temperature sensor. Now the sensing software is started.

The real-time graph of the temperature rise is displayed on the screen  (Fig. 2).  The temperature is recorded until the maximum temperature is reached. The reaction is then complete.

In addition the experiment is carried out using a 0.1075, 0.3225 and a 0.43 molar solution of potassium iodide.






























Messbildschirm
Fig. 2: Realtime graph     0.215 molar potassium iodide solution


Data analysis using Excel (Download):


A plot of T [ °C ] against t [ s ] is created. A best fit straight line is drawn through the highlighted data points of the linear portion of the individual temperature curves. The coefficient before x in the straight line equations (y = ax + b) specifies the value for the slope m   (Fig. 3),  which also can be determined directly on the measuring screen of Chemex  (Fig. 2).


temperature
Fig. 3: Effect of concebntration on rate
1:   0.215 M     2:   0.3225 M    3:   0.43 M     potassium iodide solution



Results:


slope
Fig. 4: Plot of the slope m versus the molarity of the iodide solution


The reaction rate is proportinal to the concentration of the catalyst  (Fig. 4)   - see experiment   Decomposition of Hydrogen Peroxide catalyzed by Potassium Dichromate. The temperature curves show the reaction process typical for catalytic reactions. After an induction phase the reaction proceeds  (Fig. 2 and 3).


References:
Computer-Interfaced Experiments   Kinetics: Catalyzed Decomposition of Hydrogen Peroxide - First Order Reaction
Computer-Interfaced Experiments   Kinetics: Decomposition of Hydrogen Peroxide catalyzed by Dichromate
Computer-Interfaced Experiments   Enzyme Kinetics: Enzymatic Decomposition of Hydrogen Peroxide
  Demonstration Experiment on Video   Decomposition of Hydrogen Peroxide with Catalase
Kyle Smith und Mark Iannone   Improved Data Analysis for an Adiabatic Kinetics Experiment


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