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Write 3 pages thesis on the topic rate of decomposition of hydrogen peroxide. The rate of decomposition of hydrogen peroxide at room temperature is so small that measurement cannot be performed. There
Write 3 pages thesis on the topic rate of decomposition of hydrogen peroxide.
The rate of decomposition of hydrogen peroxide at room temperature is so small that measurement cannot be performed. Therefore, hydrogen peroxide appears to exhibit a metastable characteristic in solution or its pure state (Egan and Nills, 2005). Oxygen evolution is rapid at room temperature and in concentrated solutions, the released heat may increase the temperature so that an explosion occurs. On heating, hydrogen peroxide decomposes and it may be explosive. The stability of hydrogen peroxide at room temperature is attributed to the fact that the first step in its thermolysis involves the splitting of the molecule into hydroxide radicals whose formation demands much heat. Catalysts such as silver, gold, platinum, manganese dioxide act as heterogeneous catalysts whereas ions such as I-, IO-, OH-,Fe3+, or copper act as homogenous catalysts.
 . . . . . . . . . . . Catalysis of hydrogen peroxide decomposition by iron ions is important in redox catalysis. The steps in the process as demonstrated by Evgenil, Oleg, and Gerts (2005), give data on the mechanisms of redox catalysis. This decomposition is also important in processes in living organisms. The decomposition may be represented as below.
2H2O2 . . (l) → 2H2O(l) + O2(g)
Method
Apparatus
 . . . . . . . . . . . 200ml Dewar flask, Standard potassium permanganate solution, 2M sulphuric acid solution, Fe3+ solution catalyst, Pipette.
Procedure
 . . . . . . . . . . . 25 mL of the ten‐volume hydrogen peroxide was diluted to about 200 ml with distilled water. A Dewar flask was rinsed with distilled water and then with a few mL of the dilute H2O2 solution. Hydrogen peroxide solution was added into the Dewar flask, and the solution temperature was noted at a constant value. 10 ml of Fe3+(a) catalyst solution was added into the beaker while stirring gently. A stopwatch was used to keep track of time.
Thirty seconds after the addition of the catalyst, a 10 mL aliquot of the reaction solution was pipetted and transferred into an Erlenmeyer flask containing 18 mL of 2 M H2SO4. The acid provides an acid medium for the titration and also quenches the decomposition reaction. 10 mL samples were drawn from the reaction mixture at 5 min intervals and titrated with potassium permanganate. The titration reaction follows the equation.
2MnO4 (aq) + 5H2O2 (aq) + 6H+(aq) → 2Mn2+(aq) + 5O2(g) + 8H2O(l)
 . . . . . . . . . . . The volumes of potassium permanganate were noted and recorded as per table 1(Laboratory Manual Semester 1, 2014).
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Results
Table 1 Results from the titration
mins
Titre volume(Vt)
ln Vt
[A]
ln[A]
0
24.1
3.18221
1.24481
0.21899
5
36.3
3.59182
0.82645
-0.1906
10
45.8
3.82428
0.65502
-0.4231
15
6.6
1.88707
4.54545
1.51413
20
10.9
2.38876
2.75229
1.01243
25
13.6
2.61007
2.20588
0.79113
30
16
2.77259
1.875
0.62861
35
18
2.89037
1.66667
0.51083
40
19.8
2.98568
1.51515
0.41552
45
21
3.04452
1.42857
0.35667
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Discussions
From the results obtained in table 1, the plot of the volume Vt versus the time t is a smooth curve from 15minutes to 45minutes (Egan and Nills, 2005).
Figure 1 The plot of Vt against time t
Reaction rate at 5 minutes
Reaction at 25 minutes
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Reaction rate at 45minutes
 . . . . . . . . . . . . . . . . . . . The reaction rate increased with time but eventually remained constant during the decomposition. This can be attributed to the fact that the rate of decomposition of hydrogen peroxide and the removal of its by-products was efficient therefore the reaction mixture maintained a constant reaction rate
Figure 2 The plot of [H2O2] against time(minutes
Figure 3 Plot of ln Vt against t (mins)
Rate Constant k= = (3-2.5)15 = 0.03333min-1
 . . . . . . . . . . . From the results obtained the plot of ln Vt against time t is linear. This conforms to the expected first-order reaction of graphs. The iron catalyst does not initiate the decomposition of hydrogen peroxide. Hydrogen peroxide decomposes even in the absence of the Fe3+ through the amounts of O2 liberated is negligible for measurement. The Fe3+ provides adsorption sites thereby increasing the rate of reaction (Evgeny T. Denisov, Igor B. Afanas'ev).
 .  .  .  .  .  . The temperature has a high influence on the rate of reaction. Depending on whether the reaction is exothermic or endothermic the temperature will either increase or decrease the rate of reaction respectively. In the case of hydrogen peroxide, an increase in temperature will increase the rate of reaction. Egan and Nills, (2005), explain that at room temperature the thermolysis of H2O2 takes place at high temperatures as it follows the formation of hydroxide radicals.
 .Conclusion
 . . . . . . . . . . . The rate of reaction can be estimated using an elaborate laboratory experiment. In this experiment, by measuring the concentration of hydrogen peroxide at specific time intervals it has been possible to find the rate of reaction and the reaction constant. Also, graphs that comply with the first-order reaction have been obtained.
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