Activation Energy Final

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Roman SEGALOWITCH

Determining the Activation Energy of a Reaction


Table 1: Time for the reaction of 10cm3 of Na2S2O3 with 10cm3 of fixed concentration HCl
to form a precipitate, at different temperatures.

1 -1 1
k= /s /K-1
T /oC T /K Time /s t T ln(k)
24.8 297.8 64.13 0.01559333 0.00335796 -4.1609123
32.3 305.3 48.13 0.02077706 0.00327547 -3.8739057
45.6 318.6 21.56 0.04638219 0.00313873 -3.0708397
49.9 322.9 17.72 0.05643341 0.00309693 -2.8746939
54.1 327.1 14.32 0.0698324 0.00305717 -2.6616572
Table 2: Vertical Error Bar Calculations
Max Error Max ln(k) Min ln(k) Min Error Error Bar Value
ln(k)
= Max ln(k) - = ln(k) - Min = (Max Error -
= ln(1/t)
ln(k) = ln(1/t-5) = ln(1/t+5) ln(k) Min Error)/2
0.08117389 -4.07973841 -4.1609123 -4.23598879 0.07507649 0.0030487
0.109686889 -3.764218811 -3.8739057 -3.97274174 0.09883604 0.005425424
0.263849551 -2.806990149 -3.0708397 -3.279406325 0.208566625 0.027641463
0.331518342 -2.543175558 -2.8746939 -3.123245594 0.248551694 0.041483324
0.429494571 -2.232162629 -2.6616572 -2.961140829 0.299483629 0.065005471
Table 3: Horizontal Error Bar Calculations
1 1
Max /K-1 Min /K-1
Max Error T 1 -1 T Min Error Error Bar Value
/K
T = (Max Error -
= (1/T-1) - (1/T) = 1/T-1 = 1/T+1 = (1/T) - (1/T+1) Min Error)/2
1.13122E-05 0.003369272 0.00335796 0.00334672 1.12398E-05 3.62257E-08
1.07607E-05 0.003286231 0.00327547 0.003264773 1.06969E-05 3.18958E-08
9.88461E-06 0.003148615 0.00313873 0.003128911 9.81886E-06 3.28742E-08
9.62483E-06 0.003106555 0.00309693 0.003087373 9.55735E-06 3.37383E-08
9.374E-06 0.003066544 0.00305717 0.003047851 9.31874E-06 2.76349E-08
Note: The horizontal error bar value is minimal and thus is not taken into account on the graph.

Deviation of Arrhenius’ Equation:


− Ea
k = Ae RT
−Ea
lnk = lnA + ln ⁡(e ¿ ¿ )¿
RT

−Ea
lnk = lne + lnA
RT

−Ea
lnk = + lnA
RT
Roman SEGALOWITCH

−Ea 1
lnk = ( )( ) + lnA
R T

This is written under the form y = mx + b

1
To find the Ea (activation energy), ln k againstneeds to be plotted.
T
Graph 1: ln(k) over the reciprocal of the temperature (K -1)
-2

f(x) = − 6661.87759234017 x + 18.1343296899746

-2.5

f(x) = − 5136.17443836528 x + 13.0316081421519


R² = 0.994057433710276
-3 f(x) = − 3718.86559061139 x + 8.40806348864943
R² = 1
ln k

-3.5

-4

-4.5
0.003 0.00305 0.0031 0.00315 0.0032 0.00325 0.0033 0.00335 0.0034

1/T /K-1

The equation of the line is


y = -5136.2x + 13.032
−Ea
Gradient = m = -5136.2 =
R
Ea = -mR = -(-5136.2)(8.31) = 42,681.822 J/mol-1

The activation energy is of approximately 42.7 kJ/mol -1


The activation energy of the maximum gradient line is 55.4 kJ/mol-1
The activation energy of the minimum gradient line is 31.4 kJ/mol-1

Absolute Error:
Maximum Error−Minimum Error
¿
2
55.4−31.4
= =12kJ/mol-1
2

Percentage Error:
Roman SEGALOWITCH

Lit. Value of Ea – 47 kJ/mol-1 (source - uwaterloo.ca)


42.7−47
= x 100
47
= 9.15%

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