Solving Kinetics & Arrhenius Equation: Find A & Ea

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SUMMARY

The discussion focuses on calculating the Arrhenius parameters, A and Ea, using the Arrhenius equation, k=Aexp(-Ea/RT), based on temperature-dependent k values. The user successfully determined Ea and A by plotting lnk against 1/T, with Ea calculated as the negative slope multiplied by the gas constant R (8.314 J/(mol·K)). For the second question, the user is guided to use collision theory to show that A is proportional to the square root of temperature, allowing for the calculation of A at different temperatures (300K and 500K) and confirming that the ratio A(500K)/A(300K) is approximately 1.29, validating the assumption of A being temperature-independent.

PREREQUISITES
  • Understanding of the Arrhenius equation and its components
  • Familiarity with plotting and interpreting linear graphs
  • Knowledge of collision theory in chemical kinetics
  • Basic proficiency in using the gas constant R (8.314 J/(mol·K))
NEXT STEPS
  • Learn how to derive the Arrhenius equation from first principles
  • Study the implications of temperature on reaction rates in chemical kinetics
  • Explore advanced topics in collision theory and its applications
  • Investigate the effects of varying activation energy on reaction mechanisms
USEFUL FOR

Chemistry students, researchers in physical chemistry, and professionals involved in reaction kinetics and thermodynamics will benefit from this discussion.

chemphys1
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Homework Statement



The activation energy and Arrhenius paramter can be found from its temperature dependence
the Arrhenius equation

k=Aexp(-Ea/RT) --> lnk=lnA - Ea/RT

Given data is 5 temperatures with their corresponding k values

Q1) From this data calculate A and Ea

q2)
Here A has been considered independent of temperature. Show this is a good approximation by comparing ratios A(T2)/A(T1) and exp(-Ea/RT2)/exp(-Ea/RT1)
(T1 300K T2 500K)
(use collision theory expression for A)

The Attempt at a Solution



Q1) Ok so this bit I think is fine. To find Ea and A I plotted lnk vs 1/T to get a straight line

Ea = -k x R = slope of the line x 8.314

then A is exp(intercept)

So I got both the values from the graph.

Not sure about the second part though:

Q2)can only find collision theory 'A' as d^2(8kbT/u)^1/2
So I don't really understand which equation I'm supposed to be using to find A at T1 and A at T2?


Then for exp(-Ea/RT2)/exp(-Ea/RT1) I'm just using the Ea value I found from the graph, just changing the temperatures.

I'm guessing the ratios are supposed to turn out to be similarHelp much appreciated!
 
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chemphys1 said:
Not sure about the second part though:

Q2)can only find collision theory 'A' as d^2(8kbT/u)^1/2
So I don't really understand which equation I'm supposed to be using to find A at T1 and A at T2?


Then for exp(-Ea/RT2)/exp(-Ea/RT1) I'm just using the Ea value I found from the graph, just changing the temperatures.

I'm guessing the ratios are supposed to turn out to be similarHelp much appreciated!
You've already found Ea and A at 300K from the graph that you plotted. The thing to focus on from collision theory is that A is proportional to the square root of T:
$$A \propto \sqrt{T}$$
The proportionality constant isn't going to change with temperature, so you're just going to get
$$A = k_{prop}T$$
You can plug in the value you found for A in part 1 of your question, and plug in T=300K to find ##k_{prop}##. Then you can put this back in the above equation along with T=500K to get the value for what A would be at 500K.

Another option is simply to notice that
$$\frac{A_{500K}}{A_{300K}} = \sqrt{\frac{500K}{300K}} \approx 1.29$$
since the other constants in your collision theory expression for A all cancel. So even over a range of 200 degrees, the prefactor only changes by less than 30%. Thus constant A turns out to be a decent approximation.
 

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