INGENIA

CHM-28

Arrhenius k

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Physical chemistryArrhenius

Governing equation

k=Ae−Ea/RTk=A e^{-E_a/RT}

T∈[250,800]T \in \left[250, 800\right]

where

A
A (1/s)
E_a
Ea (kJ/mol)
T
T (K)
k
k (1/s)

The figure, part by part

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CHM-28 · reactor
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①

Governing law — red

k=Ae−Ea/RTk=A e^{-E_a/RT}

T∈[250,800]T \in \left[250, 800\right]

T=250T = 250k=1.92×10−4k = 1.92\times 10^{-4}

②

Domain of the variable — blue

Tmin⁡=250,Tmax⁡=800T_{\min} = 250,\quad T_{\max} = 800

T∈[250,800]T \in \left[250, 800\right]

T=250T = 250T=250T = 250

③

Response curve — green

k=Ae−Ea/RTk=A e^{-E_a/RT}

T∈[250,800]T \in \left[250, 800\right]

T=250T = 250k=1.92×10−4k = 1.92\times 10^{-4}

④

Rate of change — amber

dkdT\frac{\mathrm{d}k}{\mathrm{d}T}

T∈[250,800]T \in \left[250, 800\right]

T=253.5T = 253.5k′=5.06×10−5k^{\prime} = 5.06\times 10^{-5}

Lecture brief

Historical brief

Ideal-gas law, van ’t Hoff, Nernst, Michaelis–Menten and Clausius–Clapeyron are physical chemistry’s working equations of equilibrium and rate. The lab is pressure, potential and kinetics. This sheet (CHM-28 — Arrhenius k) is the form associated with Arrhenius. Working symbols: AA, EaE_a, TT →\rightarrow kk. Activated rate.

Purpose

Purpose: compute kk from AA, EaE_a, TT in Physical chemistry via k=Ae−Ea/RTk=A e^{-E_a/RT} Activated rate. Use it when a real physical chemistry question must be answered in SI before a code check.

Live realistic example

In symbols

Live case. Given A=1.000e+13 1/sA = 1.000e+13\,\mathrm{1/s}, Ea=80.000 kJ/molE_a = 80.000\,\mathrm{kJ/mol}, T=350.000 KT = 350.000\,\mathrm{K}, the governing relation k=Ae−Ea/RTk=A e^{-E_a/RT} yields k=11.487420 1/sk = 11.487420\,\mathrm{1/s}. Activated rate. Move a slider: the numbers are this situation, not a canned story.

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  • k k11.487420 1/s
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CHM-28 · reactor
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