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Arrhenius equation graph

Activation energies are found from the Arrhenius equation (Eq. 13). We plot In k against 1/T, with T in kelvins, and multiply the slope of the graph by — R to find the activation energy, with R = 8.3145 J-K 1-mol l. A spreadsheet, curve-fitting program,... [Pg.676]

Arrhenius equation The equation In k = In A — EJRT for the commonly observed temperature dependence of a rate constant k. An Arrhenius plot is a graph of In k against 1/T. [Pg.941]

As an alternative to this traditional procedure, which involves, in effect, linear regression of equation 5.3-18 to obtain kf (or a corresponding linear graph), a nonlinear regression procedure can be combined with simultaneous numerical integration of equation 5.3-17a. Results of both these procedures are illustrated in Example 5-4. If the reaction is carried out at other temperatures, the Arrhenius equation can be applied to each rate constant to determine corresponding values of the Arrhenius parameters. [Pg.98]

The activation energy can be determined from the gradient of a plot of In D versus 1 IT (Fig. 5.19). Such graphs are known as Arrhenius plots. Diffusion coefficients found in the literature are usually expressed in terms of the Arrhenius equation D0 and Ea values. Some representative values for self-diffusion coefficients are given in Table 5.2. [Pg.231]

Such a plot is seen in Figure 8.25. Its gradient is equal to —EA/R. This graph is seen to be linear, with a gradient of —2400 K. From the Arrhenius equation, the value of activation energy is obtained as —gradient x R. Therefore ... [Pg.413]

Calculations show that this quotient does not vary much with pH, resulting in a bunched-up graph from which no useful data can be found. This aspect of the graphical data should be compared with the similar conclusion mentioned in connection with determination of AS X and A factors using the Arrhenius equation, Worked Problems 3.22 and 7.6. [Pg.339]

According to the Arrhenius equation, a plot of log k against 1/T has a gradient of -E /2.303R. From the graph ... [Pg.120]

To graph the activation energy we need to find its equation. It is the Arrhenius equation. [Pg.681]

Give the Arrhenius equation. Take the natural log of both sides and place this equation in the form of a straight-line equation y = mx + b). What data would you need and how would you graph those data to get a linear relationship using the Arrhenius equation What does the slope of the straight line equal What does the >--intercept equal What are the units of A in the Arrhenius equation Explain how if you know the rate constant value at two different temperatures, you can determine the activation energy for the reaction. [Pg.579]

Hunt J. M., Lew an M. D. and Hennet R. J. C. (1991) Modeling oil generation with time-temperature index graphs based on the Arrhenius equation. Am. Assoc. Petrol. Geol. Bull. 75, 795-807. [Pg.355]

The numerical value of constant p was given for each enzyme on the basis of experimental data for catalase, p = 3.699 for lipase, p = 4.880 and for alkaline phosphatase, p= 11.366. The effect of moisture content X on Ea and k o is illustrated in Figure 39.7 and Figure 39.8. From these graphs the values of k o (s ) and Ea (J/mol) can be read out for a bone-dry product (subscript 0) and for a product with moisture content X = 1 and more (subscript infinity). Figure 39.9 presents a change of reaction rate constant kd of enzyme inactivation as a function of moisture content X calculated from the Arrhenius equation for temperature 60°C. [Pg.931]

In everything we have done so far, we have drawn many graphs of modu-lus/loss against temperature/time/frequency, but nowhere did we have a specific equation for these curves. We shall now derive formulae for compliance and loss against time and frequency.The equations for temperature are more complex, but can be obtained quite simply from those for frequency by applying a frequency-temperature relationship such as the Arrhenius equation. [Pg.132]

The Effect of Temperature on Reaction Rates—The principal basis for describing the effect of temperature on the rate of a chemical reaction is the Arrhenius equation (20.21) or a variant of it (20.22). A graph of In k versus 1/T is linear, with the slope of the line equal to —E R (Fig. 20-12). [Pg.965]

This equation can be rearranged into the form y = mx + b, so a graph of In k versus 1 /T (called an Arrhenius plot) gives a straight line with slope m = —EJR and intercept b = In A ... [Pg.503]

Though the reaction mechanism here is more complex than in the previous example and the kinetic equation also has non-Arrhenius parameters, it is possible to determine all the reaction rate constants. The fact is that there is a sufficient quantity of the Arrhenius complexes. In this case it appears that all "mixed complexes, i.e. complexes containing parameters of both direct and inverse reactions, are independent. Here these complexes evidently corresponding to the mixed spanning trees of the graph are coefficients for various concentration characteristics. It is this fact that permitted us to obtain the convenient eqns. (82). [Pg.231]

An Arrhenius plot for the apparent kinetic constant at the start of run, ka, for catalyst A, is shown in Rgure 4. From this kind of graph the apparent kinetic expressions [equation (1)] were obtained ... [Pg.89]

Calculations using Arrhenius plots, such as those described above, are carried out in the pharmaceutical industry every day. It should be made clear, however, that they involve a number of assumptions. It is assumed that the linearity of the graph obtained from equation (9.9) extends to room temperature, or, mathematically, that A and E are independent of temperature. If the line cannot be extrapolated to room temperature, shelf-life predictions are invalid. Second, it is assumed that the same chemical reaction is occurring with decomposition at high temperature as at low temperature. This is usually the case, but until proven it remains an assumption in most calculations. [Pg.237]

This equation is in the form of a straight line so that a plot of In /cr versus MT should be linear. This assumes that both A and are constants, independent of temperature. This is a reasonable assumption for most reactions when studied over a limited range of temperature, say of the order of 100 K. A graph of In A r versus MT is referred to as an Arrhenius plot, and it involves reciprocal temperature or inverse temperature. [Pg.69]


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