EFN and Sustainable Growth Redo Problem 23 using sales growth rates of 30 and 35 percent in addition to 20 percent. Illustrate graphically the relationship between EFN and the growth rate, and use this graph to determine the relationship between them.
Reference:
Calculating EFN In Problem 21, suppose the firm wishes to keep its debt–equity ratio constant. What is EFN now?
d)
Mole fraction of methanol in liquid phase \(\left(x_{1}\right)\) is \(0.8\)
From subpart (a) the bubble pressure \((P)\) at mole fraction of \(0.8\) is \(1.489\) bar. At the bubble point, the state of the system will be liquid.
Fugacity of a component at liquid state is defined as the product of mole fraction of component in liquid phase, activity coefficient of the component, and saturated pressure of the component.
$$ f_{1}=x_{1} \gamma_{1} P_{1}^{5 a t} $$
Substitute \(1.81\) bar for \(P_{1}^{\text {sat }}, 0.992\) for \(\gamma_{1}\), and \(0.8\) for \(x_{1}\) in equation (3) to calculate the fugacity of methanol.
$$ \begin{aligned} f_{1} &=x_{1} \gamma_{1} P \\ &=0.8 \times 0.992 \times 1.81 \mathrm{bar} \\ &=1.436 \mathrm{bar} \end{aligned} $$
Therefore, the required fugacity is \(1.436 \mathrm{bar}\).
e)
Write the equation for chemical potential for methanol as follows:
$$ \mu_{1}=G_{1}+R T \ln \left(\gamma_{1} x_{1}\right) $$
Here, \(\mu_{1}\) is chemical potential of methanol, \(G_{1}\) Gibbs free energy of methanol, \(R\) is gas constant, \(x_{1}\) is mole fraction of methanol, and \(\gamma_{1}\) is activity coefficient.
Mole fraction of methanol in liquid phase \(\left(x_{1}\right)\) is \(0.8\).
Pressure of the system \((P)\) is \(0.4\) bar.
Temperature of the mixture \((T)\) is \(353.15 \mathrm{~K}\).
From subpart (a), \(0.8\) mole fraction and \(353.15 \mathrm{~K}\) activity coefficient of methanol \(\left(\gamma_{1}\right)\) is \(0.992\)
Since the system is pure ethanol liquid, the Gibbs free energy is neglected.
Substitute the corresponding values in the above equation to calculate the chemical potential.
$$ \begin{aligned} \mu_{1} &=G_{1}+R T \ln \left(\gamma_{1} x_{1}\right) \\ &=8.314 \mathrm{~J} / \mathrm{molK} \times 353.15 \mathrm{~K} \times \ln (0.992 \times 0.8) \\ &=-678.8 \mathrm{~J} / \mathrm{mol} \end{aligned} $$
Therefore, the required chemical potential is \(-678.8 \mathrm{~J} / \mathrm{mol}\)