Change in system entropy in relation to heat transfer

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Homework Statement
Establishing the Relationship Between Input Heat for Energy Conservation and Input Heat Defined by Entropy.
Relevant Equations
entropy balance equation.
entropy definition formula.
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Q: What are the differences between the heat transfer calculated by the energy conservation equation and the heat transfer determined by the Gibbs relation? ##why\ \left( ans\_1 \right) \ne \left( ans\_2 \right) ##
reference

Energy balance:
$$
Q_{in,net}-W_{out,net}=\cancel{\bigtriangleup U_{cv}}\cdots \left( 1 \right)
$$
$$
Q_{in,net}=-Q
$$
$$
W_{out,net}=-W_{in}
$$
$$
\therefore \left( 1 \right) =-Q+W_{in}=0
$$
$$
\therefore Q=W_{in}=200KJ\cdots \cdots \left( ans\_1 \right)
$$

entropy balance equation.
entropy definition formula.
Gibbs relation.
$$
dS_{sys}=\left( \frac{\delta Q}{T_k} \right) _{int.rev}\cdots \left( 2 \right)
$$
$$
\bigtriangleup S_{sys}=m\left( \frac{\cancel{du}+p\cancel{dv}}{T_k} \right) =0
$$
$$
\therefore \left( 2 \right) =0
$$
$$
\therefore Q=0KJ\cdots \cdots \left( ans\_2 \right)
$$
 
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tracker890 Source h said:
Homework Statement: Establishing the Relationship Between Input Heat for Energy Conservation and Input Heat Defined by Entropy.
Relevant Equations: entropy balance equation.
entropy definition formula.

View attachment 330839
Q: What are the differences between the heat transfer calculated by the energy conservation equation and the heat transfer determined by the Gibbs relation? ##why\ \left( ans\_1 \right) \ne \left( ans\_2 \right) ##
reference

Energy balance:
$$
Q_{in,net}-W_{out,net}=\cancel{\bigtriangleup U_{cv}}\cdots \left( 1 \right)
$$
$$
Q_{in,net}=-Q
$$
$$
W_{out,net}=-W_{in}
$$
$$
\therefore \left( 1 \right) =-Q+W_{in}=0
$$
$$
\therefore Q=W_{in}=200KJ\cdots \cdots \left( ans\_1 \right)
$$

entropy balance equation.
entropy definition formula.
Gibbs relation.
$$
dS_{sys}=\left( \frac{\delta Q}{T_k} \right) _{int.rev}\cdots \left( 2 \right)
$$
$$
\bigtriangleup S_{sys}=m\left( \frac{\cancel{du}+p\cancel{dv}}{T_k} \right) =0
$$
$$
\therefore \left( 2 \right) =0
$$
$$
\therefore Q=0KJ\cdots \cdots \left( ans\_2 \right)
$$
The entropy change of the system is zero since the gas temperature and volume are constant. The entropy transferred from the system to the surroundings is ##200/(30 + 273)=0.660\ kJ/K##. From the Clausius relationship, $$\Delta S=\frac{Q}{T_{surr}}+\sigma$$where ##\sigma## is the amount of entropy generated within the system during the process. So, $$0=-0.660+\sigma$$and the amount of generated entropy is equal to 0.660 kJ/K.

This question is a little ambiguous since, if the system is at 40 C and the surroundings are at 30 C, the system should be transferring heat to the surroundings until it too is at 30 C. But its final temperature is stated to be 40 C. It isn't clear what one should take as the temperature at the interface between the system and surroundings when the heat transfer Q and entropy transfer ##Q/T_{interface}##is occurring.
 
Last edited:
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Chestermiller said:
The entropy change of the system is zero since the gas temperature and volume are constant. The entropy transferred from the system to the surroundings is ##200/(30 + 273)=0.660\ kJ/K##. From the Clausius relationship, $$\Delta S=\frac{Q}{T_{surr}}+\sigma$$where ##\sigma## is the amount of entropy generated within the system during the process. So, $$0=-0.660+\sigma$$and the amount of generated entropy is equal to 0.660 kJ/K.

This question is a little ambiguous since, if the system is at 40 C and the surroundings are at 30 C, the system should be transferring heat to the surroundings until it too is at 30 C. But its final temperature is stated to be 40 C. It isn't clear what one should take as the temperature at the interface between the system and surroundings when the heat transfer Q and entropy transfer ##Q/T_{interface}##is occurring.
You've provided a detailed explanation, thank you. I finally understand.
 

FAQ: Change in system entropy in relation to heat transfer

What is entropy in the context of thermodynamics?

Entropy is a measure of the disorder or randomness of a system. In thermodynamics, it quantifies the amount of energy in a system that is not available to do work. It is a central concept in the second law of thermodynamics, which states that the total entropy of an isolated system can never decrease over time.

How does heat transfer affect the entropy of a system?

Heat transfer affects the entropy of a system by changing the energy distribution within it. When heat is added to a system, its entropy increases because the added energy increases the system's disorder. Conversely, when heat is removed from a system, its entropy decreases as the system's energy becomes more ordered.

What is the mathematical relationship between heat transfer and change in entropy?

The mathematical relationship between heat transfer (Q) and change in entropy (ΔS) is given by the equation ΔS = Q/T, where T is the absolute temperature at which the heat transfer occurs. This relationship assumes a reversible process. For an irreversible process, the change in entropy is greater than Q/T.

Can the entropy of a system decrease, and under what conditions?

The entropy of a system can decrease locally, for example, when heat is removed from the system or when work is done on the system. However, for an isolated system, the second law of thermodynamics states that the total entropy can never decrease. In a non-isolated system, the decrease in entropy of the system is accompanied by an equal or greater increase in the entropy of the surroundings, ensuring that the total entropy does not decrease.

What is the significance of entropy change in practical applications?

Entropy change is significant in various practical applications such as in engines, refrigerators, and other heat engines. It helps in determining the efficiency of these systems. For instance, in an ideal Carnot engine, the efficiency is determined by the entropy change during the heat transfer processes. Understanding entropy changes also aids in designing more efficient thermal systems and in predicting the feasibility of chemical reactions and processes.

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