Internal energy vs. Enthelpy vs. Entropy

Click For Summary
SUMMARY

The discussion clarifies the distinctions between internal energy (U), enthalpy (H), and entropy (S) in thermodynamic processes. It establishes that for constant volume processes, heat transfer (Q) is calculated using the formula Q = m(u2 - u1), while for constant pressure processes, Q = m(h2 - h1) applies. The first law of thermodynamics is fundamental in determining these relationships, particularly in open systems like steam turbines, where the equation dE/dt = Q̇ - Ẇ + Σ(ṁh_i) - Σ(ṁh_j) is utilized. Understanding these concepts is crucial for accurately analyzing heat transfer in various thermodynamic scenarios.

PREREQUISITES
  • Understanding of the first law of thermodynamics
  • Familiarity with internal energy and enthalpy definitions
  • Knowledge of heat transfer equations
  • Basic concepts of open and closed thermodynamic systems
NEXT STEPS
  • Study the first law of thermodynamics in detail
  • Learn about heat transfer calculations in closed systems
  • Explore the application of enthalpy in open systems, particularly in steam turbines
  • Investigate the relationship between entropy and heat transfer in reversible processes
USEFUL FOR

Students and professionals in thermodynamics, mechanical engineers, and anyone involved in heat transfer analysis and energy systems design.

JSBeckton
Messages
224
Reaction score
0
Ok, I must admit that I am becoming a bit confused about these concepts. I understand that enthalpy is u + Pv, and entropy has something to do with molecular randomness. I was fine until we started to solve for heat transfer when dealing with entropy and now I am confused, sometimes we use:

Q=m(u2-u1) to describe heat transfer

and other times we use:

Q=m(h2-h1)

Can anyone please explain to me how to tell which should be used where? I know that its a very important concept that i must have missed.

Thanks
 
Physics news on Phys.org
Let's start with the first law. It says the change in the internal energy \Delta U is

\Delta U = Q + W

Similarly the change in enthalpy is

\Delta H = \Delta U + \Delta (PV)

From this, you can calculate the heat exchange for a constant volume process and a constant pressure process.

So for a
1) Constant volume process
The first law reduces to
\Delta U = Q
So, the heat transfer will be Q =m(u_2-u_1)

2) Constant pressure process
In this case, the first law is
\Delta U + P\Delta V = Q
But, from the definition of enthalpy, you also have
\Delta H = \Delta U + P\Delta V

So, can you complete this and figure out how you calculate Q in each case?

If you need to calculate Q for a general process, try calculating the change in internal energy and the work, then use the first law.
Finally, in some cases you may be able to calculate the heat transferred if you know the change in entropy. (For example, a reversible isothermal process)
 
Last edited:
Thanks a lot siddharth

[text]
\begin{array}{l}
Q = \Delta U + P\Delta V \\
{\rm where }\Delta H = U + P\Delta V \\
{\rm therefore }Q = \Delta H \\
\end{array}
[/text]

So, is it safe to say that I should use U for constant volume and H for constant pressure?
 
Sorry for the double post, can't figure out this text editor

Thanks a lot siddharth

Q=delta H

So would it be safe to say that i should use U for constant volume and H for constant pressure?
 
JSBeckton said:
Sorry for the double post, can't figure out this text editor

Thanks a lot siddharth

Q=delta H

So would it be safe to say that i should use U for constant volume and H for constant pressure?

For an ideal gas, and ignoring changes in Kinetic energy and such, yes.
 
When I have a steam turbine I use enthalpy not internal energy even though its not a constant pressure process. I know that steam is not an ideal gas but how do I choose which to use?

Is this true?

Q-W=U2-U1
W=(U1-U2)+Q
W=(H1-H2)

But if its adaibatic Q=0 so,
W=(U1-U2)
 
JSBeckton said:
When I have a steam turbine I use enthalpy not internal energy even though its not a constant pressure process. I know that steam is not an ideal gas but how do I choose which to use?

Is this true?

Q-W=U2-U1
W=(U1-U2)+Q
W=(H1-H2)

But if its adaibatic Q=0 so,
W=(U1-U2)

Whoops, my error. You can use it for a non-ideal gas, but the system should be closed.

For a steam turbine, you have a flow process in an open system. In that case, you'll have to use the first law for open systems.

\frac{dE}{dt} = \dot{Q} - \dot{W} + \sum_i \dot{m_i} h_i - \sum_j \dot{m_j} h_j

You'll find how you get this in any thermodynamics book. It's different from the first case, which is for closed systems.
 

Similar threads

  • · Replies 7 ·
Replies
7
Views
4K
  • · Replies 13 ·
Replies
13
Views
4K
  • · Replies 6 ·
Replies
6
Views
4K
  • · Replies 4 ·
Replies
4
Views
4K
Replies
12
Views
3K
  • · Replies 9 ·
Replies
9
Views
6K
Replies
5
Views
2K
  • · Replies 4 ·
Replies
4
Views
2K
  • · Replies 17 ·
Replies
17
Views
3K
Replies
1
Views
2K