THERMODYNAMICS - THEORY
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In the second law analysis, it is useful to plot the
process on diagrams for which has one coordinate is entropy. The two
diagrams commonly used
in second law analysis are temperature-entropy (T-s) and
enthalpy-entropy (h-s) diagrams. For some pure substance, like water,
the
entropy is tabulated with other properties.
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The T-s Diagram
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The Total Heat Transfer Equals the Total Area
under the Process Curve on the T-s Diagram
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On a
P-v diagram, the area under the
process curve is equal, in magnitude, to the work done
during a quasi-equilibrium expansion or compression process of a closed
system. On a T-s diagram, the area under an internally reversible
process curve is equal, in magnitude, to the heat transferred between
the system and its surroundings. That is,
Note the area has no meaning for irreversible processes.
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T-s Diagram of a Carnot Cycle |
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The T-s diagram of a Carnot cycle is shown on the left. The area under
process curve 1-2 (area 1-2-B-A-1) equals the heat input from a source
(QH). The area under process curve 3-4 (area 4-3-B-A-4) equals the heat rejected
to a sink (QL). The area enclosed by the 4 processes (area 1-2-3-4-1) equals the net
heat gained during the cycle, which is also the net work output.
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How to Use the Mollier Diagram
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The h-s Diagram
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The
enthalpy-entropy (h-s) diagram is valuable in the analysis of steady-flow
devices such as nozzle,
turbine, and
compressor.
The h-s diagram is also called Mollier diagram after the German
scientist R. Mollier. The Mollier diagram of water is shown on the
left. The Mollier diagram for water contains constant-quality lines,
constant-pressure lines, and constant-temperature lines. The temperature
lines in the mixture region are straight.
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The Tds Relations
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The Tds Relations for Closed System
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In the previous section, the definition of entropy is given by
Rearranging the above equation gives
(1)
The entropy change during an internally reversible process (1-2) is
Only when the relation between δQ and
T is known, the entropy change can be determined. The relations
between δQ
and T can be found by considering the energy balance of a closed system.
The differential form of the energy balance for a closed system, which
contains a simple substance and undergoes an internally reversible
process, is given by
dU = δQrev - δWrev
(2)
The
boundary work of a closed system is
δWrev = PdV (3)
Substituting equations (1) and (3) into equation (2) gives
dU = TdS- PdV TdS
= dU + PdV
or
Tds = du +Pdv (4)
where
s = entropy per unit mass
Equation (4) is known as the first relation of Tds, or Gibbs
equation.
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The Tds Relations for Open System |
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The
definition of enthalpy gives
h = u + Pv
differential the above equation yields
dh = du +Pdv + vdP
Replacing du + Pdv with Tds yields
dh = Tds + vdP Tds = dh -vdP (5)
Equation (5) is known as the second relation of Tds.
Although the Tds equations are obtained through an internally reversible process, the results can be used for both reversible or irreversible
processes since entropy is a property.
Rewriting equations (4) and (5) in the following form
ds = du/T + Pdv/T ds = dh/T + vdP/T
The entropy change during a process can be determined by integrating the above equations between the initial and the final states. |
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