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100C
p = 1.01325 bar
Figure 1
Here liquid to vapour transformation occurs; therefore saturation temperature refers to boiling
temperature.
100C
120.23C
p = 2 bar
p = 1.01325 bar
Figure 2
There will be a saturation pressure for any given temperature. It is the pressure
at which phase transformation occurs in a constant temperature process. At
100C, the saturation pressure is 1.01325 bar and at 120.23C, it is 2 bar. (Refer
Figure2)
The state at which a phase transformation begins or ends is saturated states. In
the Figures 1 and 2, states 4 and 5 are saturated states.
State 4 is saturated liquid state with respect to evaporation (at
which evaporation begins) and
State 5 is saturated vapour state with respect to evaporation (at
which evaporation ends)
The line joining saturated liquid states at different pressures is saturated liquid
line. (In Figure 3, it is the locus of state 4s at different pressure)
The line joining saturated vapour states at different pressures is saturated
vapour line. (In Figure 3, it is the locus of state 5s at different pressure)
6
5
4
p = 2 bar
p = 1.01325 bar
Figure 3
Superheated state
The state at which the temperature of steam is greater than the saturation
temperature corresponding to its pressure is known as superheated state. In
Figure 3, the state points marked as 6 refer to superheated states at different
pressures. (Eg. If the temperature of steam is 110C at a pressure of 1.01325
bar, it is superheated by 10C.)
p-V and T-V diagrams
The saturated liquid line and saturated vapour line which separate the liquid and
vapour region can be shown in p-V and T-V coordinates as shown below:
Figure4
Figure5
Critical state
The saturated liquid line and saturated vapour line meet at critical point. The
state of substance at this point is known as critical state. Beyond critical point
there is no distinct liquid-vapour transition zone. The liquid suddenly flashes
into vapour on heating in this region.
The pressure, temperature and specific volume at this state are known
respectively as critical pressure, critical temperature and critical specific
volume.
p-T diagram
Different phases of a pure substance such as water can also be represented in
p-T coordinates as shown below:
Figure 6
pVT surface
p-V, p-T and T-V diagrams can be combined and represented in a 3-D form
known as pVT surface as shown below:
Figure 7
Handout :: ME 2202 :: Unit 3
In a non-flow process,
= +
For a process, =
and
=0
(
ln
or
)
=
ln
=
Note:
=
=
( )
Rankine Cycle:
A simple Rankine cycle has the following processes for the boiler, turbine,
condenser and pump of a steam power cycle:
Process 12: Isentropic expansion of the working fluid through the
turbine from saturated
vapor at state 1 to the condenser pressure.
Process 23: Heat transfer from the working fluid as it flows at constant
pressure through
Figure 8
Reheat Rankine Cycle:
Increasing the boiler pressure can increase the thermal efficiency of the Rankine
cycle, but it also increases the moisture content at the exit of the turbine to an
unacceptable level. To correct this side effect, the simple Rankine cycle is
modified with a reheat process. The schematic of an ideal reheat Rankine cycle
is shown below in Figure 9 with its T-s diagram. In this reheat cycle, steam is
expanded isentropically to an intermediate pressure in a high-pressure turbine
(stage I) and sent back to the boiler, where it is reheated at constant pressure to
the inlet temperature of the high-pressure turbine. Then the steam is sent to a
low-pressure turbine and expands to the condenser pressure (stage II) . The total
heat input and total work output is
qin = qprimary + qreheat = (h3 - h2) + (h5 - h4)
wtotal, out = qturb, I + qturb, II = (h3 - h4) + (h5 - h6)
Figure 9
Regenerative Rankine Cycle:
In regenerative Rankine cycle, some amount of steam is bled off during
expansion in the turbine and mixed with feed water before it enters the boiler
to reduce the heat input. In the Figure 10, shown below both reheat and
regeneration (Two feed water heaters) are incorporated.
Figure 10