Chapter 3
Chapter 3
Chapter 3
Energy Transport by Heat, Work and Mass
3.1 Energy of a System
Energy can be viewed as the ability to cause change.
Energy can exist in numerous forms such as thermal, mechanical, kinetic, potential, electric,
magnetic, chemical, and nuclear, and their sum constitutes the total energy E of a system. The
total energy of a system on a unit mass basis is denoted by e and is expressed as
E
e (kJ / kg ) (3.1)
m
Macroscopic
Microscopic
Microscopic forms of energy are those related to the molecular structure of a system and the
degree of the molecular activity, and they are independent of outside reference frames.
The sum of all the microscopic forms of energy is called the internal energy of a system and is
denoted by U.
Example:-
Latent energy
Chemical energy
Nuclear energy
Sensible energy
Internal energy
A system associated with the kinetic energies of the molecules is called the sensible
energy.
The internal energy associated with the phase of a system is called the latent energy.
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The internal energy associated with the atomic bonds in a molecule is called chemical
energy.
The tremendous amount of energy associated with the strong bonds within the nucleus of
the atom itself is called nuclear energy.
The total energy of a system, can be contained or stored in a system, and thus can be
viewed as the static forms of energy.
The forms of energy not stored in a system can be viewed as the dynamic forms of
energy.
The only two forms of energy interactions associated with a closed system are heat
transfer and work.
Macroscopic forms of energy are those a system possesses as a whole with respect to some
outside reference frame, such as kinetic and potential energies.
The energy that a system possesses as a result of its motion relative to some reference
frame is called kinetic energy (KE) and is expressed as
V2
KE m (kJ ) (3.2)
2
The magnetic, electric, and surface tension effects are significant in some specialized cases only
and are usually ignored. In the absence of such effects, the total energy of a system consists of
the kinetic, potential, and internal energies and is expressed as
E U KE PE
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V2
E U m mgz (kJJ ) (3.6)
2
Per un
nit mass
e u ke pe
V2
eu gz (kJJ / kg ) (3.7)
2
Most cloosed systemss remain stattionary durinng a processs and thus experience noo change in their
kinetic annd potential energies.
Closed syystems who
ose velocity and elevatioon of the cennter of gravvity remain constant
c durring a
a frequentlly referred too as stationaary systemss. The changge in the totaal energy ∆E
process are E of a
stationaryy system is identical
i t change inn its internall energy ∆U..
to the
3.2 E
Energy trransport by
b heat and
a work
Energy can
c cross the boundary of a closed syystem in twoo distinct form
ms: heat andd work.
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Figure
F 3.2 Heat
H transferr from hot suurface to coldd surface
That is, an
a energy intteraction is heat
h only if it
i takes placee because off a temperatuure differencce.
Then it follows
fo that there
t cannot be any heatt transfer bettween two syystems that are
a at the sam
me
temperatuure.
There aree two ways a process caan be adiabattic: Either thhe system is well insulatted so that only
o a
negligiblle amount of
o heat cann pass throough the booundary, orr both the system andd the
surrounddings are at the same temperature and
a thereforee there is noo driving foorce (temperrature
differencce) for heat trransfer.
Figure 3.3
3 During an
n adiabatic process,
p a syystem exchannges no heat with its surrroundings.
As a form
m of energy,, heat has ennergy units, kJ
k being the most comm
mon one. Thhe amount off heat
transferreed during th
he process beetween two states (statees 1 and 2) is
i denoted by
b Q12, or juust Q.
Heat trannsfer per uniit mass of a system
s is dennoted q and is determineed from
Q
q (kJ / kg ) (3.8)
m
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Sometimes it is desirable to know the rate of heat transfer (the amount of heat transferred per
unit time) instead of the total heat transferred over some time interval.
Figure 3.4 The relationships among q, Q, and Q .
The heat transfer rate is denoted , where the overdot stands for the time derivative, or “per unit
time.” The heat transfer rate has the unit kJ/s, which is equivalent to kW. When varies with
time, the amount of heat transfer during a process is determined by integrating over the time
interval of the process:
t2
Q Qdt (kJ ) (3.9)
t1
If the energy crossing the boundary of a closed system is not heat, it must be work. Work is the
energy transfer associated with force acting through a distance.
Example:-
A rising piston
A rotating shaft
Work is also a form of energy transferred like heat and, therefore, has energy units such as kJ.
The work done during a process between states 1 and 2 is denoted by W12, or simply W. The
work done per unit mass of a system is denoted by w and is expressed as
W
w (kJ / kg ) (3.11)
m
The work done per unit time is called power and is denoted by . The unit of power
is kJ/s, or kW.
Heat and work are energy transfer mechanisms between a system and its surroundings, and there
are many similarities between them:
Both are recognized at the boundaries of a system as they cross the boundaries. That is,
both heat and work are boundary phenomena.
Systems possess energy, but not heat or work.
Both are associated with a process, not a state. Unlike properties, heat or work has no
meaning at a state.
Both are path functions (i.e., their magnitudes depend on the path followed during a
process as well as the end states).
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F
Figure 3.6 Process
P from
m stage 1 to 2 Figu
ure 3.7 Proccess from staage 1 to 2
Path fun
nctions havee inexact diff
fferentials designated
d byy the symbool . Therefoore, a differeential
amount of heat or work is reppresented byy Q or W, respectivvely, insteadd of dQ orr dW.
Propertiees, however, are point functions
fu (i.ee., they depeend on the state
s only, and
a not on how
h a
system reeaches that state),
s and thhey have exaact differentiials designatted by the syymbol d.
A small change
c in vo
olume, for exxample, is reepresented by
b dv, and thee total volum
me change during
d
a processs between staates 1 and 2 is
2
1
dv v2 v1 v (3.12)
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F
Figure 3.8 Properties
P are point funcctions; but heat
h and worrk are path functions
f
The totall work done during proceess 1–2, how
wever, is
2
1
W W12 W )
(not (
(3.13)
3.3 Boundary
B y work
The worrk associated
d with a moving bounddary is called boundaryy work. The expansionn and
compresssion work is often called
c moviing boundaary work or
o simply boundary work.
w
E
Example:- pisston–cylinder device.
F
Figure 3.9 Th
he work assoociated with a moving booundary is called
c bounddary work.
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In this seection, we an
nalyze the moving
m bounndary work for
f a quasieqquilibrium process,
p a proocess
during which
w the system remainss nearly in eqquilibrium at
a all times. A quasi-equiilibrium proccess,
Boundaryy work is do
one by the steeam on the piston
p is calcculated from
m figure 3.10.
Figure 3.10
3 The areea under the process currve on a P-V
V diagram reppresents the boundary work.
w
2
Wb Wb (3.14)
1
F
Wb Fd s A PdV
Ads (3.15)
A
2
Wb PdV (3.16)
1
P= f (V) is simply th
he equation of
o the processs path on a P-V diagram
m. The differential area dA is
equal to PdV. The total area A under thee process curve
c 1–2 iss obtained by adding these
differentiial areas:
2 2
Arrea A dA PdV
V (3.17)
1 1
2
w the aboove ( Wb PdV ), revveals that thee area undeer the
A compaarison of thiis equation with
1
process curve on a P-v diagraam is equal,, in magnituude, to the work done during a quasi-
q
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equilibriuum expansio
on or comppression proocess of a closed
c system. (On the P-v diagraam, it
representts the boundary work doone per unit mass.)
m
2
Wb PddV (3.18)
1
Boundary
B work
w at constant preessure
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Boundary
B work
w at constant tem
mperature (Isotherma
( al)
mRT
m
P (3.21)
V
2 mRTT
Wb PdV Buut P (3.22)
1 V
2 mRT
Wb dV (3.23)
1 V
L
Let mRT C PV
2 dv
Wb C (3.24)
1 V
V2
Wb Cln (3.25)
V1
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V2 V2
Wb mRTln
m PV
1 1 ln (3.25)
V1 V1
V
Wb PV
P1 1 ln ln 2 (3.26)
V1
Polytropic
P Process
P
During actual
a expanssion and com
mpression prrocesses of gases,
g pressuure and volum
me are oftenn
related byy PVn = C. where
w n and C are constaants
2
Wb PdV
V but PVn = C
P
1
2 V n 1 V1 n 1 PV PV
Wb CV n ddV C 2 2 2 1 1 (3.27)
1
n 1 1 n
Since C PV
1 1 P2V2
n n
V = mRT), thhis equation can also be written
For an iddeal gas (PV w as
mR (T2 T1 )
Wb n 1 (3.28)
1 n
For the sppecial case of
o n = 1the system
s is isothermal proccess and the boundary work
w becomees
2 2 V2
Wb PdV CV n dV
V PV ln (3.29)
1 1 V1
Spring Work
When thee length of th
he spring chhanges by a differential
d a
amount dx unnder the influuence of a force
fo
F, the woork done is
2
Wspriing Fdx (3.30)
1
But F kx
1
Wspring k ( x22 x12 ) (3.31)
2
3.4 Energy
E tra
ansferredd by Masss
Mass flow
w into and out
o of a systeem changes the energy content
c of thhe system. When
W mass enters
e
a controll volume, th
he energy off the controll volume inccrease becauuse the enterring mass caarries
some eneergy with it. Likewise when
w some mass
m leaves the
t control volume,
v the energy contaained
within thhe control vo
olume decreaases becausee some leavinng mass takeeout some ennergy withinn it.
F
Figure 3.14 The
T energy content
c of a control voluume can be changed
c by mass
m flow
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