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Energy Transport by Heat, Work and Mass.pdf - Yidnekachew

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Thermodynamics I__________________________________________________________________ _<br />

AAiT<br />

Chapter 3<br />

<strong>Energy</strong> <strong>Transport</strong> <strong>by</strong> <strong>Heat</strong>, <strong>Work</strong> <strong>and</strong> <strong>Mass</strong><br />

3.1 <strong>Energy</strong> of a System<br />

<strong>Energy</strong> can be viewed as the ability to cause change.<br />

<strong>Energy</strong> can exist in numerous forms such as thermal, mechanical, kinetic, potential, electric,<br />

magnetic, chemical, <strong>and</strong> nuclear, <strong>and</strong> their sum constitutes the total energy E of a system. The<br />

total energy of a system on a unit mass basis is denoted <strong>by</strong> e <strong>and</strong> is expressed as<br />

E<br />

e ( kJ / kg )<br />

(3.1)<br />

m<br />

In thermodynamic analysis, energy can be group in to two forms:<br />

<br />

<br />

Macroscopic<br />

Microscopic<br />

Microscopic forms of energy are those related to the molecular structure of a system <strong>and</strong> the<br />

degree of the molecular activity, <strong>and</strong> they are independent of outside reference frames.<br />

The sum of all the microscopic forms of energy is called the internal energy of a system <strong>and</strong> is<br />

denoted <strong>by</strong> U.<br />

Example:-<br />

• Latent energy<br />

• Chemical energy<br />

• Nuclear energy<br />

• Sensible energy<br />

Internal energy<br />

<br />

<br />

A system associated with the kinetic energies of the molecules is called the sensible<br />

energy.<br />

The internal energy associated with the phase of a system is called the latent energy.<br />

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The internal energy associated with the atomic bonds in a molecule is called chemical<br />

energy.<br />

The tremendous amount of energy associated with the strong bonds within the nucleus of<br />

the atom itself is called nuclear energy.<br />

The total energy of a system, can be contained or stored in a system, <strong>and</strong> thus can be<br />

viewed as the static forms of energy.<br />

The forms of energy not stored in a system can be viewed as the dynamic forms of<br />

energy.<br />

The only two forms of energy interactions associated with a closed system are heat<br />

transfer <strong>and</strong> work.<br />

Macroscopic forms of energy are those a system possesses as a whole with respect to some<br />

outside reference frame, such as kinetic <strong>and</strong> potential energies.<br />

The energy that a system possesses as a result of its motion relative to some reference<br />

frame is called kinetic energy (KE) <strong>and</strong> is expressed as<br />

2<br />

V<br />

KE m<br />

2<br />

( kJ ) (3.2)<br />

Per unit mass<br />

<br />

2<br />

V<br />

ke ( kJ / kg ) (3.3)<br />

2<br />

The energy that a system possesses as a result of its elevation in a gravitational field is<br />

called potential energy (PE) <strong>and</strong> is expressed as<br />

Per unit mass<br />

PE<br />

pe<br />

mgz ( kJ ) (3.4)<br />

gz<br />

( kJ ) (3.5)<br />

The magnetic, electric, <strong>and</strong> surface tension effects are significant in some specialized cases only<br />

<strong>and</strong> are usually ignored. In the absence of such effects, the total energy of a system consists of<br />

the kinetic, potential, <strong>and</strong> internal energies <strong>and</strong> is expressed as<br />

E U KE<br />

PE<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

AAiT<br />

E<br />

U<br />

V<br />

m<br />

2<br />

2<br />

mgz<br />

(kJJ<br />

)<br />

(3.6)<br />

Per unit mass<br />

e uke<br />

pe<br />

Most closed systemss remain stationary during a processs <strong>and</strong> thus experience no<br />

change in their<br />

kinetic <strong>and</strong> potential energies.<br />

e<br />

u<br />

2<br />

V<br />

gz<br />

2<br />

Closed systems whose velocity <strong>and</strong> elevation of the center of gravity remain constant during a<br />

process are frequently referred to<br />

as stationary systems. The change in the total energy ∆EE of a<br />

stationary<br />

system is identical to the change in<br />

its internal<br />

energy ∆U. .<br />

3.2 <strong>Energy</strong> transport <strong>by</strong> heat <strong>and</strong> work<br />

(kJJ<br />

/ kg)<br />

(3.7)<br />

<strong>Energy</strong> can cross the boundary of a closed system in two<br />

distinct forms: heat <strong>and</strong><br />

work.<br />

Figure 3.1 <strong>Energy</strong> can cross the boundaries of a closed system in the<br />

form of heat <strong>and</strong> work.<br />

<strong>Energy</strong><br />

transportt <strong>by</strong> heat<br />

<strong>Heat</strong> is defined as the form of energy that is transferred between two<br />

systems (or<br />

a system <strong>and</strong> its<br />

surroundings) <strong>by</strong> virtue of a temperature difference.<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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Figure 3.2 <strong>Heat</strong> transferr from hot surface to cold<br />

surface<br />

That is, an energy interaction is heat only if it takes place<br />

because of<br />

a temperature difference.<br />

Then it follows that there cannot be any heat<br />

transfer between two systems that are at the same<br />

temperature.<br />

A process during which there is no heat transfer is called an adiabatic process. The<br />

adiabatic<br />

comes from<br />

the Greek word adiabatos, which means not to<br />

be passed.<br />

word<br />

There are<br />

two ways a process can be adiabatic: Either the system is well insulated so that only a<br />

negligible amount of heat can<br />

pass through the boundary, or<br />

both the system <strong>and</strong><br />

the<br />

surroundings are at the same temperature <strong>and</strong> thereforee there is no<br />

driving force (temperature<br />

difference) for heat transfer.<br />

Figure 3.3 During an<br />

adiabatic process, a system exchanges no heat with its surroundings.<br />

As a form<br />

of energy,<br />

heat has energy units, kJ being the most common one. The amount of<br />

heat<br />

transferred during the process between two states (states 1 <strong>and</strong> 2) is denoted <strong>by</strong> Q 12 , or just Q.<br />

<strong>Heat</strong> transfer per unit mass of a system is denoted q <strong>and</strong> is determined from<br />

Q<br />

q ( kJ / kg)<br />

(3.8)<br />

m<br />

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Sometimes it is desirable to know the rate of heat transfer (the amount of heat transferred per<br />

unit time) instead of the total heat transferred over some time interval.<br />

Figure 3.4 The relationships among q, Q, <strong>and</strong> Q .<br />

The heat transfer rate is denoted , where the overdot st<strong>and</strong>s for the time derivative, or “per unit<br />

time.” The heat transfer rate has the unit kJ/s, which is equivalent to kW. When varies with<br />

time, the amount of heat transfer during a process is determined <strong>by</strong> integrating over the time<br />

interval of the process:<br />

Q <br />

t <br />

2<br />

t1<br />

Qdt<br />

( kJ ) (3.9)<br />

When remains constant during a process, this relation reduces to<br />

Where: t t2 t1<br />

Q Q t<br />

( kJ ) (3.10)<br />

<strong>Heat</strong> is transferred <strong>by</strong> three mechanisms: conduction, convection, <strong>and</strong> radiation. Conduction is<br />

the transfer of energy from the more energetic particles of a substance to the adjacent less<br />

energetic ones as a result of interaction between particles. Convection is the transfer of energy<br />

between a solid surface <strong>and</strong> the adjacent fluid that is in motion, <strong>and</strong> it involves the combined<br />

effects of conduction <strong>and</strong> fluid motion. Radiation is the transfer of energy due to the emission of<br />

electromagnetic waves (or photons).<br />

<strong>Energy</strong> <strong>Transport</strong> <strong>by</strong> <strong>Work</strong><br />

<strong>Work</strong>, like heat, is an energy interaction between a system <strong>and</strong> its surroundings. As mentioned<br />

earlier, energy can cross the boundary of a closed system in the form of heat or work. Therefore,<br />

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Thermodynamics I__________________________________________________________________ _<br />

AAiT<br />

If the energy crossing the boundary of a closed system is not heat, it must be work. <strong>Work</strong> is the<br />

energy transfer associated with force acting through a distance.<br />

Example:-<br />

• A rising piston<br />

• A rotating shaft<br />

<strong>Work</strong> is also a form of energy transferred like heat <strong>and</strong>, therefore, has energy units such as kJ.<br />

The work done during a process between states 1 <strong>and</strong> 2 is denoted <strong>by</strong> W 12 , or simply W. The<br />

work done per unit mass of a system is denoted <strong>by</strong> w <strong>and</strong> is expressed as<br />

W<br />

w ( kJ / kg )<br />

(3.11)<br />

m<br />

The work done per unit time is called power <strong>and</strong> is denoted <strong>by</strong> . The unit of power<br />

is kJ/s, or kW.<br />

<strong>Heat</strong> <strong>and</strong> work are energy transfer mechanisms between a system <strong>and</strong> its surroundings, <strong>and</strong> there<br />

are many similarities between them:<br />

Both are recognized at the boundaries of a system as they cross the boundaries. That is,<br />

both heat <strong>and</strong> work are boundary phenomena.<br />

Systems possess energy, but not heat or work.<br />

Both are associated with a process, not a state. Unlike properties, heat or work has no<br />

meaning at a state.<br />

Both are path functions (i.e., their magnitudes depend on the path followed during a<br />

process as well as the end states).<br />

Sign convention for energy transported <strong>by</strong> heat <strong>and</strong> work<br />

<strong>Heat</strong> <strong>and</strong> work are directional quantities, <strong>and</strong> thus the complete description of a heat or work<br />

interaction requires the specification of both the magnitude <strong>and</strong> direction. One way of doing that<br />

is to adopt a sign convention. The generally accepted formal sign convention for heat <strong>and</strong> work<br />

interactions is as follows: heat transfer to a system <strong>and</strong> work done <strong>by</strong> a system are positive; heat<br />

transfer from a system <strong>and</strong> work done on a system are negative. Another way is to use the<br />

subscripts in <strong>and</strong> out to indicate direction<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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Figure 3.5 Specifying the directions of heat <strong>and</strong> work.<br />

Q in > 0 <strong>Heat</strong> transfer to a system (positive)<br />

Q out < 0 <strong>Heat</strong> transfer from a system (negative)<br />

Figure 3.6 Process from<br />

stage 1 to 2 Figure 3.7 Process from stage 1 to 2<br />

W ><br />

W <<br />

0 work done <strong>by</strong> the system (positive) Figure 3.6<br />

0 work done on the system (negative) Figure 3.7<br />

Path functions have<br />

inexact differentials designated <strong>by</strong><br />

the symbol . Therefore, a differential<br />

amount of heat or work is represented <strong>by</strong><br />

Q or W, respectively, instead<br />

of dQ or<br />

dW.<br />

Properties, however, are point functions (i.e., they depend on the state only, <strong>and</strong> not on how a<br />

system reaches that state), <strong>and</strong> they have exact differentials designated <strong>by</strong> the symbol d.<br />

A small change in volume, for example, is represented <strong>by</strong> dv, <strong>and</strong> the<br />

total volume change during<br />

a processs between states 1 <strong>and</strong> 2 is<br />

2<br />

1 dv<br />

v<br />

v<br />

v<br />

2 1<br />

(3.12)<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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Figure 3.8 Properties are point functions; but heat <strong>and</strong> work are path functions<br />

The total<br />

work done during process 1–2, however, is<br />

<br />

1<br />

2<br />

W<br />

<br />

W (not<br />

W)<br />

12<br />

(3.13)<br />

That is, the total work is obtained <strong>by</strong> following the process path<br />

<strong>and</strong> adding<br />

the differential<br />

amounts of work (W) done along the way. The integral of W is not W 2 - W 1 (i.e., the work at<br />

state 2 minus work at state 1), which is meaningless since work is not a property<br />

<strong>and</strong> systems do<br />

not possess work at a state.<br />

3.3 Boundary<br />

work<br />

The work associated<br />

with a moving boundary is called boundary<br />

work. The expansionn <strong>and</strong><br />

compression work is often called moving boundary work or simply boundary work.<br />

Example:- piston–cylinder<br />

device.<br />

Figure 3.9 The work associated with a moving boundary is called boundary work.<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

AAiT<br />

In this section, we analyze the moving boundary work for a quasiequilibrium process, a process<br />

during which the system remains<br />

nearly in equilibrium at all times. A quasi-equilibrium process,<br />

Boundary<br />

work is done <strong>by</strong> the steam on the piston is calculated from<br />

figure 3.10.<br />

Figure 3.10 The area under the process curve on a P-V<br />

diagram represents the boundary work.<br />

Wb<br />

<br />

W b<br />

<br />

1<br />

2<br />

Fd<br />

2<br />

Wb<br />

<br />

W b<br />

s<br />

<br />

1 PdV<br />

F<br />

Ads PdV<br />

A<br />

(3.14)<br />

(3.15)<br />

(3.16)<br />

This integral can be<br />

evaluated<br />

during the process.<br />

only if we<br />

know the functional relationship between P <strong>and</strong> v<br />

P= f (V) is simply the equation of the process path on a P-V diagram. The differential area dA is<br />

equal to PdV. The total area A under the<br />

process curve 1–2 is<br />

obtained <strong>by</strong> adding these<br />

differential areas:<br />

Area<br />

A<br />

<br />

A comparison of this equation with the above ( Wb<br />

<br />

1<br />

2<br />

dA <br />

1<br />

2<br />

PdV<br />

( 3.17)<br />

2<br />

1<br />

PdV ), reveals that the<br />

area under the<br />

process curve on a P-v diagram is equal,<br />

in magnitude, to the work done during a quasi-<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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equilibrium expansion or compression process of a closed system. (On the<br />

represents the boundary work done per unit mass.)<br />

P-v diagram, it<br />

Some typical process<br />

Wb<br />

<br />

Boundary work at constant volume process<br />

1<br />

2<br />

PdV<br />

(3.18)<br />

Figure 3.11 Schematic <strong>and</strong> P-V<br />

diagram for constant pressure process<br />

If the volume is held constant, =0 <strong>and</strong> the boundary work equation becomes<br />

W<br />

Boundary work at constant pressure<br />

b<br />

<br />

<br />

1<br />

2<br />

PdV<br />

0<br />

(3.19)<br />

Figure 3.12<br />

Schematic <strong>and</strong> P-v diagram for constant pressure<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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If the pressure is held constant the boundary<br />

work equation becomes.<br />

Wb<br />

<br />

1<br />

2<br />

PdV P dV<br />

PV ( <br />

V (3.20)<br />

Boundary work at constant temperature (Isothermal)<br />

<br />

1<br />

2<br />

2<br />

1 )<br />

Figure 3.13 Schematic <strong>and</strong> P-V diagram<br />

for a polytropic process.<br />

If the temperature of<br />

an ideal gas<br />

system held<br />

constant, then the equation of state<br />

provides the<br />

pressure volume relation.<br />

mRT<br />

P <br />

V<br />

(3.21)<br />

The boundary work is:<br />

2<br />

Wb<br />

<br />

PdV But<br />

1<br />

mRT<br />

P <br />

V<br />

(3.22)<br />

Wb<br />

<br />

<br />

1<br />

2<br />

mRT dV<br />

V<br />

(3.23)<br />

Let<br />

mRT<br />

C<br />

PV<br />

W C<br />

b<br />

<br />

1<br />

2<br />

dv<br />

V<br />

(3.24)<br />

V<br />

Wb<br />

Cln V<br />

2<br />

1<br />

(3.25)<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

AAiT<br />

Substitute the<br />

value of C<br />

Wb<br />

Wb<br />

V2<br />

<br />

mRTln PV<br />

1 1ln V<br />

V V<br />

<br />

<br />

PV<br />

1 1ln ln <br />

V 2<br />

<br />

V1<br />

<br />

1<br />

2<br />

1<br />

(3.25)<br />

(3.26)<br />

Polytropic Process<br />

During actual expansion <strong>and</strong> compression processes of gases, pressure <strong>and</strong> volume are often<br />

related <strong>by</strong><br />

PV n = C. where n <strong>and</strong> C are constants<br />

Wb<br />

<br />

1<br />

2<br />

PdV<br />

but<br />

PV n = C<br />

2<br />

n<br />

W b<br />

CV dV<br />

1<br />

V<br />

C <br />

<br />

n1 n<br />

1<br />

2<br />

V<br />

<br />

<br />

1<br />

n<br />

1<br />

<br />

<br />

<br />

PV PV<br />

1<br />

n<br />

2 2 1 1<br />

(3.27)<br />

Since C PV<br />

n<br />

PV<br />

For an ideal gas (PVV = mRT), this equation can also be written as<br />

n<br />

1 1 2 2<br />

Wb<br />

<br />

mR( T2 T1)<br />

1<br />

n<br />

n 1<br />

(3.28)<br />

For the special case of n = 1the system is isothermal process <strong>and</strong> the boundary work becomes<br />

W<br />

b<br />

<br />

1<br />

2<br />

PdV<br />

<br />

1<br />

2<br />

CV<br />

n<br />

2<br />

dV<br />

PV ln V V 1<br />

(3.29)<br />

Spring <strong>Work</strong><br />

When the<br />

length of the spring changes <strong>by</strong> a differential amount dx under the influence of a force<br />

F, the work done is<br />

Figure 3.14 Elongation of a spring under the influence of a force.<br />

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Thermodynamics I______ _____________________________________________________________ _<br />

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But<br />

F kx<br />

W spri ing<br />

<br />

1<br />

2<br />

Fdx<br />

(3.30)<br />

W<br />

spring<br />

1<br />

k (<br />

2<br />

x<br />

2 x 2<br />

) 2 1<br />

(3.31)<br />

3.4 <strong>Energy</strong> transferred<br />

<strong>by</strong> <strong>Mass</strong>s<br />

<strong>Mass</strong> flow<br />

into <strong>and</strong> out of a system changes the energy content of the system. When mass enters<br />

a control<br />

volume, the energy of<br />

the control<br />

volume increase because the entering mass carries<br />

some energy with it. Likewise when some mass leaves the control volume, the energy contained<br />

within the control volume decreases becausee some leaving mass takeout some energy within<br />

it.<br />

Figure 3.14 The energy content of a control volume can be changed <strong>by</strong> mass flow<br />

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