lecture 2 2014
TRANSCRIPT
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LAWS OF THERMODYNAMICS:
Thermodynamics rests upon two fundamental laws:
First law
Second law
First law of thermodynamics
- Principle of conservation of energy
- Energy can be neither created nor destroyed
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Net heat =J (Net work)
Here, J is a proportionality factor that depends on the units
used for work and heat.
As in SI system The unit of Heat and Work are same, so the
value of J is unity.
W in Wout
Q in
Q out
Basic statement: When any closed system is taken through a cycle, the net
work delivered to the surroundings (/ done on the system ) is proportional to the net heat taken from the surroundings (/
delivered to the surroundings ).
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W in Wout
Q in
Q out
inout out inW W QQ
W Q W Q
Net heat =Net work
Aspects of the first law:With the aid of this law it is possible to calculate the amount of
heat & work which cross the boundary of a system when given
changes in properties occur.
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1st law of thermodynamics for closed system
(control mass):
------- (1)
Considering cycle 1-A-2-B-1
---------- (2)
Considering cycle 1-C-2-B-1
---------- (3)
(2)-(3)
---------- (4)
Since A & C represent arbitrary processes, betn. states (1) & (2) we conclude that
the quantity ( Q- W ) is the same for all processes betn. states (1) & (2).
W Q
B A B A W W QQ 12211221
BC BC W W QQ 12211221
C AC A W W QQ 2
1
2
1
2
1
2
1
C AW QW Q )()( 2121
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By integrating we get,
-----------------(6)
Where, E 1 & E 2: initial & final values of the energy E of the
system: heat transferred to the system during the process from state
1 to state 2
: work done by the system during the process betn. state 1 to
state 2.
121212 W E E Q
12Q
12W
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Physical significance of E:
E represents all the energy of the system in the given state such as,
Kinetic Energy, KE
Potential energy, PE
Energy associates with the motion & position of the molecules
Internal energy,U Energy associated with the structure of the atom
Chemical energy and so on
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Since the terms comprising E are point function we can write
dE =dU + d(kE) + d(PE)
Eqn. (5) becomes;
Q = dU + d(kE) + d(PE) + W ---------------(7)
PE kE U E
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Let a system is initially at rest
The system be acted on by an external horizontal force F thatmoves the system a distance dx in the direction of force
.
SystemState-1
SystemState-2
dx
y
F
x
Here, d(PE) =0 (no change in PE) Q=0 (no heat transfer)dU =0 (no change in internal
energy)
Now from equ (7)
0=0+ d(kE)+ 0+(-Fdx) or, d(kE)=Fdx
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From Newtons 2nd law of motion;
ma F
dt dvm
dx
dv
dt
dxm
dxdv
mv
mvdvkE d )(
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Substituting the expressions for kE & PE into equ. (7)
Q=dU + mvdv + mgdz + W
Integrating for a change of state from (1) to (2);
---------- (8)
This is the integral from of First Law of Thermodynamics.
In the absence of kE & PE
---------- non-flow energy eqn.
1212
122
2
1212 )()2( W z z mg vv
mU U Q
121212U U W Q
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Internal Energy (U):
Internal Energy is an extensive property (depends on the
size/mass of the system).
The symbol is U
u: specific internal energy (internal energy per unit mass).
It is a Intensive property
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Enthalpy:
Let us consider a control mass undergoing quasi-equilibriumconstant pressure process, as shown in figure.
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Enthalpy:
Thermodynamic property
Extensive property
Independent of process
Combination of energy of the system due to temperature, pressure, and volume
A property of the system that measures its heat content.
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Specific heat (heat capacity):
Thermodynamic property
Intensive property
The amount of heat required per unit mass to raise thetemperature by one degree.
T
Q
m
c
1
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Specific heat at constant volume:
v
v T Q
mc
1
vvv
v T u
T U
mT Q
mc
11
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Rate Equation of First Law:
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Steady-State, Steady-Flow Process:
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Application to steady flow energy equation:
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Vapor-liquid-phase equilibrium in a pure substance:
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Vapor-liquid-phase equilibrium in a pure substance:
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Vapor-liquid-phase equilibrium in a pure substance:
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Property Diagrams for Phase-Change Processes:
FIGURE : T-v diagram of a pure substance
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P-v Diagram::
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By convention, the subscript f is used to designate a property of
a saturated liquid and the subscript g a property of a saturated
vapor.Thus, a saturation condition involving part liquid and part vapor,
such as that shown in Figure, can be shown on T v coordinates, as
in Figure.
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All of the liquid present is at state f with specific volume v f
and all of the vapor present is at state g with v g.
The total volume is the sum of the liquid volume and the
vapor volume, or
The average specific volume of the system v is then
The definition of quality x = mvap /m.
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Using the definition
v can also be written as
Now the quality x can be viewed as the fraction ( v v f )/v f g
of the distance between saturated liquid and saturated vapor, as
indicated in Figure:
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TABLES OF THERMODYNAMIC PROPERTIES
Tables of thermodynamic properties of many substances
are available, and in general, all these tables have the same
form.
In this section we will refer to the steam tables.
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Problem:
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Problem:
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Problem:
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