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Work and Heat

Dr. Rohit Singh Lather

Forms of Energy
Energy
Heat

Low Grade

High Grade

Macroscopic
Kinetic

Work

Microscopic

Potential
Sensible

(translational + rotational + vibrational)

Chemical

(Atomic Bonds)

Latent

(inter molecular phase change)

Atomic

(bonds within nucleolus of atoms)

Summation of all the microscopic energies is called Internal Energy

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E= U+KE+PE (kJ)
Dr. Rohit Singh Lather - Engineering Thermodynamics

Introduction
Temperature determines the direction of flow of thermal energy between two
bodies in thermal equilibrium
Temperature is also a measure of the average kinetic energy of particles in a
substance
Changes in the state of a system are produced by interactions with the
environment through heat and work
Heat and work are two different modes of energy transfer
During these interactions, equilibrium (a static or quasi-static process) is
necessary for the equations that relate system properties to one-another to be
valid
Bodies don't contain heat
Heat is identified as it comes across
system boundaries
The amount of heat needed to go from
one state to another is path dependent
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Dr. Rohit Singh Lather - Engineering Thermodynamics

Heat is the random motion of the


particles in the gas, i.e. a
degraded from of kinetic energy

Surroundings

Surroundings
System

System

System at higher temperature


looses energy as heat
QReleased = Negative (-)

System and surrounding at


same temperature, no energy
is transferred as heat

Surroundings
System

System at lower temperature


gains energy as heat
QAbsorbed = Positive (+)

U T
if T , U
if T = 0, U = 0
All of the energy inside a system is called INTERNAL ENERGY
When you add HEAT (Q), youDr. Rohit Singh Lather are adding energy
and the internal energy INCREASES 4
Engineering Thermodynamics

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Specific Heat
Note: It is easy to change the temperature of some things (e.g. air) and hard to change the
temperature of others (e.g. water, block of steel)
The amount of heat (Q) added into a body of mass m to change its temperature an amount is given
by
Q= m.C.T = m.C.(Tf Ti)
C is called the specific heat and depends on the material
Note: Temperature in either Kelvin or Celsius
The heat capacity C of an object is the proportionality constant between the heat Q
that the object absorbs or loses and the resulting temperature change T of the object

C=

cal J
Q
= o = o
mT g C kg C

# It is important to distinguish the heat transfer is done with constant volume or constant pressure
The specific heat is different for different processes, particular for gases

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Heat of Transformation
The amount of energy per unit mass that must be transferred as heat when a sample completely
undergoes a phase change is called the heat of transformation L (or latent heat)
When a sample of mass m completely undergoes a phase change, the total energy transferred is:
(# sublimation: transition from solid directly to gas phases)
When the phase change is between solid to liquid, the heat of transformation is called the
heat of fusion LF
When the phase change is between liquid to gas, the heat of transformation is called the
heat of vaporization LV

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

3-31
Heat Capacities
at Constant Volume and Constant Pressure

The amount of energy needed to raise the temperature of a unit of mass of a substance by one
degree is called the specific heat at constant volume Cv for a constant-volume process:

The amount of energy needed to raise the temperature of a unit of mass of a substance by one
degree is called the specific heat at constant pressure Cp for a constant pressure process:

For ideal gases u, h, Cv, and Cp are functions of temperature alone

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

Experimental apparatus used by Joule


Thermometer

Water

Air
(high pressure)

Evacuated

It has been demonstrated mathematically and experimentally (Joule, 1843) that for an ideal gas the
internal energy is a function of the temperature only. That is, u = u(T)

Joules reasoned, the internal energy is a function of temperature only and not a function of
pressure or specific volume
Later Joules showed that for gases that deviate significantly from ideal- gas behavior, the
internal energy is not a function of temperature alone
Using the definition of enthalpy and the equation of state of an ideal gas, we have is also a
function of temperature only
h = h(T)

Since u and h depend only on temperature for an ideal gas, the specific heats cv and cp also depend,
at most, on temperature only.
Therefore, at a given temperature, u, h, cv, and cp of an ideal gas have fixed values regard- less of
the specific volume or pressure
Thus, for ideal gases, the partial derivatives in Eqs. 419 and 420 can be replaced by ordinary
derivatives. Then, the differential changes in the internal energy and enthalpy of an ideal gas can be
expressed as
u = u(T)
For ideal gases, u, h, cv, and cp vary with temperature only
du = cv(T) dT

For ideal gases Cv, and Cp are related by:

Cp = Cv + R [kJ / (kg.K)]

Cp > Cv In an isobaric process system is heated and work is performed

The specific heat ratio is defined as: =

For incompressible substances (liquids and solids), both the constant-pressure and
constant-volume specific heats are identical and denoted by C:
Cp = Cv = C [kJ / (kg.K)]
CV

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CP

Monoatomic Gases

%
&

%
&

Diatomic Gases

%
&

%
&

Triatomic Gases

%
&

%
&

Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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Heat Transfer Mechanisms


Conduction: (solids--mostly)
Heat transfer without mass transfer

Convection: (liquids/gas)
Heat transfer with mass
transfer due to motion

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Radiation
Heat transfer through electromagnetic waves

Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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Conduction
Thickness L

TH
Hot
Reservoir

TC
Cold
Reservoir

Slab of face area A &


Thermal conductivity k

If Q be the energy that is transferred as heat through the


slab, from its hot face to its cold face, in time t, then the
conduction rate Pcond (the amount of energy transferred per
unit time) is

Here k, called the thermal conductivity, is a constant


that depends on the material of which the slab is made

We assume steady state


of heat transfer

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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Convection
In convection, thermal energy is transferred by bulk motion of materials from regions of high to
low temperatures
This occurs when in a fluid a large temperature difference is formed within a short vertical
distance (the temperature gradient is large)
Typically very complicated
Very efficient way to transfer energy

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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Radiation
Everything that has a temperature radiates energy
Method that energy from sun reaches the earth
In radiation, an object and its environment can exchange energy as heat via electromagnetic waves
Energy transferred in this way is called thermal radiation
The rate Prad at which an object emits energy via electromagnetic radiation depends on the
objects surface area A and the temperature T of that area in K, and is given by
StefanBoltzmann constant
5.6704 x10-8 W/m2 K4

If the rate at which an object absorbs energy via


thermal radiation from its environment is Pabs, then
the objects net rate Pnet of energy exchange due
to thermal radiation is

Emissivity

Note: if we double the temperature, the power radiated goes up by 24 =16


If we triple the temperature, the radiated power goes up by 34=81
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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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Quasi-Static Process
Arbitrarily slow process such that system always stays stays arbitrarily close to thermodynamic
equilibrium
Infinite slowness is the characteristics of a quasi-static process
It is a succession of equilibrium states

Final State
Weight
Piston
Initial State
System Boundary
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Pressure

A quasi-static process is also reversible process

Final State
Piston

Multiple
Weights

Such a process is locus of all the


equilibrium points passed through by
the system
1

Dots indicate
equilibrium states

dp

Initial State
Every state passed through by the
system will be Dr. Rohit Singh Lather an equilibriumEngineering Thermodynamics
state

dv

Volume
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Work
Heat is a way of changing the energy of a system by virtue of a temperature
difference only
Other means for changing the energy of a system is called work
We can have push-pull work
- (e.g. in a piston-cylinder, lifting a weight)
- electric and magnetic work (e.g. an electric motor)
- chemical work, surface tension work, elastic work, etc.
In defining work, we focus on the effects that the system (e.g. an engine) has on
its surroundings
Work as being positive when the system
does work on the surroundings
(energy leaves the system)
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If work is done on the system


the work is negative
(energy added to the system)

Dr. Rohit Singh Lather - Engineering Thermodynamics

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Pressure

Pressure Volume Diagrams and Work Done

Changes that happen during a


thermodynamic process can usefully be
shown on a pV diagram
This area represents the work
done by the gas
(on the surroundings)
when it expands
from state A to state B

Volume

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Dr. Rohit Singh Lather - Engineering Thermodynamics

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Work Done by a Gas (Constant Pressure)


Thermal Reservoir

Work = force x distance


= force x x
= PAx
(Pressure = F/A so F = PA)
= pV
(Ax = V)

Pressure

PI = PF = P
V
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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

V1

V2

Volume
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W = - P V
V = Positive + Work done by System
V = Negative (-) done on system
Work done by System is Negative (-)
Work done on system is Positive (+)

The negative sign in the equation for WORK is often misunderstood


Since work done by a gas has a positive volume change we must understand that the gas itself is
USING UP ENERGY or in other words, it is losing energy, thus the negative sign
When work is done ON a gas the change in volume is negative, this cancels out the negative sign in
the equation, this makes sense as some EXTERNAL agent is ADDING energy to the gas
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Dr. Rohit Singh Lather - Engineering Thermodynamics

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Expansion and Non-Expansion Work

Electrical work (kJ):


Boundary work (kJ):
Gravitational work (kJ):
Acceleration work (kJ) :
Shaft work (kJ):

Spring work (kJ):

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

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NEGATIVE WORK

Pressure

Pressure

POSITIVE WORK

2
W<0

W > 0

Volume

Volume
MORE WORK

Pressure

Pressure

LESS WORK

W > 0

W > 0

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Volume
Dr. Rohit Singh Lather - Engineering Thermodynamics

Volume

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To go from the state (Vi, Pi) by the path (a) to the state (Vf, Pf) requires a different amount of
work then by path (b).
To return to the initial point (1) requires the work to be nonzero
The work done on a system during a closed cycle can be non-zero
The work done on a system depends on the path taken in the PV diagram
CYCLIC POSITIVE NET WORK

Pressure

CONTROL WORK

Pressure

Wnet > 0

1
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Dr. Rohit Singh Lather Volume Engineering Thermodynamics

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Volume

How do you change Internal Energy (U)

Change in Volume

Supplying Heat

Work

Thermal Reservoir

All the energies received are turned into the energy of the system: this is a form of the
energy conservation law

U = Q + W

OR

U = Q - W

AS

Won

the gas

= Wby the gas

The first law of thermodynamics (closed system) states that the change in internal energy (DU)
is the sum of the work and heat changes: it is applicable to any process that begins and ends
in equilibrium
states
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Dr. Rohit Singh Lather Engineering Thermodynamics
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Internal Energy (U) is a state function: a property that depends only on the current
state of the system and is independent of how that state was prepared

Energy can cross the boundaries of a closed system in the form of heat or work
If the energy transfer across the boundaries of
to a temperature difference, it is heat; otherwise, it is work
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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: Yunus A. Cengel and Michael A. Boles Thermodynamics: An Engineering Approach, McGraw Hill, 8th Edition

closed

system

is
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due

Thermodynamic Processes - Ideal Gas Processes


States of a thermodynamic system can be changed by interacting with its
surrounding through work and heat. When this change occurs in a system, it is
said that the system is undergoing a process.
A thermodynamic cycle is a sequence of different processes that begins and ends
at the same thermodynamic state.

Some sample processes:

Isothermal Process: Temperature is constant T=C


Isobaric Process: Pressure is constant, P=C
Constant Volume Process: Volume is V=C
Adiabatic Process: No heat transfer, Q=0
Isentropic Process: entropy is constant, (n = ), s=C
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Dr. Rohit Singh Lather - Engineering Thermodynamics

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Isothermal Process
Assumptions: Ideal gas
(closed system)

U = Q - WWork done by System


U = Q - WWork done by System
Q = WWork done by System

Pressure

T = 0, then U = 0

To keep the temperature constant both the


pressure and volume change to compensate (Volume
goes up, pressure goes down)
BOYLES LAW

Q = W
W =

W =

V1

W = mRT In

W = mRT In

Internal Energy
Does not Change

W = mRT

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Isotherm

T2 = T1

Volume

V2

V1
V2

Dr. Rohit Singh Lather - Engineering Thermodynamics

W
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Reversible process can be reversed by an infinitesimal change in a variable


E.g. reversible, isothermal expansion of an ideal gas

Work done is the area beneath the ideal


gas isotherm lying between the initial and
the final volumes

Pi
Pressure

P=nRT/V

Pf
w
Vi
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Vf

Volume

Dr. Rohit Singh Lather - Engineering Thermodynamics

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Isobaric Process
In isobaric process P = C , then U = Q W

W =
W =

U = Q - W can be used
since the in this case

Pressure

The path of an isobaric process is a


horizontal line called an isobar

T2 = T1

W = P (V2 V1)
2

Heat is added to the gas which increases the


Internal Energy (U)

V1
Q

p
V2 V1

V2

Volume

V1
V2

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P2 = P1

Dr. Rohit Singh Lather - Engineering Thermodynamics


Work is done

W = p (V2 V1)

by the gas as it changes in 28volume

Isochoric / Isometric Process


Ideal gas assumption
(closed system)

In isobaric process V = C U = Q W

W = =
Q = m.U =

No work done

Pressure

Since, V = 0

V2

U = Q Wby
U = Q 0

V2 = V1
T2 > T1

V1 1

U = Q

Volume
Q

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V2 = V1

Dr. Rohit Singh Lather - Engineering Thermodynamics

W=0
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Adiabatic Process
Adiabatic process Q = 0 U = Q W
U = - W
(infinitesimal increment
of work and energy)

dW = dU
dU + PdV = 0
345
) dV = 0
6
45
+ ( 6 ) dV = 0

m.CV.dT + (
CV.dT

Cv lnT + R lnV = C

;<
(;= - 1) InV + In T = C
( - 1) In V + In T = C

InV

(- 1) +

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5&
57

Adiabat

Integrate and R = Cp - Cv
T1
2

T1 V1 (- 1) = T2 V2 (- 1)

In (T V (- 1) ) = C
TV

Loosing internal energy


T1 > T2
1

In T = C
(- 1) =

P,V, T Change

Pressure

Ideal gas assumption


(closed system)

( 1)

1
=(
)
2

Q =0
Dr. Rohit Singh Lather - Engineering Thermodynamics

V1

V2

T2

Volume

V1
V2

Wby
30 = - U

( 1)

1
=(
)
2

5&
57

Relation of Temperature with Volume


PV= nRT

T1 V1 (- 1) = T2 V2 (- 1)
> 76 7
>&6&
(1)
V1
= ?4
?4

V2 (- 1)

P1V1 = P2V2

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T = PV/nR

Relation of Pressure with Volume

Dr. Rohit Singh Lather - Engineering Thermodynamics

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Polytropic Process
Polytropic" describes any reversible process on any open or closed system of gas or vapor which
involves both heat and work transfer, such that a specified combination of properties were
maintained constant throughout the process
The expression relating the properties of the system throughout the process is called
the Polytropic path

Polytropic Process: its P-V relation can be expressed as


PVn = Constant (c)
Where, n is a constant for a specific process
- Isothermal, T = constant, if the gas is an ideal gas then P.V = R.T = constant, n = 1
- Isobaric, P = constant, n = 0 (for all substances)
- Constant-volume, V = constant, V = constant(P)(1/n), n =, (for all substances)
- Adiabatic Process, n = k for an ideal gas

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Dr. Rohit Singh Lather - Engineering Thermodynamics

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W =

W =

Pressure

P1 V1 = P2 V2 = PVn

Isobaric

n < 1 Polytropic

W =
W =
W

B B)
(

n=0

n = 1 Isothermal
Isochoric
n = infinity

n > 1 Adiabatic

Volume
PV Diagram for various Polytropic Processes

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Dr. Rohit Singh Lather - Engineering Thermodynamics

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In Summary
Process

Important Point to Remember

Gas Law that identifies it

Isothermal

Constant T, dU = 0, Q = W

Boyles Law

Isochoric

Constant V, W = 0, dU = Q

Charles Law

Isobaric

Constant P, dU = Q ( - PdV)

Gay Lussacs Law

Adiabatic

Nothing is Constant , Q = 0, dU = - W

Combined Gas Law

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Dr. Rohit Singh Lather - Engineering Thermodynamics

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Dr. Rohit Singh Lather - Engineering Thermodynamics

Source: http://www.learneasy.info/MDME/MEMmods/MEM23006A/thermo/gases_files/gas_equations.png

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