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Chapter 1 Basic Concepts in Thermodynamics

Chapter 1 of the Chemical Engineering Thermodynamics course introduces fundamental concepts such as thermodynamics definitions, dimensions, units, systems, and properties. It covers the distinction between open and closed systems, the measures of amount, and essential thermodynamic properties like temperature, pressure, and work. The chapter emphasizes the importance of understanding these concepts for analyzing energy changes and heat transfer in engineering applications.

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0% found this document useful (0 votes)
15 views51 pages

Chapter 1 Basic Concepts in Thermodynamics

Chapter 1 of the Chemical Engineering Thermodynamics course introduces fundamental concepts such as thermodynamics definitions, dimensions, units, systems, and properties. It covers the distinction between open and closed systems, the measures of amount, and essential thermodynamic properties like temperature, pressure, and work. The chapter emphasizes the importance of understanding these concepts for analyzing energy changes and heat transfer in engineering applications.

Uploaded by

nurye.zewdu
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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CLB 20703

Chemical Engineering
Thermodynamics

Chapter 1:
Basic Concepts in Thermodynamics
Objective of Chapter 1

Introduce the students towards some of


the fundamental concepts and definitions
that are used in the study of Engineering
Thermodynamics.
Outline
 Introduction  Temperature
 Pressure
 Dimensions And Units
 System  Energy
 Measure Of Amount  Heat
 Force  Work
1.1 INTRODUCTION
What is Thermodynamics?
 Thermodynamics is the Science that deals
with Heat and Work and those properties of
substances that bear a relation to Heat and
Work.
 Thermodynamics is the study of the effects
of Work, Heat and Energy on a System.
Thermodynamics is only concerned with
large scale observation.
1.1 INTRODUCTION
Scopes of Thermodynamics
 First and Second Laws of Thermodynamics

 To cope with variety of problems especially


in the calculation of Energy Changes, Heat
and Work requirements for processes
 Property Values are essential to application
of Thermodynamics
 Development of “Generalized Correlations”
to provide property estimates in the
absence of data
1.2 DIMENSIONS AND UNITS
DIMENSIONS
(= measure of
physical quatity)

FUNDAMENTAL / DERIVED /
PRIMARY SECONDARY
DIMENSIONS DIMENSIONS*

Mass (m), Length (L), Time Velocity (v), Energy (E),


(t), Temperature (T), Current Volume (V), Force (F),
(I) & Amount of matter (mol) Power (P), etc.

Derived dimensions = combination of a few primary dimensions.


Eg: Velocity = Distance/Time = L/t
1.2 DIMENSIONS AND UNITS
UNITS
(= magnitudes assigned
to the dimensions)

DERIVED /
FUNDAMENTAL /
SECONDARY
PRIMARY UNITS
UNITS*

-accompany primary -accompany derived dimensions


dimensions

2 types of unit systems widely used:


i) English System / United States Customary Systems (USCS)
ii) Metric System, SI (International System)
1.2 DIMENSIONS AND UNITS
Differences of Unit Systems
Fundamental / Derived Dimensions SI Unit ES Unit

Mass (m) kg lbm, oz


Length (L) m ft, in
Time (t) s s
Temperature (T) K oC, oF, R

Ammount of matter (mol) kmol lb mol


Velocity (v) ms-1 ft s-1
Energy (E) J (Joule) Btu, cal
Volume (V) m3 gal
Force (F) N (Newton) lbf
Power (P) W (Watt) hp
Pressure N/m2 (Pascal) psia, psig
1.2 DIMENSIONS AND UNITS

 Multiples and Decimal Fractions of SI units


are designated by prefixes
 Standard prefixes in SI units:

Prefix Multiple Prefix Multiple


tera, T 1012 centi, c 10-2
giga, G 109 milli, m 10-3
mega, M 106 macro,  10-6
kilo, k 103 nano, n 10-9
deci, d 10-1 pico, p 10-12
1.3 SYSTEM
 System is a quantity of matter or a region in
space being chosen for study.
 Boundary is the one that separates System
from its surrounding. Can be real or
imaginary. BOUNDARY
 2 types of system:
 Closedsystem/control mass
 Open system/control volume
SYSTEM

SURROUNDING
1.3 SYSTEM
Open system
 Also known as control volumes
 Both mass and energy can cross the boundary
of a control volume

OPEN Mass
SYSTEM Energy

 Its volume always fixed but its mass not


necessarily fixed.
Example of open system: compressor, turbine,
pump, nozzle
1.3 SYSTEM

Closed System
 Also known as control mass
 It has fixed amount of mass and no mass can
cross the boundary.
 Energy in theform of heat and work can cross
the boundary
 Volume does not have to be fixed.
 In special case, when energy is not allowed to
cross the boundary -> Isolated system
 Example: Rigid tank, piston cylinder device
1.3 SYSTEM

An example of closed
Mass cannot cross system with a moving
the boundaries of a boundary  piston-
closed system, but cylinder device
energy can
1.3 SYSTEM
Properties of a system
 Any characteristic of a system  property.

-independent of the
mass of a system
Intensive
Eg: Temperature T
Property
Pressure P
Density 
PROPERTY
-depend on the size of
Extensive a system
Property Eg: Mass m
Volume V
Total Energy E
1.3 SYSTEM
State and Equilibrium
m = 2 kg
 For a system not undergoing any T1 = 20oC
V1 = 1.5 m3
change, at this point all the properties
can be measured or calculated State 1
throughout the entire system  a set
of properties that completely describes
the condition  the state of the
system.
 At a given state, all the properties of a m = 2 kg
system have fixed values. If the value T2 = 20oC
V2 = 2.5 m3
of even one property changes, the
state will change to a different state.
State 2
1.3 SYSTEM
 Equilibrium indicate the State Of Balance.
 A System that is in equilibrium
experiences no changes when it is
isolated from its surroundings.
 Types of Equilibrium:
Thermal
Mechanical
Phase
Chemical
1.3 SYSTEM
 Thermal equilibrium if the temperature is the
same throughout the entire system.
 Mechanical equilibrium if there is no change
in pressure at any point of the system with
time.
 Phase equilibrium when the mass of each
phase reaches an equilibrium level and stays
there such as water and ice inequilibrium.
 Chemical equilibrium if its chemical
composition does not change with time, that
is, no chemical reactions occur.
1.3 SYSTEM
Process, Path And Cycle
 Any change that a system undergoes from
one equilibrium state to another  process,
and the series of states through which a
system passes during a process  the
process path.
 Example of process – A
compression process in
a piston-cylinder device
1.3 SYSTEM
 Quasi-static/Quasi Equilibrium Process.
“Process that proceeds in the manner that
the System remains infinitesimally/approx.
close to Equilibrium State at all time.”
 Is a slow and Ideal process that allow the
System to adjust itself internally in order
that properties in one part of the system
do not change any faster than those at
other parts.
1.3 SYSTEM

 Processes in which one thermodynamic


property is kept constant:

Process Constant property


Isobaric Pressure
Isothermal Temperature
Isochoric/isometric Volume
Isentropic Entropy
1.3 SYSTEM
 A system is said to have undergone a
cycle if it returns to its initial state at the
end of the process
 For a cycle, the initial and final states are
identical.
P
2 Process
A

1
Process
B

V
1.4 MEASURES OF AMOUNT / SIZE

 Three common measures of amount/size:


 Mass, m
 Number of moles, n = m/M
 Total volume, Vt
1.5 FORCE
 From Newton’s second law:

Force = mass x acceleration (F = ma)


 Unit: N or kg/ms2 (SI unit), lbf (ES unit)
 The Newton, N is defined as
a force required to accelerate
A mass of 1 kg at the rate of
1 meter per second.
F

Acceleration,a
1.6 TEMPERATURE
 Temperature - a measure of “hotness” or
“coldness” or the energy content of a body.
 The temperature difference causes the heat
transfer from a hot body (with higher
temperature) to an another cold body (with a
lower temperature).
 When heat is transferred to a body, E  T.
 Two bodies are in thermal equilibrium when
both of the bodies achieve similar temperature.
 Temperature applied in thermodynamic
problems must be in absolute units. Absolute
temperature scale in SI unit is Kelvin and
Rankine in ES unit.
1.6 TEMPERATURE
Unit SI ES
Property
Temperature scale oC oF

Absolute temperature scale K R


Melting point 0oC 32oF
Boiling point 100oC 212oC
Relation between temperature scales:

T(oF) = 1.8T(oC) + 32 (oC to oF)


T(K) = T(oC) + 273.15 (oC to K)
T(R) = T(oF) + 459.67 (oF to R)
T(R) = 1.8T(K) (K to R)
1.6 TEMPERATURE
1.7 PRESSURE
 Pressure is defined as the normal force exerted
by a fluid per unit area of the surface
P = F/A = mg/A
 Pressure only deal with gas or liquid
 SI unit: Pascal(Pa)/Nm-2
 ES unit: psi = lbf/in2 (pound-force per square
inch)
 psia = pound-force per square inch absolute
 psig = pound-force per square inch gage.
 Other units: bar, standard atmosphere (atm).
1.7 PRESSURE
 Pressure at any point in a fluid is same in all
directions.
 Pressure varies in vertical directions due to gravity
effects but does not vary in the horizontal directions.
Pa
Pa=Pb=Pc

P1 Pc P2

P3
Pb P1=P2P3
1.7 PRESSURE
 Absolute Pressure - The actual pressure at a
given position. Measured relative to absolute
vacuum ( absolute zero ).
 Gage Pressure - The difference between
absolute pressure and local atmospheric
pressure.
 Vacuum Pressure – Pressure below
atmospheric pressure.
Absolute P must be used in
Thermodynamics
calculations
1.7 PRESSURE

Pvac = Patm – Pabs Pgage = Pabs – Patm


(for P<Patm) (for P>Patm)
1.7 PRESSURE
Pressure measuring device
 Manometer is used to measure small and moderate
pressure differences.
 The height of the fluid in the tube represents the
pressure difference between the system and the
surroundings of the manometer which is equal to the
gage pressure:
Patm
Pgage  P  P1  Patm  ρgh
P1  P2  Patm  ρgh
 Pgas  Patm  ρgh
Patm  atmospheric pressure,
P1  gas pressure in the tank,
ρ  density of the fluid in the manometer tube,
h  the height of fluid between two points in the U - tube,
g  gravitatio nal acceleration  9.8 m/s 2 .
1.8 WORK
 Energy can cross the boundary of a closed system in the form
of heat or work. Therefore, if the energy crossing the
boundary of a closed system is not heat, it must be work.
 Work is the energy transfer associated with a force acting
through a distance:
W  F .s

 Work is also a form of energy transferred like heat and,


therefore, has energy units such as kJ/kNm
 The work done per unit time  power and is denoted W  . The
unit of power is kJ/s, or kW.
1.8 WORK
Path function
 Work, as heat, is path function  its magnitude
depend on the path followed during a process as
well as the end states.
 Path functions have inexact differentials
designated by the symbol  - a differential amount
of heat or work is represented by Q or W,
respectively:
 W  W
2
12
1

 The total work is obtained by adding the


differential amounts of work (W) done along the
way or can represented by the area under the
followed path.
1.8 WORK
 Properties, however, are point functions - depend
on the state only, and not on how a system reaches
that state, and they have exact differentials
designated by the symbol d. For eg. a small change
in volume, is represented by dV, and the total
volume change during a process between states 1
and 2:
2

1
dV  V2  V1  V
 The volume change is the
same regardless the path
followed.
1.8 WORK
Mechanical forms of work
In many thermodynamic problems, mechanical
work is the only form of work involved.
Mechanical works is associated with the movement
of the boundary of a system or with the movement
of the entire system as a whole.
Some common forms of mechanical work are:
Boundary work
Accelerational work
Shaft work
Spring work
Gravitational work
1.8 WORK
Boundary Work
One form of mechanical work frequently encountered in
practice is associated with the expansion or compression of
a gas in a piston–cylinder device  boundary work – when a
body within a system boundary causes a force to its
boundary surface to move.
Expansion work (W=+ve) and compression work (W=-ve) are
categorized as boundary work.
The boundary work can be determined by,
2 2 2 F 2
Wb   δWb   Fds  Ads  PdV
1 1 1 A 1

Thisintegral can be evaluated only if we


know the functional relationship between
P and V during the process: P  f (V )
1.8 WORK
The area under the process curve on a
P-V diagram is equal, in magnitude, to
the work done during a expansion or
compression process of a closed
system

P represents the absolute pressure and is


always positive. Hence,
When dV=+ve, Wb=+ve  expansion work
When dV=-ve, Wb=-ve  compression work

Work is path function  each path will


have a different area underneath it 
the work done will be different for each
process although the initial and final
states are the same.
1.8 WORK
Net work for a cycle

The cycle shown produces a net


work output because the work
done by the system during the
expansion process (area under
path A) is greater than the work
done on the system during the
compression part of the cycle
(area under path B), and the
difference between these two is
the net work done during the
cycle (the pink area) =Wnet
1.8 WORK
Common processes
Constant Volume/Isochoric/Isometric

 If the volume is constant, dV=0, the boundary work :


2
Wb   PdV  0
1

 for constant volume process, the boundary work = 0.


1.8 WORK
Constant Pressure/Isobaric

 If the pressure is constant, the boundary work:


Wb   PdV  Po  dV  Po (V2  V1 )
2 2

1 1

or Wb  mPo (v2  v1 )

 The magnitude of the work can also be determined


through the area under the curve of P-V diagram.
1.8 WORK
Constant temperature/Isothermal

 Ifthe temperature of an ideal gas is constant, hence the


equation of state for the ideal gas:
mRT
P
V

 And the boundary work:


2 2 mRTo V2
Wb   PdV   dV  mRTo ln
1 1 V V1
 The above equation is applicable for ideal gases only. For real
gases, PV=zmRT should be used.
1.8 WORK
Polytropic process
 A process which occurs with an interchange of both heat and work
between the system and its surroundings. The non-adiabatic expansion
or compression of a fluid is an example of a polytropic process.
 During actual processes of real gases, pressure and volume are often
related by PVn=C, (n, C = constants)
2 2 C
Wb   PdV   dV
1 1 Vn
P2V2  P1V1
 , for n  1
1 n
 For an ideal gas that undergoing
polytropic process, 2 2 C
Wb   PdV   dV
1 1 Vn
mR(T2  T1 )
 , for n  1 Similar to the
1 n isothermal process
V of an ideal gas if
 mRT ln 2 , for n  1
V1 n=1
Example 1.3
A rigid tank contains air at 500kPa and
150OC. As a result of heat transfer to the
surrounding, the temperature and pressure
inside the tank drop to 65OC and 400kPa,
respectively. Determine the work done
during the process.
Example 1.4
A piston cylinder device initially contains
0.07m3 of nitrogen gas at 130kPa and 120 OC.
The nitrogen is now expand politropically to a
state of 100kPa and 100OC. Determine the
boundary work done during this expansion.
1.9 ENERGY
 Exist in variable forms : heat, mechanical, kinetic, potential,
electric, magnetic, chemical and nuclear.
 Definition: Energy = Force x Distance (Unit = N.m = J)
 Total energy, E = Total amount of all forms of energies that
exist in a system.
 Specific energy- Total energy based on a unit of mass,
e(kJ/kg)
 Total energy can be divided into 2 groups:
1) Macroscopic energies – related to motion and the
influence of some external effects such as gravity,
magnetism, electricity, surface tension, kinetic and
potential energies.
2) Microscopic energies – related to the molecular structure
of a system. Eg : chemical, nuclear, latent heat, sensible
heat. The sum of microscopic energies- internal energy,
U.
1.9 ENERGY
Microscopic Energy
 The sum of microscopic energies  internal energy, U.

- Phase change of a system such as


liquid phase changes to gas phase.

- Atom bonding in a molecule in


chemical reactions.

- Strong bonds within the nucleus of


atoms.
1.9 ENERGY
Macroscopic Energy
 2 main forms of macroscopic energies:
1) Kinetic energy – a system possesses as a result of
its motion relative to some reference frame:
KE  2 mV 2 (kJ)

with, V = velocity of the system relative to a fixed


reference frame.
2) Potential energy – a system possesses as a result
of its elevation in a gravitational field.
PE  mgz (kJ)
with, g = gravitational acceleration, z = elevation of
the gravity centre of a system.
 Other forms of macroscopic energies:
 gravity, magnetism, electricity, surface tension.
1.9 ENERGY
Total energy
 By ignoring the effects of gravity, magnetism,
electricity and surface tension, hence the total
energy is the sum of kinetic energy, potential
energy and internal energy:
E  U  KE  PE  U  mV2  mgz (kJ)
2

 Almost all closed systems remain stationary


(KE=PE=0) during a process (unless stated) 
stationary systems. Hence, the change in total
energy of a stationary system is equal to the
change of its internal energy:
E  U
1.10 HEAT
Heat - A type of energy transfer through a system
boundary due to temperature difference.
Heat has energy units, kJ (or Btu) and denoted by
Q.
Heat transfer per unit mass of a system is denoted
q (kJ/kg) and is determined from:
Q
q
m
The rate of heat transfer (the amount of heat
transferred per unit time) = the total heat
transferred over some time interval.
The heat transfer rate is denoted Q .
The heat transfer rate has the unit kJ/s (=kW).
1.10 HEAT
3mechanisms of heat transfer: conduction,
convection and radiation.
1.10 HEAT
A process during which there is no heat
transfer (Q=0)  adiabatic process.
There are two ways a process can be
adiabatic: Either the system is well
insulated - only a negligible amount of
heat can pass through the boundary,
or both the system and the
surroundings are at the same
temperature - there is no driving force
(temperature difference) for heat
transfer.
Adiabatic
An adiabatic process  an isothermal process when
process. Isothermal process refers to insulated or
the temperature of the system that when
are the same at different state. Tsystem=Tsurr

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