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Thermodynamics I 1
Chapter 3
Properties of Pure Substances
2
PROPERTY TABLES
• For most substances, the relationships among thermodynamic properties are too
complex to be expressed by simple equations.
• Therefore, properties are frequently presented in the form of tables.
• Some thermodynamic properties can be measured easily, but others cannot and
are calculated by using the relations between them and measurable properties.
• The results of these measurements and calculations are presented in tables in a
convenient format.
Enthalpy—A Combination Property
The
combination
u + Pv is
frequently
encountered
in the analysis
of control
volumes.
The product pressure
volume has energy units.
3-3
Steam Tables
►Tables of properties for different substances are
frequently set up in the same general format. The
tables for water, called the steam tables, provide a
good example of the format (presented in Appendix:
tables A-4 through A-8)
►Table A-6 is for water
as a superheated vapor.
►Table A-7 is for compressed
liquid water.
►Tables A-4(T) and A-5 (p)
apply to the saturated water,
(liquid-vapor)
► Table A-8 is for saturated
solid states
Tables in English units are designated by letter “E”
Table A-4 & A-5
Table A-4E & A-5E
Table A-6
Table A-6E
Table A-7
Table A-7E
4
Saturated Liquid and Saturated Vapor States
• Table A–4: Saturation properties of water under temperature.
• Table A–5: Saturation properties of water under pressure.
A partial list of Table A–4.
Enthalpy of vaporization, hfg (Latent
heat of vaporization): The amount of
energy needed to vaporize a unit mass
of saturated liquid at a given
temperature or pressure.
Example
5
Discuss Example 3-1 in class:
Example
6
Discuss Example 3-2 in class:
Example
7
Discuss Example 3-3 in class:
8
Saturated Liquid–Vapor Mixture
Quality, x : The ratio of the mass of vapor to the total mass of the mixture.
Quality is between 0 and 1 0: sat. liquid, 1: sat. vapor.
The properties of the saturated liquid are the same whether it exists alone or in
a mixture with saturated vapor.
The relative
amounts of
liquid and
vapor phases
in a saturated
mixture are
specified by
the quality x.
A two-phase system can be
treated as a homogeneous
mixture for convenience.
Temperature and
pressure are dependent
properties for a mixture.
9
Quality is related
to the horizontal
distances on P-v
and T-v
diagrams.
The v value of a
saturated liquid–
vapor mixture lies
between the vf and vg
values at the
specified T or P.
y v, u, or h.
Example
10
Discuss Example 3-4 in class:
Example
11
Discuss Example 3-5 in class:
12
Superheated VaporIn the region to the right of the
saturated vapor line and at
temperatures above the critical
point temperature, a substance
exists as superheated vapor.
In this region, temperature and
pressure are independent
properties.
A partial
listing of
Table A–6.
At a specified
P, superheated
vapor exists at
a higher h than
the saturated
vapor.
Compared to saturated vapor,
superheated vapor is characterized by
13
Compressed Liquid
Compressed liquid is characterized by
At a given P and T, a pure
substance will
exist as a compressed liquid if
Property Approximations for Liquids
► Approximate values for v, u, and h at liquid states can be
obtained using saturated liquid data.
► Since the values of v and u for liquids
change very little with pressure at a fixed
temperature, Eqs. 3.11 and 3.12 (from the
textbook) can be used to approximate their
values.
v(T, p) ≈ vf(T)
u(T, p) ≈ uf(T)
(Eq. 1)
(Eq. 2)
► An approximate value for h at liquid states can be obtained using
Eqs. 1 and 2 in the definition h = u + pv: h(T, p) ≈ uf(T) + pvf(T) or
alternatively
h(T, p) ≈ hf(T) + vf(T)[p – psat(T)] (Eq. 3)
where psat denotes the saturation pressure at the given temperature
► When the underlined term in Eq. 3 is small
h(T, p) ≈ hf(T) (Eq. 4)
Saturated
liquid
14
Example
15
Discuss Example 3-9 in class:
►When a state does not fall exactly on the grid of values
provided by property tables, linear interpolation between
adjacent entries is used.
► Example: Specific volume (v) associated with
superheated water vapor at 1 MPaand 215oC is found by
linear interpolation between adjacent entries in Table A-6.
Table A-6
(0.23275 – 0.20602) (v – 0.20602)
(250 – 200) (215 – 200)
tan α = slope = = → v = 0.21404 m3/kg
Linear Interpolation
α
17
Reference State and Reference Values
• The values of u, h, and s cannot be measured directly, and they are calculated from
measurable properties using the relations between properties.
• However, those relations give the changes in properties, not the values of properties at
specified states.
• Therefore, we need to choose a convenient reference state and assign a value of zero for
a convenient property or properties at that state.
• The referance state for water is 0.01°C and for R-134a is -40°C in tables.
• Some properties may have negative values as a result of the reference state chosen.
• Sometimes different tables list different values for some properties at the same state as a
result of using a different reference state.
• However, In thermodynamics we are concerned with the changes in properties, and the
reference state chosen is of no consequence in calculations.
18
THE IDEAL-GAS EQUATION OF STATE
• Equation of state: Any equation that relates the pressure, temperature,
and specific volume of a substance.
• The simplest and best-known equation of state for substances in the gas
phase is the ideal-gas equation of state. This equation predicts the P-v-T
behavior of a gas quite accurately within some properly selected region.
R: gas constant
M: molar mass (kg/kmol)
Ru: universal gas constant
Ideal gas equation of state
Different substances have different
gas constants.
19
Properties per
unit mole are
denoted with a
bar on the top.
• The ideal-gas relation often is not
applicable to real gases; thus, care should
be exercised when using it.
• Real gases behave as an ideal gas at low
densities (i.e., low pressure, high
temperature).
Mass = Molar mass Mole number
Various
expressions
of ideal gas
equation
Ideal gas equation at two
states for a fixed mass
Example
20
Discuss Example 3-10 in class:
The gage pressure of an automobile tire is measured to be 210 kPa
before a trip and 220 kPa after the trip at a location where the
atmospheric pressure is 95 kPa. Assuming the volume of the tire
remains constant and the air temperature before the trip is 25 C,
determine air temperature in the tire after the trip.
21
Is Water Vapor an Ideal Gas?
• At pressures below 10 kPa, water
vapor can be treated as an ideal
gas, regardless of its
temperature, with negligible error
(less than 0.1 percent).
• At higher pressures, however, the
ideal gas assumption yields
unacceptable errors, particularly in
the vicinity of the critical point and
the saturated vapor line.
• In steam power plant
applications, however, the
pressures involved are usually very
high; therefore, ideal-gas relations
should not be used.
Percentage of error ([|vtable - videal|/vtable] 100) involved in
assuming steam to be an ideal gas, and the region where steam
can be treated as an ideal gas with less than 1 percent error.
22
COMPRESSIBILITY FACTOR—A MEASURE
OF DEVIATION FROM IDEAL-GAS BEHAVIOR
The compressibility factor is
unity for ideal gases.
Compressibility factor Z
A factor that accounts for
the deviation of real gases
from ideal-gas behavior at
a given temperature and
pressure.
The farther away Z is from unity, the more the
gas deviates from ideal-gas behavior.
Gases behave as an ideal gas at low densities
(i.e., low pressure, high temperature).
Question: What is the criteria for low pressure
and high temperature?
Answer: The pressure or temperature of a gas
is high or low relative to its critical temperature
or pressure.
At very low pressures, all gases approach
ideal-gas behavior (regardless of their
temperature).
23Comparison of Z factors for various gases.
Gases deviate from the
ideal-gas behavior the
most in the neighborhood
of the critical point.
Reduced
temperature
Reduced
pressure
Pseudo-reduced
specific volume
Z can also be determined from
a knowledge of PR and vR.
Example
24
Discuss Example 3-11 in class:
Determine the specific volume of refrigerant-134a at 1 MPa and 50 C
using (a) the ideal-gas equation of state and (b) the generalized
compressibility chart. Compare the values obtained to the actual value
of 0.021796 m3/kg and determine the error involved in each case.
25
Summary
• Pure substance
• Phases of a pure substance
• Phase-change processes of pure substances
 Compressed liquid, Saturated liquid, Saturated vapor, Superheated vapor
 Saturation temperature and Saturation pressure
• Property diagrams for phase change processes
 The T-v diagram, The P-v diagram, The P-T diagram, The P-v-T surface
• Property tables
 Enthalpy
 Saturated liquid, saturated vapor, Saturated liquid vapor mixture,
Superheated vapor, compressed liquid
 Reference state and reference values
• The ideal gas equation of state
 Is water vapor an ideal gas?
• Compressibility factor
Homework #3 Due: Thursday, March 6
26
Problems: 3.13C
3.20C
3.37E
3.44
3.61
3.81
3.93
3.15C
3.28
3.42
3.57
3.78
3.89

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How to Give a Domain for a Field in Odoo 17
 

Rayegan thermo i-cengel-chapter 3-p2

  • 1. Thermodynamics I 1 Chapter 3 Properties of Pure Substances
  • 2. 2 PROPERTY TABLES • For most substances, the relationships among thermodynamic properties are too complex to be expressed by simple equations. • Therefore, properties are frequently presented in the form of tables. • Some thermodynamic properties can be measured easily, but others cannot and are calculated by using the relations between them and measurable properties. • The results of these measurements and calculations are presented in tables in a convenient format. Enthalpy—A Combination Property The combination u + Pv is frequently encountered in the analysis of control volumes. The product pressure volume has energy units.
  • 3. 3-3 Steam Tables ►Tables of properties for different substances are frequently set up in the same general format. The tables for water, called the steam tables, provide a good example of the format (presented in Appendix: tables A-4 through A-8) ►Table A-6 is for water as a superheated vapor. ►Table A-7 is for compressed liquid water. ►Tables A-4(T) and A-5 (p) apply to the saturated water, (liquid-vapor) ► Table A-8 is for saturated solid states Tables in English units are designated by letter “E” Table A-4 & A-5 Table A-4E & A-5E Table A-6 Table A-6E Table A-7 Table A-7E
  • 4. 4 Saturated Liquid and Saturated Vapor States • Table A–4: Saturation properties of water under temperature. • Table A–5: Saturation properties of water under pressure. A partial list of Table A–4. Enthalpy of vaporization, hfg (Latent heat of vaporization): The amount of energy needed to vaporize a unit mass of saturated liquid at a given temperature or pressure.
  • 8. 8 Saturated Liquid–Vapor Mixture Quality, x : The ratio of the mass of vapor to the total mass of the mixture. Quality is between 0 and 1 0: sat. liquid, 1: sat. vapor. The properties of the saturated liquid are the same whether it exists alone or in a mixture with saturated vapor. The relative amounts of liquid and vapor phases in a saturated mixture are specified by the quality x. A two-phase system can be treated as a homogeneous mixture for convenience. Temperature and pressure are dependent properties for a mixture.
  • 9. 9 Quality is related to the horizontal distances on P-v and T-v diagrams. The v value of a saturated liquid– vapor mixture lies between the vf and vg values at the specified T or P. y v, u, or h.
  • 12. 12 Superheated VaporIn the region to the right of the saturated vapor line and at temperatures above the critical point temperature, a substance exists as superheated vapor. In this region, temperature and pressure are independent properties. A partial listing of Table A–6. At a specified P, superheated vapor exists at a higher h than the saturated vapor. Compared to saturated vapor, superheated vapor is characterized by
  • 13. 13 Compressed Liquid Compressed liquid is characterized by At a given P and T, a pure substance will exist as a compressed liquid if
  • 14. Property Approximations for Liquids ► Approximate values for v, u, and h at liquid states can be obtained using saturated liquid data. ► Since the values of v and u for liquids change very little with pressure at a fixed temperature, Eqs. 3.11 and 3.12 (from the textbook) can be used to approximate their values. v(T, p) ≈ vf(T) u(T, p) ≈ uf(T) (Eq. 1) (Eq. 2) ► An approximate value for h at liquid states can be obtained using Eqs. 1 and 2 in the definition h = u + pv: h(T, p) ≈ uf(T) + pvf(T) or alternatively h(T, p) ≈ hf(T) + vf(T)[p – psat(T)] (Eq. 3) where psat denotes the saturation pressure at the given temperature ► When the underlined term in Eq. 3 is small h(T, p) ≈ hf(T) (Eq. 4) Saturated liquid 14
  • 16. ►When a state does not fall exactly on the grid of values provided by property tables, linear interpolation between adjacent entries is used. ► Example: Specific volume (v) associated with superheated water vapor at 1 MPaand 215oC is found by linear interpolation between adjacent entries in Table A-6. Table A-6 (0.23275 – 0.20602) (v – 0.20602) (250 – 200) (215 – 200) tan α = slope = = → v = 0.21404 m3/kg Linear Interpolation α
  • 17. 17 Reference State and Reference Values • The values of u, h, and s cannot be measured directly, and they are calculated from measurable properties using the relations between properties. • However, those relations give the changes in properties, not the values of properties at specified states. • Therefore, we need to choose a convenient reference state and assign a value of zero for a convenient property or properties at that state. • The referance state for water is 0.01°C and for R-134a is -40°C in tables. • Some properties may have negative values as a result of the reference state chosen. • Sometimes different tables list different values for some properties at the same state as a result of using a different reference state. • However, In thermodynamics we are concerned with the changes in properties, and the reference state chosen is of no consequence in calculations.
  • 18. 18 THE IDEAL-GAS EQUATION OF STATE • Equation of state: Any equation that relates the pressure, temperature, and specific volume of a substance. • The simplest and best-known equation of state for substances in the gas phase is the ideal-gas equation of state. This equation predicts the P-v-T behavior of a gas quite accurately within some properly selected region. R: gas constant M: molar mass (kg/kmol) Ru: universal gas constant Ideal gas equation of state Different substances have different gas constants.
  • 19. 19 Properties per unit mole are denoted with a bar on the top. • The ideal-gas relation often is not applicable to real gases; thus, care should be exercised when using it. • Real gases behave as an ideal gas at low densities (i.e., low pressure, high temperature). Mass = Molar mass Mole number Various expressions of ideal gas equation Ideal gas equation at two states for a fixed mass
  • 20. Example 20 Discuss Example 3-10 in class: The gage pressure of an automobile tire is measured to be 210 kPa before a trip and 220 kPa after the trip at a location where the atmospheric pressure is 95 kPa. Assuming the volume of the tire remains constant and the air temperature before the trip is 25 C, determine air temperature in the tire after the trip.
  • 21. 21 Is Water Vapor an Ideal Gas? • At pressures below 10 kPa, water vapor can be treated as an ideal gas, regardless of its temperature, with negligible error (less than 0.1 percent). • At higher pressures, however, the ideal gas assumption yields unacceptable errors, particularly in the vicinity of the critical point and the saturated vapor line. • In steam power plant applications, however, the pressures involved are usually very high; therefore, ideal-gas relations should not be used. Percentage of error ([|vtable - videal|/vtable] 100) involved in assuming steam to be an ideal gas, and the region where steam can be treated as an ideal gas with less than 1 percent error.
  • 22. 22 COMPRESSIBILITY FACTOR—A MEASURE OF DEVIATION FROM IDEAL-GAS BEHAVIOR The compressibility factor is unity for ideal gases. Compressibility factor Z A factor that accounts for the deviation of real gases from ideal-gas behavior at a given temperature and pressure. The farther away Z is from unity, the more the gas deviates from ideal-gas behavior. Gases behave as an ideal gas at low densities (i.e., low pressure, high temperature). Question: What is the criteria for low pressure and high temperature? Answer: The pressure or temperature of a gas is high or low relative to its critical temperature or pressure. At very low pressures, all gases approach ideal-gas behavior (regardless of their temperature).
  • 23. 23Comparison of Z factors for various gases. Gases deviate from the ideal-gas behavior the most in the neighborhood of the critical point. Reduced temperature Reduced pressure Pseudo-reduced specific volume Z can also be determined from a knowledge of PR and vR.
  • 24. Example 24 Discuss Example 3-11 in class: Determine the specific volume of refrigerant-134a at 1 MPa and 50 C using (a) the ideal-gas equation of state and (b) the generalized compressibility chart. Compare the values obtained to the actual value of 0.021796 m3/kg and determine the error involved in each case.
  • 25. 25 Summary • Pure substance • Phases of a pure substance • Phase-change processes of pure substances  Compressed liquid, Saturated liquid, Saturated vapor, Superheated vapor  Saturation temperature and Saturation pressure • Property diagrams for phase change processes  The T-v diagram, The P-v diagram, The P-T diagram, The P-v-T surface • Property tables  Enthalpy  Saturated liquid, saturated vapor, Saturated liquid vapor mixture, Superheated vapor, compressed liquid  Reference state and reference values • The ideal gas equation of state  Is water vapor an ideal gas? • Compressibility factor
  • 26. Homework #3 Due: Thursday, March 6 26 Problems: 3.13C 3.20C 3.37E 3.44 3.61 3.81 3.93 3.15C 3.28 3.42 3.57 3.78 3.89