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Engineering Thermodynamics I

Part 1: Introduction, control volume, state of a system


Prof. Alberto Passalacqua Department of Mechanical Engineering Iowa State University, Ames, IA, 50011-2161 Academic year: 2013/2014
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What is Thermodynamics?

The word comes from the combination of two Greek words:


(therme): heat (dynamis): power

The development of thermodynamics started with the study of energy transfers, between two forms of energy:
heat work
Joule's heat apparatus
(Picture from Wikipedia)

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Example applications of Thermodynamics

(Pictures from Wikipedia)

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Thermodynamics

Classical
Observer is outside the system and looks at its interactions with the external environment Macroscopic effects of the motion of particles Statistical means of properties Individual particles are not considered!

Statistical
Observer is inside the system and considers the interactions among particles Quantum mechanics studies the elementary interactions in the system Statistical chemistry uses quantum mechanics to compute macroscopic quantities
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Some information on this course

Instructor
Dr. Alberto Passalacqua Office: 2074 Black Engineering E-mail: albertop@iastate.edu Office hours

When does it work for you?

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Course material

Textbook M. J. Moran and H. N. Shapiro, D. D. Boettner, M. B. Bailey, Fundamentals of Engineering th Thermodynamics, 7 Edition, Wiley, 2011 Lecture slides Available on Blackboard in PDF format

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Course outcomes
Upon completion of this course, you will be able to:

Demonstrate appropriate use of thermodynamic terminology and concepts. Define appropriate system boundaries for analyzing a variety of thermodynamic components and systems. Fix the states of pure substances and determine the relationships among pressure, temperature, specific volume, internal energy, enthalpy, and entropy using tables, charts and equations. Determine and calculate the appropriate mass and energy transfers and properties to solve steady state and transient open and closed system applications with any number of heat, work, and mass flows. Determine when a process is reversible, irreversible, or impossible.

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Prerequisites
The following courses are prerequisites for ME 231:

MATH 265 CHEM 167 PHYS 222

Prerequisites test on Blackboard to be completed by Friday, Aug. 30th.

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Expectations

Read the syllabus


Exam dates Course rules

Solve homework problems


Homework does not have to be turned in, and won't be graded. Solving homework problems is key to prepare for exams. The solutions for the homework assignments will be posted automatically on Blackboard at 3 PM on the assigned due date. If you have questions concerning homework problems, ask the Instructor!

Attend each lecture


Sign the attendance sheet at every lecture Inform the instructor if you are unable to attend the lecture

Study regularly
Learning thermodynamics requires time and effort. Spread the effort over time: don't wait until the last minute! It is not recommended to wait until the week of the exam to study. Study the book chapters corresponding to each lecture. The chapters you have to read are listed at the beginning of each section in the lecture notes.

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Exams and grading


Your final grade is calculated as follows:
5% - attendance and class participation 20% - first exam 25% - second exam 25% - third exam 25% - fourth exam

Percentage grade 85 100% 80 85% 75 80% 70 75% 65 70% 60 65% 55 60% 50 55% 0 50%

Letter grade A AB+

B BC+ C CF
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Exams

This course had four exams. Exam dates are in the syllabus The first three exams will be at the same time of the lecture on the exam day

Problems given in the exams are similar to those solved during class lectures, homework assignments and in the textbook. Attending class, studying regularly, and reading the assigned textbook chapters are the best way to prepare for each exam. Each student must follow the policy of academic honesty of Iowa State University. With regard to graded assignments and exams, any failures to abide by the academic honesty policy of Iowa State University will be dealt with as specified in the ISU student handbook.

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Exam rules

Exams are closed book. You may not use


Textbook (theory part). Lecture slides. Handwritten notes. Cellular phones, smart phones, tablet computers, laptop computers and any other device capable of connecting to the Internet or to a cellular network.

You may use


A scientific calculator (not programmable) Steam tables (you may use the steam tables in the printed version of the book).

Bring them with you at exams!

You are not allowed to refer to the theory chapters of the book during an exam.
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Exam rules

You are required to indicate the steps you followed to obtain the solution of the problems exam problems. Your solution must be written clearly and in a readable manner. Poorly written or unclear parts will not be graded.

If you cannot take the exam because of a medical problem or a conflict with another university-sponsored activity, obtain my approval at least one week in advance.

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Special accommodation

Disabilities If you have a documented disability that requires assistance, you will need to go to the Disability Resource (DR) Office first, for me to make any accommodations The DR is located in the Student Services Building, Room 1076. Their phone number is 515-294-7220 TDD 515-294-6335.

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Part 1: Introduction, control volume, state of a system

Topics
Thermodynamic systems Control volume Properties of a system State of a system and process Dimensional units Equation of state p-v-T surface and diagrams

Readings
Chapter 1 Chapter 3

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Learning outcomes

Understand the concepts of thermodynamic system Distinguish between open, closed, adiabatic and isolated system Understand the concepts of control volume, state, property, process Use the SI and Imperial unit system Apply problem-solving methodology Understand the concept of equation of state Read a p v T diagram Understand the concept of saturation pressure and temperature Read phase diagrams and explain phase change phenomena Understand the concepts of two-phase liquid-vapor mixture

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The concept of thermodynamic system

We call system the subject of our study


All the examples we have seen before are thermodynamic systems We did not mention one important and very complex example of thermodynamic system...

Our body!
(Picture from Wikipedia, Luc Viatour / www.Lucnix.be)

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Basic concepts about thermodynamic systems


External environment

System

Boundary

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Types of thermodynamic systems

A system is classified based on its interactions with the surrounding environment:


Isolated system

It cannot exchange any property with the external environment No mass exchange No energy exchange It cannot exchange matter and heat with the external environment It can exchange other forms of energy It cannot exchange mass with the external environment It can exchange energy It can exchange any property with the external environment Mass and energy exchanges are possible
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Adiabatic system

Closed system

Open system

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Control volume

A tree is an open system


Mass exchanges

Carbon dioxide Oxygen Nutrients Water Sun

Energy exchanges

Where does the exchange happen?


(Picture from Wikipedia, Brian Green)

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Control volume

A tree is an open system


Mass exchanges

Carbon dioxide Oxygen Nutrients Water Sun

Energy exchanges

Where does the exchange happen?


At the boundary!
(Picture from Wikipedia, Brian Green)

Roots included
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How to choose the control volume

The control volume is chosen based on


What is the goal of the analysis of the system What is known about the system

What is known at the boundary of the specific control volume we are thinking to choose? If we choose this control volume, we need to know what happens inside the tree!

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Properties of a system

A property is a characteristic of a system to which we can at any given time assign a numerical value without knowing the history of the system (properties can be measured!) Examples
Mass Energy Pressure Temperature

Extensive property
Unique value for the overall system Additive Depend on system size May depend on time Mass, energy, volume

Intensive property
Value depends on position Does not depend on system size May depend on time Temperature, pressure, density, concentration

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Phase
Definition: We call phase a quantity of matter that is homogeneous in both physical structure and chemical composition.

Homogeneity in structure: all solid, all liquid, all gas, More than one phase can coexist in a system:
Water (liquid) Ice (solid) Steam (vapor)

A system with more than one phase is called heterogeneous The zones of the system that separate different phases are called inter-phase surfaces (improperly interface)

(Picture from Wikipedia)

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Pure substance
Definition: A pure substance is a system with homogeneous, defined and constant composition, characterized by specific physical and chemical properties.

Various examples:

Metals: Fe, Cr, Au, Cu Noble gases: He, Ne, Ar, Kr, Xe, Rn Covalent solids: C, Si, B, Sb Molecular substances: H2, N2, H2O, CH4, Drinking water is not a pure substance (salts, impurities, )
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A pure substance can exist in multiple phases, as long as its chemical composition is the same in all the phases

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State of a system and process

The state of a system is the condition the system has, as it is described by its properties Typically, a subset of properties of the system defines its state, and the other properties can be found from those used to define the system state
Example: the state of an ideal gas is define once we specify its temperature and pressure. The volume can be found from the equation of state.

A system whose properties do not change in time is said to be at steady state (Note: none of the system properties have to change to be at steady state!) A process is a transformation which involves a change of some of the properties of a system in time. A process corresponds to a change of the system state.
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Equilibrium state
Definition: A state of a thermodynamic system is said to be an equilibrium state if the properties of the system remain unchanged and its intensive properties are uniform.

Consider a gas in a closed volume

Volume is constant (piston does not move) Temperature is constant and uniform Pressure is constant and uniform Mass of gas is constant

The gas is in equilibrium conditions We will study the equilibrium thermodynamics in this course
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State of a thermodynamic system


Observation: the state of a thermodynamic system is exactly defined by the three thermodynamic quantities pressure p, volume V and temperature T.

Once the set of data (p, V, T) is known, the thermodynamic state of the system is known too We have to learn to measure
Pressure Volume (density) Temperature

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Dimensional units

SI units (Systme International d'Units)


Preferred: decimal system Seven base units
Unit name meter kilogram second Ampere Kelvin mole candela Unit symbol m kg s A K mol cd Quantity length mass time electric current temperature amount of substance luminous intensity Quantity symbol l m t I T n Iv Dimension symbol L M T I N J
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SI multiples and fractions


Multiples
Name Symbol Factor deca da 101 hecto h 102 kilo k 103 mega M 106 giga G 109 tera T 1012 peta P 1015 exa E 1018 zetta Z 1021 yotta Y 1024

Fractions
Name Symbol Factor deci d 10-1 centi c 10-2 milli m 10-3 micro 10-6 nano n 10-9 pico p 10-12 femto f 10-15 atto a 10-18 zepto z 10-21 yocto y 10-24

Symbols of multiples and fractions always precede the main unit symbol (Example: mm, cm, dm, ) There is no space between the two symbols
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How to write SI unit symbols

Unit symbols are written after the numerical value of the quantity, separated by a space (Example: 10 m, not 10m) Derived units obtained by multiplication are indicated either with a dot or with a non-break space (Example: Pas or Pa s) Derived units obtained by division are indicated with / or a negative exponent (Example: m/s, ms-1 or m s-1). Note that / can be used only once (Example: kg/(m s), not kg/m/s) Unit symbols are not followed by a period Unit symbols must be written in Roman font (m for meter). Italic is reserved to quantity symbols (m for mass) Unit symbols are not pluralized (Example: kg, not kgs) Line breaks involving numerical values and its unit should be avoided. If required, the numerical value can be separated from its unit, while breaks inside composed units should be avoided
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Other systems of dimensional units

Imperial
Not rational Difficult conversion factors Adoption limited to a few countries You must know it. It is extensively used in the profession and in many manuals. Find a complete conversion table and keep it in your notes. You may use it during tests.

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Volumic mass and specific volume

The volumic mass (or density) is the mass per unit volume of a body Units
SI: [kg/m3] Imperial: [lb/ft3]

The specific volume is the reciprocal of the volumic mass In terms of moles, it is defined as vol/(n. of moles):
Molecular weight
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Amount of substance

Moles Avogadro's number


Number of molecules in a mole of a substance 6.02214129(27)1023 1/mol (~ 6.022 x 1023 1/mol)

Example
30g of N2, M = 28 g/mol, n = 15/14 mol 30kg of N2, M = 28 kg/kmol, n = 15/14 kmol

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Pressure

What is pressure? Measured with


Manometers Transducers

SI units
Pascal [Pa] 1 Pa = 1 N / 1 m2

Other units
1 bar = 105 Pa 1 atm = 101325 Pa = 14.7 psi = 14.7 lbf/in2 = 760 mmHg
= 29.2 inHg

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Absolute and relative pressure

Relative pressure (gage)

To avoid negative values

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Temperature and zeroth law of Thermodynamics


Temperature indicates how hot a system is. If the temperature is constant and uniform, there is no heat transfer
Thermal equilibrium

Zeroth law of Thermodynamics: If a system is in thermal equilibrium with two other systems, then also the two other bodies are in equilibrium Two systems in thermal equilibrium have the same temperature

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Measuring temperature

SI units
Kelvin [K] Fundamental SI unit Absolute scale: reference is the absolute zero (not reachable, based on the third law of Thermodynamics)

Celsius
T(K) = T(C) + 273.15

Fahrenheit
T(K) = 5[T(F) 32]/9 + 273.15

Rankine
T(R) = T(F) + 459.67

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Problem solving strategies

Carefully extract all the known data from the text of the problem
Most mistakes are caused by rushed reading of the problem text!

List what you have to calculate


Focus your effort Do not forget to answer all the questions

Sketch a diagram of the problem


Include the relevant elements Define the control volume Consider interactions, exchanges,

Make assumptions to simplify the problem Apply physical laws and write equations to describe the system Solve the equations to find the solution to the physical problem Check that results are meaningful
Example: A negative mass, or a negative absolute temperature are not acceptable! You must develop the ability of recognizing unphysical results

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An example of problem solving sheet


Data Unknowns m = 2.4 kg 1) Summarize data with symbols 2) Write down unknowns 4) Write results back here: it's easier to find if you need them!

Solution The definition of density is

3) Explain steps clearly

So we have

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Equation of state

We know from Physics that, for a gas we have three laws that relate temperature T, pressure p, and volume V:
T = T(p, V) p = p(V, T) V = V(p, T)

Such relations, due to Boyle, Charles and Gay-Lussac, are independent only for ideal gases. For real gases or condensed phases, such relations depend on the system, and only two among T, p, V are independent
A relation among these variables exists, and it is called equation of state:

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Equation of state

The equation of state f(p, V, T) = 0 defines a surface in the Cartesian space p, V, T

A process (thermodynamic transformation), namely any continuous set of values of the three variables p, V, T, is represented by a line in the same diagram

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Euler's relations

Let's assume f(x, y, z) = 0 is defined. If we consider x = x(y, z), then

If we consider y = y(x, z), then

Substituting the second expression in the first and collecting

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The p V T surface

The p V T surface is the three-dimensional representation of the equation of state


f(p, V, T) = 0

Single-phase regions on the surface include solid, liquid, and vapor Two-phase regions are located between single-phase regions, where two phases exist in equilibrium: liquidvapor, solid-vapor, solid-liquid Specific volume is used!
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The p V T surface

The dome-shaped region composed of the two-phase liquid-vapor states is called the vapor dome A state at which a phase change begins or ends is called a saturation state. Lines bordering the vapor dome are called the saturated liquid and saturated vapor lines
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The p V T surface

At the top of the dome, where saturated liquid and saturated vapor lines meet, is the critical point Critical temperature (Tc) is the maximum temperature at which liquid and vapor phases can coexist in equilibrium Critical pressure (pc) is pressure at the critical point.

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Phase diagrams

Phase diagrams are projections of the p V T surface onto the p T plane Saturation temperature designates the temperature at which a phase change takes place at a given pressure Saturation pressure is the pressure at which a phase change takes place at a given temperature Within two-phase regions pressure and temperature are not independent.
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The three phases coexist here: triple point


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Phase diagrams

Melting/solidification point Vaporization/ condensation point

Sublimation point
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p v and T v diagrams

Projection of the p v T surface onto the pressurespecific volume plane results in a p v diagram Projection of the p v T surface onto the temperaturespecific volume plane results in a T v diagram

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More details on p v diagrams

l compressed liquid

s superheated vapor

g saturated vapor Between f and g liquid and vapor coexist


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f saturated liquid
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More details on p v diagrams

When a mixture of liquid and vapor exists in equilibrium, the liquid phase is a saturated liquid and the vapor phase is a saturated vapor Vapor mass fraction (quality):

Saturated liquid: x = 0 Saturated vapor: x = 1 Superheated vapor (point s): vapor at T > saturation temperature
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Euler's relations

If we choose x and z as independent variables, such relation has to be valid for all the values of x and z, so coefficients must be identically null, leading to:

Euler's relations
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Equation of state

If we assume the function f of the equation of state f(p, V, T) is defined, we can define the following quantities:

Expansion coefficient at constant pressure Isothermal compressibility factor

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Equation of state

Since we can write, with good approximation

Using Euler's relation

If we consider the equation of state of an ideal gas

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End Part 1

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