Neng 301 Lecture 2 - The Structure of Thermodynamics (Dehoff, Chap. 2)
Neng 301 Lecture 2 - The Structure of Thermodynamics (Dehoff, Chap. 2)
Neng 301 Lecture 2 - The Structure of Thermodynamics (Dehoff, Chap. 2)
This is a system.
The subset of the universe in
focus in a particular application
of thermodynamics is usually
called the system
At any given instant of
observation the condition of
the system is described by an
appropriate set of properties
Limitations on changes in these
properties are set by the nature
of its boundary
Classification of systems
Thermodynamic systems can be classified into several categories:
1. unary (one chemical component) versus multicomponent (two
or more chemical components in multicomponent systems,
the chemical composition may vary
2. homogeneous (single phase) versus heterogeneous (two or more
phases, eg. ice/water)
3. closed (no exchange of matter by the system across its boundary
with the surroundings) versus open (exchange of matter by the
system with the surroundings) [note: also isolated]
4. non-reacting versus reacting (specifically chemical reactions)
5. simple versus complex
o simple: only energy exchanges involve thermal, mechanical or
chemical changes
o complex: gravitational, electrical, magnetic or surface factors
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More definitions
State functions (or state variables): a system is said
to be in a certain state when all of its properties
have these specific values depend on the current
condition of the system and not on how the system
got there
temperature
pressure
volume
chemical composition
(internal) energy
entropy
others.
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Simple Exercise
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What is Thermodynamics?
The study of energy transformations and the relationships among
physical properties of substances which are affected by these
transformations.
-- K. Wark, Thermodynamics, 5th Edition (1988)
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Work
The easiest way to discuss work
is through classical mechanics
Consider the application of a
force F: if the point of
application of the force moves,
then the force does work
The increment of work done by
the displacement is:
w F dx
F=Pext A
w Pext A dx Pext dV
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Work
intensity factor
capacity factor
formula
mechanical
force
change in distance
f x
gravitational
gravitational potential
(a function of height)
mass
mgh
electrical
potential difference
quantity of charge
QV
surface
surface energy/tension
change in area
g DA
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Heat
Heat and work are both measured in energy units, so
they must both represent energy
Energy can take many forms: mechanical, chemical,
electrical, radiation (light), and thermal, or heat
Heat is a form of energy, but it differs from all the
others in one crucial way: complete conversion of heat
into other forms of energy is impossible
Thermal energy can be transferred from one body (i.e.,
one system) to another (we often refer to this as a
"flow" of heat)
Heat can only flow spontaneously from a system at a
higher temperature to one at a lower temperature
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Mass
Mass
Piston
Piston
Pi, Vi
Ti
P f, V f
mechanical
stops
Tf
x2
dx x2 x1 Dx
In other words: an exact differential integrates to a finite
difference, independent of the path of the integration
x1
inexact
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The system in either the initial state or the final state does not
have any work W1 or W2, nor does it have any heat Q1 or Q2
Work and heat appear during a change in state; they are not
properties of the state, but instead are properties of the path
Properties of the state of the system (T, P, V, U) have
differentials which are exact, while differentials of properties
of the path (Q and W) are inexact
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More definitions
equations of state or state functions: relationships
between dependent variables of state and
independent variables of state
intensive property: a property that is independent
of the quantity of matter in a system (temperature,
pressure, concentration, etc.)
extensive property: a property that is dependent of
the quantity of matter in a system (volume, heat
capacity)
Note that we can derive intensive properties from
extensive properties (example: mole fraction)
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Classification of relationships
Just wait and see: you will become familiar with a large
number of thermodynamic relationships!
In order to sort through the coming confusion it will be useful
to classify these relationships
1. Laws of thermodynamics these form the physical basis
for all subsequent relationships
There exists a property of the universe, called its energy (U),
which cannot change no matter what processes occur in the
universe
There exists a property of the universe, called its entropy (S),
which can only change in one direction no matter what
processes occur in the universe
A universal absolute temperature scale exists and has a
minimum value, defined to be absolute zero, and the
entropy of all substances is the same at that temperature 24
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Answer to 2.6.
Attributes of equilibrium:
1. A state of rest: state of the system does not change with time.
2. A stable state: if the state is displaced from the equilibrium state,
it will return to it.
3. A state of internal uniformity; (in the absence of external fields)
gradients of intensive properties vanish.
The equilibrium state is the final state of every process. The
primary goal of thermodynamics is the prediction of the
properties of the final equilibrium state for any given initial
condition of any system. "How far the system is" from the
equilibrium state is a measure of the driving force for processes
changing the system toward equilibrium, and controls the rate
of approach to the final state of rest.
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Classification of relationships
2. Definitions new parameters, quantities and variables
based on prior ones
Energy:
U = U(S,V)
dU = T dS P dV
Enthalpy: H = U + PV dH = T dS + V dP
Helmholtz free energy: F = U TS dF = S dT P dV
Gibbs free energy: G = U + PV TS = H - TS
dG = S dT + V dP
2. Coefficient relationships describe how the value of state
variable changes during an infinitesimal step in a process:
dZ MdX NdY
X, Y, Z are all
state variables
dX
dY
X Y
Y X
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dX
dY
X Y
Y X
If Z = f(X,Y) represents a
surface in (X,Y,Z) space,
then dZ is the sum of the
components in the X and Y
directions
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Z
Z
dX
dY
X Y
Y X
2 ;
P
P T
T P P
So the final relationship for dV is:
RT
R
dV 2 dP dT
P
P
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M
N
dZ MdX NdY
X
Y
Where did this come from? Go back to:
Z
Z
M
and
N
X
Now take the derivatives:
Z
Z
M
N
and
X
Y X
X Y
Since the order of differentiation doesnt matter:
Z
Z N
M
X
Y X
X Y
Y
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T
T
P
the isothermal pressure dependence of entropy is
given by the easily-measured thermal expansion
Simple Exercise
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Group Exercise
Group V: N, S (7)
dX =
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number of components
number of phases
nature of the system boundary
chemical reactivity
complexity with respect to non-mechanical forces
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