* Reading Assignments:

1.1
1.1.1
1.1.2
1.2
1.2.1
1.2.2

2.1
2.1.1
2.1.2
2.1.3
2.1.4
2. Basic Concepts of Thermodynamics

2.1 Thermodynamic system

A specified collection of matter is called a system,

which is defined by the mass and the composition.

a. Open system: mass is exchanged with its

surroundings;

b. Closed system: NO mass is exchanged with its

surroundings.

What type of system does atmospheric thermodynamics

deal with?
The systems that atmospheric thermodynamics deal with include

1) an air parcel;
2) a cloud;
3) the atmosphere;
4) an air mass etc.

Precisely speaking, they are open systems because mass can

be changed by the entrainment and mixing processes.

But, we will treat them as a closed system in this course.

Assumptions:

1) the volume is large that mixing at the edges is negligible; or

2) the system is imbedded in a much larger mass which has the

same properties.
2.2 Thermodynamic properties
The properties define the thermodynamic state of a system.

a. Intensive property: does not depend on the mass (m)

or does not change with subdivision of the system,
denoted by lowercase letters, e.g., z.

b. Extensive property: does depend on the mass (m) or

does change with subdivision of the system, denoted by
uppercase letters, e.g., Z.

Exception to the convention: T for temperature and m for mass

* An intensive property is also called a specific property if

Z
z
m

For example, volume V is an extensive property, so v=V/m

(i.e., volume per unit mass) is a specific property and an
intensive property.
* Homogeneous vs heterogeneous

a. A system is considered to be homogeneous if every intensive

property has the same value for every point of the system.

Z  mz

b. A system is said to be heterogeneous if the intensive property

of one portion is different from the property of another portion.

Z   mi zi
i
* A system can exchange energy with its surroundings through
two mechanisms:

1) Mechanical exchange (Expansion work)

performing work on the surroundings

2) Thermal exchange (Heat transfer)

transferring heat across the boundary

* A system is in thermodynamic equilibrium if it is in
mechanical and thermal equilibrium.

Mechanical equilibrium: the pressure difference between

the system and its surroundings is infinitesimal;

Thermal equilibrium: the temperature difference between

the system and its surroundings is infinitesimal.
2.3 Expansion work

If a system is not in mechanical equilibrium with its surrounding

it will expand or contract.

The incremental expansion work:

W  pdSdn  pdV
p: the pressure exerted by the surroundings over the system

dV: the incremental volume p

dS: the displaced section of surface

dn: the normal distance between

original and expanded surface
2.4 Heat transfer

Adiabatic process: no heat is exchanged between the system

and the environment.

Diabatic process: heat is exchanged between the system

and the environment.

Which one will we use the most? Why?

 2.5 State variables and equation of state
* A system, if its thermodynamic state is uniquely determined by
any two intensive properties, is defined as a pure substance.
The two properties are referred to as state variables.

* From any two state variables, a third can be determined by an

equation of state,

f ( z1 , z 2 , z3 )  0.
A pure substance only has two degrees of freedom. Any two state
variables fix the thermodynamic state,
* Any third state variable as a function of the two independent
state variables forms a state surface of the thermodynamic
states, i.e.,

z3  g ( z1 , z 2 ).
2.6 Thermodynamic process

* The transformation of a system between two states describes

a path, which is called a thermodynamic process.

* There are infinite paths to connect two states.

* Exact differentials
Consider
z  M ( x, y )dx  N ( x, y )dy.
If
z z
M ( x, y )  , N ( x, y )  ,
x y
which is the same as
M ( x, y ) N ( x, y )
 ,
y x
we have
z z
z  dx  dy  dz ,
x y
dz is an exact differential, z ( x, y ) is a point function
which is path independent,

 dz  0 .
2.7 Equation of state for ideal gases
2.7.1 How to obtain the ideal gas equation?

The most common way to deduce fundamental equations is to

observe controlled experiments.
* Based on Boyle’s observation, if the temperature of a fixed
mass of gas is constant, the volume of the gas (V) is inversely
proportional to its pressure (p), i.e.,

pV  const (1)

* From Charles’ observation, for a fixed mass of gas at constant

pressure, the volume of the gas is directly proportional to its
absolute temperature (T), i.e.,
V
 const (2)
T
* For a fixed mass of gas, consider three different equilibrium states
that have ( p,V , T ), ( ps ,Vs , T ), and ( ps ,V0 s , T0 ) , respectively.

* From (1) and (2), we have

Vs V0 s
pV  psVs , 
T T0
Combine them,
pV psV0 s
 (3)
T T0
Divide (3) by the molar abundance (or number of moles)
m
n
M
which is constant since the mass (m) and molecular weight (M)
are constant, we have
pV psV0 s
 (4)
Tn T0 n
* For a standard condition,

T0  273.15K , ps  1 atm  1013.25mb  1.01325105 kgm1s 2

V0 s / n  22.4 103 m3 / mol

psV0 s
R*   8.3143 Jmol 1K 1
T0 n

is called the universal gas constant.

Now, (4) can be rearranged to get the equation of state

for the ideal gas

pV  nR T * (5)
2.7.2 Equivalent forms of ideal gas equation

Ideal gas equation (5) can be written in several forms,

m *
pV  R T  mRT (6)
M
R*
R is the specific gas constant.
M
Since the specific volume

V 1
v 
m 
,  is the density,
(6) can be also written as

pv  RT , or p  RT (7)
2.7.3 Equation of state for mixture of ideal gases

Each gas obeys its own state equation, for the i th gas

piVi  mi RiTi (8)

Since in a mixture of gases,

* The partial pressure pi is:

the pressure the i th gas would have if the same mass existed
alone at the same temperature and occupied the same volume
as the mixture;

* The partial volume Vi is:

the volume the i th gas would occupy if the same mass existed
alone at the same temperature and pressure.
(8) can be written in form,

piV  mi RiT (9)

Sum (9) over all gases in the mixture, and apply Dalton’s law,

p   pi
i
we get the equation of state for the mixture,

pV  m RT (10)

which is similar to the ideal gas equation (6).

m   mi
i

m R i i
R i is the mean specific gas constant
m
The mean molecular weight of the mixture is defined by

n M i i m i
m
M i
 i
 (11)
n n n
Since
mi
n   ni  
i i Mi

(11) can be written as

R *m R *m R*
M  
 mi ( R / M i )  mi Ri R
i
*

i
The absolute concentration of the i th gas is measured by its density i .

The molar fraction is used to measure the relative concentration

of the i th gas over the total abundance air in the mixture,
ni
Ni 
n
Using the state equations for the i th gas and the mixture of gases, we
can also have
ni pi Vi
Ni    (12)
n p V
The mass fraction is also used to measure the relative concentration.
Using n  m / M , and ni  mi / M i in (12), we can get

mi ni M i Mi
  Ni
m n M M
The mixing ratio is used to measure the relative concentration of the
i th gas over dry air, e.g., the mass mixing ratio is defined in form,
mi
ri  (13)
md
md is the mass of dry air; ri is dimensionless and expressed in g kg 1
for tropospheric water vapor.

Since the mass of air in the presence of water vapor and ozone is virtually
identical to the mass of dry air, (13) can be related to the molar fraction,
mi ni M i ni n M i
ri     N i i (14)
md nd M d n nd M d
Mi n
where i  , 1
Md nd
We can also have the volume mixing ratio related to the molar fraction,

Vi Vi Ni
  (15)
Vd V  Vi 1  N i
(d)
2.8 Atmospheric composition

Atmospheric air is composed of

1) A mixture of gases (Nitrogen, Oxygen, Argon and Carbon dioxide etc.)

* Remarkably constant up to 100 km height (except for CO2);

* These four gases are the main components of dry air.

1 1
The specific gas constant: Rd  287.05 J kg K
The mean molecular weight: M d  28.96 g mol 1

2) Water substance in any of its three physical states (vapor,

droplets and ice particles)

* very important in radiative processes, cloud formation and interaction

with the oceans, and highly variable.

3) Solid or liquid particles of very small size (atmospheric aerosols)

Problem: Find the average molecular weight M and specific
constant R for air saturated with water vapor at 0oC and 1 atm
of total pressure. The vapor pressure of water at 0oC is
6.11mb.
2.9 Hydrostatic balance
When an incremental air column experiences no net force in the
vertical direction, it is considered to be in hydrostatic balance
(or hydrostatic equilibrium).
From
pdA  ( p  dp)dA  gdAdz  0

we have

dp
  g (16)
dz

g is the acceleration of gravity.

 Homework (1)
1. Using the equations of state for the ith gas and the mixture of gases, demonstrate that

ni pi Vi
Ni    .
n p V
2. Test the following equations for exactness. If it is exact, find the point function.

z  ( x  y  6)dx  ( y  x)dy
3. Problem 3.4 d) and e)

4. a) Determine the mean molar mass of the atmosphere of Venus, which consists of 95% CO 2
and 5% N2 by volume.
b) What is the corresponding gas constant?
c) The mean surface temperature T on Venus is a scorching 740K as compared to only 288K
for Earth; the surface pressure is 90 times that on Earth. By what factor is the density of the
near-surface Venusian atmosphere greater or less than that of Earth?

5. Two sealed containers with volumes V1 and V2, respectively, contain dry air at pressures p1
and p2 and room temperature T. The containers are connected by a thin tube (negligible volume)
That can be opened with a valve. When the valve is opened, the pressures equalize, and the
system reequilibrates to room temperature. Find an expression for the new pressure.

6. Show that 1 atm of pressure is equivalent to that exerted by a 760 mm column of mercury
at 0oC (density is 13.5951 g cm-3) and standard gravity g =9.8 ms-2.