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Summary of Lecture 21, 22, 23 & 24

Zeroth Law : Law of thermal equilibrium, n = no. of moles


i.e no net heat flow between 2 objects. V = Volume in m3
Linear Expansion : L = Lo +Lo T P = Pressure in Pa
Where
L = expanded length Thermometers
Lo = original length Temperature is related to KE of the
= coefficient of linear expansion molecules.
Temperature cant be measured
Volume expansion : V = Vo + VoT directly so we measure properties that
V = expanded volume change with temperature.
Vo = original volume
= coefficient of volume expansion Thermometric properties => volume
change, resistance change, EMF change,

Simplest approximation : = 3 pressure change at constant volume.

Mole concept : 1 mole of something = 1 Celsius Scale

Avogadros number of that something ( ) ()


=
() ()
Avogradros Number NA = 6.022 X 1023
2 fixed points are ice point and steam point
Not scientific because ice & steam points
No of moles = mass of sample (in gram) /
are not unique.
molar mass (in g)

Kelvin Scale
Ideal Gas : A gas with KE only (no PE) =>
Fixed scale is triple point of water, set it as
molecules do not interact.
273.16 K.
Real gases ideal when the real gases are
Measured with the constant volume gas
at low pressure and/or low density.
thermometer. (but with a real gas inside)

Ideal gas equation of state


Short answer to the problem of using real
=
gases :
T = thermodynamic temperature (K)
Measure with decreasing pressure
R = molar gas constant 8.31 J/mol K
Then extrapolate the graph to zero Internal energy : For real gas, internal
pressure. energy = KE + PE, for ideal gas, internal
The extrapolated temperature is the energy = KE only.
Kelvin temperature. Monoatomic ideal Gas
3 3
= =
2 2
For processes that change in Temperature :
Diatomic ideal Gas
=
5 5
= =
2 2
For processes that change in state : Heat exchange Q
= Q > 0 when heat enters gas
l = lf(fusion) & lv (vaporization) Q < 0 when heat leaves gas
Q = heat exchange
c = specific heat capacity Work Done by gas

=
Gas equation in kinetic theory :

= < >

First Law of thermodynamics
Vrms = root <v2>
= ()
Combine PV = nRT with PV = 1/3 Nm
Process 1: Isochoric (constant volume)
<v2>

< > =


= =

m = mass of 1 molecule (in kg)


M = molar mass (in kg)

Work done by Gas :


Processes in gas are presented on PV
diagram. (P in y axis, V in x axis) => W=0 (no area under graph)

= =
WD by gas : positive when there is
expansion, negative when there is From 1st Law : Q = U
compression. For this process, a new definition can be
given
=
Cv = 3/2 R (mono) or 5/2R (dia)

Process 2 Isobaric (constant pressure)

Expansion => left to right, Compression


=> right to left
T = 0, U = 0
Q = W => 1st law

= =

Process 4 Adiabatic Process (definition
= ( )
Q=0)

= Equation: PV = constant => steeper than

5 isothermal curves
For mono, = 2
7 = Cp/Cv
For dia, =
2

For this process, a new definition can be


given
=
Cv = 5/2 R (mono) or 7/2R (dia)

Mayers relation : Cp- Cv = R


Extra definition : = Cp/Cv


Process 3 Isothermal (constant
= =
temperature)
From PV = nRT, P = nRT/V => y=k/x U = -W
reciprocal graphs = isothermal lines Note that PV = nRT applies to any
process

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