Section 3: Thermal Physics Flashcards
Temperature
The measure of how ‘cold’ or ‘hot’ a substance is
The common property that two bodies possess when they are in thermal equilibrium with each other
A measure of a body’s ability to transfer heat to other bodies
Human blood temp
37°C
98.6°F
Volume and temperature
V ∝ T
When T is below fusion point…
Gas becomes liquid
Triple point of water
A specific combination of pressure and temp at which all three phases of water co-exist simultaneously
Defined as 0.01°C
Celsius and Kelvin
Granularity are same (difference of 1°C is same as difference of 1K)
If problem involves a difference in temp, doesn’t matter if you use °C or K, as long its in the same units
If problem only involves a single temp, must use K
Absolute scale of temperature
Kelvin scale (K)
Using a thermometer
Essentially only gives a reading of its own temp
Thus, it’s critical to wait until the temp of the thermometer becomes the same as the substance you are measuring
i.e. must wait until thermometer is in thermal equilibrium with the substance
Thermal equilibrium
When objects are in thermal contact, their temperatures eventually equalise –> thermal equilibrium
Heat flows from hot to cold objects
Human body - thermal equilibrium?
Human body is NOT at thermal equilibrium with its surroundings
Zero-th law of thermodynamics
If A and B are separately in thermal equilibrium with C, then A and B are in thermal equilibrium with each other
i.e. they are all the same temp
Thermal expansion
Where the size of an object changes with temperature, typically increasing with increasing temp
Length and temperature
L ∝ T
α
Linear expansion coefficient - quantifies change in linear dimensions of an object
Fractional change in length per unit of temp change
Unit K^-1 or °C^-1
β
Volumetric expansion coefficient
Fractional change in volume per unit of temp change
Unit K^-1 or °C^-1
α and β
β = 3α
Solids usually use α (linear)
Liquids and gas usually use β (volume)
Hollows and cavities - heating
Hollows and cavities in solids expand on heating as do the solid parts of the object
Gases - coefficient
All gases have same coefficient, irrespective of their nature
β = 3.4 x 10^-3 K
Solids, liquids and gases - β
Generally:
β(gas)»_space; β(liquid)»_space; β(solid)
Solids: β < 10^-4 K^-1
Liquids: β < 10^-3 K^-1
Gases: β > 10^-3 K-1
Density (ρ) and temperature
ρ ∝ T
Thermal stress
Stress created in objects constrained to a precise, fixed dimension when temp changes occur
Gas
A state of matter where the diff atoms/molecules constituting the material have no bonds betwen them, are v far apart, and are moving around randomly in all directions at high speed
Compressible and deformable
Pressure
The average force (F) per unit of surface area (A)
Pressure - units
Standard unit of pressure is N/m^2 = 1 Pa (pascal)
1 bar = 10^5 Pa
Standard atmospheric pressure
The mean pressure exerted by our atmosphere at mean sea level at the latitude of Paris
1 atm is roughly equal to…
1 bar to within 1%
i.e. 10^5 Pa
Gauge pressure
Refers to pressure measured wrt atmospheric pressure
e.g. if you inflate a tyre to x bar of gauge pressure, that means the absolute (total) pressure inside the tyre is x bar + the current atmospheric pressure (i.e. about 1.5 bar)
1 atm (or 1 bar) pressure = ? of water
Roughly 10m of water
Ideal gas law - points to remember
P is the absolute pressure (not gauge pressure)
T is the absolute temp (in K)
Boltzmann constant
Proportionality constant in gas law, k
Avogadro number
N(A)
Unit is /mol (mol^-1)
Atomic masses
Atomic masses given in periodic table = masses in grams of one mole of that element
Kinetic theory
Describes the behaviour of gases as that obtained by the averaged effect of many microscopic particles (atoms or molecules) moving and colliding rapidly
Volume and pressure
Decreased volume –> increase no of collisions per unit of surface –> increased pressure
Number of particles and pressure
Increased no of particles –> more collisions –> increased pressure
Velocity of particles and pressure
Increased velocity of particles –> stronger collisions –> increased pressure
Kinetic theory - assumptions
Collisions of molecules with other molecules and the container walls are perfectly elastic and of zero time duration
Molecules occupy a negligible volume compared to size of container
Molecules obey Newton’s law of motion (F = ma)
Molecules exert no forces on each other except elastic forces during instantaneous collisions
Average kinetic energy
AKA thermal energy
Shows temp is a measure of the average energy of the particles in the gas
Existence of absolute zero of temp
Can be inferred from average kinetic energy
To lower the temp of a body, one needs to remove energy from its constitutive particles
Since energy is finite, once we have removed all the energy they have, one can’t lower the temp anymore - this is the absolute zero
RMS velocity
The square root of the mean of the square of the velocities of all particles
Molar mass and velocities of particles
Increased molar mass = heavier particles, which are harder to put in motion (have more inertia) –> decreased speed
Distribution of velocities
A graph showing the percentage of particles in a gas having such and such velocity
Bell-shaped curve that depends on temp
Starts from origin and tends towards zero for very large velocities
Tail extends to large velocities for increasing temp
Distribution of velocities - curve max and RMS
Curve maximum (‘most probable’ velocity) is slightly diff that RMS (RMS is slightly lower)
Solid
Can be seen as a collection of bound particles, each of them vibrating due to their averaged kinetic energy
Heating a material - particles
Particles will vibrate more strongly –> increase in average distances –> thermal expansion
Expansion of water
Water density decreases with increasing temp across majority of its liquid range, but does the opp in range of 0 to 4°C
Freezing a cell
Will burst because of the water expanding as it freezes
To determine which phase a substance is, must specify..
Temperature (T)
Pressure (P)
Volume (V)
Phase diagram
Represents which phase a given substance will be found in as a function of T, P and V
Types of phase diagrams (2D)
V-T diagram
P-V diagram
P-T diagram
V-T diagram
P is constant
V varies linearly with T - straight line
Below the bpt, the gas becomes liquid, and as molecules are bound together, volume shrinks significantly - gives discontinuity in V-T curve
Same occurs for liquid to solid, but less obvious
P-V diagram
Hyperbola on right part (vapour phase) of diagrams
Liquid phase curves pretty much verticle
Liquids - compression
Most liquids are largely incompressible - V barely changes when applying pressure because molecules are v close and intermolecular forces resist the applied pressure
P-V diagram - grey zone
Liquid-vapour region
Where liquid and vapour can coexist
Pressure stays constant while volume varies
P-V diagram - critical pressure
The pressure where the co-existence zone of liquid and vapour disappears
This is because the pressure is so large that molecules of a gas would be brought so close tgt that it starts to behave like a liquid
P-V diagram - above the critical point
There is no more distinction between liquid and gas phase
P-T diagram
Volume is constant
Typically contains 3 curves separating the solid, liquid and gas phase
P-T diagram - melting/fusion curve
Line separating solid from liquid
P-T diagram - boiling curve
Line separating liquid from gas
Does not extend indefinitely - it ends at the critical point, above which liquid and gas becomes indistinguishable
P-T diagram - sublimation curve
Line separating solid from gas (lower part)