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1 - Thermal concepts
The three states of matter
Solid
- Fixed shape and volume so, therefore, molecules have fixed positions
- Strong IM forces
- Molecules cannot move, but free to vibrate
Liquid
- No fixed shape, but a fixed volume, so molecules can slide past each other
- Weak IM forces
- Pressure increases with depth in liquids - molecules below are forced together by weight
above
Gas
- No fixed shape or volume, so molecules are free to move at high speeds
- Virtually negligible IM forces
- Collisions with the wall of its container create gas pressure
Temperature and energy transfer
Temperature is a property that determines the direction of thermal energy transfer (heat) between two
bodies in contact. Temperature is a measurement of the average kinetic energy of a body. It is measured
in °C or °K. Energy tends to pass from the hotter to the colder object until they are both at the same
temperature (thermal equilibrium). Thermal energy (heat) is energy transferred between two
substances by non-mechanical means (conduction, convection, or radiation).
Thermometers
A thermometer can be constructed from any object that has a property that varies with temperature (a
thermometric property). Liquid-in-glass thermometers need to be calibrated in °C, a scale based on two
fixed points, the ice point, and the steam point. The assumption with thermometers is that the
expansion of the liquid is linear. The different rate of expansion between 0°C and 100°C is not too
significant.
Absolute temperature
The absolute temperature scale is the standard SI temperature scale, measured in °K. Absolute
temperature i s defined to be zero kelvin at absolute zero. The difference of 1°C = 1°K
T (°K) = θ (°C) + 273
Internal energy
The internal energy of a substance is the total of all the potential energy and random kinetic energy of all
the particles in a substance: I nternal energy (U) = Ek (molecules) + Ep (bonds)
● Potential energy is associated with IM forces
● Kinetic energy is associated with translational, rotational, and vibrational motion
Heat capacity
Heat capacity i s the energy required to raise the temperature of a substance by 1°K
Heat capacity (J°K-1) = Energy (J)/ Change in temperature (°K) C = Q/Δt
Specific heat capacity
Specific heat capacity is the energy required to raise the temperature of 1kg of a substance by 1°K
Specific heat capacity (JK-1kg-1) = Energy (J) / Change in temperature (°K) x Mass (kg)
c = Q/mΔt
The specific heat capacities of different substances vary because:
● Different number of molecules
● Different mass of molecules
● The average charge of molecules is different
● Temperature changes different
Finding SHC experimentally
● Electric method (placing an electric heater into a beaker of water (calorimeter))
Energy supplied = Energy to the water + Energy to the calorimeter
VIt = mwcw(tf-ti) + mccc(tf-ti)
If it’s just a solid block
VIt = mbcmaterial of block(tf-ti)
● Method of mixtures
Drop a hot block of metal into the water at room temperature [Heat lost block = heat gainedwater)
mbcb(ti-tf) = mwcw(tf-ti)
Specific latent heat
Specific latent heat is the thermal energy required to change the phase of 1kg of a substance without a
temperature change. Its equation is given by Energy = mass x specific latent heat (Q = mL).
SLH of fusion = solid to liquid
SLH of vaporization = liquid to gas
Finding SLH (ice cube case)
Heat lost by water = heat gained by the ice
mwcw(ti-tf) = miL + micw(tf - ti)
Heating curves
The heating curve shows how the temperature of a substance
changes with time. The flat regions indicate that there is no
temp. change, and so phase change occurs. The gradient of
the sections where the temperature changes can be used to
determine the heat capacity of the substance in that state. The
time for which the graph is flat can be used to find the specific
latent heat of the substance in its solid and liquid state.
Molecular explanation of phase change
The transfer of energy to a solid increases its internal energy (KE increases as vibrations and speeds
increase + IM PE increases as molecules move further apart). When IM bonds are being broken, the
energy supplied does not increase the mean random KE of the molecules but instead increases the PE of
the molecules. Eventually, molecules are sufficiently free so that the solid has melted. The mean KE and
speed of molecules increases, so the temperature rises once more. The PE does not change on average.
As the liquid approaches its boiling point, individual molecules break away and the PE increases rather
than the KE as energy is supplied. As there is no rise in KE, there is no rise in temperature again. Once
all the liquid has vaporized, energy is re-applied to raising KE, and therefore, temperature.
Boiling vs evaporation
Boiling Evaporation
● Only at boiling point ● All temperatures up to the boiling point
● Throughout the liquid ● Only at the surface
Factors affecting evaporation
● Temperature - higher temperature, higher evaporation (more particles have sufficient KE)
● Surface area - larger SA, higher evaporation (more particles on the upper surface)
● Airflow - higher airflow, higher evaporation (wind takes away particles
3.2 Modelling a gas
Boyle’s law states that for a fixed mass of gas at a constant temperature, the pressure is inversely
proportional t o the volume. p 𝝰 1/V OR P V = constant. From this, we can deduce that P1V1 = P2V2
We can change the axes to linearize this curve:
Charles’ law states that for a fixed mass of gas at The Pressure law states that for a fixed mass of
constant pressure, the volume is directly gas at a constant volume, the pressure is directly
proportional to the absolute temperature. V𝝰T proportional to the absolute temperature. p𝝰T
OR V/T = constant. T herefore, V1/T1 = V2/T2. OR P /T = constant. Therefore, P1/T1 = P2/T2.
The n
o. of particles in a gas at c onstant T and P is directly proportional to V
. n
𝝰
V
OR n
/V = constant.
The four equations can be combined to give a single constant, R, which is known as the ideal gas
constant. Combining the equations also gives us the ideal gas equation:
PV/nT = R ⇒ PV = nRT {When p is in Pa, V in m3, and T in °K, the value for R is 8 .31 JK-1mol-1}
The mole and Avogadro’s constant
One mole is the amount of substance having the same number of particles as there are neutral atoms in
12 grams of Carbon-12. One mole contains 6.02 x 1023 particles. This is A vogadro’s constant (NA).
The microscopic interpretation of gases
Diffusion
Diffusion is the movement of particles from a region of their higher concentration to a region of their
lower concentration as a result of Brownian motion. The random movement of particles in zigzag paths,
as a result of random collisions with air molecules, with no given pattern, is known as Brownian
motion. The pressure exerted by a gas in a container is caused by the change of momentum of the
particles striking the walls creating a force
Postulates of an ideal gas
● No force of attraction between atoms
● Atoms are perfect spheres
● Collisions between particles are elastic
● The duration of a collision is negligible in comparison to the time between collisions
● Each molecule produces a force on the walls of the container
The kinetic energy of an ideal gas
Imagine one ball of mass ‘m’ moving with speed ‘v’ in this cube. One length of the cube is
equal to ‘L’ . The average kinetic energy of all the particles in this cube is given by the
equations below:
KE =(3/2) x kB x T = (3/2) x (R/NA) x T
Difference between real and ideal gases
Real Ideal