Properties of Gases Notes

Properties of Gases: The Air We Breathe

Intended Learning Outcomes (ILOs)

  • Apply the Ideal Gas Law to determine properties of gases.

Properties of Gases

  • How are Gases unique?
    • A gas expands spontaneously to fill its container.
    • Gases are highly compressible.
    • Gases form homogenous mixtures with other gases, regardless of identity or composition of the gas.
    • At the same temperature and pressure:
      • Equal volumes = equal number of molecules gas.
    • These properties are unique to gases and do not apply to liquids or solids.
  • Properties of gases:
    • Volume is inversely proportional to pressure.
    • Pressure is directly proportional to temperature.
    • Pressure is directly proportional to quantity of gas.
    • Gases are miscible.
    • Densities are directly proportional to molar mass.
    • Gases expand to occupy entire volume of their container.
    • Gases effuse at rates inversely proportional to molar mass.

Pressure of Gases

  • Pressure of a gas is the collective force particles exert on the walls of the container.
  • More collisions cause more pressure.
  • More particles cause more pressure.
  • Smaller volume causes more pressure.
  • Higher temperature causes more pressure.

Kinetic Molecular Theory (KMT)

  • The behavior of gases can be described using kinetic molecular theory (KMT), which is based upon four assumptions:
    1. Gas molecules have tiny volumes compared with volume the gas occupies.
      • Gases are mostly empty space
    2. Gas particles do not interact with each other.
      • We assume there are NO interactions between gas particles, no IMFs
    3. Gas molecule collisions are elastic.
      • Gas particles collide with each other constantly, but the collisions are elastic, meaning no loss of energy
    4. The average kinetic energy of the molecules in a gas are proportional to the absolute temperature.
      • No matter the gas, if the temperature is the same, the average kinetic energy is the same.

Particle Speed

  • u_m – The most likely speed for a gas particle. The speed the most particles are moving at.
  • u{avg} – The average speed of all the particles. Slightly higher than the um.
  • u_{rms} – Root mean square speed. Square root of the average of the squared speeds of all particles.

KE and u_{rms}

  • KE: Kinetic Energy
  • m: mass
  • u_{rms}: root-mean-square speed
  • At the same temperature, all gas particles, regardless of element, have the same KE_{avg}, but that does NOT mean, the same speed.
  • Heavier molecules have slower average speeds.
  • KE{avg} = \frac{1}{2} m u{rms}^2

Comparing Particle Speeds

  • Let’s compare He and N2. According to KMT, all gases at the same temp have the same KE, but not the same speed
  • KE{avg} = \frac{1}{2} m u{rms}^2
  • KE{He} = KE{N_2}
  • \frac{1}{2} m{He} u{rms,He}^2 = \frac{1}{2} m{N2} u{rms,N2}^2
  • \frac{u{rms,He}}{u{rms,N2}} = \sqrt{\frac{m{N2}}{m{He}}}
  • \frac{u{rms,He}}{u{rms,N2}} = \sqrt{\frac{\mathcal{M}{N2}}{\mathcal{M}{He}}}
  • \mathcal{M} = molar \, mass
  • He travels 2.646 times faster than N2.
  • \frac{u{rms,He}}{u{rms,N2}} = \sqrt{\frac{\mathcal{M}{N2}}{\mathcal{M}{He}}} = \sqrt{\frac{28.02 \, g/mol}{4.003 \, g/mol}} = 2.646

Effusion

  • Process by which gas molecules escape from a container through small holes to a region of lower pressure.
  • Graham’s Law of Effusion
  • \frac{effusion \, rateA}{effusion \, rateB} = \sqrt{\frac{\mathcal{M}B}{\mathcal{M}A}}
  • \frac{u{rms,A}}{u{rms,B}} = \sqrt{\frac{\mathcal{M}B}{\mathcal{M}A}}

Determining Particle Speeds

  • KE{avg} = \frac{1}{2} m u{rms}^2
  • \frac{1}{2} m u{rms}^2 = \frac{3}{2} kB T
  • KE{avg} = \frac{3}{2} kB T
  • u{rms} = \sqrt{\frac{3kBT}{m}}
  • u_{rms} = \sqrt{\frac{3RT}{\mathcal{M}}}
  • R = 8.314 \frac{kg \cdot m^2}{s^2 \cdot mol \cdot K}

Practice

  • Calculate the root-mean-square speed of Nitrogen gas molecules at 25℃.
  • u_{rms} = \sqrt{\frac{3RT}{\mathcal{M}}}
  • R = 8.314 \frac{kg \cdot m^2}{s^2 \cdot mol \cdot K}

Diffusion

  • Spread of one substance (usually gas) through another substance.
  • Mean Free Path: average distance a particle can travel through a gas before colliding with another particle.
  • At 1 atm is about 6.8 x10^{-8} m (about 10^{10} collisions per second)
  • Gases will spontaneously fill a space through diffusion and effusion, moving from high concentration to low concentration.

Atmospheric Pressure

  • Produced by Earth’s gravity pulling with force on the air molecules.
  • At higher altitudes, there are less gas molecules, and therefore lower pressure.

Atmospheric Pressure Effects

  • Differences in pressure produces wind. Remember that gas will spontaneously move from high concentrations to lower concentrations.
  • High pressure: usually associated with clear weather.
  • Low pressure: usually associated with unstable weather.

Measuring Pressure

  • Barometer
    • Pressure of the atmosphere on the mercury pool pushes the mercury up the tube. Measuring that push up the tube determines the atmospheric pressure
  • Manometer
    • When the valve is closed, Hg levels are equal.
    • Open valve and pressure will push against the atm pressure.
    • Measure the difference between the two to determine the pressure of a sample

Measuring Pressure

  • Standard pressure is the pressure at sea level:
    • 1 atm
    • 760 mm Hg
    • 760 torr

Partial Pressures

  • Gases create homogeneous mixtures
  • So, when a gas exerts a pressure, all the component gases are actually individually exerting their own pressures.
  • Dalton’s Law of Partial Pressures
  • P{Total} = P1 + P2 + P3 …
  • Where P1, P2, P_3, etc. are the partial pressures of the individual gases.

Partial Pressures

  • Can also calculate the partial pressure for an individual gas if you know how many moles of it are present in the total mixture (mole fraction).
  • P1 = \chi1 \times P_{Total}
  • \chi_1 = \frac{moles \, of \, 1}{Total \, moles}

Partial Pressures

  • One way to measure the partial pressure of a gas is over water.
  • P{total} = P{dry \, gas} + P{H2O}

Simple Gas Laws

  • Boyle’s Law – Pressure and Volume
  • Charles’s Law – Volume and Temperature
  • Amonton’s Law – Pressure and Temperature
  • Avogadro’s Law – Volume and Moles
  • When comparing two CHANGING properties, the others stay CONSTANT

Boyle’s Law

  • The volume of a gas is inversely proportional to the pressure.
  • As volume goes up, pressure goes down.
  • P1V1 = P2V2

Charles’s Law

  • The volume of a gas is directly proportional to temperature.
  • As temperature goes up, volume goes up.
  • \frac{V1}{T1} = \frac{V2}{T2}

Amonton’s Law

  • The pressure of a gas is directly proportional to temperature.
  • As temperature goes up, pressure goes up.
  • \frac{P1}{T1} = \frac{P2}{T2}

Combined Gas Law

  • Boyle’s, Charles’s, and Amonton’s Laws can be combined to produce the Combined Gas Law
  • This is useful if P, V, and T are all changing. In the individual laws, 2 things can change while one has to be held constant.
  • If you know the Combined Gas Law, you can derive Boyle’s, Charles’s, or Amonton’s
  • \frac{P1V1}{T1} = \frac{P2V2}{T2}

Avogadro’s Law

  • The volume of a gas is directly proportional to the number of moles of the gas.
  • As the moles of a gas go up, the volume goes up.
  • At STP: 22.4 L = 1 mole of gas
  • Applies to ALL gases
  • \frac{V1}{n1} = \frac{V2}{n2}

Ideal Gas Law

  • Boyle’s, Charles’s, Amonton’s, and Avogadro’s Laws can be combined along with a constant to produce the Ideal Gas Law
  • For this law, if you know 3 variables, you can determine the fourth.
  • If you know the Idea Gas Law, you can derive Boyle’s, Charles’s, Amonton’s, or Avogadro’s.
  • PV = nRT

What is an Ideal Gas

  • 2 Main Assumptions:
    • The volume of individual gas particles are insignificant.
    • Gas particles DO NOT interact with each other.
  • PV = nRT

Ideal Gas Constant

  • R is known as the gas constant.
  • Can have many combinations of units
  • The units in the constant you use MUST match your units in your measurements/variables
  • You can either choose your constant, or assure that your measurements are using the same units as your constant
  • PV = nRT

Volume at STP

  • 1 mole of ANY gas at STP is 22.4L
  • PV = nRT
  • \frac{V}{n} = \frac{RT}{P} = \frac{(0.0821 \frac{L \cdot atm}{mol \cdot K})(273 \, K)}{1 \, atm} = \frac{22.4 \, L}{1 \, mol}

Density of an Ideal Gas

  • Density is mass/volume
  • For an Ideal Gas, volume is the same from gas to gas, but mass is different, so therefore, Density is as well.
  • Can use molar mass/molar volume instead of just mass/volume
  • Density = \frac{molar \, mass}{molar \, volume} = \frac{mass/mol}{volume/mol}

Density of an Ideal Gas

  • In the Ideal Gas Equation, we know that n (moles) is the same as grams/molar mass, so we can substitute it into the Ideal Gas equation to solve for density.
  • Can also be rearranged to solve for molar mass:
  • \frac{m}{V} = \frac{P (\mathcal{M})}{RT}
  • \mathcal{M} = \frac{d (RT)}{P}

Stoichiometry Involving Gases

  • You now have a new conversion factor you can use in stoichiometry calculations.
  • H2 + O2 \rightarrow H_2O