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Applications Of Ideal Gases

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Accuracy requires taking account of deviations from ideality ... Real Gases Deviations From Ideality ... Deviation from ideality depends on. type of molecule ... – PowerPoint PPT presentation

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Title: Applications Of Ideal Gases


1
Applications Of Ideal Gases
  • Relation such as pV nRT is equation of state
    gives relation between variables in a given
    state.
  • Accuracy requires taking account of deviations
    from ideality
  • e.g. ideal gas model ? gases cannot be liquefied

2
Real Gases Deviations From Ideality
  • Breakdown of ideal gas assumptions because of
    intermolecular forces
  • long-range attractive force between molecules
  • weak (van der Waals dispersion)
  • from induced-dipole/induced-dipole force (these
    enable gases to liquefy)
  • short-range repulsive force
  • from Pauli Principle (cannot push molecules on
    top of each other, they would have same quantum
    numbers)
  • finite size of molecules

3
To Monitor Deviation...
4
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5
Size Of Non-Ideal Effects
  • Deviation from ideality depends on
  • type of molecule (strength of intermolecular
    forces) He has weakest forces, more polarizable
    molecules such as CO2 have bigger ones
  • temperature (high T ? molecules move so fast they
    do not see intermolecular forces)
  • pressure (all gases are ideal at sufficiently low
    pressures)

6
cf Textbook - Figure 5.21, page 210
7
Non-ideal Gas Equations Of State
  • Simplest van der Waals equation of state
  • ideal p ? V nRT
  • a, b are parameters measured from experiment
  • a (l2 atm mol2) b (l mol1)
  • He 0.34 0.024
  • CO2 3.59 0.042

8
Example
  • Find ideal and real (van der Waals) pressure of1
    mol of CO2 occupying 1.32 l at 48.0C.

9
cf Textbook - Figure 5.26, page 209
Intermolecular forces lessen the force of
impact with the wall - real pressure is lower
P Pideal - a (n/V)2
10
Virial Equation Of State
  • van der Waals equation has problems e.g., value
    of b for He gt b for Ne, wrong way round (Ne
    bigger than He!)
  • B, C are T-dependent
  • Can be calculated from knowledge of
    intermolecular forces
  • first to do this an Australian, John Barker
    (1969)
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