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SESM3037
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Ortho-para ratio
ratio of number of molecules occupying odd & even energy levels
State Function
Path independent measurable quantity dependent on current state and not history
Free energy
portion of internal energy converted to work, excluding heat content
Internal Energy
energy contained within system
Helmholtz Free Energy
free energy available for work at constant temperature and volume
Gibbs Free Energy
Maximum work done at constant temperature and pressure
Inversion Temperature
Temperature at which the Joule-Thompson coefficient changes sign
Inversion Temperature of Helium
43 K
Inversion Temperature of Hydrogen
202 K
Inversion Temperature of Air
603 K
Inversion Temperature of Nitrogen
623 K
Inversion Temperature of Oxygen
761 K
Triple Point of Nitrogen
63 K
Triple point of Hydrogen
14 K
Hydrogen Ortho-Para ratio at room temperature
3:1
Hydrogen ortho-para ratio at 80 K
1:1
Hydrogen ortho-para ratio at 20 K
100% para
Hydrogen Boiling Point
20 K
Advantages of Claude Cycle
Isentropic expansion of gas results in a lower temperature vs isenthalpic expansion in LH cycle.
Does not require pre-cooling or JT valve.
Examples of State Functions
P, T, V, s
Examples of Path Functions
U, H, F, G
Spin of Para Hydrogen
Antisymmetric
Spin of Ortho Hydrogen
Symmetric
Inversion Temperature of Neon
260 K
Van der Walls Pressure Term
a
Van der Walls Volume Term
b
Nitrogen Boiling Point
77 K
Negative Yield
System will not ‘start up’ with working gas warmed up after JT valve expansion
Requirement of LH cyce
Pre cooling required due to hydrogen’s inversion temperature of 202 K requiring a cryogenic liquid coolant
Liquid Yield
Ratio of work per unit compressed to work per unit liquified
Ortho Hydrogen Species
aa, ab+ba, bb
Para Hydrogen Species
ab-ba
Ortho-Para heat conversion
Heat conversion higher than heat for vaporisation