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APSC252 final exam formula sheet

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APSC252 Final Exam Formula Sheet
Pressure, temperature and specific volume
Absolute temperature: 𝑇[𝐾] = 𝑇[°πΆ] + 273.15
Pressure: 𝑃 = 𝐹/𝐴
Absolute pressure: Pabs=Patm+ ρgh
Gage pressure: Pgage=Pabs - Patm
Specific volume:
𝕍
1
𝑣=π‘š=𝜌
(𝕍: volume)
Two-phase mixture
Quality: π‘₯
=
π‘šπ‘£π‘Žπ‘π‘œπ‘’π‘Ÿ
π‘šπ‘šπ‘–π‘₯π‘‘π‘’π‘Ÿπ‘’
Specific volume: 𝑣 = 𝑣𝑓 + π‘₯𝑣𝑓𝑔 = (1 − π‘₯)𝑣𝑓 + π‘₯𝑣𝑔 , 𝑣𝑓𝑔 = 𝑣𝑔 − 𝑣𝑓
Specific internal energy: 𝑒 = 𝑒𝑓 + π‘₯𝑒𝑓𝑔 = (1 − π‘₯)𝑒𝑓 + π‘₯𝑒𝑔 , 𝑒𝑓𝑔 = 𝑒𝑔 − 𝑒𝑓
Specific enthalpy: β„Ž = β„Žπ‘“ + π‘₯β„Žπ‘“π‘” = (1 − π‘₯)β„Žπ‘“ + π‘₯β„Žπ‘” , β„Žπ‘“π‘” = β„Žπ‘” − β„Žπ‘“
Specific entropy: 𝑠 = 𝑠𝑓 + π‘₯𝑠𝑓𝑔 = (1 − π‘₯)𝑠𝑓 + π‘₯𝑠𝑔 , 𝑠𝑓𝑔 = 𝑠𝑔 − 𝑠𝑓
Compressed liquid (when tables are not available)
𝑣 ≈ 𝑣𝑓@𝑇
𝑒 ≈ 𝑒𝑓@𝑇
β„Ž ≈ β„Žπ‘“@𝑇
𝑠 ≈ 𝑠𝑓@𝑇
Ideal gas
EOS: 𝑃𝑣 = 𝑅𝑇
or 𝑃𝕍 = π‘šπ‘…π‘‡ (R: gas constant; 𝕍: volume; 𝑣: specific volume) (T in Kelvin)
Specific heats: 𝑐𝑝 = 𝑐𝑣 + 𝑅, π‘˜ = 𝑐𝑝 /𝑐𝑣 ,
π‘˜π‘…
𝑅
𝑐𝑝 = π‘˜−1 , 𝑐𝑣 = π‘˜−1
Specific enthalpy and specific internal energy: β„Ž = 𝑒 + 𝑃𝑣 = 𝑒 + 𝑅𝑇
𝑒 = 𝑐𝑣 𝑇 ,
Change in specific internal energy (assuming constant 𝑐𝑣0 )
Change in specific enthalpy (assuming constant 𝑐𝑝0 )
β„Ž = 𝑐𝑝 𝑇
𝑒2 − 𝑒1 = 𝑐𝑣0 (𝑇2 − 𝑇1 )
β„Ž2 − β„Ž1 = 𝑐𝑝0 (𝑇2 − 𝑇1 )
Change in specific entropy
𝑃
0
0 )
𝑠2 − 𝑠1 = (𝑠𝑇2
− 𝑠𝑇1
− 𝑅ln 𝑃2
•
Accurate method
•
Approximate method (assuming constant 𝑐𝑣0 and 𝑐𝑝0 )
1
𝑠2 − 𝑠1 = 𝑐𝑝0 ln
Compressibility factor: 𝑍 =
𝑇2
𝑇1
𝑃𝑣
𝑅𝑇
− 𝑅ln
𝑃2
𝑃1
or
𝑠2 − 𝑠1 = 𝑐𝑣0 ln
; reduced pressure and temperature: π‘ƒπ‘Ÿ =
𝑇2
𝑇1
𝑃
𝑃𝑐
+ 𝑅ln
𝑣2
𝑣1
𝑇
, π‘‡π‘Ÿ = 𝑇
𝑐
(T in Kelvin)
(T in Kelvin)
Solid and liquid
Specific heats: 𝑐 = 𝑐𝑝 = 𝑐𝑣
Change in specific internal energy or specific enthalpy: β„Ž2 − β„Ž1 ≈ 𝑒2 − 𝑒1 ≈ 𝑐(𝑇2 − 𝑇1 )
𝑇2
Change in specific entropy: 𝑠2 − 𝑠1 = 𝑐ln
(T in Kelvin)
𝑇1
1
Energy, work and heat
Total energy: 𝐸 = π‘ˆ + 𝐾𝐸 + 𝑃𝐸 = π‘šπ‘’ + ½ π‘šπ‘‰ 2 + π‘šπ‘”π‘§ (V: velocity)
Specific total energy: 𝑒 = 𝐸/π‘š = 𝑒 + ½ 𝑉 2 + 𝑔𝑧 (V: velocity)
Specific internal energy: 𝑒 = π‘ˆ/π‘š
Specific heat transfer: π‘ž = 𝑄/π‘š
2
Boundary work: 1W2= ∫1 𝑃𝑑𝕍 (area under the P- 𝕍 diagram; 𝕍: volume)
Specific work: 𝑀 = π‘Š/π‘š
2
1
Spring work: π‘Šspring = ∫1 𝐹𝑑π‘₯ = 𝐾(π‘₯22 − π‘₯12 )
2
Μ‡
Shaft power: π‘Š = π‘‡πœ” (T: torque)
Closed systems (control mass)
1st law: E2 − E1 = 1Q2 − 1W2
2nd law: 𝑆2 − 𝑆1 = ∑
π‘„π‘˜
π‘‡π‘˜
or
+ 𝑆𝑔𝑒𝑛
U2 − U1 = 1Q2 − 1W2 (assuming KE=0, PE=0)
(𝑆𝑔𝑒𝑛 ≥ 0)
(T in Kelvin)
Volume flow rate and mass flow rate
Volume flow rate: 𝕍̇ = π‘‰π‘Žπ‘£π‘”,𝑛 𝐴 = π‘šΜ‡π‘£ (𝕍: volume, V: velocity, 𝑣 : specific volume)
Mass flow rate: π‘šΜ‡ = πœŒπ•Μ‡ = πœŒπ‘‰π‘Žπ‘£π‘”,𝑛 𝐴
Steady-state, steady flow through a control volume (open system)
Conservation of mass: ∑ π‘šΜ‡π‘– = ∑ π‘šΜ‡π‘’
1
1
1st law: 𝑄̇𝑐𝑣 + ∑ π‘šΜ‡π‘– (β„Žπ‘– + 𝑉𝑖2 + 𝑔𝑧𝑖 ) = π‘ŠΜ‡π‘π‘£ + ∑ π‘šΜ‡π‘’ (β„Žπ‘’ + 𝑉𝑒2 + 𝑔𝑧𝑒 )
2
2nd law: ∑ π‘šΜ‡π‘’ 𝑠𝑒 − ∑ π‘šΜ‡π‘– 𝑠𝑖 = ∑
2
𝑄̇𝑐.𝑣.
𝑇
Μ‡
+ 𝑆𝑔𝑒𝑛
Μ‡
(𝑆𝑔𝑒𝑛
≥ 0)
(T in Kelvin)
Applications of the conservation of mass and the 1st law in different steady-state, steady flow devices
(note: the following derived relations are valid only if the given assumptions can be applied.)
• Throttling valve: π‘šΜ‡π‘– = π‘šΜ‡π‘’ , β„Žπ‘– = β„Žπ‘’ (assuming 𝑄̇𝑐𝑣 = 0, π‘ŠΜ‡π‘π‘£ = 0, ΔPE = 0, ΔKE = 0)
1
1
• Nozzle and diffuser: π‘šΜ‡π‘– = π‘šΜ‡π‘’ , β„Žπ‘– + 𝑉𝑖2 = β„Žπ‘’ + 𝑉𝑒2 (assuming 𝑄̇𝑐𝑣 = 0, π‘ŠΜ‡π‘π‘£ = 0, ΔPE = 0)
2
2
• Mixing chamber: ∑ π‘šΜ‡π‘– = ∑ π‘šΜ‡π‘’ , 𝑄̇𝑐𝑣 + ∑ π‘šΜ‡π‘– β„Žπ‘– = ∑ π‘šΜ‡π‘’ β„Žπ‘’ (assuming π‘ŠΜ‡π‘π‘£ = 0, ΔPE = 0, ΔKE = 0)
• Heat exchanger: π‘šΜ‡π‘– = π‘šΜ‡π‘’ (for each of the hot and cold streams, separately)
𝑄̇𝑐𝑣 + ∑ π‘šΜ‡π‘– β„Žπ‘– = ∑ π‘šΜ‡π‘’ β„Žπ‘’ (assuming π‘ŠΜ‡π‘π‘£ = 0, ΔPE = 0, ΔKE = 0)
• Turbine: π‘šΜ‡π‘– = π‘šΜ‡π‘’ = π‘šΜ‡ , π‘ŠΜ‡π‘ β„Žπ‘Žπ‘“π‘‘ = π‘šΜ‡(β„Žπ‘– − β„Žπ‘’ ) (assuming 𝑄̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)
• Compressor: π‘šΜ‡π‘– = π‘šΜ‡π‘’ = π‘šΜ‡ , π‘ŠΜ‡π‘ β„Žπ‘Žπ‘“π‘‘ = π‘šΜ‡(β„Žπ‘’ − β„Žπ‘– ) (assuming 𝑄̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)
2
Processes
• Isobaric process: P=const
• Isochoric process: v=const
• Isothermal process: T=const
• Adiabatic process: heat transfer Q=0 (for closed systems)
• Reversible process: 𝑆𝑔𝑒𝑛 = 0 (for closed systems)
𝑄̇𝑐𝑣 = 0 (for control volumes)
or
Μ‡
𝑆𝑔𝑒𝑛
= 0 (for control volumes)
or
• Isentropic process: reversible adiabatic process
• Polytropic process: 𝑃𝕍𝑛 = π‘π‘œπ‘›π‘ π‘‘. (𝕍: volume)
Boundary work in a polytropic process
o
1W2=
𝑃2 𝕍2 −𝑃1 𝕍1
o
1W2=
𝑃1 𝕍1 𝑙𝑛 𝕍2 = 𝑃2 𝕍2 𝑙𝑛 𝕍2 = π‘šπ‘…π‘‡ 𝑙𝑛 𝕍2 (𝑛 = 1)
(𝑛 ≠ 1)
1−𝑛
𝕍
𝕍
1
𝕍
1
Heat engines
• Any heat engine
o Net work output: π‘Šπ‘›π‘’π‘‘,π‘œπ‘’π‘‘ = 𝑄𝐻 − 𝑄𝐿
o
Thermal efficiency: πœ‚π‘‘β„Ž =
π‘Šπ‘›π‘’π‘‘,π‘œπ‘’π‘‘
• Carnot heat engine: πœ‚π‘‘β„Ž,π‘Ÿπ‘’π‘£ = 1 −
𝑄𝐻
𝑇𝐿
𝑄
= 1 − 𝑄𝐿
𝐻
(T in Kelvin)
𝑇𝐻
Refrigerators
• Any refrigerator
o Net work input: π‘Šπ‘›π‘’π‘‘,𝑖𝑛 = 𝑄𝐻 − 𝑄𝐿
o
Coefficient of performance: 𝐢𝑂𝑃𝑅 =
• Carnot refrigerator: 𝐢𝑂𝑃𝑅,π‘Ÿπ‘’π‘£ =
𝑇𝐿
𝑇𝐻 −𝑇𝐿
=𝑇
𝑄𝐿
π‘Šπ‘›π‘’π‘‘,𝑖𝑛
1
Coefficient of performance: 𝐢𝑂𝑃𝐻𝑃 =
• Carnot heat pump: 𝐢𝑂𝑃𝐻𝑃,π‘Ÿπ‘’π‘£ =
𝑇𝐻
𝑇𝐻 −𝑇𝐿
=𝑄
𝐻 /𝑇𝐿 −1
Heat pumps
• Any heat pump
o Net work input: π‘Šπ‘›π‘’π‘‘,𝑖𝑛 = 𝑄𝐻 − 𝑄𝐿
o
(T in Kelvin)
1
𝑄𝐻
π‘Šπ‘›π‘’π‘‘,𝑖𝑛
1
= 1−𝑇 /𝑇
𝐿
𝐻
𝑄𝐿
𝐻 −𝑄𝐿
=𝑄
1
𝐻 /𝑄𝐿 −1
(T in Kelvin)
=𝑄
𝑄𝐻
𝐻 −𝑄𝐿
1
= 1−𝑄
𝐿 /𝑄𝐻
(T in Kelvin)
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