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APSC 252 Final Exam Formula Sheet

This document provides a formula sheet for the APSC252 final exam covering: 1. Key equations for pressure, temperature, specific volume, two-phase mixtures, compressed liquids, ideal gases, solids and liquids. 2. Equations for energy, work, heat, closed and open systems. 3. Key equations for steady state, steady flow through control volumes. 4. Equations for common thermodynamic processes and cycles including heat engines, refrigerators, and heat pumps.

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0% found this document useful (0 votes)
215 views

APSC 252 Final Exam Formula Sheet

This document provides a formula sheet for the APSC252 final exam covering: 1. Key equations for pressure, temperature, specific volume, two-phase mixtures, compressed liquids, ideal gases, solids and liquids. 2. Equations for energy, work, heat, closed and open systems. 3. Key equations for steady state, steady flow through control volumes. 4. Equations for common thermodynamic processes and cycles including heat engines, refrigerators, and heat pumps.

Uploaded by

Yoslo
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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APSC252 Final Exam Formula Sheet

Pressure, temperature and specific volume

Pressure: 𝑃 = 𝐹/𝐴 Absolute temperature: 𝑇[𝐾] = 𝑇[°𝐶] + 273.15

Absolute pressure: Pabs=Patm+ ρgh


Gage pressure: Pgage=Pabs - Patm 𝕍 1
Specific volume: 𝑣=𝑚=𝜌 (𝕍: volume)

Two-phase mixture
𝑚𝑣𝑎𝑝𝑜𝑢𝑟
Quality: 𝑥 =
𝑚𝑚𝑖𝑥𝑡𝑢𝑟𝑒
Specific volume: 𝑣 = 𝑣𝑓 + 𝑥𝑣𝑓𝑔 = (1 − 𝑥)𝑣𝑓 + 𝑥𝑣𝑔 , 𝑣𝑓𝑔 = 𝑣𝑔 − 𝑣𝑓
Specific internal energy: 𝑢 = 𝑢𝑓 + 𝑥𝑢𝑓𝑔 = (1 − 𝑥)𝑢𝑓 + 𝑥𝑢𝑔 , 𝑢𝑓𝑔 = 𝑢𝑔 − 𝑢𝑓
Specific enthalpy: ℎ = ℎ𝑓 + 𝑥ℎ𝑓𝑔 = (1 − 𝑥)ℎ𝑓 + 𝑥ℎ𝑔 , ℎ𝑓𝑔 = ℎ𝑔 − ℎ𝑓
Specific entropy: 𝑠 = 𝑠𝑓 + 𝑥𝑠𝑓𝑔 = (1 − 𝑥)𝑠𝑓 + 𝑥𝑠𝑔 , 𝑠𝑓𝑔 = 𝑠𝑔 − 𝑠𝑓

Compressed liquid (when tables are not available)


𝑣 ≈ 𝑣𝑓@𝑇 𝑢 ≈ 𝑢𝑓@𝑇 ℎ ≈ ℎ𝑓@𝑇 𝑠 ≈ 𝑠𝑓@𝑇

Ideal gas
EOS: 𝑃𝑣 = 𝑅𝑇 or 𝑃𝕍 = 𝑚𝑅𝑇 (R: gas constant; 𝕍: volume; 𝑣: specific volume) (T in Kelvin)
𝑘𝑅 𝑅
Specific heats: 𝑐𝑝 = 𝑐𝑣 + 𝑅, 𝑘 = 𝑐𝑝 /𝑐𝑣 , 𝑐𝑝 = 𝑘−1 , 𝑐𝑣 = 𝑘−1
Specific enthalpy and specific internal energy: ℎ = 𝑢 + 𝑃𝑣 = 𝑢 + 𝑅𝑇
𝑢 = 𝑐𝑣 𝑇 , ℎ = 𝑐𝑝 𝑇
Change in specific internal energy (assuming constant 𝑐𝑣0 ) 𝑢2 − 𝑢1 = 𝑐𝑣0 (𝑇2 − 𝑇1 )
Change in specific enthalpy (assuming constant 𝑐𝑝0 ) ℎ2 − ℎ1 = 𝑐𝑝0 (𝑇2 − 𝑇1 )
Change in specific entropy
0 0 ) 𝑃
• Accurate method 𝑠2 − 𝑠1 = (𝑠𝑇2 − 𝑠𝑇1 − 𝑅ln 𝑃2
1
• Approximate method (assuming constant 𝑐𝑣0 and 𝑐𝑝0 )
𝑇2 𝑃2 𝑇2 𝑣2
𝑠2 − 𝑠1 = 𝑐𝑝0 ln − 𝑅ln or 𝑠2 − 𝑠1 = 𝑐𝑣0 ln + 𝑅ln (T in Kelvin)
𝑇1 𝑃1 𝑇1 𝑣1

𝑃𝑣 𝑃 𝑇
Compressibility factor: 𝑍 = ; reduced pressure and temperature: 𝑃𝑟 = , 𝑇𝑟 = 𝑇 (T in Kelvin)
𝑅𝑇 𝑃𝑐 𝑐

Solid and liquid


Specific heats: 𝑐 = 𝑐𝑝 = 𝑐𝑣
Change in specific internal energy or specific enthalpy: ℎ2 − ℎ1 ≈ 𝑢2 − 𝑢1 ≈ 𝑐(𝑇2 − 𝑇1 )
𝑇2
Change in specific entropy: 𝑠2 − 𝑠1 = 𝑐ln (T in Kelvin)
𝑇1

1
Energy, work and heat

Total energy: 𝐸 = 𝑈 + 𝐾𝐸 + 𝑃𝐸 = 𝑚𝑢 + ½ 𝑚𝑉 2 + 𝑚𝑔𝑧 (V: velocity)


Specific total energy: 𝑒 = 𝐸/𝑚 = 𝑢 + ½ 𝑉 2 + 𝑔𝑧 (V: velocity)
Specific internal energy: 𝑢 = 𝑈/𝑚

Specific heat transfer: 𝑞 = 𝑄/𝑚


2
Boundary work: 1W2= ∫1 𝑃𝑑𝕍 (area under the P- 𝕍 diagram; 𝕍: volume)
Specific work: 𝑤 = 𝑊/𝑚
2 1
Spring work: 𝑊spring = ∫1 𝐹𝑑𝑥 = 𝐾(𝑥22 − 𝑥12 )
2
̇
Shaft power: 𝑊 = 𝑇𝜔 (T: torque)

Closed systems (control mass)


1st law: E2 − E1 = 1Q2 − 1W2 or U2 − U1 = 1Q2 − 1W2 (assuming KE=0, PE=0)
𝑄𝑘
2nd law: 𝑆2 − 𝑆1 = ∑ + 𝑆𝑔𝑒𝑛 (𝑆𝑔𝑒𝑛 ≥ 0) (T in Kelvin)
𝑇𝑘

Volume flow rate and mass flow rate


Volume flow rate: 𝕍̇ = 𝑉𝑎𝑣𝑔,𝑛 𝐴 = 𝑚̇𝑣 (𝕍: volume, V: velocity, 𝑣 : specific volume)
Mass flow rate: 𝑚̇ = 𝜌𝕍̇ = 𝜌𝑉𝑎𝑣𝑔,𝑛 𝐴

Steady-state, steady flow through a control volume (open system)


Conservation of mass: ∑ 𝑚̇𝑖 = ∑ 𝑚̇𝑒
1 1
1st law: 𝑄̇𝑐𝑣 + ∑ 𝑚̇𝑖 (ℎ𝑖 + 𝑉𝑖2 + 𝑔𝑧𝑖 ) = 𝑊̇𝑐𝑣 + ∑ 𝑚̇𝑒 (ℎ𝑒 + 𝑉𝑒2 + 𝑔𝑧𝑒 )
2 2
𝑄̇𝑐.𝑣.
2nd law: ∑ 𝑚̇𝑒 𝑠𝑒 − ∑ 𝑚̇𝑖 𝑠𝑖 = ∑ ̇
+ 𝑆𝑔𝑒𝑛 ̇
(𝑆𝑔𝑒𝑛 ≥ 0) (T in Kelvin)
𝑇

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: 𝑚̇𝑖 = 𝑚̇𝑒 , ℎ𝑖 = ℎ𝑒 (assuming 𝑄̇𝑐𝑣 = 0, 𝑊̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)
1 1
• Nozzle and diffuser: 𝑚̇𝑖 = 𝑚̇𝑒 , ℎ𝑖 + 𝑉𝑖2 = ℎ𝑒 + 𝑉𝑒2 (assuming 𝑄̇𝑐𝑣 = 0, 𝑊̇𝑐𝑣 = 0, ΔPE = 0)
2 2

• Mixing chamber: ∑ 𝑚̇𝑖 = ∑ 𝑚̇𝑒 , 𝑄̇𝑐𝑣 + ∑ 𝑚̇𝑖 ℎ𝑖 = ∑ 𝑚̇𝑒 ℎ𝑒 (assuming 𝑊̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)

• Heat exchanger: 𝑚̇𝑖 = 𝑚̇𝑒 (for each of the hot and cold streams, separately)

𝑄̇𝑐𝑣 + ∑ 𝑚̇𝑖 ℎ𝑖 = ∑ 𝑚̇𝑒 ℎ𝑒 (assuming 𝑊̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)


• Turbine: 𝑚̇𝑖 = 𝑚̇𝑒 = 𝑚̇ , 𝑊̇𝑠ℎ𝑎𝑓𝑡 = 𝑚̇(ℎ𝑖 − ℎ𝑒 ) (assuming 𝑄̇𝑐𝑣 = 0, ΔPE = 0, ΔKE = 0)

• Compressor: 𝑚̇𝑖 = 𝑚̇𝑒 = 𝑚̇ , 𝑊̇𝑠ℎ𝑎𝑓𝑡 = 𝑚̇(ℎ𝑒 − ℎ𝑖 ) (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) or 𝑄̇𝑐𝑣 = 0 (for control volumes)
• Reversible process: 𝑆𝑔𝑒𝑛 = 0 (for closed systems) or ̇
𝑆𝑔𝑒𝑛 = 0 (for control volumes)
• Isentropic process: reversible adiabatic process
• Polytropic process: 𝑃𝕍𝑛 = 𝑐𝑜𝑛𝑠𝑡. (𝕍: volume)
Boundary work in a polytropic process
𝑃2 𝕍2 −𝑃1 𝕍1
o 1W2= (𝑛 ≠ 1)
1−𝑛
𝕍 𝕍 𝕍
o 1W2= 𝑃1 𝕍1 𝑙𝑛 𝕍2 = 𝑃2 𝕍2 𝑙𝑛 𝕍2 = 𝑚𝑅𝑇 𝑙𝑛 𝕍2 (𝑛 = 1) (T in Kelvin)
1 1 1

Heat engines
• Any heat engine
o Net work output: 𝑊𝑛𝑒𝑡,𝑜𝑢𝑡 = 𝑄𝐻 − 𝑄𝐿
𝑊𝑛𝑒𝑡,𝑜𝑢𝑡 𝑄
o Thermal efficiency: 𝜂𝑡ℎ = = 1 − 𝑄𝐿
𝑄𝐻 𝐻
𝑇𝐿
• Carnot heat engine: 𝜂𝑡ℎ,𝑟𝑒𝑣 = 1 − (T in Kelvin)
𝑇𝐻

Refrigerators
• Any refrigerator
o Net work input: 𝑊𝑛𝑒𝑡,𝑖𝑛 = 𝑄𝐻 − 𝑄𝐿
𝑄𝐿 𝑄𝐿 1
o Coefficient of performance: 𝐶𝑂𝑃𝑅 = =𝑄 =𝑄
𝑊𝑛𝑒𝑡,𝑖𝑛 𝐻 −𝑄𝐿 𝐻 /𝑄𝐿 −1
𝑇𝐿 1
• Carnot refrigerator: 𝐶𝑂𝑃𝑅,𝑟𝑒𝑣 = =𝑇 (T in Kelvin)
𝑇𝐻 −𝑇𝐿 𝐻 /𝑇𝐿 −1

Heat pumps
• Any heat pump
o Net work input: 𝑊𝑛𝑒𝑡,𝑖𝑛 = 𝑄𝐻 − 𝑄𝐿
𝑄𝐻 𝑄𝐻 1
o Coefficient of performance: 𝐶𝑂𝑃𝐻𝑃 = =𝑄 = 1−𝑄
𝑊𝑛𝑒𝑡,𝑖𝑛 𝐻 −𝑄𝐿 𝐿 /𝑄𝐻
𝑇𝐻 1
• Carnot heat pump: 𝐶𝑂𝑃𝐻𝑃,𝑟𝑒𝑣 = = 1−𝑇 /𝑇 (T in Kelvin)
𝑇𝐻 −𝑇𝐿 𝐿 𝐻

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