Thermodynamics

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Isothermal Process [T=C]

Condition:
𝑃𝑉 𝑛 = 𝐶
𝑤ℎ𝑒𝑟𝑒: 𝑛 = 1
1. Relationship of P and V;
𝑃1 𝑉1 = 𝑃2 𝑉2
2. Non-flow Work
𝑉2

𝑊𝑁𝐹 = ∫ 𝑃𝑑𝑉
𝑉1

𝑃𝑉 = 𝐶
𝐶
𝑃=
𝑉
𝑉2
𝑑𝑉
𝑊𝑁𝐹 =𝐶∫
𝑉
𝑉1

𝑊𝑁𝐹 = 𝐶[ln 𝑉] 𝑓𝑟𝑜𝑚 𝑉1 𝑡𝑜 𝑉2


𝑊𝑁𝐹 = 𝐶[ln 𝑉2 − ln 𝑉1 ]
𝑉2
𝑊𝑁𝐹 = 𝐶[ln ]
𝑉1
𝑏𝑢𝑡: 𝑃𝑉 = 𝐶
𝑉2
𝑊𝑁𝐹 = 𝑃𝑉[ln ]
𝑉1
𝑃1 𝑉1 = 𝑃2 𝑉2
𝑉2
𝑊𝑁𝐹 = 𝑃1 𝑉1 ln
𝑉1
𝑃1 𝑉2
=
𝑃2 𝑉1
𝑃1
𝑊𝑁𝐹 = 𝑃1 𝑉1 ln
𝑃2
𝑃1 𝑉1 = 𝑚𝑅𝑇1
𝑃1
𝑊𝑁𝐹 = 𝑚𝑅𝑇 ln
𝑃2
3. Change in Enthalpy
∆ℎ = 𝑚𝐶𝑝 ∆𝑇
𝑏𝑢𝑡: 𝑇 = 𝐶; 𝑇1 = 𝑇2
∆ℎ = 0
4. Change in Internal Energy
∆𝑈 = 𝑚𝐶𝑣 ∆𝑇 = 0
5. Heat [T=C]
𝑄 = ∆𝑃𝐸 + ∆𝐾𝐸 + ∆ℎ + 𝑊𝑁𝐹
𝑉2
𝑄 = 𝑃1 𝑉1 ln
𝑉1
6. Change in Entropy
𝑉
𝑄 𝑃1 𝑉1 ln 𝑉2
1
∆𝑠 = =
𝑇 𝑇
𝑃1 𝑉1 𝑉2
∆𝑠 = ln
𝑇 𝑉1
𝑃1 𝑉1
𝑏𝑢𝑡: = 𝑚𝑅
𝑇
𝑉2
∆𝑠 = 𝑚𝑅 ln
𝑉1
7. Work Steady Flow
𝑄 = ∆𝑃𝐸 + ∆𝐾𝐸 + ∆ℎ + 𝑊𝑆𝐹
𝑉2
𝑄 = 𝑊𝑆𝐹 = 𝑃1 𝑉1 ln
𝑉1
Isentropic Process [S=C]
Adiabatic System [Q=0]
1. Reversible adiabatic system (ideal)
2. Irreversible adiabatic system (actual)
Condition:
𝑃𝑉 𝑘 = 𝐶
1. Relationship of P, V, and T
𝑃1 𝑉1 𝑃2 𝑉2
=
𝑇1 𝑇2
𝑃1 𝑉1 𝑘 = 𝑃2 𝑉2 𝑘

𝑃1 𝑉2 𝑇1
=
𝑃2 𝑉1 𝑇2
𝑇1 𝑉2 𝑘−1
= 𝑘−1
𝑇2 𝑉1
𝑇1 𝑉2 𝑘−1
=[ ]
𝑇2 𝑉1
𝑃1 𝑉1 𝑃2 𝑉2
=
𝑇1 𝑇2
𝑃1 𝑉1 𝑘 = 𝑃2 𝑉2 𝑘
𝑉1 𝑃2 𝑇1
=
𝑉2 𝑃1 𝑇2
𝑘−1
𝑇1 𝑃1 𝑘
=[ ]
𝑇2 𝑃2
2. Work Non-Flow
𝑉2

𝑊𝑁𝐹 = ∫ 𝑃𝑑𝑉
𝑉1

𝐶𝑜𝑛𝑑𝑖𝑡𝑖𝑜𝑛: 𝑃𝑉 𝑘 = 𝐶
𝐶
𝑃= 𝑘
𝑉
𝑉2
𝑑𝑉
𝑊𝑁𝐹 =𝐶∫ 𝑘
𝑉
𝑉1
𝑉2

𝑊𝑁𝐹 = 𝐶 ∫ 𝑉 −𝑘 𝑑𝑉
𝑉1

𝑣 𝑛+1
𝑤ℎ𝑒𝑟𝑒 𝑣 = 𝑉 𝑎𝑛𝑑 𝑛 = −𝑘
𝑛+1
𝑉 −𝑘+1
𝑊𝑁𝐹 = 𝐶 [ ] 𝑓𝑟𝑜𝑚 𝑉1 𝑡𝑜 𝑉2
−𝑘 + 1
𝑉2 −𝑘+1 𝑉1 −𝑘+1
𝑊𝑁𝐹 =𝐶[ − ]
−𝑘 + 1 −𝑘 + 1
𝑉2 −𝑘+1 − 𝑉1 −𝑘+1
𝑊𝑁𝐹 =𝐶[ ]
1−𝑘
𝑃𝑉 𝑘 = 𝐶
−𝑘+1 −𝑘+1
𝑉2 − 𝑉1
𝑊𝑁𝐹 = 𝑃𝑉 𝑘 [ ]
1−𝑘
[𝑃2 𝑉2 𝑘 ][𝑉2 −𝑘+1 ] − [𝑃1 𝑉1 𝑘 ][𝑉1 −𝑘+1 ]
𝑊𝑁𝐹 =
1−𝑘
𝑃1 𝑉1 𝑘 = 𝑃2 𝑉2 𝑘
𝑃2 𝑉2 𝑘−𝑘+1 − 𝑃1 𝑉1 𝑘−𝑘+1
𝑊𝑁𝐹 =
1−𝑘
𝑃2 𝑉2 − 𝑃1 𝑉1
𝑊𝑁𝐹 =
1−𝑘
3. Change in Enthalpy
∆ℎ = 𝑚𝐶𝑝 ∆𝑇
4. Change in Internal Energy
∆𝑈 = 𝑚𝐶𝑣 ∆𝑇
5. Heat
𝑄=0
6. Change in Entropy [s=C]
∆𝑠 = 𝑠2 − 𝑠1 = 0
7. Work Steady Flow
𝑄 = ∆𝑃𝐸 + ∆𝐾𝐸 + ∆ℎ + 𝑊𝑆𝐹
𝑊𝑆𝐹 = −∆ℎ = −[ℎ2 − ℎ1 ]
𝑊𝑆𝐹 = ℎ1 − ℎ2
Polytropic Process
Condition:
𝑃𝑉 𝑛 = 𝐶
1. Relationship of P, V, and T
𝑃1 𝑉1 𝑃2 𝑉2
=
𝑇1 𝑇2
𝑃1 𝑉1 𝑛 = 𝑃2 𝑉2 𝑛
𝑇1 𝑉2 𝑛−1
=[ ]
𝑇2 𝑉1
𝑛−1
𝑇1 𝑃1 𝑛
=[ ]
𝑇2 𝑃2
2. Non-flow Work
𝑃2 𝑉2 − 𝑃1 𝑉1
𝑊𝑁𝐹 =
1−𝑛
3. Change in Enthalpy
∆ℎ = 𝑚𝐶𝑝 ∆𝑇
4. Change in Internal Energy
∆𝑈 = 𝑚𝐶𝑣 ∆𝑇
5. Heat
𝑄 = 𝑚𝐶𝑛 ∆𝑇
6. Change in Entropy
𝑇2
∆𝑠 = 𝑚𝐶𝑛 ln
𝑇1
7. Work Steady Flow
𝑄 = ∆𝑃𝐸 + ∆𝐾𝐸 + ∆ℎ + 𝑊𝑆𝐹
𝑊𝑆𝐹 = 𝑄 − ∆ℎ

Example:
Helium (k = 1.666) is compressed
isentropically from 745 kPaa, 5.1 m3/min,
5°C to 1765 kPaa. Find the following:
1. Final volume flow rate in m3/min.
2. Final temperature in °C.
3. Work non-flow in kJ/min.
Given:
P1 = 745 kPaa
Ṿ1 = 5.1 m3/min
T1 = 5°C
P2 = 1765 kPaa
Required:
1. Ṿ2 = ? m3/min
2. T2 = ? °C
3. WNF = ? kJ/min
Solution:
**Compressed isentropically
𝑃1 𝑉1 𝑘 = 𝑃2 𝑉2 𝑘
𝑃1 𝑉1 𝑘
= 𝑉2 𝑘
𝑃2
1
𝑘 𝑘 𝑃1
1 1 𝑘
𝑘 𝑘
[𝑉2 ] = [𝑉1 ] [ ]
𝑃2
1
𝑃1 𝑘
Ṿ2 = Ṿ1 [ ]
𝑃2
1
3
𝑚 745 𝑘𝑃𝑎𝑎 1.666
Ṿ2 = [5.1 ][ ]
𝑚𝑖𝑛 1765 𝑘𝑃𝑎𝑎
𝑚3
Ṿ2 = 3.038975345 (𝐴𝑁𝑆𝑊𝐸𝑅 )
𝑚𝑖𝑛

2.
𝑘−1
𝑇2 𝑃2 𝑘
=[ ]
𝑇1 𝑃1
𝑘−1
𝑃2 𝑘
𝑇2 = 𝑇1 [ ]
𝑃1
𝑤ℎ𝑒𝑟𝑒: 𝑇1 = 5℃ + 273 = 278 𝐾
1.666−1
1765 𝑘𝑃𝑎𝑎1.666
𝑇2 = [278 𝐾 ] [ ]
745 𝑘𝑃𝑎𝑎
𝑇2 = 392.4553316 𝐾 − 273
𝑇2 = 119.4553316℃ (𝐴𝑁𝑆𝑊𝐸𝑅 )

3.
Work Non-Flow in kJ/min
𝑃2 Ṿ2 − 𝑃1 Ṿ1
𝑊𝑁𝐹 =
1−𝑘
𝑘𝑁 𝑚3 𝑘𝑁 𝑚3
[1765 2 ] [3.038975345 ] − [745 2 ] [5.1 ]
𝑚 𝑚𝑖𝑛 𝑚 𝑚𝑖𝑛
𝑊𝑁𝐹 =
1 − 1.666
𝑘𝐽
𝑊𝑁𝐹 = −2348.786012 (𝐴𝑁𝑆𝑊𝐸𝑅)
𝑚𝑖𝑛

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