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Conservation of
Energy in Closed
System
Thermodynamics
Universitas Pertamina
Learning Objectives
• Students are able to determine the boundary work, internal energy, &
enthalpy of a system
• Students are able to apply the concept of energy balance in simple
thermodynamic cases for closed system
Outline
General
Boundary Specific
energy
Work Heats
balance
General energy balance
General energy balance
In rate form
In differential form
Note:
E = Energy (generalization of all kinds of energy)
Energy balance for closed system
𝑄 + 𝑊 = ∆𝐸𝑠𝑦𝑠𝑡𝑒𝑚
𝑄 + 𝑊 = ∆𝐸𝐾 + ∆𝐸𝑃 + ∆𝑈
Q, kJ W, kJ Esystem initial, kJ Esystem final, kJ m, kg Δesystem, kJ/kg
350 ... 1020 860 3 ...
350 -130 550 ... 5 ...
... -260 600 ... 2 150
-500 ... 1400 900 7 ...
... 50 1000 ... 3 -200
Moving Boundary Work (PdV work)
• Synonims: Moving boundary work/boundary work/PdV work
𝛿𝑊𝑃𝑉 = F ds = −PA ds = −P dV
𝑉2
The moving boundary 𝑊𝑃𝑉 = − න 𝑃𝑖 𝑑𝑉 (Pi= P inside the piston)
𝑉1
𝑊𝑃𝑉 = 0
Boundary work – Isobaric process
• A frictionless piston–cylinder device contains 5 kg of steam at 400 kPa and
200oC. Heat is now transferred to the steam until the temperature reaches
250oC. If the piston is not attached to a shaft and its mass is constant,
determine the work done by the steam during this process.
𝑉2
𝑊𝑃𝑉 = − න 𝑃𝑖 𝑑𝑉
𝑉1
𝑉2
𝑊𝑃𝑉 = −𝑃𝑖 න 𝑑𝑉
𝑉1
𝑊𝑃𝑉 = −𝑃𝑖 ∆𝑉
Above scheme is for ilustration only
Boundary work – Isothermal process
• A piston–cylinder device initially contains 0.4 m3 of air at 100 kPa and 80°C.
The air is now compressed to 0.1 m3 in such a way that the temperature
inside the cylinder remains constant. Determine the work done during this
process.
• Air can be assumed as ideal gas
𝑃𝑉 = 𝑛𝑅𝑇
At constant n & T : 𝑃𝑉 = 𝐶
𝑉2 𝑉2 𝑉2
𝑊𝑃𝑉 = − 𝑉𝑑𝑃 𝑉 = −𝐶 𝑙𝑛 = −𝑃1 𝑉1 𝑙𝑛
1 𝑉1 𝑉1
Energy balance for closed system 𝑄 + 𝑊 = ∆𝐸𝑠𝑦𝑠𝑡𝑒𝑚
Note that the Δu and Δ h relations given here are not restricted to
any kind of process. They are valid for all processes.
Ideal Gas
• PV = nRuT • PV=mRT
• Ru= universal gas constant • R = gas constant (table A-1, A-2)
(same for all gases) 𝑅𝑢
• 𝑅 = depends on the
• Ru= 8.31447 kJ/kmol K 𝑀
substance
• 8.31447 kPa.m3/kmol K • M = molecular weight
• 0.0831447 bar.m3/kmol.K
substance R, kJ/kg.K
• 1545.37 ft.lbf/lbmol.R Air 0.2870
Helium 2.0769
Argon 0.2081
Nitrogen 0.2968
Specific Heats of Ideal Gases
• Ideal gas (ig) Pv=RT
• uig only a function of T u=u(T)
Ideal gas u, h, cv, & cp are f(T)
h=h(T)
• Thus, Cp & Cv are functions of T only • At low P real gases behave like
(at most) the partial derivative can ideal gas
be replaced by ordinary derivative • Called ideal-gas specific heats or
zero-pressure specific heats, Cp0
𝜕𝑢 and Cv0
𝑐𝑣 = 𝑑𝑢 = 𝑐𝑣 (𝑇)𝑑𝑇
𝜕𝑇 𝑣 • Specific heats data table A-2
𝜕ℎ
𝑐𝑃 = 𝑑ℎ = 𝑐𝑃 (𝑇)𝑑𝑇
𝜕𝑇 𝑃
Specific Heats of Ideal Gases
Ideal Cp0 for some gases
• Ideal-gas specific heats of monoatomic gases remain
constant
• Complex molecules (>2 atoms) higher Cp0 and
increase with T
• Variation of specific heat with T is smooth & may be
approximated as linear over small T intervals (a few
hundred degrees or less), so
2
𝑑𝑢 = 𝑐𝑣 (𝑇)𝑑𝑇 ∆𝑢 = න 𝑐𝑣 (𝑇)𝑑𝑇 ∆𝑢 = 𝑐𝑣,𝑎𝑣𝑔 (𝑇2 − 𝑇1 )
1
2
𝑑ℎ = 𝑐𝑃 (𝑇)𝑑𝑇 ∆ℎ = න 𝑐𝑃 (𝑇)𝑑𝑇 ∆ℎ = 𝑐𝑃,𝑎𝑣𝑔 (𝑇2 − 𝑇1 )
1
Specific heat relations of Ideal Gases