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1. (a) Determine the particular gas constants for the following substances, assuming
them to be perfect gases; argon, carbon dioxide and steam. Take the molar
masses to be 39.95, 44.01 and 18.015 kg/kmol respectively.
(b) What is the density of argon at 10 bar and 200oC, assuming it to be a perfect
gas? Calculate the percentage error if the actual density is 10.14kg/m3.
2. Air occupies a volume of 0.1m3 at a pressure and temperature of 2.0 bar and 25oC
respectively. Assuming the air to be a perfect gas, determine its mass.
The temperature of the air is raised to 150oC during a reversible non-flow constant
volume process. Taking cv to have a constant value of 0.723kJ/kg K, calculate the
changes in internal energy and enthalpy and the energy transferred as heat. What is
the pressure after heating? For air, R = 0.287kJ/kg K.
4. A perfect gas for which = 5/3 undergoes processes such that the state changes from
1 bar, 0.1m3 to 2 bar, 0.2m3. What are the changes in internal energy and enthalpy?
Why is it that the work done and the heat transferred cannot be calculated from the
information given?
If the change were carried out during a reversible non-flow constant pressure process
followed by a reversible non-flow constant volume process, what would be the
amount of work done and the heat transferred? Sketch the processes on a p, V
diagram.
1.
(a)
Argon
𝑅̃ 8.3145 kJ
𝑅= = = 0.2081
𝑚
̃ 39.95 kg K
Similarly
kJ
𝑅𝐶𝑂2 = 0.1889
kg K
kJ
𝑅𝐻2 𝑂 = 0.4615
kg K
(b)
𝑝𝑣 = 𝑅𝑇
𝑝
𝜌=
𝑅𝑇
Argon
𝑝 10 × 105 kg
𝜌= = 3
= 10.16 3
𝑅𝑇 0.2081 × 10 (200 + 273) m
(c)
Percentage error in densities:
Argon
(10.16 − 10.14)
100 = 0.2%
10.14
2.
𝑝1 𝑉1 = 𝑚𝑅𝑇1
𝑝1 𝑉1 2 × 105 × 0.1
𝑚= = = 0.2338kg
𝑅𝑇1 0.287 × 103 × (25 + 273)
𝑈2 − 𝑈1 = 𝑚𝑐𝑣 (𝑇2 − 𝑇1 )
𝐻2 − 𝐻1 = 𝑚𝑐𝑝 (𝑇2 − 𝑇1 )
Thus
kJ
𝑐𝑝 = 𝑅 + 𝑐𝑣 = 0.287 + 0.723 = 1.01
kgK
(𝑇 )
𝐻2 − 𝐻1 = 𝑚𝑐𝑝 2 − 𝑇1 = 0.2338 × 1.01 × 125 = 29.52kJ
𝑄12 + 𝑊12 = 𝑈2 − 𝑈1
For a reversible constant volume process 𝑊12 = 0
𝑄12 = 𝑈2 − 𝑈1 = 21.3kJ
𝑝1 𝑉1 𝑝2 𝑉2
= and 𝑉1 = 𝑉2
𝑇1 𝑇2
𝑝1 𝑇2 2 × (150 + 273)
𝑝2 = = 2.84bar
𝑇1 (25 + 273)
3.
𝑅̃ 8.3145 kJ
𝑅= = = 0.2968
𝑚
̃ 28.01 kg K
𝑅𝑇2 𝑅𝑇1
𝑣2 − 𝑣1 = − and 𝑝1 = 𝑝2 = 2bar
𝑝2 𝑝1
0.2968 × 103 m3
𝑣2 − 𝑣1 = (750 − 500) = 0.371
2 × 105 kg
𝑞12 = 𝑐𝑝 (𝑇2 − 𝑇1 )
kJ
𝑞12 = 𝑐𝑝 (𝑇2 − 𝑇1 ) = 1.083(750 − 500) = 270.8
kg
kJ
𝑤12 = −𝑅(𝑇2 − 𝑇1 ) = −0.2968 × (750 − 500) = −74.2
kg
4.
𝑝2 𝑉2 𝑝1 𝑉1
𝑈2 − 𝑈1 = 𝑚𝑐𝑣 (𝑇2 − 𝑇1 ) = 𝑚𝑐𝑣 ( − )
𝑚𝑅 𝑚𝑅
but
𝑅
𝑐𝑣 =
𝛾−1
𝑊12 and 𝑄12 are not properties. They depend upon the process and this is not specified in the
first part of the question. However, for the given process
𝑊12 = 𝑊1𝑎 + 𝑊𝑎2 = −𝑝1 (𝑉2 − 𝑉1 ) + 0 = −1 × 105 (0.2 − 0.1) × 10−3 = −10kJ
5.
𝑊12 = −75kJ and 𝑄13 = 95kJ
𝑝1 𝑉1 40 × 105 × 0.01
𝑚= = = 0.2615kg
𝑅𝑇1 0.287 × 103 × (260 + 273)
But
20 × 103
𝑇3 = + 260 = 360K
0.2615 × 0.76 × 103
𝑝1 𝑝1 75 × 105
𝑊12 = −𝑚𝑅𝑇1 𝑙𝑛 ( ) ∴ 𝑙𝑛 ( ) =
𝑝2 𝑝2 0.2615 × 0.287 × 103 × 533
Thus
𝑝1
𝑙𝑛 ( ) = 1.875
𝑝2
or
𝑝1
= 6.52 ∴ 𝑝2 = 6.13 bar
𝑝2
But
𝑝3 𝑝2 633.6
= ∴ 𝑝3 = 6.13 × = 7.29bar
𝑇3 𝑇2 533