SECOND LAW OF THERMODYNAMICS AND ENTROPY 263dharm
/M-therm/th5-3.pm5= cv loge T
T2
1- R 1
n− 1
F
HGI
KJ
loge T
T2
1
= cv loge T
T2
1- (cp – cv) ×^1
n− 1
F
HGI
KJloge T
T2
1[Q R = cp – cv]= cv loge T
T2
1- (γ. cv – cv) ×^1
n− 1
F
HGI
KJ
loge T
T2
1[Q cp= γ. cv]=−
−
−F
HGI
KJL
NM
MO
QP
Pc
v n
1
1
1γ
logeT
T2
1
=−− −
−L
NM
O
Qc P
n
v n()()
()11
1γ
logeT
T2
1= −− +
−F
HGI
KJc n
v n11
1γ ) log
e^T
T2
1= cv. n
n−
−F
HGI
KJγ
1
loge T
T2
1per kg of gas∴ s 2 – s 1 = cv n
n−
−F
HGI
KJγ
1loge
T
T2
1per kg of gas ...(5.35)5.17.7. Approximation for heat absorbed
The curve LM shown in the Fig. 5.30 is obtained by heating 1 kg of gas from initial state L
to final state M. Let temperature during heating increases from T 1 to T 2. Then heat absorbed by
the gas will be given by the area (shown shaded) under curve LM.
s 1T 1T 2s 2 sQMTLFig. 5.30
As the curve on T-s diagram which represents the heating of the gas, usually has very
slight curvature, it can be assumed a straight line for a small temperature range. Then,
Heat absorbed = Area under the curve LM
= (s 2 – s 1 ) TT^12
2F +
HGI
KJ
...(5.36)