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ME 306 Applied Thermodynamics 1
Terminology
2
Four stroke engine
Different strokes of
4-stroke engine
35
30
25
Pressure
20
15
10
5
0
-180 -120 -60 0 60 120 180
Crank angle Valve-time diagram
Theoretical p-q diagram
Two stroke engine
5
Otto cycle
6
Otto cycle
Work done = Heat supplied - Heat rejected
= cv (T3 - T2 ) - cv (T4 - T1 )
Work done
Efficiency =
Heat supplied
cv (T3 - T2 ) - cv (T4 - T1 ) T4 - T1
= = 1-
cv (T3 - T2 ) T3 - T2
Otto cycle
T4 - T1
Efficiency = 1 -
T3 - T2
T2 = T1r k -1
T3 = T4 r k -1
1 Efficiency is a
Efficiency = 1 - k -1 function of r
r
and k
Otto cycle
Assumptions:
1. The air in the piston–cylinder assembly is the closed system.
2. The compression and expansion processes are isentropic.
3. All processes are internally reversible.
4. The air is modelled as an ideal gas.
5. Kinetic and potential energy effects are negligible.
11
Diesel Cycle
12
Diesel or Constant Pressure cycle
Work done = Heat supplied - Heat rejected
= c p (T3 - T2 ) - cv (T4 - T1 )
Work done
h =
Heat supplied
c p (T3 - T2 ) - cv (T4 - T1 ) T4 - T1
= = 1-
c p (T3 - T2 ) k (T3 - T2 )
Diesel Cycle
1.6
1.5
>1
14
Dual Cycle
1 é rp c -1
r k
ù
Efficiency = 1 - k -1 ê ú
r êë (rp - 1) + rp k (rc - 1) úû
15
Numerical Problems
At the beginning of the compression process of an air-standard Diesel cycle operating with a
compression ratio of 18, the temperature is 300 K and the pressure is 0.1 MPa. The cutoff ratio
for the cycle is 2. Determine (a) the temperature and pressure at the end of each process of the
cycle, (b) the thermal efficiency, (c) the mean effective pressure, in MPa.
At the beginning of the compression process of an air-standard dual cycle with a compression
ratio of 18, the temperature is 300 K and the pressure is 0.1 MPa. The pressure ratio for the
constant volume part of the heating process is 1.5:1. The volume ratio for the constant pressure
part of the heating process is 1.2:1. Determine (a) the thermal efficiency and (b) the mean
effective pressure, in MPa.
16
RECAP (Ref: 6th Chapter M&S)
T2 dT p
Starting from TD basics, entropy s (T , p ) - s (T , p ) =
change between 2 states
2 2 1 1 òT1
c p (T )
T
- R ln 2
p1
T c p (T )
Defining a new variable s0 s (T ) = ò
0
dT
T' T
T2 c p (T ) T2 c p (T ) T1 c p (T )
Then òT1 T
dT = ò
T' T
dT - ò
T' T
dT = s 0 (T2 ) - s 0 (T1 )
p1
For a constant entropy process
p2
0 = s (T2 ) - s (T1 ) - R ln
0 0
p1
p2
Þ s (T2 ) = s (T1 ) + R ln
0 0
p1
é s 0 (T2 ) - s 0 (T1 ) ù
Þ p2 = p1 exp ê ú
ë R û
p2 exp é
ë s 0
(T2 ) / R ùû Only a function of
Þ = temperature
p1 exp éë s 0 (T1 ) / R ùû
p2 pr 2
= ( s1 = s2 , air only )
p1 pr1
where pr = exp éë s 0 (T ) / R ùû
v2 æ RT2 ö æ p1 ö
From ideal gas equation =ç ÷ç ÷
v1 è p2 ø è RT1 ø
v2 æ RT2 öæ pr (T1 ) ö vr 2
=ç ÷ç ÷= ( s1 = s2 , air only )
v1 è pr (T2 ) øè RT1 ø vr1
pr and vr are tabulated in Table A22