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Otto Cycle Modeling

Otto Cycle Modeling

Thermodynamic Cycles

Air-standard analysis is a simplification of the real cycle that includes the following assumptions: 1) Working fluid consists of fixed amount of air ()

2) Combustion process represented by transfer into and out of the cylinder from an external source

3) Differences between intake and exhaust processes not considered (i.e. no pumping )

4) friction and heat losses not considered SI Engine Cycle vs Air Standard Otto Cycle

FUEL A I Ignition R

Fuel/Air Mixture Combustion Actual Products Cycle

Intake Compression Power Exhaust Stroke Stroke Stroke

Qin Qout

Air Otto TC Cycle BC

Compression Const Expansion Const volume Process heat addition Process heat rejection Process Process Air-Standard Otto cycle

Process 1→ 2 Isentropic compression Process 2 → 3 Constant volume heat addition Process 3 → 4 Isentropic expansion Process 4 → 1 Constant volume heat rejection

Compression ratio: v v r = 1 = 4 v v Qin 2 3

Qout

v v 2 1 TC TC BC BC First Law Analysis of Otto Cycle

1→2 Isentropic Compression AIR Q W (u − u ) = − (− in ) 2 1 m m W in = (u − u ) m 2 1

vr v 1 P v Pv P T v 2 = 2 = R = 2 2 = 1 1 → 2 = 2  1 v v r T T P T v r1 1 2 1 1 1 2 First Law Analysis of Otto Cycle

2→3 Constant Volume Heat Addition

Qin W (u − u ) = (+ ) − Qin 3 2 m m AIR TC Q in = (u − u ) m 3 2 P P P T v = 2 = 3 → 3 = 3 RT2 RT3 P2 T2 First Law Analysis of Otto Cycle

3 → 4 Isentropic Expansion

Q Wout (u − u ) = − (+ ) AIR 4 3 m m W out = (u − u ) m 3 4

vr v 4 4 P v P v P T v = = r 4 4 = 3 3 → 4 = 4  3 vr v3 3 T4 T3 P3 T3 v4 First Law Analysis of Otto Cycle

4 → 1 Constant Volume Heat Removal

Qout W (u1 − u4 ) = (− ) − Q m m AIR out

Qout = (u − u ) BC m 4 1 P P P P v = 4 = 1 → 4 = 1 RT4 RT1 T4 T1 First Law Analysis

Net cycle work:

Wcycle =Wout −Win = m(u3 −u4 )− m(u2 −u1)

Cycle :

Wcycle Wout −Win (u3 − u4 )− (u2 − u1 ) th = = = Qin Qin (u3 − u2 )

(u3 − u2 )− (u4 − u1 ) u4 − u1 th = =1− u3 − u2 u3 − u2 Cold Air-Standard Analysis • For a cold air-standard analysis the specific are assumed to be constant evaluated at ambient temperature values (k = cp/cv = 1.4).

• For the two isentropic processes in the cycle, assuming ideal gas with constant specific heat using Pv k = const. Pv = RT yields:

k−1 k−1 k 1 → 2 : T2  v1  k−1 T2  P2  =   = r =   T1  v2  T1  P1 

k−1 k−1 k−1 k 3 → 4 : T4  v3  1 T4  P4  =   =   =   T3  v4   r  T3  P3 

cv (T4 −T1) T1 1 th =1− =1− =1− k−1 const cV cv (T3 −T2 ) T2 r Effect of Specific Heat Ratio

1 th =1− k−1 const cV r

Specific heat ratio (k)

Cylinder temperatures vary between 20K and 2000K where 1.2 < k < 1.4