RELAXATION OF THE AIR IN TURBINE Dr Mohammed Saleh AlAnsari Bahrain Centre for Studies and Research April 2010 The paper presents the practical case of the irreversible adiabatic pressure drop, when the presence of friction leads to a mechanical deficit of energy, and that the heat of friction resulted from this energy produces the irreversible increase in the entropy of air. This study contains also the energy and exergy assessment, as calculates it sizes specific to the process of the expansion. 1. THE ADIABATE IRREVERSIBLE (NOT ISENTROPIQUE) 2. I=m·cpT [J] p1 1 nd γ p2 Qfd·mcp 0 ΔSirev.d S [J/K] Fig. 1. The adiabatic (reversible and irreversible) of air. n d 1 Consider a mass flow ( m ) to look perfect which expands adiabatically in a turbine. The gas is considered stabilized if any section of the stream, its thermal parameters (p, v, T) and speed (w) remain unchanged during the observation period. In Figure 1 are represented: • 1-2s - the reversible adiabatic (S = ct.) • 1-2 - the irreversible adiabatic expansion (with friction); On note: d p2 p1 - degree of gas p T2 s T1 2 p1 1 1 T1 d p 2 nd T 2 T 1 p1 n dT n 1 (3) (2) n d 1 nd T1 d T 2 s (4) The frictional heat accumulated by the gas is: Q fd L fd mcv nd T2 T1 0 nd 1 (5) The irreversible increase of entropy gas is: S irev.d T2 T1 expansion. The study has been realized to a quantity m of ideal gas. In the case of the reversible adiabatic expansion (12s) we can calculate the mechanical work received technical and final temperature: L12 s L sd mc p T1 T 2 s 0 (1) The adiabatic and friction can be likened to a transformation of nature polytropic named "pseudopolytrope. The difference between a 1-2 and a polytropic "pseudopolytrope" is that, while relations between the thermal parameters of state (p, v, T) follow the rules of the polytrope, the energy exchange is different . For a polytropic process, the elementary exchange of heat is: where: n -adiabatic exponent; γ -adiabatic exponent; cv [J/kg·K]-specific heat at constant volume. For relaxation 1-2, dTd<0,and because-as δQfd>0, and that the gas receives the heat, it follows that the exponent of the adiabatic and friction will be 1-2 nd<γ, that is to say nd(1,γ). The temperature at the end of the trigger will be: 2 2s This frictional heat will determine the increase in irreversible entropy gas. It will be shown later that the trigger 1-2 is a nonisentropic adiabatic change. This frictional heat will determine the increase of irreversible entropy gas. It will be shown later that the trigger 1-2 is a nonisentropic adiabatic transformation. Qn m c n dT m c v Lsd Lrd For the adiabatic irreversible (1-2), we lose by frottment mechanical energy is transformed into heat of friction, Qfd,, which will be fully received by the gas if the turbine is completely isolated from the thermal point of view, that is to say that the enclosure is adiabatic. Q fd T mcv n d T2 ln 0 (6) n d 1 T1 The friction heat, Qfd, results from a loss of mechanical work polytropic technique, so that the mechanical work real trigger is: Lt12 Lrd Lt12 Q fd n d pol 1 nd 1 Q fd n d Lext12 For any reversible polytropic expansion (1-2), with the introduction of heat through the walls, the mechanical work is technical: m c v T1 T2 n mc T T T2 T1 v 1 2 (7) mcv d nd 1 nd 1 n d ( 1) n d mcv T1 T2 mc p T1 T2 I 1 I 2 m(i1 i 2 ) 0 We see that this mechanical work, Lrd, is adiabatic; if in the first principle of thermodynamics (QLt=ΔI) we put Q=0, we obtain: L t I mc p T1 T 2 I 1 I 2 (8) We define an internal efficiency of the trigger, or yield adiabatic by the formula: d ad 2 ( L t 12 ) pol E 1 E 2 T T0 1 T Q d E 1 E 2 Q 12 T 0 S 12 (12) for pseudopolytrope 1-2 (adiabatic with friction), where Q12=Qfd, mechanical technique will work: L rd L t 12 ( L t 12 ) pol Q fd E 1 E 2 T 0 S irrev . d (13) where T 0 S irrev . d thermodynamic system. 2 L I I2 T T2 (9) rd 1 1 Lsd I 1 I 2 s T1 T2 s 1 anergy represents (8) the T T0 Q d T Figure no.2 shows the graph of energy balance for adiabatic irreversible. L t pol 12 L t pol L pol Q fd Q fd E1 12 E2 a). L t12 L rd T0ΔSirev.d I1 Lrd I2 E1 E2 Fig. 2. The energy balance for the adiabatic irreversible 2. EXERGY ANALYSIS For an open thermodynamic system, the exergy is: E I I 0 T0 ( S S 0 ) Fig. 3. Exergy analysis in the case of the polytropic expansion (a) and in the case of pseudopolytrope. 3. LABORATORY STAND (10) where T0 – the temperature of the atmosphere. In the case of gas expansion, mechanical work is technical: • for a reversible adiabatic-2s, the mechanical work will be technical ( S 12 0 ) L sd E 1 E 2 s I 1 I 2 s mc p ( T1 T 2 s ) b). (11) For the practical study was made a stand (Fig. 4) which contains a compressed air reservoir R, a centripetal radial turbine T and a breakdown of adjusting the pressure at the inlet of the turbine. We measured pressures and temperatures at the inlet and outlet of the turbine. For each value of the pressure p1 is the inlet temperature in a turbine is constant: We measured pressures and temperatures at the inlet and outlet of the turbine. For each pressure value p1 is the inlet temperature in a turbine is constant T1=293 K (t1=200C);; cella was possible because the evidence were made at long intervals of time and therefore compressed air tank has had time to cool to ambient laboratory (200C). For air were considered: specific heats: cp=1004,5 J/kgK; cv=717,5 J/kgK; the adiabatic exponent: =1,4 ; the pressure at the outlet of the turbine: p2=1 bar. Air Compressor T1 M obtained by measurements and 2 245,4 241,3 0,9206 1,34 6,026 47,81 22,44 4 205 197,36 0,9201 1,34 11,14 88,39 45,2 6 185 175,83 0,921 1,34 13,67 108,49 58,21 8 172 161,75 0,917 1,34 15,32 121,54 67,39 p1 1 140 T Qfd[KJ/KG] m 2 T2 p2 300 T2[K] 5 24 120 250 5 22 100 IT12[KJ/KG] lt12 sirev.d[KJ/KG] VR R Table 1. Results calculated. p1 bar T2 K T2s K ηad ηd qfd kJ/kg lt12=lrd kJ/kg Δsirev.d kJ/kg·K 5 20 5 19 5 18 8 17 80 2 17 200 150 60 100 40 50 20 0 0 2 3 4 5 6 7 8 p1[bar] M Atmosphere Fig. 4. Laboratory Stand: R-compressed air tank;Tturbine; VR- breakdown of control; T1, T2thermistor thermometers; M- manometres. 4. LES RESULTATS OBTENUS The rolling process of the air in RVs and relaxation in the turbine T are shown in the diagram i-s (Fig. 5) VR calculation is done for the amount of air m = 1 kg. i=cp·T p1=6 bar p1=4 bar p2=1 bar 1' 1 nd lsd γ lrd 2 2s 2s 0 sirev.d[KJ/KG] IT12[KJ/KG] T2[K] Fig. 6. The variations l t12 , q fd et s irrev . d No function of pressure at the entry into turbine (p1). 5. CONCLUSIONS Because the process of friction during the real adiabatic (1-2), on receives less energy than in the case of the reversible adiabatic (1-2s). receives less energy than in the case of the reversible adiabatic: L d L12 s L t 12 mc p ( T1 T 2 s ) (14) mc p ( T1 T 2 ) mc p ( T 2 T 2 s ) and is equal to the heat (module): p1=8 bar i1=cp·T1 Qfd[KJ/KG] 2 s [J/kg·K] Q 2 2 s mc p ( T 2 s T 2 ) (15) required for the return of the thermodynamic system of the state 2 to state 2s by cooling down at constant pressure (p2). For various values of p1 we obtain almost constant values for the yield and the adiabatic exponent of the adiabatic irreversible (nd). The value of the adiabatic efficiency is relatively small because the turbine was conducted in the laboratory by non-performing technical procedures Increasing pressure p1 is proportional to the degree of irreversibility of the process of relaxation, that is to say qfd and sirrev.d increase both Fig. 5. The diagram i-s; 1-1 ': Rolling VR. The results are presented in Table 1 is in Figure 6. SYMBOLES cv [J/kg·K]- the specific heat at constant volume E[W]- exergy of a thermodynamic system openadiabatic exponent of n - Q fd [J]- frictional heat accumulated by the gas - Qn [J]- Basic heat exchange -p1[Pa]- departure of the pressure relaxation -p2[Pa]- the pressure at the end of the trigger [Pa] - S irev.d [J/kgK - irreversible increase of entropy of gas] -T1[K]- the temperature departure from the relaxation -T2[K]- the temperature at the end of the trigger - d - degree of gas expansion - d - internal efficiency of relaxation or adiabatic efficiency -γ- adiabatic exponent BIBLIOGRAPHIE Bejan, A., 1996, Entropy generation minimization, CRC Press, New York. Bejan, A., Tsatsaronis, G., Moran, M., 1996, Thermal Design & Optimization, John Wiley & Sons, New York. Bejan, A., 1988, Advanced Engineering Thermodynamics, John Wiley & Sons, New York. Bogdan, C., 1981, Termotehnică şi maşini termice, Universitatea din Galaţi (in Roumanian). Mattarolo, L., 1977, Termodinamica applicata, L’Università di Padova, Ed. CLEUP (in Italian). Radcenco, V., 1977, Criterii de optimizare a proceselor termice, Ed. Tehnică, Bucureşti (in Roumanian). Moran, M., Shapiro, H., 2000, Fundamentals of engineering thermodynamics, John Wiley & Sons, New York. AlAnsari, M, 2008, Thermodynamics Notes, BCSR, Bahrain Anderson, E., 1994, Thermodynamics, International Thomsom Publishing, Boston. Russel, L., Adebiyi, G., 1993, Classical Thermodynamics, Saunders College Publishing, Fort Worth. Dr Mohammed AlAnsari, 2009, Thermodynamics and Exergy Analysis for Technicians, Short Course Notes.