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OCTOBER 19-20, 2012 - YMCA University of Science & Technology

OCTOBER 19-20, 2012 - YMCA University of Science & Technology

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Proceedings <strong>of</strong> the National Conference on<br />

Trends and Advances in Mechanical Engineering,<br />

<strong>YMCA</strong> <strong>University</strong> <strong>of</strong> <strong>Science</strong> & <strong>Technology</strong>, Faridabad, Haryana, Oct <strong>19</strong>-<strong>20</strong>, <strong>20</strong>12<br />

supply <strong>of</strong> air, may be considered as the ideal situation for every inlet air temperature. This ideal efficiency again<br />

increases with the increase in the inlet air temperature which increases the temperature <strong>of</strong> the product gas.<br />

Adebiyi [17] showed from a similar analysis in an adiabatic combustor, assuming complete combustion without<br />

dissociation and constant specific heats <strong>of</strong> air and product gas, that the maximum second-law efficiency<br />

attainable for a combustion engine is 70% with CH 4 as the fuel and keeping the product temperature within the<br />

acceptable limit guided by the metallurgical constraint. The second-law efficiency obtained from the exergy<br />

approach gives a direct measurement <strong>of</strong> the performance <strong>of</strong> the combustor. The larger the irreversibilities, lower<br />

will be the value <strong>of</strong> the second-law efficiency. However, this approach does not throw any light on the causes <strong>of</strong><br />

the irreversibilities. In a combustor, several transport and chemical processes take place simultaneously, which<br />

are irreversible. The contribution <strong>of</strong> the processes towards entropy generation at different locations within the<br />

combustor is required to be known to investigate the primary causes <strong>of</strong> exergy loss. It is also not practically<br />

possible to improve the performance <strong>of</strong> a combustor without such information.<br />

The present approach fails to provide this data and calls for a methodology, which considers the irreversibility as<br />

a field variable to find its distribution within the entire combustor. In the flow field <strong>of</strong> a combustor, the<br />

nonequilibrium conditions are due to the exchange <strong>of</strong> momentum, energy and mass <strong>of</strong> different species<br />

(multicomponent) within the fluid and at the solid boundaries. These nonequilibrium phenomena cause a<br />

continuous generation <strong>of</strong> entropy in the flow field. The entropy generation is due to the irreversible nature <strong>of</strong> heat<br />

transfer, mass diffusion, viscous effects within the fluid and at the solid boundaries, chemical reaction, coupling<br />

effects between heat and mass transfers and body force effects. Every irreversible process can be viewed as the<br />

relevant flux driven by the corresponding potential, e.g. the flux <strong>of</strong> heat is driven by the temperature gradient.<br />

The highest exergy exists in the fuel, which represents the maximum potential <strong>of</strong> the fuel to perform work. When<br />

this chemical energy is transformed into thermal energy, some portion (which depends on the final temperature)<br />

<strong>of</strong> the initial availability is destroyed. The amount <strong>of</strong> the exergy that is destroyed increases for lower final<br />

temperatures <strong>of</strong> the product, i.e. for lower flame temperature. The higher initial temperature <strong>of</strong> the reactant<br />

decreases the destruction in exergy in the combustion process due to the higher temperature <strong>of</strong> the product,<br />

which retains more exergy contained in it.<br />

Nomenclature<br />

E = Exergy rate (kJ/s)<br />

Hf = Heat supplied by fuel {kJ/kg (dry air)}<br />

∆Hr = Heat <strong>of</strong> reaction <strong>of</strong> fuel (kJ/kg <strong>of</strong> fuel)<br />

R = Gas constant (kJ/kg K)<br />

T = Absolute temperature (K)<br />

TP = Process heat temperature (°C)<br />

W = Work (kJ/kg (dry air))<br />

cp = Specific heat at constant pressure (kJ/kg K)<br />

cv = Specific heat at constant pressure (kJ/kg K)<br />

e = Specific exergy (kJ/kg (dry air))<br />

eP = Specific exergy associated with process heat (kJ/kg (dry air))<br />

gr = Gibbs function <strong>of</strong> fuel (kJ/kg)<br />

h = Enthalpy (kJ/kg (dry air))<br />

hf = Enthalpy <strong>of</strong> saturated water at process steam pressure (kJ/kg)<br />

hg = Enthalpy <strong>of</strong> saturated vapor at process steam pressure (kJ/kg)<br />

m = Mass (kg)<br />

n = Number <strong>of</strong> moles<br />

p = Pressure (bar)<br />

Q p = Process heat (kJ/kg (dry air))<br />

re = Expansion ratio<br />

rp = Pressure ratio<br />

s = Entropy (kJ/kg K)<br />

t = Temperature (°C)<br />

v = Specific volume (m 3 /kg)<br />

Greek Symbols<br />

ω = Humidity ratio (kilogram <strong>of</strong> water vapor per kilogram <strong>of</strong> dry air)<br />

φ = Relative humidity (%)<br />

ε = Effectiveness (%)<br />

η = Efficiency (%)<br />

186

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