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Analysis of cyclic variations during mode switching between spark ignition and controlled auto-ignition combustion operations
© IMechE 2014. Controlled auto-ignition, also known as homogeneous charge compression ignition, has been the subject of extensive research because of their ability to provide simultaneous reductions in fuel consumption and NOx emissions from a gasoline engine. However, due to its limited operation range, switching between controlled auto-ignition and spark ignition combustion is needed to cover the complete operating range of a gasoline engine for passenger car applications. Previous research has shown that the spark ignition -controlled auto-ignition hybrid combustion (SCHC) has the potential to control the ignition timing and heat release process during the mode transition operations. However, it was found that the SCHC is often characterized with large cycle-to-cycle variations. The cyclic variations in the in-cylinder pressure are particularly noticeable in terms of both their peak values and timings while the coefficient of variation in the indicated mean effective pressure is much less. In this work, the cyclic variations in SCHC operations were analyzed by means of in-cylinder pressure and heat release analysis in a single-cylinder gasoline engine equipped with Variable Valve Actuation (VVA) systems. First, characteristics of the in-cylinder pressure traces during the spark ignition-controlled auto-ignition hybrid combustion operation are presented and their heat release processes analyzed. In order to clarify the contribution to heat release and cyclic variation in SCHC, a new method is introduced to identify the occurrence of auto-ignition combustion and its subsequent heat release process. Based on the new method developed, the characteristics of cyclic variations in the maximum rate of pressure rise and different stages of heat release process have been analyzed and discussed
Generalized Haldane Equation and Fluctuation Theorem in the Steady State Cycle Kinetics of Single Enzymes
Enyzme kinetics are cyclic. We study a Markov renewal process model of
single-enzyme turnover in nonequilibrium steady-state (NESS) with sustained
concentrations for substrates and products. We show that the forward and
backward cycle times have idential non-exponential distributions:
\QQ_+(t)=\QQ_-(t). This equation generalizes the Haldane relation in
reversible enzyme kinetics. In terms of the probabilities for the forward
() and backward () cycles, is shown to be the
chemical driving force of the NESS, . More interestingly, the moment
generating function of the stochastic number of substrate cycle ,
follows the fluctuation theorem in the form of
Kurchan-Lebowitz-Spohn-type symmetry. When $\lambda$ = $\Delta\mu/k_BT$, we
obtain the Jarzynski-Hatano-Sasa-type equality:
1 for all , where is the fluctuating chemical work
done for sustaining the NESS. This theory suggests possible methods to
experimentally determine the nonequilibrium driving force {\it in situ} from
turnover data via single-molecule enzymology.Comment: 4 pages, 3 figure
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