Modes of reaction front propagation and end-gas combustion of hydrogen/air mixtures in a closed chamber
KAUST DepartmentClean Combustion Research Center
Mechanical Engineering Program
Physical Science and Engineering (PSE) Division
Online Publication Date2017-01-05
Print Publication Date2017-04
Permanent link to this recordhttp://hdl.handle.net/10754/622791
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AbstractModes of reaction front propagation and end-gas combustion of hydrogen/air mixtures in a closed chamber are numerically investigated using an 1-D unsteady, shock-capturing, compressible and reacting flow solver. Different combinations of reaction front propagation and end-gas combustion modes are observed, i.e., 1) deflagration without end-gas combustion, 2) deflagration to end-gas autoignition, 3) deflagration to end-gas detonation, 4) developing or developed detonation, occurring in the sequence of increasing initial temperatures. Effects of ignition location and chamber size are evaluated: the asymmetric ignition is found to promote the reactivity of unburnt mixture compared to ignitions at center/wall, due to additional heating from asymmetric pressure waves. End-gas combustion occurs earlier in smaller chambers, where end-gas temperature rise due to compression heating from the deflagration is faster. According to the ξ−ε regime diagram based on Zeldovich theory, modes of reaction front propagation are primarily determined by reactivity gradients introduced by initial ignition, while modes of end-gas combustion are influenced by the total amount of unburnt mixture at the time when autoignition occurs. A transient reactivity gradient method is provided and able to capture the occurrence of detonation.
CitationShi X, Ryu JI, Chen J-Y, Dibble RW (2017) Modes of reaction front propagation and end-gas combustion of hydrogen/air mixtures in a closed chamber. International Journal of Hydrogen Energy. Available: http://dx.doi.org/10.1016/j.ijhydene.2016.12.095.
SponsorsThe authors thank Professor Zheng Chen at Peking University for providing ASURF source code. This work at the University of California, Berkeley was supported by the National Science Foundation and U.S. Department of Energy under award CBET-1258653. This work at King Abdullah University of Science and Technology was supported by Clean Combustion Research Center (CCRC) FUELCOM project.