4.7 Article

Combustion stability and hetero-/homogeneous chemistry interactions for fuel-lean hydrogen/air mixtures in platinum-coated microchannels

Journal

COMBUSTION AND FLAME
Volume 173, Issue -, Pages 370-386

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.combustflame.2016.08.011

Keywords

Hetero-/homogeneous combustion of hydrogen over platinum; Combustion stability limits of hydrogen; Microreactors; Detailed catalytic and gas-phase chemistry; Extinction pressure dependence of stability limits

Funding

  1. European Union project Hybrid Renewable energy Converter for continuous and flexible power production (HRC-Power)

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The hetero-/homogeneous combustion and stability limits of fuel-lean hydrogen/air mixtures (equivalence ratio phi=0.40) were investigated numerically in a platinum-coated planar microchannel with a length of 10 nun and a height of 1 mm. A two-dimensional numerical model was used for both the gas and the solid, which included elementary heterogeneous and homogeneous reaction mechanisms, detailed transport, heat conduction in the solid, surface radiation heat transfer, and external losses via a heat transfer coefficient h. Pressures of 1 and 5 bar and solid thermal conductivities K-s = 1 and 16Wm(-1)K(-1) were analyzed, while stability maps were constructed in terms of the critical extinction heat transfer coefficient h(cr). versus inlet velocity U-IN (or mass throughput). For a given solid thermal conductivity, there existed a crossover mass throughput above (below) which the stability envelope was broader at 5 bar (1 bar). Simulations with a surface perfectly stirred reactor (SPSR) model qualitatively reproduced the crossover points, which originated from a shift in the pressure dependence of the catalytic reactivity of hydrogen. For the low solid thermal conductivity k(s) = 1 Wm(-1)K(-1), a non-monotonic dependence of the stability limits on the mass throughput was shown, with local minima created below the crossover point. The stability limits of hydrogen were solely determined by catalytic chemistry, as it sustained combustion at temperatures down to 320-380 K, at which gas-phase chemistry was frozen. Away from the critical extinction points, both catalytic and gas-phase reaction pathways were controlling. The diffusional imbalance of hydrogen, which led to catalytically-induced superadiabatic surface temperatures, and the suppression of the surface superadiabaticity by gaseous chemistry resulted in rich combustion phenomena, such as increasing peak wall temperatures with increasing heat transfer coefficients h. Critical extinction heat transfer coefficients for hydrogen were three to four orders of magnitude higher than those reported for methane and propane fuels in a similar channel geometry. (C) 2016 The Combustion Institute. Published by Elsevier Inc. All rights reserved.

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