Second stage porous media burner for syngas enrichment

The syngas production from hydrocarbons by porous media combustion (or conventional gasification) processes has been intensively and extensively studied due its calorific value and its applications in the energy sector. However, the syngas produced in a first stage gasifier can still have concentrations of light hydrocarbons (e.g., methane) which can be post-processing for further enrichment of hydrogen and carbon monoxide. The present work numerically investigates the performance of a second stage porous media burner to enrich the syngas content, mainly hydrogen and carbon monoxide. A one-dimensional model based on a two-temperature approximation is implemented, based on the PREMIX code, and supported by CHEMKIN and GRI-MECH 3.0 database and routines. From hybrid porous bed reactor experiments, five types of mixtures in the equivalence ratio range be-tween 0.4 and 2.4 are tested: pure methane as baseline, pure Eucalyptus nitens syngas, pure Pinus radiata syngas, and two mixtures of methane with each of the biomass syngas in equal volume quantities, as transition points. The results obtained show that in the enriched syngas, in comparison to the first content after the first stage reactor, the con-centrations of hydrogen and carbon monoxide increase, due to the partial oxidation of methane, however part of the hydrogen is consumed in the process. The intermediate species present in methane processing for pure syngas mixtures have broader reaction zones and in lower concentrations compared to the use of pure methane. For equivalence ratios greater than 1.9, pure syngas mixtures show higher conversion efficiencies compared to the baseline. At the equivalence ratio of 2.4, the pure syngas from Eucalyptus nitens and Pinus radiata has an energy return over energy invested (EROI) of 58.27% and 53.95%, respectively, and a maximum hydrogen and carbon monoxide yields of 31.66% and 48.40%, respectively. In the case of the Pinus radiata, the outlet syngas concentrations of the hydrogen and carbon monoxide on dry basis expose an increment about two times in comparison to the initial concentrations.