G. Loffler et al., NOx and N2O formation mechanisms - A detailed chemical kinetic modeling study on a single fuel particle in a laboratory-scale fluidized bed, J ENERG RES, 123(3), 2001, pp. 228-235
Citations number
46
Categorie Soggetti
Environmental Engineering & Energy
Journal title
JOURNAL OF ENERGY RESOURCES TECHNOLOGY-TRANSACTIONS OF THE ASME
NOx (i.e., NO and NO2) and N2O are known as harmful pollutants. In fluidize
d bed combustion these are formed front the nitrogen in the fuel. To develo
p effective primary measures reducing the emissions, more knowledge on the
mechanism of formation and destruction ongoing in fluidized beds has to be
obtained. lit this work, a detailed chemistry model is combined with a two-
phase model for a stationary fluidized bed to calculate the emissions of a
single fuel particle in a laboratory-scale stationary fluidized bed. The si
ngle particle model consists of a simple model for the H2O release during d
rying, a model for the volatiles composition, and a model for the nitrogen
chemistry during char combustion. The detailed reaction mechanism consists
of a homogeneous part, heterogeneously catalyzed reactions on the bed mater
ial, and radical recombination reactions oil the solids' surface. The resul
ts confirm that devolatilization and char combustion are of nearly equal im
portance for NO and N2O formation. During devolatilization, NO is formed fr
om HCN and NH3, while N2O is formed almost exclusively front HCN. During ch
ar combustion, NO is mostly formed by heterogeneous oxidation of char nitro
gen, while N2O is formed from homogeneous oxidation of HCN. On the other ha
nd, there is also a back coupling of NO on the homogeneous burnout of the c
arbon containing species, by sensitizing the oxidation of CH4.