TY - JOUR
T1 - Effect of bed material on ammonia dissociation in a bubbling fluidised bed
AU - Guo, Zipeng
AU - Li, Jianbo
AU - Zhao, Mengjia
AU - Cao, Jia
AU - Zhang, Yuanyuan
AU - Lu, Xiaofeng
AU - Zhang, Dongke
N1 - Publisher Copyright:
© 2025 Hydrogen Energy Publications LLC
PY - 2025/4/15
Y1 - 2025/4/15
N2 - Ammonia (NH3) dissociation is a crucial first step during its combustion. This study systematically examines the characteristics of NH3 dissociation in a lab-scale bubbling fluidised bed (BFB), with a special concern to the effect of the type of bed material. The dissociation experiments are performed with an initial NH3 concentration of 11.1 % in NH3/Ar mixture under incipient fluidisation and different temperatures (750–950 °C) conditions in the presence of SiO2, Al2O3, CaO, Fe2O3, and a bottom ash from a coal-fired circulating fluidised bed (CFB) boiler as bed materials, respectively. The reactor exit stream is analysed using a gas chromatograph (GC) for its gas composition, from which the NH3 conversion is calculated. The bed materials before and after the NH3 dissociation experimentation are characterised using X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) and NH3 temperature-programmed desorption (NH3-TPD) for changes in their physicochemical properties. Results showed that while the NH3 conversion generally increases with increasing temperature, it is strongly influenced by the bed material at a given temperature, where the NH3 conversion decreases with the bed material following the order of Fe2O3 > CFB bottom ash > CaO > Al2O3 > SiO2. It is believed that the metallic iron formed due to NH3 reduction of Fe2O3 and iron oxides in the CFB bottom ash, as confirmed by XRD analysis, catalyses NH3 dissociation during experimentation. The effect of CaO, Al2O3 and SiO2 as bed materials is found to depend on the surface acidity and pore structure. The CaO bed material incurs an increase in both pore volume and pore size following the NH3 dissociation experiment.
AB - Ammonia (NH3) dissociation is a crucial first step during its combustion. This study systematically examines the characteristics of NH3 dissociation in a lab-scale bubbling fluidised bed (BFB), with a special concern to the effect of the type of bed material. The dissociation experiments are performed with an initial NH3 concentration of 11.1 % in NH3/Ar mixture under incipient fluidisation and different temperatures (750–950 °C) conditions in the presence of SiO2, Al2O3, CaO, Fe2O3, and a bottom ash from a coal-fired circulating fluidised bed (CFB) boiler as bed materials, respectively. The reactor exit stream is analysed using a gas chromatograph (GC) for its gas composition, from which the NH3 conversion is calculated. The bed materials before and after the NH3 dissociation experimentation are characterised using X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) and NH3 temperature-programmed desorption (NH3-TPD) for changes in their physicochemical properties. Results showed that while the NH3 conversion generally increases with increasing temperature, it is strongly influenced by the bed material at a given temperature, where the NH3 conversion decreases with the bed material following the order of Fe2O3 > CFB bottom ash > CaO > Al2O3 > SiO2. It is believed that the metallic iron formed due to NH3 reduction of Fe2O3 and iron oxides in the CFB bottom ash, as confirmed by XRD analysis, catalyses NH3 dissociation during experimentation. The effect of CaO, Al2O3 and SiO2 as bed materials is found to depend on the surface acidity and pore structure. The CaO bed material incurs an increase in both pore volume and pore size following the NH3 dissociation experiment.
KW - Ammonia (NH)
KW - Bed material
KW - Bubbling fluidised bed
KW - Conversion
KW - Dissociation
UR - http://www.scopus.com/inward/record.url?scp=105000561479&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2025.03.259
DO - 10.1016/j.ijhydene.2025.03.259
M3 - Article
AN - SCOPUS:105000561479
SN - 0360-3199
VL - 119
SP - 444
EP - 456
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -