Numerical Simulation of Fluidized Bed Gasifier Coupled with Solid Oxide Fuel Cell Fed with Solid Carbon

A model of a fluidized bed coupled with direct carbon solid oxide fuel cell (SOFC) is developed to explore the effect of coupling between fluidized bed and solid oxide fuel cell. Three gas–solid flow regimes are involved including fixed bed, delayed bubbling bed and bubbling bed. The anode reaction of SOFC is treated as the coupling processes of Boudouard gasification of carbon and electrochemical oxidation of CO. The effects of inlet velocity of the fluidizing agent CO2, carbon activity, channel width and coupling extent on the system performance are investigated. The results show that the inlet velocity of CO2 can promote the gasification rate in the anode, but too high velocities may lower CO molar fraction. The gasification rate generally increases with the increase of the channel width and carbon activity. The overlapping area between the anode surface and the initial carbon bed, gas–solid regime and carbon activity have a significant influence on the gasification rate and the maximum current density the system can support. Overall, the mass transport in the anode is dramatically enhanced by the expansion of the carbon bed, back-mixing, solid mixing and gas mixing, especially for the delayed bubbling bed and bubbling bed. This indicates that the adopted coupling method is feasible to improve the anode performance of direct carbon solid oxide fuel cell.

Sorption of Hydrogen Chloridein The Fluidized Bed Reactor

Combustion of fuels, including renewable fuels and thermal treatment of waste (CFCs, pesticides), is associated with emissions of pollutants including halogens. The reversible process of sorption/desorption of HCl, in a fluidized (bubbling) bed reactor (BFB), during co-combustion of Cl-materials, was carried out. The thermal decomposition of methylene chloride (DCM, CH2Cl2) in an inert sand bed with the addition of the hydroxyapatite sorbent (HAp, Ca5(PO4)3(OH)) was investigated. The process parameters were as follows: temperature - 930 °C, the air excess - 1.3, stream rate of CH2Cl2 - 50 cm3/h. The concentration of HCl, CCl4, CHCl3, CH2Cl2, CH3Cl, COCl2 in the exhaust gases were monitored online with FTIR spectroscopy. The main chlorine product was hydrogen chloride. Samples of unprocessed HAp, taken from the bed during the process, and solid apatite residues were analyzed by X-ray diffraction (XRD). The content of chlorapatite (Ca5(PO4)3Cl) in the analyzed samples was respectively 11, 53 and 19 %. X-ray fluorescence (XRF) analysis showed the molar ratio of Ca:P:Cl was: 1.00:0.36:0.01, 1.00:0.36:0.09, 1.00:0.37:0.04 respectively. The HAp could be used as an sorbent of the HCl(g) during combustion of materials containing chlorine.