TY - GEN
T1 - Effect of water-gas shift reaction on reduction of iron oxide powder packed bed with H 2-CO mixtures
AU - Usui, Tateo
AU - Ono-Nakazato, Hideki
AU - Yonezawa, Toshinari
PY - 2004
Y1 - 2004
N2 - Although the hydrogen reduction is thermally more disadvantageous than the CO reduction, it' is advantageous that the reduction rate with H 2 is much larger than that with CO. In order to examine the effective use of hydrogen, the reduction of FeO 1.05 powder packed bed with H 2-CO mixture was conducted, and the results were analyzed by a proposed model. In the proposed model, when the water-gas shift reaction is taken into account, the additivity is established on the dependence of the rate constant of the reaction on the gas composition. When the water-gas shift reaction is not taken into account, the rate constant deviates negatively from the additivity. The apparent rate constants of the reduction determined in the present study take the middle values, and the contribution of the water-gas shift reaction is estimated to be 3% against its equilibrium. In reducing FeO 1.05 with CO, the time when the sample is perfectly reduced is shortened by adding a small amount of H 2, and the enhancement effect of H 2 on the gaseous reduction remarkably appears at 1093K. The effect originates in the proceeding of the water-gas shift reaction.
AB - Although the hydrogen reduction is thermally more disadvantageous than the CO reduction, it' is advantageous that the reduction rate with H 2 is much larger than that with CO. In order to examine the effective use of hydrogen, the reduction of FeO 1.05 powder packed bed with H 2-CO mixture was conducted, and the results were analyzed by a proposed model. In the proposed model, when the water-gas shift reaction is taken into account, the additivity is established on the dependence of the rate constant of the reaction on the gas composition. When the water-gas shift reaction is not taken into account, the rate constant deviates negatively from the additivity. The apparent rate constants of the reduction determined in the present study take the middle values, and the contribution of the water-gas shift reaction is estimated to be 3% against its equilibrium. In reducing FeO 1.05 with CO, the time when the sample is perfectly reduced is shortened by adding a small amount of H 2, and the enhancement effect of H 2 on the gaseous reduction remarkably appears at 1093K. The effect originates in the proceeding of the water-gas shift reaction.
KW - Equilibrium constant
KW - Gaseous reduction
KW - Water-gas shift reaction
UR - http://www.scopus.com/inward/record.url?scp=33644985330&partnerID=8YFLogxK
M3 - 会議への寄与
AN - SCOPUS:33644985330
SN - 8586778753
SN - 9788586778759
T3 - 2nd International Meeting on Ironmaking and 1st International Symposium on Iron Ore and Parallel Event- 5th Japan-Brazil Symposium on Dust Processing-Energy-Environment on Metallurgical Industries
SP - 561
EP - 570
BT - 2nd International Meeting on Ironmaking and 1st International Symposium on Iron Ore and parallel event - 5th Japan-Brazil Symposium on Dust Processing-Energy-Environment on Metallurgical Industries
T2 - 2nd International Meeting on Ironmaking and 1st International Symposium on Iron Ore and Parallel Event- 5th Japan-Brazil Symposium on Dust Processing-Energy-Environment on Metallurgical Industries
Y2 - 12 September 2004 through 15 September 2004
ER -