Kinetics of the conversion of NO to N2 during the oxidation of iron particles by NO in a hot fluidised bed

被引:66
作者
Hayhurst, AN [1 ]
Ninomiya, Y [1 ]
机构
[1] Univ Cambridge, Dept Chem Engn, Cambridge CB2 3RA, England
基金
日本学术振兴会;
关键词
NOx; fluidised bed; gas-solid reaction; pollutant removal; oxidation of iron;
D O I
10.1016/S0009-2509(98)00009-8
中图分类号
TQ [化学工业];
学科分类号
0817 [化学工程与技术];
摘要
The kinetics of the conversion of poisonous NO gas to N-2 in Fe + qNO --> FeOq + q/2 N-2 have been measured in hot fluidised beds of sand from 973 to 1173 K at 1 bar. The reaction involves NO (in N-2) reacting with tiny (diam. 139-400 mu m) iron particles and, because NO is thereby converted to harmless N-2, the reaction is of interest for removing NO from, e.g. fluidised bed or other combustors. Whether the oxide produced is FeO, Fe3O4 or Fe2O3 is one subject of discussion and it is concluded that the product is mainly FeO. Two stages were found for the reaction. Initially, the rate of oxidation of iron is first order in NO and, in fact, is kinetically controlled. The outer layer of oxide produced on each iron particle is found to be very porous at the highest temperature (1173 K), but much less porous at the lowest temperature (973 K). The associated rate constant has a low activation energy (41 +/- 4 kJ/mol) and a pre-exponential factor close to the theoretical upper limit of the collision frequency. During the second stage of reaction, the observed rate is independent of the concentration of NO. This is because the rate is controlled by diffusion of Fe2+ ions and electrons from a particle's metallic core, through vacancies in the layer of FeO (covering the unreacted Fe), to the outer surface of the particle. Interestingly, the second stage has a larger activation energy (155 +/- 20 kJ/mol) than the first stage. At the highest temperature (900 degrees C) these iron particles can be oxidised completely, but at 700 degrees C the reaction stops after only a conversion of similar to 20% of Fe to FeO. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1481 / 1489
页数:9
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