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Simulation of reduction of iron-oxide-carbon composite pellets in a rotary hearth furnace.

机译:旋转炉床式炉中还原铁-碳-碳复合颗粒的模拟。

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The primary motivation of this work is to evaluate a new alternative ironmaking process which involves the combination of a Rotary Hearth Furnace (RHF) with an iron bath smelter. This work is concerned primarily, with the productivity of the RHF. It is known that the reduction in the RHF is controlled by chemical kinetics of the carbon oxidation and wustite reduction reactions as well as by heat transfer to the pellet surface and within the pellet. It is heat transfer to the pellet which limits the number of layers of pellets in the pellet bed in the RHF and thus, the overall productivity. Different types of carbon like graphite, coal-char and wood charcoal were examined.; Part of the research was to investigate the chemical kinetics by de-coupling it from the influence of heat and mass transfer. This was accomplished by carrying out reduction experiments using small iron-oxide-carbon powder composite mixtures. The reaction rate constants were determined by fitting the experimental mass loss with a mixed reaction model. This model accounts for the carbon oxidation by CO2 and wustite reduction by CO, which are the primary rate controlling surface-chemical reactions in the composite system. The reaction rate constants have been obtained using wustite-coal-char powder mixtures and wustite-wood-charcoal mixtures. The wustite for these mixtures was obtained from two iron-oxide sources: artificial porous analytical hematite (PAH) and hematite ore tailings.; In the next phase of this study, larger scale experiments were conducted in a RHF simulator using spherical composite pellets. Measurement of the reaction rates was accomplished using off-gas analysis. Different combinations of raw materials for the pellets were investigated. These included artificial ferric oxide as well as naturally existing hematite and taconite ores. Graphite, coal-char and wood-charcoal were the reductants. Experiments were conducted using a single layer, a double layer and a triple layer of composite pellets to look into the different aspects associated with multi-layer reduction in the RHF. The reduced pellets were examined for morphology and phase distribution using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) analysis. Efforts were made to interpret the differences in the observed rates from one kind of pellet to the other on the grounds of chemical kinetics of the carbon oxidation and wustite reduction reactions and the issues of external and internal heat transport to and within the pellets.; It was concluded from the experiments that in the ore containing pellets, wood-charcoal appeared to be a faster reductant than coal-char. However, in the PAH containing pellets, the reverse was found to be true. This is because of the internal heat transport limitations imposed by two factors (a) lower thermal conductivity of wood-charcoal in comparison to coal-char and (b) swelling of the PAH-Wood-Charcoal pellets during the initial heat-up stage. For the same type of reductant, hematite containing pellets were observed to reduce faster than taconite containing pellets. This is in accordance with the higher reducibility of hematite because of development of internal porosity due to cracking and fissure formation during the Fe2O3 to Fe 3O4 transformation stage. This is however, absent during the reduction of taconite, which is primarily Fe3O4. The PAH-Wood-Charcoal pellets were found to undergo significant amounts of swelling under low temperature conditions. This behavior of the PAH-Wood-Charcoal pellets of a certain layer impeded the external heat transport to the lower layer and consequently, resulted in a relatively lower reduction rate for a multi-layer bed.; The volume change phenomena associated with the reduction of composites were also studied. Volume changes influence the external heat transport, especially to the lower layers of a multi-layer bed. The volume change of the different kinds of composite pellets was studied as a func
机译:这项工作的主要目的是评估一种新的替代炼铁工艺,该工艺涉及将旋转炉膛炉(RHF)与铁浴熔炼炉相结合。这项工作主要涉及RHF的生产率。已知RHF的减少是通过碳氧化和钙铁矿还原反应的化学动力学以及通过热传递到颗粒表面和颗粒内部来控制的。热量传递到粒料,这限制了RHF中粒料床中粒料的层数,从而限制了整体生产率。研究了不同类型的碳,例如石墨,煤焦和木炭。研究的一部分是通过将化学动力学与传热和传质的影响分离开来研究化学动力学。这是通过使用小型氧化铁-碳粉复合混合物进行还原实验来完成的。通过将实验质量损失与混合反应模型拟合来确定反应速率常数。该模型说明了CO2引起的碳氧化和CO引起的纤铁矿还原,这是控制复合体系中表面化学反应的主要速率。反应速率常数是使用硅镁石-木炭粉混合物和硅镁石-木炭混合物获得的。这些混合物的钙铁矿是从两种氧化铁来源获得的:人工多孔分析赤铁矿(PAH)和赤铁矿尾矿。在本研究的下一阶段,在RHF仿真器中使用球形复合材料小球进行了较大规模的实验。使用废气分析完成反应速率的测量。研究了用于颗粒的原料的不同组合。这些包括人造三氧化二铁以及天然存在的赤铁矿和石矿。石墨,煤焦和木炭是还原剂。使用单层,双层和三层复合颗粒进行实验,以研究与RHF多层还原相关的不同方面。使用扫描电子显微镜(SEM)和能量分散X射线(EDX)分析检查还原的颗粒的形态和相分布。基于碳氧化和钙铁矿还原反应的化学动力学以及颗粒内部和外部的内部和内部传热问题,努力解释一种颗粒与另一种颗粒之间观察到的速率的差异。从实验得出的结论是,在含有球团矿的矿石中,木炭似乎是比煤炭更快的还原剂。然而,在含有PAH的颗粒中,发现相反。这是由于两个因素(a)木炭的热导率比煤炭低,以及(b)在初始加热阶段PAH-木炭粒料的溶胀导致的内部传热限制。对于相同类型的还原剂,观察到含赤铁矿的颗粒比含滑石的颗粒减少得更快。这符合赤铁矿的更高还原性,因为在Fe2O3到Fe 3O4的转化阶段,由于开裂和裂缝形成而导致内部孔隙的发展。但是,在钙钛矿(主要是Fe3O4)的还原过程中不存在这种情况。发现PAH-木炭颗粒在低温条件下会发生大量溶胀。某层的PAH-木炭颗粒的这种行为阻碍了外部热量向下层的传递,因此导致多层床的还原率相对较低。还研究了与复合材料还原相关的体积变化现象。体积变化会影响外部传热,尤其是传到多层床下层的传热。研究了不同种类复合颗粒的体积变化

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