H2-reduction Behavior of FeS-CaO Mixture during Microwave Heating

A. Amini, K. Ohno, T. Maeda, K. Kunitomo, K. Kashimura
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Abstract

Microwave irradiation is an energy-efficient and a rapid-heating method to decrease the activation energy of chemical reactions via both thermal and non-thermal effects of microwave photons 1). Recently, hydrogen-reduction during microwave heating has been proposed for magnetite reduction to combine the advantages of microwave irradiation and using H2 as a reducing agent during iron production 2). In the present study, as a novel idea, the traditional microwave heating system was equipped with thermobalance to investigate the kinetics of H2-reduction of FeS-CaO mixture (FeS(s) + CaO(s) + H2(g) = Fe(s) + CaS(s) + H2O(g)) under microwave heating at 2.45 GHz to further mitigate CO2 emission and prevent SO2 release during iron production from a sulfide mineral. Microscope observations revealed that the un-reacted core model can be employed for such a kinetic study. Linearity (R2) of different rate-controlling mechanisms after a 10-minute reduction reaction demonstrated that the gas diffusion in micropores of reduced metallic Fe is a dominant rate-controlling mechanism while the interfacial chemical reaction is progressed rapidly. This is attributed to extraordinary effects of microwave irradiation on speeding up the chemical reactions 3), while the formation of Fe shell on the surface of FeS/FeO particles decreases the accessibility of gas to un-reacted parts, resulting in a lower rate of gas diffusion in micropores. Moreover, the diffusion coefficients (De) at 460, 570, and 750 °C were calculated from the plot of the gas diffusion, as illustrated in Fig. 1, wherein the X is reduction degree: where Wi (g) is the initial weight of the sample, Wt (g) is the weight of the sample after treatment for t seconds, Wht (g) is the weight change of the sample owing to the dehydration reaction, and WO (-) is the stoichiometric weight ratio of oxygen in the sample, which is 0.111. Consequently, the activation energy of 22.3 kJ.mol-1 was attained from the Arrhenius equation for the hydrogen-reduction reaction of FeS-CaO mixture under microwave heating.
微波加热过程中FeS-CaO混合物的h2还原行为
微波辐射是一种高效、快速的加热方法,通过微波光子的热效应和非热效应降低化学反应的活化能1)。近年来,结合微波辐射的优点和铁生产过程中H2作为还原剂的优点,提出了微波加热过程中的氢还原用于磁铁矿还原2)。利用传统的微波加热系统配备热平衡装置,研究了在2.45 GHz微波加热下FeS-CaO混合物(FeS(s) + CaO(s) + H2(g) = Fe(s) + CaS(s) + H2O(g))的H2还原动力学,以进一步减少硫化矿物制铁过程中CO2的排放和SO2的释放。显微镜观察表明,未反应的核心模型可以用于这样的动力学研究。还原反应10 min后不同速率控制机制的线性(R2)表明,还原金属铁微孔内气体扩散是主要的速率控制机制,界面化学反应快速进行。这是由于微波辐射对加速化学反应的特殊作用(3),而FeS/FeO颗粒表面铁壳的形成降低了气体对未反应部分的可及性,导致气体在微孔中的扩散速率降低。此外,扩散系数(De)在460年,570年和750°C计算气体扩散的情节,如图1中所示,其中X是减少学位:Wi (g)在哪里初始样本的重量,Wt (g)是治疗t秒后样品的重量,什么(g)是样品的重量变化由于脱水反应,和我们(-)是氧的化学计量重量比在示例中,它是0.111。因此,活化能为22.3 kJ。由微波加热下FeS-CaO混合物氢还原反应的Arrhenius方程得到mol-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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