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On the prevailing reaction pathways during magnesium production via carbothermic reduction of magnesium oxide under low pressures

机译:在低压下通过氧化镁减少氧化镁在镁生产过程中的普遍反应途径

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In this work we identify the prevailing reaction pathways of carbothermic reduction of MgO for the tem- perature and pressure ranges of 1375-1450 °Cand1-2 kPa, respectively, and normalized reduction extents of up to 0.4. It has been previously suggested that Mg(g) is produced by either (i) MgO dissociation forming O2 as the reaction intermediate or (ii) MgO(s)-C(s) boundary reaction producing CO that then reduces MgO while forming CO2 as the reaction intermediate. Either of the intermediates (O2 or CO2) are then con- sumed by C, which is necessary to sustain further Mg(g) production. To identify the prevailing pathways, O2 or CO2 was co-fed with Ar to sweep reacting MgO-C blends with the intent to shift the equilibrium of one of the suspected Mg(g)-producing reactions. After accounting for envisaged effects of both the C/MgO ra- tio in the reacting blends and the CO concentration in the reaction atmosphere, it is demonstrated that Mg(g) is produced (1) MgO thermal dissociation and (2) MgO reduction with CO that take place in paral- lel. At 1375 °C and 1400 °C, roughly twice as much Mg(g) was produced pathway (1) as compared to pathway (2). There is no evidence supporting the relevance of a direct MgO(s)-C(s) boundary reaction.
机译:在这项工作中,我们鉴定了MgO的碳水降低的普遍反应途径,用于分别为1375-1450°Cand1-2 kPa的温度和压力范围,并归一化降低范围高达0.4。先前已经表明,Mg(g)通过(i)MgO解离形成O 2作为反应中间体或(II)MgO(S)-C(S)边界反应产生Co,其在形成CO 2的同时减少MgO反应中间体。然后通过C的中间体(O 2或CO 2)中的任一个,这是维持更多Mg(g)生产所必需的。为了鉴定普遍的途径,将O 2或CO 2与AR共送,以扫描反应MgO-C混合物,意图改变疑似Mg(g) - 发产反应之一的平衡。在考虑反应混合物中C / MGO RA-TiO的设量效果和反应气氛中的CO浓度后,证明Mg(g)产生(1)MgO热解离和(2)MgO减少在Paral-Lel中发生的CO。与途径(2)相比,在1375℃和1400℃下,大致两倍于Mg(G)的途径(1)。没有证据表明直接MgO(S)边界反应的相关性。

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