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Influence Of Sio_2 And/or Mno_2 On The Reduction Behaviour And Structure Changes Of Fe_2o_3 Compacts With Co Gas

机译:Sio_2和/或Mno_2对Co气对Fe_2o_3压块还原行为和结构变化的影响

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Pure Fe_2O_3 and Fe_2O_3 doped with either 2.5-7.5 mass% SiO_2, 6.0mass% MnO_2 and (6.0%MnO_2+ 7.5%SiO_2) compacts annealed at 1 473 K for 6h were prepared. The different phases were identified by X-ray diffraction (XRD) and their structures were examined by optical and scanning electron microscopes. The magnetic properties were measured with Vibrating Sample Magnetometer (VSM). Total porosity and pore size distribution were determined and their external volume was also measured. Unlike in SiO_2 doped samples where no new phases were detected, manganese ferrite (MnFe_2O_4) was identified in MnO_2-containing samples. Annealed compacts were isothermally reduced with CO at 1 073-1 373 K and the O_2-weight loss was continuously recorded. It was found that the reduction rate of SiO_2-Fe_2O_3 samples increases at the early stages with SiO_2 mass% due to the increase in their original porosity. At final stages, the rate was retarded due to the formation of hardly reducible fayalite (Fe_2SiO_4). In MnO_2-containing samples, the reduction rate was retarded at initial stages due to the presence of manganese ferrite. At later stages, the formation of fayalite-manganoan [(Fe, Mn)_2SiO_4] greatly hindered the reduction process. A catastrophic swelling (ΔV= 405%) was recorded in 6%MnO_2-Fe_2O_3 compacts and was greatly diminished to 55.95% in presence of 7.5% SiO_2 due to the decrease in size and number of metallic iron whiskers and plates. The reduction mechanism of pure and doped samples was predicted from the correlations between reduction kinetics and the microscopic examinations of partially and completely reduced samples.
机译:制备了掺杂有2.5-7.5质量%SiO_2、6.0质量%MnO_2和(6.0%MnO_2 + 7.5%SiO_2)压块的纯Fe_2O_3和Fe_2O_3,该压​​块在1473 K退火6h。通过X射线衍射(XRD)鉴定不同的相,并通过光学和扫描电子显微镜检查其结构。用振动样品磁强计(VSM)测量磁性能。确定总孔隙率和孔径分布,并测量其外部体积。与未检测到新相的SiO_2掺杂样品不同,在含MnO_2的样品中鉴定出锰铁氧体(MnFe_2O_4)。在1 073-1 373 K用CO等温还原压坯,并连续记录O_2的重量损失。发现SiO_2-Fe_2O_3样品的还原速率在早期阶段以SiO_2质量%增加,这是由于其原始孔隙率的增加所致。在最后阶段,由于难以还原的铁橄榄石(Fe_2SiO_4)的形成,导致速率降低。在含MnO_2的样品中,由于锰铁氧体的存在,还原速率在初始阶段受阻。在后期阶段,铁橄榄石-锰锰[(Fe,Mn)_2SiO_4]的形成大大阻碍了还原过程。在6%MnO_2-Fe_2O_3压坯中记录到灾难性的溶胀(ΔV= 405%),由于金属晶须和板的尺寸和数量减少,在存在7.5%SiO_2的情况下,溶胀大大降低至55.95%。从还原动力学与部分还原和完全还原的样品的显微镜检查之间的相关性,可以预测纯掺杂样品的还原机理。

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