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方铁矿中的缺陷工程:开启气固还原中铁形态的控制

Defect Engineering in Wüstite: Unlocking Control Over Iron Morphologies in Gas-Solid Reduction.

作者信息

Wu Qinghui, Wang Shuai, Zhang Han, Zhang Fuchuan, Ma Kaihui, Xu Jian

机构信息

College of Materials Science and Engineering, Chongqing University, Chongqing, 400044, China.

出版信息

Adv Sci (Weinh). 2025 Jun;12(22):e2416713. doi: 10.1002/advs.202416713. Epub 2025 May 8.

Abstract

Hydrogen-based direct reduction (HyDR) technology has emerged as a promising pathway for sustainable steelmaking. However, the efficiency and stability of HyDR are critically influenced by the microstructure evolution of iron during gas-solid reduction reactions. Despite significant research on the reduction mechanisms of hydrogen (H) and carbon monoxide (CO) with iron oxides, key aspects of the interplay between internal defects, pore dynamics, and reduction chemistry remain unresolved. In this study, the morphological evolution of iron during reduction with H and CO across a full concentration range at 900 °C is explored, establishing a direct link between lattice distortions in wüstite (FeO) and the resultant iron microstructure. Complementary analyses reveal that the concentration of defects in FeO governs these distortions. Specifically, low CO concentrations (< 80%) induce limited large-scale defects, leading to single-point nucleation and the growth of filament-shaped iron whiskers. Conversely, H₂ and high CO concentrations (> 80%) create a high density of large-scale defects, promoting multi-point nucleation and the aggregation of tumor-shaped iron structures. This work provides a multiscale perspective on how defect engineering in FeO modulates the morphologies of iron during reduction, offering valuable insights into optimizing reaction pathways to enhance efficiency and sustainability in materials processing.

摘要

基于氢的直接还原(HyDR)技术已成为可持续炼钢的一条有前景的途径。然而,HyDR的效率和稳定性在很大程度上受到气固还原反应过程中铁微观结构演变的影响。尽管对氢气(H)和一氧化碳(CO)与铁氧化物的还原机理进行了大量研究,但内部缺陷、孔隙动力学和还原化学之间相互作用的关键方面仍未得到解决。在本研究中,探索了在900°C的全浓度范围内用H和CO还原过程中铁的形态演变,建立了方铁矿(FeO)中的晶格畸变与所得铁微观结构之间的直接联系。补充分析表明,FeO中的缺陷浓度控制着这些畸变。具体而言,低CO浓度(<80%)会诱导有限的大规模缺陷,导致单点成核和丝状铁须的生长。相反,H₂和高CO浓度(>80%)会产生高密度的大规模缺陷,促进多点成核和瘤状铁结构的聚集。这项工作从多尺度角度阐述了FeO中的缺陷工程如何在还原过程中调节铁的形态,为优化反应途径以提高材料加工的效率和可持续性提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78a3/12165032/9a9e0216c758/ADVS-12-2416713-g004.jpg

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