Unraveling the thermodynamics and mechanism behind the lowering of direct reduction temperatures in oxide mixtures

Shiv Shankar*, Barak Ratzker*, Alisson Kwiatkowski da Silva, Tim M. Schwarz, Hans Brouwer, Baptiste Gault, Yan Ma*, Dierk Raabe*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Hydrogen-based direct reduction offers a sustainable pathway to decarbonize the metal production industry. However, stable metal oxides, like Cr2O3, are notoriously difficult to reduce, requiring extremely high temperatures (above 1300 °C). Herein, we explain how reducing mixed oxides can be leveraged to lower hydrogen-based reduction temperatures of stable oxides and produce alloys in a single process. Using a newly developed thermodynamic framework, we predict the precise conditions (oxygen partial pressure, temperature, and oxide composition) needed for co-reduction. We showcase this approach by reducing Cr2O3 mixed with Fe2O3 at 1100 °C, significantly lowering reduction temperatures (by ∼200 °C). Our model and post-reduction structural and chemical analyses elucidate that the temperature-lowering effect is driven by the lower chemical activity of Cr in the Fe-Cr solid solution phase. This strategy achieves low-temperature co-reduction of mixed oxides, dramatically reducing energy consumption and CO2 emissions, while unlocking transformative pathways toward sustainable alloy design.
Original languageEnglish
Pages (from-to)43-51
Number of pages9
JournalMaterials Today
Volume90
DOIs
Publication statusPublished - 2025

Keywords

  • Alloy design
  • Atom probe tomography
  • Ellingham diagram
  • Hydrogen
  • Microstructure
  • Reduction

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