Abstract
Hydrogen-based reduction of iron ore for iron and steel production has emerged as a promising alternative to coal and natural gas. Unlike other hydrogen-based iron ore reduction studies, this research focuses on a wide temperature range across 900-1590 degrees C, encompassing reduction in solid, mixed, and liquid (slag) phases. For a 20 min exposure to hydrogen, the reduction degree increased monotonically from ~35% at 900 degrees C to >90% at 1550 degrees C, except between 1100 degrees C and 1400 degrees C, where it stagnated ~60%. This experimental work challenges the widely accepted notion that higher temperatures enhance the reduction process. Instead, it reveals an overlooked kinetic bottleneck, suggesting complex thermodynamic and mass transfer limitations influenced by phase transformations, diffusion barriers, and microstructural changes. Density functional theory-based molecular dynamics simulations indicate that oxygen diffusivity in BCC iron is 3.88 x 10-5 cm2/s which is ~5-10 times higher than that in FCC iron. This study reports that this stagnant reduction degree in the mixed solid-liquid phase is due to competition of multiple mechanisms, such as surface- and bulk-diffusion, pore collapse mechanisms, and crystallographic transitions.
| Original language | American English |
|---|---|
| Pages (from-to) | 17726-17732 |
| Number of pages | 7 |
| Journal | ACS Sustainable Chemistry and Engineering |
| Volume | 13 |
| Issue number | 42 |
| DOIs | |
| State | Published - 2025 |
NLR Publication Number
- NLR/JA-5K00-93610
Keywords
- green steel
- hematite ore reduction
- hydrogen reduction
- solid-liquid slag phase