Effects of oxygen concentration on nanoparticle formation during combustion of iron powders

• This research examined the formation of products from the combustion of powdered iron. • Products were magnetite/hematite micro-particles and agglomerated hematite nano-particles. • Micro-particles were spherical and bigger than their iron particle precursors. • Nano-particles were 30–100 nm spherules accounting for up to 7.4% of the product mass, increasing with [O 2 ] in the gas. • Iron evaporation and nano-particle formation mechanisms were evaluated with a heuristic model. Powdered iron is being investigated for its potential use as a carbon-free fuel due to its ability to burn heterogeneously and produce oxide particles, which can be collected, reduced back to iron and burned again. However, high temperature oxidation of iron particles can induce partial vaporization/decomposition and evolution of nanometric iron oxide particles. To investigate the formation process of nanoparticles in iron combustion, iron powders (consisting of spheroidal 45–53 µm particles) were injected in an electrically-heated drop tube furnace, operated at a maximum gas temperature of 1375 K, where they experienced high heating rates (10 4 K/s). The particles reacted with oxygen at concentrations of 15, 21, 35, 50 and 100 % by volume in nitrogen diluent gas. Particles ignited and burned brightly, with peak temperatures reaching 2344–2884 K, depending on the oxygen concentration. The observed distribution of the combustion products of iron was bimodal in size and composition, containing (a) dark gray spherical micrometric particles bigger than their iron particle precursors composed of both magnetite and hematite, and (b) highly agglomerated orange-reddish nanometric particles composed of hematite. The mass fraction of nanometric particles accounted for up to 1.7–7.4 % of the collected products, increasing with the oxygen partial pressure. The nanometric particles were spherules, 30–100 nm in diameter. However, they were highly agglomerated with aggregate aerodynamic diameters peaking at 180–560 nm. The yield of nanoparticles increased with increasing oxygen concentration in the furnace. A heuristic model was used to investigate the impact and sensitivity of various strategies for modeling evaporation, aiming to identify key mechanisms that limit the evaporation rate. This study highlights that understanding the type of liquid at the particle surface is crucial, as evaporation can increase significantly with a homogeneous liquid Fe-O particle compared to a core–shell morphology. Additionally, the analysis suggests that evaporation likely occurs in an intermediate regime where gaseous Fe-containing species oxidize in the boundary layer. Understanding these boundary layer processes is essential for accurately modeling the evaporation rate while maintaining computational efficiency.

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Publication Details

Journal
Fuel
Published
2025-04-17
DOI
https://doi.org/10.1016/j.fuel.2025.135366
Citations
12
Primary Topic
Energetic Materials and Combustion
Type
article
Field-Weighted Citation Impact
10.36

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article

Effects of oxygen concentration on nanoparticle formation during combustion of iron powders

Yiannis A. Levendis, Jeffrey M. Bergthorson, Leon C. Thijs, XiaoCheng Mi et al.
12 citations
Fuel
Energetic Materials and Combustion
10.36
article

Effects of oxygen concentration on nanoparticle formation during combustion of iron powders

Yiannis A. Levendis, Jeffrey M. Bergthorson, Leon C. Thijs, XiaoCheng Mi, Aidin Panahi, Di Chang
article en
12 citations

Abstract

• This research examined the formation of products from the combustion of powdered iron. • Products were magnetite/hematite micro-particles and agglomerated hematite nano-particles. • Micro-particles were spherical and bigger than their iron particle precursors. • Nano-particles were 30–100 nm spherules accounting for up to 7.4% of the product mass, increasing with [O 2 ] in the gas. • Iron evaporation and nano-particle formation mechanisms were evaluated with a heuristic model. Powdered iron is being investigated for its potential use as a carbon-free fuel due to its ability to burn heterogeneously and produce oxide particles, which can be collected, reduced back to iron and burned again. However, high temperature oxidation of iron particles can induce partial vaporization/decomposition and evolution of nanometric iron oxide particles. To investigate the formation process of nanoparticles in iron combustion, iron powders (consisting of spheroidal 45–53 µm particles) were injected in an electrically-heated drop tube furnace, operated at a maximum gas temperature of 1375 K, where they experienced high heating rates (10 4 K/s). The particles reacted with oxygen at concentrations of 15, 21, 35, 50 and 100 % by volume in nitrogen diluent gas. Particles ignited and burned brightly, with peak temperatures reaching 2344–2884 K, depending on the oxygen concentration. The observed distribution of the combustion products of iron was bimodal in size and composition, containing (a) dark gray spherical micrometric particles bigger than their iron particle precursors composed of both magnetite and hematite, and (b) highly agglomerated orange-reddish nanometric particles composed of hematite. The mass fraction of nanometric particles accounted for up to 1.7–7.4 % of the collected products, increasing with the oxygen partial pressure. The nanometric particles were spherules, 30–100 nm in diameter. However, they were highly agglomerated with aggregate aerodynamic diameters peaking at 180–560 nm. The yield of nanoparticles increased with increasing oxygen concentration in the furnace. A heuristic model was used to investigate the impact and sensitivity of various strategies for modeling evaporation, aiming to identify key mechanisms that limit the evaporation rate. This study highlights that understanding the type of liquid at the particle surface is crucial, as evaporation can increase significantly with a homogeneous liquid Fe-O particle compared to a core–shell morphology. Additionally, the analysis suggests that evaporation likely occurs in an intermediate regime where gaseous Fe-containing species oxidize in the boundary layer. Understanding these boundary layer processes is essential for accurately modeling the evaporation rate while maintaining computational efficiency.

FuelVol. 397
Worcester Polytechnic Institute (US), Northeastern University (US), McGill University (CA), Eindhoven University of Technology (NL)
National Science Foundation, European Commission, Canadian Space Agency, Division of Materials Research
Clean water and sanitation
Openalex Percentile: Top 1%
Energetic Materials and Combustion
10.36
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