% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Choisez:604233,
author = {Choisez, Laurine and Hemke, Kira and Özgün, Özge and
Pistidda, Claudio and Jeppesen, Henrik and Raabe, Dierk and
Ma, Yan},
title = {{H}ydrogen-based direct reduction of combusted iron powder:
{D}eep pre-oxidation, reduction kinetics and microstructural
analysis},
journal = {Acta materialia},
volume = {268},
issn = {1359-6454},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {PUBDB-2024-01035},
pages = {119752},
year = {2024},
note = {Funding: F.R.S.FNRS chargée de recherche mandate (ID
40011141); Walter Benjamin Programme of the Deutsche
Forschungsgemeinschaft (project number 468209039); ERC
Advanced grant ROC (Grant Agreement No 101054368)},
abstract = {Iron powder can be a sustainable alternative to fossil
fuels in power supply due to its high energy density and
abundance. Iron powder releases energy through exothermic
oxidation (combustion), and stores back energy through its
subsequent hydrogen-based reduction, establishing a circular
loop for renewable energy supply. Hydrogen-based direct
reduction is also gaining global momentum as possible future
backbone technology for sustainable iron and steel
production, with the aim to replace blast furnaces. Here, we
investigate the microstructural formation mechanisms and
reduction kinetics behind hydrogen-based direct reduction of
combusted iron powder at moderate temperatures (400–500
°C) using thermogravimetry, ex-situ X-ray diffraction,
scanning electron microscopy coupled with energy dispersive
spectroscopy and electron backscatter diffraction, as well
as in-situ high-energy X-ray diffraction. The influence of
pre-oxidation treatment was studied by reducing both
as-combusted iron powder (50 $\%$ magnetite and 50 $\%$
hematite) and the same powder after pre-oxidation (100 $\%$
hematite). A gas diffusion-limited reaction was obtained
during the in-situ high-energy X-ray diffraction experiment,
with successive hematite and magnetite reduction, and a
strong increase in reduction kinetics with initial hematite
content. Faster reduction kinetics were obtained during the
thermogravimetry experiment, with simultaneous hematite and
magnetite reduction. In this case, the reduction reaction
was limited by a mix of phase boundary and nucleation and
growth models, as analyzed by multi-step model fitting
methods as well as by microstructural investigation. When
not limited by gas diffusion, the pre-oxidation treatment
showed almost no influence on the reduction time but a
strong effect on the final microstructure of the reduced
powder.},
cin = {FS-PET-D / Hereon / FS-PS / DOOR ; HAS-User},
ddc = {670},
cid = {I:(DE-H253)FS-PET-D-20190712 / I:(DE-H253)Hereon-20210428 /
I:(DE-H253)FS-PS-20131107 / I:(DE-H253)HAS-User-20120731},
pnm = {632 - Materials – Quantum, Complex and Functional
Materials (POF4-632) / 6G3 - PETRA III (DESY) (POF4-6G3) /
FS-Proposal: I-20211077 (I-20211077)},
pid = {G:(DE-HGF)POF4-632 / G:(DE-HGF)POF4-6G3 /
G:(DE-H253)I-20211077},
experiment = {EXP:(DE-H253)P-P02.1-20150101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:001187989800001},
doi = {10.1016/j.actamat.2024.119752},
url = {https://bib-pubdb1.desy.de/record/604233},
}