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  5. Magnetite Nanoparticles Enhancing H<sub>2</sub>‐Driven Biomethanation in a Mixed Microbial Community
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Magnetite Nanoparticles Enhancing H2‐Driven Biomethanation in a Mixed Microbial Community

Author(s)
Tucci, Matteo
Sabangan, Jasper I
Cruz Viggi, Carolina
Bertaccini, Lucia
Iosi, Francesca
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Date Issued
August 19, 2025
Type
article
Journal
Global Challenges
Volume
9
Issue
9
DOI
10.1002/gch2.202500367
ISSN
2056-6646
Journal
Global Challenges
Abstract
Biological methanation is increasingly considered for biogas upgrading. Here, the supplementation of conductive magnetite (Fe3O4) nanoparticles is investigated as a strategy to enhance H2-driven biomethanation in a mixed hydrogenotrophic methanogenic community. An enrichment culture, maintained for over 180 days in a fill-and-draw anaerobic bioreactor under H2/CO2 feeding, is used to inoculate batch microcosms containing 0, 1.25, and 2.5 gFe L−1 of magnetite. Magnetite addition resulted in a dose-dependent increase in maximum methane production rates—up to 13-fold compared to controls—and sustained high hydrogen-to-methane conversion yields (78–107%). 16S rRNA gene sequencing reveals that archaeal community composition remained dominated by hydrogenotrophic Methanobrevibacter and Methanobacterium spp., whereas bacterial populations shifted from acetogenic Sporomusa and Acetobacterium spp. toward H2-oxidizing Paracoccus and Thauera spp. at higher magnetite concentrations. Electron microscopy and energy-dispersive X‑ray spectroscopy show that magnetite nanoparticles formed conductive networks bridging microbial cells, and fluorescence in situ hybridization confirmed co-localization of methanogens and Paracoccus within these aggregates. The findings support a direct interspecies electron transfer (DIET) mechanism facilitated by magnetite, whereby Paracoccus spp. oxidize H2 and shuttle electrons to methanogens, accelerating biomethanation. These results highlight the potential of magnetite-mediated DIET to improve power-to-methane processes and advance biogas upgrading technologies.
Handle
https://dspace.unitus.it/handle/2067/63378
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