The use of zero-valent iron nanoparticles in the remediation of metal-contaminated soils has received considerable attention. Upon introduction into the soil, zero-valent iron particles corrode into iron oxides, known for their high adsorption capacity for potentially toxic metals. While limited research has directly compared zerovalent iron micro- and nanoparticles, it is important to investigate whether particle size contributes to effective soil remediation. This study focuses on elucidating the comparative kinetics of iron corrosion using iron powder and a nano-iron-biochar composite. In a model experiment, these materials were exposed to a cellulose/ biochar mixture and peat for five months. Mo<spacing diaeresis>ssbauer spectroscopy, X-ray diffraction, scanning electron microscopy with energy dispersive X-ray spectroscopy, and transmission electron microscopy with electron diffraction were used to analyze the corrosion products. The results show a slow corrosion rate in the nano-iron-biochar composite in cellulose due to the protective effect of biochar on the embedded iron nanoparticles. In addition, iron corrosion in peat was inhibited, likely due to the presence of humic substances. Transmission electron microscopy after five months of corrosion revealed round metal particles encased in a graphite capsule with visible channels. Large dissolved organic matter molecules in the peat likely block these channels, inhibiting metallic iron corrosion. Consequently, the nano-iron-biochar composite emerges as a slow-reacting option for immobilizing soil metals in peat. This study highlights the need for further research involving long-term field experiments.