Fe-Ni-Cr-Co-P alloys were exposed to 17.3% CO 2 -H 2 gas mixtures to investigate the oxidation of minor elements in metallic alloys in the early solar system. Reaction temperatures varied between 700 and 1000°C. Gas-phase equilibrium was attained at 800, 900, and 1000°C, yielding H 2 -H 2 O-CO-CO 2 gas mixtures. Experiments at 700 and 750°C did not achieve gas-phase equilibrium and were performed in H 2 -CO 2 gas mixtures. Reaction timescales varied from 1 to 742 h. The experimental samples were characterized using optical microscopy, electron microprobe analysis, wavelength-dispersive-spectroscopy X-ray elemental mapping, and X-ray diffraction. In all experiments Cr experiences internal oxidation to produce inclusions of chromite (FeCr 2 O 4 ) and eskolaite (Cr 2 O 3 ) and surface layers of Cr-bearing magnetite [(Fe,Cr) 3 O 4 ]. At 900 and 1000°C, P is lost from the alloy via diffusion and sublimation from the metal surface. Analysis of P zoning profiles in the remnant metal cores allows for the determination of the P diffusion coefficient in the bulk metal, which is constant, and the internally oxidized layer, which is shown to vary linearly with distance from the metal surface. At 800 and 900°C, P oxidizes to form a surface layer of graftonite [Fe 3 (PO 4 ) 2 ] while at 700 and 750°C P forms inclusions of the phosphide-mineral schreibersite [(Fe,Ni) 3 P].