“…In fact, the poorer metal dispersion on dolomite and olivine catalysts, and therefore the lower amount of Fe active sites available for reforming and WGS reactions, enhances catalyst deactivation, either by sintering, coke deposition or iron phase change (reduction in metal active sites by the oxidation of iron species). As reported by other researchers, iron is more active for tar cracking/reforming when it is in the metal state than oxidized, but the oxidizing nature of steam at high temperatures promotes the oxidation of Fe metal sites [37,83]. Furthermore, given the lower dispersion of Fe on Fe/olivine and Fe/dolomite catalysts, most of it will be deposited on the catalyst surface, which leads to faster coke deposition, and therefore faster deactivation [24].…”