“…Furthermore, X-ray photoelectron, 13 where coke is mainly present in catalysts with a low porosity [215,220]. On the other hand, 13 C NMR and IR are intended for the bulk sample structure [184,279,280], thus being more adequate for the study of coke in highly porous catalysts. However, since coke in reforming catalysts is routinely analyzed together with the catalyst on which it is deposited, 13 C NMR analysis is not recommended due to the ferromagnetic nature of some base transition metals (Fe, Ni, Co) used in reforming catalysts, and, to a lesser extent, the paramagnetic nature of noble transition metals (Pt, Pd and Rh, among others).…”