“…Generally, two distinct mechanisms are responsible for this improvement, depending on the nature of the metal matrix: (1) the carbonaceous nanomaterials react with the metal phase in a molten state, generating carbides with high hardness [12,16], or (2) they do not dissolve into the metal phase, providing, in turn, mechanical strengthening, either through load transfer effect, through refinement of metal grains (the CNTs are located at the grain boundaries), or through interaction with dislocations at the atomic level [7,17]. The former mechanism was reported for titanium [12,15], aluminium-copper alloys [18], and silicon-rich metal alloys [19], while the latter was reported, for example, in the case of mild steel [20], pure iron [21], nickel [14], aluminium [22,23], magnesium [8], and copper [9,24,25]. When embedded in the metal, good interfacial adhesion between CNT and the metal phase has been observed, due to the formation of a thin intermediary layer of metal carbide on the nanomaterial surface, avoiding delamination [26].…”