Microalloyed steels have evolved in terms of their chemical composition, processing, and metallurgical characteristics since the beginning of the 20th century in the function of fabrication costs and mechanical properties required to obtain high-performance materials needed to accommodate for the growing demands of gas and hydrocarbons transport. As a result of this, microalloyed steels present a good combination of high strength and ductility obtained through the addition of microalloying elements, thermomechanical processing, and controlled cooling, processes capable of producing complex microstructures that improve the mechanical properties of steels. These controlled microstructures can be severely affected and result in catastrophic failures, due to the atomic hydrogen diffusion that occurs during the corrosion process of pipeline steel. Recently, a martensite–bainite microstructure with acicular ferrite has been chosen as a viable candidate to be used in environments with the presence of hydrogen. The aim of this review is to summarize the main changes of chemical composition, processing techniques, and the evolution of the mechanical properties throughout recent history on the use of microalloying in high strength low alloy steels, as well as the effects of hydrogen in newly created pipelines, examining the causes behind the mechanisms of hydrogen embrittlement in these steels.

The aim of the present work is to evaluate the activation energy (Ea) at different cathodic overpotentials (η) by potentiodynamic tests which were carried out at different temperatures of Ni-based, NiCr-m, and NiCr-p porous electrodes, during the alkaline electrolysis processes. On the other hand, the electrochemical stability of the electrodes was evaluated by cyclic voltammetry after 1000 cycles of operation and by potentiostatic tests after 10 h at −1.5 V vs. SCE. The electrodes were sintered with a heating rate of 25 °C/min up to a temperature of 1000 °C (Ni-based and NiCr-m) and 1200 °C (NiCr-p) for 60 min. The results showed that the Ea value was lower for the Ni-based system at equilibrium; however, the NiCr-p electrode had a better performance due to higher negative apparent Ea values as a function of η (dEa/dη). The cyclic voltammetry tests suggest that the NiCr-p electrode improves its activity by about 71% in its long-term operation in comparison with Ni-based and NiCr-m. A similar behavior was observed in the potentiostatic test which showed a higher cathodic current density associated with a charge transfer process after 10 h. The higher stability of the NiCr-p is attributed to a homogeneous Cr distribution in the nickel matrix.

Ti6Al4V (Ti64) alloy is the most used metal material for bone implants because of its good biocompatibility and adapted mechanical properties. Nevertheless, it shows low antibacterial activity, which may favor its failure. Addition of antibacterial elements such as copper should avoid this drawback. This work studies the addition of Cu into a Ti64 matrix resulting in Ti64/xCu composites. Powder mixtures of Ti64/xCu were compacted in a die and then sintered at 1100 °C. Sintering kinetics indicate that densification is achieved by pore filling due to eutectic liquid formed by the reaction of Ti and Cu. The microstructure of the sintered samples is composed mainly of α-Ti and Ti₂Cu phases, but TixCuy intermetallics were also found. Microhardness is increased by the addition of Cu due to densification and the formation of harder phases such as T_i2Cu. However, the stiffness and compression strength are barely the same for all composites. The corrosion resistance is significantly improved by the addition of Cu. Finally, the material with 15 wt% of copper showed the best compromise.