The review presented herein is regarding the stress corrosion cracking (SCC) phenomena of carbon steel pipelines affected by the corrosive electrolytes that comes from external (E) and internal (I) environments, as well as the susceptibility and tensile stress on the SCC. Some useful tools are presented including essential aspects for determining and describing the E-SCC and I-SCC in oil and gas pipelines. Therefore, this study aims to present a comprehensive and critical review of a brief experimental summary, and a comparison of physicochemical, mechanical, and electrochemical data affecting external and internal SCC in carbon steel pipelines exposed to corrosive media have been conducted. The SCC, hydrogen-induced cracking (HIC), hydrogen embrittlement, and sulfide stress cracking (SSC) are attributed to the pH, and to hydrogen becoming more corrosive by combining external and internal sources promoting cracking, such as sulfide compounds, acidic soils, acidic atmospheric compounds, hydrochloric acid, sulfuric acid, sodium hydroxide, organic acids (acetic acid, mainly), bacteria induced corrosion, cathodic polarization, among others. SCC growth is a reaction between the microstructural, chemical, and mechanical effects and it depends on the external and internal environmental sources promoting unpredictable cracks and fractures. In some cases, E-SCC could be initiated by hydrogen that comes from the over-voltage during the cathodic protection processes. I-SCC could be activated by over-operating pressure and temperature at flowing media during the production, gathering, storage and transportation of wet hydrocarbons through pipelines. The mechanical properties related to I-SCC were higher in comparison with those reviewed by E-SCC, suggesting that pipelines suffer more susceptibility to I-SCC. When a pipeline is designed, the internal fluid being transported (changes of environments) and the external environment concerning SCC should be considered. This review offers a good starting point for newcomers into the field, it is written as a tutorial, and covers a large number of basic standards in the area.

To date, the formation mechanisms of TiO₂, as well as its heterostructures, have not been clarified. Moreover, detailed research on the transition from a tetragonal anatase phase to the monoclinic phase of the TiO₂(B) phase and their interface structure has been quite limited until now. In the present study, we report on the sonochemical synthesis of TiO₂-anatase with a crystallite size of 5.2 ± 1.5 nm under different NaOH concentrations via the hydrothermal method. The use of alkaline solution and the effect of the temperature and reaction time on the formation and structural properties of TiO₂-anatase nanopowders were studied. The effects of NaOH concentration on the formation and transformation of titanate structures are subject to thermal effects that stem from the redistribution of energy in the system. These mechanisms could be attributed to three phenomena: (1) the self-assembly of nanofibers and nanosheets, (2) the Ostwald ripening process, and (3) the self-development of hollow TiO₂ mesostructures.