2-hydroxyethilammonium oleate protic ionic liquid as corrosion inhibitor for aluminum in neutral medium

Protic ionic liquid (PIL) 2‐hydroxyethylammonium oleate (2HEAOl) proved to be a good lubricant for aluminum‐forming processes. However, with the aim of keeping the formed component integrity, it is interesting that the same substance employed during forming does not need to be removed and works out as corrosion inhibitor. Then, the aim of this study was to test the performance of 2HEAOl as corrosion inhibitor for aluminum in neutral 0.5 mol/L NaCl medium by electrochemical characterization. Results showed that the concentration of 5 × 10−4 mol/L was a suitable concentration to promote corrosion inhibition until 72 h at the high chloride concentration studied. The PIL worked out as mixed‐type organic corrosion inhibitor, as it promoted the diminution of the oxygen reduction reaction rate and, in consequence, the pit initiation by its adsorption on the metal surface

An amino-based protic ionic liquid as a corrosion inhibitor of mild steel in aqueous chloride solutions

Protic ionic liquids (PILs) have shown to be promising substances as corrosion inhibitors (CIs). In line with this, the aim of this study is to study the performance and propose the corrosion inhibition mechanism of N‐methyl‐2‐ hydroxyethylamine (M‐2HEAOL) and bis‐2‐hidroxyethylamine (B‐HEAOL) oleate, for mild steel, in a neutral chloride solution. Electrochemical characterization was conducted under static and hydrodynamic conditions, and it was revealed that M‐2HEAOL and B‐HEAOL worked as mixed‐type CIs with more interference on the anodic reaction. Inhibition efficiency depended on the concentration reaching 97% of inhibition efficiency in 5 mmol/L concentration. Scanning electron microscopy, optical interferometry, Raman spectroscopy, and Fourier‐transform infrared spectroscopy are used to elicit the chemical composition of the surface film and corrosion morphology of steel in the presence of CIs, the adsorption processes of which involved physical and chemical adsorption between metal and different parts of ionic liquids. The results allowed the proposition of a corrosion inhibition mechanism

N-methyl-2-hydroxyethylammonium oleate ionic liquid performance as corrosion inhibitor for mild steel in hydrochloric acid medium

The aim of the present study is to evaluate the performance of N‐methyl‐2‐ hydroxyethylammonium oleate ([m‐2HEA][Ol]) as a corrosion inhibitor for mild steel in a 0.1‐mol/L hydrochloric acid solution and also investigate the role of chloride in the inhibition mechanism. This protic ionic liquid (PIL) has formerly shown a high efficiency as a corrosion inhibitor in a neutral chloride medium. Electrochemical and weight loss measurements, surface contact angle determination, scanning electron microscopy, and Raman spectroscopy were used to understand the factors that influence the response of the studied inhibitor. Results revealed that [m‐2HEA][Ol] behaves as a mixed‐type adsorption inhibitor, by blocking cathodic sites and by modifying the activation energy of the anodic reaction, and it can reach up to 94–97% of inhibition efficiency. PIL adsorption was enhanced by the excess of positive charge of the mild steel. The effect of inhibitor molecule has been discussed to propose a mechanism that explains the inhibitory action of the corrosion inhibitor, pointing out the role of chloride in the inhibition mechanism

Correlation between morphology and electrochemical behavior of chromium-free conversion coatings for aluminum alloys corrosion protection

Chromium(III)-based, tungstate-based and cerium(III)-based conversion coatings on AA2024-T3 are compared in terms of morphology and electrochemical behavior. The durability of coatings is studied under neutral salt spray conditions and in a weakly aggressive electrolyte composed of 0.1 mol/L Na2SO4 and 10−3 mol/L NaCl. The use of both microscopic and electrochemical analyses such as fitting of electrochemical impedance spectroscopy diagrams allows one to have a better insight into the influence of the interfacial and conversion layers on the degradation phenomena. The role of the remaining native interfacial oxide layer is particularly highlighted, its resistance being the highest at the beginning of the exposure. The degradation of the barrier effect of this interfacial layer is demonstrated to be closely related to the performances of the conversion layer both in terms of passive protection and a reservoir of corrosion inhibitor. Finally, coupled analyses from EIS fitting and microscopic observations allow one to reach a precise interpretation of the strengths and weak points of such system. This diagnostic is an important step towards the optimization of the chromium-free systems

Niobium and niobium-iron coatings on API 5LX 70 steel applied with HVOF

The present study aimed to create and characterize niobium and niobium-iron60% coatings applied to steel API 5L X70 using the hypersonic thermal spray process (HVOF). The morphologies of the coatings were analyzed using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and profilometry, while the coatings’ hardnesses was evaluated using the Vickers hardness test. The coatings’ corrosion resistance was evaluated by monitoring their open circuit potential and potentiodynamic polarization and performing electrochemical impedance spectroscopy in a 0.05 M NaCl solution. The results showed that the niobium-iron coating contained minor porosity regions, while such defects occurred over large regions of the niobium coating. In terms of corrosion resistance, the coatings obtained in this work promoted a reduction in the substrate’s corrosion rate, but the presence of discontinuities such as porosity compromised the barrier effects of these coatings

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Abstract: Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk. FANCM, which encodes for a DNA translocase, has been proposed as a breast cancer predisposition gene, with greater effects for the ER-negative and triple-negative breast cancer (TNBC) subtypes. We tested the three recurrent protein-truncating variants FANCM:p.Arg658*, p.Gln1701*, and p.Arg1931* for association with breast cancer risk in 67,112 cases, 53,766 controls, and 26,662 carriers of pathogenic variants of BRCA1 or BRCA2. These three variants were also studied functionally by measuring survival and chromosome fragility in FANCM−/− patient-derived immortalized fibroblasts treated with diepoxybutane or olaparib. We observed that FANCM:p.Arg658* was associated with increased risk of ER-negative disease and TNBC (OR = 2.44, P = 0.034 and OR = 3.79; P = 0.009, respectively). In a country-restricted analysis, we confirmed the associations detected for FANCM:p.Arg658* and found that also FANCM:p.Arg1931* was associated with ER-negative breast cancer risk (OR = 1.96; P = 0.006). The functional results indicated that all three variants were deleterious affecting cell survival and chromosome stability with FANCM:p.Arg658* causing more severe phenotypes. In conclusion, we confirmed that the two rare FANCM deleterious variants p.Arg658* and p.Arg1931* are risk factors for ER-negative and TNBC subtypes. Overall our data suggest that the effect of truncating variants on breast cancer risk may depend on their position in the gene. Cell sensitivity to olaparib exposure, identifies a possible therapeutic option to treat FANCM-associated tumors