Mechanisms of Inhibitor Action: Passivation and Self-Healing

In this chapter, we will briefly review the systematics of corrosion inhibitors and the classical mechanisms of action of corrosion inhibitors, the latter with an emphasis on inhibitors interacting with the material surface. The different roles corrosion inhibitors have in protecting materials surfaces will be described - with examples from applications in the oil and gas sector, but also more general. We will discuss in some detail the interaction of an imidazoline-based surfactant inhibitor with mild steel and the interaction of 2-mercaptobenzothiazole (MBT) with copper and zinc. By adsorbing to surfaces, molecules in general block sites for metal dissolution. Good inhibitors furthermore react with dissolution products to form insoluble films, in analogy to the formation of conversion coatings. Furthermore, inhibitors may interfere with the kinetics of the cathodic reaction. Over decades, a challenge for the use of inhibitors has been leaching into the environment of inhibiting molecules. Modern triggered release concepts ensure that inhibitors become available only if a corrosion attack has begun. Such triggered release systems have successfully been used for the self-healing of coatings, and we will discuss one example of the interaction of a cyclodextrin with MBT to see how this works for inhibitors. Future applications in the oil and gas sector may consider the use of intelligent coatings. © 2020 Wiley-VCH Verlag GmbH Co. KGaA. All rights reserved

Genome-wide association study identifies five new schizophrenia loci

We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects. The combined stage 1 and 2 analysis yielded genome-wide significant associations with schizophrenia for seven loci, five of which are new (1p21.3, 2q32.3, 8p23.2, 8q21.3 and 10q24.32-q24.33) and two of which have been previously implicated (6p21.32-p22.1 and 18q21.2). The strongest new finding (P = 1.6 × 10 -11) was with rs1625579 within an intron of a putative primary transcript for MIR137 (microRNA 137), a known regulator of neuronal development. Four other schizophrenia loci achieving genome-wide significance contain predicted targets of MIR137, suggesting MIR137-mediated dysregulation as a previously unknown etiologic mechanism in schizophrenia. In a joint analysis with a bipolar disorder sample (16,374 affected individuals and 14,044 controls), three loci reached genome-wide significance: CACNA1C (rs4765905, P = 7.0 × 10 -9), ANK3 (rs10994359, P = 2.5 × 10 -8) and the ITIH3-ITIH4 region (rs2239547, P = 7.8 × 10 -9). © 2011 Nature America, Inc. All rights reserved