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The electrochemical behavior of UNS(1) N08031 was investigated as a function of electrode potential in Green-Death(2) solution at 40 °C. The UNS N08031 surface is in a stable passive state during cyclic potentiodynamic polarization without an initiation and/or propagation of localized corrosion. In potentiostatic polarization of UNS N08031 for 3600 s, passive current density increases with an increase in the passivation potential from 0.7 to 1.0 VSSE (silver/silver chloride reference electrode in saturated potassium chloride) Electrochemical impedance spectroscopy (EIS) and Mott-Schottky (M-S) analysis showed that a more defective n-type semiconductive passive film forms as the potential increases. X-ray photoelectron spectroscopy (XPS) revealed that passive film consists of mainly chromium and minor iron and nickel oxides. The mechanism of the defective passive film formation is discussed. The increase of the applied potential is considered to be a reason for the change in passive film stability.
Geothermal brine is a complex system containing a wide variety of dissolved salts resulting from the condition s in a geothermal well. These fluids lead to corrosion in pipes and other parts of geothermal system construction and necessitate intense research efforts in finding new suitable materials. Carbon steel is susceptible to corrosion in geothermal brine especially when it is exposed to a high temperature and high-pressure medium, which is considered to be an aggressive environment. An artificial geothermal water, bas ed on a brine composition found in Indonesia, was used to investigate the performance of high alloyed materials. The electrolyte has pH 4 and contains 1,500 mg/l Cl-, 20 mg/l SO4 2-, 15 mg/l HCO3 -, 200 mg/l Ca 2+, 250 mg/l K+, and 600 mg/l Na+. In order to protect the bare material in geothermal application, it is necessary to either use high alloyed material s or coatings. In this research, a coating system consisting of polyaniline and silicon dioxide was investigated regarding its behavior to protect carbon steel. In detail, the effect of SiO2 and polyaniline (PANi) addition was evaluated by exposure and electrochemical tests for 7 days, i.e. electrochemical impedance spectroscopy (EIS) and open circuit potential (OCP ) at room temperature and 150 °C with 1 MPa pressure .
Finally, it can be summarized that the second edition of this popular textbook provides a comprehensive overview on the practical basics and applications of conducting polymers. It fulfills its intension of assisting various researchers from diverse fields to become familiar with fundamentals and applications of conducting polymers.
The electrochemical behavior of UNS N08031 was investigated as a function of electrode potential in Green-Death solution at 40 °C. The UNS N08031 surface is in a stable passive state during cyclic potentiodynamic polarization without an initiation and/or propagation of localized corrosion. In potentiostatic polarization of UNS N08031 for 3600 s, passive current density increases with an increase in the passivation potential from 0.7 to 1.0 VSSE (silver/silver chloride reference electrode in saturated potassium chloride) Electrochemical impedance spectroscopy (EIS) and Mott-Schottky (M-S) analysis showed that a more defective n-type semiconductive passive film forms as the potential increases. X-ray photoelectron spectroscopy (XPS) revealed that passive film consists of mainly chromium and minor iron and nickel oxides. The mechanism of the defective passive film formation is discussed. The increase of the applied potential is considered to be a reason for the change in passive film stability.
Aging of passive film formed on UNS N08031 was investigated as a function of passivation time in Green-Death solution at 40°C. The specimen surface was in a stable passive state in the solution.
The passive current density increased with an increase in the passivation potential. Electrochemical Impedance Spectroscopy and Mott–Schottky (M–S) analyses revealed that a more defective n-type
semiconductive passive film formed as the potential increased while the film became stable as the defects in the film decreased at potential lower than 1.0 VSSE. The increase of the applied potential and the polarisation time are likely reasons for the change in passive film stability.
Wie schon in den vorherigen Ausgaben bietet dieses Buch Studierenden der technischen Fach- und Hochschulen eine gute Unterstützung und ist insbesondere für die in der Industrie tätigen Techniker, Konstrukteure und Ingenieure zu empfehlen. Die aktualisierte Bibliographie von zum Thema einschlägigen Dissertationsschriften am Ende des Werkes bietet auch einen hohen Nutzen für den wissenschaftlichen Gebrauch.
Trotz teilweise nicht exakter Formulierungen und Terminologie bietet dieses Buch der angesprochenen Leserschaft einen umfassenden Einstieg in die Korrosionsthematik. Die am Ende jedes Kapitels aufgeführte Literatur liefert Beispiele zum vertiefenden Studium.
Erwähnenswert ist auf jeden Fall die haptisch interessante Einbandgestaltung, die die Neugierde auf dieses Buch fördert.
Abschließend kann gesagt werden, dass dieses Buch umfassend in die einzelnen Bereiche der Physik einführt. Aufgrund seines modularen Aufbaus und der Kombination von Lehr- und Arbeitsbuch eignet es sich sehr gut zum Selbststudium. Für den Weg zum Seminar ist es aufgrund seines Gewichtes eher nichts. Es wird jedoch seinem Anspruch, ein unentbehrlicher Begleiter für das Physikgrundstudium zu sein, in jeder Hinsicht gerecht.
Zusammenfassend kann gesagt werden, dass dieses Lehrbuch einen prägnanten und verständlichen Einstieg in die Korrosion und den Korrosionsschutz liefert. Nicht nur der adressierten Zielgruppe, sondern auch anderen Interessenten bietet es einen kompakten Überblick über korrosionsrelevante Grundlagen und Aspekte. Jedoch vermisst der Rezensent eine Übersicht zu weiterführender Literatur, die für den interessierten Nutzer dieses Lehrbuches sicherlich für einen tieferen Einstieg in
die Thematik nützlich wäre.