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Purpose: This study aims to investigate the effect of different pore diameter and pore length on corrosion properties of anodic aluminum oxide (AAO) film. Design/methodology/approach: AAO layer was produced by two-step anodization aluminum in oxalic acid. The surface morphology was investigated using field emission scanning electron microscopy. The pore diameters were ranging from 25 ± 5 to 65 ± 5 nm and the pore length ranging from 5 to 17 µm. The corrosion properties of the AAO films was analyzed by potentiodynamic polarization and electrochemical impedance spectroscopy tests. Corrosion properties and morphology of the anodic films depending on anodization times and pore expansion times were evaluated. Findings: All highlights of this work can be summarized with the following specified below: more treatment with the protective barrier layer of the solution as the pore diameter increases depends on the morphology of the nanotube structured AAO layer. The excellent corrosion resistance renders AAO films without pore expansion very promising. The oxide layer thickness does not affect the corrosion resistance. The better corrosion resistance of AAO films at low pore length can be ascribed to the barrier layer thickness and the more homogeneous structure. The presence of defects for the higher pore length decreases its corrosion resistance. Originality/value: The AAO films were fabricated by a two-step anodization method in oxalic acid. The anodization times and pore expansion times affect the corrosion performance. The AAO film without pore expansion has good corrosion resistance. The corrosion resistance decreases as the pore length increases. [ABSTRACT FROM AUTHOR]

Copyright of Bilecik Seyh Edebali University Journal of Science / Bilecik Şeyh Edebali Üniversitesi Sosyal Bilimler Dergisi is the property of Bilecik Seyh Edebali University Journal of Science and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Thermochemical heat storage (THS) systems have recently attracted a lot of attention in research and development. In this study, an anodic aluminum oxide (AAO) template, fabricated by a two-step anodization method, was used for the first time as the matrix material for a THS system. Different salts were studied as thermochemical materials for their suitability in low-grade heat storage application driven by solar energy for an open system. Compositions were prepared by absorbing CaCl2, MgCl2, LiCl, LiNO3 and mixtures of these salts under a vacuum in an AAO matrix. Field Emission Scanning Electron Microscopy was used to examine the morphology of the produced AAO composites. Thermal energy storage capacities of the composites were characterized using a differential scanning calorimeter. Characterization analysis showed that anodized Al plates were suitable matrix materials for THS systems, and composite sorbent prepared with a 1:1 ratio LiCl/LiNO3 salt mixture had the highest energy value among all composites, with an energy density of 468.1 kJ·kg−1. [ABSTRACT FROM AUTHOR]

Our previous article (Özkan, Philos. Mag. 2014) described a practical method to determine temperature dependence of the bulk modulus by using pressure dependence of the bulk modulus and the related analytical equations. The present study extended the method at low temperatures to obtain the bulk modulus of the superconducting peroxide MgCNi3, below room temperature. The bulk modulus of MgCNi3, decreases with temperature at a rate less than -0.008 GPa/K below 100K, then it decreases at a higher rate, -0.020GPa/K near 300 K, being close to corresponding theoretical values for the other non-oxide perovskites. Moreover, the Gruneisen parameter of MgCNi3, decreases from 300 K to 120 K, goes through a minimum and increases at lower temperatures. The thermal pressure, otvKT gradually increases from 1.1 MPa/K at 40 K to 2.0 at 100K then, increases with slightly reduced rate to 4.9 MPa/K at 300 K being in reasonable agreement with the related data in the literature. This study verifies that the outlined method may be used to predict bulk moduli data below room temperature to substantiate the related studies. [ABSTRACT FROM AUTHOR]

Mixed-phase TiO2 nanocomposite thin films consisting of anatase and rutile prepared on commercially pure Ti sheets via the electrochemical anodization and annealing treatments were investigated in terms of their photocatalytic activity for antibacterial use around dental implants. The resulting films were characterized by scanning electron microscopy (SEM), and X-ray diffraction (XRD). The topology was assessed by White Light Optical Profiling (WLOP) in the Vertical Scanning Interferometer (VSI) mode. Representative height descriptive parameters of roughness Rα and Rz were calculated. The photocatalytic activity of the resulting TiO2 films was evaluated by the photodegradation of Rhodamine B (RhB) dye solution. The antibacterial ability of the photocatalyst was examined by Aggregatibacter actinomycetemcomitans suspensions in a colony-forming assay. XRD showed that anatase/rutile mixed-phase TiO2 thin films were predominantly in anatase and rutile that were 54.6 wt% and 41.9 wt%, respectively. Craters (2-5 µm) and protruding hills (10-50 µm) on Ti substrates were produced after electrochemical anodization with higher Rα and Rz surface roughness values. Anatase/rutile mixed-phase TiO2 thin films showed 26% photocatalytic decolorization toward RhB dye solution. The number of colonizing bacteria on anatase/rutile mixed-phase TiO2 thin films was decreased significantly in vitro. The photocatalyst was effective against A. actinomycetemcomitans colonization. [ABSTRACT FROM AUTHOR]

The Ni-B-Mo coating on steel by electroless plating and the evaluation of the morphology and corrosion performance after applying heat treatments at different temperatures for 1 h were investigated in this study. The 25-μm-thick coating was uniform and adhesion between the substrate and the coating was good. The coating consisted of an amorphous-like structure in their as-plated condition, and after annealing at 400 °C for 1 h, crystallized nickel, nickel borides, and molybdenum carbide were formed. Immersion tests in 10% HCl solution and potentiodynamic polarization measurements in 3.5% NaCl aqueous solution were applied to investigate corrosion resistance. The corrosion performance of heat-treated coatings was compared with steel and the as-plated coating. By increasing the annealing temperature, corrosion potential shifted toward a noble direction, corrosion current density decreased and the weight loss of specimens decreased, demonstrating an increase in corrosion resistance. Best corrosion performance was achieved by the coating heat treated at 550 °C . [ABSTRACT FROM AUTHOR]

Copyright of ITU Journal Series D: Engineering is the property of Istanbul Technical University and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)