Study of Ybco Superconductor Coating on Austenitic Stainless Steel By Electrophoretic Deposition Method

2020 ◽  
Vol MA2020-02 (68) ◽  
pp. 3591-3591
Author(s):  
Shuya Sato ◽  
Setsuko Koura
2020 ◽  
Vol 840 ◽  
pp. 336-344
Author(s):  
Martinus Kriswanto ◽  
Muhammad Khairurrijal ◽  
Dave Leonard Junior Wajong ◽  
Tofan Maliki Kadarismanto ◽  
Yusril Yusuf

Hydroxyapatite (HAp) made of capiz shell has been successfully coated onto stainless steel 316L substrate using electrophoretic deposition (EPD) method. In this study, three variations were applied, they were the voltages of 25 V and 50 V, the withdrawal speeds of 0.1 mm/s, 0.5 mm/s, and 1 mm/s, and the sintering temperatures of 750, 850, and 950 °C. These variations were applied to determine the differences in morphology and crystal structure of the layers so that the most suitable result was obtained as a candidate for the bone implant. Characterization was done by Scanning Electron Microscope and X-Ray Diffractometer. The EPD process and the application of sintering temperature eliminated the phase of B type apatite carbonate which made the purity of the HAp layer higher. The SEM results show that the layer was more homogeneous and free of cracking at a voltage of 50 V and the withdrawal speed of 0.1 mm/s. The layer density was higher as the voltage and sintering temperature increased. Higher sintering temperature also made the layer more homogeneous, but at 950 °C, stainless steel 316L substrate underwent a phase transformation which caused the decreasing of the purity of the HAp layer. The best results were obtained by applying a50 V voltage, a withdrawal speed of 0.1 mm/s, and a sintering temperature of 850 °C.


2021 ◽  
Author(s):  
Shuya Sato ◽  
Setsuko Koura

Yttrium-based superconductors (YBCO) haven’t been widely applied. One reason is because of its high cost. In this study, we replaced the substrate and the fabrication method with lower-cost one, and found the possibility of making high-performance superconducting wires. Specifically, YBCO layer was fabricated by Electrophoretic deposition (EPD). Fabrication by this method needs calcination. The phenomenon that Fe in the substrate diffuses to YBCO layer during calcinating was confirmed. It was caused a decrease in YBCO performance. Therefore, CeO2 as an intermediate layer of substrate and YBCO was fabricated by EPD. It showed the possibility of preventing the spread of Fe. On the other hand, textured CeO2 layer was also fabricated in order to increase the characteristics of superconductor by EPD. And then it was also shown that to obtain a priority orientation is possible by controlling the current value.


2021 ◽  
pp. 088391152110635
Author(s):  
Zahra Sadeghinia ◽  
Rahmatollah Emadi ◽  
Fatemeh Shamoradi

In this research, bioglass nanoparticles were synthesized via sol-gel method and a polycaprolactone-chitosan-bioglass nanocomposite coating was formed on SS316L substrate using electrophoretic deposition method. Then, the effects of voltage and deposition time on morphology, thickness, roughness, and wettability of final coating were investigated. Finally, biocompatibility and toxicity of the coating were evaluated. The results showed that increase of both time and voltage enhanced the thickness, roughness, and wettability of coating. Also, increase of deposition time increased the agglomeration. Therefore, it can be concluded that voltage of 20 V and time of 10 min are suitable for the formation of a uniform agglomerate-free coating. The presence of bioglass nanoparticles also led to the increase of roughness and improvement of polycaprolactone hydrophobicity. The results also showed higher bioactivity in polycaprolactone-chitosan-1% bioglass nanocomposite coating sample. This sample had a roughness ( Ra) of 1.048 ± 0.037 μm and thickness of 2.54 ± 0.14 μm. In summary, the results indicated that coating of polycaprolactone-chitosan-bioglass nanocomposite on SS316L substrate could be a suitable surface treatment to increase its in vivo bioactivity and biocompatibility.


Author(s):  
R. Gonzalez ◽  
L. Bru

The analysis of stacking fault tetrahedra (SFT) in fatigued metals (1,2) is somewhat complicated, due partly to their relatively low density, but principally to the presence of a very high density of dislocations which hides them. In order to overcome this second difficulty, we have used in this work an austenitic stainless steel that deforms in a planar mode and, as expected, examination of the substructure revealed planar arrays of dislocation dipoles rather than the cellular structures which appear both in single and polycrystals of cyclically deformed copper and silver. This more uniform distribution of dislocations allows a better identification of the SFT.The samples were fatigue deformed at the constant total strain amplitude Δε = 0.025 for 5 cycles at three temperatures: 85, 293 and 773 K. One of the samples was tensile strained with a total deformation of 3.5%.


Author(s):  
G. Fourlaris ◽  
T. Gladman

Stainless steels have widespread applications due to their good corrosion resistance, but for certain types of large naval constructions, other requirements are imposed such as high strength and toughness , and modified magnetic characteristics.The magnetic characteristics of a 302 type metastable austenitic stainless steel has been assessed after various cold rolling treatments designed to increase strength by strain inducement of martensite. A grade 817M40 low alloy medium carbon steel was used as a reference material.The metastable austenitic stainless steel after solution treatment possesses a fully austenitic microstructure. However its tensile strength , in the solution treated condition , is low.Cold rolling results in the strain induced transformation to α’- martensite in austenitic matrix and enhances the tensile strength. However , α’-martensite is ferromagnetic , and its introduction to an otherwise fully paramagnetic matrix alters the magnetic response of the material. An example of the mixed martensitic-retained austenitic microstructure obtained after the cold rolling experiment is provided in the SEM micrograph of Figure 1.


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