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Secotom

Manufactured by Struers
Sourced in Denmark

The Secotom is a precision cutting machine designed for sample preparation in materials analysis and research. It is capable of accurately cutting a wide range of materials, including metals, ceramics, and composites, with minimal damage to the sample.

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6 protocols using secotom

1

Microstructural Analysis of Humeral Head

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To determine the microstructure of the humeral head components, cross sections were custom cut using a precision cutting machine (Secotom; Struers). Cross sections were subjected to a hot mounting process with a quick-forming resin (PolyFast; Struers) and were then polished to achieve a mirror finish. Subsequently, chemical etching of the polished surface was performed to expose the microstructure of the alloy. The presence or absence of banding—segregation bands within the alloy microstructure—of each head was recorded and delineated on by 2 authors (A.H. and R.P.).
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2

Homogeneous Alloy Microstructure Analysis

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Alloy samples were directly sectioned from the implant components. To ensure that the alloy microstructure was homogeneous, samples were cut along the longitudinal and the transverse direction using a cut-off machine (Secotom, Struers). The longitudinally and transverse oriented samples were then embedded in an epoxy resin with a hot mounting press (CitoPress, Struers). The metallographic preparation was performed with an automatic grinding/polishing machine (Tegramin, Struers) using the following steps: sequential grinding using SiC paper with 220 grit (2 minutes) and 320 grit (4 minutes), followed by mechanical polishing with 9 μm diamond suspension (10 minutes) and by 0.04 μm colloidal silica suspension (8 minutes). A final ion polishing (Cross-section polisher IB-19530 CP, JEOL) step at 4kV for 10 min, followed by 3kV for 15 min at 4°, was also performed to provide optimal conditions for microstructural analysis.
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3

Fabrication of Sintered Zirconia Blocks

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Zpex Smile (Tosoh, Tokyo, Japan) were used as raw materials for 5Y zirconia containing 0.05 wt% of alumina. The raw material was press-molded by a uniaxial press molding machine (Sansho Industry, OSAKA, JAPAN) to obtain a block having a diameter of 19 mm × 19 mm and a disc having a diameter of 100 mm × 17 mm. After that, CIP treatment was performed at 200 MPa using a cold hydrostatic isotropic press (Sansho Industry, Osaka, Japan).
The obtained zirconia block/disc was degreased at 500 °C in an inert gas oven (INH-21CD, KOYO THERMO, Nara, Japan) and then fired in a firing furnace (SC-3035F, MOTOYAMA, Osaka, Japan) at 970 °C, to obtain a semi-sintered zirconia block/disk (φ18 mm × 18 mm/φ98.5 mm × 16 mm).
The semi-sintered zirconia block/disk was cut with a cutting machine (Secotom, Struers, Ballerup, Denmark), and the surface was polished with SiC water-resistant polishing paper (# 1000), to reach a shape suitable for each test.
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4

Mg-Y-RE-Zr Alloy Degradation Study

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A Mg-Y-RE-Zr based magnesium alloy (WE43MEO, Meotec GmbH, Aachen, Germany) nominally containing app. 4% yttrium, 3% Rare Earths and less than 0.6% zirconium with magnesium being the remainer was included in this study. Samples were cut-grinded from a rod (Secotom, Struers GmbH, Willich, Germany), followed by chemical polishing in nitric acid (HNO3) (65% in volume). The samples with a final diameter of 18.8 mm and 0.2 mm height were washed in water and ethanol and preserved in a dry-air closet to prevent further oxidation. Prior to the degradation experiments, test samples were degreased in an ultrasonic bath of ethanol for 10 min. Mg WE43 samples further underwent PEO treatment in a stainless-steel container forming the counter-electrode. A layer thickness of 9 +/− 6 µm was targeted for both PEO variants by adjusting current density between 1.35–3.5 A/dm2 and the corresponding treatment time between 8–25 min. As electrolytes, two phosphate-rich electrolytes supplemented with different conductivity agents were used (Table 2). For each experiment, n = 11 test samples of Mg WE43 and the two types of PEO treatments (PEO-A and PEO-B) were used each.
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5

Fabrication of Pre-Sintered Zirconia Specimens

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Commercially available 5Y zirconia powder containing 0.05 wt% of alumina (Zpex Smile, Tosoh, Tokyo, Japan) was used for a starting powder. The powder was pressed uniaxially by a press molding machine (Sansho Industry, Osaka, Japan) to obtain zirconia blocks having a diameter of 19 mm × thickness of 19 mm and discs having a diameter of 100 mm × thickness of 17 mm. Next, the blocks and discs were isostatically pressed at 200 MPa using a cold hydrostatic isotropic press (Sansho Industry, Osaka, Japan).
The pressed zirconia blocks/discs were degreased at 500 °C in an inert gas oven (INH-21CD, KOYO THERMO, Nara, Japan) and then fired in a firing furnace (SC-3035F, MOTOYAMA, Osaka, Japan) at 970 °C to obtain a pre-sintered zirconia block/disk (φ18 mm × 18 mm/φ98.5 mm × 16 mm).
The pre-sintered zirconia blocks and disks were cut with cutting equipment (Secotom, Struers, Ballerup, Denmark), and surface polished with SiC water resistant polishing paper (# 1000) to reach the dimension required by each test.
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6

Undecalcified Histomorphometric Analysis

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After micro-CT, defect areas including a 5-mm edge of native bone at both the anterior and posterior margins were excised from the hemi-mandible I-12. The segments were fixed for at least 7 days in 10% phosphate-buffered formaldehyde solution.
Undecalcified segments were sectioned with a diamond saw (Secotom, Struers) along the anteroposterior direction thereafter dehydrated with methanol, and then embedded in methyl-methacrylate-based resin. The hardened specimen blocks were cut in the longitudinal direction along the axis of the implant. Sections of interest were sawn off with the diamond saw, ground and finally polished up with a Buelher micro-grinding device to reach 100 mm thickness.
Finally, sections were stained with modified Masson -Goldner's trichrome dye to evaluate bone healing efficiency by histomorphometry and examined under a light microscopy (DMRB Leica, DXC930 Camera Sony).
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