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Failure modes were studied by sectioning the samples and observing under optical microscope.
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By sectioning the bone samples in midlength and perpendicular to the original drill hole the stage and ratio of new bone formation versus material resorption could be optimally visualized and calculated at its most remote location.
The protein samples were collected by sectioning the OCT-embedded frozen prostate tissues.
Although, the cells in the tissue sections were dead but most of them were cut open by sectioning and became rehydrated during sample preparation, rendering a suitable environment for interactions between drug and protein molecules.
Z-stacks were generated by obtaining optical sections through the samples at 0.35 µm intervals along the z axis.
As mentioned above, the corrosion penetration and Fdet were estimated by observing the mounted cross section of the samples [23].
By observation of the cross sections of the samples, it possible to localise the wax on the pictorial surface.
Drop size distribution was measured as a function of time by computer controlled 3D optical sectioning of the sample and offline image analysis.
The cross-sections were prepared by embedding the samples between acrylic resin cubes.
After microscopic observations and documentation of the sample particles using a digital microscope Keyence VHX-500FD, cross-sections were prepared by embedding the samples in epoxy resin (EpoFix® Resin and Hardener supplied by Struers) and further by polishing them with Micromesh® abrasive cloths of decreasing granulometry (from 1500 to 12000 mesh size).
Cross-section images are obtained by cleaving the samples.
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