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Nanostructured C/SiC/ZrB2–SiC oxidation protective gradient coating was prepared by a two‐step reactive melt infiltration method. In order to reduce production cost, ZrB2 phase was synthesized by the in situ reactive that included low‐cost ZrO2 and B2O3 powders as raw materials. High‐temperature oxidation behavior of coatings was evaluated by isothermal oxidation test at 1773 K in air for 10 hours. Thermodynamical behavior of the coatings at various temperatures during oxidation test and coating process was predicted by HSC Chemistry 6.0 software. Compressive residual stresses of 36.9 MPa and 41 MPa were calculated for in situ and ex situ coatings by Williamson‐Hall method. After 10 hours of isothermal oxidation at 1773K, in situ and ex situ coatings showed 12.84% and 15.69% of weight losses with oxidation rates of 1.87 × 10−2 g cm−3 h−1 and 0.91 × 10−2 g cm−3 h−1, respectively. These results indicated that the oxidation protection ability of the coating produced by the in situ method was very close to ex situ coating.

We proposed a method to investigate the effects of the tumor existence that appear on the surface of the tissue. Finite element analysis provided properties such as the shape, depth, and location of the tumor which are important parameters for physicians to distinguish the correct condition of the patients. Several different cases were created and solved by the ANSYS software and Tactile Images and Stress Graphs were extracted. These results clearly showed the existence of the tumor in the tissue. Having made an artificial tactile sensing system, called "Tactile Tumor Detector", which consists of three main components namely: tactile probe, tactile data processor and tactile display and having performed a number of experiments, we obtained good agreements between the numerical and experimental results. In addition to anticipating the presence of a tumor in the tissue and locating the exact place of the tumor, the experimental results help the user to predict the depth of the tumor inside the tissue

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