Microstructure and Mechanical Properties of Directional Order Porous Tisic Through Reactive Synthesis
SSRN, ISSN: 1556-5068
2022
- 170Usage
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
Directional order porous TiSiC has been prepared by freezing casting, which is embodied in lamellar porous and material structure. The maximum compression stress is higher than the disorder structure and increases with an increase of solid content with 22 MPa 49 MPa and 89 MPa with a solid content of 15%, 20% and 25%. While elastic deformation shows the opposite trend. And the Young modulus of directional order porous TiSiC is nearly linear, which indicated the mechanism can be explained by the parallel model. The reason why the fitting value deviates from the theoretical value has been investigated. Besides the deviation of the porous structure from the theoretical model. Unique properties provide porous TiSiC2 energy dissipation mechanism, cyclic loading at elastic stage indicated that energy dissipation (Wd) with each loop is from 0.0009 to 0.0139 MJ/m with the increase of porosity. The fracture failure behavior was explored, and it was found that there were two main forms of macroscopic failure: splitting and fragmentation. Found by microscopic observation, the absorbed-in-fracture energy in irreversible deformation in the plastic stage includes kink bands, crack extension and delamination.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85179528852&origin=inward; http://dx.doi.org/10.2139/ssrn.4052264; https://www.ssrn.com/abstract=4052264; https://dx.doi.org/10.2139/ssrn.4052264; https://papers.ssrn.com/sol3/papers.cfm?abstract_id=4052264; https://ssrn.com/abstract=4052264
Elsevier BV
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