\begin{document}$ {10^{6}}\;{{\rm{s}}^{ - 1}} $\end{document}. However, in contrast with the strain rate range where the phase diagram is a good predictor of the crystal structure of a material, at higher strain rate (\begin{document}$ > {10^{6}}\;{{\rm{s}}^{ - 1}} $\end{document}) the phase diagram measured can be quite different not only in shifting the boundary line between various phases, but also in giving a different sequence of crystal structure. High-power laser facility can drive shock wave and simultaneously provide a precisely synchronized ultra-short and ultra-intense X-ray source. Here, based on the Prototype laser facility, an in situ X-ray diffraction platform for diagnosing shock-induced phase transition of polycrystalline material is established. The in situ observation of material phase transition under high-strain-rate shock loading is carried out with typical metals of vanadium and iron. Diffraction results are consistent with vanadium remaining in the body-centered-cubic structure up to 69 GPa, while iron transforms from the body-centered-cubic structure into hexagonal-close-packed structure at 159 GPa. The compressive properties of vanadium and iron obtained in in situ X-ray diffraction experiment are in good agreement with their macroscopic Hugonoit curves. The decrease in the lattice volume over the pressure step period yields a strain rate on the order of \begin{document}$ {10^{8}} - {10^{9}}\;{{\rm{s}}^{ - 1}} $\end{document}. The available of the presented in situ X-ray diffraction plateform offers the potential to extend our understanding of the kinetics of phase transition in polycrystalline under high-pressure high-strain-rate shock compression."> <i>In situ</i> observation of phase transition in polycrystalline under high-pressure high-strain-rate shock compression by X-ray diffraction - 必威体育下载

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Chen Xiao-Hui, Tan Bo-Zhong, Xue Tao, Ma Yun-Can, Jin Sai, Li Zhi-Jun, Xin Yue-Feng, Li Xiao-Ya, Li Jun
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  • Abstract views:7122
  • PDF Downloads:150
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  • Received Date:16 June 2020
  • Accepted Date:15 July 2020
  • Available Online:27 November 2020
  • Published Online:20 December 2020

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