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Wetting of calcium fluoride by liquid metals

Barzilai, Shmuel ; Froumin, Natalya ; Glickman, Eugene ; Fuks, David ; Frage, Nahum

Journal of Materials Science, 2012, Vol.47(24), pp.8404-8418 [Tạp chí có phản biện]

ISSN: 0022-2461 ; E-ISSN: 1573-4803 ; DOI: 10.1007/s10853-012-6680-z

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  • Nhan đề:
    Wetting of calcium fluoride by liquid metals
  • Tác giả: Barzilai, Shmuel ; Froumin, Natalya ; Glickman, Eugene ; Fuks, David ; Frage, Nahum
  • Chủ đề: Thermodynamics -- Chemical Properties ; Thermodynamics -- Analysis ; Fluorides -- Chemical Properties ; Fluorides -- Analysis ; Liquid Metals -- Chemical Properties ; Liquid Metals -- Analysis ; Density Functional Theory -- Chemical Properties ; Density Functional Theory -- Analysis
  • Là 1 phần của: Journal of Materials Science, 2012, Vol.47(24), pp.8404-8418
  • Mô tả: The results of wetting experiments for the CaF 2 /Me and CaF 2 /Me–Ti systems (Me = Cu, Ge, Al, In, Ga, Sn, and Au) are presented and discussed. It was found that pure metals do not wet the CaF 2 substrate, while a small quantity of Ti added to the melt improves the wetting. The effect of Ti depends on its thermodynamic activity in the melts. According to the thermodynamic analysis and experimental observations, Ti dissolved in the metals does not react with the substrate to form any new condensed phase at the interface and its effect cannot be attributed to the “reactive wetting” phenomenon. Density functional theory (DFT) was applied to focus on the nature of chemical bonding between the atoms in the melt and the surface of the substrate in these systems. It was demonstrated that partly filled d-states of Ti stimulate its adsorption onto F ions. Ab initio calculations show that Ti may segregate to the interface, decreasing the energy of CaF 2 /Me–Ti system. Based on the results of thermodynamic and DFT analyses, it is proposed that Ti segregation at the interface may be considered as the source of the improved wetting.
  • Ngôn ngữ: English
  • Số nhận dạng: ISSN: 0022-2461 ; E-ISSN: 1573-4803 ; DOI: 10.1007/s10853-012-6680-z

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