Abstract
AbstractComplex metallic phases in the Al–Cr–Fe system are considered to be interesting because of their enhanced resistance against corrosion. Single crystal growth of the Al4(Cr,Fe) and Al13(Fe,Cr)4 phases, which is a prerequisite for detailed studies is presented herein for the first time. Along with their binary end members Al4Cr and Al13Fe4 growth of cm3‐size crystals was achieved by using the Czochralski method from Al‐rich solutions at temperatures of approximately 1000 °C. Special emphasis is put on the refinement of the Al‐rich corner of the ternary phase diagram in determining the 1000 °C equilibria between the incongruent melts and the corresponding ternary solid solutions. Our findings confirm earlier data on the existence region of Al13(Fe,Cr)4, but significantly differ from those with respect to the so called Al4(Cr,Fe) phase. It is shown that the existence region of Al4(Cr,Fe) decomposes into four regions of structurally different phases depending on the Cr/Fe ratio. Binary μ‐Al4Cr crystallizes in the hexagonal space group P63/mmc and can dissolve only up to about 1 At‐% iron. More Fe‐rich alloys crystallize in the orthorhombic space group Cmcm (about 2 At‐% iron) or Immm (containing between 3 and about 6 At‐% iron). For crystals containing about 7 At‐% iron the structure belongs to the space group R$\bar{3}$. The grown single crystals were characterized by electron probe microanalysis revealing only weak segregation effects. The structural perfection of the orthorhombic phase was studied using X‐ray topography with the Lang technique. Significant anisotropic properties of this phase allow to discuss structural similarities with decagonal quasicrystals.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Zeitschrift für anorganische und allgemeine Chemie
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.