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Title: Interactions between zirconia–yttria–tantala thermal barrier oxides and silicate melts

Journal Article · · Acta Materialia
ORCiD logo [1];  [2];  [2];  [2];  [2];  [2]
  1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Univ. of California, Santa Barbara, CA (United States)
  2. Univ. of California, Santa Barbara, CA (United States)

The effects of TaO2.5 additions to Y4Zr3O12 (YZO) on its interactions with calcium-magnesium alumino-silicate (CMAS) melts are investigated herein. YZO is a candidate material for the protection of novel ZrO2-YO1.5-TaO2.5 based thermal barrier coatings (TBCs) against CMAS attack, but thermochemical considerations dictate that YZO contain TaO2.5 for interfacial compatibility. Oxides based on Y4Zr3-xTaxO12+0.5x (x = =0, 0.7, 1.4) were mixed with various ternary and quinary silicate compositions ranging in Ca:Si ratio from 0.35 to 1.13 and equilibrated at 1300 °C. The results show that all combinations form the desired apatite phase except for the mixture of the higher Ta5+ content with the lowest Ca:Si melt. It is found that the addition of Ta5+ increases the capture of Y3+ by the reprecipitated fluorite, decreasing the amount available to form apatite and eventually suppressing it at low Ca:Si. The effect is ascribed to the attractive interactions between Y3+ and Ta5+ in solid solution, similar to that found in tetragonal zirconia, but with concurrent incorporation of anion vacancies associated with excess Y3+ that stabilize the cubic form. As the Ca2+ content of the melt increases, so does the amount of Ca2+ incorporated in fluorite. The latter also interacts attractively with Ta5+ and leads to a reduction of captured Y3+ in fluorite as the Ca content in the reacting deposit increases. This serves to increase the amount of Y3+available in the melt to form apatite in TBC-CMAS interactions.

Research Organization:
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Sponsoring Organization:
USDOE National Nuclear Security Administration (NNSA); National Science Foundation (NSF); US Department of the Navy, Office of Naval Research (ONR)
Grant/Contract Number:
89233218CNA000001; DMR 1720256; DMR 1105672; N00014-16-1–2702
OSTI ID:
1601623
Report Number(s):
LA-UR-19-25329
Journal Information:
Acta Materialia, Vol. 185, Issue C; ISSN 1359-6454
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English