skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Structure and thermodynamics of uranium-containing iron garnets

Authors:
; ; ; ; ; ; ; ;
Publication Date:
Research Org.:
Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Sponsoring Org.:
DOE - BASIC ENERGY SCIENCESDOE - OTHERDOE - BIOLOGICAL AND ENVIRONMENTAL RESEARCH
OSTI Identifier:
1306622
Resource Type:
Journal Article
Resource Relation:
Journal Name: Geochimica et Cosmochimica Acta; Journal Volume: 189
Country of Publication:
United States
Language:
ENGLISH

Citation Formats

Guo, Xiaofeng, Navrotsky, Alexandra, Kukkadapu, Ravi K., Engelhard, Mark H., Lanzirotti, Antonio, Newville, Matthew, Ilton, Eugene S., Sutton, Stephen R., and Xu, Hongwu. Structure and thermodynamics of uranium-containing iron garnets. United States: N. p., 2016. Web. doi:10.1016/j.gca.2016.05.043.
Guo, Xiaofeng, Navrotsky, Alexandra, Kukkadapu, Ravi K., Engelhard, Mark H., Lanzirotti, Antonio, Newville, Matthew, Ilton, Eugene S., Sutton, Stephen R., & Xu, Hongwu. Structure and thermodynamics of uranium-containing iron garnets. United States. doi:10.1016/j.gca.2016.05.043.
Guo, Xiaofeng, Navrotsky, Alexandra, Kukkadapu, Ravi K., Engelhard, Mark H., Lanzirotti, Antonio, Newville, Matthew, Ilton, Eugene S., Sutton, Stephen R., and Xu, Hongwu. 2016. "Structure and thermodynamics of uranium-containing iron garnets". United States. doi:10.1016/j.gca.2016.05.043.
@article{osti_1306622,
title = {Structure and thermodynamics of uranium-containing iron garnets},
author = {Guo, Xiaofeng and Navrotsky, Alexandra and Kukkadapu, Ravi K. and Engelhard, Mark H. and Lanzirotti, Antonio and Newville, Matthew and Ilton, Eugene S. and Sutton, Stephen R. and Xu, Hongwu},
abstractNote = {},
doi = {10.1016/j.gca.2016.05.043},
journal = {Geochimica et Cosmochimica Acta},
number = ,
volume = 189,
place = {United States},
year = 2016,
month = 9
}
  • Use of crystalline garnet as a waste form phase appears to be advantageous for accommodating actinides from nuclear waste. Previous studies show that large amounts of uranium (U) and its analogues such as cerium (Ce) and thorium (Th) can be incorporated into the garnet structure. In this study, we synthesized U loaded garnet phases, Ca 3U xZr 2–xFe 3O 12 (x = 0.5–0.7), along with the endmember phase, Ca 3(Zr 2)SiFe 3+ 2O 12, for comparison. The oxidation states of U were determined by X-ray photoelectron and absorption spectroscopies, revealing the presence of mixed pentavalent and hexavalent uranium in themore » phases with x = 0.6 and 0.7. The oxidation states and coordination environments of Fe were measured using transmission 57Fe-Mössbauer spectroscopy, which shows that all iron is tetrahedrally coordinated Fe 3+. U substitution had a significant effect on local environments, the extent of U substitution within this range had a minimal effect on the structure, and unlike in the x = 0 sample, Fe exists in two different environments in the substituted garnets. The enthalpies of formation of garnet phases from constituent oxides and elements were first time determined by high temperature oxide melt solution calorimetry. The results indicate that these substituted garnets are thermodynamically stable under reducing conditions. Furthermore, our structural and thermodynamic analysis further provides explanation for the formation of natural uranium garnet, elbrusite-(Zr), and supports the potential use of Ca 3U xZr 2–xFe 3O 12 as viable waste form phases for U and other actinides.« less
  • Use of crystalline garnet as a waste form phase appears to be advantageous for accommodating actinides from nuclear waste. Previous studies show that large amounts of uranium (U) and its analogues such as cerium (Ce) and thorium (Th) can be incorporated into the garnet structure. In this study, we synthesized U loaded garnet phases, Ca3UxZr2-xFe3O12 (x = 0.5 - 0.7), along with the endmember phase, Ca3(Zr2)SiFe3+2O12, for comparison. The oxidation states of U were determined by X-ray photoelectron and absorption spectroscopies, revealing the presence of mixed pentavalent and hexavalent uranium in the phases with x = 0.6 and 0.7. Themore » oxidation states and coordination environments of Fe were measured using transmission 57Fe-Mössbauer spectroscopy, which shows that all iron is tetrahedrally coordinated Fe3+ (x = 0 and substituted sample), U substitution had a significant effect on local environments, the extent of U isubstitution within this range had a minimal effect on the structure, and unlike in the x = 0 sample, Fe exists in two different environments in the substituted garnets. The enthalpies of formation of garnet phases from constituent oxides and elements were determined by high temperature oxide melt solution calorimetry. The results indicate that these substituted garnets are thermodynamically stable under reducing conditions. Our structural and thermodynamic analysis further provides explanation for the formation of natural uranium garnet, elbrusite-(Zr), and supports the potential use of Ca3UxZr2-xFe3O12 as viable waste form phases for U and other actinides.« less
  • Some new compounds with garnet-related structures have been examined by {sub 57}Fe Moessbauer spectroscopy. The results show that in compounds of the type YCa{sub 2}SbFe{sub 4-x}Ga{sub x}O{sub 12} (x = 2,3) the gallium is distributed over both the octahedral and tetrahedral sites. In these compounds, together with materials of composition Y{sub 3-2x}Ca{sub 2x}Sb{sub x}Fe{sub 5-x}O{sub 12} (x = 1.25, 1.5) and Y{sub 3-x}Ca{sub x}Sn{sub x}Fe{sub 5-x}O{sub 12}(x = 1,2), the results show evidence of more than one tetrahedral environment for the Fe{sup 3+} ions. The quadrupole splitting data for the Fe{sup 3+} ions in tetrahedral sites in some of thesemore » compounds are significantly larger than those previously reported for Fe{sup 3+} in tetrahedral sites in other garnets.« less