Figures & data
Figure 1. X-ray diffraction (XRD) patterns of UO2–ZrO2 samples with different UO2/ZrO2 ratios after heat treatment at 1473 K in Ar + 10% H2 for 1 h. Circles represent UO2 solid solution (s.s.), and triangles represent t-ZrO2.
![Figure 1. X-ray diffraction (XRD) patterns of UO2–ZrO2 samples with different UO2/ZrO2 ratios after heat treatment at 1473 K in Ar + 10% H2 for 1 h. Circles represent UO2 solid solution (s.s.), and triangles represent t-ZrO2.](/cms/asset/161b9602-79f5-43a5-8c37-4ef51fe5be27/tnst_a_1055315_f0001_oc.jpg)
Figure 2. X-ray diffraction (XRD) patterns of UO2–ZrO2 samples with different UO2/ZrO2 ratios after heat treatment at 1473 K in N2+2% O2 for 1 h. Diamonds represent U3O8, squares represent t-ZrO2, and triangles represent m-ZrO2.
![Figure 2. X-ray diffraction (XRD) patterns of UO2–ZrO2 samples with different UO2/ZrO2 ratios after heat treatment at 1473 K in N2+2% O2 for 1 h. Diamonds represent U3O8, squares represent t-ZrO2, and triangles represent m-ZrO2.](/cms/asset/e2a7e16b-031e-42ad-9c90-a2d614884862/tnst_a_1055315_f0002_oc.jpg)
Table 1. Properties of solid solution samples: major phase conditions, initial inventory of nuclides Ai, and the half-life and the energy of peaks assigned.
Figure 3. Time dependence of the uranium molar concentration after filtration through a 0.45-μm-pore-size membrane in seawater (left) and Milli-Q water (right).
![Figure 3. Time dependence of the uranium molar concentration after filtration through a 0.45-μm-pore-size membrane in seawater (left) and Milli-Q water (right).](/cms/asset/399649a0-cd2a-4e55-a798-61f1c37da9ae/tnst_a_1055315_f0003_b.gif)
Figure 4. Uranium molar concentrations after filtration through 3 kDa and 0.45-μm-pore-size membranes.
![Figure 4. Uranium molar concentrations after filtration through 3 kDa and 0.45-μm-pore-size membranes.](/cms/asset/342e8d6f-a7f4-4a47-8077-448d05fe4165/tnst_a_1055315_f0004_b.gif)
Figure 5. Typical gamma ray spectra measured for the filtrate of #U-O (15 d of leaching in seawater), which was passed through the 0.45-μm membrane. The characteristic gamma ray emitters for quantification are marked above the corresponding peaks with underlining.
![Figure 5. Typical gamma ray spectra measured for the filtrate of #U-O (15 d of leaching in seawater), which was passed through the 0.45-μm membrane. The characteristic gamma ray emitters for quantification are marked above the corresponding peaks with underlining.](/cms/asset/fb3a75fc-6e49-4039-99a9-413c66f17f21/tnst_a_1055315_f0005_b.gif)
Figure 7. Time dependence of RM/RU in the seawater sample system; #U-O and #UZ-O series (upper) and #U-H and #UZ-H series (lower).
![Figure 7. Time dependence of RM/RU in the seawater sample system; #U-O and #UZ-O series (upper) and #U-H and #UZ-H series (lower).](/cms/asset/9828ba29-5a00-4f6b-aa4f-1868247152da/tnst_a_1055315_f0007_b.gif)