A series of compositions with general stoichiometry Ca 1−x Zr 1−x Nd 2x Ti 2 O 7 has been prepared by high-temperature solid-state reaction of component oxides and characterized by powder X-ray diffraction and electron probe for microanalyses (EPMA). The phase fields in CaZrTi 2 O 7 -Nd 2 Ti 2 O 7 system and distribution of ions in different phases have been determined. Four different phase fields, namely monoclinic zirconolite, cubic perovskite, cubic pyrochlore, and monoclinic Nd 2 Ti 2 O 7 structure types are observed in this system. The 4Mpolytype of zirconolite structure is stabilized by substitution of Nd 3+ ion. The addition of Nd 3+ ions form a cubic perovskite structure-type phase and thus observed in all the compositions with 0.05 ≤ x ≤ 0.80. Cubic pyrochlore structure-type phase is observed as a coexisting phase in the nominal composition with 0.20 ≤ x ≤ 0.90. Only a subtle amounts of Ca 2+ and Zr 4+ are incorporated into the perovskite-type Nd 2 Ti 2 O 7 structure. EPMA analyses on different coexisting phases revealed that the pyrochlore and perovskite phases have Nd 3+ -rich compositions.L. Vance-contributing editor Manuscript No. 33424.
Gd2Zr2O7 is being contemplated as a futuristic matrix for the incorporation of high-level radioactive nuclear waste. This compound has the unique ability to incorporate several fission products and heavy metal ions like uranium and thorium into its lattice sites without undergoing structural changes. X-ray diffraction analyses of Gd2-xUxZr2O7+δ samples indicate that the parent compound can incorporate a substantial amount of uranium, both under oxidizing and reducing conditions. The oxidation state of these samples was investigated by X-ray photoelectron spectroscopy. The thermodynamic stability of uranium-substituted Gd2Zr2O7 is an important parameter that will govern the long-term storage of uranium and minor actinides in this matrix. High-temperature calorimetry has been used to investigate the stability of the Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) compositions. The standard molar free energy of the formation of Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) compositions has been estimated. From the free energy of formation data, the sample corresponding to x = 0.15 was found to be most stable in the Gd2-xUxZr2O7+δ (0.00 ≤ x ≤ 0.15) series. The relative stabilities of U(4+) and U(6+) substituted gadolinium zirconate have been discussed on the basis of the charge on the uranium ion and the incorporation of corresponding extra oxygen atoms into the lattice for charge compensation.
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