2015
DOI: 10.1016/j.jssc.2014.09.030
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Structural study of (N2H5,H)2.9U1.1Ce0.9(C2O4)5·10H2O from a conventional X-ray diffraction diagram obtained on a powder synthesized by a fast vortex process

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“…On this basis, one can conclude that the precipitation step yielded to the formation of (Th,Y)(C2O4)2.2H2O solid solutions. Conversely, the sample prepared for x = 0.22 presented additional XRD lines assigned to the hexagonal structure (space group P63/mmc) already reported by Arab-Chapelet et al for mixed An(IV)/Ln(III) or An(IV)/An(III) oxalates [33,34]. Also, the position of the PXRD lines observed for this composition appeared to be closed to that noted for x = 0.…”
Section: Characterization and Conversion Of Oxalate Precursorssupporting
confidence: 59%
“…On this basis, one can conclude that the precipitation step yielded to the formation of (Th,Y)(C2O4)2.2H2O solid solutions. Conversely, the sample prepared for x = 0.22 presented additional XRD lines assigned to the hexagonal structure (space group P63/mmc) already reported by Arab-Chapelet et al for mixed An(IV)/Ln(III) or An(IV)/An(III) oxalates [33,34]. Also, the position of the PXRD lines observed for this composition appeared to be closed to that noted for x = 0.…”
Section: Characterization and Conversion Of Oxalate Precursorssupporting
confidence: 59%