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Browsing Chemistry by Subject "brannerite"
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Item Assessing the oxidation states and structural stability of the Ce analogue of brannerite(Wiley, 2017) Aluri, Esther Rani; Bachiu, Lisa; Grosvenor, Andrew; Forbes, Scott; Greedan, JohnThe Ce‐containing analogue of brannerite (ie, UTi2O6) was previously considered to be stoichio- metric (ie, CeTi2O6); however, it has recently been determined that the material is O deficient. This oxygen‐deficient material has been suggested to be charged balanced by the presence of a minor concentration of Ce3+ or by the A‐site being cation deficient with the Ce oxidation state being 4+. A variety of Ti‐containing oxides (including brannerite) have been investigated as potential nuclear wasteforms, and it is necessary to understand the electronic structure of a proposed nuclear wasteform material as well as how the structure responds to radiation from incorporated waste elements. The radiation resistance of a material can be simulated by ion implantation. The objective of this study was to confirm the Ce oxidation state in the cation‐ and oxygen‐deficient material (ie, Ce0.94Ti2O6 − δ) and to determine how radiation damage affects this material. X‐ray photoelectron spectroscopy (XPS) and X‐ray absorption near‐edge spectros- copy were used to study Ce0.94Ti2O6 − δ before and after being implanted with 2 MeV Au− ions. Analysis of the Ce 3d XPS spectra from the as‐synthesized samples by using a previously developed fitting method has unequivocally shown that Ce adopts both 4+ (major) and 3+ (minor) oxidation states, which was confirmed by examination of magnetic susceptibility data. Analysis of XPS and X‐ray absorption near‐edge spectroscopy spectra from ion‐implanted materials showed that both Ce and Ti were reduced because of radiation damage and that the local coordination environments of the cations are greatly affected by radiation damage.Item Investigation of CeTi2O6- and CaZrTi2O7-containing glass–ceramic composite materials(NRC Research Press, 2017) Paknahad, Elham; Grosvenor, AndrewGlass–ceramic composite materials are being investigated for numerous applications (i.e., textile, energy storage, nuclear waste immobilization applications, etc.) due to the chemical durability and flexibility of these materials. Borosilicate and Fe–Al–borosilicate glass–ceramic composites containing brannerite (CeTi2O6) or zirconolite (CaZrTi2O7) crystallites were synthe- sized at different annealing temperatures. The objective of this study was to understand the interaction of brannerite or zirconolite-type crystallites within the glass matrix and to investigate how the local structure of these composite materials changed with changing synthesis conditions. Powder X-ray diffraction (XRD) and Backscattered electron (BSE) microprobe images have been used to study how the ceramic crystallites dispersed in the glass matrix. X-ray absorption near edge spectros- copy (XANES) spectra were also collected from all glass–ceramic composite materials. Examination of Ti K-, Ce L3-, Zr K-, Si L2,3-, Fe K-, and Al L2,3-edge XANES spectra from the glass–ceramic composites have shown that the annealing temperature, glass composition, and the loading of the ceramic crystallites in the glass matrix can affect the local environment of the glass–ceramic composite materials. A comparison of the glass–ceramic composites containing brannerite or zirconolite crystallites has shown that similar changes in the long range and local structure of these composite materials occur when the synthesis conditions to form these materials or the composition are changed.