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Journal ArticleDOI

Increased oxidation of UO2in molten alkali-metal carbonate based mixtures by increasing oxygen solubility and by controlled generation of superoxide ions, and evidence for a new sodium uranate

TLDR
In this paper, a ternary alkali-metal carbonate melt (Li-Na-K)2CO3 containing added chlorides or sulfates has been studied in the range 723-1023 K and a variety of uranium(VI) species was obtained.
Abstract
The oxidation of uranium dioxide to uranates in the ternary alkali-metal carbonate melt (Li–Na–K)2CO3 containing added chlorides or sulfates has been studied in the range 723–1023 K and a variety of uranium(VI) species was obtained. Increased oxygen solubility in fused carbonates was achieved by adding alkali-metal chloride or sulfate. The yield of uranates in chloride-containing melts decreased with increasing radius of the alkali-metal chloride cation, Li Na > K > Cs. When UO2 was oxidised in alkali chloride containing carbonate melts no intermediate uranium chloride complexes were observed. The temperature required for complete oxidation of UO2 can be lowered by 100–150 K by the addition of alkali-metal chlorides to carbonate melts. The addition of chloride and aluminium ions to form AlCl4− effected UO2 oxidation by a different mechanism, through intermediate formation of uranyl complexes, but the yield of uranates was not significantly altered. Attempts at oxidation by direct addition of potassium superoxide at 723 K were inefficient owing to thermal instability of the reagent, but UO2 oxidation was enhanced, by more than 10%, by superoxide formed insitu by the reaction of peroxide and nitrate, compared with oxidation by peroxide or nitrate individually. Optimum conditions for complete oxidation at 723 K required a peroxide:nitrate mole ratio of ca. 3. The major reaction pathway in melts containing nitrate and peroxide, at various concentrations of these reactants, was determined. At a mole ratio of oxidiser to UO2 of 0.3, the percentage of UO2 oxidised and the yield of uranates, increased in the order Na2O2 ≈ KO2 < KNO2 < KNO3 < KNO3 + Na2O2. Evidence has been obtained for a new sodium uranate, Na2O(UO3−y)x (1 < x <2 ; y < 0.02).

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Oxidative Dehydrogenation of Ethane: Common Principles and Mechanistic Aspects

TL;DR: In this paper, the current state of the ODH of light olefins is compared with other routes for light-olefin production, with a focus on the catalyst and reactor system variants.
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Kinetic Study of the Oxidative Dissolution of UO2 in Aqueous Carbonate Media

TL;DR: In this paper, a spectrophotometric titration was used to confirm peroxide coordination to the U(VI) metal center and the disappearance of characteristic absorbance maxima associated with UO2(CO3)34- (e.g., 448.5 nm) and a subsequent change in solution coloration upon titration with hydrogen peroxide indicated a change in speciation.
Journal ArticleDOI

Molten salt oxidation: A versatile and promising technology for the destruction of organic-containing wastes

TL;DR: The history and development of MSO is described, as well as design and engineering details, and reaction mechanisms and its potential applications in various wastes, including hazardous wastes, medical wastes, mixed wastes, and energetic materials are focused on.
Journal ArticleDOI

Strategies and new developments in the field of molten carbonates and high-temperature fuel cells in the carbon cycle

TL;DR: A special issue dedicated to the International Workshop on Molten carbonates and Related Topics (IWMC2011) was published in 2011 as mentioned in this paper, where molten carbonates are used as electrolytes in molten carbonate fuel cells (MCFCs).
Journal ArticleDOI

Oxidative Dehydrogenation of Light Alkanes on Supported Molten Alkali Metal Chloride Catalysts

TL;DR: In this article, the potential and limitations of molten alkali metal (Li, Na, and K) chlorides supported on Dy2O3/MgO were explored for the oxidative dehydrogenation of lower alkanes, such as ethane and propane.
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