2021
DOI: 10.1002/zaac.202100118
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Selective separation of Yttrium and Uranium from Xenotime Concentrate

Abstract: A new process suggested for the selective dissolution of rare earth elements REEs from xenotime concentrate produced after physical beneficiation namely; shaking table and froth flotation were proposed using ammonium sulfate. The suggested procedure was established upon the selectivity of ammonium sulfate as a leaching agent of rare earth element. The Dissolution kinetic analysis of valuable elements of the dissolution process and the suggested reaction mechanism concerning the rare earth and ammonium sulfate … Show more

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Cited by 12 publications
(8 citation statements)
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“…To investigate the thermodynamic performance of the Co +2 ion sorption reaction system on the TZAB, enthalpy (ΔH), Gibbs free energy (ΔG), and entropy (ΔS) were calculated. These thermodynamic parameters were calculated by using Equations (14) and (15) [ 53 , 54 , 55 ]: ∆G° = ∆H° − T∆S° where K is the reaction constant, T (°K) is the absolute temperature, and R is the universal constant of gas (8.314 J/mol·K).…”
Section: Resultsmentioning
confidence: 99%
“…To investigate the thermodynamic performance of the Co +2 ion sorption reaction system on the TZAB, enthalpy (ΔH), Gibbs free energy (ΔG), and entropy (ΔS) were calculated. These thermodynamic parameters were calculated by using Equations (14) and (15) [ 53 , 54 , 55 ]: ∆G° = ∆H° − T∆S° where K is the reaction constant, T (°K) is the absolute temperature, and R is the universal constant of gas (8.314 J/mol·K).…”
Section: Resultsmentioning
confidence: 99%
“…It is now apparent that the 1st-order modelling and the empirical data are not alike, and therefore the modelling is not suitable for the system under investigation. Conversely, the pseudo-2nd-order modelling is symbolized by the subsequent Equation (2) [ 35 , 36 , 37 , 38 ]: …”
Section: Resultsmentioning
confidence: 99%
“…In the case of CTPO, the appearance of a new peak at 6.8° and inhibited in the strength of the second peak, as shown in Figure 3, suggests that the polymeric structure has been changed, likely because of the addition of functional groups in the polymer backbone, which facilitate the destruction of hydrogen bonds in the original main chains. In order to preserve stability, the crystallinity of chitosan mirrored the polymer's intramolecular and intermolecular hydrogen bonds [52–54] . Orientation shifts in the initial polymeric chains because of the predicted hydrogen bond disruption are reflected in the crystallinity actions after introducing moiety chains with new functional groups.…”
Section: Resultsmentioning
confidence: 99%
“…In order to preserve stability, the crystallinity of chitosan mirrored the polymer's intramolecular and intermolecular hydrogen bonds. [52][53][54] Orientation shifts in the initial polymeric chains because of the predicted hydrogen bond disruption are reflected in the crystallinity actions after introducing moiety chains with new functional groups. Journal of Inorganic and General Chemistry…”
Section: X-ray Diffraction Of Native Chitosan and Modified Chitosanmentioning
confidence: 99%