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Monazite uranyl

Fig. 4.70. Laser-induced steady-state luminescence spectra of thorite (a) and monazite (b-d) natural and heated demonstrating uranyl, Eu ", Sm and Nd " centers. Straight line-vertical polarization, dashed Zi e-horizontal polarization... Fig. 4.70. Laser-induced steady-state luminescence spectra of thorite (a) and monazite (b-d) natural and heated demonstrating uranyl, Eu ", Sm and Nd " centers. Straight line-vertical polarization, dashed Zi e-horizontal polarization...
Appendix C contains the chemical formulae for the minerals used in this book. There are very few minerals that have the ideal crystalline structures discussed above. There are sufficient substitutional impurities, crystal defects, and distortions that make the CBPC structure significantly different from the models discussed above. Several well-established minerals exhibit these features, as are many of those listed in Appendix C. For example, Ca(UO2)2(PO4)2T0H2O is formed by the substitution of Ca in autunite by uranyl (UO2) ions, making the autunite a mineral of radioactive uranium. Similarly, (Ce,Th)P04 is formed by the substitution of the Ce in monazite by Th. Numerous minerals can be formed by substitutions and provide a researcher sufficient degree of freedom to synthesize very complex minerals to produce useful CBPCs. [Pg.94]

Preparation and Characterization of Lanthanide and Actinide Solids. Crystalline / element phosphates were prepared as standards for comparison to the solids produced in the conversion of metal phytates to phosphates. The europium standard prepared was identified by X-ray powder diffiaction as hexagonal EuP04 H20 (JCPDS card number 20-1044), which was dehydrated at 204-234 °C and converted to monoclinic EUPO4 (with the monazite structure) at 500-600 °C. The standard uranyl phosphate solid prepared was the acid phosphate, U02HP04 2H20 (JCPDS card number 13-61). All attempts to prepare a crystalline thorium phosphate failed, though thorium solubility was low. In the latter case the solids were identified as amorphous Th(OH)4 with some minor crystalline inclusions of Th02. [Pg.279]

Because of the complications introduced by ferric iron, Audsley et al. concluded that a solvent that would be selective for thorium in the presence of ferric iron and that would not be inhibited by phosphate would be preferable to the Dapex solvent. They concurred with the conclusion of Crouse and co-workers at Oak Ridge National Laboratory [CS], that long-chain primary amines selectively extract thorium in the presence of uranyl, ferric, and phosphate ions. Compounds of this type are now the preferred extractant for thorium in such systems. Application of this so-called Amex process to thorium extraction from monazite is described in Sec. 8.6. [Pg.294]

Fig. 4.170 (a-i) Laser-induced time-resolved luminesc ce spectra of uranyl minerals (zippeite, autunite, zeunerite, agate, orangite, thorite, monazite, xenotime)... [Pg.195]


See other pages where Monazite uranyl is mentioned: [Pg.83]    [Pg.889]    [Pg.272]    [Pg.889]    [Pg.504]    [Pg.748]    [Pg.7034]    [Pg.861]    [Pg.89]    [Pg.1010]   
See also in sourсe #XX -- [ Pg.116 ]




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