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The lanthanum hydroxide fluoride carbonate system: The preparation of synthetic bastnaesite

dc.contributor.authorHaschke, John M.en_US
dc.date.accessioned2006-04-07T16:41:01Z
dc.date.available2006-04-07T16:41:01Z
dc.date.issued1975-01-01en_US
dc.identifier.citationHaschke, John M. (1975/01/01)."The lanthanum hydroxide fluoride carbonate system: The preparation of synthetic bastnaesite." Journal of Solid State Chemistry 12(1-2): 115-121. <http://hdl.handle.net/2027.42/22168>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WM2-4B6NPPX-H8/2/3d6d8aee2ba15c19e7da6fcd326c1bc3en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/22168
dc.description.abstractHydrothermal phase equilibria in the lanthanum + hydroxide + fluoride + carbonate system have been investigated along an isobaric and isothermal section of variable metal to fluoride ratio, x. Quantitative substitution of fluoride into LaOHCO3 proceeds with the formation of a continuous solid solution, La(OH)1-xFxCO3, for 0 0 [les] x [les] 1 and a two-phase region, LaFCO3 + LaF3, for 1 x 3 is an orthorhombic phase (a = 21.891(5), B = 12.639(3) and C = 10.047(2) A) which is not isostructural with LaFCO3. Hydrolysis of the La(OH)1-xFxCO3 phase to the corresponding UCl3-type La(OH)3-xFx compositions has been observed. Thermal decomposition reactions of the hydroxide fluoride carbonates are described, and a geochemical process for the formation of bastnaesite and tysonite is proposed.en_US
dc.format.extent575864 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleThe lanthanum hydroxide fluoride carbonate system: The preparation of synthetic bastnaesiteen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48104, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/22168/1/0000599.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-4596(75)90186-3en_US
dc.identifier.sourceJournal of Solid State Chemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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