dc.creatorSILVA, M. F. P. da
dc.creatorMATOS, J. R.
dc.creatorISOLANI, P. C.
dc.date.accessioned2012-10-20T05:23:44Z
dc.date.accessioned2018-07-04T15:49:30Z
dc.date.available2012-10-20T05:23:44Z
dc.date.available2018-07-04T15:49:30Z
dc.date.created2012-10-20T05:23:44Z
dc.date.issued2008
dc.identifierJOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, v.94, n.1, p.305-311, 2008
dc.identifier1388-6150
dc.identifierhttp://producao.usp.br/handle/BDPI/31267
dc.identifier10.1007/s10973-007-8906-x
dc.identifierhttp://dx.doi.org/10.1007/s10973-007-8906-x
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1627905
dc.description.abstractThe synthesis and characterization of lanthanide(III) citrates with stoichiometries 1:1 and 2:3; [LnL center dot xH(2)O] and [Ln(2)(LH)(3)center dot 2H(2)O], Ln=La, Ce, Pr, Nd, Sm and Eu are reported. L stands for (C6O7H5)(3-) and LH for (C6O7H6)(2-). Infrared absorption spectra of both series evidence coordination of carboxylate groups through symmetric bridges or chelation. X-ray powder patterns show the amorphous character of [LnL center dot xH(2)O]. The compounds [Ln(2)LH(3)center dot 2H(2)O] are crystalline and isomorphous. Emission spectra of Eu compounds suggest C-2v symmetry for the coordination polyhedron of [LnL center dot xH(2)O] and C-4v for [Ln(2)(LH)(3)center dot 2H(2)O]. Thermal analyses (TG-DTG-DTA) were carried out for both series. The thermal analysis patterns of the two series are quite different and both fit in a 4-step model of thermal decomposition, with lanthanide oxides as final products.
dc.languageeng
dc.publisherSPRINGER
dc.relationJournal of Thermal Analysis and Calorimetry
dc.rightsCopyright SPRINGER
dc.rightsrestrictedAccess
dc.subjectcharacterization
dc.subjectcrystalline citrate
dc.subjectemission spectra
dc.subjectlanthanide citrate
dc.subjectthermal analysis
dc.titleSYNTHESIS, CHARACTERIZATION AND THERMAL ANALYSIS OF 1:1 AND 2:3 LANTHANIDE(III) CITRATES
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución