dc.creatorSCHNEIDER, José Fabian
dc.creatorLOPES, L. V. S.
dc.creatorTAMBELLI, Caio Eduardo de Campos
dc.creatorDONOSO, José Pedro
dc.creatorLOZANO, H.
dc.creatorGONZALEZ, G.
dc.date.accessioned2012-10-20T04:22:08Z
dc.date.accessioned2018-07-04T15:44:16Z
dc.date.available2012-10-20T04:22:08Z
dc.date.available2018-07-04T15:44:16Z
dc.date.created2012-10-20T04:22:08Z
dc.date.issued2008
dc.identifierMOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.483, p.130-140, 2008
dc.identifier1542-1406
dc.identifierhttp://producao.usp.br/handle/BDPI/30065
dc.identifier10.1080/15421400801904336
dc.identifierhttp://dx.doi.org/10.1080/15421400801904336
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1626705
dc.description.abstractMeasurements of H-1 and C-13 Nuclear Magnetic Resonance (NMR) for the nano-composite materials formed by the intercalation of hexadecylamine (HDA) in metal oxides (TiO2, V2O5 and MoO3), are reported. The H-1 NMR spin-lattice relaxation in the rotating frame was described by using the spectral density due to Davidson and Cole, which incorporates a distribution of correlation times characterized by a width parameter epsilon. The fitting of the data was obtained for epsilon = 0.74, indicating that the correlation times are distributed over a narrow range in this system. High-resolution C-13 NMR techniques were used to resolve the NMR lines of middle-chain methylene groups in the spectra and variable contact time cross-polarization {H-1-}C-13 experiments were employed to analyze the reorientation dynamics of the CH3 and CH2 groups in the HDA chains.
dc.languageeng
dc.publisherTAYLOR & FRANCIS LTD
dc.relationMolecular Crystals and Liquid Crystals
dc.rightsCopyright TAYLOR & FRANCIS LTD
dc.rightsrestrictedAccess
dc.subjectfoam
dc.subjecthexadecylamine
dc.subjectintercalation compound
dc.subjectnanostructure
dc.subjectNMR
dc.titleNMR study of slow motions of HDA hydrocarbons chains inside lamellar structures
dc.typeArtículos de revistas


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