Synthesis of mesoporous silica-coated magnetic nanoparticles modified with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole and its application as Cu(II) adsorbent from aqueous samples

dc.contributor.authorWONDRACEK, MARCOS H.P.
dc.contributor.authorJORGETTO, ALEXANDRE O.
dc.contributor.authorSILVA, ADRIELLI C.P.
dc.contributor.authorIVASSECHEN, JANAINE do R.
dc.contributor.authorSCHNEIDER, JOSE F.
dc.contributor.authorSAEKI, MARGARIDA J.
dc.contributor.authorPEDROSA, VALBER A.
dc.contributor.authorYOSHITO, WALTER K.
dc.contributor.authorCOLAUTO, FABIANO
dc.contributor.authorORTIZ, WILSON A.
dc.contributor.authorCASTRO, GUSTAVO R.
dc.coverageInternacionalpt_BR
dc.date.accessioned2016-08-03T17:52:33Z
dc.date.available2016-08-03T17:52:33Z
dc.date.issued2016pt_BR
dc.description.abstractThis study presents an alternative, rapid, and environment-friendly synthesis procedure of a magnetic core–shell mesoporous SBA-15 silica composite, its functionalization with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole (Purpald), and its application in dispersive solid-phase microextraction (DSPME) for Cu(II) from water. The materials were characterized through magnetization measurements, scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), Fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) of 29Si and 13C, elemental analysis, and surface area measurements. FTIR and NMR analyses indicated the presence of the ligand on the functionalized material and that it was coupled through a Csingle bondS bond. TEM images clearly show that the magnetite core particles were effectively coated with a silica shell. The material presented a surface area of 287.99 m2 g−1 and an average pore diameter of approximately 15.1 nm. The material had its point of zero charge (PZC) determined (6.17) and its adsorption capacity was evaluated as a function of time, pH, and metal concentration. Dynamic adsorption equilibrium was reached in 120 min, and it had a good correlation with the pseudo-second-order kinetic model (r2 = 0.9997). The maximum experimental adsorption capacity (0.0786 mmol g−1) and the value calculated by the linearized Langmuir model (0.0799 mmol g−1) are very approximate, indicating the formation of a monolayer over the material. Furthermore, the material proved to be very stable, because their adsorption capacity remained greater than 95% even after 10 cycles of adsorption/desorption. A high enrichment factor of 98.1-fold was observed, indicating that this material is suitable for the preconcentration of trace Cu(II) ions before analysis through flame atomic absorption spectrometry (FAAS).
dc.format.extent533-541pt_BR
dc.identifier.citationWONDRACEK, MARCOS H.P.; JORGETTO, ALEXANDRE O.; SILVA, ADRIELLI C.P.; IVASSECHEN, JANAINE do R.; SCHNEIDER, JOSE F.; SAEKI, MARGARIDA J.; PEDROSA, VALBER A.; YOSHITO, WALTER K.; COLAUTO, FABIANO; ORTIZ, WILSON A.; CASTRO, GUSTAVO R. Synthesis of mesoporous silica-coated magnetic nanoparticles modified with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole and its application as Cu(II) adsorbent from aqueous samples. <b>Applied Surface Science</b>, v. 367, p. 533-541, 2016. Disponível em: http://repositorio.ipen.br/handle/123456789/26536.
dc.identifier.issn0169-4332pt_BR
dc.identifier.percentilfi79.36
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/26536
dc.identifier.vol367pt_BR
dc.language.isoeng
dc.relation.ispartofApplied Surface Sciencept_BR
dc.rightsopenAccesspt_BR
dc.subjectsynthesis
dc.subjectsilica
dc.subjectnanoparticles
dc.subjectadsorbents
dc.subjectwater
dc.subjectextraction
dc.subjectadsorption
dc.subjectcomposite materials
dc.subjectcopper ions
dc.subjectscanning electron microscopy
dc.subjecttransmission electron microscopy
dc.subjectfourier transform spectrometers
dc.subjectinfrared spectra
dc.subjectnuclear magnetic resonance
dc.subjectsurface area
dc.titleSynthesis of mesoporous silica-coated magnetic nanoparticles modified with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole and its application as Cu(II) adsorbent from aqueous samplespt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorWALTER KENJI YOSHITO
ipen.codigoautor161
ipen.contributor.ipenauthorWALTER KENJI YOSHITO
ipen.date.recebimento16-08pt_BR
ipen.identifier.fi3.387pt_BR
ipen.identifier.ipendoc22447pt_BR
ipen.identifier.iwosWoSpt_BR
ipen.range.fi3.000 - 4.499
ipen.range.percentilfi75.00 - 100.00
ipen.type.genreArtigo
relation.isAuthorOfPublication33f9c3eb-85be-4023-936e-37b3df51c1fc
relation.isAuthorOfPublication.latestForDiscovery33f9c3eb-85be-4023-936e-37b3df51c1fc
sigepi.autor.atividadeYOSHITO, WALTER K.:161:720:N

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