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Synthesis and characterization of core-shell superparamagnetic nanomaterials for biomedical and catalytic applications

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Author(s):
Watson Beck Júnior
Total Authors: 1
Document type: Doctoral Thesis
Press: São Carlos.
Institution: Universidade de São Paulo (USP). Instituto de Química de São Carlos (IQSC/BT)
Defense date:
Examining board members:
Laudemir Carlos Varanda; Daniel Reinaldo Cornejo; Watson Loh; Joelma Perez; Celso Valentim Santilli
Advisor: Laudemir Carlos Varanda
Abstract

The most diverse technological applications of magnetic nanoparticles (MNP) have intensifiedthe interest for materials with different magnetic properties such as enhanced saturationmagnetization (MS) and superparamagnetic behavior. Despite the high MS values of metalparticles of Fe, Co, FeCo and FePt, their low chemical stability hinders most applications at thenanoscale. This thesis reports the synthesis of metallic Fe and Co and bimetallic FeCo and FePtMNP with high chemical stability and strict morphological control. MNP of iron oxide and mixediron-cobalt oxide were also synthesized. Two methods were employed. The first method, basedon nanoheterogeneous systems (micellar or reverse microemulsion systems), was used toprepare magnetite and metallic Co NPM. The method applies cation-substituted surfactants:iron(III) dodecyl sulfate iron (FeDS) and cobalt(II) dodecyl sulfate (CoDS). Before the MNPsyntheses, it were studied e determined the critical micelle concentration of FeDS in 1-octanol(cmc = 0.90 mmol L-1) and the pseudo-ternary phase diagram of n-heptane/CoDS/nbutanol/H2O. Spheroidal MNP of magnetite with 3.4 nm in diameter and quasi-paramagneticbehavior were prepared in octanolic FeDS micellar systems. Despite their broad sizedistribution and low MS, metallic Co MNP were produced in reverse microemulsions withchemical stability and superparamagnetic behavior. The second synthesis method, based onthermal decomposition of metal complexes, was employed to prepare spherical FePt and metaloxides (Fe3O4, FeXO1-X, (Co, Fe)XO1-X and CoFe2O4) MNP. Strict morphological control and highchemical stability were reached. Such method does not show the same effectiveness tosynthesize FeAg and FeCo MNP: the FeAg bimetallic alloy was not obtained while FeCo MNPwith chemical stability and compositional control were prepared with no morphological control.Fe and FeCo MNP were produced by thermal reduction of silica-coated Fe3O4 and CoFe2O4 MPN. The coating, beyond to prevent inter-particle sintering, provides biocompatibility andhydrophilic character. The reduced samples showed a significant increase in MS values(between 21.3 and 163.9%), which is directly proportional to MNP size. The silica coating wasaccomplished by tetraethylorthosilicate (TEOS) hydrolysis in reverse microemulsions. Thethickness of the silica layer is controlled by varying the reaction time and concentration of TEOSand NPM. The observations during coating process allowed to propose its probable mechanism.An additional coating of TiO2 (anatase phase) was performed onto silica layer for somesamples. Anatase coating was achieved by using ethylene glycol as both solvent and ligand toproduce an intermediate complex Ti precursor. The variation of the relative amounts of NPMand the Ti precursor allows to control the thickness of the anatase layer between 2 and 12 nm. Assays of magnetic hyperthermia were performed for silica-coated samples. The heating rate of the reduced samples increases after thermal reduction, even for dilute MNP dispersions (0.6 to4.5 mg mL-1). Heating rates between 0.3 and 3.0o C min-1 and SAR in the range of 37.2 96.3 Wg-1 were obtained. The photocatalytic activities of pure anatase particles and TiO2 -coated MNPwere close, but the magnetic samples has the advantage of being recovered from reactionmedia by applying the external magnetic fields. The preliminary results of magnetichyperthermia and photocatalysis assays indicate such materials have strong potential forapplications in biomedicine and photocatalysis. (AU)

FAPESP's process: 11/12210-4 - Synthesis and characterization of core-shell superparamagnetic nanomaterials for catalysis and biomedical applications.
Grantee:Watson Beck Junior
Support Opportunities: Scholarships in Brazil - Doctorate