Magnetic properties of Fe3O4 nanoparticles coated with oleic and dodecanoic acids

Magnetic nanoparticles (NP) of magnetite (Fe3O4) coated with oleic acid (OA) and dodecanoic acid (DA) were synthesized and investigated through Transmission Electron Microscopy (TEM),magnetization M, and ac magnetic susceptibility measurements. The OA coated samples were produced with different magnetic concentrations (78, 76, and 65%) and the DA sample with 63% of Fe3O4. Images from TEM indicate that the NP have a nearly spherical geometry and mean diameter ~ 5.5 nm. Magnetization measurements, performed in zero field cooled (ZFC) and field cooled (FC) processes under different external magnetic fields H, exhibited a maximum at a given temperature TB in the ZFC curves, which depends on the NP coating (OA or DA), magnetite concentration, and H. The temperature TB decreases monotonically with increasing H and, for a given H, the increase in the magnetite concentration results in an increase of TB. The observed behavior is related to the dipolar interaction (DI) between NP which seems to be an important mechanism in all samples studied. This is supported by the results of the ac magnetic susceptibility Xac measurements, where the temperature in which X' peaks for different frequencies follows the Vogel-Fulcher model, a feature commonly found in systems with dipolar interactions. Curves of H vs. TB/TB(H=0) for samples with different coatings and magnetite concentrations collapse into a universal curve, indicating that the qualitative magnetic behavior of the samples may be described by the NP themselves, instead of the coating or the strength of the dipolar interaction. Below TB, M vs. H curves show a coercive field (HC) that increases monotonically with decreasing temperature. The saturation magnetization (MS) follows the Bloch's law and values of MS at room temperature as high as 78 emu/g were estimated, a result corresponding to ~80% of the bulk value. The overlap of M/MS vs. H/T curves for a given sample and the low HC at high temperatures suggest superparamagnetic behavior in all samples studied. The overlap of M/MS vs. H curves at constant temperature for different samples indicates that the NP magnetization behavior is preserved, independently of the coating and magnetite concentration.Comment: 8 pages and 9 figure

Role of dipolar interactions in a system of Ni nanoparticles studied by magnetic susceptibility measurements

The role of dipolar interactions among Ni nanoparticles (NP) embedded in an amorphous SiO2/C matrix with different concentrations has been studied performing ac magnetic susceptibility Chi_ac measurements. For very diluted samples, with Ni concentrations < 4 wt % Ni or very weak dipolar interactions, the data are well described by the Neel-Arrhenius law. Increasing Ni concentration to values up to 12.8 wt % Ni results in changes in the Neel-Arrhenius behavior, the dipolar interactions become important, and need to be considered to describe the magnetic response of the NPs system. We have found no evidence of a spin-glasslike behavior in our Ni NP systems even when dipolar interactions are clearly present.Comment: 7 pages, 5 figures, 3 table

Caffeine as an indicator of estrogenic activity in source water

Caffeine has already been used as an indicator of anthropogenic impacts, especially the ones related to the disposal of sewage in water bodies. In this work, the presence of caffeine has been correlated with the estrogenic activity of water samples measured using the BLYES assay. After testing 96 surface water samples, it was concluded that caffeine can be used to prioritize samples to be tested for estrogenic activity in water quality programs evaluating emerging contaminants with endocrine disruptor activity.Caffeine has already been used as an indicator of anthropogenic impacts, especially the ones related to the disposal of sewage in water bodies. In this work, the presence of caffeine has been correlated with the estrogenic activity of water samples measur16818661869FAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOCNPQ - CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO2008/57808-1 ; 2012/00303-0573894/2008-6This is a contribution of the INCTAA (FAPESP, proc. 2008/57808-1 and CNPq proc. 573894/2008-6). C.C.M. is grateful to FAPESP for the PhD fellowship (proc. 2012/00303-0)

Chromatographic comparison of self-immobilized and radiation-immobilized poly(methyloctylsiloxane) stationary phases on various silicas

Self-immobilized and radiation-immobilized stationary phases were prepared with poly(methyloctylsiloxane) on eight silica supports having different particle sizes, particle shapes and pore sizes. Columns prepared by the two immobilization procedures had similar efficiencies, resolutions and separation factors but columns with self-immobilized stationary phases had lower percent loadings and, thus, lower retention factors. Results show structural differences between the phases.Dois tipos de fase estacionária, auto-imobilizada e imobilizada por radiação, foram preparadas com poli(metiloctilsiloxano) sobre oito suportes de sílica com tamanho e forma de partículas, e tamanho de poros diferentes. As colunas recheadas com as fases estacionárias preparadas através dos dois procedimentos de imobilização apresentaram eficiências, resoluções e fatores de separação similares, mas as colunas recheadas com a fase estacionária auto-imobilizada tiveram percentagens de carga menores e, portanto, fatores de retenção menores. Os resultados evidenciam diferenças estruturais entre as fases.116121Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

Effects of Lorentz violation in superconductivity

This paper presents the effects of Lorentz violation in superconductivity. Constructing a Lorentz-Violating Ginzburg-Landau theory of superconductivity we discuss the influence of the Lorentz-Violating tensors $\hat{k}_{c}^{ij}$ and $\hat{k}_a^i$ in the London's depth penetration, in the coherence length and critical magnetic field.Comment: 5 pages, 1 figure, two columns. Matches version to be published at EP

Environmental chemistry in Brasil

Defining environmental chemistry is a not an easy task because it encompasses many different topics. According to Stanley E. Manahan, author of a classical textbook of Environmental Chemistry, this branch could be defined as the one centered in the study of the sources, transport, effects and fates of chemical species in the water, soil, and air environments, as well as the influence of human activity upon these processes. More recently, new knowledge emerged from the Environmental Toxicology allowed to go even deeper in the meaning of 'effects' and 'fates' of a continuous growing number of organic and inorganic species disposed in water bodies, soils and atmosphere. Toxicity tests became an important tool to evaluate the environmental impact of such species to a great number of organisms, thus allowing to set quality criteria for drinking water, sediments and biota. The state of art shows that environmental chemistry is a multi-inter disciplinary science by nature; therefore, it needs more than a limited, unique-approach and non-oriented set of data to understand the nature of natural processes. Taking all these aspects into consideration, one can say that Environmental Chemistry in Brazil is now a well established area of research within the classical areas of the Chemistry, with a large number of emerging groups as well research groups with worldwide recognition.71

Métodos para a determinação de multiresíduos de agrotóxicos em produtos agrícolas.

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