1000 resultados para Óxido de níquel


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A preocupação com metais pesados provenientes de fertilizantes minerais deve-se à possibilidade de entrada desses elementos na cadeia alimentar. O objetivo deste trabalho foi determinar o teor de metais pesados e comparar três métodos de extração (Embrapa, USEPA 3051A e USEPA 3050B) de Cd, Cr, Cu, Ni, Pb e Zn em fosfatos de rochas nacionais e importados. A quantificação dos teores desses elementos foi feita em espectrofotômetro de absorção atômica de chama ar-acetileno. Entre os fosfatos estudados, o termofosfato apresentou concentrações significativamente superiores de Cr, Cu, Ni e Zn e o fosfato natural 2, de Cu, Ni, Pb e Zn. O fosfato reativo 3 apresentou a maior quantidade de Cd (145±13 mg kg-1) e o fosfato natural 2, a maior quantidade de Pb (234±9 mg kg-1). Os métodos avaliados podem ser aplicados em estudos de teor de metais pesados em fertilizantes fosfatados.

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O objetivo deste trabalho foi avaliar o efeito da adição de Ni ao solo (0, 2,3, 10,5, 47 e 210 mg kg-1), na presença e ausência de calcário, sobre: o desenvolvimento do feijoeiro; a fitodisponibilidade de Ni e algumas características biológicas do solo. O experimento foi conduzido em casa de vegetação, em Latossolo Vermelho distrófico. A dose de Ni de 210 mg kg-1 causou a morte de todas as plantas, tanto na presença como na ausência de calcário. Houve aumento da produção de grãos de feijão no tratamento que recebeu calcário. A concentração de Ni dos grãos aumentou com o incremento de Ni no solo, ultrapassando o limite máximo permitido, de 5 mg kg-1 de matéria fresca, na dose de 2,3 mg kg-1, indicando que a aplicação de calcário não foi suficiente para reduzir os teores de Ni no grão de feijão a níveis apropriados para o consumo. Observou-se diminuição da biomassa microbiana do solo nos tratamentos com altas concentrações de Ni, que foi acompanhada por aumento no qCO2. O qCO2 foi um indicador adequado do grau de estresse que teve a comunidade microbiana do solo com a adição de Ni.

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O objetivo deste trabalho foi comparar as emissões de óxido nitroso (N2O) para a atmosfera depois da aplicação de dejetos líquidos de suínos, em plantio direto (PD) e preparo reduzido (PR) do solo. O delineamento experimental utilizado foi o de blocos inteiramente casualizados com cinco repetições. Os tratamentos consistiram na aplicação (40 m³ ha-1), ou não, de dejetos líquidos em PD e PR. As emissões de N2O foram medidas in situ depois da aplicação dos dejetos, por 28 dias. Os fluxos de N2O aumentaram com a aplicação dos dejetos e, em apenas 20% das avaliações realizadas, foram superiores no PD. As emissões de N2O relacionaram-se com o aumento do espaço poroso ocupado pela água. Quantidades acumuladas de N na forma de N2O, emitidas em 28 dias, representaram 0,20 e 0,25% do N total aplicado com os dejetos no PD e PR, respectivamente. Os resultados demonstram que a aplicação de dejetos líquidos de suínos em PD não aumenta a emissão acumulada de N2O em relação à aplicação em PR.

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In this paper is presented electrochemical evidences of the influence of the light on the electrochemical behavior of nickel electrode in diluted sulfuric acid. The current densities related with the electrooxidation of the metal decreases when the electrode is under illumination. The corrosion potential, Ecorr , shift to a more positive value in this condition. This effect was observed with polychromatic light and with different wavelength glass filters such as 700 nm and 520 nm. It was observed that increasing the temperature of the solution, the current densities related with cathodic and anodic processes, increases instead of decreases. The activation energy related with the electrooxidation of the electrode was higher under illumination than in the dark. It is suggested that this behavior may be related or with a photo-inhibition effect either with dessorption of adsorbed water involved in the electrooxidation mechanism.

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Alumina supported niobium oxide was prepared by chemical vapor deposition (CVD) of NbCl5. The alumina was calcined and pretreated at differents temperatures in order to vary the density of OH groups on the surface which was determined by thermogravimetric analysis. A good correlation was found between the amount of anchored niobium and the total number of anionic sites (oxide and hydroxyl groups) on the surface of the alumina. The infrared spectra on the OH stretching region indicate that OH groups coordinated to at least one tetrahedral aluminum were more reactive towards NbCl5.

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The simultaneous determination of cobalt and nickel is a classical analytical problem. A great number of reagents associated with several techniques of analysis have been applied to achieve this determination. In this review 117 references, which appeared between 1996-1980, are described and classified according to the technique applied.

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The strong reducing action of L-ascorbic acid (Vitamin C) are of fundamental interest in biochemical and related process. The oxidation of ascorbic acid by molecular oxygen and others oxidants are of fundamental importance, involving the intervention of transition metal ions as catalysts and the formation transition metal complexes of ascorbic acid as intermediates. The present article is intended to cover some aspects of the reactions of ascorbic acid and related compounds involving some transition metal ions.

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Nitric Oxide has been shown to be involved in many important biological functions. It serves as a vasodilator and a neurotransmitter in the brain and peripheral nervous system. It is also involved in the bacteria-killing process by macrophages. In this review we will discuss progress in nitric oxide chemistry and we will also attempt to explain its action in the cardiovascular, nervous and immune systems.

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Capsules were prepared from chitosan (QTS)-poly(vinyl alcohol) (PVA) blend by saline coacervation and then by formalization. A adsorbent based on chitosan, insoluble on acid solution, was obtained. The morphology, average diameters of QTS/PVA capsules and their pores were studied by using scanning electron microscopy. The entrapment-adsorption of dimethylglioxime and ethylenediaminetetracetate by the capsules were studied. The removal of the ion nickel (II) and copper (II), was more effective than by using unloaded capsules.

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Methylene blue (AM) was immobilised on surface of the silica gel modified with niobium oxide. This material was incorporated in a carbon paste electrode, which showed a redox couple in a potential of E= -113 mV vs SCE in KCl solution at pH 7.0. The formal potential, in 0.5 mol L-1 KCl at pH 7.0, shifted about 290 mV towards more positive values compared to those observed for AM solubilized in aqueous solution. The dependence on the formal potential with solution pH between 2 and 7 was much lower than those observed for AM solubilized in aqueous solution.

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Nickel metal hydride (Ni-MH) batteries have emerged as an alternative for replacement of nickel-cadmium batteries, because of their more environmental compatibility and high energy capacity. In this article, we described the properties and applications for Ni-MH batteries, giving some emphasis on the metal-hydride electrode, including the description of composition, the charge storage capacity and the discharge profile. The key component of the nickel-metal hydride electrode is a hydrogen storage alloy whose composition is formulated to obtain a high stable material over a large number of charge-discharge cycles.

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Bottom ash has been used as raw material to glass and glass ceramic production because it is a source of SiO2 and Al2O3. However, the high concentration of iron (about 10% wt.) difficulty the control of the nucleation and the crystallization processes. The iron content was reduced by magnetic process, where the magnetite phase was mainly removed. In order to compare glass ceramics obtained from original and low iron bottom ashes, microstructural and dilatometric characterizations were performed.

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Nickel, palladium and platinum micro-crystals were dispersed in films covering a vitreous carbon plate electrode by ion exchange followed by electroreduction of their ions. These modified electrodes were used in the electrocatalytic hydrogenation of several substrates of different classes and their efficiency is reported. A comparison among them was performed based on the structural characteristics of the metals. A modified electrode containing platinum showed to be more efficient than a palladium modified electrode and the one of nickel was the less efficient.

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This review deals with the homo- and copolymerization of styrene with nickel catalysts. The catalytic activity, polymer stereoregularity, polymer molecular weight and polydispersity are dependent upon nickel ligands and reaction parameters. Catalysts supported on silica, treated with methylaluminoxane (MAO), have shown higher stereospecificity and activity compared to homogeneous ones. The influence of these parameters is discussed focusing on the elucidation of some aspects of the polymerization mechanism.

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In this work, we report the synthesis and the photoluminescence features of Eu(III)-doped yttrium-aluminium oxide obtained by non-hydrolytic sol-gel routes. After heating the powders above 600 ºC the XRD patterns show the presence of the Y4Al2O9 (YAM) and Y3Al5O12 (YAG) phases. At 800 and at 1500 ºC the PL spectra display the Eu(III) lines characteristic of the YAM monoclinic phase. The 5D0->7F2 transition is favored relatively to the 5D0->7F1 lines. However, at 1100 ºC the cubic YAG is the preferential phase and the 5D0->7F1 transition dominates the spectrum. The Eu(III) ions lie in a centrosymmetrical site. The different solvents used in the sol-gel synthesis also change the relative proportion between these two phases. This is monitored analyzing the modifications in the relative intensity between the 5D0->7F2 and the 5D0->7F1 transitions.