997 resultados para Ni-Cd batteries


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This paper reports results from electrochemical evaluations of electrodes used as cathodes for a hydrogen evolution reaction and anodes in Ni-MH batteries that had been surface-modified by micro-encapsulation, co-deposition and sol-gel methods. The surface modifications produced actual improvements in the corresponding electrochemical reactions by enhancing the performance and/or the mechanical stability of the electrode material. (c) 2005 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.

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This work describes a recovery process of cadmium from spent nickel-cadmium batteries by a new hydrometallurgical route based on the selective extraction in hydrochloric acid medium with tributylphosphate (TBP), alone or dissolved in kerosene. The best results were obtained when TBP concentration was at least 75 vol%. Nickel extraction was negligible under these conditions. It was isolated after processing the rafinate through an anionic ion-exchange column. Final wastes generated are basically sodium chloride solutions, with no turbidity, color or heavy metals present in significant amounts.

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Spent nickel-cadmium (Ni-Cd) batteries and salts of nickel and cadmium were placed in two different columns of soil for a period of two years. A leaching solution was passed through them at ambient temperature in this period. The behavior of metals in each column was then evaluated. Under the conditions of the experiment, cadmium and nickel demonstrated the potential to contaminate and affect the natural cycles of soil. The disposal of Ni-Cd batteries directly to the soil also increased the concentration of nickel (349 mg kg-1) and cadmium (2890 mg kg-1), sometimes exceeding the intervention values defined in CONAMA resolution 420/09.

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Akkuteknologia on kehittynyt viime vuosina erityyppisten litium-ioniakkujen hallitessa markkinoita. Uutta teknologiaa kaupallisissa litium-pohjaisissa akuissa edustavat litium-polymeeri- ja litium-rautafosfaattiakut. Työn tarkoituksena oli selvittää soveltuvatko litium-polymeeri- ja litium-rautafosfaattiakut kannettavaan audiolaitteeseen ja verrata näitä Ni-Cd- ja Ni-Mh-akkuihin sekä LiCoO2- ja LiMnO4-kemian litium-ioniakkuihin. Kyseisten akkutyyppien soveltuvuutta kannettavaan audiolaitteeseen ei kirjallisuudessa ole juuri tutkittu. Työ toteutettiin kirjallisuustutkimuksena.

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The Mg-Ni metastable alloys (with amorphous or nanocrystalline structures) are promising candidates for anode application in nickel-metal hydride rechargeable batteries due to its large hydrogen absorbing capacity, low weight, availability, and relative low price. In spite of these interesting features, improvement on the cycle life performance must be achieved to allow its application in commercial products. In the present paper, the effect of mechanical coating of a Mg-50 at.% Ni alloy with Ni and Ni-5 at.% Al on the structure, powder morphology, and electrochemical properties is investigated. The coating additives, Mg-Ni alloy and resulting nanocomposites (i.e., Mg-Ni alloy + additive) were investigated by means of X-ray diffraction and scanning electron microscopy. The Mg-Ni alloy and nanocomposites were submitted to galvanostatic cycles of charge and discharge to evaluate their electrode performances. The mechanical coating with Ni and Ni-5% Al increased the maximum discharge capacity of the Mg-Ni alloy from of 221 to 257 and 273 mA h g(-1), respectively. Improvement on the cycle life performance was also achieved by mechanical coating.

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In recent years, Mg-Ni-based metastable alloys have been attracting attention due to their large hydrogen sorption capacities, low weight, low cost, and high availability. Despite the large discharge capacity and high activity of these alloys, the accelerated degradation of the discharge capacity after only few cycles of charge and discharge is the main shortcoming against their commercial use in batteries. The addition of alloying elements showed to be an effective way of improving the electrode performance of Mg-Ni-based alloys. In the present work, the effect of Ti and Pt alloying elements on the structure and electrode performance of a binary Mg-Ni alloy was investigated. The XRD and HRTEM revealed that all the investigated alloy compositions had multi-phase nanostructures, with crystallite size in the range of 6 nm. Moreover, the investigated alloying elements demonstrated remarkable improvements of both maximum discharge capacity and cycling life. Simultaneous addition of Ti and Pd demonstrated a synergetic effect on the electrochemical properties of the alloy electrodes. Among the investigated alloys, the best electrochemical performance was obtained for the Mg(51)Ti(4)Ni(43)Pt(2) composition (in at.%), which achieved 448 mAh g(-1) of maximum discharge capacity and retained almost 66% of this capacity after 10 cycles. In contrast, the binary Mg(55)Ni(45) alloy achieved only 248 mAh g(-1) and retained 11% of this capacity after 10 cycles. (C) 2010 Elsevier By. All rights reserved.

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Neste trabalho foi estudado o método de preparação de amostras baseado numa extracção ácida assistida por ultra-sons para a quantificação de metais pesados (Pb, Ni, Cd e Cr), em amostras de solo. Usou-se a espectrometria de absorção atómica com câmara de grafite (GFAAS) para quantificar os metais nestas amostras recolhidas em diferentes locais da cidade de Lisboa. A optimização dos parâmetros que influenciam a extracção dos metais por ultra-sons foi realizada a cinco variáveis: quantidade de amostra, volume de extractor (água-régia), tempo de sonificação, potência de sonificação e ciclo de sonificação. A eficiência do método foi testada por comparação dos resultados com os obtidos pela digestão ácida “tradicional” em banho de areia. A optimização do processo foi realizada para o metal chumbo. Os resultados analíticos obtidos por ambos os métodos apresentaram diferenças significativas. A extracção de chumbo das amostras, por ultra-sons, apresentou uma eficiência entre 65 a 78% quando comparada com o método “tradicional”. A recuperação de cádmio apresentou percentagens entre 36 e 90%. No caso do níquel e crómio, concluiu-se haver necessidade de optimizar o processo para cada um dos metais, pois apresentaram uma baixa taxa de recuperação.

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Dissertação apresentada na Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa para obtenção do Grau de Mestre em Tecnologia Alimentar/ Qualidade

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Dissertação apresentada na Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa para obtenção do grau de Mestre em Engenharia Sanitária

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Este estudo apresenta dados sobre a mineralogia e a química de dois solos urbanos em Manaus (Horto Minicipal e Novo Israel) formados a partir da disposição e degradação de resíduo urbano em condições tropicais úmidas. Foi determinada a concentração de Pb, Cu, Ni, Zn, Mn, Fe, Cd e Cr, investigado o grau de contaminação desses elementos no solo e o potencial deles comprometerem a qualidade da água subterrânea. Foi medido o fracionamento geoquímico por lixiviação sequencial dos elementos, além de determinado o pH, teor de matéria orgânica e caracterizados os grupos funcionais dos ácidos húmicos e fúlvicos. Comparativamente esses solos urbanos refletem a composição mineralógica dos solos naturais da região embora a caulinita tenha menor grau de ordenamento cristalino. Contudo, o pH e o conteúdo de matéria orgânica são bem mais elevados. Em termos absolutos ambos os solos têm aproximadamente a mesma sequência de concentração dos elementos: no Horto Municipal Fe>Zn>Mn>Cu>Pb>Cr>Ni>Cd e em Novo Israel Fe>Zn>Cu>Mn>Pb>Cr>Ni>Cd. As maiores acumulações foram nas frações hidróxido de Fe amorfo e óxi-hidróxidos de Fe seguidas da matéria orgânica. Comparativamente, essas frações tiveram maior enriquecimento no Horto Municipal, provavelmente em consequência dos efeitos de envelhecimento dos resíduos, enquanto as mais biodisponíveis e a residual se acumularam mais em Novo Israel. Esse acúmulo nas fases mais móveis em Novo Israel é a causa da contaminação da água subterrânea e indica que o mesmo deve ocorrer no Horto Municipal.

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There are currently many devices and techniques to quantify trace elements (TEs) in various matrices, but their efficacy is dependent on the digestion methods (DMs) employed in the opening of such matrices which, although "organic", present inorganic components which are difficult to solubilize. This study was carried out to evaluate the recovery of Fe, Zn, Cr, Ni, Cd and Pb contents in samples of composts and cattle, horse, chicken, quail, and swine manures, as well as in sewage sludges and peat. The DMs employed were acid digestion in microwaves with HNO3 (EPA 3051A); nitric-perchloric digestion with HNO3 + HClO4 in a digestion block (NP); dry ashing in a muffle furnace and solubilization of residual ash in nitric acid (MDA); digestion by using aqua regia solution (HCl:HNO3) in the digestion block (AR); and acid digestion with HCl and HNO3 + H2O2 (EPA 3050). The dry ashing method led to the greatest recovery of Cd in organic residues, but the EPA 3050 protocol can be an alternative method for the same purpose. The dry ashing should not be employed to determine the concentration of Cr, Fe, Ni, Pb and Zn in the residues. Higher Cr and Fe contents are recovered when NP and EPA 3050 are employed in the opening of organic matrices. For most of the residues analyzed, AR is the most effective method for recovering Ni. Microwave-assisted digestion methods (EPA3051 and 3050) led to the highest recovery of Pb. The choice of the DM that provides maximum recovery of Zn depends on the organic residue and trace element analyzed.

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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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A comparative study of elements deposited on tree bark was carried out for urban and periurban areas of two of the most important cities in Argentina. The content of Fe, Mg, Al, Mn, Zn, Pb, Ba, Cr, Hg, Cu, Ni, Cd and Sb was determined by inductively coupled plasma atomic emission spectrometry (ICP-OES) in Morus alba tree bark collected in the cities of Buenos Aires and Mendoza. The main air pollutants detected in the Buenos Aires urban area were Ba, Cr, Cu and Ni and indicate significative difference from the Mendoza urban and periurban areas. Significantly, higher concentrations of Zn, Ba, Cr and Cu were recorded in the periurban area of the city of Buenos Aires than in Mendoza. Bark samples were strongly influenced by dust and show Al, Fe, Mg and other element accumulations that indicate that soil particles were carried out by wind. Elements like Ba and Zn, commonly linked to traffic emissions, showed the highest concentrations in the Buenos Aires metropolitan area, possibly due to more intensive vehicular traffic. Our results indicated that intensity of vehicular traffic and not city structure is responsible for air pollution.