991 resultados para Caqui - Secagem


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No presente trabalho é proposto um método para determinação de cobre, manganês e selênio em amostras de vegetais de cultura orgânica e convencional utilizando ultra-som no processo de extração dos analitos e posterior quantificação por espectrometria de absorção atômica em forno de grafite (GFAAS). Utilizando como solução extratora HCl 0,10 mol L-1, as condições ótimas de extração estabelecidas foram: massa de amostra de 100 mg; granulometria da amostra < 60 m; tempo de sonificação de cinco ciclos de 40 s e potência de sonificação de 136 W. As determinações dos analitos por GFAAS foram feitas utilizando-se temperaturas de secagem de 90-250 oC, temperatura de pirólise de 1300 oC, temperatura de atomização de 2300 oC e temperatura de limpeza de 2800 oC. Foi utilizado como modificador químico nitrato de paládio co-injetado junto com as amostras e tungstênio como modificador permanente. A exatidão e precisão do método de extração proposto foram avaliadas utilizando-se padrão certificado Corn Bran, RM 8433 – National Institute of Standards and Technology. Os resultados obtidos pelo método de extração por ultra-som mostraram-se equivalentes aos obtidos pelo método utilizando-se mineralização ácida das amostras em forno de microondas. No entanto, a metodologia proposta diminui consideravelmente o tempo de análise, o que favorece a velocidade analítica. Além disso, a quantidade de resíduos gerados para o ambiente também é bastante minimizada

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The growth of urban population associated with the shortage of supply of public infrastructure such as hospitals, kindergartens, schools, among others, has reinforced the need to develop alternative methods that simplify the construction processes and allows for a reduction in these costs works. The conventional processes have increasingly been shown ineffective to solve the problem of demand for different types of urban and rural buildings. Given this fact, industrial construction processes can gain space and have proven to be highly interesting to solve the above problems, in particular, considering the cost-effective and time. Therefore, this study aimed to determine the influence of moisture on the strength of metal plate connections connectors (printed plate with teeth). For the sizing of the links between structural lumber using metal connectors with teeth prints; controlled process variables (drying of the wood and the different moisture contents), and finally found results and compare them with different literatures order to obtain a qualitative efficiency of the process. Some specimens had very low expectations, can be explained by the presence of bone marrow, and pre-existing cracks. Thus, the results were discarded for further analysis and more accurate results

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This work aims to study the structural characteristics of silica gels obtained from the acid hydrolysis of tetraethoxysilane (TEOS) in water solutions with different concentrations of sodium dodecyl sulfate (SDS). The structural characteristics were studied in stages ranging from the wet gel to the dry stages of the gels (aerogels and xerogels). Aerogels were obtained by ambient pressure drying (APD) after silylation process using trimethylchlorosilane (TMCS) as silylating agent. Xerogels were obtained by conventional evaporating the liquid phase from non silylated gels. The samples were characterized by nitrogen adsorption and small angle X-ray scattering (SAXS). The structure of the wet gels and of the aerogels prepared with the surfactant exhibited characteristics of mass-fractal structures with fractal dimension D in the range 2.1-2.2 for the wet gels and 2.3-2.4 for the aerogels. The characteristic size  of the fractal domain reduces while the size a0 of the primary silica particle composing the fractal structure increases with the drying of the gels, in a process in which share of the porosity is eliminated. Aerogels exhibited typical values for the specific surface of 900 m2g-1 and of 3.5 cm3.g-1 for the total pore volume. These values are correspondingly comparable to those of the aerogels prepared by supercritical drying, since the silylation process replaces hydrophilic –OH groups by hydrophobic –Si-R3 ones, inhibiting the porosity elimination on drying. The silica particle size also increases lightly with the silylation because the attachment of the –Si-R3 groups on the silica surface. The pore size distribution curves of the aerogels are similar for all samples exhibiting a maximum in around 40 nm, independent the concentration of surfactant. This suggests that the characteristic size of 40 nm is due to the association of surfactant micelles... (Complete abstract click electronic access below)

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Pós-graduação em Odontologia Restauradora - ICT

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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Objectives: the aim of this work was to define the range of possible values for each isotope of carbon-13 and nitrogen-15 for cocaine and marijuana seized in Botucatu-SP, with the intention of distinguishing the geographical origin of the drug. Materials and Methods: samples of marijuana and cocaine were collected at the time of incineration. Then, at the Stable Isotope Center from São Paulo State University in Botucatu, São Paulo, Brazil, samples of marijuana were subjected to the drying process and subsequent grinding. Samples of cocaine were not submitted to the processes of drying and grinding because they were already in adequate granulometry. Subsequently, the samples of both drugs were weighed in accordance with the standards for carbon-13 and nitrogen-15. Lastly, CO2 and N2 gases were obtained from the samples through the elemental analyzer. They were then analyzed in a mass spectrometer to obtain values of δ13C and δ15N in ‰. Results and Discussion: the results of marijuana allowed for comparison with regions of Queensland, Australia, according to the range of δ13C between -29.9 ‰ and -29.3 ‰ and δ15N range from 4.1 ‰ to 5.8 ‰. The results were also consistent with those of the state of Pará, Brazil, where the values of δ13C and δ15N were -30.3 ± 0.7 ‰ and 5.0 ± 1.3 ‰, respectively. Also the results were in accordance with those from the state of Mato Grosso do Sul, Brazil, in which δ13C values varied by -28.7 ± 1.3 ‰, and δ15N values varied by 6.6 ± 1.1 ‰, respectively. In both regions, the samples identified as being from Pará and Mato Grosso do Sul showed an overlap. In addition, the results fitted with data from the state of Maranhão, in which the values of δ13C and δ15 N were -28.8 ± 1.6 ‰ and 2.9 ± 2.5 ‰, respectively. In the case of cocaine, the present study could not be related to the results from the literature. One possible explanation may be related to the non-purification of ...

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)