994 resultados para Tesouraria líquida (TL)
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Dissertação de Mestrado apresentada ao Instituto de Contabilidade e Administração do Porto para a obtenção do grau de Mestre em Contabilidade e Finanças, sob orientação de Cláudia Maria Pereira Esta versão contém as críticas e sugestões dos elementos do júri.
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A crise económica e financeira despoletada nos EUA em 2007 teve um impacto devasto na economia dos países, empresas e famílias, e que ainda hoje se fazem sentir. Portugal foi um dos países fortemente afetados, culminando com o resgate financeiro em 2011, pelo que todos os seus efeitos limitaram e dificultaram o crescimento económico do país e consequentemente o crescimento das empresas. O estudo tem como principal objetivo analisar o desempenho económico e financeiro da média das PME portuguesas não financeiras e identificar quais as determinantes da tesouraria líquida, em períodos de estabilidade ou de crise económica. Os dados utilizados, indicadores económicos e financeiros, foram obtidos na plataforma do Banco de Portugal, e após o tratamento destes dados, foi efetuada a regressão linear múltipla com dados em painel. Embora o estudo contribua com evidência empírica para a temática da gestão de tesouraria, a utilização de outro tipo de dados além de dados financeiros complementaria o estudo. A análise descritiva mostra que a média das PME em estudo apresentam uma tesouraria líquida negativa, apresentando uma melhoria a partir do ano de 2009. Os resultados da regressão revelam que as variáveis independentes (dimensão, endividamento, maturidade do passivo, oportunidades de crescimento e o ciclo de conversão de caixa) são determinantes da tesouraria líquida. Os resultados revelam ainda que a crise não possui capacidade explicativa quanto à tesouraria líquida, resultado divergente de estudos efetuados anteriormente. Este estudo contribui para uma melhor compreensão das decisões quanto à gestão de tesouraria das empresas portuguesas, auxiliando como instrumento de gestão para as empresas e os seus gestores.
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Synthetic dyes are much used in processed foods. HPLC was applied to different types of snacks, such as colored cereals, chocolate confetti, chewing gums and candies for the determination of those additives. In the case of artificially colored breakfast cereals, 71% of the samples exceeded the allowed limits. Regarding the portions recommended for consumption by the makers of two of the samples, the amounts exceeded those allowed by the Brazilian legislation. In the case of chocolate confetti and candies none of the samples showed higher amounts than those allowed. However 37% of the chewing gum samples presented larger contents than the authorized ones, and one sample contained five times more synthetic dyes than allowed.
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High-temperature liquid chromatography (HTLC) is a technique that presents a series of advantages in liquid phase separations, such as: reduced analysis time, reduced pressure drop, reduced asymmetry factors, modified retentions, controlled selectivities, better efficiencies and improved detectivities, as well as permitting green chromatography. The practical limitations that relate to instrumentation and to stationary phase instability are being resolved and this technique is now ready to be applied for routine determinations.
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A method to quantify lycopene and β-carotene in freeze dried tomato pulp by high performance liquid chromatography (HLPC) was validated according to the criteria of selectivity, sensitivity, precision and accuracy, and uncertainty estimation of measurement was determined with data obtained in the validation. The validated method presented is selective in terms of analysis, and it had a good precision and accuracy. Detection limit for lycopene and β-carotene was 4.2 and 0.23 mg 100 g-1, respectively. The estimation of expanded uncertainty (K = 2) for lycopene was 104 ± 21 mg 100 g-1 and for β-carotene was 6.4 ± 1.5 mg 100 g-1.
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Emerging organic pollutants (EOP) include many environmental contaminants based on commercial products such as pharmaceuticals, personal care products, detergents, gasoline, polymers, etc. EOP may be candidates for future regulation as they offer potential risk to environmental and human health due to their continual entrance into the environment and to the fact that even the most modern wastewater treatment plants are not able to totally transform / remove these compounds. High performance liquid chromatography is recommended to separate emerging organic pollutants with characteristics of high polarity and low volatility, especially pharmaceuticals, from environmental matrices.
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This review describes the advantages and disadvantages of using capillary liquid chromatography (CLC), which is considered the newest member in the analytical separation science arsenal. Although CLC has tremendous potential for being the next major innovation in separatory analysis, it has not yet obtained great popularity compared to conventional high performance (and ultra-high performance) liquid chromatography. Comparisons are made between these techniques and some of the reasons that CLC has not yet reached its potential will be advanced.
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This review considers some of the difficulties encountered with the analysis of basic solutes using reversed-phase chromatography, such as detrimental interaction with stationary phase silanol groups. Methods of overcoming these problems in reversed-phase separations, by judicious selection of the stationary phase and mobile phase conditions, are discussed. Developments to improve the chemical and thermal stability of stationary phases are also reviewed. It is shown that substantial progress has been made in the manufacturing of stationary phases, enabling their use over a wide variety of experimental conditions. In addition, general measures to significantly extend their lifespan are discussed.
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A method using ultrasonication extraction for the determination of 17 polycyclic aromatic hydrocarbons (PAHs), selected by the USEPA and NIOSH as "consent decree" priority pollutants, in soil by High Performance Liquid Chromatography (HPLC) was studied. Separation and detection were completed in 20 min with a C18 columm, acetonitrile-water gradient elution and ultraviolet absorption and fluorescence detections. The detection limits, for a 10 µL of solution injection, were less than 9,917 ng/g in UV detection and less than 1,866 ng/g in fluorescence detection. Several organic solvents were tested for extraction of the 17 PAHs from soils. Acetone was the best solvent among the three solvents tested, and the order of the extraction efficiencies was: acetone>methanol>acetonitrile. Ultrasonication using acetone as solvent extraction was used to evaluate the biodegradation of those compounds in contaminated soil during a vermicomposting process.
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Thermoluminescence (TL) and Optically Stimulated Luminescence (OSL) properties of KAlSi(3)O(8):Mn glasses obtained through the sol gel technique were investigated. Samples were obtained with five different molar concentrations of 0.25, 0.5, 1, 2 and 5 mol% of manganese. Transmission Electronic Microscopy (TEM) indicated the occurrence of nanoparticles composed by glass matrix elements with Mn. Best results for TL response were obtained with 0.5 mol% Mn doped sample, which exhibits a TL peak at 180 degrees C. The TL spectrum of this sample presents a broad emission band from 450 to 700 nm with a peak at 575 nm approximately. The emission band fits very well with the characteristic lines of the Mn(2+) emission features. According to this fact, the band at 410 nm can be ascribed to (6)A(1)(S) -> (4)A(1)(G), (4)E(G) transition, while the 545 nm band can be attributed to the superposition of the transitions (6)A(1)(S) -> (4)T(2)(G) and (6)A(1)(S) -> (4)T(1)(G). The dependence of the TL response with the energy of X-rays (27-41 keV) showed a small decrease of the TL intensity in the high energy region. Excitation with blue LEDs showed OSL in the UV region with a fast decay component. (C) 2011 Elsevier Ltd. All rights reserved.
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Resumo: A dívida pública é um importante elemento das finanças públicas e sua sustentabilidade é o indicativo da boa gestão da política fiscal de um governo. Este estudo tem o objetivo de verificar a sustentabilidade da dívida estadual, de forma agregada, a partir da análise de cointegração e da reação fiscal entre o resultado primário e a dívida líquida estadual, usando dados mensais de dezembro/2001 a maio/2014. Os resultados apontam a existência de cointegração entre as séries de resultado primário e de dívida líquida estadual e, além disso, revelam que os governos estaduais geraram superávits primários em face do crescimento da dívida. Assim, tem-se a indicação de que existiu sustentabilidade para a dívida dos estados no período estudado. Contudo, desafios recentes como o afrouxamento fiscal e a redução da atividade econômica colocam em dúvida a sustentabilidade futura.
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Trabalho Final de Mestrado para obtenção do grau de Mestre em Engenharia Química e Biológica
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Trabalho Final de Mestrado para obtenção do grau de Mestre em Engenharia Química e Biológica
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Trabalho Final de Mestrado para obtenção do grau de Mestre em Engenharia Química e Biológica
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Dissertação de Mestrado Apresentado ao Instituto de Contabilidade e Administração do Porto para a obtenção do grau de Mestre em Contabilidade e Finanças, sob orientação de Mestre Adalmiro Álvaro Malheiro de Castro Andrade Pereira.