117 resultados para Multi-Resolução


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This paper present an overview of way covered for the spectrometry of atomic absorption (AAS), tracing a line of the historical events in its development and its establishment as a multielement technique. Additionally, the efforts carried by through several researchers in the search for the instrumental evolution, the advances, advantages, limitations, and trends of this approach are related. Several works focusing its analytical applications are cited employing simultaneous multielement determination by flame (FAAS) and/or graphite furnace (GF AAS), and fast sequential multielement determination using FAAS are reported in the present review.

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The development of modern analytical tools plays an important role in quality control. The main purpose of this study was to explore the use of subcritical water as a versatile analytical tool, employed simultaneously as a reagent and solvent, as well as the application of high temperature-high resolution gas chromatography (HT-HRGC) to develop a procedure for the analysis of triacylglycerides and fatty acids in Azadirachta indica A. Juss. (Neem) oil without the need for solvents, chemical reagents, or catalytic agents. The developed method presented satisfactory results and is in agreement with the concepts of Green Analytical Chemistry (GAC).

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This work shows results on the characterization, by liquid chromatography coupled to high resolution tandem mass spectrometry (LC-IT-TOF-MS) with electrospray ionization, of organic compounds present in raw and treated effluents from a combined sewage treatment systems (upflow anaerobic sludge blanket-trickling filter). The sewage samples were prepared by C18 solid phase extraction and the spectra obtained from the various extracts were submitted to principal component analysis to evaluate their pattern and identify the major deprotonated species. Some target compounds were submitted to semiquantitative analysis, using phenolphtalein as internal standard. The results showed the anaerobic step had little impact on the removal of anionic surfactants (LAS), fatty acids, and some contaminantes such as bisphenol A and bezafibrate, whereas the aerobic post-treatment was very efficient in removing these organics.

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A practical and didactic sequence of experiments was proposed to illustrate the stereochemistry concept, optically active compounds, resolution of racemates, and use of the NMR technique, including 2D-COSY for identification of organic compounds, on a laboratory course for undergraduate students. The sequence was: extractions of racemic ibuprofen and chiral naproxen from commercial tablets; syntheses of diastereoisomeric amides reacting chiral (S)-(-)-α-methylbenzylamine with (±)-ibuprofen; separation and determination of absolute configuration of amides by ¹H NMR spectroscopy and GC analysis, and hydrolysis of amides to obtain (+)- and (-)-ibuprofen.

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The purpose of this study was to develop a rapid, simple and sensitive quantitation method for pseudoephedrine (PSE), paracetamol (PAR) and loratadine (LOR) in plasma and pharmaceuticals using liquid chromatography-tandem mass spectrometry with a monolithic column. Separation was achieved using a gradient composition of methanol-0.1% formic acid at a flow rate of 1.0 mL min-1. Mass spectral transitions were recorded in SRM mode. System validation was evaluated for precision, specificity and linearity. Limit of detection for pseudoephedrine, paracetamol, and loratadine were determined to be 3.14, 1.86 and 1.44 ng mL-1, respectively, allowing easy determination in plasma with % recovery of 93.12 to 101.56%.

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We describe a synthetic route consisting of five steps from aniline to obtain liquid crystal compounds derived from nitroazobenzene. Syntheses were performed during the second half of the semester in organic chemistry laboratory classes. Students characterized the liquid crystal phase by the standard melting point techniques, differential scanning calorimetry and polarized optical microscopy. These experiments allow undergraduate students to explore fundamentally important reactions in Organic Chemistry, as well as modern concepts in Chemistry such as self-assembly and self-organization, nanostructured materials and molecular electronics.

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Multivariate Curve Resolution with Alternating Least Squares (MCR-ALS) is a resolution method that has been efficiently applied in many different fields, such as process analysis, environmental data and, more recently, hyperspectral image analysis. When applied to second order data (or to three-way data) arrays, recovery of the underlying basis vectors in both measurement orders (i.e. signal and concentration orders) from the data matrix can be achieved without ambiguities if the trilinear model constraint is considered during the ALS optimization. This work summarizes different protocols of MCR-ALS application, presenting a case study: near-infrared image spectroscopy.

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This work addresses the use of chiral gas chromatography in resolving optically active stereoisomers and racemates found in fruit flavours. It presents the types of chiral selectors applied to terpene-derived metal coordination compounds, polysiloxane-linked α-amino acid and mixed chiral stationary phases, and focuses on derivatized cyclodextrins, the most popular chiral stationary phases presently used in chromatographic analysis. Knowledge about the techniques involved in chiral recognition and enantiomer identification in the fruit flavour field is given along with examples from the latest studies.

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Spatiotemporal pattern formation in reaction-transport systems takes place spontaneously when the system is kept far from thermodynamic equilibrium. Targets, reaction fronts, waves, spirals, spots and stripes are some typical examples of selforganized structuring. In electrochemical systems, monitoring spatiotemporal patterns of potential in the solid/liquid interface can be done by the use of equally distributed microprobes located close to the working electrode. However, the physical size of each probe can limit the spatial resolution and alter mass transport properties. In contrast, the direct measurement of discrete electrodes does not suffer from this limitation and allows the accurate manipulation of the spatial coupling through changes in resistors connected to the electric circuit. In this paper, the development of an electrochemical setup for multichannel data acquisition with spatiotemporal resolution is described, especially to monitor low levels of currents usually observed in the electro-oxidation of small organic molecules.

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Os óleos vegetais comestíveis foram introduzidos na dieta humana em substituição as gorduras animais nas últimas décadas sendo amplamente consumidos em todo o mundo. O presente artigo descreve o desenvolvimento de uma metodologia para análise de aldrin, dieldrin, endrin e endosulfan em óleos vegetais por cromatografia gasosa de alta resolução (HRGC) utilizando-se extração em fase sólida (SPE). As médias de recuperação dos pesticidas estiveram entre 70 e 110%[1].

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An experiment conducted in the field the action of mancozeb, a fungicide of multi-site action was tested, to control soybean rust caused by Phakopsora pachyrhizi. Its performance was compared to that of the mixture cyproconazole (DMI) + azoxystrobin (QoI). The soybean cultivar NA 7337 RR was used with a population of 400,000 plants/ha cultivated in 20m2 plots. Treatments consisted of mancozeb levels (1.5 and 2.0 kg/ha) applied four, six and eight times. The DMI + QoI mixture was applied three times at 0.3 L/ha + Nimbus. Rust severity was assessed six times in the plots and data were integrated as the area under the disease progress curve (AUDPC). The plots were harvested and grain yield was expressed as kg/ha. Data on AUDPC and yield were subjected to analysis of variance and means compared according to Turkey's test (p = 0.005). Treatments with mancozeb were superior to DMI + QoI mixture both for rust control and grain yield. Four applications of 2.0 k/ha mancozeb were more efficient than three applications of the mixture used as standard. Mancozeb has the potential to be added to fungicide mixtures in the establishment of soybean rust anti-resistance strategy.

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Imagens do sensor TM/Landsat-5 referentes às bandas de TM1 a TM5 e TM7 do município de Altamira-PA, Brasil, da passagem de 20/7/1991, modificadas para 60, 100, 120, 200 e 250 m, foram utilizadas para avaliar a influência da resolução espacial na identificação de floresta, capoeira nova, capoeira madura e não-floresta. Mapas temáticos (um para cada resolução espacial) foram elaborados, considerando a aplicação de um algoritmo de classificação digital Bhattacharya (supervisionado), seguido da interpretação visual. A área de cada uma dessas categorias foi determinada em cada um dos mapas temáticos, tomando as imagens com 30 m de resolução espacial como referência. A exatidão de mapeamento foi avaliada, utilizando a exatidão global, o índice kappa e o índice Tau. Verificou-se que: a) as maiores discrepâncias em termos quantitativos ocorreram nos mapas gerados a partir das imagens com 200 m de resolução espacial; b) as categorias que dominavam a cena em termos espectrais e espaciais aumentaram à medida que a resolução espacial foi degradada; c) os mapas elaborados a partir de imagens com resolução espacial de 200 m apresentaram ligeira confusão na identificação dos temas; e d) a confusão espectral entre os temas não apresentou tendência linear com a gradativa degradação da resolução espectral.

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O presente artigo trata do delineamento semi-automático de copas de árvores através de suas sombras periféricas observadas em fotografia aérea de alta resolução. O estudo foi realizado em área de dois hectares de Floresta Ombrófila Mista da Floresta Nacional de Irati, PR, utilizando-se a técnica de interpretação, nos formatos analógico e digital, em uma fotografia aérea de 70 mm colorida normal, na escala de 1:1.000, e dados obtidos em campo. A metodologia consistiu na transformação das três bandas originais da fotografia colorida digital em apenas uma e na separação da componente sombra dos demais alvos restantes da imagem, através de um limiar. A partir dos resultados, verificou-se que: a) as sombras podem ser visualizadas em clareiras existentes na floresta, entre os galhos e entre as copas das árvores; b) a imagem resultante evidencia a inconsistência de se mapearem as copas exclusivamente pelas sombras periféricas; c) o resultado insatisfatório foi atribuído ao tipo de floresta natural considerado; d) a técnica mostrou-se promissora como ferramenta adicional de realce de imagem; e e) faz-se necessário desenvolver maior número de pesquisas para se obterem resultados conclusivos.

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O uso de recursos de sensoriamento remoto orbital constitui um grande avanço no levantamento de dados sobre a cafeicultura, sobretudo por seu caráter temporal e baixo custo. Sendo assim, o objetivo do trabalho foi avaliar a utilização da imagem do satélite QUICKBIRD na determinação de parâmetros biofísicos importantes para a cultura cafeeira. Foram utilizados 25 talhões com plantios de café localizados entre os municípios de Ribeirão Corrente, Franca e Cristais Paulista (SP). Os parâmetros biofísicos utilizados foram os espaçamentos entre linhas e plantas, altura, IAF, diâmetro da copa, porcentagem de cobertura vegetal, rugosidade, variedade e biomassa. Foram utilizados valores de refletância real das bandas espectrais do satélite QUICKBIRD e os índices de vegetação NDVI, GVI, SAVI e RVI. A partir desses dados, foram feitas análises de regressão linear e não linear para a geração dos modelos de estimativa. A utilização de modelos de regressão baseados em equações não lineares mostrou-se mais adequado para determinar os parâmetros IAF e a porcentagem de biomassa, importantes como indicativos da produtividade da cultura cafeeira.