551 resultados para Métodos Analíticos

em Scielo Saúde Pública - SP


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Neste trabalho são descritos os métodos analíticos empregados para a determinação de micronutrientes (Fe, Mn, Cu, Zn e Mo), cobalto, fósforo orgânico e inorgânico, silica, matéria orgânica e carbono orgânico em torta de filtro rotativo. São apresentadas as marchas analíticas preconizadas e os resultados obtidos nas determinações efetuadas em vinte e duas amostras do material.

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Os solos cultivados com arroz irrigado no Estado de Santa Catarina apresentam características mineralógicas e químicas distintas dos solos utilizados nos estudos de calibração do extrator Mehlich-1, para estimar a disponibilidade de fósforo do solo para as plantas. Desse modo, o objetivo deste trabalho foi avaliar a eficiência dos extratores Mehlich-1, Mehlich-3, Resina em lâminas, Olsen e EDTA na predição da disponibilidade P para plantas de arroz cultivadas em sistema de alagamento em solos representativos de lavouras orizícolas do Estado de Santa Catarina. O experimento foi conduzido em casa de vegetação, com cinco solos oriundos de várias lavouras orizícolas, em 2014. Foram adicionados aos solos quatro concentrações de P, correspondendo a 0, ¼, ½ e 1,0 vez a quantidade de P para atingir 0,2 mg L-1 de P na solução do solo (com base na capacidade de adsorção de cada solo). Foram usadas três repetições por tratamento, dispostas no delineamento completamente casualizado. Após cinco dias da adição dos níveis de P, as unidades experimentais constituídas por vasos de 8 L contendo 3,5 kg de solo seco foram amostradas para determinar o P disponível do solo por cinco métodos químicos. Na sequência, essas foram alagadas e cultivadas com seis plantas de arroz por 46 dias, quando se quantificaram a massa de matéria seca e o P absorvido pela parte aérea das plantas. A eficácia dos métodos Mehlich-1, Mehlich-3, Resina em lâminas, Olsen e EDTA foi avaliada por correlação linear entre a quantidade de P extraída dos solos e a quantidade absorvida pelas plantas. A quantidade de P absorvida pelas plantas de arroz aumentou com o acréscimo das doses de P aplicadas, variando com o tipo de solo. A maior recuperação do P adicionado aos solos foi obtida pelo extrator EDTA, seguido pelo Olsen. O P extraído pelo EDTA e Mehlich-3 evidenciou melhor correlação com quantidade de P absorvida pelo arroz. O agrupamento dos solos segundo características relacionadas à adsorção de P no solo melhora a eficiência de todos os métodos em predizer a disponibilidade de P em solos cultivados com arroz no sistema de inundação.

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Foram comparados dois métodos analíticos para a determinação da lignina (lignina em detergente ácido - LDA e lignina permanganato de potássio - LPer) bem como para averiguar a possível relação dos teores desse componente com a digestibilidade da fibra dos seguintes fenos: andropogon (Andropogon gayanus); aveia (Avena sativa); e dois tipos de coast-cross (Cynodon dactylon), um bem fenado e outro de baixa qualidade. Os valores de LDA e LPer foram diferentes (p <= 0,05) entre as gramíneas estudadas, com as concentrações de LPer consistentemente mais baixas do que as de LDA. Foram detectadas diferenças (p <= 0,05) nos valores de digestibilidade da fibra em detergente neutro (FDN) e da fibra em detergente ácido (FDA), porém, não foi detectada clara relação desses valores com teores de lignina. Os dados sugerem que a concentração de lignina não é o principal fator a explicar um dado valor de digestibilidade.

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Among the emergent laser based spectrometric methods, thermal lensing and other photothermal techniques present a great potential for solving a variety of problems in the fields of chemistry, physics and biology. Their main advantages are high concentration sensitivity, sensibility to physical-chemical properties of the medium, excellent spatial resolution and noninvasive characteristics. In this article, theoretical principles, main applications and practical hints as well as fundamental limitations of these techniques will be carefully described. It is hoped that this will give the reader a clear picture of this field of investigation as well as provide to the ones who are not specialists in the area, the necessary background to understand, implement and use photothermal techniques. In the final sections the development frontiers of photothermal spectrometry will be discussed.

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Increasing attention is being paid to the use of biomarkers for determining the exposure of humans to air toxics. Biomarkers include the nonreacted toxic substance, their metabolites, or the reaction products of these toxics with naturally substances in the body. Significant progress has been made in the measurement of biomarkers during the past several years. Much of this progress has been because of the development of advanced analytical techniques for identification and quantification of the chemical species in complex matrix, such as biological fluids. The assessment of the potential cancer risk associated with exposure to benzene at occupational and non-occupational ambient is necessary because of the toxicological implications of this air pollutant. Thus, in this review, the analytical methodologies used to determine the benzene metabolites, in special, urinary muconic acid and S-phenylmercapturic acid, are described and several problems affecting the precision of these procedures are discussed. Finally, in view of the difficulty pointed out for selecting the more adequate biomarker, further studies to evaluate the human exposure levels to benzene should be done.

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The acidity and ester index are suggested, as simple and cheap methods, adequate to be employed in the study of the authenticity of copaíba oil by small drugstores and export firms. The acidity index permits both the detection and the evaluation of the content of adulteration of copaíba oil. The ester index permits to know if the adulterant either contain ester compounds,as the case of fatty oils, or contain only non saponifiable compounds as is the case of ethyl alchool or mineral oil. The results of the aplication of the methods to eight commercial samples, of copaiba oil, where three samples were adultered, are coherent with those obtained by more sophisticated instrumental methods.

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A review of polypeptides and proteins that influence, direct or indirectly, beer foam quality, as well as the most relevant analytical methods used in their study, are presented. Protein Z, LTP1 and hordein/glutelin fragments originated from malt have a direct influence on beer foam quality. Other proteins, like malt hordeins and albumins and wheat puroindolines, are, to some degree, also important for beer foam quality. Protein hydrophobicity is pointed out as a key parameter to enhance foam quality. Electrophoretic, chromatographic and immunological analytical methods are currently used to study polypeptides and proteins present in barley, malt, wort, beer, and foam. Best results are obtained when combinations of these methods are applied.

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We review here the chemistry of reactive oxygen and nitrogen species, their biological sources and targets; particularly, biomolecules implicated in the redox balance of the human blood, and appraise the analytical methods available for their detection and quantification. Those biomolecules are represented by the enzymatic antioxidant defense machinery, whereas coadjutant reducing protection is provided by several low molecular weight molecules. Biomolecules can be injured by RONS yielding a large repertoire of oxidized products, some of which can be taken as biomarkers of oxidative damage. Their reliable determination is of utmost interest for their potentiality in diagnosis, prevention and treatment of maladies.

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This work presents the VALIDATION SPREADSHEET, a public domain tool that can be used to evaluate the figures of merit for univariate analytical methods. A real example of BTEX determination in environmental samples is included to illustrate its use. The spreadsheet has been developed for Excel® and Open Office®, and is available on the internet at http//lqta.iqm.unicamp.br.

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Plastic packaging materials intended for use in food packaging is an area of great interest from the scientific and economic point of view due to the irreversible internationalization and globalization process of food products. Nevertheless, a debate related to food safety aspects has emerged within the scientific community. Therefore, the development of analytical methods that allow identifying and quantifying chemical substances of toxicological potential in the packaging is considered essential. This article focuses on the main analytical methods, including validation parameters, as well as extraction and quantification techniques for determination of volatile organic compounds from food packaging materials.

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In this work is proposed, a simple experiment for the simultaneous determination of losartan (L) and hydrochlorothiazide (H) in synthetic and real samples by derivative spectrophotometry technique. For the students it is relevant to know this technique for simultaneous determinations of drugs, allowing that the students recognize that this technique is simple, rapid and applicable to quality control. This experimental work, it is proposed in order to being applied to undergraduates into laboratories of analytical chemistry. Furthermore, it is given the integration of the theoretical knowledge with the experimental work; this correlation is of interest for the students.

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The establishment of quality standards for biodiesel was a key step to win the confidence of the market and the automotive industry, thus ensuring the success of the new fuel. In this review are presented standard methods and other analytical methods suggested for analysis of biodiesel. The methods of analysis were divided into groups according to information that may be provided on the contaminants from the raw material of the production process, the molecular structures of biodiesel and its degradation during storage.

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Three analytical methods for the determination of BTEX in water were optimized and validated. With the best method the analytes were extracted of 10 mL of sample with 2.50 g of NaCl in headspace vial of 20 mL by HS and SPME to 40 ºC for 30 min for adsorption and to 250 ºC for 4 min for desorption and were analyzed by GC-MS. The recovery was between 97.9% and 104.3%, and the limit of detection was 2.4 ng L-1 for o-xylene. This method was using to analyze BTEX in water supply and surface water in Ouro Preto city. No sample had concentrations of BTEX above the legislation.

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The development of analytical methods for determination of eight pesticides of different chemical classes (trichlorfon, propanil, fipronil, propiconazole, trifloxystrobin, permethrin, difenoconazole and azoxystrobin) in sediments with gas chromatography-micro-electron capture detector (GC/µECD) and comprehensive two-dimensional gas chromatography with micro-electron capture detector (GCxGC/µECD) is described. These methods were applied to real sediment samples, and the best results were obtained using a 5% diphenyl-methylpolysiloxane column for 1D-GC. For GCxGC the same column was employed in the first dimension and a 50%-phenyl-methylpolysiloxane stationary phase was placed in the second dimension. Due to the superior peak capacity and selectivity of GCxGC, interfering matrix peaks were separated from analytes, showing a better performance of GCxGC.

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The use of dyes in the commercialization of fuel is usually associated with protection of the source and destination. It is used as "markers" to identify and guarantee the identity of the specific product of a particular manufacturer to discourage theft, tampering and disclosure of the quality of solvent or fuel. This work presents a critical analysis on the state of the art about the available analytical methods for identification and quantification of dyes used as markers of solvents and fuels, as well as evaluation of the physical-chemical staining and laws surrounding their use and commercialization.