137 resultados para HUMAN CU,ZN-SUPEROXIDE DISMUTASE


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The multi-element determination of Al, Cr, Mn, Ni, Cu, Zn, Cd, Ba, Pb, SO4= and Cl- in riverine water samples was accomplished by inductively coupled plasma mass spectrometry (ICP-MS). The sample passed through a column containing the anionic resin AG1-X8 and the metals were determined directly. The retained anionic species were eluted and SO4= and Cl- were determined at m/z 48 and 35 correspondent to the ions SO+ and Cl+ formed at the plasma. Accuracy for metals was assessed by analysing the certified reference TM-26 (National Water Research Institute of Canada). Results for SO4= and Cl- were in agreement with those obtained by turbidimetry and spectrophotometry. LOD's of 0.1 µg l-1 for Cd, Ba and Pb; 0.2 µg l-1 for Al, Mn and Cu; 0.5 µg l-1 for Cr; 0.9 for Zn; 2.0 µg l-1for Ni , 60 µg l-1 for S and 200 µg l-1 Cl were attained.

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An on-line electrodissolution procedure implemented in a flow injection system for determination of copper, zinc and lead in brasses alloys by ICP-AES is described. Sample dissolution procedure was carried out by using a PTFE chamber and a DC power supply with constant current. Solid sample was attached to chamber as anode and a gold tubing coupled in the chamber was used as cathode. An electrolytic solution flowing through the gold tubing closed the electric circuit with sample, in order to provide condition for electric dissolution when the DC power supply was switched on. The best results were achieved by using a 1.5 mol l-1 nitric acid solution as electrolyte and a 2.5 A current intensity. The procedure presented a good performance characterized by a relative standard deviation better than < 5% (n=5) and a sample throughput of 180 determinations per hour for Cu, Zn and Pb. Results were in agreement with those obtained by conventional acid dissolution (99% confidence level).

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The most relevant advances on the analytical applications of glutathione determination based on glutathione redox cycle and the antioxidant system are given. The main enzymes that participate of the glutathione metabolism are the glutathione peroxidase and glutathione reductase. The glutathione peroxidase has a major role in the removal of hydrogen peroxide and lipid peroxides from the cells. These enzymes, operating in tandem with catalase and superoxide dismutase promote a scavenging of oxyradical products in tissues minimizing damages caused by these species. Reduced glutathione is the major intracellular thiol found in mammals and changes in the glutathione concentration in biological fluids or tissues may provide a useful marker in certain disorders like hemolytic anemia, myocardial oxidative stress and in the investigation of some kinds of cancers. Particular attention is devoted to the main advantages supplied by biosensors in which there is an incorporation of bioactive materials for the glutathione determination. The correlation between stability and sensitivity of some reduced glutathione electrochemical sensors is discussed.

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The aquatic humic substances (AHS) investigated in this study were conventionally isolated from Rio Negro waters - Amazonas State/Brazil by means of the collector XAD 8. A special five-stage tangential-flow ultrafiltration device was used for analytical fractionation of AHS. The fractionation patterns (6 fractions each) showed that metal traces remaining in AHS after their XAD 8 isolation have different size distributions. For instance, the major percentage of traces of Ni, Cu, Zn, Cd and Pb (determined using ICP-AES) was preferably complexed by molecules with relatively high molecular size (30-100 kDa) and the following complexation order was characterized: F2 >> F1 = F4 = F5 > F3 > F6. Moreover, the species formed between AHS and metals prepared by spiking, showed distribution patterns changing as a function of the complexation time (ageing process), indicating a slow transformation process and an inner rearrangements in the binding sites within the AHS molecules.

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In this work the metal distribution and exchange constants between metal species and aquatic humic fractions with different molecular sizes were studied. The aquatic humic substances (AHS) were extracted by XAD-8 resin from water sample collected from Itapitanguí river, São Paulo State, Brazil. The AHS were fractionated in six fractions with different molecular sizes (>100 - <5 kDa) and characterized by several techniques. Molar ratios H/C suggested higher aromaticity for fractions F1 and F6 whereas molar ratios C/N didn´t show any differences regarding the humification degree between the fractions. The UV-Vis absorbance a254/a436 ratio showed higher results for F4 and F5, probably by less condensed features. FTIR studies showed high similarity in the functional groups in the fractions. The highest percentage of traces of Co, Al, Fe, Mn, Cu, Zn and Ni (determined by ICP-AES) was preferably complexed by fractions F3 and F4 with a greater amount of dissolved organic carbon (DOC). In addition, the exchange constants, determined by ultrafiltration method, showed complexes AHS-Fe and AHS-Al with higher stability than complexes AHS-Co in all fractions.

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The concentrations of Cu, Pb, Zn, Cr, Ni, Al, Mn and Fe were measured by atomic absorption spectrometry, of 19 topsoil samples collected in the Teresina city urban area to discriminate natural and anthropic contributions and identify possible sources of pollution. The average concentrations of Cu, Zn, Pb and Cr of the urban soils were 6.11, 8.56, 32.12 and 7,17 mg/kg-1, respectively. Statistical analysis techniques, such as principal component analysis (PCA) and hierarchical cluster analysis (HCA), were used to analyze the data. Mn, Ni and Cr levels were interpreted as natural contributions, whereas Pb, Zn and, in part, Cu were accounted for mainly by anthropic activities. High Pb levels were observed in the ancient avenues.

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The effect of operational variables and their interaction in TPR profiles was studied using a fractional factorial experimental design. The heating rate and the reducing agent concentration were found to be the most important variables determining the resolution and sensitivity of the technique. They showed opposite effects. Therefore, they should be manipulated preferentially in order to obtain optimized TPR profiles. The effect of sample particle size was also investigated. The tests were carried out within a Cu/Zn/Al2O3 catalyst used for the water-gas shift reaction that presented two distinct species of Cu2+ in TPR profiles.

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This work evaluated the kinetics as well as the retention capacity of Cu, Zn, Cd, and Pb by arbuscular mycorrhizal fungi (AMF) mycelium. The metal retention is a fast process with Cu being retained 3, 30, and 60 times faster than Zn, Cd, and Pb, respectively. Metal retention capacity varied amongst the different tested AMF species and decreased in the following order: Cu>Zn>>Cd>Pb. The Glomus clarum mycelium showed the highest retention capacity for Cu, Cd and Pb, whereas Zn was mostly retained by Gigaspora gigantea mycelium. The simultaneous application of all tested metals in solution decreased Cu and Zn retention by AMF mycelium. The high retention capacity of Cu and Zn by mycelium of G. clarum and G. gigantea suggests a promising use of these isolates in phytoremediation.

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Copper toxicity in soil was evaluated using biomarkers of oxidative stress (catalase enzyme activity, superoxide dismutase and lipid peroxidation) in the earthworm Eisenia foetida. Agricultural topsoils from mining areas of the Aconcagua river basin were collected. Total copper concentrations were in the range of 94-959 mg kg-1, while the exchangeable copper concentrations were in the range of 46-2225 µg kg-1. Earthworms exposed to soil with exchangeable copper concentrations above 32 µg kg-1 showed an increase in catalase activity. Parameters of antioxidant activity were more sensitive than the weight change and thus can be used as appropriate biomarkers in Eisenia foetida.

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This study aimed to evaluate the chemical elements levels in soil, submitted to different management systems and use by the Energy Dispersive X-Ray Fluorescence Spectrometry - EDXRF. The systems were T1 - agro forestry (SAF), T2 - Native Field (CN), T3 - Native Forest (NM), T4 - Tillage Forest (PF); T5 - conventional tillage system (SPC) and T6 - System tillage (NT). Samples were collected at 0-10 and 10-20 cm, dried and ground for analysis in EDX-720. The soil showed no difference in the average concentrations of chemical elements analyzed in the profiles, but the systems presented different concentrations of metal elements, and T3 had the highest K, Ca and Zn at 0-10 cm and higher contents of K, Ca, Cu, Zn and Mn in the layer of 10-20 cm.

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The construction and optimization of a device that can be applied to electrochemical studies in flat micro regions are described. This was developed as an attempt to study small regions of metallic samples, whose properties may differ completely from its macroscopic behavior and for studies in highly resistive medium. Some results were obtained for individual grains of polycrystalline samples, welded regions, pure copper, platinum, glassy carbon, single crystals of Cu-Zn-Al alloy, and steel in biodiesel without electrolyte intentionally added. The device showed to be useful for the proposed purpose, allowing to be automated and has potential possibilities of other applications.

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Solid state M-L compounds, were M stands for bivalent Mn, Fe, Co, Ni, Cu, Zn and L is pyruvate, have been synthesized. Thermogravimetry and derivative thermogravimetry (TG/DTG), differential scanning calorimetry (DSC), X-Ray powder diffractometry, infrared spectroscopy, elemental analysis, and complexometry were used to characterize and to study the thermal behaviour of these compounds. The results led to information about the composition, dehydration, ligand denticity, and thermal decomposition of the isolated compounds.

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O objetivo do presente trabalho foi estimar o conteúdo e a exportação de micronutrientes (Mn, B, Cu, Zn e Fe) e o Na nos diferentes componentes de árvores de um povoamento de acácia-negra (Acacia mearnsii De Wild.), procedência australiana Batemans Bay, com 2,4 anos de idade, em Butiá-RS (Brasil). A biomassa total estimada foi de 36.155 kg/ha, apresentando distribuição de 46,0, 20,0, 19,5, 12,0 e 3,0%, na madeira do lenho, nas folhas, nos galhos vivos, na casca e nos galhos mortos, respectivamente. A proporção de micronutrientes acumulados na biomassa dos componentes da árvore foram 43,76% nas folhas, 26,94% na madeira do tronco, 19,56% nos galhos vivos, 7,21% na casca e 2,54% nos galhos mortos. A quantidade estimada de micronutrientes contidos na biomassa acima do solo foi 10,4 kg/ha, acumulados da seguinte forma: Na (58,84%), Fe (21,79%), Zn (9,16%), B (4,09%), Mn (4,59%) e Cu (1,54%). A casca e a madeira do lenho acumulou Na (21,47%), Fe (6,71%), Mn (2,11%), Zn (1,66%), B (1,58%) e Cu (0,63%). A copa (folhas e galhos vivos e mortos) acumularam Na (37,36%), Fe (15,07%), Zn (7,49%), B (2,53%), Mn (2,48%) e Cu (0,91%). A exploração intensiva de áreas com a procedência Batemans Bay gera suspeitas de possíveis ocorrências de deficiências nutricionais de Na nas rotações futuras, tornando necessário o emprego de fertilizantes para manter a produtividade do sítio.

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Objetivou-se avaliar a eficiência nutricional de micronutrientes (Mn, B, Cu, Zn e Fe) e Na nos diferentes componentes das árvores de três procedências de acácia-negra (Acacia mearnsii), com 2,4 anos de idade, plantadas em Butiá-RS (Brasil). As procedências selecionadas foram Lake George, Bodalla e Batemans Bay. Constatou-se grande variação na eficiência nutricional entre as procedências. A Lake George, além de acumular maior biomassa total, foi também a mais eficiente na utilização dos nutrientes na produção de biomassa total das árvores. No entanto, a Bodalla mostrou ser a procedência mais eficiente no uso dos nutrientes para produção de biomassa da casca e da madeira.

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Lodos gerados em Estações de Tratamento de Efluentes de fábricas de celulose kraft branqueada podem conter metais pesados e compostos organoclorados mesmo para fábricas que possuam sequências de branqueamento ECF (livres de cloro elementar), devido à presença de dióxido de cloro. Neste trabalho, buscou-se avaliar o potencial de absorção de metais pesados e compostos organoclorados (PCDD e PCDF) por Brassica juncea, utilizando como substrato o composto orgânico constituído por lodo biológico de uma Estação de Tratamento de Efluentes por lodos ativados misturado com cascas de eucalipto de uma fábrica de celulose brasileira. As plantas de Brassica juncea foram cultivadas em vasos de 0,63 dm³ em casa de vegetação, durante 73 dias. Os seguintes parâmetros foram monitorados no substrato e nas plantas: Fe, Mn, Pb, Ni, Cu, Zn, Cr, Cl-, carbono orgânico total e AOX (compostos organo-halogenados adsorvíveis). Os níveis de metais pesados presentes no solo após a aplicação do composto ficaram dentro de faixas permissíveis da legislação brasileira para aplicação de composto orgânico para uso agrícola. Traços de PCDD e PCDF foram encontrados no substrato em concentrações menores do que 0,5 ng I-TEQ/kg (ppt). Tais valores ficaram abaixo de 17 ng I-TEQ/kg, considerado o limite mais exigente de qualidade de compostos adotados na Alemanha e no Canadá.