887 resultados para anion
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Pós-graduação em Química - IQ
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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The canola (Brassica napus, L.) cultivation was encouraged for grain and oil production at the 80's, and it is also considered a good option for crop rotation. The nitrogen is one of the most required nutrients by the plant to increase its production, while sulfur is essential to provide seed quality. Thus, the objective of this study was, at Cerrado region, evaluate the effects of nitrogen and sulfur fertilization at yield and contents of oil and crude protein in the grains. We also sought relate to grain yield the S content in the soil and concentrations of N and S in the diagnosis leaf. The experiment was conducted in Uberaba County, State of Minas Gerais, Brazil, in an Oxisol, utilizing the Hyola 401 hybrid. The treatments consisted in a factorial scheme 5 x 4 (five N rates: 0, 60, 100, 140 and 180 kg ha(-1) and; four S rates: 0, 15, 30 and 60 kg ha(-1)) in a randomized blocks design, with four replicates. The nitrogen and sulfur fertilization increased canola grain yield, without significantly alter contents of oil and crude protein. Rates higher than to 140 kg ha(-1) of N and 15 kg ha(-1) of S provided grain yield above 1100 kg ha(-1). Plots with yield higher than to 1000 kg ha(-1) presented foliar concentration of N above 52 g kg(-1). The highest S content was observed at the 0.15-0.30 m layer, proving the sulfate anion mobility. The lowest grain yield were observed when the S content in the soil at this layer were less than 4 mg dm(-3). The N concentrations in the diagnostic leaf and S-SO4-2 content in the 0.15-0.30 m layer correlated positively with crop yield.
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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)
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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)
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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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Apocynin, a methoxy-catechol originally extracted from the root of Picrorhiza kurroa, has been used as an inhibitor of the NADPH oxidase complex in phagocytic and nonphagocytic cells. Its mechanism of inhibition is linked to their prior activation through the action of peroxidases leading to oxidation of the dimeric product, diapocynin. In this study, dipocinina was synthesized and investigated its effect as an inhibitor of activation NADPH oxidase in neutrophils (PMN) and peripheral blood mononuclear cells (PBMC). The synthesis of diapocinina was performed by oxidation of apocinina by potassium persulphate in the midst of water for 5 minutes at room temperature. The precipitate was filtered and washed with water and methanol. Diapocinina was characterized by mass spectrometry. PMN and PBMC were obtained from peripheral blood of healthy donors and purified for gelatin sedimentation, or centrifugation with Histopaque ®, the red cells were lysed with ice water or ammonium chloride. Diapocinina or apocinina were incubated with opsonized zymosan, activation of PMNs and release of superoxide anion, these monitored by chemiluminescent assay dependent lucigenina. We found that diapocinina inhibitor was no better than the apocinina in PMN. However, diapocinina was more efficient than apocinina as an inhibitor of NADPH oxidase in PBMC. In conclusion, whereas PBMC are relatively poor compared with peroxidases PMN, our results are consistent with the need for oxidation apocinina for its effect as an inhibitor of NADPH oxidase
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In the eld of synthetical materials, often called in the literature as organic/molecular conductors or charge-transfer salts, the most prominient examples are the quasi onedimensional systems (TMTTF)2X and (TMTSF)2X, where TMTTF, TMTSF and X refers to tetrametiltetratiafuvaline, tetrametiltetraselenafuvaline and a monovalent anion (X = PF6
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It is known that there is a wide variety of bioavailable trace metals in aquatic systems, and its determination is fundamental to predict impacts to organisms in these environments. However, the determination of the total concentration of chemicals in aquatic systems, despite its importance, does not provide necessary information for decision making or even may lead to misinterpretation of the procedures and potential risks to the system in question. This study aimed to use the technique of diffusion in thin films by concentration gradients (DGT) to evaluate the anion exchange membrane Whatman DE 81 as binder alternative in determining Cr (VI). Experiments were carried out to determine the diffusion coefficients for the material used diffusion (agarose gel). The behaviors of the binders were analyzed before the main variables of the systems, immersion time, pH and ionic strength. Then was made the assessment of potential interferences, to finally proceed with testing using actual samples in the laboratory and in situ
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Peruvian carrot and cassava starches were isolated, adjusted to 30 and 35% moisture, and heatedat 90°C for 8 h. Structural and physicochemical characteristics of the treated starches wereevaluated and compared. High performance anion exchange chromatography with pulsedamperometric detector (HPAEC-PAD), gel permeation chromatography (GPC), and amylosecontent, revealed that the HMT did not change the chemical structures of the starches. A largeagglomeration of granules was observed from SEM, particularly in the Peruvian carrot starch.Crystalline patterns in Peruvian carrot and cassava starches changed from B to C and CAto A,respectively. Relative crystallinity decreased from 30 to 25% in Peruvian Carrot starch, andincreased from 35 to 37% in cassava starch adjusted to 30% moisture. SF and peak viscositydecreased, breakdown was almost completely eliminated (particularly in the Peruvian carrotstarch), and final viscosity increased. WAI and WSI increased as moisture levels of bothstarches increased. Gelatinization temperatures increased and enthalpy decreased. Degrees ofgelatinization increased as the moisture level increased, reaching 33 and 72% in the cassavaand Peruvian carrot starches, respectively. HMT strengthened the intra- and intermolecularinteractions of starches and increased their stability during heating and shearing, but also causeda partial gelatinization in the starches, particularly in Peruvian carrot starch.