1000 resultados para fracionamento do fósforo


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Com objetivo de avaliar o efeito da aplicação de calcário e fósforo sobre o desenvolvimento de duas variedades de maracujazeiro, foi desenvolvido experimento em casa de vegetação no Instituto de Ciências Agrárias da Universidade Federal Rural da Amazônia (UFRA). Utilizou-se como substrato Latossolo Amarelo distrófico, textura média. O delineamento experimental foi em blocos casualizados, em esquema fatorial 4x4x2, com 32 tratamentos e 4 repetições, totalizando 128 parcelas. Os fatores estudados foram quatro doses de fósforo (0; 100; 200 e 300 mg dm-3 de P) na forma de superfosfato triplo (SFT); quatro níveis de saturação por bases (inicial = 15%, 40%, 65% e 90%) e duas variedades de maracujazeiro (Golden Star e CPATU-Casca fina). Como corretivo de acidez do solo, foram utilizados carbonato de cálcio (CaCO3) e carbonato de magnésio (MgCO3). Após 50 dias da instalação do experimento, realizaram-se as avaliações nas variáveis biológicas indicativas do desenvolvimento da planta, como: altura, diâmetro do caule e massa seca da parte aérea. A aplicação combinada de fósforo e de calcário influenciou positivamente no desenvolvimento e na massa seca de plantas de maracujazeiro. A maior produção de massa seca foi obtida com aplicação combinada de 160 mg dm-3 de P em solo com saturação por bases estimada de 47%, que esteve associada às concentrações de P e de Ca de 143 mg dm-3 e 2,9 cmol c dm-3 no solo; e a teores de 2,6 e 10,8 g kg-1 na massa seca da parte aérea, respectivamente. A variedade CPATU Casca fina foi superior, em termos de diâmetros médios de caule e massa seca da parte aérea.

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Conduziu-se o experimento em casa de vegetação com o objetivo de avaliar os efeitos da inoculação de fungos micorrízicos arbusculares (FMAs) e de bactérias diazotróficas endofíticas no crescimento de mudas de maracujazeiro-doce sob diferentes doses de fósforo. O delineamento experimental foi em blocos casualizados, em arranjo fatorial 3x2x4, sendo três tratamentos com fungos: Gigaspora margarita, Glomus clarum e controle (sem fungo); dois tratamentos com bactérias: Burkholderia sp. + Burkholderia silvatlantica e controle (sem bactéria); e quatro doses de fósforo: 0; 15; 30 e 60 mg dm-3, com quatro repetições. A unidade experimental foi composta por um vaso de 3,5 dm³ com três plantas. As mudas foram produzidas a partir de sementes e transplantadas para vasos, contendo mistura de solo e areia (1:2 v:v) esterilizada. Aos noventa dias após o transplante das mudas, foram avaliados: altura, diâmetro do caule, área foliar, massa seca da parte aérea, porcentagem de raízes colonizadas por fungos e enumeração de bactérias nas raízes. Independentemente da presença de bactérias diazotróficas, a inoculação com FMAs proporcionou incrementos na altura, massa seca de parte aérea, área foliar e diâmetro do caule das mudas de maracujazeiro-doce, nas doses de 0 e 15 mg dm-3 de P. As bactérias promoveram incrementos na altura e área foliar das mudas quando associadas ao FMA G. margarita, entretanto, sem a presença dos FMAs, estas reduziram a massa seca da parte aérea, independentemente das doses de P no substrato.

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A cultivar de abacaxi 'Vitória' tem como principais características a resistência à fusariose, ausência de espinhos nas folhas, frutos de forma cilíndrica e de polpa branca. O objetivo deste trabalho foi avaliar o efeito de doses de N, P2O5 e K2O no desenvolvimento da folha "D", massa dos frutos, produtividade, produção de mudas e qualidade da polpa do fruto - sólidos solúveis (SS) e acidez titulável (AT). Os tratamentos foram constituídos de cinco níveis de N: 0; 214; 428; 642 e 856 kg ha-1; cinco níveis de P2O5: 0; 75; 150; 225 e 300 kg ha-1, e cinco níveis de K2O: 0; 150; 300; 450 e 600 kg ha-1 dispostos em fatorial fracionado do tipo (1/5) 5³ em blocos. Doses crescentes de N promoveram maior crescimento da folha "D", produção de mudas, desenvolvimento do fruto e produtividade. A produtividade e a massa média do fruto com coroa alcançaram os valores máximos de 65,0 t ha-1 com 647 kg ha-1 de N e 1.247 g com 660 kg ha-1 de N, respectivamente. Os valores de AT e SS cresceram linearmente em função das doses de potássio implementadas, ao passo que a elevação das doses de nitrogênio apresentou efeito oposto. Mesmo com a baixa disponibilidade de P, não houve resposta a este nutriente.

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Com o objetivo de avaliar a interferência da relação fósforo-zinco sobre o crescimento inicial de pitaia para fornecer informações que subsidiem a definição de sistemas de produção mais adequados para a exploração desta cultura no Brasil, realizou-se o experimento, testando cinco doses de P (0; 75; 150; 225 e 300 mg dm-3) e Zn (0; 2; 4; 6 e 8 mg dm-3), sendo os níveis de cada nutriente arranjados em esquema fatorial 5x5, com quatro blocos. Para a interação significativa (p<0,05), procedeu-se ao ajuste em superfícies de resposta do tipo Y = β0 + β1(A) + β2(A)² + β3(B) + β4(B)² + β5(A).( B) + e. As estimativas das correlações fenotípicas foram obtidas considerando apenas o intervalo das doses de P e Zn que promoveram as melhores respostas do acesso de pitaia para os caracteres estudados. A aplicação de P e Zn, e a interação P x Zn afetam a disponibilidade de ambos os nutrientes no substrato, sistema radicular e parte aérea, influenciando, assim, o crescimento inicial de plantas de pitaia. Os rendimentos mais satisfatórios ocorrem quando há 60 - 75 mg de P dm-3 e 3,0 - 4,0 mg de Zn dm-3 no substrato, e 4,5 - 6,0 g kg-1 de P e 150 mg de Zn kg-1 na parte aérea. Esses níveis foram obtidos para a combinação de 150 - 225 mg dm-3 de P, com 4 - 6 mg dm-3 de Zn. Os teores de P e Zn na parte aérea e o somatório do comprimento dos cladódios (SCC) säo os caracteres explicativos que apresentam maiores efeitos diretos sobre a massa seca dos cladódios (MSC).

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A method for the determination of phosphorus in steel samples by graphite furnace atomic absorption spectrometry, using the Zeeman effect background correction and the STPF conditions is proposed. The effect of iron (III) on the phosphorus signal was studied. It was verified, through the pyrolysis temperature curves, that iron (III) is an efficient chemical modifier, thermically stabilizing phosphorus up to 1400ºC. The phosphorus signal increases with the iron (III) concentration, but in the range, which corresponds to the usual concentrations of iron in the sample solutions, the increase is small. Phosphorus was determined in three standard reference materials, after its dissolution in a mixture of hydrochloric and perchloric acids in a PTFE bomb. The agreement with the certified concentration values was excellent. Iron (III) was added to the reference analytical solutions prepared in the blank of the dissolution, while the sample solutions were measured directly, since they already contained the modifier. The detection limit (k = 2) was 0.0042% of phosphorus in the steel sample.

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Results on the optimization of analytical methods for the determination of phosphorus in phosphino-polycarboxylate (PPCA), used frequently as scale inhibitor during oil production, by ICP-AES and ICP-MS are presented. Due to the complex matrix of production waters (brines) and their high concentration in inorganic phosphorus, the separation of organic phosphorus prior to its determination is necessary. In this work, minicolumns of silica immobilized C18 were used. Optimization of the separation step resulted in the following working conditions: (1) prewashing of the column with methanol (80% v/v); (2) use of a flow rate of 5 mL/min and 10 mL/min, respectively, for the preconditioning step and for percolation of the water sample; (3) final elution of organic phosphorus with 7 mL of buffer of H3BO3/NaOH (0.05 M, pH 9) with a flow rate of 1 mL/min. Sample detection limits (3s) for different combinations of nebulizers and spectrometric methods, based on 10 mL water aliquots, are: ICP-AES -Cross flow (47 mg/L) and Ultrasonic (18 mug/L); ICP-MS -Cross flow (1.2 mug/L), Cyclonic (0.7 mug/L) and Ultrasonic (0.5 mug/L). Typical recoveries of organic phosphorus are between 90 and 95% and the repeatability of the whole procedure is better than 10%. The developed methodology was applied successfully to samples from the oil-well NA 46, platform PNA 2, Campos basin, Brazil. Assessment of the PPCA inhibitor was possible at lower concentrations than achieved by current analytical methods, resulting in benefits such as reduced cost of chemicals, postponed oil production and lower environmental impacts.

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Cp'Mn(CO)3 (Cp'=h5-C5H4-CH 3) reacts with P(C6H5)2H in THF to give Cp'(CO)2MnPPh2H (Ph = Phenyl) (1), by substitution of one CO ligand. The reaction of 1 with CH3COCl and CH3S(O)2Cl in the presence of triethylamine occurs under electrophilic substitution on the diphenylphosphan ligand to yield the acetyl- and sulfonylphosphane complexes of manganese(I) Cp'(CO)2MnPPh2COCH3 (2) and Cp'(CO)2MnPPh2S(O)2 CH3 (3). The complex stabilisation of these molecules, wich are hitherto unknown in the free state, is only accomplished by blocking the free electron pair on phosphorus by coordination. The new complexes 1, 2 and 3 were analysed by IR, ¹H-NMR and 31P-MNR spectroscopy and their similar structures are discusssed.

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A sequential system for fractionation by ultrafiltration (SSFU) equipped with advanced membranes filters (molecular size cut-off: 5, 10, 30, 50 and 100 kDalton) of the polyethersulfone type was developed for analytical fractionation of humic substances (HS) extracted from aquatic systems or soils. The device consists of five membrane filters (Sartocon® Micro) operated by a multi-channel peristaltic pump, enabling an easy handling, working in a closed system and with simple collection of the six obtained fractions (F1>100; F2: 100-50; F3: 50-30; F4:30-10; F5: 10-5 and F6 <5 kDalton). Then, the HS sample (250 mL solution 1.0 mg/mL, pH 5.0 to 6.0) to be fractionated is pumped by pump through the series of membrane filters with a tangential flow of 85 mL/min, initial pressure 0.2 to 0.3 bar and permeation flux through the membranes of 0.8 to 1.4 mL/min. The overall time for fractionation and cleaning of the device is about 10 h and 25 mL of each fraction is obtained.

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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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This study was developed with a soil contaminated by heavy metals, with the purpose of evaluating the action of silicon and phosphorus as protection agents through simple extractions by DTPA. The collected samples were prepared and incubated with five doses of silicon and five doses of phosphorus, with four replicates, amounting to 100 experimental units. After 30 and 60 days, samples of each treatment were collected, submitted to pH analyses and simple extraction by DTPA. The amounts of DTPA-extracted metals depended on the doses of silicon and phosphorus and on the pH. Treatments with silicon and phosphorus was efficient in decreasing the availability of heavy metals in soil.

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The present study evaluated the influence of nitrogen, phosphorus and ºBrix on the production of MSCT through a factorial design methodology and analysis of response surface. The objective was to propose a statistically significant probabilistic model for the alcoholic fermentation. In order to obtain less MSCT, the medium under fermentation needs to present low sugar concentration. It was observed that phosphorus and nitrogen, even with no significant individual effects, presented interactions with each other decreasing the production of MSCT, which improves alcohol quality.

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Hydrological samples were collected on the continental shelf of the Amazon river to determine particulate organic and inorganic matter, dissolved organic phosphorus (DOP), phosphate, total particulate phosphorus (TPP), chlorophyll a, temperature, salinity, pH, water transparency, dissolved oxygen (DO) and saturation rate. The objective was to study the forms of DOP, phosphate and TPP. In the euphotic layer, the fluvial discharge from the Amazon river favored the distribution of phosphate, TPP and DOP. In the aphotic layer, the phosphate concentration increased due to the decomposition of DOP and TPP. This increase is due to the absence of photosynthetic processes.

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Phosphorus geochemistry as a proxy of environmental estuarine processes at the Jaguaribe River, Northeastern Brazil. Sedimentation of different phosphorus geochemical fractions can characterize the natural or anthropogenic processes dominant in the watershed. Selective chemical extraction of different phosphorus geochemical forms in estuarine sediments showed the predominance of inorganic over organic forms suggesting an increase in inorganic phosphorus input from anthropogenic sources. Local hydrochemistry favors the dominance of inorganic ferric and carbonatic phosphorus. Ongoing changes in the estuarine throphy, from mesothrophic to euthrophic, may decrease the immobilization of these forms, increasing dissolved phosphorus and favoring euthrophy. Detritic phosphorus suggests a fluvial origin of this fraction and acts as a tracer of river influence upon the estuary.

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The gold and iron mining activities in the Velhas River yield considerable amounts of suspended solids as well as metals to the hydrological system of the region. The risks were assessed by sequential extraction procedures. They were carried out in sediment samples, aiming to evaluate the presence of Co, Cr, Cu, Ni, Zn and As. Although being at high levels in some parts of the river (e.g. As 527 mg g-1 and Cr 475 mg g-1) they are associated with the residual fraction. Mobility factors were also calculated and show that these species are enriched along the river, e.g. for As 0.02 at the spring and 0.33 at the high course of the river.

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The objective of the present work was to evaluate the distribution of Cd, Cu, Mn, Pb and Zn among the different fractions of contaminated soil, before and after rice cultivation. Seven soil samples with different degrees of contamination were studied using a randomized experimental design, with four replicates. Using an ICP-OES we analyzed the contents of heavy metals in fractions of soil, the organic matter therein, the oxides and the residual content before and after rice cultivation. The largest concentrations of Cd, Cu, Mn and Zn in the soil are found in the fractions with stable chemical bonds.