985 resultados para ammonium glufosinate


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Pós-graduação em Agronomia (Agricultura) - FCA

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Os objetivos deste trabalho foram avaliar a eficácia dos dessecantes e determinar a melhor época de aplicação na cultura de soja. O delineamento experimental utilizado foi em blocos casualizados, estando os tratamentos dispostos em esquema fatorial 3x3 e 4x4 de produtos (dessecantes) e épocas de aplicação, nos anos agrícolas 1996/97 e 1997/98, respectivamente. Os dessecantes utilizados foram: paraquat, diquat e paraquat + diquat em 1996/97 e paraquat, diquat, paraquat + diquat e glufosinato de amônio em 1997/98, respectivamente nas dosagens de 0,4, 0,3 e 0,2 + 0,15; e 0,4, 0,3, 0,2 + 0,15 e 0,4 kg i.a. ha¹. Como épocas, foram realizadas três aplicações em 1996/97 e quatro em 1997/98, com intervalos de cinco dias a partir do estádio R6. Após análise e interpretação dos resultados, concluiu-se que os dessecantes foram eficazes na dessecação e que o teor de umidade das sementes entre 50 e 60%, as plantas com baixa incidência de vagens amarelas e marrons e a relação peso de biomassa verde de vagens/biomassa verde total de cerca de 0,5 foram características marcantes na determinação da melhor época de aplicação dos dessecantes.

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Este trabalho foi conduzido no município de Selvíria-MS, semeando soja do cultivar IAC-15. O delineamento experimental utilizado foi o de blocos casualizados, estando os tratamentos dispostos em um esquema fatorial 3x3 e 4x4, sendo os fatores os produtos (dessecantes) e as épocas de aplicação, nos anos agrícolas 1996/97 e 1997/98, respectivamente. Os dessecantes utilizados foram: paraquat, diquat e mistura paraquat + diquat, nas dosagens de 0,4; 0,3 e 0,2+0,15 em 1996/97, respectivamente, e os mesmos tratamentos em 1997/98, além do glufosinato de amônio na dosagem de 0,4 kg i.a. ha-1 em 1997/98. Como épocas, foram realizadas três aplicações em 1996/97 e quatro em 1997/98, todas espaçadas de cinco dias a partir do estádio fenológico médio da cultura R6. Concluiu-se que os dessecantes utilizados mostraram-se eficientes na dessecação da soja; foi possível obter antecipação da colheita de sementes de soja, sem alterar a produção, por um período máximo de sete dias.

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The objective of this paper was to verify the ideal moment of application of desiccants on the soybeans crop, to obtain seeds with maximum physiological and sanitary quality. The cultivar IAC-15 was sowed at the experimental area of FE/UNESP - Campus of Ilha Solteira, located in the district of Selvíria, State of Mato Grosso do Sul (20° 22′S, 51° 22′W at approximately 335 m of altitude). The experimental design was a randomized block, with treatments in a factorial scheme of 3×3 and 4×4 (dessicant x application time), in 1996/97 and 1997/98, respectively. The desiccants applied during the season agricultural year 1996/97 were: paraquat, diquat, paraquat+diquat mix at the doses 400; 300; 200+150 e 400 g a.i.ha -1, respectively. In 1997/98 the same desiccants were used, at the same doses, with additional treatment application of ammonium glufosinate at the dose of 400 g a.i.ha -1. The desiccants were applied three times in 1996/97 and four times in 1997/98 with 5 days intervals starting at the R 6 stage. According to the environmental conditions of this research the best desiccation time was when soybean plants had 80% to 90% of pods with yellow and brown coloration and seeds with 45% to 60% of water content. There were no effects of any of the desiccants tested in the physiological and sanitary potential required for commercialization of the seeds.

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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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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Dynamic and controlled rate thermal analysis (CRTA) has been used to characterise alunites of formula [M(Al)3(SO4)2(OH)6 ] where M+ is the cations K+, Na+ or NH4+. Thermal decomposition occurs in a series of steps. (a) dehydration, (b) well defined dehydroxylation and (c) desulphation. CRTA offers a better resolution and a more detailed interpretation of water formation processes via approaching equilibrium conditions of decomposition through the elimination of the slow transfer of heat to the sample as a controlling parameter on the process of decomposition. Constant-rate decomposition processes of water formation reveal the subtle nature of dehydration and dehydroxylation.

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In the structure of the title compound, cis NH4+ C8H11O4-, the carboxylic acid and carboxyl groups of the cation adopt C-C-C-O torsion angles of 174.9(2) and -145.4(2)deg. respecticely with the alicyclic ring. The ammonium H atoms of the cations give a total of five hydrogen-bonding associations with carboxyl O-atom acceptors of the anion which, together with a carboxylic acid O-H...O(carboxyl) interaction give two-dimensional sheet structures which lie in the (101) planes in the unit cell.

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In wastewater treatment plants based on anaerobic digestion, supernatant and outflows from sludge dewatering systems contain significantly high amount of ammonium. Generally, these waters are returned to the head of wastewater treatment plant (WWTP), thereby increasing the total nitrogen load of the influent flow. Ammonium from these waters can be recovered and commercially utilised using novel ion-exchange materials. Mackinnon et al. have described an approach for removal and recovery of ammonium from side stream centrate returns obtained from anaerobic digester of a typical WWTP. Most of the ammonium from side streams can potentially be removed, which significantly reduces overall inlet demand at a WWTP. However, the extent of reduction achieved depends on the level of ammonium and flow-rate in the side stream. The exchange efficiency of the ion-exchange material, MesoLite, used in the ammonium recovery process deteriorates with long-term use due to mechanical degradation and use of regenerant. To ensure that a sustainable process is utilised a range of potential applications for this “spent” MesoLite have been evaluated. The primary focus of evaluations has been use of ammonium-loaded MesoLite as a source of nitrogen and growth medium for plants. A MesoLite fertiliser has advantage over soluble fertilisers in that N is held on an insoluble matrix and is gradually released according to exchange equilibria. Many conventional N fertilisers are water-soluble and thus, instantly release all applied N into the soil solution. Loss of nutrient commonly occurs through volatilisation and/or leaching. On average, up to half of the N delivered by a typical soluble fertiliser can be lost through these processes. In this context, use of ammonium-loaded MesoLite as a fertiliser has been evaluated using standard greenhouse and field-based experiments for low fertility soils. Rye grass, a suitable test species for greenhouse trials, was grown in 1kg pots over a period of several weeks with regular irrigation. Nitrogen was applied at a range of rates using a chemical fertiliser as a control and using two MesoLite fertilisers. All other nutrients were applied in adequate amounts. All treatments were replicated three times. Plants were harvested after four weeks, and dry plant mass and N concentrations were determined. At all nitrogen application rates, ammonium-loaded MesoLite produced higher plant mass than plants fertilised by the chemical fertiliser. The lower fertiliser effectiveness of the chemical fertliser is attributed to possible loss of some N through volatilisation. The MesoLite fertilisers did not show any adverse effect on availability of macro and trace nutrients, as shown by lack of deficiency symptoms, dry matter yield and plant analyses. Nitrogen loaded on to MesoLite in the form of exchanged ammonium is readily available to plants while remaining protected from losses via leaching and volatilisation. Spent MesoLite appears to be a suitable and effective fertiliser for a wide range of soils, particularly sandy soils with poor nutrient holding capacity.

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Magnetic zeolite NaA with different Fe3O4 loadings was prepared by hydrothermal synthesis based on metakaolin and Fe3O4. The effect of added Fe3O4 on the removal of ammonium by zeolite NaA was investigated by varying the Fe3O4 loading, pH, adsorption temperature, initial concentration, adsorption time. Langmuir, Freundlich, and pseudo-second-order modeling were used to describe the nature and mechanism of ammonium ion exchange using both zeolite and magnetic zeolite. Thermodynamic parameters such as change in Gibbs free energy, enthalpy and entropy were calculated. The results show that all the selected factors affect the ammonium ion exchange by zeolite and magnetic zeolite, however, the added Fe3O4 apparently does not affect the ion exchange performance of zeolite to the ammonium ion. Freundlich model provides a better description of the adsorption process than Langmuir model. Moreover, kinetic analysis indicates the exchange of ammonium on the two materials follows a pseudosecond-order model. Thermodynamic analysis makes it clear that the adsorption process of ammonium is spontaneous and exothermic. Regardless of kinetic or thermodynamic analysis, all the results suggest that no considerable effect on the adsorption of the ammonium ion by zeolite is found after the addition of Fe3O4. According to the results, magnetic zeolite NaA can be used for the removal of ammonium due to the good adsorption performance and easy separation method from aqueous solution.

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The structures of two ammonium salts of 3-carboxy-4-hydroxybenzenesulfonic acid (5-sulfosalicylic acid, 5-SSA) have been determined at 200 K. In the 1:1 hydrated salt, ammonium 3-carboxy-4-hydroxybenzenesulfonate monohydrate, NH4+·C7H5O6S-·H2O, (I), the 5-SSA- monoanions give two types of head-to-tail laterally linked cyclic hydrogen-bonding associations, both with graph-set R44(20). The first involves both carboxylic acid O-HOwater and water O-HOsulfonate hydrogen bonds at one end, and ammonium N-HOsulfonate and N-HOcarboxy hydrogen bonds at the other. The second association is centrosymmetric, with end linkages through water O-HOsulfonate hydrogen bonds. These conjoined units form stacks down c and are extended into a three-dimensional framework structure through N-HO and water O-HO hydrogen bonds to sulfonate O-atom acceptors. Anhydrous triammonium 3-carboxy-4-hydroxybenzenesulfonate 3-carboxylato-4-hydroxybenzenesulfonate, 3NH4+·C7H4O6S2-·C7H5O6S-, (II), is unusual, having both dianionic 5-SSA2- and monoanionic 5-SSA- species. These are linked by a carboxylic acid O-HO hydrogen bond and, together with the three ammonium cations (two on general sites and the third comprising two independent half-cations lying on crystallographic twofold rotation axes), give a pseudo-centrosymmetric asymmetric unit. Cation-anion hydrogen bonding within this layered unit involves a cyclic R33(8) association which, together with extensive peripheral N-HO hydrogen bonding involving both sulfonate and carboxy/carboxylate acceptors, gives a three-dimensional framework structure. This work further demonstrates the utility of the 5-SSA- monoanion for the generation of stable hydrogen-bonded crystalline materials, and provides the structure of a dianionic 5-SSA2- species of which there are only a few examples in the crystallographic literature.