137 resultados para 356


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Oxidative dehydrogenation of propane (ODP) to propylene was investigated in a dense tubular membrane reactor made of Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) at 700degreesC and 750degreesC. The propylene selectivity in the membrane reactor (44.2%) is much higher than that in the fixed-bed reactor (15%) at the similar propane conversion (23-27%). Higher propylene selectivity in the membrane reactor was attributed to the lattice oxygen (O2-) supplied through the membrane.

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The density function theory was used to calculate the potential energy surface for the decomposition of CF3OF. The geometries, vibrational frequencies and energies of all stationary points were obtained. The calculated harmonic frequencies agreed well with the experimental ones. Three decomposition channels of CF3OF were studied. The calculated reaction enthalpy (29.85 kcal/mol) of the elimination reaction CF3OF --> CF2O + F-2 was in good agreement with the experimental value (27.7 kcal/mol). The O-F bond of CF3OF is broken easily by comparing the energies, while the decomposition channel to yield the CF30 and F radicals is the main reaction path. (C) 2002 Published by Elsevier Science B.V.

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The optimization of the organic modifier concentration in micellar electrokinetic capillary chromatography (MECC) has been achieved by a uniform design and iterative optimization method, which has been developed for the optimization of composition of the mobile phase in high performance liquid chromatography. According to the proposed method, the uniform design technique has been applied to design the starting experiments, which can reduce the number of experiments compared with traditional simultaneous methods, such as the orthano design. The hierarchical chromatographic response function has been modified to evaluate the separation quality of a chromatogram in MECC. An iterative procedure has been adopted to search the optimal concentration of organic modifiers for improving the accuracy of retention predicted and the quality of the chromatogram. Validity of the optimization method has been proved by the separation of 31 aromatic compounds in MECC. (C) 2000 John Wiley & Sons, Inc.

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We present an analysis of extensive nutrient data sets from two river-dominated coastal ecosystems, the northern Adriatic Sea and the northern Gulf of Mexico, demonstrating significant changes in surface nutrient ratios over a period of 30 years. The silicon:nitrogen ratios have decreased, indicating increased potential for silicon limitation. The nitrogen:phosphorus and the silicon:phosphorus ratios have also changed substantially, and the coastal nutrient structures have become more balanced and potentially less limiting for phytoplankton growth. It is likely that net phytoplankton productivity increased under these conditions and was accompanied by increasing bottom water hypoxia and major changes in community species composition. These findings support the hypothesis that increasing coastal eutrophication to date may be associated with stoichiometric nutrient balance, due to increasing potential for silicon limitation and decreasing potential for nitrogen and phosphorus limitation. On a worldwide basis, coastal ecosystems adjacent to rivers influenced by anthropogenic nutrient loads may experience similar alterations.

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The effect of metal ions on the conformation of thymine-containing poly-D-lysine was studied by CD spectra in aqueous solution. Of the metal ions studied,only copper(Ⅱ)ion affected the conformation of mucleic acid analogs .copper(Ⅱ)ion also affected the specifically interacting system made up of thymine-containing poly-D-lysine and polyadenylic acid.

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在黄土高原沟壑区长期施肥对土壤剖面中的 NH4- N、NO3 - N含量分布影响不同。长期不同施肥处理对 NH4- N含量和分布保持相对稳定 ;但不同施肥对 NO3 - N含量分布影响显著。凡施氮肥处理中 ,土壤剖面中出现了 NO3 - N深层富集分布。土壤剖面中 NO3 - N深层富集分布是作物降雨等条件的综合影响下经多年累积而形成的。其中 N处理中 ,NO3 - N富集深度的最大为 12 0 cm~ 2 0 0 cm,富集量为 2 91.4kg/ hm2。NPM处理中 ,NO3 - N富集量最大356.8kg/ hm2 ,但富集分布深度降低 60 cm~ 12 0 cm。 NP处理可有效降低 NO3 - N富集量169.9kg/ hm2和富集分布深度 80 cm~ 140 cm。不施氮肥处理中 ,NO3 - N含量分布在整个土壤剖面显著降低。

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根据旱地作物长期田间试验数据 ,论述了旱作农业生产中作物产量波动性是一个规律性现象 ,并用波动系数加以表述。研究结果表明旱作高产田与低产田相比 ,存在相似的产量波动性 ,区别是它在较高产量水平上波动。高产田作物耗水量较高 ,从而导致土壤相对干燥化。土壤干燥化是高产田产量产生波动性的直接原因 ;而低产田则因作物吸水能力低 ,土壤储水不能充分利用所致

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硝化/脲酶抑制剂对于解决氮肥,特别是尿素及含尿素肥料施用带来的问题已经显示其效果和很好的应用前景。大量的实验室和田间实验表明,与传统肥料相比,添加硝化/脲酶抑制剂的肥料对尿素氮的转化、氨的挥发、土壤中的硝化、反硝化作用以及作物产量、环境效益等方面起到了积极的作用。当今,在世界肥料市场已经有几十种抑制剂申请了专利,其中有四种抑制剂西吡(Nitrapyrin)、双氰胺(DCD)、n-丁基硫代磷酰三胺(NBPT)和氰醌(HQ)大量应用于农业生产。

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Gold nanoparticles were used to enhance the immobilization amount and retain the immunoactivity of recombinant dust mite allergen Der f2 immobilized on a glassy carbon electrode (GCE). The interaction between allergen and antibody was studied by electrochemical impedance spectroscopy (EIS). Self-assembled Au colloid layer (Phi = 16 nm) deposited on (3-mercaptopropyl)trimethoxysilane (MPTS)-modified GCE offered a basis to control the immobilization of allergen Der f2. The impedance measurements were based on the charge transfer kinetics of the [Fe(CN)(6)](3-/4-) redox pair, compared with bare GCE, the immobilization of allergen Der f2 and the allergen-antibody interaction that occurred on the electrode surface altered the interfacial electron transfer resistance and thereby slowed down the charge transfer kinetics by reducing the active area of the electrode or by preventing the redox species in electrolyte solution from approaching the electrode. The interactions of allergen with various concentrations of monoclonal antibody were also monitored through the change of impedance response. The results showed that the electron transfer resistance increased with increasing concentrations of monoclonal antibody.

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系统地研究了2-乙基己氧基甲基膦酸二(2-乙基己基)酯(代号PT28)对硫酸、磷酸、硝酸、高氯酸、盐酸和醋酸六种酸的萃取行为,发现PT-28对硫酸、磷酸、高氯酸和盐酸均不萃取,只对硝酸和醋酸萃取,这与中性磷氧萃取剂甲基膦酸二甲庚酯(P350)和磷酸三正丁酯(TBP)对强酸的萃取有显著的不同,并对其萃取机理进行了讨论。

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Both dinuclear [3] ferrocenophane derivatives of the type Fe(C5H4E)(2)[MLn] [E = S,Se; MLn = Cp* - Cr(NO) (1), Cp* Mo(NO) (2a,2b), CpMo(NO) (3), Cp* W(NO) (4a,4b), Ca2Mo (6b), Cp2W (7a)] and trinuclear 1,1' - ferrocene dichalcogenato complexes Fe(C5H4E)(2)[MLn](2)[MLn = Cp* Cr(NO)(2), E = S(8a), Se(8b)] were synthesized and characterized by their IR, H-1 MMR and EI - MS spectra as well as their elemental analyses.