928 resultados para potassium fertilizing


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研究结果表明不同坡度谷子地 ,高 N处理小区径流中铵态氮、硝态氮和有效氮浓度平均为 1.0 6、0 .76和1.82 mg/kg,低 N分别为 0 .6 4、1.2 9和 1.93mg/kg;高氮处理土壤铵态氮、硝态氮和有效氮平均流失量分别达到17.90、12 .93和 30 .84kg/(km2 · a) ,低 N流失量为 11.90、2 3.86和 35 .77kg/(km2 · a)。高氮处理小区泥沙中有机质和全氮浓度平均为 5 .2 1和 0 .5 36 g/kg,而低氮处理分别为 4.94和 0 .481g/kg;高氮和低氮处理土壤有机质流失量分别为 5 70 2和 5 743kg/(km2 · a) ,土壤全氮流失量为 498和 5 5 9kg/(km2 · a)

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通过大田试验 ,研究了不同供钾方式对烟叶含钾量的影响及提高石灰性土壤上烤烟含钾量的可能途径。结果表明 ,施钾能显著提高烟叶产量 ,其中以粉肥结合喷优丰处理效果最好。在干旱条件下 ,增施钾肥可以显著提高烟叶含钾量 ,尤其能较大幅度提高中上部烟叶含钾量。粉肥对提高烟叶含钾量的效果稍优于粒肥。采用喷施“优丰 98- 2”进行根外补钾 ,可显著提高烟叶含钾量。在石灰性土壤上 ,干旱是提高烟叶含钾量的障碍因子。仅凭土壤施钾来提高烟叶含钾量 ,效果不稳定 ,受气候影响较大。土施结合喷施叶肥 ,是提高该区烤烟烟叶含钾量的有效途径。

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根据黄土高原因水肥不协调而形成大面积低效林的问题 ,以水肥耦合为中心 ,以 1龄杨树幼苗为研究对象 ,采用三因子五水平正交旋转组合回归设计方法 ,利用盆栽试验和定量分析的手段 ,研究探讨了不同水肥条件下 ,水、N、P三因子对杨树生物量的影响 ,结果表明三因素对杨树生物量存在着耦合交互效应 ,不同的水、N、P配合有不同的生物量积累 .因此 ,合理施肥、量水配肥是改善黄土高原因水肥不协调而形成大面积低效林的有效途径

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应用时空互代方法,以柠条林为例,对黄土丘陵沟壑区不同利用年限人工林土壤养分特征、空间变异及其演变进行了系统的研究。结果表明,该区人工林土壤肥力处于较低水平;人工林表层土壤养分中速效磷和速效钾的空间变异性较大;各环境因子对土壤养分有一定的影响,海拔、坡度和坡向等环境因子与人工林地土壤养分间呈负相关关系,坡位和地形与人工林地土壤养分间呈正相关关系。随着利用年限的增加,人工林土壤养分各指标含量均增加,与利用年限有显著的相关性。有机质、全氮、有效氮和速效磷的增加量不明显,全磷含量保持相对稳定的水平,速效钾经过多年积累有明显的增加。从土壤养分指数模型可以算出该区的人工林土壤有机质、全氮、有效氮约需35a能达到中上等养分水平,速效钾则约需27a才能达到中上等养分水平。

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In this paper, marine brown algae Laminaria japonica was chemically modified by crosslinking with epichlorohydrin (EC1 and EC2), or oxidizing by potassium permanganate (PC), or crosslinking with glutaraldehyde (GA), or only washed by distilled water (DW). They were used for equilibrium sorption uptake studies with Cd2+, Cu2+, Ni2+ and Zn2+.

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An industrial waterproof reagent [(potassium methyl siliconate) (PMS)] was used for fabricating a superhydrophobic surface on a cellulose-based material (cotton fabric or paper) through a solution-immersion method. This method involves a hydrogen bond assembly and a polycondensation process. The silanol, which was formed by a reaction of PMS aqueous solution with CO2, Was assembled on the cellulose molecule surface via hydrogen bond interactions. The polymethylsilsesquioxane coatings were prepared by a polycondensation reaction of the hydroxyl between cellulose and silatiol. The superhydrophobic cellulose materials were characterized by FTIR spectroscopy, thermogravimetry, and surface analysis (XPS, FESEM, AFM, and contact angle measurements).

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Weak epitaxy growth (WEG) can afford high-mobility thin films of disk-like organic semiconductor of which mobility is up to the level of the corresponding single crystals. We investigated the WEG behavior and mechanism of planar phthalocyanine in the model system of metal-free phthalocyanine (H2Pc) grown on p-sexiphenyl (p-6P) ultrathin films (monolayers and double layers). Highly oriented H2Pc films with molecules standing up exhibited two kinds of different in-plane orientations, i.e., three sets of in-plane orientations and only one set of in-plane orientation, on p-6P monolayer and double-layer films, respectively.

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Monodispersed KY3F10:Eu3+ nanospheres with bimodal size distribution have been successfully synthesized via a facile and efficient sonochemical method in a surfactant-free system. Rare-earth nitrate (Y, Eu)(NO3)(3) and potassium fluoborate (KBF4) were used as precursors. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and photoluminescence (PL) spectra were used to characterize the samples.

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The fabrication of organic semiconductor thin films is extremely important in organic electronic devices. This tutorial review-which should particularly appeal to chemists and physicists interested in organic thin-film growth, organic electronic devices and organic semiconductor materials-summarizes the method of weak epitaxy growth (WEG) and its application in the fabrication of high quality organic semiconductor thin films.

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Weak epitaxy growth (WEG) behavior and mechanism of copper hexadecafluorophthalocyanine (F16CuPc) on p-sexiphenyl (p-6P) monolayer film were investigated by atomic force microscopy (AFM), selected area electron diffraction (SEAD), and wide-angle X-ray diffraction (WAXD). High-quality F16CuPc films with high order, large size, and molecular-level smoothness were obtained successfully by WEG method. It was identified that there exists incommensurate epitaxial relation between highly oriented F16CuPc and p-6P films. The geometrical channels of p-6P monolayer surface induce the nucleation and growth of F16CuPc molecules.

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In this paper, marine brown algae Laminaria japonica was chemically modified by crosslinking with epichlorohydrin (EC1 and EC2), or oxidizing by potassium permanganate (PC), or crosslinking with glutaraldehyde (GA), or only washed by distilled water (DW). They were used for equilibrium sorption uptake studies with Cd2+, Cu2+, Ni2+ and Zn2+. The experimental data have been analyzed using Langmuir, Freundlich and Redlich-Peterson isotherms. The results showed that the biosorption equilibrium was well described by both the Langmuir and Redlich-Peterson isotherms.

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In this paper, the characterization and application of a chemically reduced graphene oxide modified glassy carbon (CR-GO/GC) electrode, a novel electrode system, for the preparation of electrochemical sensing and biosensing platform are proposed. Different kinds of important inorganic and organic electroactive compounds (i.e., probe molecule (potassium ferricyanide), free bases of DNA (guanine (G), adenine (A), thymine (T), and cytosine (C)), oxidase/dehydrogenase-related molecules (hydrogen peroxide (H2O2/beta-nicotinamide adenine dinucleotide (NADH)), neurotransmitters (dopamine (DA)), and other biological molecules (ascorbic acid (AA), uric acid (UA), and acetaminophen (APAP)) were employed to study their electrochemical responses at the CR-GO/GC electrode, which shows more favorable electron transfer kinetics than graphite modified glassy carbon (graphite/GC) and glassy carbon (GC) electrodes.

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A facile and practical one-pot synthesis of beta-oxo thioamides from beta-oxo amides has been developed. By treatment with isothiocyanates in ethanol in the presence of potassium carbonate, a series of beta-oxo amides was converted, under reflux, in high yields into the corresponding beta-oxo thioamides.

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We have developed a simple, efficient, economical, and general approach to construct diverse multifunctional Fe3O4/metal hybrid nanostructures displaying magnetization using 3-aminopropyltrimethoxysilane (APTMS) as a linker. High-density Au nanoparticles (NPs) could be supported on the surface of superparamagnetic Fe3O4 spheres and used as seeds to construct Au shell-coated magnetic spheres displaying near-infrared (NIR) absorption., which may make them promising in biosensor and biomedicine applications. High-density flower-like Au/Pt hybrid NPs could be supported on the surface of Fe3O4 spheres to construct multifunctional hybrid spheres with high catalytic activity towards the electron-transfer reaction between potassium ferricyanide and sodium thiosulfate. High-density Ag or Au/Ag core/shell NPs could also be supported on the surface of Fe3O4 spheres and exhibited pronounced surface-enhanced Raman scattering (SERS), which may possibly be used as an optical probe with magnetic function for application in high-sensitivity bioassays.

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Four individual quadruplexes, which are self-assembled in ammonium acetate solution from telomeric sequences of closely related DNA strands - d(G(4)T(4)G(4)), d(G(3)T(4)G(4)), d(G(3)T(4)G(3)), and d(G(4)T(4)G(3)) - have been detected in the gas phase using electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS). The bimolecular quadruplexes associate with the same number of NH4+ in the gas phase as NMR shows that they do in solution. The quadruplex structures formed in solution are maintained in the gas phase. Furthermore, the mass spectra show that the bimolecular quadruplexes generated by the strands d(G(3)T(4)G(3)) and d(G(4)T(4)G(3)) are unstable, being converted into trimolecular and tetramolecular structures with increasing concentrations of NH4+ in the solution. Circular dichroism (CD) spectra reveal structural changes during the process of strand stoichiometric transitions, in which the relative orientation of strands in the quadruplexes changes from an antiparallel to a parallel arrangement. Such changes were observed for the strand d(G(4)T(4)G(3)), but not for the strand d(G(3)T(4)G(3)). The present work provides a significant insight into the formation of various DNA quadruplexes, especially the higher-order species.