有机肥料中氮磷钾测定前处理方法改进研究

为提高有机肥料中氮、磷、钾的测定效率,对有机肥料前处理过程进行了改进,并与农业标准NY525-2012的分析结果进行了比较。结果表明,改进方法与NY525-2012分析结果无显著性差异,可以代替NY525-2012对有机肥料中氮、磷、钾测定时进行前处理。     

Surface structural and solar absorptance features of nitrate-based copper-cobalt oxides composite coatings: Experimental studies and molecular dynamic simulation

The copper and cobalt oxides composites coatings on aluminum substrates have been successfully synthesized via sol-gel method using nitrate-based sol precursors. The composites were characterized by X-ray Diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Field Emission Scanning Electron Microscopy (FESEM), Atomic Force Microscopy (AFM), and UV–Vis–NIR spectrophotometry. The sol-gel reactions were discussed and Molecular Dynamics (MD) simulation was integrated into the study to predict molecules assembly properties. The XRD analyses revealed that the CuO and the Co₃O₄ composites were formed after the annealing process with the average difference of the calculated lattice parameters compared to ICDDs was 1.17%. The surface electronic structure was mainly consisted of tetrahedral Cu(I), octahedral Cu(II), tetrahedral Co(II), octahedral Co(III) as well as surface, sub-surface and lattice oxygen O^?. The XRD, XPS and MD simulation results showed that there was minimal (or possibly non-existing) indication of copper-cobalt mixed phase oxides formations. FESEM and AFM surveys revealed that the coating had a porous surface composed of interlinked nanoparticles in the range of ~?10 to ~?40?nm. UV–Vis–NIR reflectance spectra showed that the sol precursors concentration and the dip-drying cycle significantly influenced the absorptance value with optimum absorptance (α) of 88.7% exhibited by coating synthesized using sol concentration of 0.1?M and 10 dip-drying cycles. High absorptance value and simplicity in the synthesis process render the coatings to be very promising candidates for solar selective absorber (SSA) applications.     

Two‐Dimensional Nanomaterials for Biomedical Applications: Emerging Trends and Future Prospects

Two‐dimensional (2D) nanomaterials are ultrathin nanomaterials with a high degree of anisotropy and chemical functionality. Research on 2D nanomaterials is still in its infancy, with the majority of research focusing on elucidating unique material characteristics and few reports focusing on biomedical applications of 2D nanomaterials. Nevertheless, recent rapid advances in 2D nanomaterials have raised important and exciting questions about their interactions with biological moieties. 2D nanoparticles such as carbon‐based 2D materials, silicate clays, transition metal dichalcogenides (TMDs), and transition metal oxides (TMOs) provide enhanced physical, chemical, and biological functionality owing to their uniform shapes, high surface‐to‐volume ratios, and surface charge. Here, we focus on state‐of‐the‐art biomedical applications of 2D nanomaterials as well as recent developments that are shaping this emerging field. Specifically, we describe the unique characteristics that make 2D nanoparticles so valuable, as well as the biocompatibility framework that has been investigated so far. Finally, to both capture the growing trend of 2D nanomaterials for biomedical applications and to identify promising new research directions, we provide a critical evaluation of potential applications of recently developed 2D nanomaterials.     

Sol-gel processed high-k aluminum oxide dielectric films for fully solution-processed low-voltage thin-film transistors

High-k oxide dielectric films have attracted intense interest for thin-film transistors (TFTs). However, high-quality oxide dielectrics were traditionally prepared by vacuum routes. Here, amorphous high-k alumina (Al₂O₃) thin films were prepared by the simple sol-gel spin-coating and post-annealing process. The microstructure and dielectric properties of Al₂O₃ dielectric films were systematically investigated. All the Al₂O₃ thin films annealed at 300–600?°C are in amorphous state with ultrasmooth surface (RMS ~ 0.2?nm) and high transparency (above 95%) in the visible range. The leakage current of Al₂O₃ films gradually decreases with the increase of annealing temperature. Al₂O₃ thin films annealed at 600?°C showed the low leakage current density down to 3.9?×?10^?7 A/cm² at 3?MV/cm. With the increase of annealing temperature, the capacitance first decreases then increases to 101.1?nF/cm² (at 600?°C). The obtained k values of Al₂O₃ films are up to 8.2. The achieved dielectric properties of Al₂O₃ thin films are highly comparable with that by vapor and solution methods. Moreover, the fully solution-processed InZnO TFTs with Al₂O₃ dielectric layer exhibit high mobility of 7.23?cm² V^?1 s^?1 at the low operating voltage of 3?V, which is much superior to that on SiO₂ dielectrics with mobility of 1.22?cm²/V^?1 s^?1 at the operating voltage of 40?V. These results demonstrate that solution-processed Al₂O₃ thin films are promising for low-power and high-performance oxide devices.     

Preparation of nanocrystalline nickel oxide from nickel hydroxide using spark plasma sintering and inverse Hall-Petch related densification

Nanocrystalline nickel oxide (NiO) was prepared from nickel hydroxide by Spark plasma sintering (SPS) and the mechanisms involved in the densification of NiO were studied. Reverse precipitated nickel hydroxide powders were SPS processed at 400, 600 and 700?°C with 70?MPa pressure. Pure NiO with 12?nm crystallite size formed after 400?°C sintering process. However NiO grains had grown to 18 and 38?nm after 600 and 700?°C sintering respectively. NiO pellets prepared using 600 and 700?°C SPS sintering schedules had relative densities of 83% and 94% respectively. Two displacement rate regimes were observed during densification of NiO in both 600 and 700?°C sintering processes. Decomposition of nickel hydroxide and particle sliding of NiO led to first displacement rate maximum while inverse Hall-Petch based plastic deformation facilitated densification during the constant second displacement rate regime. No densification occurred during sintering holding times indicating the limited role that diffusion played during densification.     

Relationships between ammonia volatilization and nitrogen fertilizer application rate,intake and excretion of herbage nitrogen by cattle on grazed swards

Grazed pastures emit ammonia (NH₃) into the atmosphere; the size of the NH₃ loss appears to be related to nitrogen (N) application rate.The micrometeorological mass balance method was used to measure NH₃ volatilization from rotationally grazed swards on three plots in the autumn of 1989 and throughout the 1990 growing season. The aim of the research was to derive a mathematical relationship between NH₃ volatilization and N application rate, which would vary between soil type and weather conditions. In both years the plots received a total of 250, 400 or 550 kg N ha^–1 as calcium ammonium nitrate (CAN) split over 6 to 8 dressings. The number of grazing cycles ranged from 7 to 9 for the three N plots.In the last two grazing cycles of 1989, NH₃ losses were 3.8, 12.0 and 14.7 kg N ha^–1 for the 250N, 400N and 550N plots, which was equivalent to 5.3%, 13.9% and 14.4% of the amount of N excreted on the sward, respectively. In 1990, NH₃ losses were 9.1, 27.0 and 32.8 kg N ha^–1 for the 250N, 400N and 550N plots, which was equivalent to 3.3%, 6.9% and 6.9% of the N excreted, respectively. Differences in urine composition between the plots were relatively small. Rainfall and sward management affected the size of the NH₃ volatilization rate. Volatilization of NH₃ was related to N excretion and N application rate.A calculation procedure is given to enable the estimation of NH₃ volatilization from N application rate. Adjustments can be made for grazing efficiency, grazing selectivity, N retention in milk and liveweight gain, concentrate N intake and milking duration. Losses of NH₃ increase progressively with an increase in N application rate until herbage yield reaches a maximum at an application rate of about 500 kg N ha^–1 yr^–1.     

Sol-gel processed highly (100)-textured (K,Na)NbO3-based lead-free thin films: Effect of pyrolysis temperature

Recently, lead-free piezoelectric thin films have received increasing attention due to the growing demands for mircoelectromechanical systems and the significant progress in lead-free piezoelectric research. Here, potassium sodium niobate [(K, Na)NbO₃ (KNN)]-based thin films were fabricated via a sol-gel method. The effects of pyrolysis temperature on the resulting microstructure and electrical properties of KNN-based films were investigated. The KNN-based film pyrolyzed at 550°C and annealed at 700°C shows a dominant (100) orientation with a high texturing degree of 91.7%. The microstructures, morphologies, piezo- and ferroelectric properties of the KNN-based films were discussed in association with different pyrolysis temperatures. The crystallization mechanism of the (100) textured KNN-based thin films was elaborated in detail.     

An Engineering Approach for Estimating the Formation of Nitric Oxide from Fuel‐Nitrogen

Explicit approximate equations for estimating the conversion factor of fuel‐nitrogen into nitric oxide are presented. They depend on the fuel‐nitrogen mole fraction, the initial nitric oxide mole fraction, and the kinetics‐equilibrium mole fraction of nitric oxide. This last parameter expresses a limiting value of fuel‐nitrogen conversion; it includes the complex nitrogen chemistry and depends thus on combustion conditions. Experimental results demonstrate that the kinetics‐equilibrium mole fraction for fuel‐lean and high‐temperature conditions can be well estimated by the chemical‐equilibrium mole fraction, but for lower temperatures the kinetics‐equilibrium mole fraction has to be described by other correlations.     

Study on thermolysis process of a new hydrated and protonated perovskite-like oxides H2K0.5Bi2.5Ti4O13·yH2O

A protonated form of the n?=?4 layered bismuth containing perovskite-like titanate K_2.5Bi_2.5Ti₄O₁₃ belonging to Ruddlesden-Popper phases was prepared via ion exchange reaction of interlayer K⁺ with protons. Its composition was investigated by TG ICP and EDX analysis was found to be H₂K_0.5Bi_2.5Ti₄O₁₃·H₂O. The thermal behavior of the obtained phase was investigated by STA coupled with mass-spectrometry, the structural changes, happening with the sample during heating, were examined by XRD. It was shown that the as-prepared hydrated phase undergoes two-stage dehydration at low temperatures (up to 160?°C). The further heating leads to the gradual decomposition and crystallization of new phases, notably Bi₂Ti₂O₇, Bi₄Ti₃O₁₂ and Bi₂Ti₄O₁₁. The morphology of the as-prepared sample and samples after heat treatment was examined using SEM.