This article reports an easy chemical method of synthesizing boehmite nanofibers by a modified sol-gel process involving aluminum isopropoxide precursor. Nanorods of gamma-alumina have been successfully prepared after dehydration of the viscous sol at 600 degrees C for 4 h in air. The boehmite nanofibers and gamma-alumina nanorods were characterized by X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy for surface chemistry and functional groups, scanning electron microscopy, high-resolution transmission electron microscopy with selected area electron diffraction, and energy-dispersed spectroscopy for morphology and structure identification. The length of the boehmite nanofibers was found to be more than 10 mum with a crystalline lattice structure. The mechanism of formation of the boehmite nanofibers included the preferential growth along the longitudinal axis due to interaction between the solvent molecules and the surface OH- groups of hydrogen bonds. It is also suggested that the boehmite nanofibers may have formed due to the inherent instability of the planar structure of the boehmite lattice. The diameter of the gamma-alumina nanorods was found to be less than 10 nm with a varying length in the range of 50-200 nm. Boehmite to gamma-Al2O3 transformation was attributed to the loss of water molecules by internal condensation of protons and hydroxyl ions. 相似文献
For the ferrites NixCd1–xFe2O4 (x=0.3, 0.4,1) the lattice parameter, grain size, electrical resistivity, initial permeability, Curie temperature and squareness of the magnetization curve were measured. The results are discussed in terms of the model of the canted spin structure taking into account the domain structure of the polycrystalline ferrite. 相似文献
Domestic fund transfers are all the time immediate, handier and obtainable however in overseas fund transfer, funds are transferred from payers account to payees account through the correspondent banks, central bank and messaging network which involves intermediaries and allied charges. Blockchain Technology has grabbed the interest of financial systems due to its inventive benefits such as decentralised structure, faster speed, cost-effectiveness and more security over conventional approaches. Adopting Blockchain Technology for overseas fund transfer can overcome the transaction delays, intermediaries’ failures and recurring costs involved in the current system. In this paper, a Consortium Blockchain based overseas fund transfer process is proposed to achieve faster operations, security and transparency. Hyperledger Fabric Blockchain framework has been used for overseas fund transfer process and web-user interface is developed for the same. Simulation results demonstrate the significance of Blockchain as a promising technology for overseas fund transfer process to facilitate speed, security, transparency and efficiency for overseas fund transfer.
Summary A simple and rapid method is described for synergetic extraction and spectrophotometric determination of iron(II). The Fe(II)--furildioxime-pyridine complex extracted into chloroform has a characteristic pink color measurable at 570 nm. Iron is also separated from associated elements and the results of the analysis of synthetic mixtures and standard steel samples are reported.
Zusammenfassung Eine einfache und rasche Methode zur Extraktion und Bestimmung von Eisen(II) wurde beschrieben. Der Komplex Fe(II)--Furildioxim-Pyridin wird mit Chloroform extrahiert. Seine charakteristische rosa Farbe ist bei 570 nm meßbar. Eisen läßt sich so auch von Begleitelementen trennen. Die Analysenergebnisse für synthetische Gemische und Standard-Stahlproben werden mitgeteilt.
A stereoselective conversion of the readily available (+)-car-3-ene into (+)-carvone by two different routes is described. This is the first report on synthesis of carvone from car-3-ene. 相似文献
A sensitive and reproducible method is described for the quantitative determination of metadoxine in the presence of its degradation products. The method was based on high performance liquid chromatographic separation of the drug from its degradation products on the reversed phase, kromasil column [C18 (5-micron, 25 cm × 4.6 mm, i.d.)] at ambient temperature using a mobile phase consisting of methanol and water (50: 50, v/v). Flow rate was 1.0 mL min?1 with an average operating pressure of 180 kg cm?2 and tR was found to be 2.85 ± 0.05 min. Quantitation was achieved with UV detection at 286 nm based on peak area with linear calibration curves at concentration range 10–100 μg mL?1. This method has been successively applied to pharmaceutical formulation. No chromatographic interference from the tablet excipients was found. The method was validated in terms of precision, robustness, recovery and limits of detection and quantitation. Drug was subjected to acid, alkali and neutral hydrolysis, oxidation, dry heat, wet heat treatment and photo and UV degradation. As the proposed method could effectively separate the drug from its degradation products, it can be employed as stability indicating one. Moreover, the proposed HPLC method was utilized to investigate the kinetics of the acidic, alkaline and oxidative degradation processes at different temperatures and their respective apparent pseudo first order rare constant, half-life and activation energy was calculated with the help of Arrhenius plot. In addition the pH-rate profile of degradation of metadoxine in constant ionic strength buffer solutions with in the pH range 2–11 was studied. 相似文献
Fine particle cobalt doped-Fe2O3 and Mn-Zn ferrites have been prepared by the thermal decomposition of N2H5CoxFe1–x(N2H3COO)3.H2O wherex=1–10 atom% and (N2H5)3MnxZn1–xFe2(N2H3COO)9· 3H2O wherex=0.2–0.8, respectively. Formation of these oxide materials has been confirmed by thermogravimetry and X-ray powder diffraction patterns. The fine particle nature of these oxide materials is evident from particle size analysis and surface area measurements.
Zusammenfassung Mit fein verteiltem Kobalt versetztes-Fe2O3 sowie Mn-Zn Ferrite wurden durch thermische Zersetzung von N2H5CoxFe1–x(N2H3COO)3·H2O mit jc=1–10 Atomprozent bzw. (N2H5)3MnxZn1–xFe2(N2H3COO)9·3H2O mitx=0,2–0,8 hergestellt. Die Bildung dieser Oxidstoffe wurde durch Thermogravimetrie und Pulverdiffraktionsmethoden bekräftigt. Die Feinkornstruktur dieser Oxidstoffe wird durch Korngrößenverteilungs- und Oberflächenmessungen augenscheinlich.
Tracer-diffusion of Zn2+ ions in the presence of CoSO4 is studied at 25°C in 1% agar gel over a concentration range of 10–5 to 0.25M using a zone-diffusion technique. The deviations observed between experimental and theoretical values of diffusion coefficients are explained by considering different types of interactions occurring in the ion-gel-water system. Further, study of the obstruction, effect in the diffusion of Zn2+ ions at different concentrations of CoSO4 reveals that the -value decreases with increasing concentration of the electrolyte. This observation is accounted on the basis of competitive hydration between ions and agar molecules. 相似文献