Catalysis Letters - A new zirconium based carbonaceous solid acid catalyst Zr@CC-PA with both Lewis and Bronsted acidic sites was prepared by simultaneous carbonization and phosphonation of glucose... 相似文献
Fresh niobium hydroxide was first precipitated from NbF5 solution using an aqueous ammonium hydroxide under basic conditions. Then a simple procedure of mixing lithium and niobium hydroxides together and heating at a low temperature (400 °C) produced pure ultrafine single phase LiNbO3 (LN). In the literature, this is the lowest temperature so far reported on the formation of LN. The phase content and lattice parameters are determined by X-ray diffraction (XRD). The average particle size and morphology were studied by transmission electron microscopy (TEM). 相似文献
The samples of the series Co1+ySnyFe2- 2y- xCrxO4 ferrites with x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5 and y = 0.05, were prepared by the usual double sintering ceramic technique. The single- phase spinel structure of the samples was confirmed by using X- ray diffractometry technique. The lattice parameter ’a’ with an accuracy of ± 0.002 Å were determined using Bragg peaks of XRD pattern. The lattice parameter ’a’ decreases with concentration, x, which is due to the difference in the ionic radii of Cr3+ and Fe3+ ions. The X- ray intensity calculations were carried out in order to determine the possible cation distribution amongst tetrahedral (A) and octahedral [B] sites. The X- ray intensity calculations show Cr3+ ions occupying B site. The saturation magnetization, σs, and magneton number, nB (the saturation magnetization per formula unit), measured at 300 K determined from high field hysteresis loop technique decrease with increase in concentration, x, suggesting a decrease in ferrimagnetic behaviour. Thermal variation of low field a.c. susceptibility measurements from room temperature to about 800 K exhibits almost normal ferrimagnetic behaviour and the Curie temperature, TC determined from a.c. susceptibility data decreases with increase in x.
Cyclic urea SD146, a potent HIV protease inhibitor bearing a flat resistance profile, possessed poor solubility and bioavailability, which precluded further development of the compound. In an effort to improve upon the pharmacokinetic profile of the compound, several analogs modified at the P1/P1' residues were prepared and evaluated. Several of those compounds displayed significant improvement of physical properties. 相似文献
There is an extensive possibility of improving characteristics of fibers used in hard tissue engineering, being hydrophobic and less osteoconductive, resulting in the dynamic growth of new tissues. The current work focuses on the fabrication of nanofibers incorporated with titanium dioxide (TiO2) ''as osteoconductive'' and silver (Ag) ''as self-healing'' nanoparticles (NPs). The incorporation of AgNO3 by in situ method not only helped to impart the antibacterial activity but also changed the contact angle from 81 ± 03° in the case of pristine nanofibers to 74 ± 03°, 61 ± 03°, 50 ± 08°, and 39 ± 1.1°, in the composite scaffolds containing 0.01, 0.03, 0.05, and 0.07 M of Ag salts. The incubation in simulated body fluid at 37°C to induce mineralization on nanofiber scaffolds indicated Ca and P crystals' formation. The antibacterial activity showed significantly more toxicity toward E. coli (8.3 ± 0.9 mm) than S. aureus (1.2 ± 0.1 mm). Biocompatibility studies using MTT assay on the pre-osteoblasts showed that both TiO2 and Ag NPs present in the nanofibers are non-toxic to the bone-like cells. However, results show that a higher concentration of Ag NPs (i.e., 0.07 M) is toxic to cells growing. Finally, all the results suggest that the nanofiber scaffolds have considerable scope for future bone tissue engineering materials. 相似文献
In this report, we studied various structural and optical properties of pure and copper-doped cadmium oxide (CdO) thin films. Nanostructured Cu-doped CdO films were deposited using sol–gel spin-coating technique. The structural and morphological changes have been observed by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and atomic force microscopy (AFM) studies. The optical and electrical properties of the pure and Cu-doped CdO thin films were studied by UV–vis spectroscopy and four-point probe method, respectively. The XRD peaks show the formation of nanocrystalline CdO with cubic face-centered crystal structure. The band gaps of the as deposited films were found in the range of 2.32–2.73 eV, while after doping, it decreases due to structural deformation. The electrical resitivity was found to decrease approximately ~10 in Cu-doped CdO thin films. 相似文献
The present study reports a novel, facile, biosynthesis route for the synthesis of carbon nanodots (CDs) with an approximate quantum yield of 38.5%, using Musk melon extract as a naturally derived‐precursor material. The synthesis of CDs was established by using ultraviolet–visible (UV–vis) spectroscopy, Dynamic light scattering, photoluminescence spectroscopy, X‐ray diffraction, transmission electron microscopy and Fourier transform infrared (FTIR) spectroscopy. The as‐prepared CDs possess an eminent fluorescence under UV–light (λex = 365 nm). The size range of CDs was found to be in the range of 5–10 nm. The authors further explored the use of such biosynthesised CDs as a photocatalyst material for removal of industrial dye. Degradation of methylene blue dye was performed in a photocatalytic reactor and monitored using UV–vis spectroscopy. The CDs show excellent dye degradation capability of 37.08% in 60 min and reaction rate of 0.0032 min−1. This study shows that synthesised CDs are highly stable in nature, and possess potential application in wastewater treatment.Inspec keywords: carbon, nanostructured materials, nanofabrication, catalysis, photochemistry, ultraviolet spectra, visible spectra, photoluminescence, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectra, fluorescence, dyesOther keywords: green synthesis, highly stable CD, photocatalytic performance, biosynthesis route, carbon nanodots, quantum yield, Musk melon extract, naturally derived‐precursor material, ultraviolet‐visible spectroscopy, dynamic light scattering, photoluminescence spectroscopy, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, FTIR spectroscopy, fluorescence, biosynthesised CD, photocatalyst material, industrial dye, methylene blue dye degradation, photocatalytic reactor, UV‐vis spectroscopy, wastewater treatment, size 5 nm to 10 nm, time 60 min相似文献
Conventional gait recognition schemes has poor recognition accuracies in presence of covariates. It is mainly due to ineffective and inefficient representation and discriminative feature extraction schemes. The paper presents new technique to extract discriminative features from masked gait energy image based on curvelet transform and PCANet. The binary gait silhouette video sequence obtained from pre-processing of video sequence is converted in to masked gait energy image and then direction and edge representation ability of fast discrete curvelet transform is employed. Nonlinear and non invertible, image space to feature space mapping scheme of PCANet is used to extract discriminative robust features. The suitability and effectiveness of newly proposed scheme is demonstrated by experimentation on standard publicly available benchmark USF HumanID database. 相似文献
We present a haptic telerehabilitation framework for patients with upper-limb dysfunction that is well-suited for deployment in patients' homes. Specifically, a commercial-off-the-shelf (COTS) haptic force-feedback driving wheel interfaces with a PC to create a haptic Virtual Driving Environment (hVDE). Coupling this framework with parametric exercise/ movement protocols-structured as driving exercises along paths of varying complexity-is the key to the creation of an inexpensive, immersive, and yet individualized personal-movement trainer. 相似文献
ABSTRACTA simple, rapid and accurate reverse phase high-performance liquid chromatographic (RP-HPLC) method was developed for the quantitative determination of cilostazol. The developed method is also applicable for the related substance determination in bulk drugs. The chromatographic separation was achieved on reversed-phase C-18 column. Eluents were monitored on photo-diode array detector at a wavelength of 210 nm using a mixture (50:50) of water and acetonitrile. Solution concentrations were quantified by external calibration. In the developed HPLC method, resolution between cilostazol and its potential impurities, namely Imp-A, Imp-B, and Imp-C were found greater than two. The drug was subjected to stress condition of hydrolysis, oxidation, photolysis and thermal degradation. Considerable degradation was found to occur in alkaline medium stress condition. The developed RP-HPLC method was validated with respect to linearity, accuracy, precision, stability of analytical solutions, and robustness. 相似文献