2D assembly of gold-PNIPAM core-shell nanocrystals

2D arrays of Au-PNIPAM core-shell nanocrystals were fabricated using convective deposition and spin-coating. The particle density and ordering were studied by AFM. Annealing at 700 °C removes the polymer shell, while retaining a monolayer of well-separated gold nanoparticles. The surface plasmon modes of the colloid monolayers could be measured by spectroscopic ellipsometry.     

Fabrication of a magmolecule using nanoparticle and evaluation of its adsorption capacity for selenium ions from nuclear wastewater

The purpose of present study is to fabrication of a magmolecule (amino-functionalized magnetite nanoparticles) and evaluation of its adsorption capacity for selenite (SeO₃ ^2?) ions from nuclear wastewater. To accomplish this, synthesized magnetite nanoparticles is coated with a layer of SiO₂ in order to be chemically stable and then functionalized with 3-aminopropyl triethoxysilane (APTES) to be more effective. Adsorption of SeO₃ ^2? ions was investigated in batch technique. The effect of parameters such as solution pH, presence of competing anions using sulfuric acid and nitric acid (NO₃ ^?, HSO₄ ^? and SO₄ ^2?) and temperature were studied. Maximum adsorption occurred at pH 2.4 for magnetite (naked nanoparticle) and 1.7 for functionalized nanoparticles, while the dose of adsorbent was 1 g/L and selenite ion concentration was 50 mg/L. sulfuric acid was selected as the better acidic agent for controlling pH of solution. Thermodynamic parameters were also calculated and it has been found that the adsorption was endothermic. The obtained result showed that the naked particles had more adsorption capacity but it has been suggested usage of functionalized particles in the magmolecule process duo to stability and reusable capability.     

A Facile Synthesis of Stable Phosphorus Ylides Containing Chlorine and Sulfur Derived from 6-Chloro-2-benzoxazolethiol and 2-Chloro-phenothiazine

Stable crystalline phosphorus ylides containing chlorine and sulfur were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylene-dicarboxylates in the presence of 6-chloro-2-benzoxazolethiol and 2-chloro-phenothiazine. These stable ylides exist in solution as a mixture of two geometrical isomers. This is caused by the conjugation of the ylide moiety with the adjacent carbonyl group, which results in a restricted rotation around the respective carbon-carbon bond.     

Internal resonance in the higher-order modes of a MEMS beam: experiments and global analysis

This work investigates the dynamics of a microbeam-based MEMS device in the neighborhood of a 2:1 internal resonance between the third and fifth vibration modes. The saturation of the third mode and the concurrent activation of the fifth are observed. The main features are analyzed extensively, both experimentally and theoretically. We experimentally observe that the complexity induced by the 2:1 internal resonance covers a wide driving frequency range. Constantly comparing with the experimental data, the response is examined from a global perspective, by analyzing the attractor-basins scenario. This analysis is conducted both in the third-mode and in fifth-mode planes. We show several metamorphoses occurring as proceeding from the principal resonance to the 2:1 internal resonance, up to the final disappearance of the resonant and non-resonant attractors. The shape and wideness of all the basins are examined. Although they are progressively eroded, an appreciable region is detected where the compact cores of the attractors involved in the 2:1 internal resonance remain substantial, which allows effectively operating them under realistic conditions. The dynamical integrity of each resonant branch is discussed, especially as approaching the bifurcation points where the system becomes more vulnerable to the dynamic pull-in instability.

     

Investigating parameters on the preparation of mesoporous activated carbons by the combination of chemical and physical activations using the Taguchi method

Mesoporous activated carbons were prepared from coconut shell by the combination of chemical and physical activation methods. Zinc chloride and CO₂ were used as chemical and physical agents, respectively. Optimum parameters were obtained from investigating the effect of various factors at different levels on the methane storage of wet activated carbons using the Taguchi experimental design method. Soaking time, carbonization temperature, and carbonization time were found as effective parameters in the methane storage. Finally, after achieving optimum levels for each factors based on the enhancement of methane storage, a confirmation experiment was conducted. Methane uptakes of the activated carbons were measured at temperature of 2?^°C up to the pressure of 80 bar and it turned out that the maximum amount of methane storage (241?V/V) had a good agreement with the predicted result from the Taguchi method.     

Fe3O4@SiO2‐imid‐PMAn Magnetic Porous Nanosphere as Reusable Catalyst for Synthesis of Polysubstituted Quinolines under Solvent‐free Conditions

In this research, a facile one‐pot synthesis of poly‐substituted quinoline derivatives has been demonstrated by using 2‐aminobenzophenones and ethylacetoacetate or ketones in the presence of Fe₃O₄@SiO₂‐imid‐PMAⁿ and Fe₃O₄@SiO₂‐imid‐PMA^b nanoparticles as green and reusable catalysts under solvent‐free conditions. The reaction proceeds efficiently in excellent yields and in a state of excellent purity. The nanocatalysts can be recycled and reused for at least four times without noticeably decreasing in catalytic activity.     

Synthesis of Hollow SiO2 Nanoparticles from Dy2O3@SiO2 Core–Shell Nanocomposites via a Recyclable Sonochemical Method

Hollow silica nanoparticles were prepared from Dy₂O₃@SiO₂ core–shell nanocomposites, for the first time, by a simple ultrasonic assisted sol–gel method. The Dy₂O₃@SiO₂ core–shell nanocomposites were prepared by the deposition of a SiO₂ layer onto the surface of Dy₂O₃ nanoparticles using a three-step coating process. The hollow SiO₂ nanostructures were obtained by selective removal of the Dy₂O₃ cores. The structure, morphology and composition of the products were determined by the techniques of X-ray diffraction, Fourier transfom infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy. The results indicated that hollow SiO₂ nanostructures were sphere-like shape with the average size of 20?nm and had an amorphous crystal structure. The important advantage of this process is the recyclability of the Dy₂O₃ nanoparticles as the starting material of the reaction.     

Synthesis and structure revision of calyxin natural products

Tandem Prins cyclization and Friedel-Crafts reaction with an electron-rich aromatic ring were used to prepare the core structures of calyxin natural products. The proposed structure of epicalyxin F was prepared and shown to be incorrect. Several calyxin natural products, including calyxin F and L, were synthesized, and the structures were reassigned on the basis of NMR data and synthetic correlations.