Comparison of photonic crystal narrow filters with metamaterials and dielectric defects

The photonic band-gap of the two kinds of 1D photonic crystal structure which is composed of the form of (AB) ^N1 C ^m (BA) ^N2 , one with a metamaterial defect layer (MDL) and the other one with a dielectric defect layer (DDL) are studied. Our results show that in both cases, where there is only one defect layer, m=1, no defect mode exists, but for two defect layers (m=2) there is a single defect mode which is centered in the middle of the band-gap. The width of the defect mode in DDL is narrower than that in MDL. For a number of defects of more than two (m>2) and even, in both of the MDL and DDL structures, there is only one defect mode. For m>2 and odd, the defect mode in the MDL vanishes, but for DDL there is two defect-mode symmetrically centered in the middle of the band-gap. The effects of the defect layers refractive index value, the periodicity number of the structures and the incident angle on the properties of the defect modes and the transmittance spectrum are discussed.     

Exact electrostatic solitons in a magnetoplasma with degenerate electrons

Fully nonlinear planar ion-acoustic solitary waves (IASWs) moving obliquely to an external magnetic field are studied in a collisionless magnetoplasma with degenerate electrons. The features of the nonlinear IASWs are investigated through the derivation of an energy balance-like equation involving the Sagdeev-type potential as well as the nonlinear dispersion relation.     

Electrospun Nylon-66/5-(4-dimethylaminobenzyliden) rhodanine composite nanofibres for solid phase extraction of palladium ions from wastewater samples

In the present work, a simple procedure is presented for the extraction and determination of pre-concentrated trace amounts of palladium ions through solid phase extraction (SPE) and flame atomic absorption spectrophotometry. This process was performed using Nylon-66/5-(4-dimethylaminobenzylidene) rhodanine composite nanofibres. These nanofibres were produced under optimised conditions via two-axial electrospinning technique and characterised by scanning electron microscopy and Fourier-transform infrared spectroscopy. The effect of experimental parameters including solution pH, the type and volume of eluent and contact time was investigated in extraction and desorption process. Under the optimised conditions, good linearity in the range of 0.07–8 μg L^?1 and low detection limit of 0.015 μg L^?1 were obtained. High enrichment factor of 187.5 and good relative standard deviation of ±2.2% at 5 μg L^?1 of palladium had been achieved. The sorbent capacity for palladium adsorption was obtained 27 mg palladium per gram of nanofibres. So, the SPE was successfully applied to pre-concentrate and determine Pd(II) ions with flame atomic absorption spectrophotometer in real samples.     

Poly (3-aminobenzoic acid) @ MWCNTs hybrid conducting nanocomposite: preparation,characterization, and application as a coating for copper corrosion protection

Nowadays, corrosion is a widely observed phenomenon in metal and one of the most important reasons of degradation in industrial parts. As a result, developing and applying the methods to reduce corrosion costs in industry is essential. In this research, emulsion polymerization route was used to prepare poly (3-aminobenzoic acid) @ multi-walled carbon nanotubes (P3ABA@MWCNTs) hybrid conducting nanocomposite film. Different techniques like Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermal gravimetric analysis (TGA) were used to evaluate structure and morphology of resultant materials. P3ABA@MWCNTs hybrid conducting nanocomposite demonstrated an improvement in the crystallinity as well as thermal stability. In this literature for the first time, P3ABA and P3ABA@MWCNTs hybrid conducting nanocomposite films were used as a coating for corrosion protection of copper metal. The corrosion inhibition applicability of the P3ABA and P3ABA@MWCNTs hybrid conducting nanocomposite films on copper immersed in salt solution (3.5 wt.%) was investigated by potentiodynamic polarization, electrochemical impedance spectroscopic (EIS), and open circuit potential (OCP) measurements. The results showed that the presence of MWCNTs in P3ABA matrix considerably improved the corrosion inhibition efficiency of copper metal where corrosion potential (E_corr) and corrosion current density (I_corr) were ?103 mV and 0.562 μA cm^?2, respectively. The good anti-corrosion activity of P3ABA@MWCNTs hybrid nanocomposite was most likely due to physical barrier effect, and anodic protection performance of P3ABA together enhances the overall compactness of the MWCNTs.     

Fe3O4@SiO2@ADMPT/H6P2W18O62: a novel Wells–Dawson heteropolyacid-based magnetic inorganic–organic nanohybrid material as potent Lewis acid catalyst for the efficient synthesis of 1,4-dihydopyridines

A novel Wells–Dawson heteropolyacid-based magnetic Inorganic–organic nanohybrid, Fe₃O₄@SiO₂@ADMPT/H₆P₂W₁₈O₆₂, was fabricated and used as a green, efficient, eco-friendly, and highly recyclable catalyst for the one-pot and multi-component synthesis of 1,4-Dihydopyridine (1,4-DHP) derivatives from the reaction of various aromatic aldehydes with ethyl acetoacetate and ammonium acetate with good to excellent yields and in a short span of time. The nanohybrid catalyst was prepared by the chemical anchoring of Wells–Dawson heteropolyacid H₆P₂W₁₈O₆₂ onto the surface of functionalized Fe₃O₄ nanoparticles with 2,4-bis(3,5-dimethylpyrazol)-triazine (ADMPT) linker. These nanocatalysts were identified by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), infrared spectroscopy (IR) and vibrating sample magnetometer (VSM). This protocol is developed as a safe, cost-effective and convenient alternate method for the synthesis of 1,4-DHP derivatives utilizing an eco-friendly, and a highly reusable catalyst.     

Zirconium borohydride piperazine complex, an efficient, air and thermally stable reducing agent

A zirconium borohydride piperazine complex (Ppyz)Zr(BH₄)₂Cl₂, obtained by the reaction of an ethereal solution of ZrCl₄ and LiBH₄ with piperazine is a stable, selective and efficient reducing agent. (Ppyz)Zr(BH₄)₂Cl₂ reduces aldehydes, ketones, silylethers, α,β-unsaturated carbonyl compounds and esters. The reactions were performed in diethyl ether at room temperature or under reflux, and the yields of the corresponding alcohols were excellent. The selective reduction of aldehydes in the presence of ketones and complete regioselectivity in the reduction of α,β-unsaturated carbonyl groups were observed.     

Determination of Buprenorphine (BUP) with Molecularly Imprinted Polymer Zn/La3+ Metal Organic Framework on Modified Glassy Carbon Electrode (GCE)

In this study we report the Zn/La³⁺ metal organic frameworks (MOFs) were synthesized with the co-precipitation assisted microwave method. Zn/La³⁺ MOFs were used as a new nanocomposite for the design and construction of a nanosensor based on glassy carbon electrode (GCE). MOFs due to their unique and excellent physicochemical properties can be used in sensors based on glassy carbon electrode (GCE). The synergistic effect of MOFs on glassy carbon electrode increases the power of the limits of detection (LOD). In this study, a new chemical sensor was fabricated by electro polymerization to measure buprenorphine with MOFs based on molecularly imprinted polymer. Zn/La³⁺ MOFs nanostructures were identified with scanning electron microscopy (SEM), Dynamic light scattering (DLS), Transmission electron microscopy (TEM) and the Fourier-transform infrared spectroscopy (FT-IR) spectra. Buprenorphine was used as a template, pyrrole was used as a monomer, potassium ferrocyanide as an electrochemical active tracer in electropolymerization processes and the parameters affecting the sensor response were optimized. At the Zn/La³⁺ MOF/MIP electrode, the calibration curve in the linear region was obtained in the concentration range between 4 to 50 ng/ml and the detection limit was 1.08 ng/ml. In a new strategy, Zn/La³⁺ MOFs nanostructures can be introduced as new materials with high efficiency which used at chemical sensors for detection of the opiates in all over the world.     

Ionene-Bound Borohydrides: Efficient, Selective, and Versatile Polymer-Supported Reducing Agents

Summary. Reduction of structurally different carbonyl compounds, such as aldehydes, ketones, α,β-unsaturated enals and enones, acid chlorides, and imines was accomplished efficiently using high capacity ionene based borohydride reagents. Aldehydes and imines were reduced to the corresponding alcohols and amines in excellent yields in methanol at ambient temperature while ketones and acid chlorides were reduced in iso-propanol and THF-MeOH at reflux. Chemoselective reduction of aldehydes over ketones was achieved successfully with these reagents. Complete regioselectivity was also observed in the reduction of α,β-unsaturated aldehydes and ketones.     

银纳米颗粒的合成及用于抗癌药氟他胺的电化学检测（英文）

Ag nanoparticles were synthesized on the surface of a glassy carbon electrode modified with p‐tert‐butylcalix[4]arene and p‐tert‐butylcalix[6]arene by the deposition of Ag+ at an open circuit potential followed by the electrochemical reduction of the Ag+.The presence of the calixarene layer on the electrode surface controlled the particle size and prevented agglomeration.Cyclic voltam‐metry showed that the Ag nanoparticles on the modified glassy carbon electrode had good catalytic ability for the reduction of flutamide.The effects of calixarene concentration,potential applied for the reduction of Ag+,number of calixarene layers,and p H value on the electrocatalytic activity of the Ag nanoparticles were investigated.The modified electrode had a linear range in differential pulse voltammetry of 10-1000 μmol/L with a detection limit of 9.33 μmol/L for flutamide at an S/N = 3.The method was applied to the detection of flutamide in practical samples.     

Efficient removal of heavy metal ions using hydrophilic thiacalix[4]arene doped polyaniline prepared by emulsion polymerization: conductivity,isotherm and kinetic study

The adsorption capacity of conductive polyaniline doped by thiacalix[4]arene tetrasulfonate (PANI–TCAS) towards Cu(II), Cd(II), Co(II) and Cr(III) was investigated through batch adsorption techniques, and the extent of adsorption was measured as a function of pH, initial metal ion concentration and contact time. It was found that the metal ion removal reached maximum at pH 8.0 and remained constant after 60 min. Experimental data was fitted to Langmuir, Freundlich, Redlich–Peterson and Temkin equation models with the maximum adsorption capacity calculated to be 833.3, 555.5, 526.3 and 500 for Cr³⁺, Cu²⁺, Co²⁺ and Cd²⁺, respectively, from the Langmuir isotherm model. The kinetic study was carried out through pseudo‐first‐order, pseudo‐second‐order, Elovich kinetic and intraparticle diffusion models in which the related correlation coefficient for each kinetic model showed that the pseudo‐second‐order rate equation was better described by the adsorption process. XRD spectra, SEM and TEM images of the adsorbent revealed a homogeneous distribution of nano‐sized particle structure with a porous surface, the morphology of which brings about high adsorption capacity for the PANI–TCAS molecular nanocomposite which in turn was observed by the AFM micrograph. The conductivity of thiacalix[4]arene tetrasulfonate doped polyaniline after metal ion adsorption was also assessed, and the four‐probe measurement technique revealed conductivity increment as high as 102.4 S cm^?1 with a 100 order of magnitude enhancement. Copyright © 2015 John Wiley & Sons, Ltd.