Pristine and cadmium-doped zinc oxide: chemical synthesis and characterizations

The chemical synthesis of pristine and cadmium-doped ZnO powders using a simple, cost-effective at 65 °C is reported and characterized for their structures, optical and morphological studies using X-ray diffraction, UV–visible–Near Infra-Red (UV–Vis–NIR) spectroscopy, scanning electron microscopy measurement techniques where XRD spectra confirm the formation of ZnO and Cd-doped ZnO with hexagonal crystal structure. The particle size of ZnO is reduced on Cd-doping from 16 to 14 nm. Plane-view surface morphology analysis supported for spherical-type crystallites and UV–Vis–NIR spectra reveal shift in the band edge of ZnO after Cd-doping. Photo-degradation study of Methylene Blue dye shows Pristine ZnO degrades dye faster than Cd-doped ZnO.     

Design of fructose-2,6-bisphosphatase inhibitors: a novel virtual screening approach

Fructose-2,6-bisphosphatase (FBPase-2) is a switch between gluconeogenesis and glycolysis in the hepatic cells. The structural features required for inhibitory activity of FBPase-2 were unidentified; no leads are available for inhibiting this important enzyme. In this paper pharmacophore mapping, molecular docking methods were employed in a virtual screening strategy to identify leads for FBPase-2. A receptor based pharmacophore map was modeled which comprised of important interactions as observed in co-crystal of rat liver isozyme with the product inhibitor fructose-6-phosphate. The pharmacophore model was validated against two databases of best docked structural analogues of fructose-2,6-bisphosphate and fructose-6-phosphate. The query generated was submitted for flexible search of ligands in chemical databases, namely LeadQuest, Maybridge and NCI. The hits obtained were further screened by molecular docking using FlexX.     

Synthesis,solution properties and scale‐inhibiting behaviour of a diallylammonium/sulfur dioxide cyclocopolymer bearing phospho‐ and sulfopropyl pendents

Zwitterion (Z) monomer 3‐[diallyl{3‐(diethoxyphosphoryl)propyl}ammonio]propane‐1‐sulfonate underwent cyclocopolymerization with sulfur dioxide to give a new alternating copolymer poly(Z‐alt‐SO₂) in excellent yield (ca 90%). The polyzwitterion (±) (PZ) (i.e. poly(Z‐alt‐SO₂), bearing a diethylphosphonate as well as a sulfonate functionality in each repeat unit, upon ester hydrolysis gave its corresponding pH‐responsive polyzwitterionic acid (±) (PZA). The pH‐induced equilibrations (+) cationic polyelectrolyte ? (±) PZA ? polyzwitterion/anion (± ?) (PZAN) ? polyzwitterion/dianion (± =) (PZDAN) permitted us to examine the effects of charge types and their densities on the interesting solubility and viscosity behaviours. The apparent protonation constants of the basic functionalities &tbond;N^±PO₃^2? in (± =) PZDAN and &tbond;N^±PO₃H^1? in (± ?) PZAN in salt‐free water and 0.1 mol L^?1 NaCl were determined using potentiometric titrations. (±) PZA at a meagre concentration of 20 ppm was found to be an effective antiscalant to inhibit the precipitation of CaSO₄ from its supersaturated solution: after 500 and 800 min, the respective scale inhibitions of 86 and 98% indicated its potential use as an effective antiscalant in reverse osmosis plant. © 2014 Society of Chemical Industry     

Nanostructured MIEC Ba0.5Sr0.5Co0.6Fe0.4O3−δ (BSCF5564) cathode for IT-SOFC by nitric acid aided EDTA–citric acid complexing process (NECC)

Ba_0.5Sr_0.5Co_0.6Fe_0.4O_3−δ(BSCF5564) was synthesized by nitric acid aided EDTA–citric acid complexing sol-gel method (NECC). Both, the phase formation temperature and time of BSCF5564 synthesized NECC were found to be low i.e. single perovskite phase formation temperature is 200 °C less as compared to the conventional method of synthesis. The orthorhombic perovskite structure has been formed after calcination at 800 °C for 5 h. Scanning electron microscopy reveals the formation of porous material constituting nano-sized and irregularly shaped rod-like structure with particle size approximately ranges from 90 to 160 nm. The total weight loss of the BSCF5564 sample comes out to be 6.6%, indicating that quadrivalence state Co⁴⁺ and Fe⁴⁺ in the sample have been completely reduced to the trivalent state Co³⁺ and Fe³⁺ due to thermal analysis. The value of E_a for BSCF5564 prepared by NECC was 0.2288 eV. The electrical conductivity of BSCF5564 synthesized by NECC is observed to be steady at high temperature (above 700 °C).     

Thermally stable and durable superhydrophobic surfaces on stainless steel sheets with microholes via acid pretreatment and modification with self-assembled monolayers

Microfluidics and Nanofluidics - Single-cell nucleic acid analysis aims at discovering the genetic differences between individual cells which is well known as the cellular heterogeneity. This...     

Effect of cooling methods on residual compressive strength and cracking behavior of fly ash concretes exposed at elevated temperatures

This paper presents the effects of cooling methods on residual compressive strength and cracking behavior of concretes containing four different class F fly ash contents of 10%, 20%, 30% and 40% as partial replacement of cement at various elevated temperatures. The residual compressive strength of the aforementioned fly ash concretes is measured after being exposed to 200, 400, 600 and 800 °C temperatures and two different cooling methods, for example, slow cooling and rapid water cooling. Results show that the residual compressive strengths of all fly ash concretes decrease with increase in temperatures irrespective of cooling regimes, which is similar to that of ordinary concrete. Generally, control ordinary concrete and all fly ash concretes exhibited between 10% and 35% more reduction in residual compressive strength because of rapid cooling than slow cooling except few cases. Cracks are observed over concrete specimens after being exposed to temperatures ranging from 400 to 800 °C. Samples that are slowly cooled developed smaller cracks than those rapidly cooled. At 800 °C, all fly ash concretes that are exposed to rapid cooling showed the most severe cracking. X‐ray diffraction analysis shows reduction of Ca(OH)₂ peak and formation of new calcium silicate peak in concretes containing 20% and 40% fly ash when subjected to 800 °C in both cooling methods. Thermo gravimetric analysis and differential thermal analysis results show increase in thermal stability of concrete with increase in fly ash contents. The existing Eurocode also predicted the compressive strength of fly ash concretes with reasonable accuracy when subjected to the aforementioned elevated temperatures and cooling methods. Copyright © 2014 John Wiley & Sons, Ltd.     

Synthesis of a terpolymer and a tetrapolymer using monomers of diallylamine salts and SO<Subscript>2</Subscript> and their application as antiscalants

An aqueous solution of diallylammonium salts (CH₂ = CHCH₂)₂NH⁺(CH₂)₃A^? having A^? as: CO₂ ^? (I), PO₃H₂ Cl^? (II) and SO₃ ^? (III) in 1:1:1 mol ratio underwent ammonium persulfate-initiated ter cyclopolymerization to yield pH-responsive zwitterionic polymer IV with random placements of the monomers in the same ratio. During dialysis, PO₃H₂Cl^? of the incorporated monomer units of II upon depletion of HCl became PO₃H^?. Likewise, azobisisobutyronitrile-initiated cyclopolymerization of I, II, III, and SO₂ in a mole ratio of 1:1:1:3 provided pH-responsive tetrapolymer V in over 90 % yield with random and alternative placements of I–III and SO₂ units, respectively, in the same ratio as the feed. Polyzwitterions (PZs) IV and V were insoluble in salt-free water but soluble in the presence of salts. The critical salt concentrations required to promote water solubility of PZ IV were determined to be 0.356 M NaCl, 0.237 M NaBr and 0.128 M NaI, whereas for PZ V the corresponding values were found to be 2.25, 1.26 and 0.862 M, respectively. PZs IV and V were converted into anionic polyelectrolytes VI and VII upon basification with NaOH. The viscosity and antiscalant behaviors of VI and VII were examined. The polymers demonstrated remarkable scale inhibition efficacies; at a dose of 10 ppm, both IV (+NaOH) and V (+NaOH) delayed the precipitation of CaSO₄ from its supersaturated solution up to 920 and over 4000 min, respectively. For a small concentration of 5 ppm of polymer V, a scale inhibition of 100 % over 100 min verified it to be a potential effective antiscalant additive in reverse osmosis plants.     

Synthesis of a polyaminophosphonate and its evaluation as an antiscalant in desalination plant

The cationic monomer, N,N‐diallyl‐3‐(diethylphosphonato)propylammonium chloride, was cyclopolymerized in aqueous solutions using t‐butylhydroperoxide (TBHP) or ammonium persulfate (APS) as initiators to afford a cationic polyelectrolyte (CPE) having a (diethylphosphonato)propyl pendent. The CPE on acidic hydrolysis of the diester groups gave pH‐responsive polyzwitterionic acid (PZA) which on treatment with one and two equivalents NaOH gave zwitterionic/anionic polyelectrolyte (ZAPE) and dianionic polyelectrolyte (DAPE), respectively. The solution properties of the CPE, PZA, ZAPE, and DAPE were investigated in detail by viscometric technique. For the purpose of comparison, the solution properties of the polymers were correlated to a structurally similar polyzwitterion (PZ) having monoethylphosphonate and NH⁺ groups. When performance evaluation was carried out for application in reverse osmosis (RO) plants, DAPE at a concentration of 10 ppm in brackish water feed proved very effective as an inhibitor against calcium sulfate scale. POLYM. ENG. SCI., 54:166–174, 2014. © 2013 Society of Plastics Engineers     

FPGA：挑战带来新机遇

Aitera:依靠40nm与灵活性突围 谈及未来FPGA的发展趋势,Altera亚太区副总裁兼董事总经理Erhaan Shaikh认为对于面向全球市场采用了单芯片方案的新产品,在不同地区市场上推出时需要提供各种各样的型号产品.