DC Electrical Resistivity and Magnetic Property of Single-Phase α-Fe2O3 Nanopowder Synthesized by a Simple Chemical Method

Nanocrystalline pure α-Fe₂O₃ powder, with an average particle size of 35 nm, has been synthesized by using an aqueous solution-based synthetic route. DC electrical resistivity of the synthesized material was measured with respect to temperature by the two-probe method from 28° to 225°C. Room temperature resistivity of the nanopowder was ∼10⁸Ω·cm. Magnetic hysteresis measurement revealed that the synthesized α-Fe₂O₃ nanopowder exhibited ferromagnetic behavior at room temperature. The hysteretic features are high saturation magnetization of 5.1 emu/g, high remanence of 2.2 emu/g, and coercivity of 200.5 Oe.     

An investigation of the flocculation characteristics of polyacrylamide‐grafted chitosan

To investigate the flocculation characteristics of polyacrylamide (PAM)‐grafted chitosan, a series of PAM‐grafted chitosan copolymer (Chito‐g‐PAM1 to Chito‐g‐PAM4) have been synthesized by ceric ammonium nitrate‐induced solution polymerization technique in nitrogen atmosphere. The flocculation characteristics of the polymer samples (PAM, grafted and ungrafted chitosan) were studied by settling test and jar test methods in the colloidal suspensions of kaolin, iron ore, silica, and bentonite powder. It was found that the settling performance of Chito‐g‐PAM3 is best among the polymer samples. The jar test results indicate that the ungrafted chitosan has better water clarifying performance than both the PAM and grafted chitosan. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Synthesis of trideuteratedO-alkyl platelet activating factor and lyso derivatives

Racemic heavy isotope analogs of 1-O-alkyl-sn-glycero-3-phosphocholine (lysoPAF) and 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine (PAF) were prepared for use as internal standards to facilitate quantitative studies based on mass spectrometry. Starting from pentadencane-1,15-diol andrac-glycerol-1,2-acetonide, a convergent synthesis of 1-O-[16′-²H₃]hexadecyl and 1-O-[18′-²H₃]octadecylrac-glycero-3-phosphocholine and their acetyl derivatives is described. Three deuterium atoms were introduced at the terminal position of the 1-O-alkyl group by displacement of thep-toluensulfonyl group from 1-O-alkyl-15′-p-toluensulfonate and 1-O-alkyl-17′-p-toluensulfonate with [²H₃]-methylmagnesium iodide. The 1-O-alkyl-17′-p-toluensulfonate was obtained by reaction of the 1-O-alkyl-15′-p-toluensulfonate with allylmagnesium bromide, followed by reductive ozonolysis and treatment withp-toluenesulfonyl chloride. The hydroxyl group at C-2 was protected by a benzyl group and removed at a late stage in the synthesis. This provided the corresponding lysoderivatives or allowed preparation of racemic PAF by subsequent acetylation of the free hydroxy group. The phosphocholine moiety was introduced at glycerol C-3 by reaction with bromoethyldichlorophosphate and trimethylamine. The synthetic compounds were analyzed by FAB/MS and GC/NICIMS. They were shown to contain less than 0.6% protium impurity.     

A Novel Oxidation of Valine by N-Bromophthalimide in the Presence of Ruthenium(III) Chloride as a Homogeneous Catalyst

Kinetics of Ruthenium(III) [Ru(III)] chloride catalyzed oxidation of valine (Val) has been studied by N-bromophthalimide (NBP) in the acidic medium at 35 °C. The reaction rate follows first-order and zero-order dependence with respect to [NBP] and [Val]. First-order kinetics was observed for Ru(III) chloride at low range of concentrations and tending towards zero-order at higher concentrations. A negative effect was observed for [H⁺] and [phthalimide], while a positive effect was observed for [Cl^?] on the reaction rate. Hg(OAc)₂, ionic strength (I), and dielectric constant (D) of the medium did not change significantly the reaction rate. The rate constants as a function of temperature (298–318 K) were used to calculate activation parameters of the oxidation of Val by NBP. A plausible mechanism was proposed to explain the results of kinetic studies, reaction stoichiometry and product analysis.     

Phosphotungstic Acid: An Efficient Catalyst for the Aqueous Phase Synthesis of Bis-(4-hydroxycoumarin-3-yl)methanes

In this present work, we report that phosphotungstic acid provides a simple, efficient and environmentally benign route is a two-component one-pot domino Knoevenagel-type condensation/Michael reaction between 4-coumarin derivative and an aldehyde in water as a solvent in shorter duration with high yields.      

Influence of Cobalt Doping on the Physical Properties of Zn<Subscript>0.9</Subscript>Cd<Subscript>0.1</Subscript>S Nanoparticles

Zn_0.9Cd_0.1S nanoparticles doped with 0.005–0.24 M cobalt have been prepared by co-precipitation technique in ice bath at 280 K. For the cobalt concentration >0.18 M, XRD pattern shows unidentified phases along with Zn_0.9Cd_0.1S sphalerite phase. For low cobalt concentration (≤0.05 M) particle size, d _XRD is ~3.5 nm, while for high cobalt concentration (>0.05 M) particle size decreases abruptly (~2 nm) as detected by XRD. However, TEM analysis shows the similar particle size (~3.5 nm) irrespective of the cobalt concentration. Local strain in the alloyed nanoparticles with cobalt concentration of 0.18 M increases ~46% in comparison to that of 0.05 M. Direct to indirect energy band-gap transition is obtained when cobalt concentration goes beyond 0.05 M. A red shift in energy band gap is also observed for both the cases. Nanoparticles with low cobalt concentrations were found to have paramagnetic nature with no antiferromagnetic coupling. A negative Curie–Weiss temperature of −75 K with antiferromagnetic coupling was obtained for the high cobalt concentration.     

Corrosion Behavior of Bare,Cr3C2-25%(NiCr), and Cr3C2-25%(NiCr)+0.4%CeO2-Coated Superni 600 Under Molten Salt at 900 °C

Cr₃C₂-25(NiCr) and Cr₃C₂-25(NiCr)+0.4%CeO₂ coatings were deposited on nickel-based superalloy Superni 600 by Detonation-gun technique. Studies were conducted on bare and coated alloys in molten salt environment (Na₂SO₄-25%NaCl) at 900 °C under cyclic condition. Characterization of the corrosion product was done using field emission scanning electron microscopy/energy dispersive spectroscopy and x-ray diffraction techniques. The bare Superni 600 shows penetration of corrosion beneath the metal layer thereby indicating internal oxidation. The coating of Cr₃C₂-25(NiCr) with 0.4%CeO₂ leads to the formation of adherent scale.     

Structural,Optical, and Ferroelectric Behaviors of Cu_(1-x)Li_xO(0≤x≤0.09) Nanostructures

We report structural,optical,and ferroelectric behaviors of lithium-doped copper oxide(Cu1-xLixO with x =0.0,0.05,0.07,and 0.09) nanostructures synthesized by hydrothermal method.The XRD pattern indicates the pure phase formation of CuO without any impurity,and the crystallite size is found to be increases for x =0–0.07 and decreases for x =0.09.FESEM analysis shows that the average size of Cu1-xLixO nanostructures increases with the increasing the Li-doping concentrations up to 7% and then decreases for 9% Li doping concentration.Moreover,Raman and photoluminescence spectrum also confirm the phase formation of CuO.A significant reduction in optical band gap is observed up to x =0.07,and then band gap increases for x =0.09 due to segregation of the impurities on the surface or grain boundaries,which may suppress the grain growth and results the enhancement in optical band gap.Moreover,a weak ferroelectricity is observed in CuO nanostructures for pure and 9% Li doping through polarization versus electric field(P–E).     

Low-Temperature Sintering of La(Ca)CrO3 Powder Prepared through the Combustion Process

Ultrafine La(Ca)CrO₃ (LCC) powder was prepared through the glycine–nitrate gel combustion process. It was shown for the first time that the use of relatively inexpensive CrO₃ as a starting material for chromium has potential for the bulk preparation of sinter-active LCC powder. As-prepared powder, when calcined at 700°C, resulted in LCC along with a small amount of CaCrO₄. The calcined powder was found to be composed of soft agglomerates with a particle size of ≈70–290 nm. The cold pressing and sintering of the calcined powder at 1200°C resulted in the mono-phasic La_0.7Ca_0.3CrO₃ with density ≈98% of its theoretical value. This is the lowest sintering temperature ever reported for La_0.7Ca_0.3CrO₃. The conductivity of the sintered La_0.7Ca_0.3CrO₃ at 1000°C was found to be ≈57 S/cm in air. The sintering and electrical behavior achieved for La_0.7Ca_0.3CrO₃ may find application as an interconnect material for high-temperature solid oxide fuel cells if problems with chemical expansion and poor conductivity in fuel can be overcome.     

Investigations of ruthenium pyrochlores as bifunctional oxygen electrodes

The lead–ruthenates oxides were synthesized and characterized by X-ray diffraction and thermogravimetric analysis. Compounds in which part of the ruthenium is substituted with iridium were also prepared. The performance of these oxides for oxygen reduction and generation reactions was investigated in porous, gas-fed electrodes. The performance of pyrochlore oxide electrodes was shown to be excellent for oxygen reduction and generation reactions. It was observed that iridium substituted pyrochlores exhibit somewhat better performance for oxygen reduction than the unsubstituted compounds. The anodic corrosion resistance of pyrochlore-based porous electrodes was improved by using two different anionically conducting polymer overlayers, which slow down the diffusion of ruthenates and plumbate out of the electrode. The use of the conducting polymer overlayers resulted in improved performance of these electrodes.