Assessment of nanocomposites based on unsaturated polyester resin/nanoclay under impact loading

The aim of this study is to investigate the performance of nanoclay reinforced unsaturated polyester (UP) resin under impact loads. Nanocomposite specimens containing nanoclay in 0, 1.5, and 3 (wt%) were prepared by melt mixing method. X‐ray diffraction, transmission electron microscopy analysis, scanning electron microscope photographs, and viscosity changes in liquid state resin confirmed exfoliation and intercalation of the nanoclay in the UP resin system used. Tensile modulus showed an increase with increase in nanoclay content. However, the tensile strength and elongation at break exhibited reducing performance with increase in nanoclay content. Izod impact test results indicated better performance for the specimens containing nanoclay reinforcements, with 1.5 (wt%) of nanoclay specimens showing the highest value. High velocity impact tests were carried out using gas gun in velocity range of 20–100 m/sec and harden steel hemispherical tip projectile with diameter of 8.7 mm and weight of 11.54 g. Results for high velocity impact test indicated better performance by the specimens containing nanoclay, with 1.5 (wt%) nanoclay showing the highest attained value. Damage assessments of impact area for all specimens showed spalling type brittle failure with punch out and sever fragmentation pattern. Copyright © 2011 John Wiley & Sons, Ltd.     

Effects of Magnetic Nanofluid Fuel Combustion on the Performance and Emission Characteristics

Although the compression ignition engines are a significant source of power, their detrimental emissions create considerable problems to the environment as well as to humans. The objective of the present experimental investigation is to examine the effects of the magnetic nanofluid fuels on combustion performance characteristics and exhaust emissions. In this regard, the Fe₃O₄ nanoparticles dispersed in the diesel fuel with the nanoparticle concentrations of 0.4 and 0.8 vol% were employed for combustion in a single-cylinder, direct-injection diesel engine. After a series of experiments, it was demonstrated that the nanoparticle additives, even at very low concentrations, have considerable influence in diesel engine characteristics. Furthermore, the results indicated that the nanofluid fuel with nanoparticle concentration of 0.4 vol% shows better combustion characteristics in comparison with that of 0.8 vol%. Based on the experimental results, NO _x and SO₂ emissions dramatically reduce, while CO emissions and smoke opacity noticeably increase with increasing the dosing level of nanoparticles.     

Efficient and selective oxidation of hydrocarbons with tert-butyl hydroperoxide catalyzed by oxidovanadium(IV) unsymmetrical Schiff base complex supported on γ-Fe2O3 magnetic nanoparticles

The catalytic activity of an oxidovanadium(IV) unsymmetrical Schiff base complex supported on γ-Fe₂O₃ magnetic nanoparticles, γ-Fe₂O₃@[VO(salenac-OH)] in which salenac-OH?=?[9-(2′,4′-dihydroxyphenyl)-5,8-diaza-4-methylnona-2,4,8-trienato](-2), was explored in the oxidation of hydrocarbons with tert-butyl hydroperoxide (TBHP, 70% aqueous solution) as oxidant. High catalytic activity and selectivity were demonstrated by this magnetic nanocatalyst in alkane hydroxylation and alkene epoxidation, and the corresponding products were obtained with good to excellent yields in acetonitrile at 50 °C. Reasonable catalytic activity was presented by this supported catalyst in the epoxidation of linear alkenes under optimal reaction conditions. In addition, alkylbenzene derivatives and cycloalkanes can be oxidized to their corresponding alcohols and ketones with good yields in this catalytic system. It is possible to magnetically separate the γ-Fe₂O₃@[VO(salenac-OH)] catalyst and reuse it four times without losing the activity significantly. Moreover, the catalyst structure and morphology do not change after recovery, as indicated by comparing scanning electron microscopy (SEM) image, Fourier transform infrared (FT-IR) and diffuse reflectance spectrum (DRS) of the recovered catalyst with those of the fresh catalyst.

     

On the resonant behavior of the16O+15N reaction

The ¹⁶ O+ ¹⁵ N reaction products have been studied by the γ-ray detection method in the CM energy range 15.5 to 36.1 MeV and by the kinematical coincidence method at energies ranging from E _CM =20.6 to 33.5MeV. The γ-ray yield excitation function of the ¹⁶O 3^? inelastic channel shows the existence of resonant structures. Two structures with ～ 1.6 MeV width are observed in the large angle elastic scattering excitation function, they are correlated with the resonances seen in the inelastic channel. Angular momentum assignments were made from the elastic backward angular distributions.     

Sur le carré d'un opérateur non linéaire

Sans résumé     

Hydroxylation of Aromatics by H2O2 Catalyzed by Mononuclear Non-heme Iron Complexes: Role of Triazole Hemilability in Substrate-Induced Bifurcation of the H2O2 Activation Mechanism

Rieske dioxygenases are metalloenzymes capable of achieving cis-dihydroxylation of aromatics under mild conditions using O₂ and a source of electrons. The intermediate responsible for this reactivity is proposed to be a cis-Fe^V(O)(OH) moiety. Molecular models allow the generation of a Fe^III(OOH) species with H₂O₂, to yield a Fe^V(O)(OH) species with tetradentate ligands, or {Fe^IV(O); OH^.} pairs with pentadentate ones. We have designed a new pentadentate ligand, mtL₄², bearing a labile triazole, to generate an “in-between” situation. Two iron complexes, [(mtL₄²)FeCl](PF₆) and [(mtL₄²)Fe(OTf)₂]), were obtained and their reactivity towards aromatic substrates was studied in the presence of H₂O₂. Spectroscopic and kinetic studies reflect that triazole is bound at the Fe^II state, but decoordinates in the Fe^III(OOH). The resulting [(mtL₄²)Fe^III(OOH)(MeCN)]²⁺ then lies on a bifurcated decay pathway (end-on homolytic vs. side-on heterolytic) depending on the addition of aromatic substrate: in the absence of substrate, it is proposed to follow a side-on pathway leading to a putative (N₄)Fe^V(O)(OH), while in the presence of aromatics it switches to an end-on homolytic pathway yielding a {(N₅)Fe^IV(O); OH^.} reactive species, through recoordination of triazole. This switch significantly impacts the reaction regioselectivity.     

Homonuclear chalcogen–chalcogen bond interactions in complexes pairing YO3 and YHX molecules (Y = S,Se; X = H,Cl, Br,CCH, NC,OH, OCH3): Influence of substitution and cooperativity

MP2/aug‐cc‐pVTZ calculations are performed on complexes of YO₃ (Y = S, Se) with a series of electron‐donating chalcogen bases YHX (X = H, Cl, Br, CCH, NC, OH, OCH₃). These complexes are formed through the interaction of a positive electrostatic potential region (π‐hole) on the YO₃ molecule with the negative region in YHX. Interaction energies of the binary O₃Y???YHX complexes are in the range of ?4.37 to ?12.09 kcal/mol. The quantum theory of atoms in molecules and the natural bond orbital analysis were applied to characterize the nature of interactions. It was found that the formation and stability of these binary complexes are ruled mainly by electrostatic effects, although the electron charge transfer from YHX to YO₃ unit also seems to play an important role. In addition, mutual influence between the Y???N and Y???Y interactions is studied in the ternary HCN???O₃Y???YHX complexes. The results indicate that the formation of a Y???N interaction tends to weaken Y???Y bond in the ternary systems. Although the Y???Y interaction is weaker than the Y???N one, however, both types of interactions seem to compete with each other in the HCN???O₃Y???YHX complexes. © 2016 Wiley Periodicals, Inc.     

Determination of the chloride and fluoride contents in the ebrie lagoon and the underground waters in ivory Coast by means of X-ray fluorescence analysis and potentiometric method

This study is devoted to the determination of percentages of fluoride and chloride in Ebrié located in Abidjan and wells located in the central and southern areas of Ivory Coast. Nondispersive X-Ray Fluorescence method and potentometric method with ion sensitive electrodes have been used. For underground water, the concentrations obtained are, with the exception of some isolated cases, lower than the upper limits tolerated for drinking water. These waters are drinkable. In a lagunal environment, the results show that the elements drawn from the bottom of the sea, through the Vridi Canal, spread in the lagoon. The ratio of the concentration of elements and the corresponding salinity confirm the fact that chloride undergoes an essential dilution in the lagoon due to contact with continental waters. A semi-diurnal periodicity of the concentration of elements has been firmly established. This period is the same as the tidal one.