Synthesis of Nickel Sulfides by Mechanical Alloying

The feasibility and kinetics of synthesizing various nickel sulfides by milling of elemental mixtures of Ni and S in a high-energy shaker mill have been investigated. The phases Ni₃S₂ and the high-temperature polymorph of NiS are formed readily via such processing. In distinction, it requires prolonged milling to obtain Ni₇S₆; NiS₂ can only be obtained as a minor reaction product; and Ni₃S₄ cannot be formed by milling for the conditions of this study. Structural evolution during synthesis and the kinetics of Ni₃S₂ formation are investigated in depth. S coats the Ni particles and sulfide formation takes place at the interface of the elements after a certain degree of microstructural refinement due to the plastic deformation accompanying milling. Ni₃S₂ forms rapidly at this stage. However, a stasis in the reaction is then observed. This is associated with NiS formation and a slight decrease in the amount of Ni₃S₂. The stasis is of approximately 5-min duration and is followed by a recurrence in the formation of Ni₃S₂ and a disappearance of the NiS phase. The kinetics can be mimicked through a model of the mechanical alloying process. The model is able to predict the time dependence of the initial and later stages of Ni₃S₂ formation and the effect of other parameters, such as mill atmosphere and use of premilled powder, on the reaction kinetics. The microstructures found in the intermediate to later stages of milling are similar to those associated with self-sustaining reactions.     

Atomic snapshots using lattice agreement

Summary Thesnapshot object is an important tool for constructing wait-free asynchronous algorithms. We relate the snapshot object to thelattice agreement decision problem. It is shown that any algorithm for solving lattice agreement can be transformed into an implementation of a snapshot object. The overhead cost of this transformation is only a linear number of read and write operations on atomic single-writer multi-reader registers. The transformation uses an unbounded amount of shared memory. We present a deterministic algorithm for lattice agreement that usedO (log² n) operations on 2-processorTest & Set registers, plusO (n) operations on atomic single-writer multi-reader registers. The shared objects are used by the algorithm in adynamic mode, that is, the identity of the processors that access each of the shared objects is determined dynamically during the execution of the algorithm. By a randomized implementation of 2-processorsTest & Set registers from atomic registers, this algorithm implies a randomized algorthm for lattice agreement that uses an expected number ofO (n) operations on (dynamic) atomic single-writer multi-reader registers. Combined with our transformation this yields implementations of atomic snapshots with the same complexity.Cambridge Research Laboratory, Digital Equipment Corporation Hagit Attiya received the B.Sc. degreeiin Mathematics and Computer Science from the Hebrew University of Jerusalem, in 1981, the M.Sc. and Ph.D. degrees in Computer Science from the Hebrew University of Jerusalem, in 1983 and 1987, respectively. She is presently a senior lecturer at the departtment of Computer Science at the Technion, Israel Institute of Technology. Prior to this, she has been a post-doctoral research associate at the Laboratory for Computer Science at M.I.T. Her general research interests are distributed computation and theoretical computer science. More specific interests include fault-tolerance, timing-based and asynchronous algorithms. Maurice Herlihy received the A.B. degree in Mathematics from Harvard University, and the M.S. and the Ph.D. degrees in Computer Science from M.I.T. From 1984 to 1989 he was a faculty member in the Computer Science Department at Carnegie Mellon University in Pittsburgh, PA. In 1989 he joined the research staff at the Digital Equipment Corporation's Cambridge Research Laboratory in Cambridge MA. Since 1994, he has been on the faculty at the Computer Science Department at Brown University. Dr. Herlihy's research interests encompass practical and theoretical aspects of distributed and concurrent computation. Ophir achman received a B.A. in computer science from the Technion, Haifa, Israel in 1989 and M.Sc. in computer science from the Technion, Haifa, Israel, in 1992. He is now studying for a D.Sc. in computer science at the Technion. His currentarea of research is distributed computing, and in particular, asynchronous shared memory systems.This work appeared in preliminary form in proceedings ofthe 6th International Workshop on Distributed Algorithms [12]. This research was partially supported by grant No. 92-0233 from the United States-Israel Binational Science Foundation (BSF), Jerusalem, Technion V.P.R. funds — B. and G. Greenberg Research Fund (Ottawa), and the fund for the promotion of research in the TechnionPart of the work of this author was performed while visiting DEC Cambridge Research Laboratory     

The Influence of Cooling Rate on the Specific Volume of Isotactic Poly(propylene) at Elevated Pressures

Summary: We used a custom designed dilatometer to measure quantitatively the time evolution of the specific volume of (semi‐crystalline) polymers for an unusual combined wide range of cooling rates and elevated pressures, covering processing conditions. For an isotactic poly(propylene), applying the Schneider rate equations for quiescent crystallization, experimental results are compared to numerical predictions. Average cooling rates imposed during crystallization of the material vary from 0.1 to 35 °C · s^?1 while pressures range from 20 to 60 MPa. The results show the well‐known profound influence of pressure and cooling rate on the specific volume. An increasing cooling rate shifts the crystallization temperature T_c towards lower temperatures, increases the final specific volume, and the transition due to crystallization is more gradual and widespread. For the highest cooling rate applied, the shift in T_c is as much as 30 °C, while the final specific volume increases up to 1.4%. Increasing pressure has an opposite effect on the shift in T_c, while the final specific volume, after pressure release, also increases. Finally, a comparison of numerical predictions with experimental data shows that the crystallization temperature T_c is consistently predicted too low, and that the predictions at high cooling rate are sensitive to (small) variations in model parameters.

Influence of cooling rate on the specific volume of iPP.     

Enhanced removal of Cr(VI) from aqueous solution using polypyrrole/Fe3O4 magnetic nanocomposite

Fe(3)O(4) coated polypyrrole (PPy) magnetic nanocomposite was prepared via in situ polymerization of pyrrole monomer for the removal of highly toxic Cr(VI). Structure and morphology of the prepared nanocomposite were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray diffraction pattern, Field emission scanning electron microscopy (FE-SEM) and high resolution transmission electron microscopy (HR-TEM). Electron spin resonance (ESR) studies confirmed that the nanocomposite is magnetic in nature. Up to 100% adsorption was found with 200mg/L Cr(VI) aqueous solution at pH 2. Adsorption of Cr(VI) on the surface of the adsorbent was confirmed by the ATR-FTIR and X-ray photoelectron spectroscopy (XPS). XPS studies also suggested that ion exchange and reduction on the surface of the nanocomposite may be the possible mechanism for Cr(VI) removal by the PPy/Fe(3)O(4) nanocomposite. Adsorption results showed that Cr(VI) removal efficiency by the nanocomposite decreased with an increase in pH. Adsorption kinetics was best described by the pseudo-second-order rate model. Isotherm data fitted well to the Langmuir isotherm model. Thermodynamic study revealed that the adsorption process is endothermic and spontaneous in nature. Desorption experiment showed that in spite of the very poor recovery of the adsorbed Cr(VI); the regenerated adsorbent can be reused successfully for two successive adsorption-desorption cycles without appreciable loss of its original capacity.     

Functionalization of Polymer Surfaces Using Excimer VUV Systems and Silent Discharges. Application to Electroless Metallization

New approaches for electroless plating of nonconductive polymers or polymer-based materials are described. In this work, polyimide substrates were surface-functionalized (i) in nitrogenated (ammonia at reduced pressure) and oxygenated (air at atmospheric pressure) atmospheres under assistance of vacuum-ultraviolet (VUV) irradiation (use of a xenon silent discharge excimer source) or (ii) directly in air at atmospheric pressure using a dielectric-barrier discharge (DBD) device. After functionalization, the substrates were “activated” by dipping in a dilute acidic PdCl₂ solution or by spin-coating of a thin metal-organic film (from a solution of palladium acetate (PdAc) in chloroform). The catalytic activity of the so-deposited palladium species toward the electroless deposition of nickel was studied before and after a VUV post-irradiation (in air at atmospheric or reduced pressure) with a view to understanding better the role of the reducer (sodium hypophosphite) within the electroless bath.

This work confirms the specific interest of grafting nitrogenated functionalities onto polymer surfaces for attaching covalently the palladium-based catalyst (in particular in the case of the PdCl₂ route), forming thus strong Pd - N - C bonds at the metal/polymer interface. This results from the strong chemical affinity of palladium toward nitrogen. On the other hand, when oxygenated functionalities are surface-grafted, the conventional two-step procedure using SnCl₂ and PdCl₂ solutions can be proposed due to the strong chemical affinity of tin toward oxygen. The Ni deposits obtained under these different conditions pass the standard Scotch^®-tape test and, therefore, exhibit a good practical adhesion. For this same purpose, it is interesting to note that the DBD treatment operating in air at atmospheric pressure causes an increase of the surface roughness and, therefore, an improvement in adhesion of metallic films when their initiation is catalyzed through the PdAc route. In addition, this work demonstrates that extensive research still has to be performed to understand and improve the Ni/polymer adhesion when the PdAc route associated with a VUV irradiation is considered.     

Vertically oriented nickel nanorod/carbon nanofiber core/shell structures synthesized by plasma-enhanced chemical vapor deposition

Plasma-enhanced chemical vapor deposition, without a nickel-containing gaseous precursor, was used to synthesize continuous nickel (Ni) nanorods inside the hollow cavity of carbon nanofibers (CNFs), thus forming vertically aligned Ni/CNF core/shell structures. Scanning and transmission electron microscopic images indicate that the elongated Ni nanorods originate from the catalyst particles at the tips of the CNFs and that their formation is due to the effect of extrusion induced by the compressive force of the graphene layers during growth. Different from previous work, each vertically-aligned core/shell structure reported is totally isolated from its neighbors. Continuous Ni nanorods are found to separate into smaller ones with increasing growth time, which was ascribed to (i) the limited amount of Ni available in the tip of the CNF, (ii) the polycrystalline nature of the Ni nanorods and (iii) the combined effects of the compressive stresses on the side of the Ni nanorods and of the tensile stress along their axis.     

COMPARISON OF TWO ANALYTICAL METHODS FOR THE DETERMINATION OF AZAARENES IN ATMOSPHERIC PARTICULATE MATTER

In this paper, the development of an analytical method for the separation and quantification of 20 azaarenes is described. Two methods are compared: high performance liquid chromatography with fluorescence detection (HPLC-fluorescence) and gas chromatography with mass spectrometry detection (GC-MS).

Although HPLC-fluorescence was proven to be the most sensitive method, GC-MS was selected in particular for the efficiency of the separation of the 20 azaarenes. The detection limits of the HPLC-fluorescence and GC-MS methods varied between 0.04 μ g.L^?1 (dibenz[a,c]acridine) and 1.30 μ g.L ^?1 (acridine) and between 1.50 μ g.L ^?1 (benz[c]acridine) and 2.56 μ g.L ^?1 (dibenz[a,c]acridine) respectively.

The GC-MS method was applied to particulate matter (PM ₁₀ ) samples collected over 48–72 h periods between April 2006 and February 2007 in Strasbourg (East of France). Before analysis aerosol samples were Soxhlet extracted and concentrated to a final volume of about 1 mL of hexane.

The seasonally mean concentrations of all azaarenes for this urban site have shown a seasonal variation in which the maximum concentration occurred in the winter (6.0 ng.m ³ ) and the minimum in the summer (0.90 ng.m³). For all the seasons the 2 rings species were the predominant azaarenes while the > 4 rings species were the less abundant.     

Parvovirus B19 infection in AIDS patients

We report a 16-year-old boy, born to consanguineous parents, with mental retardation, gait disturbances and dysarthria; brain magnetic resonance showed features consistent with rhombencephalosynapsis. This condition is characterised by a hypoplastic single-lobed cerebellum. The interest of this case is the presence of common ancestors, pointing to an autosomal recessive inheritance of the malformation.     

Effect of alum treatment on the trihalomethane formation and bacterial regrowth potential of natural and synthetic waters

Waters from five reservoirs and "synthetic waters", prepared using terrestrially derived dissolved organic matter (DOM) extracted from vegetation and reservoir catchment soils, were studied for their treatability with alum using a jar test procedure. DOM in drinking water is a precursor for the formation of trihalomethanes (THM) following chlorine disinfection and can also be a substrate for microbial growth in the drinking water distribution system. The trihalomethane formation potential (THMFP) represents an upper concentration limit on THMs formed by chlorination, while bacterial regrowth potential (BRP) is an indicator of the bioavailability of DOM. BRP and THMFP were measured before and after alum treatment and the results were related to the source of the DOM. It was found that freshly derived terrestrial DOM in synthetic water resulted in higher THMFP and BRP than DOM in reservoir waters. For the samples investigated, conventional alum treatment did not always reduce the THM precursor levels formed in laboratory tests below the NH&MRC (1996) guideline level of 250 microg/L nor produce microbially stable waters.     

Interaction between laser beam and BaTiO3 powders in selective laser sintering treatments

The research work reported in this paper is an investigation of the behavior of barium titanate powders under selective laser irradiation. Our goal is to determine suitable conditions to sinter the powders and form dense layers usable in some electronic components. On that purpose, compacts of micro/nano BaTiO₃ powder mixes are used for a parametric investigation of the laser scans parameters (power, speed, etc.) with a Nd-YVO₄ laser (23 W). The microstructures obtained after laser treatments are evaluated by XRD, SEM and EDS and compared to a reference specimen manufactured in a conventional way. From this work it can be concluded that a high laser beam power is required to obtain a consolidation of the powder grains and the use of a high scan speed avoids the melting. The scanning speed also influences the final crystallographic state of BaTiO₃. Optimal parameters were founded in order to form a dense and homogeneous tetragonal BaTiO₃ surface.