Effect of Co,Pd and Pt ultra-thin films on the Ni-silicide formation: investigating the sandwich configuration

The effect of Co, Pd and Pt ultrathin films on the kinetics of the formation of Ni-silicide by reactive diffusion is investigated. 50 nm Ni/1 nm X/ 50 nm Ni (X?=?Co, Pd, Pt) deposited on Si(100) substrates are studied using in-situ and ex-situ measurements by X-ray diffraction (XRD). The presence of Co, Pd or Pt thin films in between the Ni layers delays the formation of the metal rich phase compared to the pure Ni/Si system and thus these films act as diffusion barriers. A simultaneous silicide formation (δ-Ni₂Si and NiSi phases) different from the classic sequential formation is found during the consumption of the top Ni layer for which Ni has to diffuse through the barrier. A model for the simultaneous growth in the presence of a barrier is developed, and simulation of the kinetics measured by XRD is used to determine the permeability of the different barriers. Atom probe tomography (APT) of the Ni/Pd/Ni system shows that the Pd layer is located between the Ni top layer and δ-Ni₂Si during the silicide growth, in accordance with a silicide formation controlled by Ni diffusion through the Pd layer. The effect of the barrier on the silicide formation and properties is discussed.

     

Software HEVC video decoder: towards an energy saving for mobile applications

Multimedia Tools and Applications - With the explosive growth of mobile video consumption over the Internet, delivering video at high quality while controlling the energy consumption of embedded...     

Dynamic response of ferrofluidic deformable mirrors using elastomer membrane and overdrive techniques

The experimental results obtained with a ferrofluidic deformable mirror controlled by electro-magnet actuators are presented here. Using a step input through a single actuator, we obtained a steady-state settling time of 100?ms; however, different combinations of overdrive inputs can be used to decrease it to 25?ms. A new technique which consists of laying down an elastomer membrane, coated with an aluminum film, on the ferrofluid is also discussed. By adding the membrane on the ferrofluid, it further decreases the time response by a factor of 2. Furthermore, the thin aluminum layer improves the reflectivity of the mirror. Finally, using the membrane and the overdrive techniques combined, the time response is improved by a factor of 20. Numerical simulations show that ferrofluidic mirrors using membranes and improved electronics should reach settling times of the order of a millisecond. Presumably, even lower settling times could be possible.     

Substrate Flexibility of the Flavin-Dependent Dihydropyrrole Oxidases PigB and HapB Involved in Antibiotic Prodigiosin Biosynthesis

In the biosynthesis of the tripyrrolic pigment prodigiosin, PigB is a predicted flavin-dependent oxidase responsible for the formation of 2-methyl-3-amylpyrrole (MAP) from a dihydropyrrole. To prove which dihydropyrrole is the true intermediate, both possibilities, 5-methyl-4-pentyl-3,4-dihydro-2H-pyrrole ( 5 a , resulting from transamination of the aldehyde of 3-acetyloctanal) and 2-methyl-3-pentyl-3,4-dihydro-2H-pyrrole ( 6 , resulting from transamination of the ketone), were synthesised. Only 5 a restored pigment production in a strain of Serratia sp. ATCC 39006 blocked earlier in MAP biosynthesis. PigB is membrane-associated and inactive when its transmembrane domain was deleted, but HapB, its homologue in Hahella chejuensis, lacks the transmembrane domain and is active in solution. Two colourimetric assays for PigB and HapB were developed, and the HapB-catalysed reaction was kinetically characterised. Ten analogues of 5 a were synthesised, varying in the C2 and C3 side chains, and tested as substrates of HapB in vitro and for restoration of pigment production in Serratia ΔpigD in vivo. All lengths of side chain tested at C3 were accepted, but only short side chains at C2 were accepted. The knowledge that 5 a is an intermediate in prodigiosin biosynthesis and the ease of synthesis of analogues of 5 a makes a range of prodigiosin analogues readily available by mutasynthesis.     

Multivariate Analysis of Multiple Datasets: a Practical Guide for Chemical Ecology

Chemical ecology has strong links with metabolomics, the large-scale study of all metabolites detectable in a biological sample. Consequently, chemical ecologists are often challenged by the statistical analyses of such large datasets. This holds especially true when the purpose is to integrate multiple datasets to obtain a holistic view and a better understanding of a biological system under study. The present article provides a comprehensive resource to analyze such complex datasets using multivariate methods. It starts from the necessary pre-treatment of data including data transformations and distance calculations, to the application of both gold standard and novel multivariate methods for the integration of different omics data. We illustrate the process of analysis along with detailed results interpretations for six issues representative of the different types of biological questions encountered by chemical ecologists. We provide the necessary knowledge and tools with reproducible R codes and chemical-ecological datasets to practice and teach multivariate methods.     

Fate of N-nitrosodimethylamine, trihalomethane and haloacetic acid precursors in tertiary treatment including biofiltration

The presence of disinfection by-products (DBPs) such as trihalomethanes (THMs), haloacetic acids (HAAs) and N-nitrosamines in water is of great concern due to their adverse effects on human health. In this work, the removal of N-nitrosodimethylamine (NDMA), total THM and five HAA precursors from secondary effluent by biological activated carbon (BAC) is investigated at full and pilot scale. In the pilot plant two filter media, sand and granular activated carbon, are tested. In addition, we evaluate the influence of ozonation prior to BAC filtration on its performance. Among the bulk of NDMA precursors, the fate of four pharmaceuticals containing a dimethylamino moiety in the chemical structure are individually investigated. Both NDMA formation potential and each of the studied pharmaceuticals are dramatically reduced by the BAC even in the absence of main ozonation prior to the filtration. The low removal of NDMA precursors at the sand filtration in comparison to the removal of NDMA precursors at the BAC suggests that adsorption may play an important role on the removal of NDMA precursors by BAC. Contrary, the precursors for THM and HAA formation are reduced in both sand filtration and BAC indicating that the precursors for the formation of these DBPs are to some extent biodegradable.     

WO3 nano-ribbons: their phase transformation from tungstite (WO3·H2O) to tungsten oxide (WO3)

Tungsten oxide (WO₃) nano-ribbons (NRs) were obtained by annealing tungstite (WO₃·H₂O) NRs. The latter was synthesized below room temperature using a simple, environmentally benign, and low cost aging treatment of precursors made by adding hydrochloric acid to diluted sodium tungstate solutions (Na₂WO₄·2H₂O). WO₃ generates significant interests and is being used in a growing variety of applications. It is therefore important to identify suitable methods of production and better understand its properties. The phase transformation was observed to be initiated between 200 and 300 ^°C, and the crystallographic structure of the NRs changed from orthorhombic WO₃·H₂O to monoclinic WO₃. It was rigorously studied by annealing a series of samples ex situ in ambient air up to 800 ^°C and characterizing them afterward. A temperature-dependent Raman spectroscopy study was performed on tungstite NRs between minus 180 and 700 ^°C. Also, in situ heating experiments in the transmission electron microscope allowed for the direct observation of the phase transformation. Powder X-ray diffraction, electron diffraction, electron energy-loss spectroscopy, and X-ray photoelectron spectroscopy were employed to characterize precisely this transformation.     

Parametric study of riveted joints

As one of the most reliable fasteners, solid riveted joints are widely utilized in many industrial areas. In the present work, the authors recalled some results on the riveting process and the strength of one kind of riveted joints obtained by simulation and experimental investigations in a previous paper. The numerical results were in very good agreement with the experimental results, allowing us to validate our simulation approach and its use for further studies. We selected several engineering parameters for the riveted joint: initial assembly, friction coefficient, rivet’s geometry and sheets’ geometry, in order to carry out a parametric study and determine their relative importance. These were conducted in FEA software. The results showed the impact on riveting process and the strength of the riveted joint by varying each parameter which was interesting for the industry.