Carbon reaction and diffusion on Ni(111), Ni(100), and Fe(110): Kinetic parameters from x-ray photoelectron spectroscopy and density functional theory analysis

This paper investigates the reactivity of elemental carbon films deposited from the vapor phase with Fe and Ni substrates at room temperature. X-ray photoelectron spectroscopy (XPS) measurements are presented as a method for evaluating kinetic reaction data. Carbon films are deposited on different surface orientations representing geometries from a dense atom packing as in fcc (111) to an open surface structure as in fcc (100). During annealing experiments several reactions are observed (carbon subsurface diffusion, carbide formation, carbide decomposition, and graphite ordering). These reactions and the respective kinetic parameters are analyzed and quantified by XPS measurements performed while annealing at elevated temperatures (620–820 K). The resulting activation barriers for carbon subsurface diffusion are compared with calculated values using the density functional theory. The determined kinetic parameters are used to reproduce the thermal behavior of carbon films on nickel surfaces

Disordered actomyosin networks are sufficient to produce cooperative and telescopic contractility

While the molecular interactions between individual myosin motors and F-actin are well established, the relationship between F-actin organization and actomyosin forces remains poorly understood. Here we explore the accumulation of myosin-induced stresses within a two-dimensional biomimetic model of the disordered actomyosin cytoskeleton, where myosin activity is controlled spatiotemporally using light. By controlling the geometry and the duration of myosin activation, we show that contraction of disordered actin networks is highly cooperative, telescopic with the activation size, and capable of generating non-uniform patterns of mechanical stress. We quantitatively reproduce these collective biomimetic properties using an isotropic active gel model of the actomyosin cytoskeleton, and explore the physical origins of telescopic contractility in disordered networks using agent-based simulations

Chemical vapor deposition and infiltration for the production of tungsten fiber reinforced tungsten composite material

Contribution submission to the conference Regensburg 2016Chemical vapor deposition and infiltration for the productionof tungsten fiber reinforced tungsten composite material —∙Martin Aumann1, Jan Willem Coenen1, Hanns Gietl2, TillHoeschen2, Johann Riesch2, Klaus Schmid2, Rudolf Neu2, andChristian Linsmeier1 — 1Forschungszentrum Juelich GmbH, Institutfür Energie- und Klimaforschung, 52425 Juelich — 2Max-Planck-Institut für Plasmaphysik, 85748 GarchingDue to its high melting point, high corrosion resistance and its preferableproperties in terms of hydrogen retention, tungsten is a promisingcandidate in future nuclear fusion devices. However, the mechanicalbehavior of tungsten is crucial, as it is inherently brittle at room temperature.As possibility to overcome this brittleness, a composite materialcan be formed, which shows pseudo-ductility and therefore avoidscatastrophic failure of the material. A possibility to produce such aWf/W-composite is chemical vapor deposition and chemical vapor infiltration,where tungsten is deposited on small tungsten wires throughthe reaction of WF6 and H2. With ongoing infiltration time, pores areformed between the fibers, which decrease in size through the chemicalreaction. For better process understanding, a pore model was established,which solves the mass balance inside the pore and the resultingpore diameter simultaneously. It shows a significant difference in diameterfor longer infiltration times. This behavior shall be proved inexperiments with an experimental pore, which is similar to the simulatedone. Furthermore also kinetic investigations on the chemicalsurface reaction are carried out to increase the process understanding.Part: MMType: Vortrag;TalkTopic: Transport (Diffusion, Leitfähigkeit,Wärme)/ Transport (Diffusion,conductivity, heat)Email: [email protected]

Smart Tungsten-based Alloys for a First Wall of DEMO

During an accident with loss-of-coolant and air ingress in DEMO, the temperature of tungsten first wall cladding may exceed 1000 °C and remain for months leading to tungsten oxidation. The radioactive tungsten oxide can be mobilized to the environment at rates of 10–150 kg per hour. Smart tungsten-based alloys are under development to address this issue. Alloys are aimed to function as pure tungsten during regular plasma operation of DEMO. During an accident, alloying elements will create a protective layer, suppressing release of W oxide. Bulk smart alloys were developed by using mechanical alloying and field-assisted sintering technology. The mechanical alloying process was optimized leading to an increased powder production by at least 40 %. Smart alloys and tungsten were tested under a variety of DEMO-relevant plasma conditions. Both materials demonstrated similar sputtering resistance to deuterium plasma. Under accident conditions, alloys feature a 40-fold reduction of W release compared to that of pure tungsten.</p

Active removal of waste dye pollutants using Ta[sub]3N[sub]5/W[sub]18O[sub]49 nanocomposite fibres

A scalable solvothermal technique is reported for the synthesis of a photocatalytic composite material consisting of orthorhombic Ta3N5 nanoparticles and WOx≤3 nanowires. Through X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(VI) sub-oxide was identified as monoclinic W18O49. The composite material catalysed the degradation of Rhodamine B at over double the rate of the Ta3N5 nanoparticles alone under illumination by white light, and continued to exhibit superior catalytic properties following recycling of the catalysts. Moreover, strong molecular adsorption of the dye to the W18O49 component of the composite resulted in near-complete decolourisation of the solution prior to light exposure. The radical species involved within the photocatalytic mechanisms were also explored through use of scavenger reagents. Our research demonstrates the exciting potential of this novel photocatalyst for the degradation of organic contaminants, and to the authors’ knowledge the material has not been investigated previously. In addition, the simplicity of the synthesis process indicates that the material is a viable candidate for the scale-up and removal of dye pollutants on a wider scale