Solid state reaction in sandwich-type Al/Cu thin films

Al/Cu/Al and Cu/Al/Cu triple layers with approximately 10 nm single layer thickness deposited on tungsten substrates were analyzed in the early stages of reactive interdiffusion by means of atom probe tomography. The first reaction product is found after 5 min thermal treatment at 110 degrees C and identified by direct chemical analysis to be Al2Cu. Surprisingly, we found a significant asymmetry in the reaction rate of the new phase with the stacking sequence: the thickness of the product grown at the interfaces, at which Cu is deposited on top of the Al layer, is approximately 1.5-2 times thicker than the other one at the interfaces at which Al is deposited onto a Cu layer. On the other hand, at both interfaces the thickness of the product layer depends parabolically on time. No precursory interdiffusion and no distinct nucleation process of the product are observed.     

Mass-controlled capillary viscometer for a Newtonian liquid: viscosity of water at different temperatures

The operation principle of the mass-controlled capillary viscometer is presented for a Newtonian liquid. The derived equation for the temporal changes of the mass in a liquid column draining under gravity through a discharge capillary tube accounts self-consistently for the inertial convective term associated with the acceleration effect. The viscosity of water measured at different temperatures using the new approach is in good agreement with literature data.     

Pressure cell for investigations of solid-liquid interfaces by neutron reflectivity

We describe an apparatus for measuring scattering length density and structure of molecular layers at planar solid-liquid interfaces under high hydrostatic pressure conditions. The device is designed for in situ characterizations utilizing neutron reflectometry in the pressure range 0.1-100 MPa at temperatures between 5 and 60?°C. The pressure cell is constructed such that stratified molecular layers on crystalline substrates of silicon, quartz, or sapphire with a surface area of 28 cm(2) can be investigated against noncorrosive liquid phases. The large substrate surface area enables reflectivity to be measured down to 10(-5) (without background correction) and thus facilitates determination of the scattering length density profile across the interface as a function of applied load. Our current interest is on the stability of oligolamellar lipid coatings on silicon surfaces against aqueous phases as a function of applied hydrostatic pressure and temperature but the device can also be employed to probe the structure of any other solid-liquid interface.     

Spatially resolved characterization of cellulose nanocrystal-polypropylene composite by confocal Raman microscopy

Raman spectroscopy was used to analyze cellulose nanocrystal (CNC) -polypropylene (PP) composites and to investigate the spatial distribution of CNCs in extruded composite filaments. Three composites were made from two forms of nanocellulose (CNCs from wood pulp and the nano-scale fraction of microcrystalline cellulose) and two of the three composites investigated used maleated PP as a coupling agent. Raman maps, based on cellulose and PP bands at 1098 and 1460 cm(-1), respectively, obtained at 1 μm spatial resolution showed that the CNCs were aggregated to various degrees in the PP matrix. Of the three composites analyzed, two showed clear existence of phase-separated regions: Raman images with strong PP and absent/weak cellulose or vice versa. For the third composite, the situation was slightly improved but a clear transition interface between the PP-abundant and CNC-abundant regions was observed, indicating that the CNC remained poorly dispersed. The spectroscopic approach to investigating spatial distribution of the composite components was helpful in evaluating CNC dispersion in the composite at the microscopic level, which helped explain the relatively modest reinforcement of PP by the CNCs.     

Analysis of Polycyclic Aromatic Compounds Using Microbore Columns

The gas chromatographic analysis of polycyclic aromatic compounds can be completed faster and with increased chromatographic resolution using microbore columns (Fast GC). Microbore columns contain two to three times the number of theoretical plates per meter when compared to 0.25 mm internal diameter (i.d.) capillary columns. The increased chromatographic resolving power of microbore columns enables separations to be carried out with much shorter columns giving rise to faster analysis times. Analysis times of priority polycyclic aromatic hydrocarbons on 20 m (5% phenyl, 0.1 mm i.d., 0.1 w m film thickness) and 10 m (5% phenyl, 0.1 mm i.d., 0.1 w m film thickness) columns are reduced by about 45% and 60% respectively in comparison with 30 m columns, and data quality (precision and accuracy) is not affected. All areas/parameters of the chromatographic system must be adjusted and optimized to ensure proper chromatographic performance. Smaller injection volumes (0.2-0.5 w L) and injection liners (1-2 mm i.d.) are required to obtain optimum (and reproducible) chromatography on 0.1 mm i.d. columns.     

Buckling initiation and displacement dependence in compression of vertically aligned carbon nanotube arrays

Carbon nanotube (CNT) arrays have shown the remarkable ability to react as foam-like structures and exhibit localized buckling coordinated within specific regions. Here, we report on the low-cycle compression of bulk vertically aligned CNT arrays to observe initiation and growth of the buckling as a function of compressive strain. A critical strain is found above which the buckling region length increased and below which it remained at or below the applied strain. As previously observed, the buckling region of the CNT array propagates from the surface where growth occurred, which, in the test specimen, is a free surface and later receives compressive contact by a polished silicon substrate. The results are corroborated with nanoindentation on the surfaces, which indicate a stiffening of the near surface with increasing applied strain. Observation and results of the buckling region nature are important for applications of nanotube arrays as energy absorbing cushions, tunable dampers, thermal contacts, or in sliding contact.     

Fertigung und Montage des Messeturms in Rostock

The making of a tensegrity tower. This contribution describes the making of a tensegrity tower, which is based on a triangular pattern that is rotated by 30° at each segment (twist element). The realization is based on the highest possible production accuracy, especially for the cables, and a consistent concept for tolerance compensation. A major subject is the pre‐stressing of the cables that turned out to be possible by moving the three base points of each segment inwards simultaneously by means of a horizontal frame with three jacks, each with a capacity of 100 tons. The tower was pre‐assembled from the twist elements in two parts. The upper part was finally lifted on top of the lower part by means of a 170 t mobile crane.