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Eingeladener Vortrag
- nein (2)
We present a new method for the complete three-dimensional (3D) calibration of scanning probe microscopes (SPM) and other high-resolution microscopes, e.g., scanning electron microscopes (SEM) and confocal laser scanning microscopes (CLSM), by applying a 3D micrometre-sized reference structure with the shape of a cascade slope-step pyramid. The 3D reference structure was produced by focused ion beam induced metal deposition. In contrast to pitch featured calibration procedures that require separate lateral and vertical reference standards such as gratings and step height structures, the new method includes the use of landmarks, which are well established in calibration and measurement tasks on a larger scale. However, the landmarks applied to the new 3D reference structures are of sub-micrometre size, the so-called 'nanomarkers'. The nanomarker coordinates are used for a geometrical calibration of the scanning process of SPM as well as of other instrument types such as SEM and CLSM. For that purpose, a parameter estimation routine involving three scale factors and three coupling factors has been developed that allows lateral and vertical calibration in only one sampling step. With this new calibration strategy, we are able to detect deviations of SPM lateral scaling errors as well as coupling effects causing, e.g., a lateral coordinate shift depending on the measured height position of the probe.
Oxidation of a single crystal nickel-base superalloy at 950 °C - a kinetic and microstructure study
(2008)
The nickel-base single crystal alloy investigated is a widely used material for first and second row blades in stationary gas turbines. Nickel-base superalloys are especially designed to resist high temperature oxidation by process gases. To determine this high temperature behaviour oxidation testing was carried out using samples cut perpendicular to (001)-direction. Microstructures were characterized by X-ray diffraction XRD, Light Microscopy LM, Scanning Electron Microscopy SEM, and X-ray energy dispersive spectroscopy (EDS), after a series of heat treatments (950 °C, 0 h - 1000 h). Mass gain and the respective thicknesses of the different oxide layers were measured to determine oxidation kinetics. In general, the isothermal oxidation behaviour at 950 °C, as defined by weight gain, follows a parabolic law with a parabolic rate constant around 1.4 · 10-2 mg2/(cm4 · h). A short incubation time is followed by the constitution of a multi-layered oxide scale. The oxide scale consists of a three layer structure. An outer scale contains a Ti-bearing thin film associated as TiO2 and NiTiO3 but mostly Cr attributed to Cr2O3, (Ni/Co)Cr2O4 beside NiTaO4. This outer scale is connected to a discontinuous layer of inner oxidation consisting mainly of Al2O3, which is followed by an area of γ´-depletion within the base material.
The introduction of carbon capture technology into thermal power plants benefits from combustion of fuel and pure oxygen due to high partial pressures of CO2 in the flue gas. The consumption of energy for carbon capture devices and oxygen production plants has to be compensated by higher efficiencies of the power plant. Consequently IGCC plants with 80 bar reactors and high temperature turbine equipment, boilers with 700 °C steam raising units will be the next generation power plants. All plants have in common locally in the process gas compositions with high CO2 partial pressure and steam. In our test we applied a gas composition with 30% H2O and 70% CO2 an composition in between the water content of coal burned in pure oxygen and Methane-oxygen combustion. Additional gas fractions such as SO2 will be added in coming experiments. In this paper we discuss the attack of our model gas composition on different typical power plant construction steels with chromium contents in the range of 1 to 24%. The test conditions were annealing time up to 1000 h, 80 bar pressure, fast flowing gas and temperatures between 500 and 700°C depending on the maximum working temperature of the individual steel. Dependent on the test parameters and in particular the chromium content the oxide scale growth mechanism, the scale thickness, the scale microstructure and phase sequences differed. In particular we observe the growth of FeO at temperatures lower than 570°C which is the eutectic decomposition temperature in the Oxygen-iron phase diagram. Iron carbides are primarily formed in low alloyed steels near the oxide steel interface. The steels studied containing more then 9% chromium the growth of Fe3O4 and Fe-Cr-Spinel was typical. Co and W influenced the reaction in 9 - 12% Cr-steel. The attrition of Mn and other alloying additions was monitored. In no case a dense and protective Cr2O3 or an other Metal-Cr-oxide layer was observed. The oxide scale thickness increases strongly with temperature and decrease with raising chromium content. Data of oxide scale thickness up to corrosion time of 1000 h will be presented. A model will be presented, which deals with possible reactions paths during the corrosion processes in flowing CO2 and water. The steels can be arranged according the reaction with gas and their alloying elements such as Mn, Co and W. In the test environment the maximum working temperature of the steels decreased 50K compared to working temperature in current power plant environment.
Influence of pressure and chromium content on corrosion reactions at 600°C in a CO2-H2O atmosphere
(2008)
The resistance of structural steels against corrosion in CO2-H2O and CO2-H2O-O2
atmospheres at temperatures above 550°C was observed with high magnification methods.
The test atmosphere is the basic composition of an oxyfuel coal combustion atmosphere. The
analytical information base was applied to develop reaction schemes for the oxidation of
steels. It was demonstrated that the formation of phases and the kinetics of oxidation reactions
in this atmospheres is affected by the formation of intermediate iron hydroxide and a high
carbon activity. In the temperature regime above 550°C the thermal equilibrium between H2O,
CO2 and Fe reacted and formed CO. CO triggers the formation of FeO and carbides and
increases the reaction kinetics. Porosity at the interface is established by gaseous phases
such as Fe(OH)2 or H2O. H2 formation is not limited to the steel - oxide interface but can occur
in the whole oxide scale. Examples of the experimental results were compared with a
thermodynamic approach. The objective of the work was to derive qualitative rules of the basic
corrosion reactions.
The most efficient construction materials for boiler water walls and superheaters in
steam power plants are ferritic and martensitic steels. In practical operation tubes are
simultaneously exposed to combustion gas and air/steam on their opposite surfaces. The
corrosion behaviour of ferritic-martensitic steels under such dual atmospheres is nondistinctive
and has therefore been investigated in a special designed test equipment between 500 and
620°C. The power plant conditions were simulated wi th a flowing and pressurised (80 bar)
combustion gas on the inner side of the tube which mainly consists of H2O and/or CO2. On the
outer side, the tube material was exposed to air. It was discovered that under similar
temperatures the oxides formed on the air side under dual atmosphere conditions were
significantly different to the oxide scales formed when the alloy was exposed to air only. It is
assumed that the anomalous corrosion behaviour during the dual atmosphere exposure is due
to the hydrogen transport through the bulk alloy from the combustion gas side to the air side.