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We report about investigations of typical material problems in steels. First, residual stresses in and around weld seams with low martensite transition temperature filler material were analyzed w/ and w/o additional transverse tensile load. The investigation was accompanied by x-ray diffraction measurements to track stress-induced phase transitions. Martensite formation during welding under external load yield strain gradients near the surface that improve the integrity of the weld. Further, the residual stress distribution close to laser-treated steel surfaces was analyzed. The method could be improved to reduce analysis artifacts. Finally, hydrogen diffusion in different steels was measured using neutron radiography and subsequent image analysis. Diffusion coefficients were derived by analyzing the time-dependent mass flux. In an outlook we describe the optimal ESS instrumentation from a metallurgists point of view.
Hydrogen assisted cracking of metals limits the durability of welds and constructions. Still
the failure mechanisms are not fully understood, for instance the role of hydrogen mass
transport during crack initiation. Measuring the hydrogen concentration as a function of
time (and space) would allow to determine diffusion coefficients helping to enlighten this
lack of understanding. Therefore, neutron radiography is a valuable tool for measuring in
situ hydrogen transport in iron and steels [1].
The influence of grain boundaries on the hydrogen diffusion behaviour can be determined
by comparing the diffusion behaviour of samples with e.g. different microstructure. In a
first study we investigated in situ the simplest case, the hydrogen effusion out of pure iron
(ARMCO) using neutron radiography at ANTARES [2]. Samples were charged electrochemically
ex situ with a well defined amount of hydrogen, stored in liquid nitrogen and were then
heat treated during a neutron radiography measurement whilst the change of neutron transmission
was recorded. For analysis the gray values in the pictures were transformed into
concentrations with help of an ex post calibration. Therefore, the experimental temperaturetime
profile of the heat treatment has been repeated with identical samples in the home lab
and the amount of effusing hydrogen was measured by carrier gas hot extraction. In a first
approximation the concentration of hydrogen in the sample can be calculated by subtracting
the hydrogen concentration in the atmosphere from the initial one in the sample. We
were able to measure hydrogen concentrations as low as 65 wt.ppm.
Simultaneously monitoring of hydrogenous
sample and hydrogen-free reference allowed
for in situ measurement of hydrogen effusion.
Sample heating was done by infrared radiation.
Diffusion coefficients for hydrogen effusion
from iron have been calculated. They coincide
fairly with literature data.
We report about diffusion measurements and molecular dynamic simulations
in Al-Ni and Al-Cu melts. Capillary methods were used to measure Ni and
Cu self diffusion and to measure interdiffusion. The combination of the
capillary set-up with X-ray radiography allowed in-situ detecting of
convective contributions to the interdiffusion transport by tracking the
time dependence of diffusion. Thus, the determination of the
interdiffusion coefficient can
be restricted to convection-free experiment times resulting in an
increased accuracy of the measured interdiffusion coefficient.
Additionally, quasielastic neutron scattering was used to measure
convection-free Ni and Cu self diffusion. Molecular dynamics simulations
were used to determine all diffusion coefficients and the thermodynamic
factor. The comparison between experiment and simulation shows an
excellent agreement of the interdiffusion coefficients as a function of
temperature. It was found that interdiffusion is enhanced by
thermodynamic forces with a maximum around the stoichiometric composition.
Die dehnungsinduzierte Martensitbildung wurde mittels Röntgen-Diffraktion und -Radiographie mit dem EDDI-Instrument am BESSY II in supermartensitischem Stahl mit Anlassaustenit untersucht. Die Bildung wird durch Wasserstoff im Gefüge unterdrückt. Die Duktilität von wasserstofffreiem SMSS korreliert mit dem Anteil an dehnungs-induziertem Martensit
Duplexstähle besitzen ein zweiphasiges Gefüge und werden aufgrund ihrer verbesserten Schweißeignung gegenüber den Vollausteniten häufig im Anlagen- bzw. Apparatebau eingesetzt. Aufgrund der hohen Abkühlgeschwindigkeit und dem Abbrand von Legierungselementen kommt es zu einer Ferritisierung des Schweißguts und damit zu einer Degradation der mechanischen Eigenschaften. Zur Vorhersage des Phasenverhältnisses im Schweißgut wird das WRC1992-Diagramm genutzt. Dieses Diagramm zeigt einige Ungenauigkeiten und benötigt zur genaueren Vorhersage der Phasenverhältnisse eine Überarbeitung. Um den Einfluss einzelner Elemente auf das Schweißnahtmikrogefüge besser zu verstehen, wurden drahtförmige Schweißzusatzwerkstoffe mit dem Ferrit-Bildner Nb und dem Austenit-Bildner Cu beschichtet und für Schweißungen verwendet. Die Messmethode der Laser-induzierten Plasmaspektroskopie (LIBS) bietet hier eine gute Möglichkeit der in situ Überwachung der chemischen Konzentrationen, während des WIG-Schweißens von Duplexstählen. Die LIBS-Messergebnisse, konnten mit der Ferritnummer und der Schweißnahtmikrostruktur korreliert werden.