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The interaction of hydrogen with various tungsten-inert-gas-welded austenitic stainless steels’ (AUSS) microstructure is studied by means of desorption/absorption analysis and microstructure observations. One of the limitations of welding is created by the presence of hydrogen in the weld, which can shorten the steel’s service life. The local hydrogen concentration, trapping, and its distribution along the welded samples were studied by thermal desorption spectrometry and were supported by X-ray diffraction (XRD) and electronic microstructural observations. Hydrogen content demonstrated a dependence on the welding zone. It was found that hydrogen distribution, and accepted microstructure during welding, played a significant role in the trapping mechanism of 316L AUSS. XRD analysis revealed residual stresses which were caused due to the presence of hydrogen in c-phase. It was shown that the austenite microconstituents inside 316L can have a crucial effect in preventing hydrogen-assisted cracking phenomenon. The effects of AUSS microstructure on hydrogen absorption and desorption behavior are discussed in detail.
This paper describes austenitic-ferritic duplex stainless steels, SAF 2205, in the presence of hydrogen. The duplex stainless steels (DSS) properties include excellent resistance to stress corrosion cracking, high strength and good weldability. Those steels are preferably used in industries combining hydrogen and loads. Hydrogen location in addition to hydrogen binding energy with the steel's defects are of great importance for the analysis of hydrogen embrittlement model in that steel. It is known from previously published works that the susceptibility to hydrogen embrittlement will depend on the competition between reversible and irreversible traps; meaning a direct relation to the hydrogen's state and position in the steel. In this work, we examine the local hydrogen concentration, trapping and distribution by two modern and advanced techniques: thermal desorption spectrometry (TDS) and we support it by time of flight-secondary ion mass spectrometer (ToF-SIMS). In this paper, we support and give for the first time new insights and better understanding to the hydrogen embrittlement mechanism in SAF 2205. The trapping energies levels were calculated using TDS and Lee and Lee's model. This model revealed reversible in addition to irreversible trapping sites. Also the trapping controlling mechanism was found to be a combination of detrapping controlled mechanism and diffusion controlled mechanism. The use of ToF-SIMS for local imaging the distribution of hydrogen species supports the discussion of the different hydrogen traps in this type of steel. The hydrogen embrittlemet phenomenon in SAF 2205 will be discussed in details in that paper.
The effect of electrochemical charging of hydrogen on the structure of a lean duplex stainless steel LDX 2101® (EN 1.4162, UNS S32101) was examined by both Time-of-Flight secondary ion mass spectrometry and electron back-scatter diffraction. The goal is to correlate hydrogen concentration and induced structural changes. Chemical and structural characterizations were done for the same region at the sample's surface with sub-micron spatial resolution. Regions of interest were varying in size between 50 × 50 μm and 100 × 100 μm. The results show a phase transformation of austenite to mainly a defect-rich BCC and scarcely a HCP phase. The phase transformation occurred in deuterium rich regions in the austenite.
In the present work, the influence of deuterium on the microstructure of a duplex stainless steel type EN 1.4462 has been characterized by Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) supported by scanning electron microscopy (SEM), focused ion beam (FIB), electron back scattered diffraction(EBSD) and energy dispersive x-ray (EDX) investigations. Characterization has been carried out before and after electrochemical charging with deuterium which has been used as a tracer, due to its similar behavior to hydrogen in the steel microstructure. In a first approach, the distribution of the deuterium occurring at temperatures above 58 °C has been visualized. Further it turned out that sub-surface micro blisters are formed in the ferrite-austenite interface, followed by the formation of needle shaped plates and subsequent cracking at the ferrite surface. In the austenite phase, parallel cracking alongside twins and hexagonal close packed (martensitic) regions has been observed. In both phases and even in the apparent interface, cracking has been associated with high deuterium concentrations, as compared to the surrounding undamaged microstructure. Sub-surface blistering in the ferrite has to be attributed to the accumulation and recombination of deuterium at the ferrite-austenite interface underneath the respective ferrite grains and after fast diffusing through this phase. Generally, the present application of chemometric imaging and structural analyses allows characterization of hydrogen assisted degradation at a sub-micron lateral resolution.
Hydrogen interaction with residual stresses in steel studied by synchrotron X-ray diffraction
(2014)
The residual stress state in a material has an important role in the mechanism of cracking, induced or assisted by hydrogen. In this contribution, the beamline EDDI in BESSY II instrument in Berlin was used in order to investigate the influence of hydrogen upon the residual stresses state existing in a Supermartensitic stainless steel sample. The method used for investigating the residual stresses is the sinus square ψ method. This method involves the usage of high energy X-ray diffraction in order to measure the residual stress state and magnitude. It was found that hydrogen presence has a significant influence upon the magnitude of the residual stresses, as its value decreases with high hydrogen content. This effect is reversible, as hydrogen desorbs from the sample the residual stress magnitude gains its initial value before hydrogen charging.
Hydrogen generally causes lattice distortions and phase transformations when introduced into a metallic crystal lattice. For the investigations reported in this contribution, hydrogen thermal desorption analysis has been carried out to observe the influence of hydrogen desorption on the lattice of super martensitic stainless steel during continuous heating. The lattice expansion parameter and the phase transformations have been monitored during the thermal desorption process, and the influence of hydrogen on such characteristics has been evaluated. It was found that hydrogen has a significant influence on both the lattice parameter and on the thermal expansion. However, hydrogen has no influence on phase transformation during thermal desorption. The hydrogen's desorption behavior in this process was also observed and it turned out that hydrogen desorbs in two stages, i.e., firstly diffusible hydrogen and trapped hydrogen afterward.
In situ analysis of hydrogen behaviour in stainless steels by high energy synchrotron radiation
(2011)
Hydrogen generally causes lattice distortions and phase transformations when introduced into a metal matrix. The present contribution provides a report of first in situ investigations of hydrogen effects on the lattice of the austenite and the martensite phase in a supermartensitic stainless steel using hard synchrotron radiation for respective energy dispersion diffraction measurements. Lattice distortions, such as the planar spacing expansion, have been monitored during the complete hydrogen effusion process over 24 h and are directly correlated to the dissolved hydrogen in the metal matrix. Among other results, it turned out that hydrogen at the introduced concentration level causes a reversible lattice expansion and after hydrogen effusion the lattice nearly regained its original dimensions. Hydrogen much more significantly affects the austenite phase with respect to lattice expansion than the martensite phase, but no phase transformations occur during the hydrogen desorption process.
Ein entscheidendes Problem neuer Wasserstofftechnologien ist die leichte und sichere Lagerung ausreichender Mengen an Wasserstoff insbesondere für Nutzung bei tragbaren oder mobilen Anwendungen. Eine neue und innovative Technologie basierend auf gebündelte Kapillaren wurde entwickelt. Diese Systeme garantieren eine sichere Speicherung, Lagerung und kontrollierte Freisetzung von Wasserstoff, obgleich Speicherdrücke bis 1200 bar angewendet werden. Die neue Technologie ermöglicht die Lagerung einer erheblich größeren Menge Wasserstoff als andere Systeme und übertraf bereits die Zielsetzung des DOE 2010. Es wird erwartet, die DOE-Zielsetzung für das Jahr 2015 bereits in naher Zukunft zu erreichen. Hauptaspekt für die Speichertechnologie ist die Druckfestigkeit der Glaskapillaren. Es ist weithin bekannt, dass besonders Quarz eine dreimal höhere Festigkeit als Stahl hat. Gleichzeitig ist die Dichte ungefähr dreimal niedriger, was bedeutet, dass viel weniger Material notwendig ist, um die gleiche Druckfestigkeit zu erreichen. Die Druckfestigkeit einzelner Kapillare ist in der Abhängigkeit der Materialien, der Abmessungen, der Wandstärke etc. ermittelt worden, um optimale Parameter für die "finalen" Kapillaren herauszufinden.