Filtern
Dokumenttyp
Schlagworte
- Hydrogen (8)
- Numerical simulation (3)
- hydrogen assisted cracking (3)
- Carrier gas hot extraction (2)
- Diffusion (2)
- Duplex stainless steel (2)
- Hydrogen assisted cracking (2)
- Hydrogen diffusion (2)
- Microstructure (2)
- Numerical Simulation (2)
Organisationseinheit der BAM
Industry faces a growing demand for high-strength structural steels with yield strengths of up to 1,300 MPa in order to cope with increasingly higher strength requirements in engineering. Higher strength levels are achieved by a special coordinated production process and an adapted chemical composition. Nevertheless, disastrous damage cases with high-strength steels have occurred in the past. The sensitivity to mechanical property degradation by hydrogen increases dramatically with strength. This phenomenon leads to hydrogen-assisted cold cracking. T-joints with fillet welds made from one side with an included angle of 60° were examined for their cold cracking behavior. Based on the T-joint, a modified heat input, even interpass temperature, plate thickness, and length ones were examined. The diffusion behavior and the effectiveness of different post-weld heat treatments in joints were simulated. The results of post-weld heat treatments are illustrated in practical hydrogen removal heat treatment diagrams. It is noticed that the T-joint is subject to a very high risk of hydrogen-assisted cold cracking (HACC). Contrary to other joints, its most critical area for cracking is not the weld metal but the heat-affected zone surrounding area of the root pass. The simulation shows that HACC in the T-joint can only be avoided by applying a sufficient post-weld heat treatment.
Carrier gas hot extraction (CGHE) is a commonly applied technique for determination of hydrogen in weld joints using a thermal conductivity detector (TCD) for hydrogen measurement. The CGHE is based on the accelerated hydrogen effusion due to thermal activation at elevated temperatures. The ISO 3690 standard suggests different specimen geometries as well as necessary minimum extraction time vs. temperature. They have the biggest influence on precise hydrogen determination. The present study summarizes the results and experience of numerous test runs with different specimen temperatures, geometries (ISO 3690 type B and small cylindrical samples), and factors that additionally influence hydrogen determination. They are namely specimen surface (polished/as-welded), limited TCD sensitivity vs. specimen volume, temperature measurement vs. effects of PI-furnace controller, as well as errors due to insufficient data assessment. Summarized, the temperature is the driving force of the CGHE. Two different methods are suggested to increase the heating rate up to the desired extraction temperature without changing the experimental equipment. Suggestions are made to improve the reliability of hydrogen determination depended on the hydrogen signal stability during extraction accompanied by Evaluation of the recorded data. Generally, independent temperature measurement with dummy specimens is useful for further data analysis, especially if this data is used for calculation of trapping kinetics by thermal desorption analysis (TDA).
Welded components of P91 9% Cr steel demand for careful welding fabrication with necessary post weld heat treatment (PWHT). Before the PWHT, a hydrogen removal heat treatment is necessary for avoidance of hydrogen assisted cracking (HAC). In this context, the microstructure and temperature-dependent hydrogen diffusion is important, and reliable diffusion coefficients of P91 weld metal are rare. For that reason, the diffusion behavior of P91 multi-layer weld metal was investigated for as-welded (AW) and PWHT condition by electrochemical permeation experiments at room temperature and carrier gas hot extraction (CGHE) from 100 to 400 °C. Hydrogen diffusion coefficients were calculated, and the corresponding hydrogen
concentration was measured. It was ascertained that both heat treatment conditions show significant differences. At room
temperature the AW condition showed significant hydrogen trapping expressed by to seven times lower diffusion coefficients. A preferred diffusion direction was found in perpendicular direction expressed by high permeability. The CGHE experiments
revealed lower diffusion coefficients for the AW condition up to 400 °C. In this context, a hydrogen concentration of approximately 21 ml/100 g was still trapped at 100 °C. For that reason, a certain HAC susceptibility of as-welded P91 weld metal cannot
be excluded, and hydrogen removal should be done before PWHT.
Literature provides a wide range of hydrogen diffusion coefficients for low alloyed steels used in power plants. In fact, experimental boundary conditions and calculation methods have influence on the determination of these coefficients. The diffusion and trapping behavior in creep-resistant steel 7CrMoVTiB10-10 has been studied. Based on experimental carrier gas hot extraction (CGHE) data, a numerical model has been developed to describe the hydrogen transport and respective hydrogen distribution at elevated temperatures. The numerical results suggest that common calculation methods for diffusion coefficients are limited for experimental data analysis. The sample preparation time before CGHE experiment influences the determined diffusion coefficients with the consequence that non-homogeneous hydrogen concentration profiles have to be considered in the simulations.
Modeling of Hydrogen-Assisted Cracking (HAC) in Duplex Stainless Steels (DSS):
- Hydrogen causes significant degradation in DSS and consequently HAC
- Mechanisms of HAC have not been fully understood in two-phase microstructures
- Mesoscale numerical modeling for HAC in DSS was created, coupled to the macroscale, enabling simulation of HAC in both phases independent from predefined crack paths
In the field of modelling hydrogen assisted cracking (HAC) phenomenon, hydrogen diffusivity is an important input parameter for numerical simulation. In terms of hydrogen diffusion coefficients, they have great impact on realistic assessment of the evolution of possible crack critical hydrogen concentrations. In addition, the chemical compositions of steels can have a strong effect on hydrogen diffusion. Unfortunately, literature provides a wide range of available hydrogen diffusion coefficients even for similar microstructures and equal temperatures. The scattering of the data can lead to significant deviations in the results of simulating the evolving hydrogen concentrations due to hydrogen uptake (by fabrication or service). Thus, the application of such data to crack-models or for component life tie predictions can be realized up to the present only by considering envelope curves of such value, corresponding to a work or bench case scenario, respectively. For improved reliability of numerical simulaitons, it is necessary to minimize the mentioned deviation of these data. Hence, this work focuses on the validation of hydrogen diffusion coefficients obtained from permeation experiments at room temperature. Two baintic steels with different alloying concepts were investigated, the creep-resistant 7CrMoVTiB10-10 and the reactor pressure vessel grade 20MnMoNi4-5. A numerical model is presented for simulation of the corresponding hydrogen diffusion during permeation experiments using the finite element software ANSYS. Three different diffusion coefficients (obtained from different common calculation methods) are considered and compared to numerical results. The vases of thes calculation methods are permeation transients which are a direct measure for hydrogen. The results of the simulated hydrogen diffusion coefficients show that only one procedure for calculation of diffusion coefficitnes is suitable in comparision to the experimental values. Thus, it is suggested to use this method for analysis of experimental results in case of hydrogen diffusion during permeation experiments. Furthermore, this work supplies validated values for the hydrogen diffusion coefficients of both steel grades.
Quite a number of models for hydrogen distribution in steels and welds have been developed in the past 20 years. They reach from simple analytical models to more complex two and three dimensional finite element simulations. So far, these models have been used to simulate hydrogen distribution in homogeneous microstructure. This paper contributes to numerical simulation of hydrogen distribution in heterogeneous microstructure, e. g. in a duplex stainless steel microstructure consisting of two phase fractions. Under appropriate conditions, such as cathodic protection, it is possible that hydrogen is absorbed leading to material embrittlement and possibly initiating hydrogen assisted cracking. In order to avoid hydrogen assisted cracking in duplex stainless steels, it is of great interest to know more about the diffusion behavior of the ferrite and austenite phase. A numerical model has been developed that operates on the mesoscale and enables simulation of hydrogen transport in the various phases of a metallic material. As a first application of this model, hydrogen distribution in a duplex stainless steel 1.4462, consisting of approximately equal portions of ferrite and austenite, was simulated using the finite element program package ANSYS. The results reflect the dependency of hydrogen distribution on the microstructural alignment of the ferrite and austenite phase fractions. Crack-critical areas can thus be identified, provided the critical strain-hydrogen combination is known for the respective microstructural phase.
Duplex stainless steels (DSS) are used in various industrial applications, e.g. in offshore construction as well as in chemical industry. But, at specific conditions, as for instance arc welding fabrication, cathodic protection or exposure to sour service environments, such materials can take up hydrogen which may cause significant property degradation particularly in terms of ductility losses which, in turn, may entail hydrogen assisted cracking (HAC). If HAC occurs in a duplex stainless steel the cracking mechanism is different from steels having only one phase, because hydrogen diffusion, stress-strain distribution and crack propagation are totally different in the austenite or ferrite phase. Whereas, the mechanism of hydrogen assisted crack initiation and propagation as well as hydrogen trapping in DSS have not been fully understood up to the present, as in most two-phase microstructures. In order to better understand the mechanisms of hydrogen assisted cracking in duplex stainless steels, knowledge of the diffusion behavior and of the stress-strain distribution in the ferritic and austenitic phase is of great interest. A numerical mesoscale model was created with a view to studying the hydrogen transport and the stresses and strains in each phase of duplex stainless steel. The material investigated in this work was DSS 1.4462, consisting of approximately equal portions of ferrite and austenite. Hydrogen diffusion in the duplex base metal was studied using the finite element program ANSYS. Stress-strain distribution as well as hydrogen assisted cracking in the ferritic and austenitic phase fractions were additionally investigated. The results of numerical simulation of the hydrogen diffusion process as well as structural analyses enable the identification of crack critical areas in the DSS microstructure. Numerical simulations qualitatively reflect the crack initiation and propagation process in ferrite. Crack critical combinations of hydrogen concentrations and local mechanical loads initiating HAC can be identified.