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In situ three-dimensional (3-D) X-ray diffraction experiments have been performed at a synchrotron source on low-alloyed multiphase TRIP steels containing 0.25 wt.% Si and 0.44 wt.% Al and produced with different bainitic holding times, in order to assess the influence of the bainitic transformation on the thermal stability of individual austenite grains with respect to their martensitic transformation. A detailed characterization of the austenite grain volume distribution at room temperature was performed as a function of the prior bainitic holding time. In addition, the martensitic transformation behaviour of individual metastable grains was studied in situ during cooling to a temperature of 100 K. Both the carbon content and the grain volume play a key role in the stability of the austenite grains below 15 lm 3 , while the carbon content exerts the dominant effect in the stability of the bigger grains. Measurements also suggest that the tetragonality of the thermally formed martensite is suppressed.

The stability of the retained austenite has been studied in situ in low-alloyed transformation-induced-plasticity (TRIP) steels using high-energy X-ray diffraction during tensile tests at variable temperatures down to 153 K. A detailed powder diffraction analysis has been performed to probe the austenite-to-martensite transformation by characterizing the evolution of the phase fraction, load partitioning and texture of the constituent phases simultaneously. Our results show that at lower temperatures the mechanically induced austenite transformation is significantly enhanced and extends over a wider deformation range, resulting in a higher elongation at fracture. Low carbon content grains transform first, leading to an initial increase in average carbon concentration of the remaining austenite. Later the carbon content saturates while the austenite still continues to transform. In the elastic regime the probed {h k l} planes develop different strains reflecting the elastic anisotropy of the constituent phases. The observed texture evolution indicates that the austenite grains oriented with the {2 0 0} plane along the loading direction are transformed preferentially as they show the highest resolved shear stress. For increasing degrees of plastic deformation the combined preferential transformation and grain rotation results in the standard deformation texture for austenite with the {1 1 1} component along the loading direction. The mechanical stability of retained austenite in TRIP steel is found to be a complex interplay between carbon concentration in the austenite, grain orientation, load partitioning and temperature.

We have performed in situ synchrotron X-ray diffraction experiments to assess the influence of aluminium and phosphorus on the austenite stability in low-alloyed transformation-induced plasticity steels during the high-temperature bainitic holding and the subsequent martensitic transformation during cooling to temperatures between room temperature and 100 K. Although the addition of aluminium increases the chemical driving force for the formation of bainitic ferrite plates significantly, the phosphorus exerts a larger influence on the bainitic transformation kinetics. Consequently, the addition of phosphorus leads to a higher degree of carbon enrichment and a narrower grain volume distribution of the metastable austenite. The stability of the individual austenite grains with respect to their martensitic transformation depends on both the local carbon content and the grain volume for austenite grains smaller than 20 lm 3 . The presence of aluminium and phosphorus further stabilizes the austenite grains.

The mechanically-induced transformation behaviour of the metastable austenite phase in a high-strength industrial TRIP-assisted Dual Phase steel was monitored in situ using high-energy synchrotron diffraction under uniaxial loading. This allowed direct quantification of the impact of the transformation of the metastable austenite phase (16 vol %), embedded in a ferrite-bainite-martensite matrix, on the work hardening behaviour of this steel. Our results show that the mechanically induced transformation of austenite does not begin until the onset of matrix yielding. We provide experimental evidence which demonstrates for the first time that the austenite transformation increases the work-hardening contribution, σw thereby supporting a driving force approach to transformation induced plasticity. The transformation work required leads to an increase in the macroscopic work-hardening rate after matrix yielding and continues to offset the decrease in the work-hardening rate in the ferrite and martensite phases up to the UTS. Further we show conclusively that martensite yielding does not occur until the completion of the mechanically induced transformation of austenite. Plastic deformation of martensite is immediately followed by local plastic instability leading to necking and ultimate failure of this material

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We have studied the micromechanical behaviour of two low-alloyed multiphase TRIP steels with different aluminium contents by performing in situ high-energy X-ray diffraction experiments at a synchrotron source under increasing tensile stress levels. A detailed analysis of the two-dimensional diffraction data has allowed us to unravel the interplay between the martensite formation, the texture evolution and the load partitioning, and to correlate the observed behaviour to the macroscopic response of the material. The high aluminium content TRIP steel grade presents a higher volume fraction of retained austenite at room temperature that transforms more gradually into martensite under deformation, providing a larger uniform elongation. The comparison between the observed transformation behaviour and the texture evolution indicates that the 1 0 0 component along the loading direction corresponds to a low critical stress for the transformation. The evolution of the elastic strains revealed the occurrence of a significant load partitioning before reaching the macroscopic yield strength, which becomes more pronounced in the plastic regime due to the progressive yielding of the different grains in the polycrystalline material. This opens the door to tailor the austenite stability by altering the distribution in grain size, local carbon content, and grain orientation in order to produce the optimal load partitioning and work hardening for improved combinations of strength and formability in low-alloyed TRIP steels.