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Local distribution of orientation relationship between austenite and martensite is quantitatively examined using lath martensite in an ultra-low-carbon steel. Orientation relationship is systematically deviated between near Greninger–Troiano and Nishiyama–Wasserman orientation relationships around variant boundaries of the smallest misorientation pair, which is observed as the most frequent variant pair in the steel. Misorientation between this variant pair is decreased at some boundaries of the pair. Formation mechanism of the pair is discussed using the observed boundary characters. Image, graphical abstract [ABSTRACT FROM AUTHOR]

Abstract: This study investigated the substructures of lenticular martensites with different martensite start temperatures (Ms) by transmission electron microscopy. Observation of Fe–33Ni revealed a substructural change from fine transformation twins in the midrib and twinned region to several sets of screw dislocations in the untwinned region during growth. Tangled and curved dislocations also appeared near the martensite–austenite interface of the untwinned region, as the martensite inherited the dislocations in the surrounding austenite. In contrast, curved and tangled dislocations appeared in the entire untwinned region in Fe–31Ni and in the whole martensite plate in Fe–20.5Ni–35Co, as the higher Ms temperatures facilitated the plastic deformation of the surrounding austenite. Thermally transformed thin plate martensite in Fe–31Ni–10Co–3Ti grew into a lenticular shape accompanied by a substructure with dislocations after deformation at temperatures above the Ms temperature. The change in the substructure of lenticular martensite presumably resulted from the local temperature rise in the martensite plate. [Copyright &y& Elsevier]

Abstract: The morphology and crystallography of lath martensite in two Mn-containing interstitial free steels and a maraging steel were examined in detail by a combination of transmission electron microscopy, electron backscatter diffraction in a scanning electron microscope and optical microscopy. Indirect determination of the orientation relationship between the lath martensite and the austenite was made by analysis of misorientation distributions, and a similar orientation relationship was found for the three alloys in accordance with previous observations in low-carbon steels. Furthermore, the formation of six variants in a given packet and the preferential arrangement into blocks of low-misorientation variant pairs demonstrate a universality of morphology and crystallography of lath martensite. The presence of six variants in a packet can be accounted for by the minimization of the total shape strain introduced during the transformation. The lath boundaries developed within the volume of a certain variant show alternating misorientations and a mixed tilt and twist character characterizing these structures as low-energy dislocation structures. [Copyright &y& Elsevier]

Abstract: The orientation relationship of lenticular martensite (M) with respect to austenite (A) is nearly Greninger–Troiano at the midrib and twinned region but gradually deviates towards Kurdjumov–Sachs near the M/A interface. This change is related to the change in the substructure of martensite and also to the deformation in the surrounding austenite. [Copyright &y& Elsevier]

The morphology and crystallography of lath martensite in Fe-C alloys containing various carbon contents from 0.0026 to 0.61% were studied by analyzing electron back scattered diffraction patterns in scanning electron microscopy and Kikuchi diffraction patterns in transmission electron microscopy. As carbon content increases, the sizes of both packet and block decrease. In low carbon steels (0.0026–0.38%C), a block which is observed as having different contrasts under optical microscopy contains two groups (sub-blocks) of laths which are of two K-S variants with a misorientation of about 10 degrees. On the other hand, in the high carbon alloy (0.61%C), a block consists of laths of a single K-S variant. [Copyright &y& Elsevier]

Abstract: The upper bainite structures were investigated in Fe–9Ni–(0.15–0.5)C (mass%) alloys transformed at temperatures between 723 and 623K. A bainite packet similar to lath martensite is formed and is partitioned into blocks containing lath-shaped bainitic ferrite with the same parallel close-packed plane relationship of the K–S relationship. Its feature is categorized into three types: (A) a packet contains laths of two K–S variants with a small misorientation (sub-blocks), (B) a packet is divided by blocks largely misoriented and each block contains sub-blocks and (C) a packet is divided by blocks containing a single variant of laths. A packet of type (A) is formed at 723K in each alloy whereas the packet type becomes (B) or (C) at lower temperatures. As a result, bainite blocks are refined with decreases in transformation temperature and carbon content. In contrast, blocks and packets of lath martensite are refined with increasing carbon content. [Copyright &y& Elsevier]

Abstract: The corrosion behavior of 28Cr–7Ni–O–0.34N duplex stainless steels in air-saturated 3.5-wt% NaCl solution at pH 2, 7, 10 and 27 °C was studied by the potentiodynamic method. Two types of microstructures were investigated: the as-forged duplex and microduplex (average austenite grain size 5–16 μm) structures. The austenite volume fractions of the tested steels were between 0.35 and 0.64. The nitrogen effect on corrosion behaviors of both duplex and microduplex stainless steels were the same. At pH 2, the corrosion potential increased when the nitrogen content increased, however, corrosion current density as well as corrosion rate decreased. At pH 7 and 10, the effect of nitrogen on corrosion potential and corrosion rate could not be observed. Corrosion potential at pH 10 was lower than at pH 7. Pitting potential increased when the nitrogen content in the tested steels increased at all tested pH. For the nitrogen effect on the passive current density, it seemed that only at pH 2, the average passive current densities reduced when the nitrogen content increased. Nitrogen may have participated in the passive film or has been involved in the reaction to build up passive film. The ammonium formation and nitrogen enrichment at the interface metal/passive film with adsorption mechanism were discussed. The dissolute nitrogen might have combined with the hydrogen ions in solution to form ammonium ions, resulting in increasing solution pH. The steel could then easily repassivate, hence the corrosion potential and pitting potential would increase. However, the ammonium formation mechanism could not explain the decrease of corrosion potential in basic solution. Nitrogen enrichment at the metal/passive film interface with adsorption mechanism seemed to be an applicable consideration in increasing pitting potential. However, this mechanism did not involve the ammonium ion formation. In general, for the duplex and microduplex stainless steels tested, nitrogen increased the general corrosion resistances in acid solution and pitting corrosion resistance at all solution pH. Metallographic observation in both tested duplex and microduplex steels after pitting corrosion at all tested pH revealed that, the corroded structure in the tested steels without nitrogen alloying was austenite, but those with nitrogen alloying was ferrite. Even though ferrite had a higher chromium content than austenite but higher dissolved nitrogen in austenite than in ferrite may have increased the pitting resistance equivalent number (PRE) of austenite to be higher than that of ferrite. [Copyright &y& Elsevier]