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In the phase reversion process, severe deformation of austenite at room temperature (typically ~60 80%) transforms face-centered cubic austenite to body centered cubic martensite.
The concept of phase reversion involving severe cold deformation of austenite at room temperature to generate strain-induced martensite, followed by annealing when martensite reverts to austenite via a diffusional mechanism, was used to obtain a "high strength, high ductility" combination in nanograined (NG) austenitic stainless steel.
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In this context, the innovative concept of phase reversion-induced NG/UFG structure enabled achieving high strength besides comparable ductility, for instance, in metastable austenitic stainless steels.
NG/UFG austenitic stainless steel was obtained by a novel controlled phase-reversion annealing of cold-deformed austenite.
Our recent electron microscopy study on biomimetic nanostructured coatings on nanograined/ultrafine-grained (NG/UFG) substrates [Mater Sci Eng C 2009;29:2417–27] indicated that electrocrystallized nanohydroxyapatite (nHA) on phase-reversion-induced NG/UFG substrates exhibited a vein-type interconnected and fibrillar structure that closely mimicked the hierarchical structure of bone.
On 6 July 2009 the first of the eight modified Chinook HC3s made its first test flight at MoD Boscombe Down as part of the flight testing and evaluation phase of the HC3 "reversion" program.
From the 3,698 participants with complete data on MetS at phases 3 and 5, diet and covariates at phase 5, and MetS reversion between phases 5 and 7, the 339 case subjects with MetS at phase 5 formed the study population for the main analysis.
Possible applications of the present treatment include intermediate phase formation in multilayers, pearlite reversion and "pearlite-like" reactions.
Specific isothermal experiments combined with simulations revealed the existence of two potential Ga diffusion paths during indirect reversion: (i) from the α′ phase to the δ phase and (ii) from a new transient β′ phase, preceding the appearance of β phase of pure Pu, to the δ phase.
The gradient program was as follows: initial: 35% B; 0 4.0 min: a gradient change to 98% A; from 4.0 10 min: kept at 98% A; from 10 14 min: reversion of the mobile phase to 35% B; 14.1 20.0 min; 35% B. The mass spectrometer was auto-equilibrated for 0.5 min. The channel electron multiplier (CEM) detector was set to 3290 eV with a deflection of 400.
True reversion is the reversal of the original nucleotide change.
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