Crystallographic and lattice point correlations of a new hcp-to-fco martensitic transformation observed in the Ni-Hf system
Creators
- 1. Advanced Materials Laboratory, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)
Description
A hexagonal close-packed to face-centered orthorhombic (hcp-to-fco) martensitic transformation in the Hf lattice upon dissolving Ni atoms is observed by molecular dynamics simulations based on a proven realistic Ni-Hf potential. It is proposed that the mechanism of the phase transformation takes place through four simultaneous actions, i.e. sliding, shearing, stretching and lattice constant adjusting, with a speed in an order of 100 m/s. Based on an analytical deduction, the crystallographic and lattice point correlations between the initial hcp and final fco structures are obtained, respectively, and the deduced correlations may also be of relevance for another two phase transformations: the hexagonal close-packed to body-centered tetragonal, and hexagonal close-packed to face-centered cubic martensitic phase transformations
Additional details
Identifiers
- DOI
- 10.1016/j.actamat.2004.10.025;
- PII
- S1359-6454(04)00635-4;
Publishing Information
- Journal Title
- Acta Materialia
- Journal Volume
- 53
- Journal Issue
- 3
- Journal Page Range
- p. 743-748
- ISSN
- 1359-6454
- CODEN
- ACMAFD
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36080476
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CRYSTALLOGRAPHY; FCC LATTICES; HAFNIUM; HAFNIUM COMPOUNDS; HCP LATTICES; LATTICE PARAMETERS; MOLECULAR DYNAMICS METHOD; NICKEL; NICKEL COMPOUNDS; PHASE TRANSFORMATIONS; SIMULATION
- Descriptors DEC
- CALCULATION METHODS; CRYSTAL LATTICES; CRYSTAL STRUCTURE; CUBIC LATTICES; ELEMENTS; HEXAGONAL LATTICES; METALS; REFRACTORY METAL COMPOUNDS; REFRACTORY METALS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.