Issue |
ESOMAT 2009
2009
|
|
---|---|---|
Article Number | 06025 | |
Number of page(s) | 6 | |
Section | Applied Research and Applications: Testing and Modelling | |
DOI | https://doi.org/10.1051/esomat/200906025 | |
Published online | 01 September 2009 |
DOI: 10.1051/esomat/200906025
Textural Evolution by Multiple Steps of Marforming in Ti-Rich Ni-Ti Shape Memory Alloy
A. S. Paula1, 2, K. K. Mahesh1, 2, 3 and F. M. Braz Fernandes1, 2, 31 CSN – GGDP/GPD, Rod. BR 393, km 5001 – Lúcio Meira, s/n – Vila Santa Cecília – Volta Redonda – RJ – Brazil – CEP 27260-390
2 UNIFoa – Centro Universitário de Volta Redonda, Campus Três Poços – Av. Paulo Erlei Alves Abrantes, 1325, Três Poços – Volta Redonda – RJ – Brazil – CEP 27240-560
3 CENIMAT – I3N, Campus da FCT/UNL, 2829-516 Monte de Caparica, Portugal
fbf@fct.unl.pt
Published online: 1 September 2009
Abstract
The Nickel-Titanium (Ni-Ti) alloys are the most attractive amongst shape memory alloys (SMA) due to their good functionality properties coupled with high strength and good ductility. The transformation temperatures in Ti-rich NiTi SMA can be altered with suitable thermal and/or mechanical treatments to obtain martensitic transformation in one or more steps above 0°C. The goal of the present work is to investigate the textural evolution in Ti-Rich Ni-Ti SMA (Ni-51at%Ti) that will contribute to different phase transformation sequences (one, two and multiple steps) after being subjected to (i) two distinct thermal treatments (500 °C for 30 minutes in air and 800°C for 300 minutes in vacuum), (ii) followed by multiple steps of marforming (30% thickness reduction by cold rolling), intercalated with thermal treatment at 500°C for 30 minutes in air and (iii) four distinct final thermal treatments (400, 450, 500 or 600°C for 30 minutes in air). The textural results were obtained by X-Ray Diffraction (XRD) at room temperature (B19’ phase) and at 150ºC (B2 phase). Differential Scanning Calorimetry (DSC), Electrical Resistivity (ER) and X-Ray Diffraction (XRD) were used to identify the transformation temperatures and the phases that are present after all steps of thermomechanical treatments.
© Owned by the authors, published by EDP Sciences 2009