MATERIALS TRANSACTIONS
Online ISSN : 1347-5320
Print ISSN : 1345-9678
ISSN-L : 1345-9678
Effect of Boron Concentration on Martensitic Transformation Temperatures, Stress for Inducing Martensite and Slip Stress of Ti-24 mol%Nb-3 mol%Al Superelastic Alloy
Yosuke HoriuchiTomonari InamuraHee Young KimKenji WakashimaShuichi MiyazakiHideki Hosoda
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2007 Volume 48 Issue 3 Pages 407-413

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Abstract

Effects of boron (B) addition on martensitic transformation temperature, stress for inducing martensite and slip stress of a Ti-24 mol%Nb-3 mol%Al (TiNbAl) superelastic alloy were investigated in a composition range from 0 to 0.10 mass%B. It was found that a second phase is formed by the B addition being higher than 0.05 mass%B. This second phase was estimated to be TiB. The averaged grain size of TiNbAl was decreased by the B addition being higher than 0.05 mass%B. This decrease must be explained by the suppression of grain growth by the second phase. The second phase plays a role of pining sites of grain boundary movement during the solution treatment. The martensitic transformation temperatures (Ms) measured by differential scanning calorimetry were decreased by the B addition. Superelastic behavior was evaluated by a cyclic loading-unloading tensile test at room temperature with a constant strain increment of 1%, and it was found that superelasticity appeared regardless of the amount of B addition. It was also found that stress for inducing martensitic transformation (σSIM) increased with increasing B concentration up to 0.05 mass%B. This increase of σSIM by the B addition can be explained by the lowering of Ms by the B addition. The critical stress for slip (σSLIP) increased with increasing the B concentration being up to 0.05 mass%B. The increase of σSLIP by B addition was evaluated to be 3 GPa/mass%B, and it was significantly higher than that of σSIM (500 MPa/mass%B) when the B concentration was less than 0.05 mass%B. These results indicate that B addition is effective to reduce the permanent unrecoverable strain introduced during deformation.

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© 2007 The Japan Institute of Metals and Materials
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