Microstructure of selective laser melted nickel-titanium

被引:204
作者
Bormann, Therese [1 ,2 ]
Mueller, Bert [1 ]
Schinhammer, Michael [3 ]
Kessler, Anja [2 ]
Thalmann, Peter [1 ]
de Wild, Michael [2 ]
机构
[1] Univ Basel, Univ Basel Hosp, Biomat Sci Ctr, CH-4031 Basel, Switzerland
[2] Univ Appl Sci & Arts Northwestern Switzerland, Sch Life Sci, Inst Med & Analyt Technol, CH-4132 Muttenz, Switzerland
[3] ETH, Dept Mat, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Shape memory alloy; NiTi; Selective laser melting; Differential scanning calorimetry; Electron backscatter diffraction; Anisotropic grain; GROWTH MECHANISMS; POROUS NITI; TEXTURE; SIZE; BIOCOMPATIBILITY; MANUFACTURE; TI-6AL-4V; TI;
D O I
10.1016/j.matchar.2014.05.017
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
In selective laser melting, the layer-wise local melting of metallic powder by means of a scanning focused laser beam leads to anisotropic microstructures, which reflect the pathway of the laser beam. We studied the impact of laser power, scanning speed, and laser path onto the microstructure of NiTi cylinders. Here, we varied the laser power from 56 to 100 W and the scanning speed from about 100 to 300 mm/s. In increasing the laser power, the grain width and length increased from (33 +/- 7) to (90 +/- 15) mu m and from (60 +/- 20) to (600 +/- 200) mu m, respectively. Also, the grain size distribution changed from uni- to bimodal. Ostwald-ripening of the crystallites explains the distinct bimodal size distributions. Decreasing the scanning speed did not alter the microstructure but led to increased phase transformation temperatures of up to 40 K. This was experimentally determined using differential scanning calorimetry and explained as a result of preferential nickel evaporation during the fabrication process. During selective laser melting of the NiTi shape memory alloy, the control of scanning speed allows restricted changes of the transformation temperatures, whereas controlling the laser power and scanning path enables us to tailor the microstructure, i.e. the crystallite shapes and arrangement, the extent of the preferred crystallographic orientation and the grain size distribution. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 202
页数:14
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